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    Results for Activators & Inhibitors ( 70846 )

      • Ref: 79861-1
        Sizes: 100 µl
        From: €321.00

        Guanosine 5'-triphosphate sodium salt hydrate (GTP) functions as a carrier of phosphates and pyrophosphates involved in channeling chemical energy into specific biosynthetic pathways.

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      • Ref: 79861-2
        Sizes: 500 µl
        From: €888.00

        Guanosine 5'-triphosphate sodium salt hydrate (GTP) functions as a carrier of phosphates and pyrophosphates involved in channeling chemical energy into specific biosynthetic pathways.

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      • Ref: 79888-2
        Sizes: 1 g
        From: €293.00

        3-aminobenzamide is a novel, potent inhibitor of PARP. Also acts as a mediator of oxidant-induced myocyte dysfunction during reperfusion.

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      • Ref: 79888-3
        Sizes: 5 g
        From: €488.00

        3-aminobenzamide is a novel, potent inhibitor of PARP. Also acts as a mediator of oxidant-induced myocyte dysfunction during reperfusion.

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      • Ref: 10-1365
        Sizes: 5 mg, 25 mg
        From: €91.00

        Activity: PPARγ partial agonist . Function/Pharmacology: Displays high affinity for PPARγ with excellent anti-diabetic activity in mice but poor PPARγ agonist activity in transcription and adipogenesis assays. Highly effective (30 nM) at blocking Cdk5-mediated phosphorylation of PPARγ. Cell permeable. Chemical Name: (S)-2-(3-((1-(4-Methoxybenzoyl)-2-methyl-5-(trifluoromethoxy)-1H-indol-3-yl)methyl)phenoxy)propanoic acid

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      • Ref: 04-0004
        Sizes: 2 mg
        From: €377.00

        Stemolecule CHIR99021 (2 mg)

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      • Ref: 1088-1kg
        Sizes: 1kg
        From: €36.00

        Polyethylene glycol Water-soluble and non-toxic polymer. Increases solubility of therapeutic proteins and peptides.

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      • Ref: 04-0074
        Sizes: 2 mg
        From: €377.00

        Stemolecule LDN-193189 (2 mg)

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      • Ref: 10-1186
        Sizes: 5 mg, 25 mg
        From: €70.00

        Activity: Tankyrase inhibitor, Cardiomyogenesis inducer . Function/Pharmacology: Tankyrase inhibitor (IC50=11 and 4 nM for TNKS1 and 2 respectively). Antagonizes wnt signaling via stimulation of ß-catenin degradation and stabilization of actin.1 Robustly induces cardiomyogenesis of stem cells.2 Cell Permeable Chemical Name: 2-[4-(Trifluoromethyl)phenyl]-7,8-dihydro-5H-thiino[4,3-d]pyrimidin-4-ol

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