CD1530

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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。

CD1530 

CD1530 是一种选择性的 RARγ 激动剂，其 Kd 为150 nM。CD1530 已与 bexarotene 联合使用，以抑制致癌物4-硝基喹啉 1-氧化物在人类口腔和食管鳞状细胞癌小鼠模型中诱导的口腔癌发生。

CD1530

CD1530 Chemical Structure

CAS No. : 107430-66-0

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生物活性

CD1530 is a selective RARγ agonist with an Kd of 150 nM[1]. CD1530 has been used in combination with bexarotene to inhibit oral carcinogenesis induced by the carcinogen 4-nitroquinoline 1-oxide in a mouse model of human oral-cavity and esophageal squamous-cell carcinoma[2].

IC50 & Target

RARγ

150 nM (Kd)

分子量

398.49

Formula

C27H26O3
CAS 号

107430-66-0
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]. Bernard BA, et al. Identification of synthetic retinoids with selectivity for human nuclear retinoic acid receptor gamma. Biochem Biophys Res Commun. 1992 Jul 31;186(2):977-83.

    [2]. Tang XH, et al. Combination of bexarotene and the retinoid CD1530 reduces murine oral-cavity carcinogenesis induced by the carcinogen 4-nitroquinoline 1-oxide. Proc Natl Acad Sci U S A. 2014 Jun 17;111(24):8907-12.

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