CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 535 of 1
Non-Antibody Products
Page 535 of 1,288
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| Guanylin (human) (trifluoroacetate salt) | A peptide hormone activator of GC-C; expression is reduced by 100- to 1,00… | 1 mg | 33140-1 | More Info |
| Guanylin (human) (trifluoroacetate salt) | A peptide hormone activator of GC-C; expression is reduced by 100- to 1,00… | 500 µg | 33140-500 | More Info |
| Guanylyl Imidodiphosphate (lithium salt) | A nonhydrolyzable GTP analog that binds to and irreversibly activates G pr… | 1 mg | 16880-1 | More Info |
| Guanylyl Imidodiphosphate (lithium salt) | A nonhydrolyzable GTP analog that binds to and irreversibly activates G pr… | 10 mg | 16880-10 | More Info |
| Guanylyl Imidodiphosphate (lithium salt) | A nonhydrolyzable GTP analog that binds to and irreversibly activates G pr… | 25 mg | 16880-25 | More Info |
| Guanylyl Imidodiphosphate (lithium salt) | A nonhydrolyzable GTP analog that binds to and irreversibly activates G pr… | 5 mg | 16880-5 | More Info |
| Gusacitinib | A dual inhibitor of JAKs (IC50s = 46, 4, and 11 nM for JAK1-3, respectivel… | 1 mg | 36554-1 | More Info |
| Gusacitinib | A dual inhibitor of JAKs (IC50s = 46, 4, and 11 nM for JAK1-3, respectivel… | 10 mg | 36554-10 | More Info |
| Gusacitinib | A dual inhibitor of JAKs (IC50s = 46, 4, and 11 nM for JAK1-3, respectivel… | 25 mg | 36554-25 | More Info |
| Gusacitinib | A dual inhibitor of JAKs (IC50s = 46, 4, and 11 nM for JAK1-3, respectivel… | 5 mg | 36554-5 | More Info |
| Guvacine (hydrochloride) | An inhibitor of GABA uptake (IC50 = 10 µM; Ki = 14 µM) in rat… | 100 mg | 23361-100 | More Info |
| Guvacine (hydrochloride) | An inhibitor of GABA uptake (IC50 = 10 µM; Ki = 14 µM) in rat… | 25 mg | 23361-25 | More Info |
| Guvacine (hydrochloride) | An inhibitor of GABA uptake (IC50 = 10 µM; Ki = 14 µM) in rat… | 250 mg | 23361-250 | More Info |
| Guvacine (hydrochloride) | An inhibitor of GABA uptake (IC50 = 10 µM; Ki = 14 µM) in rat… | 50 mg | 23361-50 | More Info |
| Guvacoline (hydrobromide) | A full agonist of atrial and ileal muscarinic receptors with 15-fold reduc… | 1 mg | 17190-1 | More Info |
| Guvacoline (hydrobromide) | A full agonist of atrial and ileal muscarinic receptors with 15-fold reduc… | 10 mg | 17190-10 | More Info |
| Guvacoline (hydrobromide) | A full agonist of atrial and ileal muscarinic receptors with 15-fold reduc… | 5 mg | 17190-5 | More Info |
| GW 0742 | A selective agonist of PPARδ (EC50 = 1.1 nM); exhibits 1,000-fold se… | 10 mg | 10006798-10 | More Info |
| GW 0742 | A selective agonist of PPARδ (EC50 = 1.1 nM); exhibits 1,000-fold se… | 25 mg | 10006798-25 | More Info |
| GW 0742 | A selective agonist of PPARδ (EC50 = 1.1 nM); exhibits 1,000-fold se… | 5 mg | 10006798-5 | More Info |
| GW 0742 | A selective agonist of PPARδ (EC50 = 1.1 nM); exhibits 1,000-fold se… | 50 mg | 10006798-50 | More Info |
| GW 1100 | A selective antagonist of GPR40-mediated Ca2+ elevations in HEK293 cells (… | 10 mg | 10008908-10 | More Info |
| GW 1100 | A selective antagonist of GPR40-mediated Ca2+ elevations in HEK293 cells (… | 25 mg | 10008908-25 | More Info |
| GW 1100 | A selective antagonist of GPR40-mediated Ca2+ elevations in HEK293 cells (… | 5 mg | 10008908-5 | More Info |
| GW 1100 | A selective antagonist of GPR40-mediated Ca2+ elevations in HEK293 cells (… | 50 mg | 10008908-50 | More Info |
| GW 1929 | An N-aryl tyrosine activator of PPARγ that binds with a Ki value of… | 1 mg | 13689-1 | More Info |
| GW 1929 | An N-aryl tyrosine activator of PPARγ that binds with a Ki value of… | 10 mg | 13689-10 | More Info |
| GW 1929 | An N-aryl tyrosine activator of PPARγ that binds with a Ki value of… | 25 mg | 13689-25 | More Info |
| GW 1929 | An N-aryl tyrosine activator of PPARγ that binds with a Ki value of… | 5 mg | 13689-5 | More Info |
| GW 2580 | A selective inhibitor of cFMS kinase (IC50 = 0.03 µM) that prevents… | 1 mg | 15411-1 | More Info |
| GW 2580 | A selective inhibitor of cFMS kinase (IC50 = 0.03 µM) that prevents… | 10 mg | 15411-10 | More Info |
| GW 2580 | A selective inhibitor of cFMS kinase (IC50 = 0.03 µM) that prevents… | 25 mg | 15411-25 | More Info |
| GW 2580 | A selective inhibitor of cFMS kinase (IC50 = 0.03 µM) that prevents… | 5 mg | 15411-5 | More Info |
| GW 405833 | A partial agonist of CB2 receptors (EC50 = 0.65 nM); demonstrates anti-inf… | 1 mg | 20219-1 | More Info |
| GW 405833 | A partial agonist of CB2 receptors (EC50 = 0.65 nM); demonstrates anti-inf… | 10 mg | 20219-10 | More Info |
| GW 405833 | A partial agonist of CB2 receptors (EC50 = 0.65 nM); demonstrates anti-inf… | 25 mg | 20219-25 | More Info |
| GW 405833 | A partial agonist of CB2 receptors (EC50 = 0.65 nM); demonstrates anti-inf… | 5 mg | 20219-5 | More Info |
| GW 406381 | A NSAID and COX-2 inhibitor (IC50 = 3 nM); selective for COX-2 over COX-1… | 1 mg | 33895-1 | More Info |
| GW 406381 | A NSAID and COX-2 inhibitor (IC50 = 3 nM); selective for COX-2 over COX-1… | 10 mg | 33895-10 | More Info |
| GW 406381 | A NSAID and COX-2 inhibitor (IC50 = 3 nM); selective for COX-2 over COX-1… | 25 mg | 33895-25 | More Info |
| GW 406381 | A NSAID and COX-2 inhibitor (IC50 = 3 nM); selective for COX-2 over COX-1… | 5 mg | 33895-5 | More Info |
| GW 4064 | A selective agonist of FXR (EC50 = 15 nM); displays no activity at other n… | 1 mg | 10006611-1 | More Info |
| GW 4064 | A selective agonist of FXR (EC50 = 15 nM); displays no activity at other n… | 10 mg | 10006611-10 | More Info |
| GW 4064 | A selective agonist of FXR (EC50 = 15 nM); displays no activity at other n… | 5 mg | 10006611-5 | More Info |
| GW 441756 | A potent, selective inhibitor of TrkA (IC50 = 2 nM); used to clarify the r… | 1 mg | 16915-1 | More Info |
| GW 441756 | A potent, selective inhibitor of TrkA (IC50 = 2 nM); used to clarify the r… | 10 mg | 16915-10 | More Info |
| GW 441756 | A potent, selective inhibitor of TrkA (IC50 = 2 nM); used to clarify the r… | 5 mg | 16915-5 | More Info |
| GW 501516 | A PPARδ agonist; binds to PPARδ (IC50 = 1 nM); 100-fold select… | 1 mg | 10004272-1 | More Info |
| GW 501516 | A PPARδ agonist; binds to PPARδ (IC50 = 1 nM); 100-fold select… | 10 mg | 10004272-10 | More Info |
| GW 501516 | A PPARδ agonist; binds to PPARδ (IC50 = 1 nM); 100-fold select… | 5 mg | 10004272-5 | More Info |
CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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