Biselyngbyasides, cytotoxic marine macrolides, are novel and potent inhibitors of the Ca2+pumps with a unique mode of binding-Reference-Cited by-同舟云学术

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Biselyngbyasides, cytotoxic marine macrolides, are novel and potent inhibitors of the Ca2+pumps with a unique mode of binding

Published:2015-05-06 Issue:13 Volume:589 Page:1406-1411
ISSN:0014-5793
Container-title:FEBS Letters
language:en
Short-container-title:

Author:

Morita Maho,Ogawa Haruo,Ohno Osamu,Yamori Takao,Suenaga Kiyotake,Toyoshima Chikashi

Funder

Ministry of Education, Culture, Sports, Science, and Technology

Publisher

Wiley

Subject

Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology,Biophysics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1016/j.febslet.2015.04.056/fullpdf

Reference40 articles.

1. Drug development from marine natural products;Molinski;Nat. Rev. Drug Discovery,2009

2. Natural product and natural product derived drugs in clinical trials;Butler;Nat. Prod. Rep.,2014

3. Natural products in medicine: transformational outcome of synthetic chemistry;Szychowski;J. Med. Chem.,2014

4. Impact of natural products on developing new anti-cancer agents;Cragg;Chem. Rev.,2009

5. Biselyngbyaside, a macrolide glycoside from the marine cyanobacterium Lyngbya sp;Teruya;Org. Lett.,2009

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