PeptideDB

WEE1-IN-7

CAS: 2924006-98-2 F: C28H28N10O W: 520.59

WEE1-IN-7 (compound 12h) is a potent and orally activeWEE1 inhibitor with an IC50 value of 2.1 nM. WEE1-IN-7 induces apo
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Bioactivity WEE1-IN-7 (compound 12h) is a potent and orally activeWEE1 inhibitor with an IC50 value of 2.1 nM. WEE1-IN-7 induces apoptosis and cell cycle arrest at the S phase. WEE1-IN-7 shows antitumor activity[1].
Target IC50: 2.1 nM (WEE1)
Invitro WEE1-IN-7 (compound 12h) 抑制细胞活力,对 A427 和 Lovo 细胞的 IC50 值分别为 84 和 82 nM[1]。WEE1-IN-7 (0-800 nM; 48 h) 以剂量依赖性方式诱导细胞凋亡和细胞周期停滞在 S 期[1]。 MCE has not independently confirmed the accuracy of these methods. They are for reference only. 0 --> WEE1-IN-7 相关抗体: Apoptosis Analysis[1] Cell Line:
In Vivo WEE1-IN-7 (60 mg/kg; p.o.; daily for 27 days) 在 Lovo CDX 异种移植小鼠模型中表现出抗肿瘤活性,肿瘤生长抑制率 (TGI) 为 88%[1]。药代动力学分析[1]. Admin.
CAS 2924006-98-2
Formula C28H28N10O
Molar Mass 520.59
Transport Room temperature in continental US; may vary elsewhere.
Storage

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

Reference [1]. Wang Y, et al. Advanced Design, Synthesis, and Evaluation of Highly Selective Wee1 Inhibitors: Enhancing Pharmacokinetics and Antitumor Efficacy. J Med Chem. 2024 Jun 7.