CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 99 of 865
Non-Antibody Products
Page 99 of 865
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| BH3I-1 | A cell permeable inhibitor that blocks the binding of BH3 peptides to Bcl-… | 5 mg | 18763-5 | 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 |
| BI-6015 | A small molecule antagonist of HNF4α that at 20 µM reduces end… | 50 mg | 12032-50 | More Info |
| BI-605906 | An IKKβ inhibitor (IC50 = 380 nM); selective for IKKβ over insul… | 1 mg | 19184-1 | More Info |
| BI-605906 | An IKKβ inhibitor (IC50 = 380 nM); selective for IKKβ over insul… | 10 mg | 19184-10 | More Info |
| BI-605906 | An IKKβ inhibitor (IC50 = 380 nM); selective for IKKβ over insul… | 5 mg | 19184-5 | More Info |
| BI-671800 | An antagonist of CRTH2 / DP2 (IC50 = 42 nM in a radioligand binding assay)… | 1 mg | 27638-1 | More Info |
| BI-671800 | An antagonist of CRTH2 / DP2 (IC50 = 42 nM in a radioligand binding assay)… | 10 mg | 27638-10 | More Info |
| BI-671800 | An antagonist of CRTH2 / DP2 (IC50 = 42 nM in a radioligand binding assay)… | 5 mg | 27638-5 | More Info |
| BI-6727 | A dihydropteridinone that inhibits Plk1, Plk2, and Plk3 (IC50s = 0.87, 5,… | 1 mg | 18193-1 | More Info |
| BI-6727 | A dihydropteridinone that inhibits Plk1, Plk2, and Plk3 (IC50s = 0.87, 5,… | 10 mg | 18193-10 | More Info |
| BI-6727 | A dihydropteridinone that inhibits Plk1, Plk2, and Plk3 (IC50s = 0.87, 5,… | 25 mg | 18193-25 | More Info |
| BI-6727 | A dihydropteridinone that inhibits Plk1, Plk2, and Plk3 (IC50s = 0.87, 5,… | 5 mg | 18193-5 | More Info |
| BI-7273 | A potent and selective BRD9 bromodomain inhibitor (Kd = 15.4 nM; IC50 = 19… | 1 mg | 20311-1 | More Info |
| BI-7273 | A potent and selective BRD9 bromodomain inhibitor (Kd = 15.4 nM; IC50 = 19… | 10 mg | 20311-10 | More Info |
| BI-7273 | A potent and selective BRD9 bromodomain inhibitor (Kd = 15.4 nM; IC50 = 19… | 25 mg | 20311-25 | More Info |
| BI-7273 | A potent and selective BRD9 bromodomain inhibitor (Kd = 15.4 nM; IC50 = 19… | 5 mg | 20311-5 | More Info |
| BI-847325 | A selective dual MEK / Aurora kinase inhibitor (IC50s = 3, 25, 15, 25, and… | 1 mg | 18301-1 | More Info |
| BI-847325 | A selective dual MEK / Aurora kinase inhibitor (IC50s = 3, 25, 15, 25, and… | 5 mg | 18301-5 | More Info |
| BI-882370 | A RAF inhibitor (IC50s = 0.8, 0.8, and 0.6 nM for B-RAFV600E, wild-type B-… | 1 mg | 24273-1 | More Info |
| BI-882370 | A RAF inhibitor (IC50s = 0.8, 0.8, and 0.6 nM for B-RAFV600E, wild-type B-… | 10 mg | 24273-10 | More Info |
| BI-882370 | A RAF inhibitor (IC50s = 0.8, 0.8, and 0.6 nM for B-RAFV600E, wild-type B-… | 25 mg | 24273-25 | More Info |
| BI-882370 | A RAF inhibitor (IC50s = 0.8, 0.8, and 0.6 nM for B-RAFV600E, wild-type B-… | 5 mg | 24273-5 | More Info |
| BI-9564 | A selective inhibitor of BRD9 and BRD7 bromodomains (Kds = 14.1 and 239 nM… | 1 mg | 17897-1 | More Info |
| BI-9564 | A selective inhibitor of BRD9 and BRD7 bromodomains (Kds = 14.1 and 239 nM… | 10 mg | 17897-10 | More Info |
| BI-9564 | A selective inhibitor of BRD9 and BRD7 bromodomains (Kds = 14.1 and 239 nM… | 500 µg | 17897-500 | More Info |
| BI-9627 | An NHE1 inhibitor (IC50s = 6 and 31 nM in pHi and human platelet swelling… | 1 mg | 27640-1 | More Info |
| BI-9627 | An NHE1 inhibitor (IC50s = 6 and 31 nM in pHi and human platelet swelling… | 10 mg | 27640-10 | More Info |
| BI-9627 | An NHE1 inhibitor (IC50s = 6 and 31 nM in pHi and human platelet swelling… | 5 mg | 27640-5 | More Info |
| BI-1467335 | An inhibitor of VAP-1 (IC50 = 50s = >1,000 and >10,000 nM, respectively);… | 1 mg | 30672-1 | More Info |
| BI-1467335 | An inhibitor of VAP-1 (IC50 = 50s = >1,000 and >10,000 nM, respectively);… | 10 mg | 30672-10 | More Info |
| BI-1467335 | An inhibitor of VAP-1 (IC50 = 50s = >1,000 and >10,000 nM, respectively);… | 25 mg | 30672-25 | More Info |
| BI-1467335 | An inhibitor of VAP-1 (IC50 = 50s = >1,000 and >10,000 nM, respectively);… | 5 mg | 30672-5 | More Info |
| BIA 10-2474 | An inhibitor of FAAH (IC50 = 4.9 nM in HEK293T cells expressing the human… | 10 mg | 23157-10 | More Info |
| BIA 10-2474 | An inhibitor of FAAH (IC50 = 4.9 nM in HEK293T cells expressing the human… | 25 mg | 23157-25 | More Info |
| BIA 10-2474 | An inhibitor of FAAH (IC50 = 4.9 nM in HEK293T cells expressing the human… | 5 mg | 23157-5 | 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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