(Z)-Orantinib Size:Contact [email protected] for quotation 4-dihydroisoquinolin-1-yl)-2-phenyl-N

4-dihydroisoquinolin-1-yl)-2-phenyl-N

3-thiazol-4-yl)ethynyl]pyridine hydrochloride

AS2863619 is a potent Foxp3 inducer in Tconv cells

Solubility: DMSO : 250 mg/mL (290

thus decreasing cancer cell proliferation

(Z)-Orantinib Size:Contact [email protected] for quotation 4-dihydroisoquinolin-1-yl)-2-phenyl-N(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