Name | Description | Size | Catalog # | Supplier | |
---|---|---|---|---|---|
A-205804 | A potent inhibitor of E-selectin and ICAM-1 expression in HUVECs stimulate… | 50 mg | 21252-50 |
CAYMAN CHEMICAL COMPANY |
More Info |
A23187 | A calcium ionophore and a microbial metabolite; induces calcium overload a… | 1 mg | 11016-1 |
CAYMAN CHEMICAL COMPANY |
More Info |
A23187 | A calcium ionophore and a microbial metabolite; induces calcium overload a… | 10 mg | 11016-10 |
CAYMAN CHEMICAL COMPANY |
More Info |
A23187 | A calcium ionophore and a microbial metabolite; induces calcium overload a… | 25 mg | 11016-25 |
CAYMAN CHEMICAL COMPANY |
More Info |
A23187 | A calcium ionophore and a microbial metabolite; induces calcium overload a… | 5 mg | 11016-5 |
CAYMAN CHEMICAL COMPANY |
More Info |
A286982 | An inhibitor that blocks the integrin-ligand interaction between LFA-1 and… | 10 mg | 27646-10 |
CAYMAN CHEMICAL COMPANY |
More Info |
A286982 | An inhibitor that blocks the integrin-ligand interaction between LFA-1 and… | 25 mg | 27646-25 |
CAYMAN CHEMICAL COMPANY |
More Info |
A286982 | An inhibitor that blocks the integrin-ligand interaction between LFA-1 and… | 5 mg | 27646-5 |
CAYMAN CHEMICAL COMPANY |
More Info |
A286982 | An inhibitor that blocks the integrin-ligand interaction between LFA-1 and… | 50 mg | 27646-50 |
CAYMAN CHEMICAL COMPANY |
More Info |
A-317491 | A P2X3 and P2X2 / 3 receptor antagonist (Kis = 22-92 nM in a calcium influ… | 1 mg | 19256-1 |
CAYMAN CHEMICAL COMPANY |
More Info |
A-317491 | A P2X3 and P2X2 / 3 receptor antagonist (Kis = 22-92 nM in a calcium influ… | 10 mg | 19256-10 |
CAYMAN CHEMICAL COMPANY |
More Info |
A-317491 | A P2X3 and P2X2 / 3 receptor antagonist (Kis = 22-92 nM in a calcium influ… | 25 mg | 19256-25 |
CAYMAN CHEMICAL COMPANY |
More Info |
A-317491 | A P2X3 and P2X2 / 3 receptor antagonist (Kis = 22-92 nM in a calcium influ… | 5 mg | 19256-5 |
CAYMAN CHEMICAL COMPANY |
More Info |
A-366 | A potent, peptide-competitive inhibitor of the lysine methyltransferase G9… | 10 mg | 16081-10 |
CAYMAN CHEMICAL COMPANY |
More Info |
A-366 | A potent, peptide-competitive inhibitor of the lysine methyltransferase G9… | 5 mg | 16081-5 |
CAYMAN CHEMICAL COMPANY |
More Info |
A-366 | A potent, peptide-competitive inhibitor of the lysine methyltransferase G9… | 50 mg | 16081-50 |
CAYMAN CHEMICAL COMPANY |
More Info |
A-419259 | An inhibitor of Src family kinases, including Src, LCK, Lyn, and Hck (IC50… | 1 mg | 25605-1 |
CAYMAN CHEMICAL COMPANY |
More Info |
A-419259 | An inhibitor of Src family kinases, including Src, LCK, Lyn, and Hck (IC50… | 10 mg | 25605-10 |
CAYMAN CHEMICAL COMPANY |
More Info |
A-419259 | An inhibitor of Src family kinases, including Src, LCK, Lyn, and Hck (IC50… | 5 mg | 25605-5 |
CAYMAN CHEMICAL COMPANY |
More Info |
A-443654 | A pan Akt inhibitor (Ki = 160 pmol / L for all three isoforms) that interf… | 1 mg | 16499-1 |
CAYMAN CHEMICAL COMPANY |
More Info |
A-443654 | A pan Akt inhibitor (Ki = 160 pmol / L for all three isoforms) that interf… | 5 mg | 16499-5 |
CAYMAN CHEMICAL COMPANY |
More Info |
A-443654 | A pan Akt inhibitor (Ki = 160 pmol / L for all three isoforms) that interf… | 500 µg | 16499-500 |
CAYMAN CHEMICAL COMPANY |
More Info |
A-484954 | An eEF-2K inhibitor; reduces eEF-2K autophosphorylation in various cancer… | 1 mg | 28279-1 |
CAYMAN CHEMICAL COMPANY |
More Info |
A-484954 | An eEF-2K inhibitor; reduces eEF-2K autophosphorylation in various cancer… | 10 mg | 28279-10 |
CAYMAN CHEMICAL COMPANY |
More Info |
A-484954 | An eEF-2K inhibitor; reduces eEF-2K autophosphorylation in various cancer… | 25 mg | 28279-25 |
CAYMAN CHEMICAL COMPANY |
More Info |