HPK1-IN-16

发表于由

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白，专注于信号通路和疾病研究领域。

HPK1-IN-16 

HPK1-IN-16 是一种有效的、选择性的 HPK1 抑制剂。最初从造血祖细胞克隆的造血祖细胞激酶1 (HPK1) 是 MAP4Ks 家族的成员。HPK1-IN-16 可用于研究、预防或改善与 HPK1 活性相关的疾病或病症，例如癌症 (信息提取自专利 WO2019051199A1，compound 39) 。

HPK1-IN-16

HPK1-IN-16 Chemical Structure

CAS No. : 2294965-95-8

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生物活性

HPK1-IN-16 is a potent and selective inhibitor of HPK1. Hematopoietic progenitor kinase 1 (HPKl) originally cloned from hematopoietic progenitor cells is a member of MAP kinase kinase kinase kinases (MAP4Ks) family. HPK1-IN-16 is useful in researching, preventing or ameliorating diseases or disorders associated with HPK1 activity such as cancer (extracted from patent WO2019051199A1, compound 39)[1].

分子量

454.54

Formula

C28H27FN4O
CAS 号

2294965-95-8
运输条件

Room temperature in continental US; may vary elsewhere.
储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.
参考文献

  • [1]. Oleg VECHORKIN, et al. 6-cyano-indazole compounds as hematopoietic progenitor kinase 1 (hpk1) modulators. Patent WO2019051199A1.

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