CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 421 of 870
Non-Antibody Products
Page 421 of 870
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| JNK1/2/3 (Total) and JNK1/2/3 (Phospho-Thr183/Tyr185) TR-FRET Assay Kit | This JNK1 / 2/3 (Total) and JNK1 / 2/3 (Phospho-Thr183 / Tyr185) TR-FRET A… | 480 Well | 500256-480WELLS | More Info |
| JNK1/2/3 (Total) TR-FRET Assay Kit | This JNK1 / 2/3 (Total) TR-FRET Assay Kit uses a homogeneous TR-FRET assay… | 2400 Well | 500255-2400WELLS | More Info |
| JNK1/2/3 (Total) TR-FRET Assay Kit | This JNK1 / 2/3 (Total) TR-FRET Assay Kit uses a homogeneous TR-FRET assay… | 480 Well | 500255-480WELLS | More Info |
| JNK1/2/3 (Total) TR-FRET Assay Kit | This JNK1 / 2/3 (Total) TR-FRET Assay Kit uses a homogeneous TR-FRET assay… | 4800 Well | 500255-4800WELLS | More Info |
| JNK1/2/3 (Total) TR-FRET Assay Kit | This JNK1 / 2/3 (Total) TR-FRET Assay Kit uses a homogeneous TR-FRET assay… | 96 Well | 500255-96WELLS | More Info |
| JNK1/2/3 (Total) TR-FRET Assay Kit | This JNK1 / 2/3 (Total) TR-FRET Assay Kit uses a homogeneous TR-FRET assay… | 9600 Well | 500255-9600WELLS | More Info |
| Josamycin | A macrolide antibiotic; active against clinical isolates of the Gram-posit… | 100 mg | 29606-100 | More Info |
| Josamycin | A macrolide antibiotic; active against clinical isolates of the Gram-posit… | 25 mg | 29606-25 | More Info |
| Josamycin | A macrolide antibiotic; active against clinical isolates of the Gram-posit… | 250 mg | 29606-250 | More Info |
| Josamycin | A macrolide antibiotic; active against clinical isolates of the Gram-posit… | 50 mg | 29606-50 | More Info |
| JP104 | An irreversible FAAH inhibitor of the carbamate class with an IC50 value o… | 10 mg | 10008661-10 | More Info |
| JP104 | An irreversible FAAH inhibitor of the carbamate class with an IC50 value o… | 100 mg | 10008661-100 | More Info |
| JP104 | An irreversible FAAH inhibitor of the carbamate class with an IC50 value o… | 5 mg | 10008661-5 | More Info |
| JP104 | An irreversible FAAH inhibitor of the carbamate class with an IC50 value o… | 50 mg | 10008661-50 | More Info |
| JP83 | An irreversible FAAH inhibitor of the carbamate class with an IC50 value o… | 10 mg | 10008660-10 | More Info |
| JP83 | An irreversible FAAH inhibitor of the carbamate class with an IC50 value o… | 5 mg | 10008660-5 | More Info |
| JP83 | An irreversible FAAH inhibitor of the carbamate class with an IC50 value o… | 50 mg | 10008660-50 | More Info |
| JPC0323 | A positive allosteric modulator of 5-HT2A and 5-HT2C receptors; selective… | 1 mg | 39470-1 | More Info |
| JPC0323 | A positive allosteric modulator of 5-HT2A and 5-HT2C receptors; selective… | 10 mg | 39470-10 | More Info |
| JPC0323 | A positive allosteric modulator of 5-HT2A and 5-HT2C receptors; selective… | 5 mg | 39470-5 | More Info |
| JPC0323 Oleate | An acylated derivative of JPC0323 | 1 mg | 39833-1 | More Info |
| JPC0323 Oleate | An acylated derivative of JPC0323 | 10 mg | 39833-10 | More Info |
| JPC0323 Oleate | An acylated derivative of JPC0323 | 5 mg | 39833-5 | More Info |
| JPH203 | An inhibitor of LAT1 (IC50 = 0.14 µM for 14C-leucine uptake in S2 ce… | 1 mg | 29715-1 | More Info |
| JPH203 | An inhibitor of LAT1 (IC50 = 0.14 µM for 14C-leucine uptake in S2 ce… | 10 mg | 29715-10 | More Info |
| JPH203 | An inhibitor of LAT1 (IC50 = 0.14 µM for 14C-leucine uptake in S2 ce… | 5 mg | 29715-5 | More Info |
| JPH203 (hydrochloride) | An inhibitor of LAT1 (IC50 = 0.14 µM for 14C-leucine uptake in S2 ce… | 1 mg | 36053-1 | More Info |
| JPH203 (hydrochloride) | An inhibitor of LAT1 (IC50 = 0.14 µM for 14C-leucine uptake in S2 ce… | 10 mg | 36053-10 | More Info |
| JPH203 (hydrochloride) | An inhibitor of LAT1 (IC50 = 0.14 µM for 14C-leucine uptake in S2 ce… | 25 mg | 36053-25 | More Info |
| JPH203 (hydrochloride) | An inhibitor of LAT1 (IC50 = 0.14 µM for 14C-leucine uptake in S2 ce… | 5 mg | 36053-5 | More Info |
| JP-1302 (hydrochloride hydrate) | An α2C-AR antagonist; selective for α2C-ARs over α2A- an… | 1 mg | 25974-1 | More Info |
| JP-1302 (hydrochloride hydrate) | An α2C-AR antagonist; selective for α2C-ARs over α2A- an… | 10 mg | 25974-10 | More Info |
| JP-1302 (hydrochloride hydrate) | An α2C-AR antagonist; selective for α2C-ARs over α2A- an… | 5 mg | 25974-5 | More Info |
| (+)-JQ1 | Displaces BET proteins from chromatin by competitively binding to the acet… | 1 mg | 11187-1 | More Info |
| (+)-JQ1 | Displaces BET proteins from chromatin by competitively binding to the acet… | 10 mg | 11187-10 | More Info |
| (+)-JQ1 | Displaces BET proteins from chromatin by competitively binding to the acet… | 25 mg | 11187-25 | More Info |
| (+)-JQ1 | Displaces BET proteins from chromatin by competitively binding to the acet… | 5 mg | 11187-5 | More Info |
| JQAD1 | A PROTAC that drives p300 degradation; selectively induces the degradation… | 1 mg | 39566-1 | More Info |
| JQAD1 | A PROTAC that drives p300 degradation; selectively induces the degradation… | 10 mg | 39566-10 | More Info |
| JQAD1 | A PROTAC that drives p300 degradation; selectively induces the degradation… | 5 mg | 39566-5 | More Info |
| JQEZ5 | An EZH2 inhibitor (IC50 = 11.1 nM); colony formation of primary human CD34… | 10 mg | 27457-10 | More Info |
| JQEZ5 | An EZH2 inhibitor (IC50 = 11.1 nM); colony formation of primary human CD34… | 25 mg | 27457-25 | More Info |
| JQEZ5 | An EZH2 inhibitor (IC50 = 11.1 nM); colony formation of primary human CD34… | 5 mg | 27457-5 | More Info |
| JQEZ5 | An EZH2 inhibitor (IC50 = 11.1 nM); colony formation of primary human CD34… | 50 mg | 27457-50 | More Info |
| (+)-JQ1 (free acid) | An inhibitor of BET family proteins; binds to BRD4 bromodomains 1 and 2 wi… | 1 mg | 9002910-1 | More Info |
| (+)-JQ1 (free acid) | An inhibitor of BET family proteins; binds to BRD4 bromodomains 1 and 2 wi… | 10 mg | 9002910-10 | More Info |
| (+)-JQ1 (free acid) | An inhibitor of BET family proteins; binds to BRD4 bromodomains 1 and 2 wi… | 25 mg | 9002910-25 | More Info |
| (+)-JQ1 (free acid) | An inhibitor of BET family proteins; binds to BRD4 bromodomains 1 and 2 wi… | 5 mg | 9002910-5 | More Info |
| (+)-JQ1 PA | A clickable form of (+)-JQ1; binds to BRD4 and displaces it from Myc in a… | 1 mg | 30414-1 | More Info |
| (+)-JQ1 PA | A clickable form of (+)-JQ1; binds to BRD4 and displaces it from Myc in a… | 10 mg | 30414-10 | More Info |
| (+)-JQ1 PA | A clickable form of (+)-JQ1; binds to BRD4 and displaces it from Myc in a… | 25 mg | 30414-25 | More Info |
| (+)-JQ1 PA | A clickable form of (+)-JQ1; binds to BRD4 and displaces it from Myc in a… | 5 mg | 30414-5 | More Info |
| JSH-23 | An inhibitor of NF-κB, blocking its translocation into the nucleus (… | 1 mg | 15036-1 | More Info |
| JSH-23 | An inhibitor of NF-κB, blocking its translocation into the nucleus (… | 10 mg | 15036-10 | More Info |
| JSH-23 | An inhibitor of NF-κB, blocking its translocation into the nucleus (… | 25 mg | 15036-25 | More Info |
| JSH-23 | An inhibitor of NF-κB, blocking its translocation into the nucleus (… | 5 mg | 15036-5 | More Info |
| JS-K | A nitric oxide donor; inhibits proliferation of HL-60 cells (IC50 = 0.5 &m… | 1 mg | 21225-1 | More Info |
| JS-K | A nitric oxide donor; inhibits proliferation of HL-60 cells (IC50 = 0.5 &m… | 5 mg | 21225-5 | More Info |
| JT010 | A TRPA1 agonist (EC50 = 0.65 nM in a calcium influx assay); selective for… | 1 mg | 29732-1 | More Info |
| JT010 | A TRPA1 agonist (EC50 = 0.65 nM in a calcium influx assay); selective for… | 10 mg | 29732-10 | More Info |
| JT010 | A TRPA1 agonist (EC50 = 0.65 nM in a calcium influx assay); selective for… | 5 mg | 29732-5 | More Info |
| JTC 801 | A selective nociceptin receptor antagonist (ORL1; Ki = 44.5 nM; IC50 = 94… | 10 mg | 21254-10 | More Info |
| JTC 801 | A selective nociceptin receptor antagonist (ORL1; Ki = 44.5 nM; IC50 = 94… | 25 mg | 21254-25 | More Info |
| JTC 801 | A selective nociceptin receptor antagonist (ORL1; Ki = 44.5 nM; IC50 = 94… | 5 mg | 21254-5 | More Info |
| JTC 801 | A selective nociceptin receptor antagonist (ORL1; Ki = 44.5 nM; IC50 = 94… | 50 mg | 21254-50 | More Info |
| JTE-013 | An S1P2 and S1P4 receptor antagonist (IC50 = 17 and 237 nM, respectively);… | 1 mg | 10009458-1 | More Info |
| JTE-013 | An S1P2 and S1P4 receptor antagonist (IC50 = 17 and 237 nM, respectively);… | 10 mg | 10009458-10 | More Info |
| JTE-013 | An S1P2 and S1P4 receptor antagonist (IC50 = 17 and 237 nM, respectively);… | 5 mg | 10009458-5 | More Info |
| JTE-013 | An S1P2 and S1P4 receptor antagonist (IC50 = 17 and 237 nM, respectively);… | 50 mg | 10009458-50 | More Info |
| JTE-607 | A cytokine synthesis inhibitor; inhibits the production of TNF-α, IL… | 10 mg | 36942-10 | More Info |
| JTE-607 | A cytokine synthesis inhibitor; inhibits the production of TNF-α, IL… | 25 mg | 36942-25 | More Info |
| JTE-607 | A cytokine synthesis inhibitor; inhibits the production of TNF-α, IL… | 5 mg | 36942-5 | More Info |
| JTE-607 | A cytokine synthesis inhibitor; inhibits the production of TNF-α, IL… | 50 mg | 36942-50 | More Info |
| JTE-907 | A CB2 receptor inverse agonist; selective for CB2 over CB1 receptors (Kis… | 1 mg | 10009857-1 | More Info |
| JTE-907 | A CB2 receptor inverse agonist; selective for CB2 over CB1 receptors (Kis… | 5 mg | 10009857-5 | 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
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