首页> 外国专利> Polypeptide compounds useful for the treatment of microbial Infections, Process for preparing them,Compositions that include Drugs and the use of such compounds and Method for prophylactic and therapeutic Treatment of infections

Polypeptide compounds useful for the treatment of microbial Infections, Process for preparing them,Compositions that include Drugs and the use of such compounds and Method for prophylactic and therapeutic Treatment of infections

机译:可用于治疗微生物感染的多肽化合物,其制备方法,包括药物的组合物以及此类化​​合物的用途以及预防和治疗感染的方法

摘要

This polypeptide compounds represented by the General formula (i) wherein: R1 is Hydrogen; arilamino alcanoilo (Lower) can have one or more appropriate Substituent (S) (S); aroilo replacementGone with a group that can teneruno Heterocyclic Substituent (S) or right (S); aroilo substituted alkyl conarilo has higherAroilo substituted aryl alkyl aryl is lower: alcanoilo (C2 - 6) has alquiloinferior substituted with aryl,Alcanoilo Lower unsaturated Heterocyclic condensate sustituidocon Group can have one or more appropriate Substituent (S) (S); alcanoiloinferior substituted piridilo can have one or moreAppropriate Substituent (S) (S) amino Group hexilnaftoilo, heptilnaftoilo protector;Aroilosustituido with carbamoilo can have one or more Heterocyclic Substituent (S) (S) alcanoilo replaced with lower Cycle (Lower alkyl) may have one or more Substituent (S)Right (S); alcanoiloinferior is replaced with tienilo Group that can teneruno Heterocyclic Substituent (S) or right (S); or alquenoilo Lower substituted Heterocyclic Group thatYou can have one or more appropriate Substituent (S) (S) r2es; R3 is Hydrogen, Hydroxy, alkoxy or Hydroxy, hidroxisulfoniloxi Lower.Hydroxy or alkoxy and R4 is lower, or one of its Salts which have actividadesantimicrobianas (especially Antifungal Activities), Inhibitory activity on 1,3 glucan synthase.Seproponen also the preparation of the same and / or Pharmaceutical compositions and Methods for the therapeutic or prophylactic Treatment of Infectious DiseasesDepneumocystis carinil including infection (e.g. carinil Pneumocystis pneumonia in humans and animals.
机译:该多肽化合物由通式(i)表示,其中:R1是氢; arilamino alcanoilo(低级)可以具有一种或多种合适的取代基(S)(S); aroilo替换与可以teneruno杂环取代基(S)或右(S)的基团一起消失;芳基取代的烷基芳基具有较高的芳基取代的芳基烷基芳基较低:芳基(C2-6)的亚芳基被芳基取代,Alcanoilo低级不饱和杂环缩合物sustituidocon基团可以具有一个或多个合适的取代基(S)(S); alcanoilo亚取代基的piridilo可以具有一个或多个合适的取代基(S)(S)氨基hexilnaftoilo,heptilnaftoilo保护基;具有carbamoilo的Arustosustituido可以具有一个或多个杂环取代基(S)(S)Alcanoilo被较低的环取代(低级烷基)或更多替代品(S)权利(S); alcanoiloinferior替换为tennuno杂环取代基(S)或右(S)的tienilo组;或alquenoilo低级取代杂环基团,您可以具有一个或多个合适的取代基(S)(S)r2es; R3是氢,羟基,烷氧基或羟基,羟基磺酰氨基低级化合物。羟基或烷氧基和R4是较低级的,或其盐之一具有活化的抗菌剂(特别是抗真菌活性),对1,3葡聚糖合酶具有抑制活性。用于感染性疾病的治疗或预防的相同和/或药物组合物和方法以及包括感染在内的卡氏肺孢子虫(例如人和动物卡氏肺孢子虫肺炎)。

著录项

  • 公开/公告号AR014554A1

    专利类型

  • 公开/公告日2001-02-28

    原文格式PDF

  • 申请/专利权人 FUJISAWA PHARMACEUTICAL CO. LTD.;

    申请/专利号AR1999P100549

  • 发明设计人

    申请日1999-02-09

  • 分类号C07K7/50;A61K38/12;

  • 国家 AR

  • 入库时间 2022-08-22 01:26:21

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