Name | Description | Size | Catalog # | Supplier | |
---|---|---|---|---|---|
852A | A TLR7 agonist; selectively induces NF-κB signaling in HEK293 cells… | 25 mg | 39512-25 |
CAYMAN CHEMICAL COMPANY |
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852A | A TLR7 agonist; selectively induces NF-κB signaling in HEK293 cells… | 5 mg | 39512-5 |
CAYMAN CHEMICAL COMPANY |
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A 83-01 | An inhibitor of ALK5, ALK4, and ALK7 (IC50s = 12, 45, and 7.5 nM, respecti… | 1 mg | 9001799-1 |
CAYMAN CHEMICAL COMPANY |
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A 83-01 | An inhibitor of ALK5, ALK4, and ALK7 (IC50s = 12, 45, and 7.5 nM, respecti… | 10 mg | 9001799-10 |
CAYMAN CHEMICAL COMPANY |
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A 83-01 | An inhibitor of ALK5, ALK4, and ALK7 (IC50s = 12, 45, and 7.5 nM, respecti… | 25 mg | 9001799-25 |
CAYMAN CHEMICAL COMPANY |
More Info |
A 83-01 | An inhibitor of ALK5, ALK4, and ALK7 (IC50s = 12, 45, and 7.5 nM, respecti… | 5 mg | 9001799-5 |
CAYMAN CHEMICAL COMPANY |
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A01 | A Smurf1 inhibitor (Kd = 3.67 nM); inhibits Smurf1-mediated ubiquitination… | 10 mg | 26137-10 |
CAYMAN CHEMICAL COMPANY |
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A01 | A Smurf1 inhibitor (Kd = 3.67 nM); inhibits Smurf1-mediated ubiquitination… | 25 mg | 26137-25 |
CAYMAN CHEMICAL COMPANY |
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A01 | A Smurf1 inhibitor (Kd = 3.67 nM); inhibits Smurf1-mediated ubiquitination… | 5 mg | 26137-5 |
CAYMAN CHEMICAL COMPANY |
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A01 | A Smurf1 inhibitor (Kd = 3.67 nM); inhibits Smurf1-mediated ubiquitination… | 50 mg | 26137-50 |
CAYMAN CHEMICAL COMPANY |
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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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