CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 533 of 1

Non-Antibody Products
Page 533 of 1,304
  • Records 26,601 - 26,650 of 65,198
Name Description Size Catalog #
GSK189254 A histamine H3 receptor antagonist (Kis = 0.13, 0.68, and 1.74 nM for the… 5 mg 36705-5 More Info
GSK1940029 A stearoyl-CoA desaturase inhibitor; increases palmitate-induced phosphory… 1 mg 36704-1 More Info
GSK1940029 A stearoyl-CoA desaturase inhibitor; increases palmitate-induced phosphory… 10 mg 36704-10 More Info
GSK1940029 A stearoyl-CoA desaturase inhibitor; increases palmitate-induced phosphory… 25 mg 36704-25 More Info
GSK1940029 A stearoyl-CoA desaturase inhibitor; increases palmitate-induced phosphory… 5 mg 36704-5 More Info
GSK2018682 An S1P1 and S1P5 receptor agonist; selective for S1P1 and S1P5 over S1P2,… 10 mg 31437-10 More Info
GSK2018682 An S1P1 and S1P5 receptor agonist; selective for S1P1 and S1P5 over S1P2,… 25 mg 31437-25 More Info
GSK2018682 An S1P1 and S1P5 receptor agonist; selective for S1P1 and S1P5 over S1P2,… 5 mg 31437-5 More Info
GSK2018682 An S1P1 and S1P5 receptor agonist; selective for S1P1 and S1P5 over S1P2,… 50 mg 31437-50 More Info
GSK2033 An antagonist of LXRα and LXRβ (IC50s = 0.1 and 0.398 µM,… 1 mg 25443-1 More Info
GSK2033 An antagonist of LXRα and LXRβ (IC50s = 0.1 and 0.398 µM,… 10 mg 25443-10 More Info
GSK2033 An antagonist of LXRα and LXRβ (IC50s = 0.1 and 0.398 µM,… 5 mg 25443-5 More Info
GSK2126458 A potent inhibitor of PI3K isoforms (Kis = 19, 130, 24, and 60 pM for p110… 1 mg 17377-1 More Info
GSK2126458 A potent inhibitor of PI3K isoforms (Kis = 19, 130, 24, and 60 pM for p110… 10 mg 17377-10 More Info
GSK2126458 A potent inhibitor of PI3K isoforms (Kis = 19, 130, 24, and 60 pM for p110… 5 mg 17377-5 More Info
GSK2126458 A potent inhibitor of PI3K isoforms (Kis = 19, 130, 24, and 60 pM for p110… 50 mg 17377-50 More Info
GSK2190915 A selective inhibitor of human FLAP (IC50 = 2.9 nM); selective for FLAP ov… 1 mg 28600-1 More Info
GSK2193874 A potent, selective antagonist of TRPV4 channels, blocking the influx of c… 1 mg 17715-1 More Info
GSK2193874 A potent, selective antagonist of TRPV4 channels, blocking the influx of c… 10 mg 17715-10 More Info
GSK2193874 A potent, selective antagonist of TRPV4 channels, blocking the influx of c… 25 mg 17715-25 More Info
GSK2193874 A potent, selective antagonist of TRPV4 channels, blocking the influx of c… 5 mg 17715-5 More Info
GSK2194069 An inhibitor of fatty acid synthase (IC50 = 7.7 nM in an assay detecting r… 1 mg 20022-1 More Info
GSK2194069 An inhibitor of fatty acid synthase (IC50 = 7.7 nM in an assay detecting r… 5 mg 20022-5 More Info
GSK2194069 An inhibitor of fatty acid synthase (IC50 = 7.7 nM in an assay detecting r… 500 µg 20022-500 More Info
GSK2245035 A TLR7 agonist; selectively induces the production of IFN-α over TNF… 1 mg 33171-1 More Info
GSK2245035 A TLR7 agonist; selectively induces the production of IFN-α over TNF… 10 mg 33171-10 More Info
GSK2245035 A TLR7 agonist; selectively induces the production of IFN-α over TNF… 5 mg 33171-5 More Info
GSK2256098 A FAK inhibitor; selective for FAK over 261 kinases; inhibits FAK autophos… 1 mg 22955-1 More Info
GSK2256098 A FAK inhibitor; selective for FAK over 261 kinases; inhibits FAK autophos… 10 mg 22955-10 More Info
GSK2256098 A FAK inhibitor; selective for FAK over 261 kinases; inhibits FAK autophos… 25 mg 22955-25 More Info
GSK2256098 A FAK inhibitor; selective for FAK over 261 kinases; inhibits FAK autophos… 5 mg 22955-5 More Info
GSK2269557 A selective PI3Kδ inhibitor (pKi = 9.9) that is active in a brown No… 1 mg 17388-1 More Info
GSK2269557 A selective PI3Kδ inhibitor (pKi = 9.9) that is active in a brown No… 10 mg 17388-10 More Info
GSK2269557 A selective PI3Kδ inhibitor (pKi = 9.9) that is active in a brown No… 25 mg 17388-25 More Info
GSK2269557 A selective PI3Kδ inhibitor (pKi = 9.9) that is active in a brown No… 5 mg 17388-5 More Info
GSK2292767 A potent and selective inhibitor of PI3Kδ (Ki = 79 pM); has >1,000-f… 1 mg 21757-1 More Info
GSK2292767 A potent and selective inhibitor of PI3Kδ (Ki = 79 pM); has >1,000-f… 10 mg 21757-10 More Info
GSK2292767 A potent and selective inhibitor of PI3Kδ (Ki = 79 pM); has >1,000-f… 25 mg 21757-25 More Info
GSK2292767 A potent and selective inhibitor of PI3Kδ (Ki = 79 pM); has >1,000-f… 5 mg 21757-5 More Info
GSK2330672 An ASBT inhibitor (IC50s = 42, 2.1, and 1.9 nM for human, mouse, and rat A… 1 mg 23843-1 More Info
GSK2330672 An ASBT inhibitor (IC50s = 42, 2.1, and 1.9 nM for human, mouse, and rat A… 10 mg 23843-10 More Info
GSK2330672 An ASBT inhibitor (IC50s = 42, 2.1, and 1.9 nM for human, mouse, and rat A… 5 mg 23843-5 More Info
GSK2334470 A selective PDK1 inhibitor (IC50 = ~10 nM) that even at 100-fold higher co… 10 mg 18095-10 More Info
GSK2334470 A selective PDK1 inhibitor (IC50 = ~10 nM) that even at 100-fold higher co… 25 mg 18095-25 More Info
GSK2334470 A selective PDK1 inhibitor (IC50 = ~10 nM) that even at 100-fold higher co… 5 mg 18095-5 More Info
GSK2334470 A selective PDK1 inhibitor (IC50 = ~10 nM) that even at 100-fold higher co… 50 mg 18095-50 More Info
GSK25 A ROCK1 inhibitor (IC50 = 7 nM for the human kinase); selective over RSK1… 1 mg 39163-1 More Info
GSK25 A ROCK1 inhibitor (IC50 = 7 nM for the human kinase); selective over RSK1… 10 mg 39163-10 More Info
GSK25 A ROCK1 inhibitor (IC50 = 7 nM for the human kinase); selective over RSK1… 5 mg 39163-5 More Info
GSK25 A ROCK1 inhibitor (IC50 = 7 nM for the human kinase); selective over RSK1… 500 µg 39163-500 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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