CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 99 of 870
Non-Antibody Products
Page 99 of 870
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| BG45 | A selective inhibitor of HDAC3 (IC50 = 289 nM) that alone or in combinatio… | 25 mg | 16918-25 | More Info |
| BG45 | A selective inhibitor of HDAC3 (IC50 = 289 nM) that alone or in combinatio… | 5 mg | 16918-5 | More Info |
| BG45 | A selective inhibitor of HDAC3 (IC50 = 289 nM) that alone or in combinatio… | 50 mg | 16918-50 | More Info |
| BGC 20-1531 (hydrochloride) | A potent and selective EP4 receptor antagonist (Kis = 11.7, >10,000, and >… | 1 mg | 19742-1 | More Info |
| BGC 20-1531 (hydrochloride) | A potent and selective EP4 receptor antagonist (Kis = 11.7, >10,000, and >… | 10 mg | 19742-10 | More Info |
| BGC 20-1531 (hydrochloride) | A potent and selective EP4 receptor antagonist (Kis = 11.7, >10,000, and >… | 5 mg | 19742-5 | More Info |
| BGC 20-1531 (hydrochloride) | A potent and selective EP4 receptor antagonist (Kis = 11.7, >10,000, and >… | 500 µg | 19742-500 | More Info |
| BGJ398 | A pan FGFR inhibitor (IC50s = 0.9, 1.4, and 1 nM for FGFR1, FGFR2, and FGF… | 1 mg | 19157-1 | More Info |
| BGJ398 | A pan FGFR inhibitor (IC50s = 0.9, 1.4, and 1 nM for FGFR1, FGFR2, and FGF… | 10 mg | 19157-10 | More Info |
| BGJ398 | A pan FGFR inhibitor (IC50s = 0.9, 1.4, and 1 nM for FGFR1, FGFR2, and FGF… | 25 mg | 19157-25 | More Info |
| BGJ398 | A pan FGFR inhibitor (IC50s = 0.9, 1.4, and 1 nM for FGFR1, FGFR2, and FGF… | 5 mg | 19157-5 | More Info |
| BGJ398 (phosphate) | A pan FGFR inhibitor (IC50s = 0.9, 1.4, and 1 nM for FGFR1, FGFR2, and FGF… | 1 mg | 39292-1 | More Info |
| BGJ398 (phosphate) | A pan FGFR inhibitor (IC50s = 0.9, 1.4, and 1 nM for FGFR1, FGFR2, and FGF… | 10 mg | 39292-10 | More Info |
| BGJ398 (phosphate) | A pan FGFR inhibitor (IC50s = 0.9, 1.4, and 1 nM for FGFR1, FGFR2, and FGF… | 25 mg | 39292-25 | More Info |
| BGJ398 (phosphate) | A pan FGFR inhibitor (IC50s = 0.9, 1.4, and 1 nM for FGFR1, FGFR2, and FGF… | 5 mg | 39292-5 | More Info |
| BGP-15 | A PARP inhibitor and insulin sensitizer; blocks self-ADP-ribosylation of n… | 1 mg | 17503-1 | More Info |
| BGP-15 | A PARP inhibitor and insulin sensitizer; blocks self-ADP-ribosylation of n… | 10 mg | 17503-10 | More Info |
| BGP-15 | A PARP inhibitor and insulin sensitizer; blocks self-ADP-ribosylation of n… | 25 mg | 17503-25 | More Info |
| BGP-15 | A PARP inhibitor and insulin sensitizer; blocks self-ADP-ribosylation of n… | 5 mg | 17503-5 | More Info |
| BHBM | An acylhydrazone with antifungal activity; active against C. neoformans in… | 1 mg | 29817-1 | More Info |
| BHBM | An acylhydrazone with antifungal activity; active against C. neoformans in… | 10 mg | 29817-10 | More Info |
| BHBM | An acylhydrazone with antifungal activity; active against C. neoformans in… | 25 mg | 29817-25 | More Info |
| BHBM | An acylhydrazone with antifungal activity; active against C. neoformans in… | 5 mg | 29817-5 | More Info |
| B7-H3/CD276 Extracellular Domain (human, recombinant) | Source: Recombinant C-terminal human IgG1 Fc-tagged B7-H3 expressed in HEK… | 1 mg | 31822-1 | More Info |
| B7-H3/CD276 Extracellular Domain (human, recombinant) | Source: Recombinant C-terminal human IgG1 Fc-tagged B7-H3 expressed in HEK… | 100 µg | 31822-100 | More Info |
| BHD | A reversible male contraceptive agent; induces spermatogenic cell apoptosi… | 1 mg | 38962-1 | More Info |
| BHD | A reversible male contraceptive agent; induces spermatogenic cell apoptosi… | 10 mg | 38962-10 | More Info |
| BHD | A reversible male contraceptive agent; induces spermatogenic cell apoptosi… | 5 mg | 38962-5 | More Info |
| B7-H4 (human, recombinant) | Source: Active recombinant C-terminal human IgG1 Fc-tagged B7-H4 expressed… | 1 mg | 31823-1 | More Info |
| B7-H4 (human, recombinant) | Source: Active recombinant C-terminal human IgG1 Fc-tagged B7-H4 expressed… | 100 µg | 31823-100 | More Info |
| BH3I-1 | A cell permeable inhibitor that blocks the binding of BH3 peptides to Bcl-… | 1 mg | 18763-1 | More Info |
| BH3I-1 | A cell permeable inhibitor that blocks the binding of BH3 peptides to Bcl-… | 10 mg | 18763-10 | More Info |
| BH3I-1 | A cell permeable inhibitor that blocks the binding of BH3 peptides to Bcl-… | 25 mg | 18763-25 | More Info |
| BH3I-1 | A cell permeable inhibitor that blocks the binding of BH3 peptides to Bcl-… | 5 mg | 18763-5 | More Info |
| Bhimanone | An acetylated tetralone | 1 mg | 40910-1 | More Info |
| BHPI | An antagonist of ERα that blocks 17β-estradiol-induced prolifer… | 1 mg | 17750-1 | More Info |
| BHPI | An antagonist of ERα that blocks 17β-estradiol-induced prolifer… | 5 mg | 17750-5 | More Info |
| BHPI | An antagonist of ERα that blocks 17β-estradiol-induced prolifer… | 500 µg | 17750-500 | More Info |
| BHT | A synthetic antioxidant; scavenges peroxide, DPPH, superoxide, and ABTS ra… | 1 g | 89910-1 | More Info |
| BHT | A synthetic antioxidant; scavenges peroxide, DPPH, superoxide, and ABTS ra… | 500 mg | 89910-500 | More Info |
| B-HT 920 (hydrochloride) | A potent agonist of D2 receptors (Ki = 5.8 nM); has neuroprotective and re… | 10 mg | 14177-10 | More Info |
| B-HT 920 (hydrochloride) | A potent agonist of D2 receptors (Ki = 5.8 nM); has neuroprotective and re… | 5 mg | 14177-5 | More Info |
| B-HT 920 (hydrochloride) | A potent agonist of D2 receptors (Ki = 5.8 nM); has neuroprotective and re… | 50 mg | 14177-50 | More Info |
| B-HT 933 (hydrochloride) | An α2-AR agonist (EC50 = 0.65 µM for contraction of canine sap… | 1 mg | 11941-1 | More Info |
| B-HT 933 (hydrochloride) | An α2-AR agonist (EC50 = 0.65 µM for contraction of canine sap… | 10 mg | 11941-10 | More Info |
| B-HT 933 (hydrochloride) | An α2-AR agonist (EC50 = 0.65 µM for contraction of canine sap… | 25 mg | 11941-25 | More Info |
| B-HT 933 (hydrochloride) | An α2-AR agonist (EC50 = 0.65 µM for contraction of canine sap… | 5 mg | 11941-5 | More Info |
| BI-01383298 | An NaCT inhibitor (IC50 = ~100 nM); irreversibly inhibits sodium-dependent… | 10 mg | 24482-10 | More Info |
| BI-01383298 | An NaCT inhibitor (IC50 = ~100 nM); irreversibly inhibits sodium-dependent… | 25 mg | 24482-25 | More Info |
| BI-01383298 | An NaCT inhibitor (IC50 = ~100 nM); irreversibly inhibits sodium-dependent… | 5 mg | 24482-5 | More Info |
| BI-01383298 | An NaCT inhibitor (IC50 = ~100 nM); irreversibly inhibits sodium-dependent… | 50 mg | 24482-50 | More Info |
| BI-187004 | An 11β-HSD1 inhibitor (IC50 = 31 nM) | 1 mg | 38786-1 | More Info |
| BI-187004 | An 11β-HSD1 inhibitor (IC50 = 31 nM) | 10 mg | 38786-10 | More Info |
| BI-187004 | An 11β-HSD1 inhibitor (IC50 = 31 nM) | 5 mg | 38786-5 | More Info |
| BI-2536 | A selective inhibitor of Plk1 (IC50 = 0.83 nM); induces mitotic arrest and… | 1 mg | 17385-1 | More Info |
| BI-2536 | A selective inhibitor of Plk1 (IC50 = 0.83 nM); induces mitotic arrest and… | 10 mg | 17385-10 | More Info |
| BI-2536 | A selective inhibitor of Plk1 (IC50 = 0.83 nM); induces mitotic arrest and… | 5 mg | 17385-5 | More Info |
| BI-2536 | A selective inhibitor of Plk1 (IC50 = 0.83 nM); induces mitotic arrest and… | 50 mg | 17385-50 | More Info |
| BI-2545 | An inhibitor of autotaxin (IC50s = 2.2 and 3.4 for the human and rat enzym… | 10 mg | 24285-10 | More Info |
| BI-2545 | An inhibitor of autotaxin (IC50s = 2.2 and 3.4 for the human and rat enzym… | 25 mg | 24285-25 | More Info |
| BI-2545 | An inhibitor of autotaxin (IC50s = 2.2 and 3.4 for the human and rat enzym… | 5 mg | 24285-5 | More Info |
| BI-3406 | An inhibitor of the K-Ras-SOS1 protein-protein interaction (IC50 = 5 nM);… | 1 mg | 35261-1 | More Info |
| BI-3406 | An inhibitor of the K-Ras-SOS1 protein-protein interaction (IC50 = 5 nM);… | 10 mg | 35261-10 | More Info |
| BI-3406 | An inhibitor of the K-Ras-SOS1 protein-protein interaction (IC50 = 5 nM);… | 25 mg | 35261-25 | More Info |
| BI-3406 | An inhibitor of the K-Ras-SOS1 protein-protein interaction (IC50 = 5 nM);… | 5 mg | 35261-5 | More Info |
| BI-409306 | A potent and selective PDE9A inhibitor (IC50s = 65 and 168 nM for the huma… | 1 mg | 30375-1 | More Info |
| BI-409306 | A potent and selective PDE9A inhibitor (IC50s = 65 and 168 nM for the huma… | 10 mg | 30375-10 | More Info |
| BI-409306 | A potent and selective PDE9A inhibitor (IC50s = 65 and 168 nM for the huma… | 25 mg | 30375-25 | More Info |
| BI-409306 | A potent and selective PDE9A inhibitor (IC50s = 65 and 168 nM for the huma… | 5 mg | 30375-5 | More Info |
| BI-4394 | An inhibitor of MMP-13 (IC50 = 0.001 µM for the recombinant human en… | 1 mg | 36855-1 | More Info |
| BI-4394 | An inhibitor of MMP-13 (IC50 = 0.001 µM for the recombinant human en… | 10 mg | 36855-10 | More Info |
| BI-4394 | An inhibitor of MMP-13 (IC50 = 0.001 µM for the recombinant human en… | 5 mg | 36855-5 | More Info |
| BI-6015 | A small molecule antagonist of HNF4α that at 20 µM reduces end… | 10 mg | 12032-10 | More Info |
| BI-6015 | A small molecule antagonist of HNF4α that at 20 µM reduces end… | 25 mg | 12032-25 | More Info |
| BI-6015 | A small molecule antagonist of HNF4α that at 20 µM reduces end… | 5 mg | 12032-5 | 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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