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碘胺强力定及其相关化合物:一类对组胺H2受体具有高亲和力和选择性的新型配体。

Iodoaminopotentidine and related compounds: a new class of ligands with high affinity and selectivity for the histamine H2 receptor.

作者信息

Hirschfeld J, Buschauer A, Elz S, Schunack W, Ruat M, Traiffort E, Schwartz J C

机构信息

Institute of Pharmacy, Freie Universität Berlin, Germany.

出版信息

J Med Chem. 1992 Jun 12;35(12):2231-8. doi: 10.1021/jm00090a013.

Abstract

The synthesis and biological evaluation of a new class of histamine H2 antagonists with N-cyano-N'-[omega-[3-(1-piperidinylmethyl)phenoxy] alkyl]guanidine partial structure are described as part of an extensive research program to find model compounds for the development of new radioligands with high H2 affinity and specific activity. High receptor affinity is achieved by an additional (substituted) aromatic ring, which is connected with the third guanidine N by a carbon chain spacer and an amine, carboxamide, ester, or sulfonamide link ("polar group"). In functional studies for H2 antagonistic activity and other pharmacological actions [e.g. H1 antihistaminic, antimuscarinic, antiadrenergic (alpha 1, beta 1), 5-HT2 blocking activity] in the isolated guinea pig atrium and ileum and rat aorta and tail artery, the compounds proved to be highly potent and selective histamine H2 receptor antagonists. The H2 antagonistic activity is mainly depending on the length of both the N'-alkyl chain (chain A) and the N"-spacer (chain B). Compounds with a C3 chain A and a C2 chain B are most potent in the preferred group of substances, i.e., the carboxamide series. A wide variety of substituents at the aromatic ring is tolerated, among them iodine, amino, and azido groups. These compounds are up to 32 times more potent than cimetidine in the isolated guinea pig right atrium. The replacement of the carboxamide by an ester group (44c) is well tolerated, while replacement of the cyanoguanidine by an urea group results in nearly 100-fold decrease in activity (46c,e). The iodinated benzamides are among the most potent H2 antagonists known so far. The [125I]-labeled form of 31f ([125I]iodoaminopotentidine, [125I]-N-[2-(4-amino-3-iodobenzamido) ethyl]-N'-cyano-N"-[3-[3-(1-piperidinylmethyl) phenoxy]propyl]guanidine) and its photolabile analogue 31h ([125I]iodoazidopotentidine, [125I]-N-[2-(4-azido-3- iodobenzamido)ethyl]-N'-cyano-N"-[3-[3-(1-piperidinyl-methyl)pheno xy] propyl]guanidine) proved to be useful probes for reversible and irreversible labeling of the histamine H2 receptor. Radioligand binding studies in guinea pig cerebral membranes revealed considerably higher H2 receptor affinity for 31f (pKi = 9.15), 31h (pKi = 8.58), and some analogues than functional experiments (guinea pig atrium), presumably reflecting an easier access to the H2 receptors in membranes.

摘要

作为一项广泛研究计划的一部分,本文描述了一类具有N-氰基-N'-[ω-[3-(1-哌啶基甲基)苯氧基]烷基]胍部分结构的新型组胺H2拮抗剂的合成及生物学评价,该研究计划旨在寻找具有高H2亲和力和比活性的新型放射性配体的模型化合物。通过一个额外的(取代的)芳环实现高受体亲和力,该芳环通过碳链间隔基和胺、羧酰胺、酯或磺酰胺连接键(“极性基团”)与第三个胍氮相连。在分离的豚鼠心房和回肠以及大鼠主动脉和尾动脉中进行的H2拮抗活性和其他药理作用[如H1抗组胺、抗毒蕈碱、抗肾上腺素能(α1、β1)、5-HT2阻断活性]的功能研究中,这些化合物被证明是高效且选择性的组胺H2受体拮抗剂。H2拮抗活性主要取决于N'-烷基链(链A)和N"-间隔基(链B)的长度。在优选的物质组即羧酰胺系列中,具有C3链A和C2链B的化合物活性最强。芳环上可耐受多种取代基,包括碘、氨基和叠氮基。在分离的豚鼠右心房中,这些化合物的活性比西咪替丁高32倍。用酯基取代羧酰胺(44c)耐受性良好,而用脲基取代氰基胍导致活性降低近100倍(46c,e)。碘化苯甲酰胺是迄今为止已知的最有效的H2拮抗剂之一。31f的[125I]标记形式([125I]碘氨基强效替丁,[125I]-N-[2-(4-氨基-3-碘苯甲酰胺基)乙基]-N'-氰基-N"-[3-[3-(1-哌啶基甲基)苯氧基]丙基]胍)及其光不稳定类似物31h([125I]碘叠氮基强效替丁,[125I]-N-[2-(4-叠氮基-3-碘苯甲酰胺基)乙基]-N'-氰基-N"-[3-[3-(1-哌啶基甲基)苯氧基]丙基]胍)被证明是用于组胺H2受体可逆和不可逆标记的有用探针。在豚鼠脑膜中进行的放射性配体结合研究表明,31f(pKi = 9.15)、31h(pKi = 8.58)和一些类似物对H2受体的亲和力比功能实验(豚鼠心房)高得多,这可能反映了在膜中更容易接近H2受体。

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