Structure–activity studies of the pelorusides: new congeners and semi-synthetic analogues-Reference-Cited by-同舟云学术

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Structure–activity studies of the pelorusides: new congeners and semi-synthetic analogues

Published:2011 Issue:12 Volume:9 Page:4456
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Singh A. Jonathan,Razzak Mina,Teesdale-Spittle Paul,Gaitanos Thomas N.,Wilmes Anja,Paterson Ian,Goodman Jonathan M.,Miller John H.,Northcote Peter T.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2011/OB/C0OB01127D

Reference24 articles.

1. Peloruside A: A Potent Cytotoxic Macrolide Isolated from the New Zealand Marine Sponge Mycale sp.

2. Peloruside A Does Not Bind to the Taxoid Site on β-Tubulin and Retains Its Activity in Multidrug-Resistant Cell Lines

3. Synergistic Effects of Peloruside A and Laulimalide with Taxoid Site Drugs, but Not with Each Other, on Tubulin Assembly

4. Peloruside A Synergizes with Other Microtubule Stabilizing Agents in Cultured Cancer Cell Lines

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1. Chemical and biological diversity of new natural products from marine sponges: a review (2009–2018);Marine Life Science & Technology;2022-08-01

2. Natural chemical control of marine associated microbial communities by sessile Antarctic invertebrates;Aquatic Microbial Ecology;2020-12-03

3. Mitotic Poisons in Research and Medicine;Molecules;2020-10-12

4. Peloruside E (22-Norpeloruside A), a Pelorusane Macrolide from the New Zealand Marine Sponge Mycale hentscheli, Retains Microtubule-Stabilizing Properties;Journal of Natural Products;2018-09-06

5. Chemistry and Biological Activities of the Marine Sponges of the Genera Mycale (Arenochalina), Biemna and Clathria;Marine Drugs;2018-06-18

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