CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 1 of 1
Non-Antibody Products
Page 1,029 of 1,288
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| Quininib | A CysLT1 and CysLT2 receptor antagonist (IC50s = 1.4 and 52 µM, resp… | 5 mg | 19838-5 | More Info |
| Quininib | A CysLT1 and CysLT2 receptor antagonist (IC50s = 1.4 and 52 µM, resp… | 500 µg | 19838-500 | More Info |
| (+)-Quinolactacin A1 | A fungal metabolite; inhibits AChE in vitro (IC50 = 280 µM), | 1 mg | 27939-1 | More Info |
| (+)-Quinolactacin A1 | A fungal metabolite; inhibits AChE in vitro (IC50 = 280 µM), | 5 mg | 27939-5 | More Info |
| Quinolactacin A | A quinolone fungal metabolite; inhibits LPS-induced TNF production in muri… | 1 mg | 27701-1 | More Info |
| Quinolactacin A | A quinolone fungal metabolite; inhibits LPS-induced TNF production in muri… | 5 mg | 27701-5 | More Info |
| Quinolactacin A | A quinolone fungal metabolite; inhibits LPS-induced TNF production in muri… | 500 µg | 27701-500 | More Info |
| 2,8-Quinolinediol | An endogenous metabolite; serum levels are increased in hemodialysis patie… | 1 g | 36376-1 | More Info |
| 2,8-Quinolinediol | An endogenous metabolite; serum levels are increased in hemodialysis patie… | 10 g | 36376-10 | More Info |
| 2,8-Quinolinediol | An endogenous metabolite; serum levels are increased in hemodialysis patie… | 25 g | 36376-25 | More Info |
| 2,8-Quinolinediol | An endogenous metabolite; serum levels are increased in hemodialysis patie… | 5 g | 36376-5 | More Info |
| Quinolinic Acid | An active metabolite of tryptophan and an NMDA receptor agonist; induces l… | 1 g | 14941-1 | More Info |
| Quinolinic Acid | An active metabolite of tryptophan and an NMDA receptor agonist; induces l… | 10 g | 14941-10 | More Info |
| Quinolinic Acid | An active metabolite of tryptophan and an NMDA receptor agonist; induces l… | 50 g | 14941-50 | More Info |
| 4-Quinolone-3-Carboxamide CB2 Ligand | A selective, high-affinity ligand of the CB2 receptor (Ki = 0.6 nM v. CB1… | 1 mg | 11093-1 | More Info |
| 4-Quinolone-3-Carboxamide CB2 Ligand | A selective, high-affinity ligand of the CB2 receptor (Ki = 0.6 nM v. CB1… | 10 mg | 11093-10 | More Info |
| 4-Quinolone-3-Carboxamide CB2 Ligand | A selective, high-affinity ligand of the CB2 receptor (Ki = 0.6 nM v. CB1… | 25 mg | 11093-25 | More Info |
| 4-Quinolone-3-Carboxamide CB2 Ligand | A selective, high-affinity ligand of the CB2 receptor (Ki = 0.6 nM v. CB1… | 5 mg | 11093-5 | More Info |
| 4-Quinolone-3-Carboxamide Furan CB2 Agonist | A high-affinity ligand of CB2 (Ki = 8.5 nM) with little affinity for CB1 (… | 1 mg | 11094-1 | More Info |
| 4-Quinolone-3-Carboxamide Furan CB2 Agonist | A high-affinity ligand of CB2 (Ki = 8.5 nM) with little affinity for CB1 (… | 10 mg | 11094-10 | More Info |
| 4-Quinolone-3-Carboxamide Furan CB2 Agonist | A high-affinity ligand of CB2 (Ki = 8.5 nM) with little affinity for CB1 (… | 25 mg | 11094-25 | More Info |
| 4-Quinolone-3-Carboxamide Furan CB2 Agonist | A high-affinity ligand of CB2 (Ki = 8.5 nM) with little affinity for CB1 (… | 5 mg | 11094-5 | More Info |
| Quin-2 (potassium salt) | A high-affinity fluorescent calcium indicator (Kd = 115 nM for calcium) th… | 5 mg | 20421-5 | More Info |
| Quinupristin (mesylate) | A streptogramin antibiotic that is usually combined with another streptogr… | 1 mg | 19764-1 | More Info |
| Quinupristin (mesylate) | A streptogramin antibiotic that is usually combined with another streptogr… | 5 mg | 19764-5 | More Info |
| Quizartinib | A selective FLT3 inhibitor (Kd = 1.6 nM) that inhibits the proliferation o… | 1 mg | 17986-1 | More Info |
| Quizartinib | A selective FLT3 inhibitor (Kd = 1.6 nM) that inhibits the proliferation o… | 10 mg | 17986-10 | More Info |
| Quizartinib | A selective FLT3 inhibitor (Kd = 1.6 nM) that inhibits the proliferation o… | 5 mg | 17986-5 | More Info |
| Quizartinib | A selective FLT3 inhibitor (Kd = 1.6 nM) that inhibits the proliferation o… | 500 µg | 17986-500 | More Info |
| Q-VD-OPH | A broad-spectrum caspase inhibitor, blocking caspases-3, -7, -8, -9, -10,… | 1 mg | 15260-1 | More Info |
| Q-VD-OPH | A broad-spectrum caspase inhibitor, blocking caspases-3, -7, -8, -9, -10,… | 5 mg | 15260-5 | More Info |
| QX-77 | An activator of chaperone-mediated autophagy; decreases paraquat- or oleic… | 10 mg | 29903-10 | More Info |
| QX-77 | An activator of chaperone-mediated autophagy; decreases paraquat- or oleic… | 25 mg | 29903-25 | More Info |
| QX-77 | An activator of chaperone-mediated autophagy; decreases paraquat- or oleic… | 5 mg | 29903-5 | More Info |
| QX-77 | An activator of chaperone-mediated autophagy; decreases paraquat- or oleic… | 50 mg | 29903-50 | More Info |
| QX-314 (bromide) | A membrane-impermeant lidocaine derivative that when combined with capsaic… | 100 mg | 10011032-100 | More Info |
| QX-314 (bromide) | A membrane-impermeant lidocaine derivative that when combined with capsaic… | 25 mg | 10011032-25 | More Info |
| QX-314 (bromide) | A membrane-impermeant lidocaine derivative that when combined with capsaic… | 50 mg | 10011032-50 | More Info |
| QX-314 (chloride) | A membrane-impermeant lidocaine derivative that when combined with capsaic… | 50 mg | 18454-50 | More Info |
| R 1530 | A multi-kinase inhibitor that targets over 20 kinases, including angiogene… | 1 mg | 15255-1 | More Info |
| R 1530 | A multi-kinase inhibitor that targets over 20 kinases, including angiogene… | 10 mg | 15255-10 | More Info |
| R 1530 | A multi-kinase inhibitor that targets over 20 kinases, including angiogene… | 25 mg | 15255-25 | More Info |
| R 1530 | A multi-kinase inhibitor that targets over 20 kinases, including angiogene… | 5 mg | 15255-5 | More Info |
| R112 | A Syk inhibitor (IC50 = 226 nM in cultured human mast cells); acts in an A… | 1 mg | 22929-1 | More Info |
| R112 | A Syk inhibitor (IC50 = 226 nM in cultured human mast cells); acts in an A… | 10 mg | 22929-10 | More Info |
| R112 | A Syk inhibitor (IC50 = 226 nM in cultured human mast cells); acts in an A… | 25 mg | 22929-25 | More Info |
| R112 | A Syk inhibitor (IC50 = 226 nM in cultured human mast cells); acts in an A… | 5 mg | 22929-5 | More Info |
| R162 | A GDH1 inhibitor (IC50 = 23 µM); decreases intracellular fumarate le… | 10 mg | 30922-10 | More Info |
| R162 | A GDH1 inhibitor (IC50 = 23 µM); decreases intracellular fumarate le… | 25 mg | 30922-25 | More Info |
| R162 | A GDH1 inhibitor (IC50 = 23 µM); decreases intracellular fumarate le… | 5 mg | 30922-5 | 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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