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Vorapaxar Vorapaxar (SCH 530348), an antiplatelet agent, is a selective, orally active, and competitive thrombin receptor protease-activated receptor (PAR-1) antagonist ( K i =8.1 nM). Vorapaxar (SCH 530348) inhibits thrombin receptor-activating peptide (TRAP)-induced platelet aggregation in a dose-dependent manner [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SCH 530348. CAS No. 618385-01-6. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10119. MedChemExpress MCE
Vorapaxar-[d5] One of the isotopic labelled form of Vorapaxar, which has been found to be an antiplatelet agent and could be potentially effective against atherothrombosis. Synonyms: (1,1,2,2,2-D5)ethyl N-[(1R,3aR,4aR,6R,8aR,9S,9aS)-9-[(E)-2-[5-(3-fluorophenyl)pyridin-2-yl]ethenyl]-1-methyl-3-oxo-dodecahydronaphtho[2,3-c]furan-6-yl]carbamate. Grade: >98%. Molecular formula: C29H28D5FN2O4. Mole weight: 497.61. BOC Sciences 2
Vorapaxar sulfate Vorapaxar sulfate. Group: Biochemicals. Alternative Names: N- [ (1R, 3aR, 4aR, 6R, 8aR, 9S, 9aS) -9- [ (1E) -2- [5- (3-Fluorophenyl) -2-pyridinyl] ethenyl] dodecahydro-1-methyl-3-oxonaphtho [2, 3-c] furan-6-yl] carbamic acid ethyl ester sulfate; Sch 530348. Grades: Highly Purified. CAS No. 705260-08-8. Pack Sizes: 1mg, 2mg, 5mg, 10mg. Molecular Formula: C29H35FN2O8S. US Biological Life Sciences. USBiological 8
Worldwide
Vorapaxar sulfate Vorapaxar sulfate (SCH 530348 sulfate), an antiplatelet agent, is a selective, orally active, and competitive thrombin receptor protease-activated receptor (PAR-1) antagonist ( K i =8.1 nM). Vorapaxar sulfate inhibits thrombin receptor-activating peptide (TRAP)-induced platelet aggregation in a dose-dependent manner [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SCH 530348 sulfate. CAS No. 705260-08-8. Pack Sizes: 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-10119A. MedChemExpress MCE
Diethyl ((5-(3-fluorophenyl)pyridin-2-yl)methyl)phosphonate An impurity of Vorapaxar. Vorapaxar, also known as SCH 530348, is a thrombin receptor (protease-activated receptor, PAR-1) antagonist based on the natural product himbacine. Synonyms: Phosphonic acid, [[5-(3-fluorophenyl)-2-pyridinyl]methyl]-, diethyl ester; [[5-(3-Fluorophenyl)-2-pyridinyl]methyl]phosphonic acid diethyl ester; Vorapaxar Impurity B. Grade: 97%. CAS No. 380894-77-9. Molecular formula: C16H19FNO3P. Mole weight: 323.30. BOC Sciences 7
ethyl ((1R,3aR,4aR,6S,8aR,9S,9aS)-9-((E)-2-(5-(3-fluorophenyl)pyridin-2-yl)vinyl)-1-methyl-3-oxododecahydronaphtho[2,3-c]furan-6-yl)carbamate An impurity of Vorapaxar. Vorapaxar, also known as SCH 530348, is a thrombin receptor (protease-activated receptor, PAR-1) antagonist based on the natural product himbacine. Synonyms: (6S)-Vorapaxar; Vorapaxar Impurity G. Grade: 99%. CAS No. 618385-10-7. Molecular formula: C29H33FN2O4. Mole weight: 492.58. BOC Sciences 8

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