首页> 外国专利> CYCLIC DEPSIPEPTIDES FROM ISOLATED CHONDROMYCES CROCATUS USEFUL AS INHIBITORS OF KALLIKREIN 7 AND HUMAN NEUTROPHIL ELASTASE

CYCLIC DEPSIPEPTIDES FROM ISOLATED CHONDROMYCES CROCATUS USEFUL AS INHIBITORS OF KALLIKREIN 7 AND HUMAN NEUTROPHIL ELASTASE

机译:分离的软骨细胞中的环二肽可用作激肽释放酶7和人中性粒细胞弹性蛋白酶的抑制剂

摘要

Disclosed herein is a cyclic depsipeptide having the structure of formula (I), wherein an ester bond is formed between the carboxy group of A7 and the hydroxyl group of A2, wherein the acyl residue X is CH3CH2CH(CH3)CO or (CH3)2CHCO, A1 is glutamine, glutamic acid, or a derivative thereof, A2 is threonine,A3 is leucine, A4 is Ahp, 3-amino-piperidine-2-one, proline, 5-hydroxy-proline or a derivative thereof, A5 is isoleucine, A6 is tyroxine, N-Me-tyrosine or a derivative thereof, A7 is isoleucine or valine;or a pharmaceutically acceptable salt thereof. Also disclosed is the extraction of said compound from isolated Chondromyces microorganism from the strain Chrondromyces crocatus (DSM 19329) as well as an alternative process for its preparation.
机译:本文公开了具有式(I)结构的环状二肽,其中在A7的羧基和A2的羟基之间形成酯键,其中酰基残基X为CH 3 CH 2 CH(CH 3)CO或(CH 3)2 CHCO。 ,A1是谷氨酰胺,谷氨酸或其衍生物,A2是苏氨酸,A3是亮氨酸,A4是Ahp,3-氨基-哌啶-2-酮,脯氨酸,5-羟基脯氨酸或其衍生物,A5是异亮氨酸,A6是酪氨酸,N-Me-酪氨酸或其衍生物,A7是异亮氨酸或缬氨酸;或其药学上可接受的盐。还公开了从分离的克氏梭菌(Chrondromyces crocatus)菌株(DSM 19329)中的分离的软骨细胞微生物中提取所述化合物,以及其制备的替代方法。

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