Non-Antibody Products — page 1 of 88,939
Non-Antibody Products
Page 1 of 88,939
| Name | Description | Size | Catalog # | Supplier | |
|---|---|---|---|---|---|
| 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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