Synthesis of (+)-7,20-Diisocyanoadociane and Liver-Stage Antiplasmodial Activity of the Isocyanoterpene Class-Reference-Cited by-同舟云学术

Synthesis of (+)-7,20-Diisocyanoadociane and Liver-Stage Antiplasmodial Activity of the Isocyanoterpene Class

Published:2016-05-31 Issue:23 Volume:138 Page:7268-7271
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Lu Hai-Hua¹,Pronin Sergey V.¹,Antonova-Koch Yevgeniya²,Meister Stephan²,Winzeler Elizabeth A.²,Shenvi Ryan A.¹

Affiliation:

1. Department of Chemistry, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, United States

2. Department of Pediatrics, University of California, San Diego, School of Medicine, 9500 Gilman Drive 0741, La Jolla, California 92093, United States

Funder

Novartis

Alfred P. Sloan Foundation

Donald E. and Delia B. Baxter Foundation

Amgen

Bristol-Myers Squibb

Boehringer Ingelheim

National Institute of General Medical Sciences

Eli Lilly and Company

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.6b03899

Reference46 articles.

1. Syntheses and biological studies of marine terpenoids derived from inorganic cyanide

2. Marine Isonitriles and Their Related Compounds

3. Naturally occurring isocyanides

4. Antimalarial Activity of Sesquiterpenes from the Marine Sponge Acanthella klethra

5. Novel Potent Antimalarial Diterpene Isocyanates, Isothiocyanates, and Isonitriles from the Tropical Marine Sponge Cymbastela hooperi

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