CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 2 of 1

Non-Antibody Products
Page 2 of 1,288
  • Records 51 - 100 of 64,374
Name Description Size Catalog #
A286982 An inhibitor that blocks the integrin-ligand interaction between LFA-1 and… 10 mg 27646-10 More Info
A286982 An inhibitor that blocks the integrin-ligand interaction between LFA-1 and… 25 mg 27646-25 More Info
A286982 An inhibitor that blocks the integrin-ligand interaction between LFA-1 and… 5 mg 27646-5 More Info
A286982 An inhibitor that blocks the integrin-ligand interaction between LFA-1 and… 50 mg 27646-50 More Info
A-317491 A P2X3 and P2X2 / 3 receptor antagonist (Kis = 22-92 nM in a calcium influ… 1 mg 19256-1 More Info
A-317491 A P2X3 and P2X2 / 3 receptor antagonist (Kis = 22-92 nM in a calcium influ… 10 mg 19256-10 More Info
A-317491 A P2X3 and P2X2 / 3 receptor antagonist (Kis = 22-92 nM in a calcium influ… 25 mg 19256-25 More Info
A-317491 A P2X3 and P2X2 / 3 receptor antagonist (Kis = 22-92 nM in a calcium influ… 5 mg 19256-5 More Info
A-366 A potent, peptide-competitive inhibitor of the lysine methyltransferase G9… 10 mg 16081-10 More Info
A-366 A potent, peptide-competitive inhibitor of the lysine methyltransferase G9… 5 mg 16081-5 More Info
A-366 A potent, peptide-competitive inhibitor of the lysine methyltransferase G9… 50 mg 16081-50 More Info
A-419259 An inhibitor of Src family kinases, including Src, LCK, Lyn, and Hck (IC50… 1 mg 25605-1 More Info
A-419259 An inhibitor of Src family kinases, including Src, LCK, Lyn, and Hck (IC50… 10 mg 25605-10 More Info
A-419259 An inhibitor of Src family kinases, including Src, LCK, Lyn, and Hck (IC50… 5 mg 25605-5 More Info
A-443654 A pan Akt inhibitor (Ki = 160 pmol / L for all three isoforms) that interf… 1 mg 16499-1 More Info
A-443654 A pan Akt inhibitor (Ki = 160 pmol / L for all three isoforms) that interf… 5 mg 16499-5 More Info
A-443654 A pan Akt inhibitor (Ki = 160 pmol / L for all three isoforms) that interf… 500 µg 16499-500 More Info
A-484954 An eEF-2K inhibitor; reduces eEF-2K autophosphorylation in various cancer… 1 mg 28279-1 More Info
A-484954 An eEF-2K inhibitor; reduces eEF-2K autophosphorylation in various cancer… 10 mg 28279-10 More Info
A-484954 An eEF-2K inhibitor; reduces eEF-2K autophosphorylation in various cancer… 25 mg 28279-25 More Info
A-484954 An eEF-2K inhibitor; reduces eEF-2K autophosphorylation in various cancer… 5 mg 28279-5 More Info
A-485 A p300 / CBP inhibitor (IC50 = 60 nM); decreases H3K27Ac levels in PC3 cel… 1 mg 24119-1 More Info
A-485 A p300 / CBP inhibitor (IC50 = 60 nM); decreases H3K27Ac levels in PC3 cel… 10 mg 24119-10 More Info
A-485 A p300 / CBP inhibitor (IC50 = 60 nM); decreases H3K27Ac levels in PC3 cel… 25 mg 24119-25 More Info
A-485 A p300 / CBP inhibitor (IC50 = 60 nM); decreases H3K27Ac levels in PC3 cel… 5 mg 24119-5 More Info
A-61603 A selective α1A-adrenergic receptor agonist that is at least 35-fold… 1 mg 17358-1 More Info
A-61603 A selective α1A-adrenergic receptor agonist that is at least 35-fold… 10 mg 17358-10 More Info
A-61603 A selective α1A-adrenergic receptor agonist that is at least 35-fold… 5 mg 17358-5 More Info
A-66 A potent, selective inhibitor of the PI3K isoform p110α (IC50 = 32 n… 1 mg 17382-1 More Info
A-66 A potent, selective inhibitor of the PI3K isoform p110α (IC50 = 32 n… 10 mg 17382-10 More Info
A-66 A potent, selective inhibitor of the PI3K isoform p110α (IC50 = 32 n… 25 mg 17382-25 More Info
A-66 A potent, selective inhibitor of the PI3K isoform p110α (IC50 = 32 n… 5 mg 17382-5 More Info
A-674563 An orally available, reversible inhibitor of Akt (Ki = 11 nM for Akt1); al… 1 mg 18715-1 More Info
A-674563 An orally available, reversible inhibitor of Akt (Ki = 11 nM for Akt1); al… 10 mg 18715-10 More Info
A-674563 An orally available, reversible inhibitor of Akt (Ki = 11 nM for Akt1); al… 5 mg 18715-5 More Info
A-674563 An orally available, reversible inhibitor of Akt (Ki = 11 nM for Akt1); al… 500 µg 18715-500 More Info
A6770 An inhibitor of S1P lyase; induces accumulation of [3H]dhS1P in IT-79MTNC3… 1 mg 29972-1 More Info
A6770 An inhibitor of S1P lyase; induces accumulation of [3H]dhS1P in IT-79MTNC3… 10 mg 29972-10 More Info
A6770 An inhibitor of S1P lyase; induces accumulation of [3H]dhS1P in IT-79MTNC3… 5 mg 29972-5 More Info
A6770 An inhibitor of S1P lyase; induces accumulation of [3H]dhS1P in IT-79MTNC3… 500 µg 29972-500 More Info
A-740003 A selective P2X7 antagonist (IC50s = 40 and 18 nM for human and rat recept… 1 mg 21256-1 More Info
A-740003 A selective P2X7 antagonist (IC50s = 40 and 18 nM for human and rat recept… 10 mg 21256-10 More Info
A-740003 A selective P2X7 antagonist (IC50s = 40 and 18 nM for human and rat recept… 25 mg 21256-25 More Info
A-740003 A selective P2X7 antagonist (IC50s = 40 and 18 nM for human and rat recept… 5 mg 21256-5 More Info
A-769662 A direct activator of AMPK (EC50 = 116 nM in a cell-free assay); allosteri… 10 mg 11900-10 More Info
A-769662 A direct activator of AMPK (EC50 = 116 nM in a cell-free assay); allosteri… 25 mg 11900-25 More Info
A-769662 A direct activator of AMPK (EC50 = 116 nM in a cell-free assay); allosteri… 5 mg 11900-5 More Info
A-769662 A direct activator of AMPK (EC50 = 116 nM in a cell-free assay); allosteri… 50 mg 11900-50 More Info
A-770041 An orally bioavailable LCK kinase inhibitor (IC50 = 0.147 µM); selec… 1 mg 32854-1 More Info
A-770041 An orally bioavailable LCK kinase inhibitor (IC50 = 0.147 µM); selec… 5 mg 32854-5 More Info
CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
1180 East Ellsworth Road
Ann Arbor MI 48108
P: (734) 971-3335
P: (800) 364-9897 (USA & Canada only)
F: (734) 971-3640

Customer Service: custserv@caymanchem.com
Technical Support: techserv@caymanchem.com
Sales: sales@caymanchem.com

http://www.caymanchem.com

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