Design, synthesis, and structure–activity relationships of 1,3,4-oxadiazol-2(3H)-ones as novel FAAH inhibitors-Reference-Cited by-同舟云学术

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Design, synthesis, and structure–activity relationships of 1,3,4-oxadiazol-2(3H)-ones as novel FAAH inhibitors

Published:2011 Issue:9 Volume:2 Page:889
ISSN:2040-2503
Container-title:MedChemComm
language:en
Short-container-title:Med. Chem. Commun.

Author:

Kiss László E.,Ferreira Humberto S.,Beliaev Alexandre,Torrão Leonel,Bonifácio Maria João,Learmonth David A.

Publisher

Royal Society of Chemistry (RSC)

Subject

Pharmaceutical Science,Biochemistry,Drug Discovery,Molecular Medicine,Pharmacology,Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2011/MD/C1MD00136A

Reference12 articles.

1. STRUCTURE AND FUNCTION OF FATTY ACID AMIDE HYDROLASE

2. Molecular characterization of an enzyme that degrades neuromodulatory fatty-acid amides

3. Fatty acid amide hydrolase: an emerging therapeutic target in the endocannabinoid system

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1. Theoretical Studies on Pd-catalyzed Oxidative N-H Carbonylation to Synthesis of 1,3,4-Oxadiazole-2(3H)-one Heterocyclic Compounds;CHEM J CHINESE U;2021

2. Regulatory safety pharmacology evaluation of BIA 10-2474;Journal of Pharmacological and Toxicological Methods;2020-03

3. Preclinical pharmacological evaluation of the fatty acid amide hydrolase inhibitor BIA 10‐2474;British Journal of Pharmacology;2020-02-12

4. A perspective review on fatty acid amide hydrolase (FAAH) inhibitors as potential therapeutic agents;European Journal of Medicinal Chemistry;2020-02

5. Synthesis of Oxadiazolones with Hydrazides: The Mechanism and the Sensing Application as Sensitive, Rapid, and Visual Fluorescent Sensors for Phosgene;Organic Letters;2019-11-13

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