Semi-synthetic modification of nimbolide to 6-homodesacetylnimbin and 6-desacetylnimbin and their cytotoxic studies

被引:6
作者
Anitha, G.
Raj, J. Josepha Lourdu
Krishnan, V. Radha
Narasimhan, S.
Solomon, K. Anand
Rajan, S. S.
机构
[1] Asthagiri Herbal Res Fdn, Madras 600059, Tamil Nadu, India
[2] Univ Madras, Dept Crystallog & Biophys, Madras 600032, Tamil Nadu, India
关键词
6-homodesacetyinimbin; nimbolide; 6-desacetylnimbin; Ti((OPr)-O-i)(4); brine shrimp;
D O I
10.1080/10286020500383742
中图分类号
Q94 [植物学];
学科分类号
071001 [植物学];
摘要
A new C-seco tetranortriterpenorid named as 6-homodesacetylnimbin 2, has been synthesised for the first time through semi-synthetic modification of nimbolide 1, a potent molecule with anticancer activity. Attempts were made to transesterify the -COOMe moiety in nimbolide using titanium (IV) isopropoxide and ethanol so as to obtain a molecule with -COOEt moiety. However, a novel product was envisaged during the course of the reaction, which was identified as 6-homodesacetylnimbin, a higher homologue of 6-desacetylnimbin 3 through spectroscopic and crystallographic methods. Also, 6-desacetylnimbin has been synthesised through acid hydrolysis of nimbolide. The compounds were screened for their cytotoxic properties through brine shrimp lethality bioassay method using Artemia salina.
引用
收藏
页码:73 / 78
页数:6
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