CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 98 of 1
Non-Antibody Products
Page 98 of 1,304
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| Aryl Hydrocarbon Receptor Bioassay | This assay kit provides the convenience of an all-inclusive cell-based rep… | 96 well | 41037-96 | More Info |
| Arylpiperazine 5k | A FATP1 inhibitor (IC50 = 4.6 nM for the human protein); reduces neutral a… | 10 mg | 38135-10 | More Info |
| Arylpiperazine 5k | A FATP1 inhibitor (IC50 = 4.6 nM for the human protein); reduces neutral a… | 25 mg | 38135-25 | More Info |
| Arylpiperazine 5k | A FATP1 inhibitor (IC50 = 4.6 nM for the human protein); reduces neutral a… | 5 mg | 38135-5 | More Info |
| Arylpiperazine 5k | A FATP1 inhibitor (IC50 = 4.6 nM for the human protein); reduces neutral a… | 50 mg | 38135-50 | More Info |
| Arylquin 1 | A Par-4 secretagogue; binds to vimentin to displace Par-4 for secretion; i… | 1 mg | 16961-1 | More Info |
| Arylquin 1 | A Par-4 secretagogue; binds to vimentin to displace Par-4 for secretion; i… | 10 mg | 16961-10 | More Info |
| Arylquin 1 | A Par-4 secretagogue; binds to vimentin to displace Par-4 for secretion; i… | 5 mg | 16961-5 | More Info |
| (-)-AS 115 | A single enantiomer of a potent and selective inactivator of KIAA1363, a M… | 1 mg | 13250-1 | More Info |
| (-)-AS 115 | A single enantiomer of a potent and selective inactivator of KIAA1363, a M… | 100 µg | 13250-100 | More Info |
| (-)-AS 115 | A single enantiomer of a potent and selective inactivator of KIAA1363, a M… | 500 µg | 13250-500 | More Info |
| (+)-AS 115 | A single enantiomer of a potent and selective inactivator of KIAA1363, a M… | 1 mg | 10009650-1 | More Info |
| (+)-AS 115 | A single enantiomer of a potent and selective inactivator of KIAA1363, a M… | 100 µg | 10009650-100 | More Info |
| (+)-AS 115 | A single enantiomer of a potent and selective inactivator of KIAA1363, a M… | 500 µg | 10009650-500 | More Info |
| 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 |
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
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