List of Publications
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2002 (Impact factor: 1.83) |
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Paper Details ( Author , title) |
Journal Details (Title, volume, issue, page.no, year, publisher, country) |
Journal Quality (Impact factor, SNIP, SJR etc.) |
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1 |
B. D. Chandler, M. Parvez, V. U. Ahmad, J. Hussain, H. Hussain, M. Zubair. Triethylammonium (3-carboxyacrylato)-dichlorodimethyltin |
Acta Crystallographica Section E:, Volume E58, pp m281-m283, 2002; Wiley-Blackwell, USA |
IF = 0.34 SJR = 0.22 SNIP: 0.18 |
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2 |
A.R. Ramirez, M. Parvez, V. U. Ahmad, J. Hussain, H. Hussain. Polymeric di-n-butyl(glutarato)tin |
Acta Crystallographica Section E:, Volume E58, pp m278-m280, 2002; Wiley-Blackwell, USA |
IF = 0.34 SJR = 0.22 SNIP: 0.18 |
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3 |
V. U. Ahmad,; H. Hussain, J. Hussain, A. R. Jassbi, I. A. Bukhari, A. Yasin, M. I. Choudhary, A. Dar. New Bioactive Diterpenoids from Euphorbia decipiens |
Zeitschrift für Naturforschung-B, Volume 57B, pp 1066-1971, 2002; Walter de Gruyter, USA |
IF = 0.76 SJR = 0.24 SNIP: 0.39 |
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4 |
V. U. Ahmad, H. Hussain, J. Hussain, A. R. Jassbi, I. A. Bukhari, A. Yasin, M. I. Choudhary. Three New Diterpenoids from Euphorbia decipiens |
Polish Journal of Chemistry, Volume 76, 1699-1706, 2002; Polish Chemical Society, Poland |
IF = 0.39 SJR = X.XX SNIP = X.XX |
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2003 (Impact factor: 7.92) |
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5 |
V. U. Ahmad, H. Hussain, J. Hussain, A. R. Jassbi, I. A. Bukhari, A. Yasin, M. I. Choudhary. Three New Bioactive Diterpene Polyesters from Euphorbia decipiens |
Journal of Natural Products, Volume 66, pp, 1221-1224, 2003; American Chemical Society, USA. |
IF = 3.79 SJR = 1.19 SNIP: 1.73 |
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6 |
V. U. Ahmad, M. A. Abbasi, H. Hussain, M. N. Akhtar, U. Farooq, N. Fatima, M. I. Choudhary. Phenolic glycosides from Symplocos racemosa: natural inhibitors of phosphodiesterase I |
Phytochemistry, Volume 63, 217-220, 2003; Elsevier, USA |
IF = 2.54 SJR = 0.99 SNIP: 1.47 |
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7 |
V. U. Ahmad, H. Hussain, J. Hussain, F. Ullah. Chemical Constituents from Arisaema flavum |
Proceedings of the Pakistan Academy of Sciencies, Volume 40, pp 85-90, 2003; Pakistan Academy of Sciences, Pakistan |
IF = 0.00 SJR = 0.00
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8 |
V. U. Ahmad, J. Hussain, H. Hussain, M. I. Lodhi, A. Yasin, M. I. Choudhary. First Natural Urease Inhibitor from Euphorbia decipiens |
Chemical Pharmaceutical Bulletins, Volume 51, pp 719-723, 2003; The Pharmaceutical Society of Japan, Japan |
IF = 1.59 SJR = 0.43 SNIP: 0.82 |
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2004 (Impact factor: 1.10) |
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9 |
V. U. Ahmad, J. Hussain, H. Hussain, E. Akber, S. A. Nawaz, M. I. Choudhary. Bioactive Ceramides from Tanacetum artemisioides |
Zeitschrift für Naturforschung-B, Volume 59B, pp 329-333, 2004; Walter de Gruyter, USA |
IF = 0.76 SJR = 0.24 SNIP: 0.39 |
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10 |
M. Parvez, V. U. Ahmad, J. Hussain, H. Hussain, U. Farooq. 3,7,17-Tri-O-acetyl-5-O-butanoyl-13,15-dihydroxy-myrsinol |
Acta Crystallographica Section E:, Volume E60, pp 148-150, 2004; Wiley-Blackwell, USA |
IF = 0.34 SJR = 0.22 SNIP: 0.18 |
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2005 (Impact factor: 9.43) |
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11 |
V. U. Ahmad, H. Hussain, J. Hussain, A. R. Jassbi, I. A. Bukhari, A. Dar. Analgesic compound from Euphorbia decipiens |
Fitoterapia, Volume 76, pp. 230-232, 2005; Elsevier, USA |
IF = 2.34 SJR = 0.81 SNIP: 1.49 |
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12 |
V. U. Ahmad, J. Hussain, H. Hussain, M. A. Lodhi, M. I. Choudhary. Two new diterpene polyesters from Euphorbia decipiens |
Natural Product Research, Volume 19, pp 267-275, 2005; Taylor & Francis, UK |
IF = 0.91 SJR = 0.37 SNIP = 0.71 |
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13 |
J. Hussain, V. U. Ahmad, H. Hussain, Z. Hassan, A. Khan, U. Farooq. One new ceramides from Tanacetum artemisioides |
Polish Journal of Chemistry, Volume 76, 1699-1706, 2002; Polish Chemical Society, Poland |
IF = 0.39 SJR = X.XX SNIP = X.XX |
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14 |
S. T. A. Shah, K. M. Khan, H. Hussain, S. Hayat, W. Voelter. Cesium fluoride-Celite: a Solid base for efficient synthesis of aromatic esters and ethers |
Tetrahedron, Volume 61, pp. 6652-6656, 2005; Elsevier, USA |
IF = 2.64 SJR = 0.87 SNIP: 0.88 |
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15 |
S. T. A. Shah, K. M. Khan, H. Hussain, M. U. Anwer, W. Voelter. CsF-Celite, an Efficient Solid State Reagent for the Syntheses of Thioesters and Thioethers |
Monatshefte für Chemie/Chemical Monthly, Volume 136, pp. 1583-1589, 2005; Springer Vienna, Austria |
IF = 1.22 SJR = 0.33 SNIP = 0.57 |
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16 |
K.O. Kenneth, K. Krohn, H. Hussain, G. N. Folefoc, A. E. Nkengfack, B. Schulz, Q. Hu. Newbouldiaquinone and newbouldiamide: A new naphthoquinone-anthraquinone coupled pigment and a new ceramide from Newbouldia laevis |
Chemical Pharmaceutical Bulletins, Volume 53, pp 616-619, 2005; The Pharmaceutical Society of Japan, Japan |
IF = 1.59 SJR = 0.43 SNIP: 0.82 |
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17 |
P. Wafo, H. Hussain, S. F. Kouam, B. T. Ngagjui, Ü. Flörke, K. Krohn 2-Hydroxy-4,4,5,6-tetramethoxychalcone |
Acta Crystallographica Section E:, Volume E61, pp 03017-3019, 2005; Wiley-Blackwell, USA |
IF = 0.34 SJR = 0.22 SNIP: 0.18 |
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2006 (Impact factor: 5.31) |
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18 |
B. Meffo, K. Krohn, H. Hussain, E. Dongo, B. Schulz, Q. Hu. Tithoniamarin and tithoniamide: A new isocoumarin dimer and a new ceramide from Tithnonia diversifolia |
Natural Product Research, Volume 20, pp 842-849, 2006; Taylor & Francis, UK |
IF = 0.91 SJR = 0.37 SNIP = 0.71 |
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19 |
K. O. Eyong, G. N. Folefoc, V. Kuete, V. P. Beng, K. Krohn, H. Hussain, A. E. Nkengfack, M. Saeftel, S. R. Sarite, A. Hoerauf. Newbouldiaquinone B: a new naphthoquinone-anthraquinone ether coupled pigment, a potential antimicrobial and antimalarial agent from Newbouldia laevis |
Phytochemistry, Volume 67, pp. 605-609, 2006; Elsevier, USA |
IF = 2.54 SJR = 0.99 SNIP: 1.47 |
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20 |
B. Meffo, K. Krohn, H. Hussain, E. Dongo, B. Schulz, Q. Hu. Tithoniaquinone A and tithoniamide B: A new anthraquinone and a new ceramide from the leaves of Tithnonia diversifolia |
Zeitschrift für Naturforschung-B, Volume 61B, pp 78-82, 2006; Walter de Gruyter, USA |
IF = 0.76 SJR = 0.24 SNIP: 0.39 |
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21 |
U. Flörke, K. Krohn, Z. Ullah, H. Hussain. An orthorhombicmodification of (R)-(-)-8-hydroxy-3-methyl-3,4- dihydro-1H-2-benzopyran-1-one [(R)-(-)-mellein] |
Acta Crystallographica Section E:, Volume E62, pp 03539-3541, 2006; Wiley-Blackwell, USA |
IF = 0.34 SJR = 0.22 SNIP: 0.18 |
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22 |
S. M. Renadin, K. Krohn, H. Hussain, E. Dongo. Paullinoside A and auallinomide A: A new cerebroside and a new ceramide from leaves of Pullinia pinnata |
Zeitschrift für Naturforschung-B, Volume 61B, pp 1123-1127, 2006; Walter de Gruyter, USA |
IF = 0.76 SJR = 0.24 SNIP: 0.39 |
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2007 (Impact factor: 21.50) |
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23 |
H. Hussain, K. Krohn, U. Floerke, B. Schulz, S. Draeger, G. Pescitelli, S. Antus, T. Kurtan. Absolute configuration of globosuxanthone A and secondary metabolites from Microdiplodia sp. |
European Journal of Organic Chemistry, pp. 292-295, 2007; WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim, Germany |
IF = 3.06 SJR = 1.05 SNIP: 0.74 |
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24 |
M. F. Tala, K. Krohn, H. Hussain, S. F. Kouam, H. K. Wabo, P. Tane, B. Schulz, Q. Hu. Laurentixanthone C: A new antifungal and algicidal xanthone from stem bark of Vismia laurentii |
Zeitschrift für Naturforschung-B, Volume 62B, pp 565-568, 2007; Walter de Gruyter, USA |
IF = 0.76 SJR = 0.24 SNIP: 0.39 |
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25 |
A. M. Aguinaldo, A. P. G. Macabeo, K. Krohn, H. Hussain. Regulation of Capsaicin synthase in Capsicum annuum L by Penicillium resedanum LK6 during drought conditions. |
Biochemical Systematics and Ecology, Volume 35, 45-47 , 2007; Elsevier Netherland |
IF = 0.96 SJR = 0.34 SNIP: 0.78 |
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26 |
K. Krohn, Z. Ullah, H. Hussain, U. Floerke, B. Schulz, S. Draeger, G. Pescitelli, P. Salvadori, S. Antus, T. Kurtan. Massarilactones E-G, new metabolites from the endophytic fungus Coniothyrium sp., associated with the plant Artimisia maritime |
Chirality, Volume 19, 464-470, 2007; Wiley, USA |
IF = 1.88 SJR = 0.51 SNIP: 0.67 |
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27 |
H. Hussain, K. Krohn, U. Floerke, B. Schulz, S. Draeger, G. Pescitelli, S. Antus, T. Kurtan. Absolute configuration of hypothemycin and new 5'-O-methylhypothemycin from Phoma sp.- A novel solid state CD/TDDFT approach to 14 membered conformationally flexible system. |
Tetrahedron Asymmetry, Volume 18, 925-930, 2007; Elsevier Netherland |
IF = 2.15 SJR = 0.66 SNIP: 0.69 |
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28 |
V. Kuete, K. O. Eyong, G. N. Folefoc, V. P. Beng, H. Hussain, K. Krohn, A. E. Nkengfac. Antimicrobial activity of the methanolic extract and of the chemical constituents isolated from Newbouldia laevis |
Pharmazie/International Journal of Pharmaceutical Sciences, Volume 62, pp. 552-556, 2007; Ingentaconnect, UK |
IF = 1.00 SJR = 0.39 SNIP: 0.48 |
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29 |
T. Dagobert, K. Krohn, H. Hussain, E. Dongo. Laportoside A and laportomide A: A new cerebroside and a new ceramide from leaves of Laportea ovalifolia |
Zeitschrift für Naturforschung-B, Volume 62B, pp 1208-1212, 2007; Walter de Gruyter, USA |
IF = 0.76 SJR = 0.24 SNIP: 0.39 |
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30 |
H. Hussain*, K. Krohn, B. Schulz, S. Draeger. Bioactive constituents of two endophytic fungi. |
Biochemical Systematics and Ecology, Volume 35, 898-900, 2007; Elsevier Netherland |
IF = 0.96 SJR = 0.34 SNIP: 0.78 |
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31 |
F. Ullah, H. Hussain, J. Hussain, I. A. Bukhari, M. T. H. Khan, M. I. Choudhary, V.U. Ahmad. Tyrosinase inhibitory pentacyclic triterpenes and analgesic and spasmolytic activities of methanolic extracts of Rhododendron collettianum. |
Phytotherapy Research, Volume 21, pp. 1076-1081, 2007; John Wiley & Sons, USA |
IF = 2.66 SJR = 0.82 SNIP: 1.18 |
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32 |
H. Hussain, K. Krohn, B. Schulz, S. Draeger. Exochromone: Structurally unique chromone dimer with antifungal and algicidal agent from Exophiala sp. |
Heterocycles, Volume 74, pp. 331–337, 2007; Elsevier, UK |
IF = 1.07 SJR = 0.37 SNIP: 0.40 |
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33 |
H. K. Wabo, S. F. Kouam, K. Krohn, H. Hussain, M. F. Tala, P. Tane, T. Ree, Q. Hu, B. Schulz. Antimicrobial prenylated anthraquinones and other constituents from the seeds of Vismia laurentii De Wild. |
Chemical Pharmaceutical Bulletins, Volume 55, pp 1640-1642, 2007; The Pharmaceutical Society of Japan, Japan |
IF = 1.59 SJR = 0.43 SNIP: 0.82 |
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34 |
H. Hussain*, K. Krohn, V.U. Ahmad, G. A. Miana. Lapachol: An overview |
ARKIVOC, 145-171, 2007; ARKAT, Inc., USA |
IF = 1.25 SJR = 0.23 SNIP: 0.37 |
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35 |
H. Hussain*, V. U. Ahmad, I. R. Green, K. Krohn, J. Hussain, A. Badshah. Antibacterial organotin(IV) compounds, their synthesis and spectral characterization |
ARKIVOC, 289-299, 2007; ARKAT, Inc., USA |
IF = 1.25 SJR = 0.23 SNIP: 0.37 |
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36 |
Z. Hassan, H. Hussain, V. U. Ahmad S. Anjum, M. I. Choudhary, G. Pescitelli, T. Kurtán, K. Krohn. Absolute configuration of 1β,10β-epoxydesacetoxymatricarin isolated from Carthamus oxycantha by means of TDDFT CD calculations |
Tetrahedron Asymmetry, Volume 18, 2905-2909, 2007; Elsevier Netherland |
IF = 2.15 SJR = 0.66 SNIP: 0.69 |
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2008 (Impact factor: 14.57) |
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37 |
M. D. Awouafack, S. F. Kouam, H. Hussain, D. Ngamga, P. Tane, B. Schulz, I. R. Green, K. Krohn. Antimicrobial prenylated dihydro chalcones from Eriosema glomerata |
Planta Medica, Volume 74, pp. 50–54, 2008; Thieme Medical Publishers, Germany |
IF = 2.15 SJR = 0.68 SNIP: 1.07 |
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38 |
V. Bertin, H. Hussain, S. F. Kouam, E. Dongo, G. Pescitelli, P. Salvadori, T. Kurtán, K. Krohn. Antialactone: A new γ-lactone from Antiaris africana and its absolute configuration by means of TDDFT CD calculations |
Natural Product Communications, Volume 3, 215-218, 2008; Natural Product Communications Inc., USA |
IF = 1.24 SJR = 0.34 SNIP: 0.59 |
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39 |
M. Ng’ang’a, S. Chhabra, C. L. Thoruwa, H. Hussain, K. Krohn. Chemical constituents from the leaves of Drypetes gerrardii
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Biochemical Systematics and Ecology, Volume 36, 320-322, 2008; Elsevier Netherland |
IF = 0.96 SJR = 0.34 SNIP: 0.78 |
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40 |
H. Hussain*, V. U. Ahmad, S. Anwar, G. A. Miana. Chemical constituents of Scutellaria linearis |
Biochemical Systematics and Ecology, Volume 36, 490-492, 2008; Elsevier Netherland |
IF = 0.96 SJR = 0.34 SNIP: 0.78 |
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41 |
J. Hussain, F. Ullah, H. Hussain, S. T. Hussain, M. R. Shah. Nepetolide: One new diterpene from Nepeta suavis |
Zeitschrift für Naturforschung-B, Volume 63B, pp 591-594, 2008; Walter de Gruyter, USA |
IF = 0.76 SJR = 0.24 SNIP: 0.39 |
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42 |
Ahmad, V.U.; Ullah, F.; H. Hussain* Colletinin A and 2,2´´-diepicolletinin A: two new bisflavan-3-ols from Rhododendron collettianum |
Natural Product Communications, Volume 3, 765-768, 2008; Natural Product Communications Inc., USA |
IF = 1.24 SJR = 0.34 SNIP: 0.59 |
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43 |
B. Vouffo, K. Krohn, S. F. Kouam, H. Hussain, E. Dongo. Dinklagenonoate: A new isobauerane-type triterpenoid and other minor constituents from the twigs of Dorstenia dinklagei |
Biochemical Systematics and Ecology, Volume 36, 655-658, 2008; Elsevier Netherland |
IF = 0.96 SJR = 0.34 SNIP: 0.78 |
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44 |
A.P. G. Macabeo, M. C. G. Villafranca, A. M. Aguinaldo, H. Hussain, K. Krohn. Clerosterols from Clerodendrum quadriloculare |
Biochemical Systematics and Ecology, Volume 36, 659-660, 2008; Elsevier Netherland |
IF = 0.96 SJR = 0.34 SNIP: 0.78 |
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45 |
B. Schulz, S. Draeger, T. Edison, J. Rheinheimer, K. Siems, S. Loesgen, J. Bitzer, O. Schloerke, A. Zeek, I. Kock, H. Hussain, J. Dai, K. Krohn. Intelligent screening of marine habitat for novel, biologically active, fungal secondary metabolites |
Botanica Marina, Volume 51, pp. 219-234, 2008; Walter de Gruyter, USA |
IF = 1.40 SJR = 0.55 SNIP: 0.81 |
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46 |
V. Bertin, H. Hussain, K. O. Eyong, E. Dongo, G. N. Folefoc, A. E. Nkengfack, K. Krohn. Chemical constituents of Dorstenia picta and Newbouldia laevis |
Biochemical Systematics and Ecology, Volume 36, 730-732, 2008; Elsevier Netherland |
IF = 0.96 SJR = 0.34 SNIP: 0.78 |
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47 |
A. M. Lannang, G. N. Louh, D. Lontsi, S. Specht, S. R. Sarite, U. Floerke, H. Hussain, A. Hoerauf, K. Krohn |
Journal of Antibiotics, Volume 61, pp. 518-523, 2008; Nature Publishing Group, UK. |
IF = 1.73 SJR = 0.57 SNIP: 0.79 |
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48 |
K. Krohn, G. Carlson, H. Köhle, H. Hussain, I. R. Green. Synthesis of daunosamyl anthraquinone and anthracyclinone analogues |
ARKIVOC, 216-233, 2008; ARKAT, Inc., USA |
IF = 1.25 SJR = 0.23 SNIP: 0.37 |
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2009 (Impact factor: 22.37) |
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49 |
V. U. Ahmad, J. Hussain, H. Hussain. Bioactive chemical constituents from Ranunculus laetus Ranunculus laetusglomerata |
Chemistry of Natural Compounds, Volume 45, pp. 720-721, 2009; Springer, Germany |
IF = 0.50 SJR = 0.30 SNIP: 0.55 |
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50 |
K. Krohn, S. F. Kouam, G. M. Kuigoua, H. Hussain, S. Cludius-Brand, U. Flörke, T. Kurtán, G. Pescitelli, L. Di Bari, S. Draeger, B. Schulz. Xanthones and new oxepino[2,3-b]chromones from three endophytic Fungi |
Chemistry-A European Journal, Volume 15, pp. 12121-12132, 2009; WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim, Germany |
IF = 5.73 SJR = 2.23 SNIP: 1.18 |
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51 |
M. Ismail, M. Ibrar, Z. Iqbal, J. Hussain, H. Hussain*, M. Ahmed, A. Ijaz, M. I. Choudhary. Chemical constituents and antioxidant activity of Geranium wallichianum |
Records of Natural Products, Volume 3, pp. 193-197, 2009; ACG Publications, Turkey |
IF = 1.20 SJR = 0.52 SNIP: 0.94 |
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52 |
F. Gallier, H. Hussain, A. Martel, A. Kirschning, G. Dujardin. Hetero-Diels- Alder reactions of cyclic ketone derived enamide. A new and efficient concept for the asymmetric robinson annulation |
Organic Letters, Volume 11, pp. 3060-3063, 2009; American Chemical Society, USA |
IF = 6.36 SJR = 2.63 SNIP: 1.29 |
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53 |
S. F. Asghar, S. Aziz, H. U. Rehman, I. Ahmed, H. Hussain, A. U. Rahman, M. I. Choudhary. Secondary metabolites isolated from Iris germanica |
Records of Natural Products, Volume 3, pp. 139-152, 2009; ACG Publications, Turkey |
IF = 1.20 SJR = 0.52 SNIP: 0.94 |
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54 |
E. Dongo, H. Hussain*, Miemenang, R.; B. Schulz, K. Krohn. Bioactive chemical constituents of Klainedoxa gabonensis and Paullinia pinnata |
Records of Natural Products, Volume 3, pp. 165-169, 2009; ACG Publications, Turkey |
IF = 1.20 SJR = 0.52 SNIP: 0.94 |
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55 |
H. Hussain*, S. Aziz, V. U. Ahmad, S. Anwar, G. A. Miana, I. Ahmed. Chemical constituents of Verbascum thapsus |
Biochemical Systematics and Ecology, Volume 37, 124-126, 2009; Elsevier Netherland |
IF = 0.96 SJR = 0.34 SNIP: 0.78 |
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56 |
H. Hussain, N. Akhtar, B. Schulz, S. Draeger, G. Pescitelli, S. Antus, T. Kurtan, K. Krohn. New bioactive 2,3-epoxycyclohexenes and isocoumarins from the endophytic fungus Phomopsis sp. from Laurus azorica |
European Journal of Organic Chemistry, pp. 749-756, 2009; WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim, Germany |
IF = 3.06 SJR = 1.05 SNIP: 0.74 |
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57 |
H. Hussain*, K. Krohn, S. Draeger, K. Meier, B. Schulz. Bioactive chemical constituents of a sterile endophytic fungus from Meliotus dentatus |
Records of Natural Products, Volume 3, pp. 114-117, 2009; ACG Publications, Turkey |
IF = 1.20 SJR = 0.52 SNIP: 0.94 |
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58 |
M. Ng’ang’a, H. Hussain, S. Chhabra, C. L. Thoruwa, K. Krohn. Chemical constituents from the root bark of Ozoroa insignis |
Biochemical Systematics and Ecology, Volume 37, 116-119, 2009; Elsevier Netherland |
IF = 0.96 SJR = 0.34 SNIP: 0.78 |
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2010 (Impact factor: 27.68) |
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59 |
M. Saleem, M. Nazir, M. S. Ali, H. Hussain, Y. S. Lee, N. Riaz, A. Jabbar. Antimicrobial natural products; an update on the future antibiotic drug candidates |
Natural Product Reports, Volume 27, 238-254, 2010; Elsevier Netherland |
IF = 10.10 SJR = 2.97 SNIP: 3.58 |
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60 |
S. Qin, H. Hussain, B. Schulz, S. Draeger, K. Krohn. Two new metabolites, epoxydine A and B, from Phoma sp. |
Helvetica Chimica Acta, Volume 93, 169-174, 2010; John Wiley & Sons, Germany |
IF = 1.47 SJR = 0.42 SNIP: 0.61 |
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61 |
J. D. Wansi, H. Hussain*, S. F. Kouam, S. Specht, S. R. Sarite, A. Hoerauf, K. Krohn. Antiplasmodial activities of furoquinoline alkaloids from Teclea afzelii Engl. |
Phytotherapy Research, Volume 24, pp. 775-777, 2007; John Wiley & Sons, USA |
IF = 2.66 SJR = 0.82 SNIP: 1.18 |
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62 |
S. Aziz, H. U. Rehman, M. Irshad, S. F. Asghar, H. Hussain, I. Ahmed. Phytotoxic and antifungal activities of essential oil of Thymus serpyllum grown in the state of Jammu & Kashmir. |
Journal Essential Oil Bearing Plants, Volume 13, pp. 224-229, 2010; Taylor & Francis, UK |
IF = 0.306 SJR = ??? SNIP: ??? |
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63 |
V. B. Tsassi, H. Hussain*, S. F. Kouam, B. Y. Meffo, E. Dongo, B. Schulz, I. R. Green, K. Krohn. Antimicrobial coumarins from the stem bark of Afraegle paniculata |
Natural Product Communications, Volume 5, 559-561, 2010; Natural Product Communications Inc., USA |
IF = 1.24 SJR = 0.34 SNIP: 0.59 |
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64 |
J. Hussain, R. Ullah, F. U. Khan, Z. Muhammad, N. U. Rehman, H. Hussain. Antiglycation and antimicrobial activities of Phlomis bracteosa |
American-Eurasian Journal of Agricultural & Environmental Sciences, Volume 7, pp. 634-636, 2010 |
IF = 0.00 SJR = 0.00 SNIP: 0.00 |
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65 |
A.Kakam, H. Hussain*, E. Dongo, S. F. Kouam, B. Schulz, K. Krohn. Cameroonemide A: A new ceramide from Helichrysum cameroonense |
Journal of Asian Natural Products Research, Volume 12, 629-633, 2010; Taylor & Francis, UK |
IF = 0.91 SJR = 0.38 SNIP: 0.72 |
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66 |
J. Hussain, N. Bukhari, H. Hussain, S. Haider, Z. Hassan. Phlomisamide and phlomisteriod: A new ceramide and a new stigmasterol derivative from Phlomis cashmeriana |
Helvetica Chimica Acta, Volume 93, 169-174, 2010; John Wiley & Sons, Germany |
IF = 1.47 SJR = 0.42 SNIP: 0.61 |
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67 |
J. Dai, H. Hussain, S. Dräger, B. Schulz, T. Kurtán, G. Pescitelli, U. Flörke, K. Krohn. Metabolites from the fungus Phoma sp. 7210, associated with Aizoon canariense |
Natural Product Communications, Volume 5, 1175-1180, 2010; Natural Product Communications Inc., USA |
IF = 1.24 SJR = 0.34 SNIP: 0.59 |
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68 |
J. Hussain, N. Bukhar, N. Bano, H. Hussain*, A. Naeem, I. R. Green. Flavonoids and terpenoids from Phlomis cashmeriana and their Chemotaxonomic significance |
Records of Natural Products, Volume 4, pp. 242-249, 2010; ACG Publications, Turkey |
IF = 1.20 SJR = 0.52 SNIP: 0.94 |
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69 |
S. F. Kouam, Y. Njonkou, G. M. Kuigoua, B. T. Ngadjui, H. Hussain, I. R. Green, B. Schulz, K. Krohn. Psorantin, a unique methylene linked dimer of vismin and kenganthranol E, two anthranoid derivatives from the seeds of Psorospermum aurantiacum (Hypericaceae) |
Phytochemistry Letters, Volume 3, pp. 185-189, 2010; Elsevier, UK |
IF = 1.45 SJR = 0.54 SNIP: 1.01 |
|||||||
70 |
J. Hussain, N. U. Rahman, H. Hussain* Chemical constituents from Nepeta clarkei |
Biochemical Systematics and Ecology, Volume 38, 823-826, 2010; Elsevier Netherland |
IF = 0.96 SJR = 0.34 SNIP: 0.78 |
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71 |
A.P. G. Macabeo, F. A. Tudla, G. J. D. Alejandro, S. F. Kouam, H. Hussain, K. Krohn. Benzoylated derivatives from Uvaria rufa |
Biochemical Systematics and Ecology, Volume 38, 857-860, 2010; Elsevier Netherland |
IF = 0.96 SJR = 0.34 SNIP: 0.78 |
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72 |
J. Hussain, N. Bukhari, H. Hussain*, N. U. Rehman, S. M. Hussain. Chemical constituents from Nepeta distans |
Natural Product Communications, Volume 5, 1785-1786, 2010; Natural Product Communications Inc., USA |
IF = 1.24 SJR = 0.34 SNIP: 0.59 |
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73 |
E. Dongoa, H. Hussain*, S. F. Kouam, K. Krohn. Pycnangloside: A new cerebroside from Pycnanthus angolensis |
Natural Product Communications, Volume 5, 1795-1798, 2010; Natural Product Communications Inc., USA |
IF = 1.24 SJR = 0.34 SNIP: 0.59 |
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74 |
A.T. Nyongha, H. Hussain*, E. Dongo, I. Ahmed, K. Krohn. Hyloglyceride and hylodiglyceride: Two new glyceride derivatives from Hylodendron gabunensis |
Natural Product Communications, Volume 5, 1939-1940, 2010; Natural Product Communications Inc., USA |
IF = 1.24 SJR = 0.34 SNIP: 0.59 |
|||||||
2011 (Impact factor: 53.89) |
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75 |
E. Dongo, H. Hussain*, I. Ahmed, K. Krohn. Ozocardic A: one new alkylanacardic acid from Ozoroa pulcherrima |
Journal of Asian Natural Products Research, Volume 13, 84-87, 2011; Taylor & Francis, UK |
IF = 0.91 SJR = 0.38 SNIP: 0.72 |
|||||||
76 |
M. Saleem, H. Hussain, I. Ahmed, S. Draeger, B. Schulz, K. Krohn. Viburspiran: A new member of new class octadride of anhydide family |
European Journal of Organic Chemistry, pp. 808-812, 2011; WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim, Germany |
IF = 3.06 SJR = 1.05 SNIP: 0.74 |
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77 |
H. Hussain*, A. Badawy, A. Elshazly, A. Elsayed, M. Riaz, K. Krohn, B. Schulz. Chemical constituents and antimicrobial activity of Salix subserrata |
Records of Natural Products, Volume 5, pp. 133-137, 2011; ACG Publications, Turkey |
IF = 1.20 SJR = 0.52 SNIP: 0.94 |
|||||||
78 |
L. Meng, P. Sun, H. Tang, L. Li, S. Draeger, B. Schulz, K. Krohn, H. Hussain, W. Zhanga, Y. Yi. Entophytic fungus Penicillium chrysogenum, a new source of hypocrellins |
Biochemical Systematics and Ecology, Volume 39, 163-165, 2011; Elsevier Netherland |
IF = 0.96 SJR = 0.34 SNIP: 0.78 |
|||||||
79 |
I.Siddiqui, A. Zahoor, H. Hussain, I. Ahmed, B. Schulz, K. Krohn. Diversonol and blennolide derivatives from the endophytic fungus Microdiplodia sp. Absolute configuration of diversonol. |
Journal of Natural Products, Volume 74, pp, 365-373, 2011; American Chemical Society, USA. |
IF = 3.79 SJR = 1.19 SNIP: 1.73 |
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80 |
T. B. Valeriea, H. Hussain*, G. Albertine, E. Dongo, I. Ahmed, M. Riaz, K. Krohn. Citropremide and citropridone: A new ceramide and a new acridone alkaloid from Stem Bark of Citropsis gabunensis |
Helvetica Chimica Acta, Volume 94, 1035-1040, 2011; John Wiley & Sons, Germany |
IF = 1.47 SJR = 0.42 SNIP: 0.61 |
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81 |
I.Ahmed, H. Hussain, B. Schulz, S. Draeger, D. Padula, G. Pescitelli, K. Krohn Three new antimicrobial metabolites from the endophytic fungus, Phomopsis sp. |
European Journal of Organic Chemistry, pp. 2867-2873, 2011; WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim, Germany |
IF = 3.06 SJR = 1.05 SNIP: 0.74 |
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82 |
H. Hussain*, B. Vouffo, E. Dongo, K. Krohn. Dorstenpictanone: A new bicyclic polyprenylated from Dorstenia picta |
Journal of Asian Natural Products Research, Volume 13, 547-550, 2011; Taylor & Francis, UK |
IF = 0.91 SJR = 0.38 SNIP: 0.72 |
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83 |
H. Hussain*, J. Hussain, M. Saleem, G. A. Miana, M. Riaz, K. Krohn, S. Anwar. Cichorin A: A new phenolic compounds from Cichorium intybus |
Journal of Asian Natural Products Research, Volume 13, 566-569, 2011; Taylor & Francis, UK |
IF = 0.91 SJR = 0.38 SNIP: 0.72 |
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84 |
Zamarrud, I. Ali, H. Hussain*, V. U. Ahmad, M. Qaiser, F. V. Mohammad. Two new antioxidant bergenin derivatives from the stem of Rivea hypocrateriformis |
Fitoterapia, Volume 82, pp. 722-725, 2011; Elsevier, USA |
IF = 2.34 SJR = 0.81 SNIP: 1.49 |
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85 |
K. Z. Antoine, H. Hussain*, E. Dongo, B. Schulz, K. Krohn. Cameroonenoside A: A new algicidal cinnamic acid glycoside ester from Helichrysum cameroonense |
Records of Natural Products, Volume 5, pp. 305-308, 2011; ACG Publications, Turkey |
IF = 1.20 SJR = 0.52 SNIP: 0.94 |
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86 |
H. Hussain*, S. Aziz, B. Schulz, K. Krohn. Synthesis of a 4H-anthra[1,2-b]pyran derivative and its antimicrobial activity |
Natural Product Communications, Volume 6, 841-843, 2011; Natural Product Communications Inc., USA |
IF = 1.24 SJR = 0.34 SNIP: 0.59 |
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87 |
F.U. Khan, J. Hussain, I. U. Khan, R. Ullah, I. Ali, Z. Muhammad, H. Hussain, M. R. Shah. Nepetasuavol: A new dammarane triterpenediol from Nepeta suavis |
Chemistry of Natural Compounds, Volume 47, pp. 234-236, 2011; Springer, Germany |
IF = 0.50 SJR = 0.30 SNIP: 0.55 |
|||||||
88 |
H. Hussain*, K. Krohn, M. Saeftel, S. R. Sarite, A. Hoerauf. A new class of phenazines with activity against a Chloroquine resistant Plasmodium falciparum strain and antimicrobial activity |
Journal of Medicinal Chemistry, Volume 47, pp. 234-236, 2011; Springer, Germany |
IF = 5.44 SJR = 1.96 SNIP: 1.61 |
|||||||
89 |
S. Lu, S. Draeger, B. Schulz, K. Krohn, I. Ahmed, H. Hussain, Y. Yi, L. Li, W. Zhang. Bioactive aromatic derivatives from endophytic fungus, Cytospora sp. |
Natural Product Communications, Volume 6, 661-666, 2011; Natural Product Communications Inc., USA |
IF = 1.24 SJR = 0.34 SNIP: 0.59 |
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90 |
M. M. Ng’ang’a, H. Hussain*, S. Chhabra, C. Langat-Thoruwa, M. Riaz, K. Krohn. Drypetdimer A: A New Flavone Dimer from Drypetes gerrardii |
Natural Product Communications, Volume 6, 1115-1116, 2011; Natural Product Communications Inc., USA |
IF = 1.24 SJR = 0.34 SNIP: 0.59 |
|||||||
91 |
T. D. Christelle, H. Hussain*, E. Dongo, O. E. Julius, J. Hussain. Cordioxime: A new dioxime γ-lactam from Cordia platythyrsa |
Natural Product Communications, Volume 6, 1135-1136, 2011; Natural Product Communications Inc., USA |
IF = 1.24 SJR = 0.34 SNIP: 0.59 |
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92 |
T. D. Christelle, H. Hussain*, E. Dongo, J. M. B. Hermine, I. Ahmed, K. Krohn. Two new alkylanacardic acids, ozorcardic A and B, from Ozoroa pulcherrima |
Natural Product Communications, Volume 6, 1133-1134, 2011; Natural Product Communications Inc., USA |
IF = 1.24 SJR = 0.34 SNIP: 0.59 |
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93 |
H. Hussain, I. Ahmed, B. Schulz, S. Draeger, U. Floerke, G. Pescitelli, K. Krohn. Solid-state circular dichroism and hydrogen bonding absolute configuration of Massarigenin A from Microsphaeropsis sp |
Chirality, Volume 23, 617-623, 2011; Wiley, USA |
IF = 1.88 SJR = 0.51 SNIP: 0.67 |
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94 |
M. Saleem, H. Hussain, I. Ahmed, T. Van Ree, K. Krohn. Platensimycin and its relatives: A recent story in the struggle to develop new naturally derived antibiotics |
Natural Product Reports, Volume 28, 1534-1579, 2011; Elsevier Netherland |
IF = 10.10 SJR = 2.97 SNIP: 3.58 |
|||||||
95 |
S. Qin, K. Krohn, H. Hussain, B. Schulz, S. Draeger. Pestalotheols E-H: antimicrobial metabolites from endophytic fungus Ascocarpe sp. |
European Journal of Organic Chemistry, pp. 5163-5166, 2011; WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim, Germany |
IF = 3.06 SJR = 1.05 SNIP: 0.74 |
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96 |
K. Krohn, U. Farooq, H. Hussain, I. Ahmed, J. Rheinheimer, S. Draeger, B. Schulz, T. Van Ree. Phomosines H–J, Novel Highly Substituted Biraryl Ethers, Isolated from the Endophytic Fungus Phomopsis sp. from Ligustrum vulgare |
Natural Product Communications, Volume 6, 1907-1912, 2011; Natural Product Communications Inc., USA |
IF = 1.24 SJR = 0.34 SNIP: 0.59 |
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97 |
J. Hussain, N. Rehman, H. Hussain*, L. Ali, A. Al-Harassi. Nepethalates A and B: Two new phthalate derivatives from Nepeta clarkei |
Helvetica Chimica Acta, Volume 94, 2106-2110, 2011; John Wiley & Sons, Germany |
IF = 1.47 SJR = 0.42 SNIP: 0.61 |
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98 |
M. Nazir, M. Sultan, N. Riaz, M. Hafeez, H. Hussain, I. Ahmed, B. Schulz, S. Draeger, A. Jabbar, K. Krohn, M. Ashraf, M. Saleem. Depsitinuside: A new depside galactoside from an endophytic fungus isolated from Viburnum tinus |
Journal of Asian Natural Products Research, Volume 13, 1056-1060, 2011; Taylor & Francis, UK |
IF = 0.91 SJR = 0.38 SNIP: 0.72 |
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99 |
H. Hussain*, K. Krohn, M. K. Tichimeme, I. Ahmed, K. Meier, M. Steinert, S. Draeger, B. Schulz. Antimicrobial Chemical Constituents from the Endophytic Fungus from Phomopsis sp. from Notobasis syriaca |
Natural Product Communications, Volume 6, 1905-1906, 2011; Natural Product Communications Inc., USA |
IF = 1.24 SJR = 0.34 SNIP: 0.59 |
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100 |
J. Hussian, N. Rehman, A. Al-Harrasi, L. Ali, R. Ullah, F. Mabood, H. Hussain, M. Ismail. Nutritional prospects and mineral compositions of selected vegetables from Dhoda sharif–Kohat |
Journal of Medicinal Plants Research, Volume 5, pp. 6505-6514, 2011; Academic Journals, Nigeria |
IF = 0.00 SJR = 0.00 SNIP: 0.00 |
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101 |
H. Hussain*, J. Hussain, A. Al-Harrasi. Chemistry of some species of genus Lantana |
Pakistan Journal of Botany, Volume 43, pp. 51-62, 2011; Pakistan Botanical Society, Pakistan |
IF = 0.82 SJR = 0.41 SNIP: 0.95 |
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102 |
K. O. Eyong, H. Hussain, G. N. Folefoc, A. E. Nkengfack, M. Saeftel, S. R. Sarite, A. Hoerauf, K. Krohn. Synthesis of novel phenazine derivatives by solid state chemistry and preliminary screening against Plasmodium falciparum in vitro |
Rasayan Journal of Chemistry, Volume 4, pp. 713-722, 2011; |
IF = 0.40 SJR = 0.20 SNIP: 0.50 |
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103 |
J. Hussain, N. U. Rehman, A. L. Khan, H. Hussain, A. Al-Harrasi, L. Ali, F. Sami, Z. H. Shinwari. Determination of macro and micronutrients and nutritional prospects of six vegetable species of Mardan, Pakistan |
Pakistan Journal of Botany, Volume 43, pp. 2829-2833, 2011; Pakistan Botanical Society, Pakistan |
IF = 0.82 SJR = 0.41 SNIP: 0.95 |
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2012 (Impact factor: 37.27) |
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104 |
J. Hussain, N. Rehman, H. Hussain*, A. Al-Harassi, L. Ali. Two new phthalate derivatives from Nepeta clarkei |
Journal of Asian Natural Products Research, Volume 14, 22-26, 2012; Taylor & Francis, UK |
IF = 0.91 SJR = 0.38 SNIP: 0.72 |
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105 |
K. Krohn, H. Hussain, H. Egold, B. Schulz, I. Green. Chemical derivatization of phomosine A, a highly antifungal secondary metabolite from Phomopsis sp |
ARKIVOC, 71-89, 2012; ARKAT, Inc., USA |
IF = 1.25 SJR = 0.23 SNIP: 0.37 |
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106 |
H. Hussain*, J. Hussain, A. Al-Harrasi, K. Krohn. Chemistry and biology of biocoumarins |
Tetrahedron, Volume 68, pp. 2553-2578, 2012; Elsevier, UK. |
IF = 2.37 SJR = 0.72 SNIP: 0.77 |
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107 |
H. Hussain*, I. Ahmed, S. Draeger, B. Schulz, K. Krohn. Pyrenocines J-M: Four New Pyrenocines from the Endophytic Fungus, Phomopsis sp. |
Fitoterapia, Volume 83, pp. 523-526, 2012; Elsevier, USA |
IF = 2.34 SJR = 0.81 SNIP: 1.49 |
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108 |
H. Hussain, K. Krohn, I. Ahmed, S. Draeger, B. Schulz, S. Pietro, G. Pescitelli. Phomopsinones A-D: Four New Pyrenocines from an Endophytic Fungus, Phomopsis sp. |
European Journal of Organic Chemistry, pp. 1783-1789, 2012; WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim, Germany |
IF = 3.06 SJR = 1.05 SNIP: 0.74 |
|||||||
109 |
M. M. Ng’ang’a, H. Hussain*, S. Chhabra, C. Langat-Thoruwa, K. Krohn, J. Hussain, A. Al-Harrasi, I. Green. Eucleanal: One new naphthalene derivative from Euclea divinorum |
Natural Product Communications, Volume 7, 193-194, 2012; Natural Product Communications Inc., USA |
IF = 1.24 SJR = 0.34 SNIP: 0.59 |
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110 |
M.M. Ng’ang’a, H. Hussain*, S. Chhabra, C. Langat-Thoruwa, K. Krohn, A. Al-Harrasi, I. Green. Eucleanal A and B: Two new naphthalene derivatives from Euclea divinorum |
Chinese Chemical Letters, Volume 23, pp. 576-578, 2012; Elsevier, UK. |
IF = 1.58 SJR = 0.42 SNIP: 0.68 |
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111 |
H. Hussain*, J. Hussain, S. Ali, A. Al-Harrasi, M. Saleem, G. A. Miana, M. Riaz, S. Anwar, S. Hussain. Cichorins B and C: Two new benzo-isochromenes from Cichorium intybus |
Journal of Asian Natural Products Research, Volume 14, 297-300, 2012; Taylor & Francis, UK |
IF = 0.91 SJR = 0.38 SNIP: 0.72 |
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112 |
J. Hussain, N. U. Rehman, H. Hussain*, A. Al-Harassi, L. Ali, Mehjabeen, M. Ahmed, T. S. Rizvi. Analgesic, anti-inflammatory, and CNS depressant activities of new constituents of Nepeta clarkei |
Fitoterapia, Volume 83, pp. 593-598, 2012; Elsevier, USA |
IF = 2.34 SJR = 0.81 SNIP: 1.49 |
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113 |
H. Hussain*, K. Krohn, B. Schulz, S. Draeger, M. Nazir, M. Saleem. Two New Antimicrobial Metabolites from the Endophytic Fungus, Seimatosporium sp. |
Natural Product Communications, Volume 7, 293-294, 2012; Natural Product Communications Inc., USA |
IF = 1.24 SJR = 0.34 SNIP: 0.59 |
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114 |
J. Hussain, H. Hussain*, V. U. Ahmad, A. A-Harrasi, A. Badshah. Organotin(IV) Compounds of n-propyl and isopropyl Glutarate: Their synthesis, spectral characterization, and antibacterial activity |
Organic Communications, Volume 5, pp. 18-26, 2012; ACG Publication, Turkey |
IF = 0.70 SJR = 0.24 SNIP: 0.80 |
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115 |
M. Irshad, S. Aziz, H. U. Rehman, H. Hussain. GC-MS Analysis and antifungal activity of essential oils of Angelica glauca, Plectranthus rugosus, and Valeriana wallichii |
Journal Essential Oil Bearing Plants, Volume 15, pp. 15-21, 2012; Taylor & Francis, UK |
IF = 0.306 SJR = ??? SNIP: ??? |
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116 |
H. Hussain*, N. Bibi, A. Al-Harrasi, S. Siddiqi, S. U. Kazmi, Y. Zhang. Antituberculosis and cytotoxic activities of triorganotin(IV) complexes |
Chinese Chemical Letters, Volume 23, pp. 731-735, 2012; Elsevier, UK. |
IF = 1.58 SJR = 0.42 SNIP: 0.68 |
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117 |
A.Al-Harrasi, A. Al-Rawahi, J. Hussain, N. Rehman, L. Ali, H. Hussain. Proximate analysis of the resins and Leaves of Boswellia sacra |
Journal of Medicinal Plants Research, Volume 6, pp. 3098-3104, 2012; Academic Journals, Nigeria |
IF = 0.00 SJR = 0.00 SNIP: 0.00 |
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118 |
J. Hussain, Naeema, H. Hussain*, F. U. Khan, N. U. Rehman, A. Al-Harrasi. Ajuganane: A new phenolic compound from Ajuga bracteosa |
Natural Product Communications, Volume 7, 615-616, 2012; Natural Product Communications Inc., USA |
IF = 1.24 SJR = 0.34 SNIP: 0.59 |
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119 |
M.M. Ng’ang’a, H. Hussain*, S. Chhabra, C. Langat-Thoruwa, B. N. Arungu, K. Krohn, A. Al-Harrasi. Antipalsmodial activity of Drypetes gerradii |
Chemistry of Natural Compounds, Volume 48, pp. 339-340, 2012; Springer, Germany |
IF = 0.50 SJR = 0.30 SNIP: 0.55 |
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120 |
H. Hussain*, J. Hussain, H. Al-Harrasi, I. R. Green. Chemistry and biology of the genus Voacanga |
Pharmaceutical Biology, Volume 50, pp. 1183-1193, 2012; Taylor & Francis, UK |
IF = 1.24 SJR = 0.48 SNIP: 0.81 |
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121 |
A.P. G. Macabeo, J. A. Avilaa, G. J. D. Alejandro, S. G. Franzblau, S. F. Kouam, H. Hussain, K. Krohn. Villarinol, a new alkenoyloxyalkenol derivative from the endemic Philippine Rubiaceae species Villaria odorata |
Natural Product Communications, Volume 7, 779-780, 2012; Natural Product Communications Inc., USA |
IF = 1.24 SJR = 0.34 SNIP: 0.59 |
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122 |
H. Hussain*, A. Al-Harrasi, M. Saleem, I. R. Green, T. Van Ree. Chemistry and biology of the genus Vismia |
Pharmaceutical Biology, Volume 50, pp. 1448-1462, 2012; Taylor & Francis, UK |
IF = 1.24 SJR = 0.48 SNIP: 0.81 |
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123 |
A.Zahoor, H. Hussain*, A. Khan, I. Ahmed, V. U. Ahmad, K. Krohn. Chemical constituents from Erigeron bonariensis L. and their chemotaxonomic importance |
Records of Natural Products, Volume 6, pp. 376-380, 2012; ACG Publications, Turkey |
IF = 1.20 SJR = 0.52 SNIP: 0.94 |
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124 |
H. Hussain*, K. Krohn, M. Saeftel, S. R. Sarite, A. Hoerauf. Synthesis of hydroxynaphthaquinones and quinoline-5,8-diones and its antiplasmodial activity |
European Journal of Medicinal Chemistry, Volume 54, pp. 936-942, 2012; Elsevier, UK |
IF = 3.44 SJR = 1.00 SNIP: 1.61 |
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125 |
E. Nosheen, A. Shah, A. Badshah, Z. Rehman, H. Hussain, R. Qureshi, S. Ali, M. Siddiq, A. M. Khan. Electrochemical oxidation of hydantoins at glassy carbon electrode |
Electrochimica Acta, Volume 80, pp. 108-117, 2012; Elsevier, UK |
IF = 4.50 SJR = 1.28 SNIP: 1.45 |
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126 |
A.Shah, S. Munir, F. Zafar, A. Badshah, X. Wang, Z. Rehman, H. Hussain, S. Lunsford. Redox behavior of a novel derivative of vitamin K at a glassy carbon electrode |
Journal of The Electrochemical Society, Volume 159, pp. G112-G116, 2012; Electrochemical Society, USA |
IF = 2.85 SJR = 1.08 SNIP: 1.23 |
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2013 (Impact factor: 82.82) |
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127 |
S. Munir, A. Shah, A. Rauf, A. Badshah, S. K. Lunsford, Z. Rehman, H. Hussain, G. S. Khan. Redox behavior of a novel menadiol derivative at glassy carbon electrode |
Electrochimica Acta, Volume 88, pp. 858-864, 2013; Elsevier, UK |
IF = 4.50 SJR = 1.28 SNIP: 1.45 |
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128 |
A.Shah, E. Nosheen, S. Munir, A. Badshah, R. Qureshi, Z. Rehman, N. Muhammad, H. Hussain Characterization and DNA binding studies of unexplored imidazolidines by electronic absorption spectroscopy and cyclic voltammetry |
Journal of Photochemistry and Photobiology B: Biology Volume 120, pp. 90-97, 2013; Elsevier, UK |
IF = 2.96 SJR = 0.72 SNIP: 1.25 |
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129 |
H. Hussain*, A. T. Nyongha, E. Dongo, A. Badshah, I. R. Green. Melicimides A and B: Two New Ceramides from Stem Bark of Melicia excelsa |
Records of Natural Products, Volume 7, pp. 141-146, 2013; ACG Publications, Turkey |
IF = 1.20 SJR = 0.52 SNIP: 0.94 |
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130 |
P. Sun, J. Huo, T. Kurtán, A. Mándi, S. Antus, H. Tang, S. Draeger, B. Schulz, H. Hussain, K. Krohn, W. Pan, Y. Yi, W. Zhang. Structural and stereochemical studies of hydroxyanthraquinone derivatives from the endophytic Fungus Coniothyrium sp |
Chirality, Volume 25, 141-148, 2013; Wiley, USA |
IF = 1.88 SJR = 0.51 SNIP: 0.67 |
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131 |
H. Hussain*, I. R. Green, K. Krohn, I. Ahmed. Advances in the total synthesis of biologically important callipeltosides: A review |
Natural Product Reports, Volume 30, 640-693, 2013; Elsevier Netherland |
IF = 10.10 SJR = 2.97 SNIP: 3.58 |
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132 |
H. Hussain*, I. R. Green, I. Ahmed. Journey describing applications of Oxone in Synthetic Chemistry |
Chemical Reviews, Volume 113, pp. 3329−3371, 2013; American Chemical Society, USA |
IF = 46.56 SJR = 16.31 SNIP: 11.13 |
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133 |
J. Hussain, N. Rehman, A. L. Khan, L. Ali, A. Al-Harrasi, Z. K. Shinwari, H. Hussain, T. S. Rizvi. Proximate based comparative assessment of five medicinal plants to meet the challenges of malnutrition |
European Journal of Medicinal Plants, Volume 3, pp. 444-453, 2013; Sciencedomain International |
IF = 0.00 SJR = 0.00 SNIP: 0.00 |
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134 |
M. Saleem, M. I. Tousif, N. Riaz, I. Ahmed, B. Schulz, M. Ashraf, R. Nasar, G. Pescitelli, H. Hussain, A. Jabbar, N. Shafiq, K. Krohn. phyto |
Phytochemistry, Volume 93, 199-202, 2013; Elsevier, USA |
IF = 2.54 SJR = 0.99 SNIP: 1.47 |
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135 |
H. Hussain*, A. T. Nyongha, E. Dongo, I. Ahmed, W. Zhang. Melicilamide A: A New Ceramide from Melicia excelsa |
Natural Product Research, Volume 27, pp 1246-1249, 2013; Taylor & Francis, UK |
IF = 0.91 SJR = 0.37 SNIP = 0.71 |
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136 |
A.Al-Harrasi, L. Ali, N. Rehman, J. Hussain, H. Hussain*, A. Al-Rawahi, T. S. Rizvi. 11α-ethoxy-β-boswellic acid and Nizwanone: one new boswellic acid derivative and new triterpene, respectively, from Boswellia sacra |
Chemistry & Biodiversity, Volume 10, pp. 1501-1506, 2013; John Wiley & Sons, USA |
IF = 1.80 SJR = 0.52 SNIP = 0.86 |
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137 |
A.Al-Harrasi, L. Ali, E. Ceniviva, A. Al-Rawahi, J. Hussain, H. Hussain, N. Rehman, A. Ghulam, R. Al-Harrasi. Antiglycation and antioxidant activities and HPTLC analysis of Boswellia sacra resin: The Sacred Frankincense |
Tropical Journal Pharmaceutical Sciences Volume 12, pp. 597-602, 2013; |
IF = 0.82 SJR = 0.23 SNIP = 0.71 |
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138 |
M. Nazir, N. Riaz, M. Ashraf, S. A. Ejaz, M. Saleem, I. Ahmad, H. Hussain, B. Schulz, S. Draeger, A. Jabbar, K. Krohn. Bioactive Secondary Metabolites of the fungus Noduliosporium sp. Isolated from Dittrichia viscose |
Journal of the Chemical Society of Pakistan, Volume 35, pp. 463-467, 2013; Chemical Society Pakistan |
IF = 1.00 SJR = 0.23 SNIP = 0.71 |
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139 |
A.Al-Harrasi, L. Ali, N. Rehman, H. Hussain*, J. Hussain, A. Al-Rawahi, G. J. Langley, N. J. Wells, G. Abbas. Nine triterpenes from Boswellia sacra Flückiger and their chemotaxonomic importance |
Biochemical Systematics and Ecology, Volume 51, 113-116, 2013; Elsevier Netherland |
IF = 0.96 SJR = 0.34 SNIP: 0.78 |
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140 |
A.ShahUllah, E. Nousheen, U.A. Rana, I. Shakir, A. Badshah, Z. Rehman, H. Hussain. Detailed electrochemical probing of the pH dependent redox behaviour of 1-methoxyphenazine |
Journal of The Electrochemical Society, Volume 160, pp. H765-H769, 2013; Electrochemical Society, USA |
IF = 2.85 SJR = 1.08 SNIP: 1.23 |
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141 |
A.Al-Harrasi, A. Al-Rawahi, J. Hussain, L. Ali, H. Hussain, N. Rehman, A. Ghulam, M. Ahmad, Mehjabeen. The first in vitro Lipid peroxidation and in vivo Anti-inflamatory activity of the Omani Frankincense obtained from Boswellia sacra |
International Journal of Phytomedicine, Volume 5, 73-77, 2013; Advance Research Journals |
IF = 1.23 SJR = x.xx SNIP: x.xx |
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142 |
H. Hussain*, H. Al-Harrasi, I. Ahmed, I. R Green, T. Van Ree, A. Ghulam. The genus Pluchea: phytochemistry, traditional uses, and biological activitie |
Chemistry & Biodiversity, Volume 10, pp. 1944-1971, 2013; John Wiley & Sons, USA |
IF = 1.80 SJR = 0.52 SNIP = 0.86 |
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143 |
S. Munir, A. Shah, A. Rauf, A. Badshah, H. Hussain, Z. Rehman, Z. Ahmad. Redox behavior of juglone in buffered aq.: Ethanol media |
Comptes Rendus Chimie, Volume 16, pp. 1140-1146, 2013; Elsevier, UK |
IF = 1.71 SJR = 0.48 SNIP = 0.66 |
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144 |
A.Ali, A. Falodun, G. C. Josephs, H. Hussain, U. Karsten, P. Langer. Characterization and antimicrobial evaluation of epiafzelechin from the stem bark of Calliandra surinamensis Benth. |
African Journal of Pharmaceutical Research & Development, Volume 5, pp. 25-29, 2013; |
IF = 0.00 SJR = 0.00 SNIP = 0.00 |
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2014 (Impact factor: 74.11) |
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145 |
H. Hussain*, A. Al-Harrasi, I. Ahmed, I. R. Green, G. Abbas, N. Rehman. meta-chloroperbenzoic acid: A versatile reagent in Organic synthesis |
RSC Advances, Volume 4, pp. 12882-12917, 2014; Royal Society Chemistry, UK |
IF = 3.84 SJR = 1.02 SNIP = 0.95 |
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146 |
H. Hussain*, I. Kock, A. Al-Harrasi, G. Abbas, I. R. Green, S. Draeger, B. Schulz, K. Krohn. Antimicrobial and phytochemical investigation of the endophytic fungus Acremonium sp. |
Topclass Journal of Herbal Medicine Volume 3, pp. 1-4, 2014; Topclass Global Enterprise, Nigeria |
IF = 0.00 SJR = 0.00 SNIP = 0.00 |
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147 |
H. Hussain*, I. Kock, A. Al-Harrasi, A. Al-Rawahi, G. Abbas, I. R. Gree, A. Shah, A. Badshah, M. Saleem, S. Draeger, B. Schulz, K. Krohn. Antimicrobial Chemical Constituents from Endophytic Fungus, Phoma sp. |
Asian Pacific Journal of Tropical Medicine Volume 7, pp. 699-702, 2014; Elsevier, UK |
IF = 1.06 SJR = 0.45 SNIP = 0.82 |
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148 |
H. Hussain*, C. Kliche-Spory, A. Al-Harrasi, A. Al-Rawahi, G. Abbas, I. R. Green, B. Schulz, K. Krohn, A. Shah. Antimicrobial constituents from three endophytic fungi |
Asian Pacific Journal of Tropical Medicine Volume 7, pp. S224-S227, 2014; Elsevier, UK |
IF = 1.06 SJR = 0.45 SNIP = 0.82 |
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149 |
K. Ahmad, A. H. Shah, B. Adhikari, U. A. Rana, S. N. Uddin, C. Vijayaratnam, N. Muhammad, S. Shujah, A. Rauf, H. Hussain, A. Badshah, R. Qureshi, H. B. Kraatz, A. Shah. pH-dependent redox mechanism and evaluation of kinetic and thermodynamic parameters of a novel anthraquinone |
RSC Advances, Volume 4, pp. 31657-31665, 2014; Royal Society Chemistry, UK |
IF = 3.84 SJR = 1.02 SNIP = 0.95 |
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150 |
A.A. Shad, S. Ahmad, R. Ullah, N. M. A. El-Salam, H. Fouad, N. U. Rehman, H. Hussain, W. Saeed. Phytochemical and biological activities of four Wild medicinal plants |
The Scientific World Journal, 1-7 (Article ID 857363) Hindawi Publishing Corporation, Egypt |
IF = 1.2 SJR = 0.00 SNIP = 0.00 |
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151 |
A.Rauf, H. Subhan, R. Abbasi, B. Adhikari, A. H. Shah, U. A. Rana, Q. Abbas, I. Z. Qureshi, H. Hussain, K. Mazhar, A. Badshah, H. B. Kraatz, A. Shah. Biological activity, pH dependent redox behavior and UV–Vis spectroscopic studies of naphthalene derivatives |
Journal of Photochemistry and Photobiology B: Biology Volume 140, pp. 173-181, 2014; Elsevier, UK |
IF = 2.96 SJR = 0.72 SNIP: 1.25 |
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152 |
A.H. Shah, A. Shah, S. U. D. Khan, U. A. Rana, H. Hussain, S. B. Khan, R. Qureshi, A. Badshah, A. Waseem Probing the pH dependent electrochemistry of a novel quinoxaline carboxylic acid derivative at a glassy carbon electrode. |
Electrochimica Acta, Volume 147, pp. 121-128, 2014; Elsevier, UK |
IF = 4.50 SJR = 1.28 SNIP: 1.45 |
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153 |
H. Hussain*, A. Al-Harrasi, A. Rawahi, I. R. Green, S. Gibbons. Fruitful decade for antileishmanial compounds from 2002 to late 2011 |
Chemical Reviews, Volume 114, pp. 10369-10428, 2013; American Chemical Society, USA |
IF = 46.56 SJR = 16.31 SNIP: 11.13 |
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154 |
A.H. Shah, A. Shah, U. A. Rana, S. U. Khan, H. Hussain, S. B. Khan, R. Qureshi, A. Badshah. Redox mechanism and evaluation of kinetic and thermodynamic parameters of 1,3-dioxolo[4,5-g]pyrido[2,3-b]quinoxaline using electrochemical techniques |
Electroanalysis Volume 26, pp. 2292-2300, 2014; John Wiley & Sons, USA |
IF = 2.13 SJR = 0.63 SNIP: 0.75 |
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155 |
I.Ali, S. Bibi, F. Bano, S. Ali, H. Hussain*, Zamarrud, V. U. Ahmad, A. Al-Harrasi. Biological activities of Suaeda heterophylla and Bergenia stracheyii |
Asian Pacific Journal of Tropical Disease Volume 4, pp. S885-S889, 2014; Elsevier, UK |
IF = 0.00 SJR = 0.34 SNIP: 0.72 |
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156 |
H. Hussain*, I. Kock, A. Al-Harrasi, G. Abbas, N. Rehman, A. Badshah, A. Shah, U. A. Raina, Z. Naureen, I. R. Green, S. Draeger, B. Schulz, K. Krohn. Coniothyren: One New Phenoxyphenyl Derivative from Endophytic Fungus, Coniothyrium sp |
Journal of Asian Natural Products Research, Volume 16, 1094-1098, 2014; Taylor & Francis, UK |
IF = 0.91 SJR = 0.38 SNIP: 0.72 |
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157 |
M. I. Tousif, N. Shazmeen, N. Riaz, N. Shafiq, T. Khatoon, B. Schulz, M. Ashraf, A. Shaukat, H. Hussain, A. Jabbar, M. Saleem. α-Glucosidase and lipoxygenase inhibitory derivatives of cryptosporioptide from the endophytic fungus Cryptosporiopsis sp. |
Journal of Asian Natural Products Research, Volume 16, 1094-1098, 2014; Taylor & Francis, UK |
IF = 0.91 SJR = 0.38 SNIP: 0.72 |
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158 |
H. Hussain*, N. Root, F. Jabeen, A. Al-Harrasi, A. Al-Rawahi, M. Ahmad, Z. Hassan, G. Abbas, F. Mabood, A. Shah, A. Badshah, A. Khan, R. Ahmad, I. R. Green, S. Draeger, B. Schulz, K. Krohn Seimatoric acid and colletonoic acid: Two new compounds from the endophytic fungi, Seimatosporium sp. and Colletotrichum sp. |
Chinese Chemical Letters, Volume 25, pp. 1575-1579, 2014; Elsevier, UK. |
IF = 1.58 SJR = 0.42 SNIP: 0.68 |
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159 |
A.Al-Harrasi, H. Hussain*, A. Al-Rawahi, J. Hussain, F. L. Hakkim, H. Y. Khan, N. U. Rehman, L. Ali, R. Al-Harrasi, S. Al-Hadrami, I. Al-Hadrami. First and reproducible pyrolysate products from Omani Frankincense smoke: First evidence of thermal aromatization of boswellic acids |
Journal of Analytical and Applied Pyrolysis Volume 110, pp. 430-434, 2014; Elsevier, UK |
IF = 3.56 SJR = 1.59 SNIP: 1.93 |
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2015 (Impact factor: 33.46) |
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160 |
H. Hussain*, K. H. E. Drogies, A. Al-Harrasi, Z. Hassan, A. Shah, U. A. Rana, I. R. Green, S. Draeger, B. Schulz, K. Krohn. Antimicrobial Constituents from Endophytic Fungus Fusarium sp. |
Asian Pacific Journal of Tropical Disease Volume 5, pp. 186-89, 2015; Elsevier, UK |
IF = 0.00 SJR = 0.34 SNIP: 0.72 |
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161 |
H. Hussain*, M. John, A. Al-Harrasi, A. Shah, Z. Hassan, G. Abbas, U. A. Rana, I. R. Green, B. Schulz, K. Krohn. Phytochemical investigation and antimicrobial activity of Edophytic Fungus Phoma sp |
Journal of King Saud University-Sciences Volume 27, pp. 92-95, 2015; Elsevier, UK |
IF = 0.00 SJR = 0.28 SNIP: 0.78 |
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162 |
A.H. Shah, W. Zaid, A. Shah, U. A. Rana, H. Hussain, M. N. Ashiq, R. Qureshi, A. Badshah, M. A. Zia, H. B. Kraatz. pH Dependent electrochemical characterization, computational studies and evaluation of thermodynamic, kinetic and analytical parameters of two phenazines |
Journal of The Electrochemical Society, Volume 162, pp. H115-H123, 2015; Electrochemical Society, USA |
IF = 2.85 SJR = 1.08 SNIP: 1.23 |
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163 |
A.Ullah, A. Rauf, U. A. Rana, R. Qureshi, M. N. Ashiq, H. Hussain, H. B. Kraatz, A. Badshah, A. Shah. pH Dependent Electrochemistry of Anthracenediones at a Glassy Carbon Electrode |
Journal of The Electrochemical Society, Volume 162, pp. H157-H163, 2015; Electrochemical Society, USA |
IF = 2.85 SJR = 1.08 SNIP: 1.23 |
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164 |
H. Hussain*, N. Root, F. Jabeen, A. Al-Harrasi, M. Ahmad, F. Mabood, Z. Hassan, A. Shah, I.R. Green, B. Schulz, K. Krohn. Microsphaerol and Seimatorone: Two New Compounds isolated from the Endophytic Fungi, Microsphaeropsis sp. and Seimatosporium sp. |
Chemistry & Biodiversity, Volume 12, pp. 289-294, 2015; John Wiley & Sons, USA |
IF = 1.80 SJR = 0.52 SNIP = 0.86 |
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165 |
S. Ahmad, S. Ahmad, I. bibi, N. M. AbdEl-Salam, H. Hussain, M. S. Ishaq, M. Adnan, A. Tariq, R. Ullah. Antibacterial and antifungal activities of the extract and fractions of aerial parts of Heliotropium bacciferum |
African Journal of Traditional, Complementary and Alternative Medicines Volume 12, pp. 32-35, 2015; African Ethnomedicines Network (Nigeria) |
IF = 0.70 SJR = X.XX SNIP = X.XX |
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166 |
H. Hussain*, F. Jabben, A. Al-Harrasi, F. Mabbod, A. Manzoor, F. Mabood, J. Hussain, A. Shah, Z. Hassan, N. Rehman, I. R. Green, A. Khan, T. Dzeha, S. Draeger, B. Schulz, K. Krohn. Seimisochromenes A and B: Two new dihydroisochromenes from the endophytic fungus, Seimatosporium sp |
Journal of Asian Natural Products Research, Volume 17, 348-351, 2015; Taylor & Francis, UK |
IF = 0.91 SJR = 0.38 SNIP: 0.72 |
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167 |
L. Rahman, A. Shah, S. B. Khan, A. M. Asiri, H. Hussain, C. Han, R. Qureshi, M. N. Ashiq, M. A. Zia, M. Ishaq, H. B. Kraatz. Synthesis, characterization, and application of Au–Ag alloy nanoparticles for the sensing of an environmental toxin, pyrene |
Journal Applied Electrochememistry Volume 45, pp. 463-472, 2015; Springer, Netherlands |
IF = 2.40 SJR = X.XX SNIP: X.XX |
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168 |
G. Abbas, M. Shahzad, Z. Saddiqe, M. J. Hassan, S. Saba, J. R. R. Malik, H. Hussain. Various fractions of Hypericum moserianum and Hypericum ericoides possess antiglycation, anti-lipid peroxidation, antioxidative activities and non-toxic effects in vitro |
Pakistan Journal of Pharmaceutical Sciences Volume 28, pp. 933-938, 2015; Faculty of Pharmacy Karachi, Pakistan |
IF = 0.95 SJR = X.XX SNIP: X.XX |
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169 |
M. A. Raeesa, H. Hussain*, N. U. Rehman, H. Y. Khan, G. Abbas, A. Al-Rawahi, A. Elyassi, I. S. Al-Amri, I. R. Green, T. Mahmood, A. Al-Harrasi. Desmiflavasides A and B: Two New Bioactive Pregnane Glycosides from the Sap of Desmidorchis flava |
Phytochemistry Letters, Volume 12, pp. 153-157, 2015; Elsevier, UK |
IF = 1.45 SJR = 0.54 SNIP: 1.01 |
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170 |
F. Mabood, A. Al-Harrasi, R. Boque, F. Jabeen, J. Hussain, A. Hafidh, K. Hind, M. A. Ahmed, A. Manzoor, H. Hussain, N. Rehman, S. H. Iman, J. J. Sajid, S. A. Hamood. Determination of sucrose in date fruits (Phoenix dactylifera L.) growing in the Sultanate of Oman by NIR spectroscopy and multivariate calibration |
Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy Volume 150, pp. 170-174, 2015; Elsevier, UK |
IF = 2.35 SJR = 0.59 SNIP: 1.16 |
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171 |
R. Ullah, S. Ahmad, A. Atiq, H. Hussain, N. Rehman, N. M. AbdElsalam, M. Adnan. Quantification and antibacterial activity of flavonoids in coffee samples |
African Journal of Traditional, Complementary and Alternative Medicines Volume 12, pp. 84-86, 2015; African Ethnomedicines Network (Nigeria) |
IF = 0.70 SJR = X.XX SNIP = X.XX |
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172 |
H. Hussain*, F. Jabben, K. Krohn, A. Al-Harrasi, A. Manzoor, F. Mabbod, A. Shah, A. Badshah, N. Rehman, I. R. Green, I. Ali, S. Draeger, B. Schulz. Antimicrobial activity of two mellein derivatives isolated from an endophytic fungus |
Medicinal Chemistry Research Volume 24, pp. 2111-2114, 2015; Springer, Netherlands |
IF = 1.40 SJR = 0.40 SNIP = 0.75 |
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173 |
H. Hussain*, F. Jabeen, A. Al-Harrasi, Ahmed Al-Rawahi, M. Ahmad, F. Mabood, I. R. Green, A. Zahoor, A. Shah, S. Draeger, B. Schulz, K. Krohn. Microdiplanol and microdiplane: A new m-anisaldehyde derivative and a new 24-methylcholestanol derivative from the endophytic fungus Microdiplodia sp. |
Journal of Asian Natural Products Research, Volume 17, 733-737, 2015; Taylor & Francis, UK |
IF = 0.91 SJR = 0.38 SNIP: 0.72 |
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174 |
K. Ahmad, A. Rauf, A. Shah, S. U. Khan, U. A. Rana, H. Hussain, R. Qureshi, A. Badshah, H. B. Kraatz. pH and temperature responsive redox behavior of hydroxyanthracenediones |
Comptes Rendus Chimie, Volume 18, pp. 823-833, 2015; Elsevier, UK |
IF = 1.71 SJR = 0.48 SNIP = 0.66 |
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175 |
H. Subhan, A. Lashin, U.A. Rana, N. Al-Arifi, K. Ahmad, H. Hussain, R. Qureshi, S. Ali, M.A. Zia, H.B. Kraatz, A. Shah. pH and temperature responsive redox behavior of biologically important aniline derivatives |
RSC Advances, Volume 5, pp. 64617-64625, 2014; Royal Society Chemistry, UK |
IF = 3.84 SJR = 1.02 SNIP = 0.95 |
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176 |
S. Ahmad, R. Ullah, N. M. AbdEl-Salam, M. Arfan, H. Hussain. Royleanumioside, A New phytotoxic Triterpenoid from Teucrium royleanum |
Journal of Asian Natural Products Research, Volume 17, 838-842, 2015; Taylor & Francis, UK |
IF = 0.91 SJR = 0.38 SNIP: 0.72 |
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177 |
H. Hussain*, A. Al-Harrasi, A. Al-Rawahi, I. R. Green, R. Csuk, I. Ahmed, A. Shah, G. Abbas, N. U. Rehman, R. Ullah. A fruitful decade from 2005-2014 for anthraquinone patents |
Expert Opinion on Therapeutic Patents, Volume 25, pp. 1053-1064, 2015; Taylor & Francis, UK |
IF = 4.29 SJR = 1.23 SNIP: 1.08 |
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178 |
H. Hussain*, A. Al-Harrasi, K. Krohn, S. F. Kouam, G. Abbas, A. Shah, M. A. Raees, R. Ullah, S. Aziz, B. Schulz. Phytochemical investigation and antimicrobial activity of Derris scandens |
Journal of King Saud University-Sciences Volume 27, pp. 375-378, 2015; Elsevier, UK |
IF = 0.00 SJR = 0.28 SNIP: 0.78 |
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179 |
J. Khan, N. Naz, N. M. AbdEl-Salam, Nayab, A. Tabassum, H. Hussain, R. Ullah. ESBL determination and antibacterial drug resistance pattern of Klebsiella pneumoniae amongst patients at PIMS Islamabad |
African Journal of Traditional, Complementary and Alternative Medicines Volume 12, pp. 70-77, 2015; African Ethnomedicines Network (Nigeria) |
IF = 0.70 SJR = X.XX SNIP = X.XX |
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180 |
S. Niaz, T. Akhter, Naser M. AbdEl-Salam, S. Ayaz, S. Shams, R. Ullah, H. Hussain, S. Bibi. Therapeutic potential of pegnum harmela against Schistosoma bovis in buffaloes |
African Journal of Traditional, Complementary and Alternative Medicines Volume 12, pp. 84-89, 2015; African Ethnomedicines Network (Nigeria) |
IF = 0.70 SJR = X.XX SNIP = X.XX |
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181 |
S. H. Ghoran, B. Azadi, H. Hussain. Chemical composition of the volatile oils of three Lamiaceae species growing wild in North of Iran |
Journal of Herbal Drugs, Volume 6, pp. 23-29, 2015; Research Centre for Medicinal Plants and Ethno-veterinary, Iran |
IF = 0.00 SJR = X.XX SNIP = X.XX |
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182 |
H. Hussain*, M. A. Raees, N. U. Rehman, A. Al-Rawahi, H. Y. Khan, G. Abbas, M. A. Al-Broumi1, A. Elyassi, T. Mahmood, A. Al-Harrasi. Nizwaside: A New Anticancer Pregnane Glycoside from the Sap of Desmidorchis flava |
Archives Pharmacal Research, Volume 38, 2137-2142; Springer, Netherlands |
IF = 2.04 SJR = 0.57 SNIP = 0.98 |
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2016 (Impact factor: 6.00) |
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183 |
G. Abbas, A. Al-Harrasi, H. Hussain, J. Hussain, R. Rashid, M. I. Choudhary. Antiglycation therapy: Discovery of promising antiglycation agents for the management of diabetic complications |
Pharmaceutical Biology, Volume 54, pp. 198-206, 2016; Taylor & Francis, UK |
IF = 1.24 SJR = 0.48 SNIP: 0.81 |
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184 |
S. Hafeez-Ghoran, S. Saeidnia, E. Babaei, F. Kiuchi, H. Hussain. Scillapersicene: a new homoisoflavonoid with cytotoxic activity from the bulbs of Scilla persica HAUSSKN |
Natural Product Research, Volume 30, IN print, 2016; Taylor & Francis, UK |
IF = 0.91 SJR = 0.37 SNIP = 0.71 |
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185 |
S. Niaz, T. Akhter, N. M. AbdEl-Salam, S. Ayaz, S. Shams, R. Ullah, H. Hussain, M. A. Wasim. Treatment of schistosomiasis by seeds of Lagenaria siceraria and its comparison with allopathic drugs in Buffaloes |
Indian Journal of Animal Research, 2016, In print; Indian Council of Agricultural Research, India |
IF = 0.00 SJR = X.XX SNIP = X.XX |
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186 |
F. Mabood, Z. Hussain, H. Haq, M. B. Arian, R. Boque, K. M. Khan, K. Hussain, F. Jabeen, J. Hussain, M. Ahmed, A. Al-Harrasi, Z. Noureen, H. Hussain, A. Khan, S. Parveen. Development of new UV-Vis spectroscopic microwave-assisted method for determination of glucose in pharmaceutical samples |
Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy Volume 153, pp. 212-215, 2016; Elsevier, UK |
IF = 2.35 SJR = 0.59 SNIP: 1.16 |
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187 |
S. Aziz, H. Rehman, M. A. Ch, K. S. Ghani, K. A. Yasin, H. Hussain, K. Krohn. Efficient synthesis and biological evaluation of topopyrone C derivatives
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Chemistry of Natural Compounds, Volume 52, pp. 58-61, 2016; Springer, Germany |
IF = 0.50 SJR = 0.30 SNIP: 0.55 |
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188 |
M. Imran Tousif, N. Shazmeen, N. Riaz, H. Hussain, A. Al-Harrasi, A. Yaqoob, F. H. Nasim, A. Jabbar, T. Khatoon, R. B. Tareen, M. Saleem. Bioactive Secondary Metabolites from Vincetoxicum stocksii |
Journal of the Chemical Society of Pakistan, Volume 38, In print, 2016; Chemical Society Pakistan |
IF = 1.00 SJR = 0.23 SNIP = 0.71 |
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Book Chapters |
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189 |
H. Hussain*, A. Al-Harrasi, I. R. Green, I. Ahmed, G. Abbas. Recent Advances in the Chemistry and Biology of Natural Dimeric Quinones |
In: Studies in Natural Products Chemistry" (Bioactive Natural Products), edited by Atta Ur Rahman; Elsevier Science Publishers, The Netherlands, 2015, vol. 46, 447-517 |
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190 |
H. Hussain*, A. Al-Harrasi, I. R. Green. Frankincense (Boswellia) Oils |
In: “Essential Oils in Food Preservation, Flavor and Safety” edited by Preedy, V.R. Academic Press, Elsevier, UK; 2016; pp. 431–440 |
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191 |
H. Hussain*, A. Al-Harrasi, I. R. Green, N. Rehman. Iris (Iris germanica) Oils |
In: “Essential Oils in Food Preservation, Flavor and Safety” edited by Preedy, V.R. Academic Press, Elsevier, UK; 2016; pp. 481–486 |
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192 |
H. Hussain*, A. Al-Harrasi, I. R. Green. Pune-sa (Nepeta) Oils |
In: “Essential Oils in Food Preservation, Flavor and Safety” edited by Preedy, V.R. Academic Press, Elsevier, UK; 2016; pp. 641–648 |
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