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A648229-5mgAc-VLPE-FMK, a tetrapeptidyl mono-fluoromethyl ketone (m-FMK), is a Cat-B and Cat-L inhibitor. Ac-VLPE-FMK can be used for the research of cancer aggressivenessIn VitroAc-VLPE-FMK (2 μM) significantly affects the cleavage of probe Ac-PLVQ-AMC by
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A646607-10mgAC1-IN-1 is a potent and selective Adenylyl cyclase type 1 (AC1) inhibitor with an IC 50 of 0.54 µM. AC1-IN-1 displays modest antiallodynic effects in a mouse model of inflammatory pain. AC1-IN-1 has CNS activityIn VitroAC1-IN-1 (compound 38: HEK293
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A646607-25mgAC1-IN-1 is a potent and selective Adenylyl cyclase type 1 (AC1) inhibitor with an IC 50 of 0.54 µM. AC1-IN-1 displays modest antiallodynic effects in a mouse model of inflammatory pain. AC1-IN-1 has CNS activityIn VitroAC1-IN-1 (compound 38: HEK293
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A646607-5mgAC1-IN-1 is a potent and selective Adenylyl cyclase type 1 (AC1) inhibitor with an IC 50 of 0.54 µM. AC1-IN-1 displays modest antiallodynic effects in a mouse model of inflammatory pain. AC1-IN-1 has CNS activityIn VitroAC1-IN-1 (compound 38: HEK293
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A654655-1mlAC1-IN-1 is a potent and selective Adenylyl cyclase type 1 (AC1) inhibitor with an IC 50 of 0.54 µM. AC1-IN-1 displays modest antiallodynic effects in a mouse model of inflammatory pain. AC1-IN-1 has CNS activityIn VitroAC1-IN-1 (compound 38: HEK293
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A646957-10mgAc32Az19 is a potent, nontoxic, and highly selective BCRP inhibitor with an EC 50 value of 13 nM in theBCRP-overexpressed HEK293/R2 cells.Form:Solid.
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A646957-25mgAc32Az19 is a potent, nontoxic, and highly selective BCRP inhibitor with an EC 50 value of 13 nM in theBCRP-overexpressed HEK293/R2 cells.Form:Solid.
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A646957-50mgAc32Az19 is a potent, nontoxic, and highly selective BCRP inhibitor with an EC 50 value of 13 nM in theBCRP-overexpressed HEK293/R2 cells.Form:Solid.
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A646957-5mgAc32Az19 is a potent, nontoxic, and highly selective BCRP inhibitor with an EC 50 value of 13 nM in theBCRP-overexpressed HEK293/R2 cells.Form:Solid.
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A654805-1mlAc32Az19 is a potent, nontoxic, and highly selective BCRP inhibitor with an EC 50 value of 13 nM in theBCRP-overexpressed HEK293/R2 cells.
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A649209-10mgAcamprosate-d 3 (calcium) is the deuterium labeled Acamprosate calcium. Acamprosate calcium is a GABA receptor agonist and modulator of glutamatergic systems.In VitroStable heavy isotopes of hydrogen, carbon, and other elements have been
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A649209-1mgAcamprosate-d 3 (calcium) is the deuterium labeled Acamprosate calcium. Acamprosate calcium is a GABA receptor agonist and modulator of glutamatergic systems.In VitroStable heavy isotopes of hydrogen, carbon, and other elements have been