首页> 外国专利> PHOSPHINIC PSEUDO-PEPTIDE DERIVATIVES FOR SELECTIVE INHIBITION OF THE ACTIVE C-TERMINAL SITE OF ANGIOTENSIN CONVERTING ENZYME (I) (ACE)

PHOSPHINIC PSEUDO-PEPTIDE DERIVATIVES FOR SELECTIVE INHIBITION OF THE ACTIVE C-TERMINAL SITE OF ANGIOTENSIN CONVERTING ENZYME (I) (ACE)

机译:用于选择性抑制血管紧张素转化酶(I)(ACE)的活性C末端位点的磷肽肽衍生物

摘要

The invention relates to the use of phosphine pseudo-peptide derivatives for the preparation of a medicament capable of selectively inhibiting the C-terminal active site of the angiotensin I converting enzyme. These derivatives respond to the following formula: (1) in which: - R1 may be a usual protective group of the amine functions in peptide chemistry, or an amino acid or a peptide protected by this same type of protective groups s, - R2 and R3 correspond to a chain lateral of natural or unnatural amino acid, and- R4 and R5 represent a hydrogen atom or a counterion. Applications: prevention and treatment of cardiovascular pathologies in humans.
机译:本发明涉及膦假肽衍生物在制备能够选择性抑制血管紧张素I转化酶的C-末端活性位点的药物中的用途。这些衍生物响应下式:(1)其中:-R1可以是肽化学中氨基官能团的常用保护基团,或者是氨基酸或被该相同类型的保护基团s保护的肽,-R2和R 3对应于天然或非天然氨基酸的侧链,并且-R 4和R 5代表氢原子或抗衡离子。应用:预防和治疗人类心血管疾病。

著录项

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号