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Synthesis and Characterization of the Selective, Reversible PKCβ Inhibitor (9 S)-9-[(Dimethylamino)methyl]-6,7,10,11-tetrahydro-9 H,18 H-5,21:12,17-dimethenodibenzo[ e,k]pyrrolo[3,4- h][1,4,13]oxadiazacyclohexadecine-18,20(19 H)-dione, Ruboxistaurin (LY333531).
ACS Chemical Neuroscience ( IF 5 ) Pub Date : 2018-09-11 , DOI: 10.1021/acschemneuro.8b00196
Anita H Lewin 1 , Larry Brieaddy 1 , Jeffrey R Deschamps 2 , Gregory H Imler 2 , S Wayne Mascarella 1 , P Anantha Reddy 1 , F Ivy Carroll 1
Affiliation  

The demonstrated role of PKCβ in mediating amphetamine-stimulated dopamine efflux, which regulates amphetamine-induced dopamine transporter trafficking and activity, has promoted the research use of the selective, reversible PKCβ inhibitor (9 S)-9-[(dimethylamino)methyl]-6,7,10,11-tetrahydro-9 H,18 H-5,21:12,17-dimethenodibenzo[ e,k]pyrrolo[3,4- h][1,4,13]oxadiazacyclohexadecine-18,20(19 H)-dione, ruboxistaurin. Despite the interest in development of ruboxistaurin as the mesylate monohydrate (Arxxant) for the treatment of diabetic retinopathy, macular edema, and nephoropathy, several crucial details in physicochemical characterization were erroneous or missing. This report describes the synthesis and full characterization of ruboxistaurin free base (as a monohydrate), including X-ray crystallography to confirm the absolute configuration, and of the mesylate salt, isolated as a hydrate containing 1.5 mol of water per mole.

中文翻译:

选择性可逆PKCβ抑制剂(9 S)-9-[((二甲氨基)甲基] -6,7,10,11-四氢-9 H,18 H-5,21:12,17-二甲基二苯并[]的合成与表征e,k] pyrrolo [3,4-h] [1,4,13]草二氮杂环己癸-18,20(19 H)-二酮,黄杨黄嘌呤(LY333531)。

PKCβ在介导安非他明刺激的多巴胺流出中的调节作用,调节苯丙胺诱导的多巴胺转运蛋白的运输和活性,已证明促进了选择性可逆PKCβ抑制剂(9 S)-9-[((二甲基氨基)甲基]- 6,7,10,11-四氢-9 H,18 H-5,21:12,17-二甲二苯并[e,k]吡咯并[3,4-h] [1,4,13]草二氮杂环十六烷-18,20 (19 H)-二酮,ruboxistaurin。尽管有兴趣开发鲁贝司他林作为甲磺酸盐一水合物(Arxxant)用于治疗糖尿病性视网膜病,黄斑水肿和肾病,但理化特性中的一些关键细节是错误的或缺失的。这份报告描述了Ruboxistaurin游离碱(作为一水合物)的合成和完整表征,包括X射线晶体学以确认其绝对构型,
更新日期:2018-08-29
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