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In vitro antituberculosis activity of diterpenoids from the Vietnamese medicinal plant Croton tonkinensis

Authors
Jang, Woong SikJyoti, Md. AnirbanKim, SukyungNam, Kung-WooHa, Thi Kim QuyOh, Won KeunSong, Ho-Yeon
Issue Date
Jan-2016
Publisher
Japanese Society of Pharmacognosy
Keywords
Diterpenoid; Croton tonkinensis; Ent-kaurane; M. tuberculosis; MDR TB; XDR TB
Citation
Natural Medicines, v.70, no.1, pp 127 - 132
Pages
6
Journal Title
Natural Medicines
Volume
70
Number
1
Start Page
127
End Page
132
URI
https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/9497
DOI
10.1007/s11418-015-0937-1
ISSN
1340-3443
Abstract
Diterpenoids from the Vietnamese medicinal plant Croton tonkinensis are rich in ent-kaurane, kaurane and the grayanane class and are valuable intermediate plant metabolites with different bioactivities. In this study, we report the antituberculosis activity of these diterpenoids against both susceptible and resistant strains of M. tuberculosis for the first time. All of the ent-kaurane, kaurane and grayanane diterpenoids showed high to moderate activity against Mycobacterium. The highest antituberculosis activity was observed for ent-1 beta,7 alpha,14 beta-triace-toxykaur-16-en-15-one (cpp604), with MIC values of 0.78, 1.56 and 3.12-12.5 mu g/ml against H37Ra, H37Rv and all other resistant strains of Mycobacterium tuberculosis examined. In addition, other ent-kaurane-type diterpenoids also showed very high activities against mycobacterium, including cpp609 (1.56 mu g/ml), cpp610 (1.56 mu g/ml), cpp601 (3.12-6.25 mu g/ml), cpp602 (3.12-6.25 mu g/ml), cpp607 (3.12-6.25 mu g/ml) and cpp608 (3.12-6.25 mu g/ml). From the structure-activity relationship, functional groups R3 and R5 of the ent-kaurane skeleton were found to modulate the antimycobacterial activity.
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