Synthesis, Structure–Activity Relationship Studies, and Antibacterial Evaluation of 4-Chromanones and Chalcones, as Well as Olympicin A and Derivatives-Reference-Cited by-同舟云学术

Synthesis, Structure–Activity Relationship Studies, and Antibacterial Evaluation of 4-Chromanones and Chalcones, as Well as Olympicin A and Derivatives

Published:2014-10-07 Issue:20 Volume:57 Page:8398-8420
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Feng Li¹,Maddox Marcus M.²,Alam Md. Zahidul³,Tsutsumi Lissa S.¹,Narula Gagandeep⁴,Bruhn David F.²,Wu Xiaoqian³,Sandhaus Shayna⁴,Lee Robin B.²,Simmons Charles J.⁵,Tse-Dinh Yuk-Ching⁴,Hurdle Julian G.³,Lee Richard E.²,Sun Dianqing¹

Affiliation:

1. Department of Pharmaceutical Sciences, The Daniel K. Inouye College of Pharmacy, University of Hawai’i at Hilo, 34 Rainbow Drive, Hilo, Hawaii 96720, United States

2. Department of Chemical Biology and Therapeutics, St. Jude Children’s Research Hospital, Memphis, Tennessee 38105, United States

3. Department of Biology, University of Texas at Arlington, Arlington, Texas 76019, United States

4. Department of Chemistry & Biochemistry, Biomolecular Sciences Institute, Florida International University, Miami, Florida 33199, United States

5. Department of Chemistry, University of Hawai’i at Hilo, Hilo, Hawaii 96720, United States

Funder

National Center for Complementary and Alternative Medicine

National Institute of Allergy and Infectious Diseases

Hawaii Community Foundation

National Institute of General Medical Sciences

American Lebanese Syrian Associated Charities

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm500853v

Reference79 articles.

1. Antimicrobial activity of flavonoids

2. Natural Products, Small Molecules, and Genetics in Tuberculosis Drug Development

3. Where will new antibiotics come from?

4. Advancing chemistry and biology through diversity-oriented synthesis of natural product-like libraries

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