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 type: Journal Article
Publication date: 1980-05-01
Journal:
Journal of Medicinal Chemistry
scimago Q1
wos Q1
SJR: 1.986
CiteScore: 12.8
Impact factor: 6.8
ISSN: 00222623, 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.
Found
Are you a researcher?
Create a profile to get free access to personal recommendations for colleagues and new articles.