1. Stem Cell/Wnt
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  3. pan-TEAD-IN-1

pan-TEAD-IN-1 (Compound 3) 是一种具有口服活性的 TEAD 泛抑制剂,通过靶向 TEAD 的棕榈酰化位点,干扰其与共激活因子 YAP/TAZ 的相互作用,从而抑制 Hippo 信号通路中癌基因(如 CtgfCyr61)的转录上调。pan-TEAD-IN-1 展现了优异的活性,对 luciferase IC50 为 0.36 nM,对 H226 细胞 IC50 为 1.52 nM,并具有较好的药代动力学特性 (AUC0–∞ = 228.7 μg/mL·min,T1/2 = 183.9 min)。在 TEAD 依赖型癌症的异种移植小鼠模型中,pan-TEAD-IN-1 显著抑制肿瘤生长。pan-TEAD-IN-1 有望用于研究 TEAD 依赖型癌症。

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pan-TEAD-IN-1 Chemical Structure

pan-TEAD-IN-1 Chemical Structure

CAS No. : 3027484-09-6

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  • 生物活性

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生物活性

pan-TEAD-IN-1 (Compound 3) is an orally active pan-TEAD inhibitor targeting the palmitoylation site of TEAD, disrupting its interaction with the coactivators YAP/TAZ, thereby suppressing the transcriptional upregulation of oncogenes (e.g., Ctgf and Cyr61) in the Hippo signaling pathway. pan-TEAD-IN-1 exhibits excellent activity with a luciferase IC50 of 0.36 nM and an H226 cell IC50 of 1.52 nM. It also shows favorable pharmacokinetics (AUC0–∞ = 228.7 μg/mL·min, T1/2 = 183.9 min). In TEAD-dependent xenograft mouse models, pan-TEAD-IN-1 significantly inhibited tumor growth, showing promise for research in TEAD-dependent cancers[1].

分子量

331.33

Formula

C19H16F3NO

CAS 号
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Room temperature in continental US; may vary elsewhere.

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产品名称:
pan-TEAD-IN-1
目录号:
HY-159912
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