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Volumn 83, Issue 1, 2012, Pages 49-54

Sesquiterpenoids and norterpenoids from Vitex negundo

Author keywords

Negundoal; Negundonorin; Negunfurol; Verbenaceae; Vitex negundo

Indexed keywords

3 EPICOROSOLIC ACID; 3 FORMYL 4,5 DIMETHYL 8 OXO 5H 6,7 DIHYDRONAPHTHO[2,3 B]FURAN; DOXORUBICIN; NEGUNDOAL; NEGUNDONORIN A; NEGUNDONORIN B; NEGUNFUROL; NORTERPENOID; SESQUITERPENOID; TERPENOID; UNCLASSIFIED DRUG;

EID: 83055194304     PISSN: 0367326X     EISSN: 18736971     Source Type: Journal    
DOI: 10.1016/j.fitote.2011.09.012     Document Type: Article
Times cited : (43)

References (20)
  • 4
    • 0026517495 scopus 로고
    • Chemical investigation and anti-inflammatory activity of Vitex negundo seeds
    • A.S. Chawla, A.K. Sharma, and S.S. Handa Chemical investigation and anti-inflammatory activity of Vitex negundo seeds J Nat Prod 55 1992 163 167
    • (1992) J Nat Prod , vol.55 , pp. 163-167
    • Chawla, A.S.1    Sharma, A.K.2    Handa, S.S.3
  • 5
    • 77952894900 scopus 로고    scopus 로고
    • Antinociceptive activities of the liposoluble fraction from Vitex negundo seeds
    • C.J. Zheng, B.K. Huang, T. Han, Q.Y. Zhang, H. Zhang, and K. Rahman Antinociceptive activities of the liposoluble fraction from Vitex negundo seeds Pharm Biol 48 2010 651 658
    • (2010) Pharm Biol , vol.48 , pp. 651-658
    • Zheng, C.J.1    Huang, B.K.2    Han, T.3    Zhang, Q.Y.4    Zhang, H.5    Rahman, K.6
  • 8
    • 0024826254 scopus 로고
    • Antiandrogenic effects of a flavonoid-rich fraction of Vitex negundo seeds: A histological and biochemical study in dogs
    • DOI 10.1016/0378-8741(89)90007-X
    • S.K. Bhargava Antiandrogenic effects of a flavonoid-rich fraction of Vitex negundo seeds: a histological and biochemical study in dogs J Ethnopharmacol 27 1989 327 339 (Pubitemid 20027681)
    • (1989) Journal of Ethnopharmacology , vol.27 , Issue.3 , pp. 327-339
    • Bhargava, S.K.1
  • 9
    • 0000482608 scopus 로고
    • Chemical investigation and anti-inflammatory activity of Vitex negundo seeds: Part i
    • A.S. Chawla, A.K. Sharma, and S. Handa Chemical investigation and anti-inflammatory activity of Vitex negundo seeds: Part I Indian J Chem 30B 1991 773 776
    • (1991) Indian J Chem , vol.30 B , pp. 773-776
    • Chawla, A.S.1    Sharma, A.K.2    Handa, S.3
  • 10
    • 79958109335 scopus 로고    scopus 로고
    • Chemical constituents and bioactivities of the liposoluble fraction from different medicinal parts of Crocus sativus
    • C.J. Zheng, L. Li, W.H. Ma, T. Han, and L.P. Qin Chemical constituents and bioactivities of the liposoluble fraction from different medicinal parts of Crocus sativus Pharm Biol 49 7 2011 756 763
    • (2011) Pharm Biol , vol.49 , Issue.7 , pp. 756-763
    • Zheng, C.J.1    Li, L.2    Ma, W.H.3    Han, T.4    Qin, L.P.5
  • 12
    • 34548833897 scopus 로고    scopus 로고
    • Pentacyclic triterpenes. Part 5: Synthesis and SAR study of corosolic acid derivatives as inhibitors of glycogen phosphorylases
    • DOI 10.1016/j.bmcl.2007.08.057, PII S0960894X07010141
    • X. Wen, J. Xia, K. Cheng, L. Zhang, P. Zhang, and J. Liu Pentacyclic triterpenes. Part 5: synthesis and SAR study of corosolic acid derivatives as inhibitors of glycogen phosphorylases Bioorg Med Chem Lett 17 21 2007 5777 5782 (Pubitemid 47446231)
    • (2007) Bioorganic and Medicinal Chemistry Letters , vol.17 , Issue.21 , pp. 5777-5782
    • Wen, X.1    Xia, J.2    Cheng, K.3    Zhang, L.4    Zhang, P.5    Liu, J.6    Zhang, L.7    Ni, P.8    Sun, H.9
  • 13
    • 67349288106 scopus 로고    scopus 로고
    • Three new sesquiterpenes from Euonymus schensianus Maxim
    • X.K. Zheng, J.H. Guo, W.S. Feng, and H.W. Li Three new sesquiterpenes from Euonymus schensianus Maxim Chin Chem Lett 20 2009 952 954
    • (2009) Chin Chem Lett , vol.20 , pp. 952-954
    • Zheng, X.K.1    Guo, J.H.2    Feng, W.S.3    Li, H.W.4
  • 14
    • 84986974386 scopus 로고
    • Stereoisomeric flavour compounds. LII: Separation and structure elucidation of the furanoid linalool oxide stereoisomers using chirospecific capillary gas chromatography and nuclear magnetic resonance spectroscopy
    • A. Christiane, and M. Armin Stereoisomeric flavour compounds. LII: separation and structure elucidation of the furanoid linalool oxide stereoisomers using chirospecific capillary gas chromatography and nuclear magnetic resonance spectroscopy Phytochem Anal 2 1991 211 214
    • (1991) Phytochem Anal , vol.2 , pp. 211-214
    • Christiane, A.1    Armin, M.2
  • 15
    • 0012585831 scopus 로고
    • Terpenoids derived from linalyl oxide. Part 1. The stereochemistry of the davanones
    • A.F. Thomas, W. Thornmen, B. Willhalm, E.W. Hagaman, and E. Wenkert Terpenoids derived from linalyl oxide. Part 1. The stereochemistry of the davanones Helv Chim Acta 57 1974 2055 2061
    • (1974) Helv Chim Acta , vol.57 , pp. 2055-2061
    • Thomas, A.F.1    Thornmen, W.2    Willhalm, B.3    Hagaman, E.W.4    Wenkert, E.5
  • 16
    • 21644482782 scopus 로고    scopus 로고
    • New norditerpenoids with trypanocidal activity from Vitex trifolia
    • DOI 10.1248/cpb.52.1492
    • F. Kiuchi, K. Matsuo, M. Ito, T.K. Qui, and G. Honda New norditerpenoids with trypanocidal activity from Vitex trifolia Chem Pharm Bull 52 12 2004 1492 1494 (Pubitemid 41364435)
    • (2004) Chemical and Pharmaceutical Bulletin , vol.52 , Issue.12 , pp. 1492-1494
    • Kiuchi, F.1    Matsuo, K.2    Ito, M.3    Qui, T.K.4    Honda, G.5
  • 19
    • 35148836262 scopus 로고    scopus 로고
    • Natural triterpenoids from Cecropia lyratiloba are cytotoxic to both sensitive and multidrug resistant leukemia cell lines
    • DOI 10.1016/j.bmc.2007.07.020, PII S0968089607006839
    • G. Rocha Gda, M. Simões, K.A. Lúcio, R.R. Oliveira, M.A. Coelho Kaplan, and C.R. Gattass Natural triterpenoids from Cecropia lyratiloba are cytotoxic to both sensitive and multidrug resistant leukemia cell lines Bioorg Med Chem 15 23 2007 7355 7360 (Pubitemid 47539142)
    • (2007) Bioorganic and Medicinal Chemistry , vol.15 , Issue.23 , pp. 7355-7360
    • Rocha, G.D.G.1    Simoes, M.2    Lucio, K.A.3    Oliveira, R.R.4    Coelho Kaplan, M.A.5    Gattass, C.R.6
  • 20
    • 33747347496 scopus 로고    scopus 로고
    • Beccaridiol, an unusual 28-nortriterpenoid from the leaves of Diplectria beccariana
    • D.S. Jang, B.N. Su, A.D. Pawlus, Y.H. Kang, L.B. Kardono, and S. Riswan Beccaridiol, an unusual 28-nortriterpenoid from the leaves of Diplectria beccariana Phytochemistry 67 16 2006 1832 1837
    • (2006) Phytochemistry , vol.67 , Issue.16 , pp. 1832-1837
    • Jang, D.S.1    Su, B.N.2    Pawlus, A.D.3    Kang, Y.H.4    Kardono, L.B.5    Riswan, S.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.