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Inhibitors of invertase in vascular diseases and addictive salts without spermatic acid, their preparation procedures and drug synthesis containing such substances

机译:血管疾病中的转化酶抑制剂和不含精氨酸的成瘾性盐,其制备方法和含有此类物质的药物合成

摘要

A formula compound (I),Among them, a is an inhibitor of angiosin converting enzyme with basic separable function; B is a compound with effective function matching a group of non donors; m is the number of acid functions separated from B and N, which is the number of basic functions separated from a; a is the number of formula (II).Wherein R1 is h, or tar (C1-C6);R2 is asphalt (C1-C6) or arilalquilo (C1-C6);R3 means lease (C1-C6) or lease (C1-C6);(I) preferably pyridine glycol, peroxide glycol, pyridine. The most popular compounds are: acid (2S) - 2 - [(3 - [5-oxide-4 - (phenylsulfonyl) - 1,2,5-oxadiazol-3-il] - oxi} - propionil) - amine] - scientific acid (2S, 3a, 7a) - 1 - [(2S) - 2 - [(1s) - 2 - [(1s) - butil] - amine] - propionil] - octahydroAcido (2S) - 2 - [(3 - [5-oxido-4 - (phenylsulfonyl-1,2,5-oxadiazol-3-il] - oxi} - propionil) - amine] - pentanodio acido (2S, 3a, 7a) - 1 - [(2S) - 2 - [(1s) - 1 - (toxic butil] - amine} - propionil] - octahydro-1There are others He also mentioned a way to prepare for drug synthesis. This ingredient is useful in the treatment of hypertension and cardiovascular disease.
机译:在式(I)化合物中,a是具有基本可分离功能的血管紧张素转化酶的抑制剂。 B是具有与非供体基团匹配的有效功能的化合物; m是从B和N分离的酸官能团的数目,是从a分离的碱性官能团的数目; a是式(II)的数字,其中R1是h或tar(C1-C6); R2是沥青(C1-C6)或阿里拉基洛(C1-C6); R3表示租赁(C1-C6)或租赁( C1-C6);(I)优选吡啶二醇,过氧化物二醇,吡啶。最受欢迎的化合物为:酸(2S)-2-[(3-[5-氧化物4-(苯磺酰基)-1,2,5-恶二唑-3-il]-氧}-丙腈)-胺]-科学酸(2S,3a,7a)-1-[[(2S)-2-[(1s)-2-[(1s)-丁醇]-胺]-丙腈]-八氢乙酰基(2S)-2-[[(3 -[5-氧化-4---(苯磺酰基-1,2,5-恶二唑-3-il]-氧化}-丙腈)-胺]-戊二酸(2S,3a,7a)-1-[((2S)- 2-[(1s)-1-(有毒的丁腈]-胺}-丙腈]-octahydro-1他还提到了其他制备药物的方法,该成分可用于治疗高血压和心血管疾病。

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