血小板活化化合物1的衍生物（PAC-1）及其抗癌活性

Title:Derivatives of Procaspase-Activating Compound 1 (PAC-1) and their Anticancer Activities

Volume: 23 Issue: 3

Author(s): Howard S. Roth and Paul J. Hergenrother

Affiliation:

关键词: 血小板活化化合物1、caspase-3蛋白、锌、凋亡、癌症、程序库。

摘要: PAC-1 induces the activation of procaspase-3 in vitro and in cell culture by chelation of inhibitory labile zinc ions via its ortho-hydroxy-N-acylhydrazone moiety. First reported in 2006, PAC-1 has shown promise in cell culture and animal models of cancer, and a Phase I clinical trial in cancer patients began in March 2015 (NCT02355535). Because of the considerable interest in this compound and a well-defined structure-activity relationship, over 1000 PAC-1 derivatives have been synthesized in an effort to vary pharmacological properties such as potency and pharmacokinetics. This article provides a comprehensive examination of all PAC-1 derivatives reported to date. A survey of PAC-1 derivative libraries is provided, with an indepth discussion of four derivatives on which extensive studies have been performed.

Cite this article as:

Howard S. Roth and Paul J. Hergenrother , Derivatives of Procaspase-Activating Compound 1 (PAC-1) and their Anticancer Activities, Current Medicinal Chemistry 2016; 23 (3) . https://dx.doi.org/10.2174/0929867323666151127201829