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V127032-250mgVinblastine inhibits microtubule formation and supresses nAChR activity with IC50 of 8.9 μM.
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V127032-50mgVinblastine inhibits microtubule formation and supresses nAChR activity with IC50 of 8.9 μM.
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V127477-100mgVismodegib (GDC-0449) is a potent, novel and specific hedgehog inhibitor with IC50 of 3 nM and also inhibits P-gp with IC50 of 3.0 μM.A potent hedgehog (Hh) signaling pathway inhibitor.
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V127477-10mgVismodegib (GDC-0449) is a potent, novel and specific hedgehog inhibitor with IC50 of 3 nM and also inhibits P-gp with IC50 of 3.0 μM.A potent hedgehog (Hh) signaling pathway inhibitor.
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V127477-1gVismodegib (GDC-0449) is a potent, novel and specific hedgehog inhibitor with IC50 of 3 nM and also inhibits P-gp with IC50 of 3.0 μM.A potent hedgehog (Hh) signaling pathway inhibitor.
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V127477-250mgVismodegib (GDC-0449) is a potent, novel and specific hedgehog inhibitor with IC50 of 3 nM and also inhibits P-gp with IC50 of 3.0 μM.A potent hedgehog (Hh) signaling pathway inhibitor.
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V127477-500mgVismodegib (GDC-0449) is a potent, novel and specific hedgehog inhibitor with IC50 of 3 nM and also inhibits P-gp with IC50 of 3.0 μM.A potent hedgehog (Hh) signaling pathway inhibitor.
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V127477-50mgVismodegib (GDC-0449) is a potent, novel and specific hedgehog inhibitor with IC50 of 3 nM and also inhibits P-gp with IC50 of 3.0 μM.A potent hedgehog (Hh) signaling pathway inhibitor.
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V413905-100mgInformationVorapaxar (MK-5348) Vorapaxar (SCH 530348, MK-5348) is a potent and orally active thrombin receptor (PAR-1) antagonist with K i of 8.1 nM.TargetsPAR-1 (Cell-free assay) 8.1 nM(Ki)In vitroSCH 530348 is a synthetic tricyclic
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V413905-25mgInformationVorapaxar (MK-5348) Vorapaxar (SCH 530348, MK-5348) is a potent and orally active thrombin receptor (PAR-1) antagonist with K i of 8.1 nM.TargetsPAR-1 (Cell-free assay) 8.1 nM(Ki)In vitroSCH 530348 is a synthetic tricyclic
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V413905-50mgInformationVorapaxar (MK-5348) Vorapaxar (SCH 530348, MK-5348) is a potent and orally active thrombin receptor (PAR-1) antagonist with K i of 8.1 nM.TargetsPAR-1 (Cell-free assay) 8.1 nM(Ki)In vitroSCH 530348 is a synthetic tricyclic
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V413905-5mgInformationVorapaxar (MK-5348) Vorapaxar (SCH 530348, MK-5348) is a potent and orally active thrombin receptor (PAR-1) antagonist with K i of 8.1 nM.TargetsPAR-1 (Cell-free assay) 8.1 nM(Ki)In vitroSCH 530348 is a synthetic tricyclic