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鉴定和表征一种血脑屏障穿透型肌醇六磷酸激酶(IP6K)抑制剂。

Identification and Characterization of a Blood-Brain Barrier Penetrant Inositol Hexakisphosphate Kinase (IP6K) Inhibitor.

机构信息

Department of Pharmacology and Molecular Sciences, Johns Hopkins School of Medicine, Baltimore, Maryland 21205, United States.

Lieber Institute for Brain Development, 855 N. Wolfe Street, Baltimore, Maryland 21205, United States.

出版信息

J Med Chem. 2024 Aug 22;67(16):13639-13665. doi: 10.1021/acs.jmedchem.4c00190. Epub 2024 Aug 3.

Abstract

Inositol hexakisphosphate kinases (IP6Ks) have been studied for their role in glucose homeostasis, metabolic disease, fatty liver disease, chronic kidney disease, neurological development, and psychiatric disease. IP6Ks phosphorylate inositol hexakisphosphate (IP6) to the pyrophosphate, 5-diphosphoinositol-1,2,3,4,6-pentakisphosphate (5-IP7). Most of the currently known potent IP6K inhibitors contain a critical carboxylic acid which limits blood-brain barrier (BBB) penetration. In this work, the synthesis and testing of a variety of carboxylic acid isosteres resulted in several new compounds with improved BBB penetration. The most promising compound has an IP6K1 IC of 16 nM with an improved brain/plasma ratio and a favorable pharmacokinetic profile. This series of brain penetrant compounds may be used to investigate the role of IP6Ks in CNS disorders.

摘要

肌醇六磷酸激酶 (IP6Ks) 的研究主要集中在其在葡萄糖稳态、代谢性疾病、脂肪肝疾病、慢性肾病、神经发育和精神疾病中的作用。IP6Ks 将肌醇六磷酸 (IP6) 磷酸化为焦磷酸,即 5-二磷酸肌醇-1,2,3,4,6-五磷酸 (5-IP7)。目前已知的大多数有效 IP6K 抑制剂都含有一个关键的羧酸,这限制了其对血脑屏障 (BBB) 的穿透。在这项工作中,对各种羧酸类似物的合成和测试导致了几种具有改善 BBB 穿透性的新型化合物。最有前途的化合物对 IP6K1 的 IC50 为 16 nM,具有改善的脑/血浆比和有利的药代动力学特征。这一系列可穿透血脑屏障的化合物可用于研究 IP6Ks 在中枢神经系统疾病中的作用。

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