| Literature DB >> 28335606 |
Russell B Williams1, Steven M Martin1, Julie A Lawrence1, Vanessa L Norman1, Mark O'Neil-Johnson1, Gary R Eldridge1, Courtney M Starks1.
Abstract
The pursuit of structurally novel compounds has led to the isolation of a series of neolignans (2-6), for which the structures have been determined from microgram quantities using microcryoprobe NMR technology. Compounds 2-6 provided some unexpectedly clear structure-activity relationship data, with compound 2 demonstrating significantly more potency in the in vitro cytotoxicity assay than the other analogues. Further screening found that compound 2 induces apoptosis with activation of caspase 3/7. The NCI Compare algorithm suggested that compound 2 acts through the inhibition of tubulin/microtubule dynamics. Compound 2 was confirmed to be a tubulin polymerization inhibitor that binds directly to tubulin.Entities:
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Year: 2016 PMID: 28335606 DOI: 10.1021/acs.jnatprod.6b00893
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050