CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 853 of 870
Non-Antibody Products
Page 853 of 870
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| 1400W (hydrochloride) | 1400W is a potent, selective inhibitor of iNOS.{4277} Using purified human… | 50 mg | 81520-50 | More Info |
| W-13 (hydrochloride) | A potent antagonist of calmodulin (IC50 = 22 µM) that is widely used… | 1 mg | 14277-1 | More Info |
| W-13 (hydrochloride) | A potent antagonist of calmodulin (IC50 = 22 µM) that is widely used… | 10 mg | 14277-10 | More Info |
| W-13 (hydrochloride) | A potent antagonist of calmodulin (IC50 = 22 µM) that is widely used… | 5 mg | 14277-5 | More Info |
| W-5 (hydrochloride) | A less active, chlorine-deficient analog of W-7, the potent calmodulin ant… | 25 mg | 14271-25 | More Info |
| W-5 (hydrochloride) | A less active, chlorine-deficient analog of W-7, the potent calmodulin ant… | 5 mg | 14271-5 | More Info |
| W-7 (hydrochloride) | A cell-permeable antagonist of calmodulin (Ki = 11 µM); also associa… | 10 mg | 14826-10 | More Info |
| W-7 (hydrochloride) | A cell-permeable antagonist of calmodulin (Ki = 11 µM); also associa… | 100 mg | 14826-100 | More Info |
| W-7 (hydrochloride) | A cell-permeable antagonist of calmodulin (Ki = 11 µM); also associa… | 50 mg | 14826-50 | More Info |
| WIC1 | An inhibitor of Wnt signaling; inhibits CHIR99021-induced Wnt signaling in… | 10 mg | 39574-10 | More Info |
| WIC1 | An inhibitor of Wnt signaling; inhibits CHIR99021-induced Wnt signaling in… | 25 mg | 39574-25 | More Info |
| WIC1 | An inhibitor of Wnt signaling; inhibits CHIR99021-induced Wnt signaling in… | 5 mg | 39574-5 | More Info |
| WIC1 | An inhibitor of Wnt signaling; inhibits CHIR99021-induced Wnt signaling in… | 50 mg | 39574-50 | More Info |
| WIKI4 | A potent and selective inhibitor of TNKS1 and TNKS2 (IC50s = 26 and 15 nM,… | 10 mg | 14057-10 | More Info |
| WIKI4 | A potent and selective inhibitor of TNKS1 and TNKS2 (IC50s = 26 and 15 nM,… | 25 mg | 14057-25 | More Info |
| WIKI4 | A potent and selective inhibitor of TNKS1 and TNKS2 (IC50s = 26 and 15 nM,… | 5 mg | 14057-5 | More Info |
| WIKI4 | A potent and selective inhibitor of TNKS1 and TNKS2 (IC50s = 26 and 15 nM,… | 50 mg | 14057-50 | More Info |
| Wilforgine | A sesquiterpene alkaloid with paralytic activity; induces paralysis in thi… | 1 mg | 35029-1 | More Info |
| Wilforgine | A sesquiterpene alkaloid with paralytic activity; induces paralysis in thi… | 10 mg | 35029-10 | More Info |
| Wilforgine | A sesquiterpene alkaloid with paralytic activity; induces paralysis in thi… | 5 mg | 35029-5 | More Info |
| Wilforlide A | A triterpene; inhibits xylene-induced ear swelling in mice at 60 or 300 &m… | 10 mg | 34654-10 | More Info |
| Wilforlide A | A triterpene; inhibits xylene-induced ear swelling in mice at 60 or 300 &m… | 25 mg | 34654-25 | More Info |
| Wilforlide A | A triterpene; inhibits xylene-induced ear swelling in mice at 60 or 300 &m… | 5 mg | 34654-5 | More Info |
| Wilforlide A | A triterpene; inhibits xylene-induced ear swelling in mice at 60 or 300 &m… | 50 mg | 34654-50 | More Info |
| WIN 18,446 | Inhibits aldehyde dehydrogenase 1a2, (IC50 = 300 nM), a testes-specific is… | 100 mg | 14018-100 | More Info |
| WIN 18,446 | Inhibits aldehyde dehydrogenase 1a2, (IC50 = 300 nM), a testes-specific is… | 250 mg | 14018-250 | More Info |
| WIN 18,446 | Inhibits aldehyde dehydrogenase 1a2, (IC50 = 300 nM), a testes-specific is… | 50 mg | 14018-50 | More Info |
| WIN 66,306 | A peptide antagonist of NK1 and NK2 receptors; binds to NK1 and NK2 recept… | 1 mg | 33161-1 | More Info |
| WIN 66,306 | A peptide antagonist of NK1 and NK2 receptors; binds to NK1 and NK2 recept… | 5 mg | 33161-5 | More Info |
| (-)-WIN 55,212-3 (mesylate) | A competitive neutral antagonist of CB2; blocks the stimulating action of… | 10 mg | 12022-10 | More Info |
| (-)-WIN 55,212-3 (mesylate) | A competitive neutral antagonist of CB2; blocks the stimulating action of… | 25 mg | 12022-25 | More Info |
| (-)-WIN 55,212-3 (mesylate) | A competitive neutral antagonist of CB2; blocks the stimulating action of… | 5 mg | 12022-5 | More Info |
| (-)-WIN 55,212-3 (mesylate) | A competitive neutral antagonist of CB2; blocks the stimulating action of… | 50 mg | 12022-50 | More Info |
| (+)-WIN 55,212-2 (mesylate) | A potent aminoalkylindole CB receptor agonist (Ki = 62.3 and 3.3 nM for hu… | 10 mg | 10009023-10 | More Info |
| (+)-WIN 55,212-2 (mesylate) | A potent aminoalkylindole CB receptor agonist (Ki = 62.3 and 3.3 nM for hu… | 25 mg | 10009023-25 | More Info |
| (+)-WIN 55,212-2 (mesylate) | A potent aminoalkylindole CB receptor agonist (Ki = 62.3 and 3.3 nM for hu… | 5 mg | 10009023-5 | More Info |
| (+)-WIN 55,212-2 (mesylate) | A potent aminoalkylindole CB receptor agonist (Ki = 62.3 and 3.3 nM for hu… | 50 mg | 10009023-50 | More Info |
| Wiskostatin | A cell-permeable, selective inhibitor of N-WASP (IC50 = ~10 µM); dir… | 1 mg | 15047-1 | More Info |
| Wiskostatin | A cell-permeable, selective inhibitor of N-WASP (IC50 = ~10 µM); dir… | 10 mg | 15047-10 | More Info |
| Wiskostatin | A cell-permeable, selective inhibitor of N-WASP (IC50 = ~10 µM); dir… | 5 mg | 15047-5 | More Info |
| Wiskostatin | A cell-permeable, selective inhibitor of N-WASP (IC50 = ~10 µM); dir… | 50 mg | 15047-50 | More Info |
| Withaferin A | A steroidal lactone with diverse biological activities; binds to and induc… | 1 mg | 11352-1 | More Info |
| Withaferin A | A steroidal lactone with diverse biological activities; binds to and induc… | 10 mg | 11352-10 | More Info |
| Withaferin A | A steroidal lactone with diverse biological activities; binds to and induc… | 25 mg | 11352-25 | More Info |
| Withaferin A | A steroidal lactone with diverse biological activities; binds to and induc… | 5 mg | 11352-5 | More Info |
| Withanolide A | A natural product that has antioxidant and neuroprotective activity; promo… | 1 mg | 11797-1 | More Info |
| Withanolide A | A natural product that has antioxidant and neuroprotective activity; promo… | 10 mg | 11797-10 | More Info |
| Withanolide A | A natural product that has antioxidant and neuroprotective activity; promo… | 5 mg | 11797-5 | More Info |
| Withanolide A | A natural product that has antioxidant and neuroprotective activity; promo… | 500 µg | 11797-500 | More Info |
| Withanolide B | A withanolide; identified as an nNOS inhibitor in an in silico docking stu… | 1 mg | 11798-1 | More Info |
| Withanolide B | A withanolide; identified as an nNOS inhibitor in an in silico docking stu… | 10 mg | 11798-10 | More Info |
| Withanolide B | A withanolide; identified as an nNOS inhibitor in an in silico docking stu… | 5 mg | 11798-5 | More Info |
| Withanone | A phytochemical with diverse biological activities; inhibits the protein-p… | 1 mg | 11804-1 | More Info |
| Withanone | A phytochemical with diverse biological activities; inhibits the protein-p… | 5 mg | 11804-5 | More Info |
| Withanone | A phytochemical with diverse biological activities; inhibits the protein-p… | 500 µg | 11804-500 | More Info |
| WKYMVm (trifluoroacetate salt) | A synthetic peptide agonist of FPR1 and FPR2; induces calcium mobilization… | 1 mg | 33589-1 | More Info |
| WKYMVm (trifluoroacetate salt) | A synthetic peptide agonist of FPR1 and FPR2; induces calcium mobilization… | 10 mg | 33589-10 | More Info |
| WKYMVm (trifluoroacetate salt) | A synthetic peptide agonist of FPR1 and FPR2; induces calcium mobilization… | 25 mg | 33589-25 | More Info |
| WKYMVm (trifluoroacetate salt) | A synthetic peptide agonist of FPR1 and FPR2; induces calcium mobilization… | 5 mg | 33589-5 | More Info |
| WM-1119 | An inhibitor of KAT6A (IC50 = 6.3 nM); binds to KAT6A (Kd = 2 nM); selecti… | 10 mg | 30509-10 | More Info |
| WM-1119 | An inhibitor of KAT6A (IC50 = 6.3 nM); binds to KAT6A (Kd = 2 nM); selecti… | 25 mg | 30509-25 | More Info |
| WM-1119 | An inhibitor of KAT6A (IC50 = 6.3 nM); binds to KAT6A (Kd = 2 nM); selecti… | 5 mg | 30509-5 | More Info |
| WM-1119 | An inhibitor of KAT6A (IC50 = 6.3 nM); binds to KAT6A (Kd = 2 nM); selecti… | 50 mg | 30509-50 | More Info |
| WM-3835 | A KAT6A and KAT7 inhibitor (IC50s = 17 and 30 nM, respectively); selective… | 10 mg | 40296-10 | More Info |
| WM-3835 | A KAT6A and KAT7 inhibitor (IC50s = 17 and 30 nM, respectively); selective… | 25 mg | 40296-25 | More Info |
| WM-3835 | A KAT6A and KAT7 inhibitor (IC50s = 17 and 30 nM, respectively); selective… | 5 mg | 40296-5 | More Info |
| WM-3835 | A KAT6A and KAT7 inhibitor (IC50s = 17 and 30 nM, respectively); selective… | 50 mg | 40296-50 | More Info |
| WNK463 | A WNK1-4 inhibitor (IC50s = 5, 1, 6, and 9 nM, respectively); selective fo… | 10 mg | 37673-10 | More Info |
| WNK463 | A WNK1-4 inhibitor (IC50s = 5, 1, 6, and 9 nM, respectively); selective fo… | 25 mg | 37673-25 | More Info |
| WNK463 | A WNK1-4 inhibitor (IC50s = 5, 1, 6, and 9 nM, respectively); selective fo… | 5 mg | 37673-5 | More Info |
| WNK463 | A WNK1-4 inhibitor (IC50s = 5, 1, 6, and 9 nM, respectively); selective fo… | 50 mg | 37673-50 | More Info |
| WNK-IN-11 | An allosteric WNK1 inhibitor (IC50 = 4 nM); 57- and 1000-fold selective fo… | 10 mg | 29676-10 | More Info |
| WNK-IN-11 | An allosteric WNK1 inhibitor (IC50 = 4 nM); 57- and 1000-fold selective fo… | 25 mg | 29676-25 | More Info |
| WNK-IN-11 | An allosteric WNK1 inhibitor (IC50 = 4 nM); 57- and 1000-fold selective fo… | 5 mg | 29676-5 | More Info |
| WNK-IN-11 | An allosteric WNK1 inhibitor (IC50 = 4 nM); 57- and 1000-fold selective fo… | 50 mg | 29676-50 | 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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