CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 97 of 1

Non-Antibody Products
Page 97 of 1,288
  • Records 4,801 - 4,850 of 64,374
Name Description Size Catalog #
AS-041164 A potent inhibitor of PI3K with selectivity for the class IB isoform PI3K&… 10 mg 13622-10 More Info
AS-041164 A potent inhibitor of PI3K with selectivity for the class IB isoform PI3K&… 25 mg 13622-25 More Info
AS-041164 A potent inhibitor of PI3K with selectivity for the class IB isoform PI3K&… 5 mg 13622-5 More Info
AS-041164 A potent inhibitor of PI3K with selectivity for the class IB isoform PI3K&… 50 mg 13622-50 More Info
AS-101 An immunomodulator; inhibits IL-10 secretion from and cell proliferation o… 1 mg 21443-1 More Info
AS-101 An immunomodulator; inhibits IL-10 secretion from and cell proliferation o… 10 mg 21443-10 More Info
AS-101 An immunomodulator; inhibits IL-10 secretion from and cell proliferation o… 5 mg 21443-5 More Info
AS-1269574 An agonist of GPR199 that is effective both in isolated cells and in vivo;… 1 mg 10626-1 More Info
AS-1269574 An agonist of GPR199 that is effective both in isolated cells and in vivo;… 10 mg 10626-10 More Info
AS-1269574 An agonist of GPR199 that is effective both in isolated cells and in vivo;… 25 mg 10626-25 More Info
AS-1269574 An agonist of GPR199 that is effective both in isolated cells and in vivo;… 5 mg 10626-5 More Info
AS1517499 A STAT6 inhibitor (IC50 = 21 nM in a reporter assay); inhibits IL-4-induce… 1 mg 29071-1 More Info
AS1517499 A STAT6 inhibitor (IC50 = 21 nM in a reporter assay); inhibits IL-4-induce… 10 mg 29071-10 More Info
AS1517499 A STAT6 inhibitor (IC50 = 21 nM in a reporter assay); inhibits IL-4-induce… 25 mg 29071-25 More Info
AS1517499 A STAT6 inhibitor (IC50 = 21 nM in a reporter assay); inhibits IL-4-induce… 5 mg 29071-5 More Info
AS-1842856 A potent FoxO1 inhibitor (IC50 = 33 nM in HepG2 cells); causes a dose-depe… 1 mg 16761-1 More Info
AS-1842856 A potent FoxO1 inhibitor (IC50 = 33 nM in HepG2 cells); causes a dose-depe… 10 mg 16761-10 More Info
AS-1842856 A potent FoxO1 inhibitor (IC50 = 33 nM in HepG2 cells); causes a dose-depe… 5 mg 16761-5 More Info
AS-1892802 A potent ROCK inhibitor (IC50s = 122, 52, and 57 nM for human ROCK1, ROCK2… 1 mg 14978-1 More Info
AS-1892802 A potent ROCK inhibitor (IC50s = 122, 52, and 57 nM for human ROCK1, ROCK2… 10 mg 14978-10 More Info
AS-1892802 A potent ROCK inhibitor (IC50s = 122, 52, and 57 nM for human ROCK1, ROCK2… 25 mg 14978-25 More Info
AS-1892802 A potent ROCK inhibitor (IC50s = 122, 52, and 57 nM for human ROCK1, ROCK2… 5 mg 14978-5 More Info
AS-19 A 5-HT7 receptor agonist (IC50 = 0.83 nM); selective for 5-HT7 over 5-HT1A… 1 mg 20642-1 More Info
AS-19 A 5-HT7 receptor agonist (IC50 = 0.83 nM); selective for 5-HT7 over 5-HT1A… 10 mg 20642-10 More Info
AS-19 A 5-HT7 receptor agonist (IC50 = 0.83 nM); selective for 5-HT7 over 5-HT1A… 5 mg 20642-5 More Info
AS-1949490 A selective inhibitor of SHIP2 (IC50s = 0.62 and 0.34 µM for human a… 1 mg 17627-1 More Info
AS-1949490 A selective inhibitor of SHIP2 (IC50s = 0.62 and 0.34 µM for human a… 10 mg 17627-10 More Info
AS-1949490 A selective inhibitor of SHIP2 (IC50s = 0.62 and 0.34 µM for human a… 5 mg 17627-5 More Info
AS-1949490 A selective inhibitor of SHIP2 (IC50s = 0.62 and 0.34 µM for human a… 50 mg 17627-50 More Info
AS-2077715 An inhibitor of fungal complex III (IC50 = 80 ng / ml for T. mentagrophyte… 1 mg 29775-1 More Info
AS-252424 A potent inhibitor of PI3K with selectivity for the g isoform; inhibits hu… 1 mg 10009052-1 More Info
AS-252424 A potent inhibitor of PI3K with selectivity for the g isoform; inhibits hu… 10 mg 10009052-10 More Info
AS-252424 A potent inhibitor of PI3K with selectivity for the g isoform; inhibits hu… 25 mg 10009052-25 More Info
AS-252424 A potent inhibitor of PI3K with selectivity for the g isoform; inhibits hu… 5 mg 10009052-5 More Info
AS-2717638 An LPA5 antagonist (IC50 = 0.038 µM); selective for LPA5 over LPA1,… 1 mg 37787-1 More Info
AS-2717638 An LPA5 antagonist (IC50 = 0.038 µM); selective for LPA5 over LPA1,… 10 mg 37787-10 More Info
AS-2717638 An LPA5 antagonist (IC50 = 0.038 µM); selective for LPA5 over LPA1,… 25 mg 37787-25 More Info
AS-2717638 An LPA5 antagonist (IC50 = 0.038 µM); selective for LPA5 over LPA1,… 5 mg 37787-5 More Info
AS-2863619 A dual inhibitor of Cdk8 and Cdk19 (IC50s = 0.6 and 4.3 nM, respectively);… 1 mg 30976-1 More Info
AS-2863619 A dual inhibitor of Cdk8 and Cdk19 (IC50s = 0.6 and 4.3 nM, respectively);… 5 mg 30976-5 More Info
AS-2863619 A dual inhibitor of Cdk8 and Cdk19 (IC50s = 0.6 and 4.3 nM, respectively);… 500 µg 30976-500 More Info
AS-604850 AS-604850 is a selective, ATP-competitive inhibitor of PI3Kγ with IC… 1 mg 10010175-1 More Info
AS-604850 AS-604850 is a selective, ATP-competitive inhibitor of PI3Kγ with IC… 10 mg 10010175-10 More Info
AS-604850 AS-604850 is a selective, ATP-competitive inhibitor of PI3Kγ with IC… 25 mg 10010175-25 More Info
AS-604850 AS-604850 is a selective, ATP-competitive inhibitor of PI3Kγ with IC… 5 mg 10010175-5 More Info
AS-605240 A potent inhibitor of PI3Kγ; inhibits human recombinant PI3Kγ,… 1 mg 10007707-1 More Info
AS-605240 A potent inhibitor of PI3Kγ; inhibits human recombinant PI3Kγ,… 10 mg 10007707-10 More Info
AS-605240 A potent inhibitor of PI3Kγ; inhibits human recombinant PI3Kγ,… 25 mg 10007707-25 More Info
AS-605240 A potent inhibitor of PI3Kγ; inhibits human recombinant PI3Kγ,… 5 mg 10007707-5 More Info
AS-703026 Selectively inhibits MEK1 / 2; potently inhibits growth and survival of hu… 1 mg 11226-1 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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