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PRT4165 10mg  | ≥98%

CSNpharm

PRT4165, an inhibitor of bim1 and ring1A, could block PRC1 (Polycomb-repressive complex 1)-mediated H2A ubiquitylation.

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PRT4165 50mg  | ≥98%

CSNpharm

PRT4165, an inhibitor of bim1 and ring1A, could block PRC1 (Polycomb-repressive complex 1)-mediated H2A ubiquitylation.

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PRT4165 5mg  | ≥98%

CSNpharm

PRT4165, an inhibitor of bim1 and ring1A, could block PRC1 (Polycomb-repressive complex 1)-mediated H2A ubiquitylation.

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NPS-2143 HCl 5mg  | ≥99%

CSNpharm

NPS-2143 HCl is a potent and selective calcium ion-sensing receptor antagonist with IC50 of 43 and 41 nM for cytoplasmic Ca2+ concentrations and parathyroid hormone secretion, respectively.

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NPS-2143 HCl 1mg  | ≥99%

CSNpharm

NPS-2143 HCl is a potent and selective calcium ion-sensing receptor antagonist with IC50 of 43 and 41 nM for cytoplasmic Ca2+ concentrations and parathyroid hormone secretion, respectively.

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NPS-2143 HCl 50mg  | ≥99%

CSNpharm

NPS-2143 HCl is a potent and selective calcium ion-sensing receptor antagonist with IC50 of 43 and 41 nM for cytoplasmic Ca2+ concentrations and parathyroid hormone secretion, respectively.

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Paradol 1mg  | ≥99%

CSNpharm

Paradol is an effective inhibitor of tumor promotion in mouse skin carcinogenesis, binds to cyclooxygenase (COX)-2 active site, it’s a pungent phenolic substance isolated and purified from ginger and other Zingiberaceae plants.

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Paradol 5mg  | ≥99%

CSNpharm

Paradol is an effective inhibitor of tumor promotion in mouse skin carcinogenesis, binds to cyclooxygenase (COX)-2 active site, it’s a pungent phenolic substance isolated and purified from ginger and other Zingiberaceae plants.

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Paradol 10mg  | ≥99%

CSNpharm

Paradol is an effective inhibitor of tumor promotion in mouse skin carcinogenesis, binds to cyclooxygenase (COX)-2 active site, it’s a pungent phenolic substance isolated and purified from ginger and other Zingiberaceae plants.

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SR-3335 50mg  | ≥99%

CSNpharm

SR3335 can selectively bind to RORα and competitively inhibit the binding of 25-hydroxycholesterol to the ligand binding domain with Ki of 220 nM.

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