[EN] THERAPEUTIC RELEASE AGENTS<br/>[FR] AGENTS DE LIBÉRATION THÉRAPEUTIQUES
申请人:ORGANON NV
公开号:WO2008100977A2
公开(公告)日:2008-08-21
[EN] Pharmacological inhibition of fatty acid amide hydrolase (FAAH) activity leads to increased levels of fatty acid amides. Esters of alkylcarbamic acids are disclosed that are inhibitors of FAAH activity. Compounds disclosed herein inhibit FAAH activity. Described herein are processes for the preparation of esters of alkylcarbamic acid compounds, compositions that include them, and methods of use thereof. [FR] L'inhibition pharmacologique de l'activité de l'amide hydrolase d'acides gras (FAAH) entraîne une augmentation des taux d'amides d'acides gras. L'invention concerne des esters d'acides alkylcarbamiques qui constituent des inhibiteurs de l'activité de la FAAH. Les composés décrits inhibent l'activité de la FAAH. L'invention concerne aussi des procédés de préparation d'esters de composés d'acides alkylcarbamiques, des compositions renfermant ceux-ci et des procédés d'utilisation de celles-ci.
Torosachrysone and physcion gentiobiosides from the seeds of Cassia torosa.
作者:SUSUMU KITANAKA、MICHIO TAKIDO
DOI:10.1248/cpb.32.3436
日期:——
Torosachrysone 8-β-D-gentiobioside (1) and physcion 8-β-D-gentiobioside (2) were isolated along with protocatechuic acid from the unripe and ripe seeds of Cassia torosa CAVANILLES, respectively. The structure of 1 was established on the basis of chemical and spectroscopic findings. In addition, the 13C nuclear magnetic resonance spectra of torosachrysone and related compounds are discussed.
Abstract A new anthraquinone diglucoside isolated fromRhamnus virgata has been shown to be physcion-8- O -β-gentiobioside on the basis of spectral and other evidence.