Chemical Synthesis Enables Structural Reengineering of Aglaroxin C Leading to Inhibition Bias for Hepatitis C Viral Infection-Reference-Cited by-同舟云学术

Chemical Synthesis Enables Structural Reengineering of Aglaroxin C Leading to Inhibition Bias for Hepatitis C Viral Infection

Published:2018-12-27 Issue:3 Volume:141 Page:1312-1323
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Zhang Wenhan¹,Liu Shufeng²,Maiga Rayelle I.,Pelletier Jerry,Brown Lauren E.¹^ORCID,Wang Tony T.²,Porco John A.¹^ORCID

Affiliation:

1. Department of Chemistry, Center for Molecular Discovery (BU-CMD), Boston University, Boston, Massachusetts 02215, United States

2. Laboratory of Vector-Borne Viral Diseases, Division of Viral Products, Center for Biologics Evaluation and Research, U.S. Food and Drug Administration, Silver Spring, Maryland 20903, United States

Funder

Canadian Institutes of Health Research

National Institute of Diabetes and Digestive and Kidney Diseases

National Institute of General Medical Sciences

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.8b11477

Reference91 articles.

1. X-Ray crystal structure of rocaglamide, a novel antileulemic 1H-cyclopenta[b]benzofuran from Aglaia elliptifolia

2. Isolation and X-ray structure determination of a novel pyrimidinone from Aglaia odorata

3. Cyclopentabenzofuran Lignan Protein Synthesis Inhibitors from Aglaia odorata

4. Insecticidal rocaglamide derivatives from Aglaia duppereana

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