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Substituted indole compounds with Inhibitory activity of nos. Pharmaceutical compositions.

机译:具有抑制活性nos的取代的吲哚化合物。药物组合物。

摘要

Pharmaceutical compositions containing same.Claim 1: a compound with the formula (1), or one of its pharmaceutically acceptable salts or prodrugs, where r1es h, alkyl, optionally substituted C1 - 6, alcarilo c1-4 optionally replaced, or alcaheterociclilo c1-4 optionally substituted; each of R2 and R3 is independent. Consequence, Hal h, alkyl, optionally substituted aryl C1 - C6 6 - 10, optionally substituted,Alcarilo C1 - C2 - 4 heterociclilo optionally substituted, optionally replaced with Bridge 9, alcaheterociclilo c1-4 optionally replaced with a Bridge, heterociclilo C2 - 9 optionally replaced, or alcaheterociclilo c1-4 optionally substituted; each R4 and R7 is independently h, F, alkyl or alkoxy C1 C1 - 6 - 6; R5 is H, r5ac (NH) NH (CH2) R5 or r5anhc (S) NH (CH2) R5,Wherein R5 is an integer from 0 to 2, r5a is C1 - 6 optionally substituted alkyl, optionally substituted aryl c6-10 alcarilo C1, C2 - 4 - 9 heterociclilo optionally substituted, optionally substituted, optionally substituted alcaheterociclilo c1-4, tioalcoxi C1 - 6 optionally replaced, tioal Carilo c1-4 optionally replaced,Ariloilo optionally replaced tioalcaheterociclilo c1-4 or optionally substituted; and R6 H or r6ac (NH (CH2) or r6anhc R6 (S) NH (CH2) R6, wherein R6 is an integer from 0 to 2, r6a is C1 - 6 optionally substituted alkyl, optionally substituted aryl c6-10, alcarilo C1 4 - optionally replaced, I Terociclilo C2 - 9 optionally replaced, alcaheterociclilo c1-4 optionally replaced,Tioalcoxi C1 - 6 optionally replaced, tioalcarilo c1-4 ariloilo optionally substituted, optionally substituted, or tioalcaheterociclilo c1-4 optionally substituted; where one, but not both, R5 and R6 H.
机译:1。具有式(1)的化合物或其药学上可接受的盐或前药之一,其中r 1为h,烷基,任选取代的C 1-6,alcarilo c1-4任选取代的或alcaheterociclilo c1- 4个可选取代的; R2和R3各自独立。结果,Halh,烷基,任选取代的芳基C1-C6 6-10,任选取代,Alcarilo C1-4-2-4杂取代基,任选被桥9取代,alcaheterociclilo c1-4任选被取代,杂桥C2-9任选取代,或alcaheterociclilo c1-4任选取代;每个R 4和R 7独立地为h,F,烷基或烷氧基C 1 -C 6-6; R5为H,r5ac(NH)NH(CH2)R5或r5anhc(S)NH(CH2)R5,其中R5为0至2的整数,r5a为C1-6任选取代的烷基,任选取代的芳基c6-10烷基C1,C2-4-9杂取代基,任选取代,任选取代,任选取代的alcaheterociclilo c1-4,tioalcoxi C1-6任选取代,tioal Carilo c1-4任选取代,Ariloilo任选取代tioalcaheterociclilo c1-4或任选取代; R6 H或r6ac(NH(CH2)或r6anhc R6(S)NH(CH2)R6,其中R6是0到2的整数,r6a是C1-6可选取代的烷基,可选取代的芳基c6-10,芳基C1 4-可选取代,I Terociclilo C2-9可选取代,alcaheterociclilo c1-4可选取代,噻唑烷C1-6可选取代,tioalcarilo c1-4 ariloilo可选取代,可选取代,或tioalcaheterociclilo c1-4可选取代;其中一个,但不仅是R5和R6H。

著录项

  • 公开/公告号AR055053A1

    专利类型

  • 公开/公告日2007-08-01

    原文格式PDF

  • 申请/专利权人 NEURAXON INC;

    申请/专利号AR2006P101505

  • 发明设计人

    申请日2006-04-17

  • 分类号C07D209/40;C07D409/12;C07D409/14;C07D405/14;C07D401/04;C07D451/02;C07D453/02;C07D471/04;A61K31/404;A61P25/00;

  • 国家 AR

  • 入库时间 2022-08-21 20:59:36

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