Name | Description | Size | Catalog # | Supplier | |
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A011 | An inhibitor of ATM kinase (IC50 = 1 nM); selective for ATM over a panel o… | 1 mg | 39183-1 |
CAYMAN CHEMICAL COMPANY |
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A011 | An inhibitor of ATM kinase (IC50 = 1 nM); selective for ATM over a panel o… | 5 mg | 39183-5 |
CAYMAN CHEMICAL COMPANY |
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A-1070722 | A GSK3β inhibitor (IC50 = <100 nM) | 1 mg | 29783-1 |
CAYMAN CHEMICAL COMPANY |
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A-1070722 | A GSK3β inhibitor (IC50 = <100 nM) | 10 mg | 29783-10 |
CAYMAN CHEMICAL COMPANY |
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A-1070722 | A GSK3β inhibitor (IC50 = <100 nM) | 25 mg | 29783-25 |
CAYMAN CHEMICAL COMPANY |
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A-1070722 | A GSK3β inhibitor (IC50 = <100 nM) | 5 mg | 29783-5 |
CAYMAN CHEMICAL COMPANY |
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A-1120 | An RBP4 antagonist (Ki = 8.3 nM for disruption of RBP4 binding to transthy… | 10 mg | 30921-10 |
CAYMAN CHEMICAL COMPANY |
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A-1120 | An RBP4 antagonist (Ki = 8.3 nM for disruption of RBP4 binding to transthy… | 5 mg | 30921-5 |
CAYMAN CHEMICAL COMPANY |
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A-1155463 | A Bcl-xL inhibitor (Ki = is = 80 and 16 nM, respectively); inhibits the gr… | 1 mg | 27369-1 |
CAYMAN CHEMICAL COMPANY |
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A-1155463 | A Bcl-xL inhibitor (Ki = is = 80 and 16 nM, respectively); inhibits the gr… | 10 mg | 27369-10 |
CAYMAN CHEMICAL COMPANY |
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A-1155463 | A Bcl-xL inhibitor (Ki = is = 80 and 16 nM, respectively); inhibits the gr… | 25 mg | 27369-25 |
CAYMAN CHEMICAL COMPANY |
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A-1155463 | A Bcl-xL inhibitor (Ki = is = 80 and 16 nM, respectively); inhibits the gr… | 5 mg | 27369-5 |
CAYMAN CHEMICAL COMPANY |
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A-1210477 | A selective Mcl-1 inhibitor (Ki = 0.43 nM; IC50 = 26.2 nM); disrupts the i… | 1 mg | 21113-1 |
CAYMAN CHEMICAL COMPANY |
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A-1210477 | A selective Mcl-1 inhibitor (Ki = 0.43 nM; IC50 = 26.2 nM); disrupts the i… | 10 mg | 21113-10 |
CAYMAN CHEMICAL COMPANY |
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A-1210477 | A selective Mcl-1 inhibitor (Ki = 0.43 nM; IC50 = 26.2 nM); disrupts the i… | 25 mg | 21113-25 |
CAYMAN CHEMICAL COMPANY |
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A-1210477 | A selective Mcl-1 inhibitor (Ki = 0.43 nM; IC50 = 26.2 nM); disrupts the i… | 5 mg | 21113-5 |
CAYMAN CHEMICAL COMPANY |
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A-1331852 | An orally bioavailable Bcl-xL inhibitor; selectively binds Bcl-xL over Bcl… | 1 mg | 22963-1 |
CAYMAN CHEMICAL COMPANY |
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A-1331852 | An orally bioavailable Bcl-xL inhibitor; selectively binds Bcl-xL over Bcl… | 10 mg | 22963-10 |
CAYMAN CHEMICAL COMPANY |
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A-1331852 | An orally bioavailable Bcl-xL inhibitor; selectively binds Bcl-xL over Bcl… | 5 mg | 22963-5 |
CAYMAN CHEMICAL COMPANY |
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A-196 | A selective inhibitor of SUV420H1 and SUV420H2 (IC50s = 25 and 144 nM, res… | 1 mg | 18317-1 |
CAYMAN CHEMICAL COMPANY |
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A-196 | A selective inhibitor of SUV420H1 and SUV420H2 (IC50s = 25 and 144 nM, res… | 5 mg | 18317-5 |
CAYMAN CHEMICAL COMPANY |
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A-196 | A selective inhibitor of SUV420H1 and SUV420H2 (IC50s = 25 and 144 nM, res… | 500 µg | 18317-500 |
CAYMAN CHEMICAL COMPANY |
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A-205804 | A potent inhibitor of E-selectin and ICAM-1 expression in HUVECs stimulate… | 1 mg | 21252-1 |
CAYMAN CHEMICAL COMPANY |
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A-205804 | A potent inhibitor of E-selectin and ICAM-1 expression in HUVECs stimulate… | 10 mg | 21252-10 |
CAYMAN CHEMICAL COMPANY |
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A-205804 | A potent inhibitor of E-selectin and ICAM-1 expression in HUVECs stimulate… | 5 mg | 21252-5 |
CAYMAN CHEMICAL COMPANY |
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