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Volumn 60, Issue 12, 1997, Pages 1229-1235

Neoclerodane diterpenoids from Scutellaria polyodon

Author keywords

[No Author keywords available]

Indexed keywords

DITERPENOID; NEOCLERODANE DITERPENOID; SCUPOLIN; UNCLASSIFIED DRUG;

EID: 0031445968     PISSN: 01633864     EISSN: None     Source Type: Journal    
DOI: 10.1021/np970213a     Document Type: Article
Times cited : (24)

References (29)
  • 1
    • 0008402749 scopus 로고
    • Although the hydrocarbon skeleton of these diterpenoids is biogenetically derived from an ent-labdane, and they should be named ent-clerodanes, we prefer to use the term "neoclerodane" proposed by Rogers et al. (Rogers, D.; Unal, G. G.; Williams, D. J.; Ley, S. V.; Sim, G. A.; Joshi, B. S.; Ravindranath, K. R. J. Chem. Soc., Chem. Commun. 1979, 97-99) because it is the nomenclature used in the majority of the articles published on this subject since 1979.
    • (1979) J. Chem. Soc., Chem. Commun. , pp. 97-99
    • Rogers, D.1    Unal, G.G.2    Williams, D.J.3    Ley, S.V.4    Sim, G.A.5    Joshi, B.S.6    Ravindranath, K.R.7
  • 4
    • 0029139998 scopus 로고    scopus 로고
    • Hanson, J. R. Nat. Prod. Rep. 1995, 12, 207-218; ibid. 1996, 13, 59-71.
    • (1995) Nat. Prod. Rep. , vol.12 , pp. 207-218
    • Hanson, J.R.1
  • 5
    • 0029139998 scopus 로고    scopus 로고
    • Hanson, J. R. Nat. Prod. Rep. 1995, 12, 207-218; ibid. 1996, 13, 59-71.
    • (1996) Nat. Prod. Rep. , vol.13 , pp. 59-71
  • 6
    • 0000002619 scopus 로고
    • Labiate-Insect Interactions: Effects of Labiate-Derived Compounds on Insect Behaviour
    • Harley, R. M., Reynolds, T., Eds.; Royal Botanic Gardens: Kew, UK
    • Simmonds, M. S. J.; Blaney, W. M. "Labiate-Insect Interactions: Effects of Labiate-Derived Compounds on Insect Behaviour". In Advances in Labiate Science; Harley, R. M., Reynolds, T., Eds.; Royal Botanic Gardens: Kew, UK, 1992; pp 375-392.
    • (1992) Advances in Labiate Science , pp. 375-392
    • Simmonds, M.S.J.1    Blaney, W.M.2
  • 29
    • 6844239864 scopus 로고    scopus 로고
    • note
    • 1H-NMR spectrum) of the 15α-methoxy epimer10,18,19 of 11, although it was homogeneous on TLC: The scarcity of the sample available precluded the complete characterization of this substance.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.