Name | Description | Size | Catalog # | Supplier | |
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A-366 | A potent, peptide-competitive inhibitor of the lysine methyltransferase G9… | 50 mg | 16081-50 |
CAYMAN CHEMICAL COMPANY |
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A-419259 | An inhibitor of Src family kinases, including Src, LCK, Lyn, and Hck (IC50… | 1 mg | 25605-1 |
CAYMAN CHEMICAL COMPANY |
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A-419259 | An inhibitor of Src family kinases, including Src, LCK, Lyn, and Hck (IC50… | 10 mg | 25605-10 |
CAYMAN CHEMICAL COMPANY |
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A-419259 | An inhibitor of Src family kinases, including Src, LCK, Lyn, and Hck (IC50… | 5 mg | 25605-5 |
CAYMAN CHEMICAL COMPANY |
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A-443654 | A pan Akt inhibitor (Ki = 160 pmol / L for all three isoforms) that interf… | 1 mg | 16499-1 |
CAYMAN CHEMICAL COMPANY |
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A-443654 | A pan Akt inhibitor (Ki = 160 pmol / L for all three isoforms) that interf… | 5 mg | 16499-5 |
CAYMAN CHEMICAL COMPANY |
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A-443654 | A pan Akt inhibitor (Ki = 160 pmol / L for all three isoforms) that interf… | 500 µg | 16499-500 |
CAYMAN CHEMICAL COMPANY |
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A-484954 | An eEF-2K inhibitor; reduces eEF-2K autophosphorylation in various cancer… | 1 mg | 28279-1 |
CAYMAN CHEMICAL COMPANY |
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A-484954 | An eEF-2K inhibitor; reduces eEF-2K autophosphorylation in various cancer… | 10 mg | 28279-10 |
CAYMAN CHEMICAL COMPANY |
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A-484954 | An eEF-2K inhibitor; reduces eEF-2K autophosphorylation in various cancer… | 25 mg | 28279-25 |
CAYMAN CHEMICAL COMPANY |
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A-484954 | An eEF-2K inhibitor; reduces eEF-2K autophosphorylation in various cancer… | 5 mg | 28279-5 |
CAYMAN CHEMICAL COMPANY |
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A-485 | A p300 / CBP inhibitor (IC50 = 60 nM); decreases H3K27Ac levels in PC3 cel… | 1 mg | 24119-1 |
CAYMAN CHEMICAL COMPANY |
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A-485 | A p300 / CBP inhibitor (IC50 = 60 nM); decreases H3K27Ac levels in PC3 cel… | 10 mg | 24119-10 |
CAYMAN CHEMICAL COMPANY |
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A-485 | A p300 / CBP inhibitor (IC50 = 60 nM); decreases H3K27Ac levels in PC3 cel… | 25 mg | 24119-25 |
CAYMAN CHEMICAL COMPANY |
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A-485 | A p300 / CBP inhibitor (IC50 = 60 nM); decreases H3K27Ac levels in PC3 cel… | 5 mg | 24119-5 |
CAYMAN CHEMICAL COMPANY |
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A-61603 | A selective α1A-adrenergic receptor agonist that is at least 35-fold… | 1 mg | 17358-1 |
CAYMAN CHEMICAL COMPANY |
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A-61603 | A selective α1A-adrenergic receptor agonist that is at least 35-fold… | 10 mg | 17358-10 |
CAYMAN CHEMICAL COMPANY |
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A-61603 | A selective α1A-adrenergic receptor agonist that is at least 35-fold… | 5 mg | 17358-5 |
CAYMAN CHEMICAL COMPANY |
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A-66 | A potent, selective inhibitor of the PI3K isoform p110α (IC50 = 32 n… | 1 mg | 17382-1 |
CAYMAN CHEMICAL COMPANY |
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A-66 | A potent, selective inhibitor of the PI3K isoform p110α (IC50 = 32 n… | 10 mg | 17382-10 |
CAYMAN CHEMICAL COMPANY |
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A-66 | A potent, selective inhibitor of the PI3K isoform p110α (IC50 = 32 n… | 25 mg | 17382-25 |
CAYMAN CHEMICAL COMPANY |
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A-66 | A potent, selective inhibitor of the PI3K isoform p110α (IC50 = 32 n… | 5 mg | 17382-5 |
CAYMAN CHEMICAL COMPANY |
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A-674563 | An orally available, reversible inhibitor of Akt (Ki = 11 nM for Akt1); al… | 1 mg | 18715-1 |
CAYMAN CHEMICAL COMPANY |
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A-674563 | An orally available, reversible inhibitor of Akt (Ki = 11 nM for Akt1); al… | 10 mg | 18715-10 |
CAYMAN CHEMICAL COMPANY |
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A-674563 | An orally available, reversible inhibitor of Akt (Ki = 11 nM for Akt1); al… | 5 mg | 18715-5 |
CAYMAN CHEMICAL COMPANY |
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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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A-867744 | A positive allosteric modulator of α7 nAChRs; selective for α7… | 100 mg | 32974-100 |
CAYMAN CHEMICAL COMPANY |
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A-867744 | A positive allosteric modulator of α7 nAChRs; selective for α7… | 50 mg | 32974-50 |
CAYMAN CHEMICAL COMPANY |
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A-922500 | A potent inhibitor of DGAT-1 (IC50s = 7 and 24 nM, for human and mouse, re… | 1 mg | 10012708-1 |
CAYMAN CHEMICAL COMPANY |
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A-922500 | A potent inhibitor of DGAT-1 (IC50s = 7 and 24 nM, for human and mouse, re… | 10 mg | 10012708-10 |
CAYMAN CHEMICAL COMPANY |
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A-922500 | A potent inhibitor of DGAT-1 (IC50s = 7 and 24 nM, for human and mouse, re… | 25 mg | 10012708-25 |
CAYMAN CHEMICAL COMPANY |
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A-922500 | A potent inhibitor of DGAT-1 (IC50s = 7 and 24 nM, for human and mouse, re… | 5 mg | 10012708-5 |
CAYMAN CHEMICAL COMPANY |
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A-939572 | A stearoyl-CoA desaturase 1 inhibitor (IC50 = 6.3 nM) that induces cell de… | 10 mg | 19123-10 |
CAYMAN CHEMICAL COMPANY |
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A-939572 | A stearoyl-CoA desaturase 1 inhibitor (IC50 = 6.3 nM) that induces cell de… | 5 mg | 19123-5 |
CAYMAN CHEMICAL COMPANY |
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A-939572 | A stearoyl-CoA desaturase 1 inhibitor (IC50 = 6.3 nM) that induces cell de… | 50 mg | 19123-50 |
CAYMAN CHEMICAL COMPANY |
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A-966492 | A dual inhibitor of PARP1 and PARP2 (Kis = 1 and 1.5 nM, respectively); re… | 1 mg | 26378-1 |
CAYMAN CHEMICAL COMPANY |
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A-966492 | A dual inhibitor of PARP1 and PARP2 (Kis = 1 and 1.5 nM, respectively); re… | 10 mg | 26378-10 |
CAYMAN CHEMICAL COMPANY |
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A-966492 | A dual inhibitor of PARP1 and PARP2 (Kis = 1 and 1.5 nM, respectively); re… | 25 mg | 26378-25 |
CAYMAN CHEMICAL COMPANY |
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A-966492 | A dual inhibitor of PARP1 and PARP2 (Kis = 1 and 1.5 nM, respectively); re… | 5 mg | 26378-5 |
CAYMAN CHEMICAL COMPANY |
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A-967079 | A potent, selective, and bioavailable inhibitor of the TRPA1 channel, with… | 10 mg | 15207-10 |
CAYMAN CHEMICAL COMPANY |
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A-967079 | A potent, selective, and bioavailable inhibitor of the TRPA1 channel, with… | 25 mg | 15207-25 |
CAYMAN CHEMICAL COMPANY |
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A-967079 | A potent, selective, and bioavailable inhibitor of the TRPA1 channel, with… | 5 mg | 15207-5 |
CAYMAN CHEMICAL COMPANY |
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A-967079 | A potent, selective, and bioavailable inhibitor of the TRPA1 channel, with… | 50 mg | 15207-50 |
CAYMAN CHEMICAL COMPANY |
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A-971432 | An S1P5 agonist that is selective for S1P5 over S1P1 and S1P3 (IC50s = 0.0… | 1 mg | 25326-1 |
CAYMAN CHEMICAL COMPANY |
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A-971432 | An S1P5 agonist that is selective for S1P5 over S1P1 and S1P3 (IC50s = 0.0… | 10 mg | 25326-10 |
CAYMAN CHEMICAL COMPANY |
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A-971432 | An S1P5 agonist that is selective for S1P5 over S1P1 and S1P3 (IC50s = 0.0… | 25 mg | 25326-25 |
CAYMAN CHEMICAL COMPANY |
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A-971432 | An S1P5 agonist that is selective for S1P5 over S1P1 and S1P3 (IC50s = 0.0… | 5 mg | 25326-5 |
CAYMAN CHEMICAL COMPANY |
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A-196 | A-196 is a small molecule which can act as a Selective inhibitor of lysine… | 5 mg, 25 mg, | abx282942 |
ABBEXA LTD |
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A-23187 | A-23187 is a small molecule which can act as a Ca2 ionophore. It is provid… | 5 mg, 25 mg, | abx076596 |
ABBEXA LTD |
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A-438079 | A-438079 is a small molecule which can act as a P2X7 antagonist. It is pro… | 5 mg, 25 mg, | abx283339 |
ABBEXA LTD |
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A-769662 | A-769662 is a small molecule which can act as an AMPK activator. It is pro… | 5 mg, 25 mg, | abx076760 |
ABBEXA LTD |
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