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鉴定 NVP-CLR457 为一种口服生物利用度、非 CNS 穿透的 pan-Class IA 磷酸肌醇-3-激酶抑制剂。

Identification of NVP-CLR457 as an Orally Bioavailable Non-CNS-Penetrant pan-Class IA Phosphoinositol-3-Kinase Inhibitor.

机构信息

Novartis Institutes for BioMedical Research, Basel CH-4002, Switzerland.

Novartis Institutes for BioMedical Research, Emeryville, California 94608, United States.

出版信息

J Med Chem. 2022 Jun 23;65(12):8345-8379. doi: 10.1021/acs.jmedchem.2c00267. Epub 2022 May 2.

Abstract

Balanced pan-class I phosphoinositide 3-kinase inhibition as an approach to cancer treatment offers the prospect of treating a broad range of tumor types and/or a way to achieve greater efficacy with a single inhibitor. Taking buparlisib as the starting point, the balanced pan-class I PI3K inhibitor (NVP-CLR457) was identified with what was considered to be a best-in-class profile. Key to the optimization to achieve this profile was eliminating a microtubule stabilizing off-target activity, balancing the pan-class I PI3K inhibition profile, minimizing CNS penetration, and developing an amorphous solid dispersion formulation. A rationale for the poor tolerability profile of in a clinical study is discussed.

摘要

平衡的泛 PI3K 抑制剂治疗癌症提供了治疗广泛肿瘤类型的前景,或者是使用单一抑制剂实现更高疗效的途径。以 buparlisib 为起点,发现了平衡的泛 PI3K 抑制剂 (NVP-CLR457),其具有被认为是同类最佳的特征。实现这一特征的关键是消除微管稳定的脱靶活性,平衡泛 PI3K 抑制特征,最大限度地减少 CNS 穿透,并开发无定形固体分散体配方。讨论了临床研究中 buparlisib 耐受性差的原因。

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