Tecarfarin sodium ahydroquinoline which is a concentration that

which is a concentration that has little or no adverse effect on the host cell (cell viability >80%)

InChi: InChI=1S/C24H19F2N5O5/c1-14(2)29(19-12-11-15(22(32)33)13-20(19)36-16-7-4-3-5-8-16)23(34)31-24(35)30(27-28-31)21-17(25)9-6-10-18(21)26/h3-14H

Comprehensive evaluation of tamoxifen sequential biotransformation by the human cytochrome P450 system in vitro: prominent roles for CYP3A and CYP2D6

InChi: InChI=1S/C4H9NO2/c1-2-3(5)4(6)7/h3H

Solubility: DMSO : ≥ 25 mg/mL (53

Tecarfarin sodium ahydroquinoline which is a concentration thatTecarfarin sodium (ATI 5923 sodium) is a novel orally active non competitive vitamin K epoxide reductase (VKOR) antagonist, impairs the activation of the vitamin K dependent clotting factors II, VII, IX and X. Tecarfarin sodium has the antithrombotic activity. Product information CAS Number: 1004551 83 0 Molecular Weight: 482. 31 Formula: C21H13F6NaO5 Chemical Name: sodium 3 [(4 {[(1,1,1,3,3,3 hexafluoro 2 methylpropan 2 yl)oxy]carbonyl}phenyl)methyl]