Name | Description | Size | Catalog # | Supplier | |
---|---|---|---|---|---|
A-769662 | A direct activator of AMPK (EC50 = 116 nM in a cell-free assay); allosteri… | 10 mg | 11900-10 |
CAYMAN CHEMICAL COMPANY |
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A-769662 | A direct activator of AMPK (EC50 = 116 nM in a cell-free assay); allosteri… | 25 mg | 11900-25 |
CAYMAN CHEMICAL COMPANY |
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A-769662 | A direct activator of AMPK (EC50 = 116 nM in a cell-free assay); allosteri… | 5 mg | 11900-5 |
CAYMAN CHEMICAL COMPANY |
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A-769662 | A direct activator of AMPK (EC50 = 116 nM in a cell-free assay); allosteri… | 50 mg | 11900-50 |
CAYMAN CHEMICAL COMPANY |
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A-770041 | An orally bioavailable LCK kinase inhibitor (IC50 = 0.147 µM); selec… | 1 mg | 32854-1 |
CAYMAN CHEMICAL COMPANY |
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A-770041 | An orally bioavailable LCK kinase inhibitor (IC50 = 0.147 µM); selec… | 5 mg | 32854-5 |
CAYMAN CHEMICAL COMPANY |
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A-77-01 | A potent inhibitor of the TGF-β1 receptor ALK5 (IC550 = 25 nM), block… | 1 mg | 18396-1 |
CAYMAN CHEMICAL COMPANY |
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A-77-01 | A potent inhibitor of the TGF-β1 receptor ALK5 (IC550 = 25 nM), block… | 10 mg | 18396-10 |
CAYMAN CHEMICAL COMPANY |
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A-77-01 | A potent inhibitor of the TGF-β1 receptor ALK5 (IC550 = 25 nM), block… | 25 mg | 18396-25 |
CAYMAN CHEMICAL COMPANY |
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A-77-01 | A potent inhibitor of the TGF-β1 receptor ALK5 (IC550 = 25 nM), block… | 5 mg | 18396-5 |
CAYMAN CHEMICAL COMPANY |
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A-771726 | An active metabolite of leflunomide; inhibits DHODH (IC50 = 0.23 µM)… | 10 mg | 14404-10 |
CAYMAN CHEMICAL COMPANY |
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A-771726 | An active metabolite of leflunomide; inhibits DHODH (IC50 = 0.23 µM)… | 25 mg | 14404-25 |
CAYMAN CHEMICAL COMPANY |
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A-771726 | An active metabolite of leflunomide; inhibits DHODH (IC50 = 0.23 µM)… | 5 mg | 14404-5 |
CAYMAN CHEMICAL COMPANY |
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A-784168 | A TRPV1 competitive antagonist; inhibits capsaicin-induced activation of T… | 1 mg | 32855-1 |
CAYMAN CHEMICAL COMPANY |
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A-784168 | A TRPV1 competitive antagonist; inhibits capsaicin-induced activation of T… | 10 mg | 32855-10 |
CAYMAN CHEMICAL COMPANY |
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A-784168 | A TRPV1 competitive antagonist; inhibits capsaicin-induced activation of T… | 25 mg | 32855-25 |
CAYMAN CHEMICAL COMPANY |
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A-784168 | A TRPV1 competitive antagonist; inhibits capsaicin-induced activation of T… | 5 mg | 32855-5 |
CAYMAN CHEMICAL COMPANY |
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A-796260 | A synthetic CB that shows high selectivity for the CB2 receptor (Ki = 0.77… | 1 mg | 11606-1 |
CAYMAN CHEMICAL COMPANY |
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A-796260 | A synthetic CB that shows high selectivity for the CB2 receptor (Ki = 0.77… | 10 mg | 11606-10 |
CAYMAN CHEMICAL COMPANY |
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A-796260 | A synthetic CB that shows high selectivity for the CB2 receptor (Ki = 0.77… | 5 mg | 11606-5 |
CAYMAN CHEMICAL COMPANY |
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A-803467 | A sodium channel blocker with high-affinity and selectivity for inhibiting… | 10 mg | 10012588-10 |
CAYMAN CHEMICAL COMPANY |
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A-803467 | A sodium channel blocker with high-affinity and selectivity for inhibiting… | 100 mg | 10012588-100 |
CAYMAN CHEMICAL COMPANY |
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A-803467 | A sodium channel blocker with high-affinity and selectivity for inhibiting… | 5 mg | 10012588-5 |
CAYMAN CHEMICAL COMPANY |
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A-803467 | A sodium channel blocker with high-affinity and selectivity for inhibiting… | 50 mg | 10012588-50 |
CAYMAN CHEMICAL COMPANY |
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A-804598 | A potent and selective competitive antagonist of the P2X7 receptor (IC50s… | 10 mg | 20060-10 |
CAYMAN CHEMICAL COMPANY |
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