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 phosphinic pseudo-peptide derivatives for production of a medicament for the selective inhibition of the active C-terminal site of angiotensin converting enzyme (I). Said derivatives are of formula (II), where, Rsb1/sb = optionally a normal protective group for amino functions in peptide chemistry or an amino acid or a peptide protected by the above type of protective group, Rsb2/sb and Rsb3/sb = a natural or synthetic amino acid side chain and Rsb4/sb and Rsb5/sb = a hydrogen atom or a counter-ion. The above finds application in the prevention and treatment of cardiovascular disease in humans.
机译:本发明涉及次膦酸假肽衍生物在制备用于选择性抑制血管紧张素转化酶(I)的活性C-末端位点的药物中的用途。所述衍生物具有式(II),其中R sb 1 =任选地为肽化学中用于氨基官能团的正常保护基或由上述类型的保护基保护的氨基酸或肽, sb> 2 和R 3 =天然或合成的氨基酸侧链,R 4 和R 5 =氢原子或抗衡离子。以上发现在预防和治疗人类心血管疾病中的应用。

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