Exploiting Enzymatic Promiscuity to Engineer a Focused Library of Highly Selective Antifungal and Antiproliferative Aureothin Analogues-Reference-Cited by-同舟云学术

Exploiting Enzymatic Promiscuity to Engineer a Focused Library of Highly Selective Antifungal and Antiproliferative Aureothin Analogues

Published:2010-07-13 Issue:30 Volume:132 Page:10407-10413
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Werneburg Martina¹,Busch Benjamin¹,He Jing¹,Richter Martin E.A.¹,Xiang Longkuan¹,Moore Bradley S.¹,Roth Martin¹,Dahse Hans-Martin¹,Hertweck Christian¹

Affiliation:

1. Leibniz Institute for Natural Product Research and Infection Biology, HKI, Dept. of Biomolecular Chemistry, Beutenbergstr. 11a, 07745 Jena, Germany, the Friedrich Schiller University, Jena, Germany, and the Scripps Institution of Oceanography and Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California at San Diego, La Jolla, California, 92093-0204

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja102751h

Reference53 articles.

1. Natural Products as Sources of New Drugs over the Last 25 Years

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