Journal of Medicinal Chemistry, volume 23, issue 5, pages 546-549

Structure-antitubulin activity relationships in steganacin congeners and analogs. Inhibition of tubulin polymerization in vitro by (.+-.)-isodeoxypodophyllotoxin

Flora Zavala
Daniel Guénard
Jean Pierre Robin
Eric Brown
Publication typeJournal Article
Publication date1980-05-01
scimago Q1
wos Q1
SJR1.986
CiteScore12.8
Impact factor6.8
ISSN00222623, 15204804
PubMed ID:  7381854
Drug Discovery
Molecular Medicine
Abstract
A new series of 23 synthetic analogues of the naturally occurring antitumor lignan steganacin was tested for the inhibition of microtubule assembly in vitro. Interestingly, (+/-)-isopicrostegane (I50 = 5 microM) was found to be almost as active as (+/-)-steganacin(I50 = 3.5 microM). On the other hand, racemic isodeoxypodophyllotoxin has an inhibiting activity of microtubule assembly comparable to that of (-)-podophyllotoxin, whereas (-)-isodeoxypodophyllotoxin is totally inactive.
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