MAILING ADDRESS

UoN Chair of Oman’s Medicinal Plants

and Marine Natural Products

University of Nizwa

P.O Box 33, Postal Code 616

Birkat Al Mauz, Nizwa,

Oman

Email: hussainchem3@gmail.com

Tel: 00986-97154164

EDUCATION

Ph.D. (Organic Chemistry)

H. E. J. Research Institute of Chemistry

University of Karachi, Karachi-75270, Pakistan

2004

M.Sc. (Organic Chemistry)

Gomal University D. I. Khan, Khyber Pakhtunkhwa, Pakistan

1999

B.Sc. (Chemistry, Zoology, Botany)
Govt Degree College Parachinar, Karachi-75270, Pakistan

1995

List of Publications

2002 (Impact factor: 1.83)

Paper Details

( Author , title)

Journal Details

(Title, volume, issue, page.no, year, publisher, country)

Journal Quality

(Impact factor, SNIP, SJR etc.)

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

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

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

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

2003 (Impact factor: 7.92)

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

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

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

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

2004 (Impact factor: 1.10)

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

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

2005 (Impact factor: 9.43)

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

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

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

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

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

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

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

2006 (Impact factor: 5.31)

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

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

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

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

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

2007 (Impact factor: 21.50)

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

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

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

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

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

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

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

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

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

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

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

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

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

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

2008 (Impact factor: 14.57)

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

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

39

M. Ng’ang’a, S. Chhabra, C. L. Thoruwa, H. Hussain, K. Krohn.

Chemical constituents from the leaves of Drypetes gerrardii

Biochemical Systematics and Ecology, Volume 36, 320-322, 2008; Elsevier Netherland 

IF = 0.96

SJR = 0.34

SNIP: 0.78

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

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

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

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

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

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

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

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

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

2009 (Impact factor: 22.37)

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

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

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

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

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

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

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

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

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

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

2010 (Impact factor: 27.68)

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

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

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

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: ???

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

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

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

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

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

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

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

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

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

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

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)

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

2012 (Impact factor: 37.27)

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

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

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

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

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

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

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

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

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

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

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: ???

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

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

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

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

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

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

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

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

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

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

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

2013 (Impact factor: 82.82)

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

2014 (Impact factor: 74.11)

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

2015 (Impact factor: 33.46)

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

2016 (Impact factor: 6.00)

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

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

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

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

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

Chemistry of Natural Compounds, Volume 52, pp. 58-61, 2016; Springer, Germany

IF = 0.50

SJR = 0.30

SNIP: 0.55

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

Book Chapters

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

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

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

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

Project Title

PI/Co P.I

Sponsoring Agency

Amount

Status

Identification of New Antiglycation agents of Natural and Synthetic Origins for the Management of Diabetic Complications in vitro and in animal model

PI

University of Nizwa

67000 USD

Funded

Synthesis of acetyl keto boswellic acids as anticancer agents

Co I.

The Oman Research Council

810,380 USD

Funded

Discovery of New Antagonists of Glucagon Receptor and New Inhibitors of Protein Glycation, α-Glucosidase, Dipeptidyl Peptidase-4 (DPP-4) Enzymes from Natural and Synthetic Products for the Management of Diabetes Mellitus and Late Diabetic Complications.

Co I.

University of Nizwa

25,450 USD

Funded

Catalytic Pyrolysis of Scrap Tires into End-uses for Fuel Oil and Carbon Black Products by using Novel Catalysts from Sultanate of Oman

Co I

University of Nizwa

25,450 USD

Funded