CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 97 of 1
Non-Antibody Products
Page 97 of 1,297
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| ARUK3001185 | An inhibitor of NOTUM (IC50 = 6.7 nM); selective for NOTUM over a panel of… | 5 mg | 37113-5 | More Info |
| Arundic Acid | An inhibitor of astrocyte activation; reduces increases in brain GFAP and… | 1 mg | 29087-1 | More Info |
| Arundic Acid | An inhibitor of astrocyte activation; reduces increases in brain GFAP and… | 10 mg | 29087-10 | More Info |
| Arundic Acid | An inhibitor of astrocyte activation; reduces increases in brain GFAP and… | 25 mg | 29087-25 | More Info |
| Arundic Acid | An inhibitor of astrocyte activation; reduces increases in brain GFAP and… | 5 mg | 29087-5 | More Info |
| ARV-110 | A PROTAC that drives AR degradation; reduces androgen receptor levels in V… | 10 mg | 39662-10 | More Info |
| ARV-110 | A PROTAC that drives AR degradation; reduces androgen receptor levels in V… | 25 mg | 39662-25 | More Info |
| ARV-110 | A PROTAC that drives AR degradation; reduces androgen receptor levels in V… | 5 mg | 39662-5 | More Info |
| ARV-110 | A PROTAC that drives AR degradation; reduces androgen receptor levels in V… | 50 mg | 39662-50 | More Info |
| ARV-771 | A PROTAC that drives BET family protein degradation; induces degradation o… | 1 mg | 21299-1 | More Info |
| ARV-771 | A PROTAC that drives BET family protein degradation; induces degradation o… | 10 mg | 21299-10 | More Info |
| ARV-771 | A PROTAC that drives BET family protein degradation; induces degradation o… | 5 mg | 21299-5 | More Info |
| ARV-825 | A hetero-bifunctional molecule composed of a BRD4 binding moiety joined to… | 1 mg | 21109-1 | More Info |
| ARV-825 | A hetero-bifunctional molecule composed of a BRD4 binding moiety joined to… | 5 mg | 21109-5 | More Info |
| ARV-825 | A hetero-bifunctional molecule composed of a BRD4 binding moiety joined to… | 500 µg | 21109-500 | More Info |
| Arvanil | A structural analog of capsaicin with complex interactions in the CB syste… | 10 mg | 90052-10 | More Info |
| Arvanil | A structural analog of capsaicin with complex interactions in the CB syste… | 100 mg | 90052-100 | More Info |
| Arvanil | A structural analog of capsaicin with complex interactions in the CB syste… | 5 mg | 90052-5 | More Info |
| Arvanil | A structural analog of capsaicin with complex interactions in the CB syste… | 50 mg | 90052-50 | More Info |
| 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 |
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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