Chemical Structure : KTI-218
Catalog No.: PC-25395Not For Human Use, Lab Use Only.
KTI-218 is a small molecule inhibitor that covalently bind to cysteine-51 (Cys-51) in HPV16 E6, specifically inhibit HPV16 E6 mediate p53 degradation with EC50 of 4.2 uM in RPE-1 cells.
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KTI-218 is a small molecule inhibitor that covalently bind to cysteine-51 (Cys-51) in HPV16 E6, specifically inhibit HPV16 E6 mediate p53 degradation with EC50 of 4.2 uM in RPE-1 cells.
KTI-218 specifically reduce HPV+ cells viability with IC50 of 1-3 uM.
KTI-218 activates p53-dependent transcriptional programs associated with apoptosis and senescence, resulting in reduced tumor cell viability.
KTI-218 (50 mg/kg, s.c. injection) inhibits growth of HPV-16 expressing human cervical and oropharyngeal tumor cells in vivo.
M.Wt | 490.58 | |
Formula | C28H31FN4O3 | |
Appearance | Solid | |
Storage |
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Solubility |
10 mM in DMSO |
1. Anne Rietz, et al. bioRxiv[Preprint]. 2025 Aug 28:2025.08.24.671874.
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