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Synthesis and biological evaluation of 10, 11-Dihydrodictyostatin, a potent analogue of the marine anticancer agent dictyostatin

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Date Issued:
2008
Title: Synthesis and biological evaluation of 10, 11-Dihydrodictyostatin, a potent analogue of the marine anticancer agent dictyostatin.
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Name(s): Paterson, Ian, creator
Gardner, Nicola M., creator
Poullennec, Karine G., creator
Wright, Amy E., creator
Type of Resource: text
Genre: Article
Issuance: single unit
Date Issued: 2008
Publisher: The American Chemical Society and American Society of Pharmacognosy
Extent: 7 p.
Physical Description: pdf
Language(s): English
Identifier: 3333013 (digitool), FADT3333013 (IID), fau:6209 (fedora), 10.1021/np070547s (doi)
Note(s): By employing a diverted total synthesis strategy with late-stage intermediates, 10,11-dihydrodictyostatin ( 5) was prepared and evaluated in vitro for growth inhibition against a range of human cancer cell lines, including the NCI/ADR Taxol-resistant cell line. This novel dictyostatin analogue was found to retain potent antimitotic activity, with a comparable profile to discodermolide and Taxol, functioning by microtubule stabilization and G2/M arrest. These SAR studies provide further insight into the interaction between dictyostatin ( 1) and its tubulin target.
This document is the accepted manuscript version of a published work that appeared in final form in Journal of Natural Products after peer review and technical editing by the publisher. To access the final edited and published work see http://dx.doi.org/10.1021/np070547s. This article may be cited as: Paterson, I., Gardner, N. M., Poullennec, K. G., & Wright, A. E. (2008). Synthesis and biological evaluation of 10, 11-Dihydrodictyostatin, a potent analogue of the marine anticancer agent dictyostatin. Journal of Natural Products, 71(3), 364-369. doi:10.1021/np070547s
Florida Atlantic University. Harbor Branch Oceanographic Institute contribution #1775.
Subject(s): Macrolides
Antineoplastic agents
Biological evaluation
Synthesis
Antimitotic agents
Persistent Link to This Record: http://purl.flvc.org/FCLA/DT/3333013
Links: http://dx.doi.org/10.1021/np070547s
Restrictions on Access: ©2008 The American Chemical Society and American Society of Pharmacognosy
Host Institution: FAU