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PX-478 has excellent activity against established human tumor xenografts
3-thiazol-4-yl)ethynyl]pyridine hydrochloride
MK-571-treated mice display lower RVSP and Fulton index and a decrease in the medial thickening of small pulmonary arteries and arterioles
Smiles: CC1=CC(C)=C(CNC(=O)C2=CC(Cl)=C3O[C@@](C)(OC3=C2C)[C@@H]2CC[C@H](CC2)N(C)C)C(=O)N1
4-dimethoxybenzamide
(Z)-Orantinib Size:Contact [email protected] for quotation PX-478 has excellent activity against(Z) Orantinib ((Z) SU6668) is a potent, selective, orally active and ATP competitive inhibitor of Flk1 KDR, PDGFR, and FGFR1, with IC50s of 2. 1, 0. 008, and 1. 2 M, respectively. (Z) Orantinib is a potent antiangiogenic and antitumor agent that induces regression of established tumors. Product information CAS Number: 210644 62 5 Molecular Weight: 310. 35 Formula: C18H18N2O3 Chemical Name: 3 (2,4 dimethyl 5 {[(3Z) 2 oxo 2,3 dihydro 1H indol 3
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