Non-Antibody Products — page 1 of 44,461
Non-Antibody Products
Page 1 of 44,461
| Name | Description | Size | Catalog # | Supplier | |
|---|---|---|---|---|---|
| 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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| A-205804 | A potent inhibitor of E-selectin and ICAM-1 expression in HUVECs stimulate… | 50 mg | 21252-50 |
CAYMAN CHEMICAL COMPANY |
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| A23187 | A calcium ionophore and a microbial metabolite; induces calcium overload a… | 1 mg | 11016-1 |
CAYMAN CHEMICAL COMPANY |
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| A23187 | A calcium ionophore and a microbial metabolite; induces calcium overload a… | 10 mg | 11016-10 |
CAYMAN CHEMICAL COMPANY |
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| A23187 | A calcium ionophore and a microbial metabolite; induces calcium overload a… | 25 mg | 11016-25 |
CAYMAN CHEMICAL COMPANY |
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| A23187 | A calcium ionophore and a microbial metabolite; induces calcium overload a… | 5 mg | 11016-5 |
CAYMAN CHEMICAL COMPANY |
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| A286982 | An inhibitor that blocks the integrin-ligand interaction between LFA-1 and… | 10 mg | 27646-10 |
CAYMAN CHEMICAL COMPANY |
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| A286982 | An inhibitor that blocks the integrin-ligand interaction between LFA-1 and… | 25 mg | 27646-25 |
CAYMAN CHEMICAL COMPANY |
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| A286982 | An inhibitor that blocks the integrin-ligand interaction between LFA-1 and… | 5 mg | 27646-5 |
CAYMAN CHEMICAL COMPANY |
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| A286982 | An inhibitor that blocks the integrin-ligand interaction between LFA-1 and… | 50 mg | 27646-50 |
CAYMAN CHEMICAL COMPANY |
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| A-317491 | A P2X3 and P2X2 / 3 receptor antagonist (Kis = 22-92 nM in a calcium influ… | 1 mg | 19256-1 |
CAYMAN CHEMICAL COMPANY |
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| A-317491 | A P2X3 and P2X2 / 3 receptor antagonist (Kis = 22-92 nM in a calcium influ… | 10 mg | 19256-10 |
CAYMAN CHEMICAL COMPANY |
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| A-317491 | A P2X3 and P2X2 / 3 receptor antagonist (Kis = 22-92 nM in a calcium influ… | 25 mg | 19256-25 |
CAYMAN CHEMICAL COMPANY |
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| A-317491 | A P2X3 and P2X2 / 3 receptor antagonist (Kis = 22-92 nM in a calcium influ… | 5 mg | 19256-5 |
CAYMAN CHEMICAL COMPANY |
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| A-366 | A potent, peptide-competitive inhibitor of the lysine methyltransferase G9… | 10 mg | 16081-10 |
CAYMAN CHEMICAL COMPANY |
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| A-366 | A potent, peptide-competitive inhibitor of the lysine methyltransferase G9… | 5 mg | 16081-5 |
CAYMAN CHEMICAL COMPANY |
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| A-366 | A potent, peptide-competitive inhibitor of the lysine methyltransferase G9… | 50 mg | 16081-50 |
CAYMAN CHEMICAL COMPANY |
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| A-419259 | An inhibitor of Src family kinases, including Src, LCK, Lyn, and Hck (IC50… | 1 mg | 25605-1 |
CAYMAN CHEMICAL COMPANY |
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| A-419259 | An inhibitor of Src family kinases, including Src, LCK, Lyn, and Hck (IC50… | 10 mg | 25605-10 |
CAYMAN CHEMICAL COMPANY |
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| A-419259 | An inhibitor of Src family kinases, including Src, LCK, Lyn, and Hck (IC50… | 5 mg | 25605-5 |
CAYMAN CHEMICAL COMPANY |
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| A-443654 | A pan Akt inhibitor (Ki = 160 pmol / L for all three isoforms) that interf… | 1 mg | 16499-1 |
CAYMAN CHEMICAL COMPANY |
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| A-443654 | A pan Akt inhibitor (Ki = 160 pmol / L for all three isoforms) that interf… | 5 mg | 16499-5 |
CAYMAN CHEMICAL COMPANY |
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| A-443654 | A pan Akt inhibitor (Ki = 160 pmol / L for all three isoforms) that interf… | 500 µg | 16499-500 |
CAYMAN CHEMICAL COMPANY |
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| A-484954 | An eEF-2K inhibitor; reduces eEF-2K autophosphorylation in various cancer… | 1 mg | 28279-1 |
CAYMAN CHEMICAL COMPANY |
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| A-484954 | An eEF-2K inhibitor; reduces eEF-2K autophosphorylation in various cancer… | 10 mg | 28279-10 |
CAYMAN CHEMICAL COMPANY |
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| A-484954 | An eEF-2K inhibitor; reduces eEF-2K autophosphorylation in various cancer… | 25 mg | 28279-25 |
CAYMAN CHEMICAL COMPANY |
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| A-484954 | An eEF-2K inhibitor; reduces eEF-2K autophosphorylation in various cancer… | 5 mg | 28279-5 |
CAYMAN CHEMICAL COMPANY |
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| A-485 | A p300 / CBP inhibitor (IC50 = 60 nM); decreases H3K27Ac levels in PC3 cel… | 1 mg | 24119-1 |
CAYMAN CHEMICAL COMPANY |
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| A-485 | A p300 / CBP inhibitor (IC50 = 60 nM); decreases H3K27Ac levels in PC3 cel… | 10 mg | 24119-10 |
CAYMAN CHEMICAL COMPANY |
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| A-485 | A p300 / CBP inhibitor (IC50 = 60 nM); decreases H3K27Ac levels in PC3 cel… | 25 mg | 24119-25 |
CAYMAN CHEMICAL COMPANY |
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| A-485 | A p300 / CBP inhibitor (IC50 = 60 nM); decreases H3K27Ac levels in PC3 cel… | 5 mg | 24119-5 |
CAYMAN CHEMICAL COMPANY |
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| A-61603 | A selective α1A-adrenergic receptor agonist that is at least 35-fold… | 1 mg | 17358-1 |
CAYMAN CHEMICAL COMPANY |
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| A-61603 | A selective α1A-adrenergic receptor agonist that is at least 35-fold… | 10 mg | 17358-10 |
CAYMAN CHEMICAL COMPANY |
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| A-61603 | A selective α1A-adrenergic receptor agonist that is at least 35-fold… | 5 mg | 17358-5 |
CAYMAN CHEMICAL COMPANY |
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| A-66 | A potent, selective inhibitor of the PI3K isoform p110α (IC50 = 32 n… | 1 mg | 17382-1 |
CAYMAN CHEMICAL COMPANY |
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| A-66 | A potent, selective inhibitor of the PI3K isoform p110α (IC50 = 32 n… | 10 mg | 17382-10 |
CAYMAN CHEMICAL COMPANY |
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| A-66 | A potent, selective inhibitor of the PI3K isoform p110α (IC50 = 32 n… | 25 mg | 17382-25 |
CAYMAN CHEMICAL COMPANY |
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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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