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苯二氮䓬类药物与其外周型位点结合的结构要求。

Structural requirements for the binding of benzodiazepines to their peripheral-type sites.

作者信息

Wang J K, Taniguchi T, Spector S

出版信息

Mol Pharmacol. 1984 May;25(3):349-51.

PMID:6328261
Abstract

The DS19 Friend erythroleukemia cells possess peripheral-type benzodiazepine recognition sites that are similar to those characterized in other tissues and cells. These sites recognize only specific and well-defined ligand structures. In order for the benzodiazepines to bind to these sites, an alkyl group of 3 carbons or less is required at position 1, together with a carbonyl group at position 2. In addition, the binding affinity is enhanced by 4'-halogen or 4'-methoxy substituents, and by 7- or 2'-halogens. However, the affinity is decreased by substitutions at position 3 or 4. Central-type benzodiazepine binding in brain, on the other hand, is not affected by 1-alkyl groups and is inhibited by 4'-substitutions. Furthermore, unlike the peripheral-type site, the brain receptor is stereo-selective. These results demonstrate that the two binding sites are fundamentally different in their recognition of benzodiazepine ligands.

摘要

DS19 友系红白血病细胞具有外周型苯二氮䓬识别位点,这些位点与其他组织和细胞中所描述的位点相似。这些位点仅识别特定且明确的配体结构。为使苯二氮䓬与这些位点结合,在第1位需要有3个或更少碳原子的烷基,同时在第2位需要有羰基。此外,4'-卤素或4'-甲氧基取代基以及7-或2'-卤素会增强结合亲和力。然而,在第3位或第4位进行取代会降低亲和力。另一方面,脑中的中枢型苯二氮䓬结合不受1-烷基的影响,而受4'-取代的抑制。此外,与外周型位点不同,脑受体具有立体选择性。这些结果表明,这两种结合位点在识别苯二氮䓬配体方面存在根本差异。

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