Name | Theliatinib tartrate |
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Description | Theliatinib (Xiliertinib) tartrate is a potent, ATP-competitive, orally active and highly selective EGFR inhibitor with a Ki of 0.05 nM and an IC50 of 3 nM. Theliatinib has an IC50 of 22 nM for EGFR T790M/L858R mutant. Theliatinib shows >50-fold selectivity for EGFR than other kinases[1]. |
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Related Catalog | |
In Vitro | Theliatinib tartrate 显着抑制 A431 细胞中的 EGFR 磷酸化,IC50 为 7 nM。Theliatinib 还抑制 A431、H292 和 FaDu 细胞存活,IC50 值分别为 80 nM、58 nM 和 354 nM[1]。 |
In Vivo | Theliatinib tartrate (2-15 mg/kg; oral administration;daily; for 21 days; NOD-SCID mice; PDECX 1T0950 model) treatment demonstrates tumor regression of 75% at the end of study, and with a dose response[1]. |
References |
Molecular Formula | C29H32N6O8 |
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Molecular Weight | 592.60 |