Name | Description | Size | Catalog # | Supplier | |
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A-674563 | An orally available, reversible inhibitor of Akt (Ki = 11 nM for Akt1); al… | 500 µg | 18715-500 |
CAYMAN CHEMICAL COMPANY |
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A6770 | An inhibitor of S1P lyase; induces accumulation of [3H]dhS1P in IT-79MTNC3… | 1 mg | 29972-1 |
CAYMAN CHEMICAL COMPANY |
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A6770 | An inhibitor of S1P lyase; induces accumulation of [3H]dhS1P in IT-79MTNC3… | 10 mg | 29972-10 |
CAYMAN CHEMICAL COMPANY |
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A6770 | An inhibitor of S1P lyase; induces accumulation of [3H]dhS1P in IT-79MTNC3… | 5 mg | 29972-5 |
CAYMAN CHEMICAL COMPANY |
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A6770 | An inhibitor of S1P lyase; induces accumulation of [3H]dhS1P in IT-79MTNC3… | 500 µg | 29972-500 |
CAYMAN CHEMICAL COMPANY |
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A-740003 | A selective P2X7 antagonist (IC50s = 40 and 18 nM for human and rat recept… | 1 mg | 21256-1 |
CAYMAN CHEMICAL COMPANY |
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A-740003 | A selective P2X7 antagonist (IC50s = 40 and 18 nM for human and rat recept… | 10 mg | 21256-10 |
CAYMAN CHEMICAL COMPANY |
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A-740003 | A selective P2X7 antagonist (IC50s = 40 and 18 nM for human and rat recept… | 25 mg | 21256-25 |
CAYMAN CHEMICAL COMPANY |
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A-740003 | A selective P2X7 antagonist (IC50s = 40 and 18 nM for human and rat recept… | 5 mg | 21256-5 |
CAYMAN CHEMICAL COMPANY |
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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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A-804598 | A potent and selective competitive antagonist of the P2X7 receptor (IC50s… | 25 mg | 20060-25 |
CAYMAN CHEMICAL COMPANY |
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A-804598 | A potent and selective competitive antagonist of the P2X7 receptor (IC50s… | 5 mg | 20060-5 |
CAYMAN CHEMICAL COMPANY |
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A-804598 | A potent and selective competitive antagonist of the P2X7 receptor (IC50s… | 50 mg | 20060-50 |
CAYMAN CHEMICAL COMPANY |
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A-834735 | An indole-derived CB that acts as a full agonist at both the CB1 and CB2 r… | 1 mg | 11163-1 |
CAYMAN CHEMICAL COMPANY |
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A-834735 | An indole-derived CB that acts as a full agonist at both the CB1 and CB2 r… | 10 mg | 11163-10 |
CAYMAN CHEMICAL COMPANY |
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A-834735 | An indole-derived CB that acts as a full agonist at both the CB1 and CB2 r… | 5 mg | 11163-5 |
CAYMAN CHEMICAL COMPANY |
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A-836339 | A synthetic CB which has a higher affinity for the peripheral CB2 receptor… | 1 mg | 13898-1 |
CAYMAN CHEMICAL COMPANY |
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A-836339 | A synthetic CB which has a higher affinity for the peripheral CB2 receptor… | 10 mg | 13898-10 |
CAYMAN CHEMICAL COMPANY |
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A-836339 | A synthetic CB which has a higher affinity for the peripheral CB2 receptor… | 5 mg | 13898-5 |
CAYMAN CHEMICAL COMPANY |
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A-839977 | A P2X7 receptor antagonist; inhibits BzATP-evoked intracellular calcium in… | 1 mg | 30934-1 |
CAYMAN CHEMICAL COMPANY |
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A-839977 | A P2X7 receptor antagonist; inhibits BzATP-evoked intracellular calcium in… | 10 mg | 30934-10 |
CAYMAN CHEMICAL COMPANY |
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A-839977 | A P2X7 receptor antagonist; inhibits BzATP-evoked intracellular calcium in… | 5 mg | 30934-5 |
CAYMAN CHEMICAL COMPANY |
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A-841720 | A noncompetitive antagonist of mGluR1 (IC50 = 10.7 nM); selective over mGl… | 1 mg | 21807-1 |
CAYMAN CHEMICAL COMPANY |
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A-841720 | A noncompetitive antagonist of mGluR1 (IC50 = 10.7 nM); selective over mGl… | 10 mg | 21807-10 |
CAYMAN CHEMICAL COMPANY |
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A-841720 | A noncompetitive antagonist of mGluR1 (IC50 = 10.7 nM); selective over mGl… | 5 mg | 21807-5 |
CAYMAN CHEMICAL COMPANY |
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A-867744 | A positive allosteric modulator of α7 nAChRs; selective for α7… | 10 mg | 32974-10 |
CAYMAN CHEMICAL COMPANY |
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