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Factor Xa

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Factor Xa

Chemical Structure Cat. No. Product Name CAS No.
BMS-962212 Chemical Structure
BCP31167 BMS-962212 1430114-34-3
BMS-962212 is a reversible, direct, and highly selective inhibitor of FXIa.
BMS-740808 Chemical Structure
BCP23400 BMS-740808 280118-23-2
BMS-740808 is a highly potent, selective, efficacious, and orally bioavailable inhibitor of blood coagulation factor Xa.
Betrixaban maleate Chemical Structure
BCP25697 Betrixaban maleate 936539-80-9
Betrixaban is a highly potent, selective, and orally efficacious factor Xa inhibitor with IC50 of 1.2 nM(inhibition of Factor 10a).
Idraparinux sodium Chemical Structure
BCP16293 Idraparinux sodium 149920-56-9
Idraparinux selectively blocks coagulation factor Xa.
Z-D-Arg-Gly-Arg-pNA   2 HCl Chemical Structure
BCP18446 Z-D-Arg-Gly-Arg-pNA 2 HCl 113711-77-6
Z-RGR-pNA is a chromogenic substrate for the determination of factor Xa.
Letaxaban Chemical Structure
BCP24734 Letaxaban 870262-90-1
Letaxaban, also known as TAK-442, is a potent, selective, and orally active factor Xa inhibitor, which is a tetrahydropyrimidin-2(1H)-one derivative.
D-PHE-PIP-ARG-PNA Chemical Structure
BCP18445 D-PHE-PIP-ARG-PNA 115388-96-0
Thrombin substrates are often cleaved as well by trypsin and trypsin-like enzymes, e.g. I-1365, I-1560, J-1120, and L-1150. Chromogenic substrate specific for thrombin but insensitive to factor Xa.
Rivaroxaban Diol Chemical Structure
BCP07255 Rivaroxaban Diol 1160170-00-2
Rivaroxaban is a highly potent and selective, direct Factor Xa (FXa) inhibitor, achieving a strong gain in anti-FXa potency (IC50 0.7 nM; Ki 0.4 nM).
5-R-Rivaroxaban Chemical Structure
BCP09021 5-R-Rivaroxaban 865479-71-6
5-R-Rivaroxaban is (R) enantiomer of Rivaroxaban. Rivaroxaban (Xarelto; BAY 59-7939) is a novel, oral, direct Factor Xa (FXa) inhibitor in late-stage development for the prevention and treatment of thromboembolic disorders.
Ozagrel hydrochloride Chemical Structure
BCP09493 Ozagrel hydrochloride 78712-43-3
Ozagrel(OKY-046) is an antiplatelet agent working as a thromboxane A2 synthesis inhibitor.
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