Chemical Structure : XL495
Catalog No.: PC-26487Not For Human Use, Lab Use Only.
XL495 is a potent, selective and orally bioavailable PKMYT1 inhibitor, demonstrates dose-dependent antitumor activity, inhibits phosphorylation of CDK1 at Thr14, and induces phosphorylation of KAP1 at Ser824 in CDX tumors.
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XL495 is a potent, selective and orally bioavailable PKMYT1 inhibitor, demonstrates dose-dependent antitumor activity, inhibits phosphorylation of CDK1 at Thr14, and induces phosphorylation of KAP1 at Ser824 in CDX tumors.
| M.Wt | 308.34 | |
| Formula | C17H16N4O2 | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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1. Zhu J, et al. J Org Chem. 2026 Apr 6. doi: 10.1021/acs.joc.6c00304.
2. Dana Gwinn, et al. Cancer Res (2025) 85 (8_Supplement_1): 1733.

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