PeptideDB

Cdc7-IN-20

CAS: F: C15H16N4OS W: 300.38

Cdc7-IN-20 (EP-05) is an orally effective and selective Cdc7 inhibitor with IC50 and Ki values of 0.93 and 0.11 nM, resp
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This product is for research use only, not for human use. We do not sell to patients.

Bioactivity Cdc7-IN-20 (EP-05) is an orally effective and selective Cdc7 inhibitor with IC50 and Ki values of 0.93 and 0.11 nM, respectively. Cdc7-IN-20 has antitumor activity[1].
Invitro Cdc7-IN-20 (0.5, 1, 2 μM, 24 h) 可抑制 COLO 205 细胞的增殖[1]。 MCE has not independently confirmed the accuracy of these methods. They are for reference only. 0 --> Cdc7-IN-20 相关抗体: Western Blot Analysis[1] Cell Line:
In Vivo Cdc7-IN-20 (2, 4, 8 mg/kg, 口服, 连续 3 天) 在 COLO 205 异种移植小鼠模型中具有抗肿瘤作用[1]。 MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model:
Formula C15H16N4OS
Molar Mass 300.38
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]. Fu M, et al. Discovery of a potent and selective cell division cycle 7 inhibitor from 6-(3-fluoropyridin-4-yl) thieno [3, 2-d] pyrimidin-4 (3H)-one derivatives as an orally active antitumor agent. Acta Pharmaceutica Sinica. B, 2024, 14(2): 893.