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Volumn 69, Issue 12, 2006, Pages 1734-1738

Clerodane diterpenoids from Salvia splendens

Author keywords

[No Author keywords available]

Indexed keywords

11 O ACETYLSALVISPLENDIN B; 2 O ACETYLSALVISPLENDIN D; 7 O ACETYLSALVISPLENDIN C; CLERODANE DERIVATIVE; DEHYDROKERLIN; DIAZOMETHANE; DITERPENOID; MARRUBIASTROL; OLEARIN; PLANT EXTRACT; SALVIA SPLENDENS EXTRACT; SALVIARIN; SALVISPLENDIN A; SALVISPLENDIN B; SALVISPLENDIN C; SALVISPLENDIN D; SPLENDIDIN; SPLENOLIDE A; SPLENOLIDE B; UNCLASSIFIED DRUG;

EID: 33846448168     PISSN: 01633864     EISSN: None     Source Type: Journal    
DOI: 10.1021/np068036d     Document Type: Article
Times cited : (19)

References (28)
  • 17
    • 33846418012 scopus 로고    scopus 로고
    • 9-11 co-occurring in the same species. Moreover, the clerodane-type diterpenoids until now isolated from plants of the Salvia genus, and whose absolute configuration has rigorously been established, belong to the enantio series. Connolly, J. D.; Hill, R. A. Dictionary of Terpenoids; Chapman & Hall: London, 1991; 2, pp 750-809.
    • 9-11 co-occurring in the same species. Moreover, the clerodane-type diterpenoids until now isolated from plants of the Salvia genus, and whose absolute configuration has rigorously been established, belong to the enantio series. (Connolly, J. D.; Hill, R. A. Dictionary of Terpenoids; Chapman & Hall: London, 1991; Vol. 2, pp 750-809.
  • 19
    • 33846430043 scopus 로고    scopus 로고
    • Rodriguez-Hahn, L.; Esquivel, B.; Cardenas, J. In Phytochemistry of Medicinal Plants; Arnason, J. T., Mata, R., Romeo, J. T., Eds.; Plenum Press: New York, 1995; Chapter 12, pp 311-332.
    • Rodriguez-Hahn, L.; Esquivel, B.; Cardenas, J. In Phytochemistry of Medicinal Plants; Arnason, J. T., Mata, R., Romeo, J. T., Eds.; Plenum Press: New York, 1995; Chapter 12, pp 311-332.)
  • 20
    • 33846409488 scopus 로고    scopus 로고
    • In accordance with the Cahn-Ingold-Prelog convention, the configuration of the C-12 chiral center must be described as 12R for 2-6, 8, and 9 and as 12S for 1, 7, and 10, although the spatial arrangement of the substituents of that asymmetric carbon is identical for all these compounds. Moreover, since we assume17 that 1-6 belong to the enantio series, the R- or S-configuration for an asymmetric carbon must be described as ent-S or ent-R, respectively Connolly, J. D, Hill, R. A. Dictionary of Terpenoids; Chapman & Hall: London, 1991; 1, pp XV-XVI, However, for clarity we use throughout the text the R/S nomenclature, omitting the prefix ent, which refers to the absolute configuration of the whole molecule. On the other hand, and also for clarity, the α- or β-configuration for a substituent indicates that it is placed, respectively, below or above the
    • 17 those configurations should be described as ent-β or ent-α, indicating that the substituent is placed, respectively, below or above the plane of the formulas.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.