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达瓦色替(NVP-LXS196)的发现,一种用于治疗转移性葡萄膜黑素瘤的泛 PKC 抑制剂。

Discovery of Darovasertib (NVP-LXS196), a Pan-PKC Inhibitor for the Treatment of Metastatic Uveal Melanoma.

机构信息

Novartis Institutes for Biomedical Research, 250 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States.

出版信息

J Med Chem. 2024 Jan 25;67(2):1447-1459. doi: 10.1021/acs.jmedchem.3c02002. Epub 2024 Jan 10.

Abstract

Uveal melanoma (UM) is the most common primary intraocular malignancy in the adult eye. Despite the aggressive local management of primary UM, the development of metastases is common with no effective treatment options for metastatic disease. Genetic analysis of UM samples reveals the presence of mutually exclusive activating mutations in the Gq alpha subunits GNAQ and GNA11. One of the key downstream targets of the constitutively active Gq alpha subunits is the protein kinase C (PKC) signaling pathway. Herein, we describe the discovery of darovasertib (NVP-LXS196), a potent pan-PKC inhibitor with high whole kinome selectivity. The lead series was optimized for kinase and off target selectivity to afford a compound that is rapidly absorbed and well tolerated in preclinical species. LXS196 is being investigated in the clinic as a monotherapy and in combination with other agents for the treatment of uveal melanoma (UM), including primary UM and metastatic uveal melanoma (MUM).

摘要

葡萄膜黑色素瘤 (UM) 是成年人眼内最常见的原发性眼内恶性肿瘤。尽管对原发性 UM 进行了积极的局部治疗,但转移的发展很常见,转移性疾病没有有效的治疗选择。UM 样本的基因分析显示 Gqα亚基 GNAQ 和 GNA11 中存在相互排斥的激活突变。组成性激活的 Gqα亚基的一个关键下游靶标是蛋白激酶 C (PKC) 信号通路。本文描述了 darovasertib(NVP-LXS196)的发现,这是一种有效的泛 PKC 抑制剂,对整个激酶组具有高选择性。该先导系列化合物经过激酶和非靶点选择性优化,得到一种在临床前物种中吸收迅速且耐受性良好的化合物。LXS196 目前正在作为单药以及与其他药物联合用于治疗葡萄膜黑色素瘤 (UM),包括原发性 UM 和转移性葡萄膜黑色素瘤 (MUM)。

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