1. Immunology/Inflammation
  2. Aryl Hydrocarbon Receptor
  3. CB7993113

CB7993113 是一种有效的 AHR 拮抗剂,IC50 为 0.33 μM。 CB7993113 直接结合 AHR 蛋白并阻断 AHR 核转位。 CB7993113 可分别抑制多环芳烃 (PAH) 和 TCDD 诱导的报告基因活性 75% 和 90%。

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CB7993113 Chemical Structure

CB7993113 Chemical Structure

CAS No. : 819827-50-4

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

CB7993113 is a potent AHR antagonist, with an IC50 of 0.33 μM. CB7993113 directly binds AHR protein and blocks AHR nuclear translocation. CB7993113 inhibits polycyclic aromatic hydrocarbon (PAH)- and TCDD-induced reporter activity by 75% and 90% respectively[1].

体外研究
(In Vitro)

当以至少高达 20 μM 的浓度添加到多种人类细胞(包括 HepG2 肝癌细胞、BP1、D3、Hs578T 或 MDA-MB-231 乳腺癌细胞以及原代人诱导多能干细胞)时,CB7993113 不会表现出毒性 [1]
CB7993113 显着降低 ER-/PR-/HER2- 乳腺癌细胞的体外侵袭表型[1]

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

体内研究
(In Vivo)

CB7993113 可有效阻断 50 mg/kg DMBA (HY-W011845) 诱导的急性肝 CYP1A1 诱导和体内骨髓毒性[1]

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

364.15

Formula

C15H10BrNO5

CAS 号
Unlabeled CAS

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.

纯度 & 产品资料
参考文献
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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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产品名称:
CB7993113
目录号:
HY-111450
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