681179-07-7Relevant academic research and scientific papers
MMPL3 INHIBITORS, COMPOSITIONS AND USES THEREOF
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Paragraph 0210; 0211, (2020/06/10)
Disclosed are inhibitors of mycobacterial membrane protein MmpL3, compositions comprising the inhibitors, and methods of preparation and use thereof.
Bioisosteric replacement of the pyrazole 3-carboxamide moiety of rimonabant. A novel series of oxadiazoles as CB1 cannabinoid receptor antagonists
Chu, Cheng-Ming,Hung, Ming-Shiu,Hsieh, Min-Tsang,Kuo, Chun-Wei,Suja,Song, Jen-Shin,Chiu, Hua-Hao,Chao, Yu-Sheng,Shia, Kak-Shan
experimental part, p. 3399 - 3407 (2009/02/05)
Based on the bioisosteric replacement of the pyrazole C3-carboxamide of rimonabant with a 5-alkyl oxadiazole ring, a novel class of oxadiazole derivatives with promising biological activity towards CB1 receptors was discovered. Among them, compounds with an alkyl linker containing a strong electron-withdrawing group (e.g., CF3) and a sterically favorable bulky group (e.g., t-butyl) exhibited excellent CB1 antagonism and selectivity, and thus might serve as potential candidates for further development as anti-obesity agents.
(1,5-DIPHENYL-1H-PYRAZOL-3-YL)OXADIAZOLE DERIVATIVES, PREPARATION METHOD THEREOF AND USE OF SAME IN THERAPEUTICS
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Page/Page column 23, (2008/06/13)
The invention relates to compounds having formula (I): Wherein R1, R2, R3 and R4 are as defined herein. The invention also relates to a method of preparing said compounds and to the application thereof in therapeutics.
Tetrazole-biarylpyrazole derivatives as cannabinoid CB1 receptor antagonists
Kang, Suk Youn,Lee, Sung-Han,Seo, Hee Jeong,Jung, Myung Eun,Ahn, Kwangwoo,Kim, Jeongmin,Lee, Jinhwa
, p. 2385 - 2389 (2008/09/20)
Cannabinoid CB1 receptors have been the focus of extensive studies since the first clinical results of rimonabant (SR141716) for the treatment of obesity and related metabolic disorders were reported in 2001. To further evaluate the properties of CB recep
Cannabinoid receptor ligands and uses thereof
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, (2008/06/13)
Compounds of Formula (I) that act as cannabinoid receptor ligands and their uses in the treatment of diseases linked to the modulation of the cannabinoid receptors in animals are described herein.
