Name | Description | Size | Catalog # | Supplier | |
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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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A77 1726 | A77 1726 is a small molecule which can act as a DHODH inhibitor. It is pro… | 5 mg, 25 mg, | abx282325 |
ABBEXA LTD |
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A-803467 | A-803467 is a small molecule which can act as a Sodium NaV1.8 channel bloc… | 10 mg, 50 mg, | abx076576 |
ABBEXA LTD |
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A83-01 | A83-01 is a small molecule which can act as an ALK inhibitor. It is provid… | 5 mg, 25 mg, | abx076740 |
ABBEXA LTD |
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A939572 | A939572 is a small molecule which can act as a SCD1 inhibitor. It is provi… | 5 mg, 25 mg, | abx283352 |
ABBEXA LTD |
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A-967079 | A-967079 is a small molecule which can act as a TRPA1 blocker. It is provi… | 5 mg, 25 mg, | abx076611 |
ABBEXA LTD |
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A 1070722 | Structural Formula: C17H13F3N4O2, Molecular Weight: 362.31 | 10 mg | sc-364392 |
SANTA CRUZ BIOTECHNOLOGY INC. |
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A 1070722 | Structural Formula: C17H13F3N4O2, Molecular Weight: 362.31 | 50 mg | sc-364392A |
SANTA CRUZ BIOTECHNOLOGY INC. |
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A 1120 | Structural Formula: C20H19F3N2O3, Molecular Weight: 392.37, CAS: 1152782-1… | 5 mg | sc-361093 |
SANTA CRUZ BIOTECHNOLOGY INC. |
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A 1120 | Structural Formula: C20H19F3N2O3, Molecular Weight: 392.37, CAS: 1152782-1… | 25 mg | sc-361093A |
SANTA CRUZ BIOTECHNOLOGY INC. |
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A 1120 | Structural Formula: C20H19F3N2O3, Molecular Weight: 392.37, CAS: 1152782-1… | 4 g | sc-361093B |
SANTA CRUZ BIOTECHNOLOGY INC. |
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A 205804 | 4-[(4-METHYLPHENYL)THIO]THIENO[2,3-C]PYRIDINE-2-CARBOXAMIDE, C15H12N2OS2,… | 10 mg | sc-203484 |
SANTA CRUZ BIOTECHNOLOGY INC. |
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A 205804 | 4-[(4-METHYLPHENYL)THIO]THIENO[2,3-C]PYRIDINE-2-CARBOXAMIDE, C15H12N2OS2,… | 50 mg | sc-203484A |
SANTA CRUZ BIOTECHNOLOGY INC. |
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A 286982 | Structural Formula: C24H27N3O4S, Molecular Weight: 453.55, CAS: 280749-17-9 | 10 mg | sc-362705 |
SANTA CRUZ BIOTECHNOLOGY INC. |
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A 286982 | Structural Formula: C24H27N3O4S, Molecular Weight: 453.55, CAS: 280749-17-9 | 50 mg | sc-362705A |
SANTA CRUZ BIOTECHNOLOGY INC. |
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A 484954 | Structural Formula: C13H15N5O3, Molecular Weight: 289.29, CAS: 142557-61-7 | 10 mg | sc-479613 |
SANTA CRUZ BIOTECHNOLOGY INC. |
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A 582941 | Structural Formula: C17H20N4, Molecular Weight: 280.37, CAS: 848591-90-2 | 10 mg | sc-362706 |
SANTA CRUZ BIOTECHNOLOGY INC. |
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A 582941 | Structural Formula: C17H20N4, Molecular Weight: 280.37, CAS: 848591-90-2 | 50 mg | sc-362706A |
SANTA CRUZ BIOTECHNOLOGY INC. |
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A 740003 | N-[1-[[(Cyanoamino)(5-quinolinylamino)methylene]amino]- 2,2-dimethylpropyl… | 10 mg | sc-291774 |
SANTA CRUZ BIOTECHNOLOGY INC. |
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A 740003 | N-[1-[[(Cyanoamino)(5-quinolinylamino)methylene]amino]- 2,2-dimethylpropyl… | 50 mg | sc-291774A |
SANTA CRUZ BIOTECHNOLOGY INC. |
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A 77-01 | Structural Formula: C18H14N4, Molecular Weight: 286.33, CAS: 607737-87-1 | 5 mg | sc-396001 |
SANTA CRUZ BIOTECHNOLOGY INC. |
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A 804598 | Structural Formula: C19H17N5, Molecular Weight: 315.37, CAS: 1125758-85-1 | 5 mg | sc-396064 |
SANTA CRUZ BIOTECHNOLOGY INC. |
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