CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 419 of 865
Non-Antibody Products
Page 419 of 865
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| 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 |
| Juglanin | A flavonol with diverse biological activities; reduces OSS-induced increas… | 1 mg | 39824-1 | More Info |
| Juglanin | A flavonol with diverse biological activities; reduces OSS-induced increas… | 10 mg | 39824-10 | More Info |
| Juglanin | A flavonol with diverse biological activities; reduces OSS-induced increas… | 25 mg | 39824-25 | More Info |
| Juglanin | A flavonol with diverse biological activities; reduces OSS-induced increas… | 5 mg | 39824-5 | More Info |
| Juglone | A natural naphthoquinone that has allelopathic actions, suppressing growth… | 1 g | 16216-1 | More Info |
| Juglone | A natural naphthoquinone that has allelopathic actions, suppressing growth… | 500 mg | 16216-500 | More Info |
| Jun9-72-2 | A SARS-CoV-2 PLpro inhibitor (IC50 = 0.67 µM); inhibits viral replic… | 1 mg | 37195-1 | More Info |
| Jun9-72-2 | A SARS-CoV-2 PLpro inhibitor (IC50 = 0.67 µM); inhibits viral replic… | 10 mg | 37195-10 | More Info |
| Jun9-72-2 | A SARS-CoV-2 PLpro inhibitor (IC50 = 0.67 µM); inhibits viral replic… | 5 mg | 37195-5 | More Info |
| Juvenile Hormone III | An acyclic sesquiterpenoid that regulates diverse processes in insects; ac… | 1 mg | 19646-1 | More Info |
| Juvenile Hormone III | An acyclic sesquiterpenoid that regulates diverse processes in insects; ac… | 10 mg | 19646-10 | More Info |
| Juvenile Hormone III | An acyclic sesquiterpenoid that regulates diverse processes in insects; ac… | 5 mg | 19646-5 | More Info |
| JW 480 | A potent, selective inhibitor of KIAA1361 (IC50s = 20 nM in mouse brain me… | 10 mg | 10879-10 | More Info |
| JW 480 | A potent, selective inhibitor of KIAA1361 (IC50s = 20 nM in mouse brain me… | 25 mg | 10879-25 | More Info |
| JW 480 | A potent, selective inhibitor of KIAA1361 (IC50s = 20 nM in mouse brain me… | 5 mg | 10879-5 | More Info |
| JW 480 | A potent, selective inhibitor of KIAA1361 (IC50s = 20 nM in mouse brain me… | 50 mg | 10879-50 | More Info |
| JW 55 | An inhibitor of the PARP domain of TNKS1 and TNKS2 (IC50s = 1.9 and 0.83 &… | 10 mg | 16260-10 | More Info |
| JW 55 | An inhibitor of the PARP domain of TNKS1 and TNKS2 (IC50s = 1.9 and 0.83 &… | 25 mg | 16260-25 | More Info |
| JW 55 | An inhibitor of the PARP domain of TNKS1 and TNKS2 (IC50s = 1.9 and 0.83 &… | 5 mg | 16260-5 | More Info |
| JW 618 | A potent, selective inhibitor of MAGL that displays IC50 values of 123, 38… | 10 mg | 11790-10 | More Info |
| JW 618 | A potent, selective inhibitor of MAGL that displays IC50 values of 123, 38… | 25 mg | 11790-25 | More Info |
| JW 618 | A potent, selective inhibitor of MAGL that displays IC50 values of 123, 38… | 5 mg | 11790-5 | More Info |
| JW 618 | A potent, selective inhibitor of MAGL that displays IC50 values of 123, 38… | 50 mg | 11790-50 | More Info |
| JW 642 | An inhibitor of MAGL (IC50s = 3.7, 7.6, and 14 nM for the human, mouse, an… | 10 mg | 11789-10 | More Info |
| JW 642 | An inhibitor of MAGL (IC50s = 3.7, 7.6, and 14 nM for the human, mouse, an… | 5 mg | 11789-5 | More Info |
| JW 74 | An inhibitor of the catalytic PARP domain of TNKS1 / 2 that blocks canonic… | 1 mg | 19124-1 | More Info |
| JW 74 | An inhibitor of the catalytic PARP domain of TNKS1 / 2 that blocks canonic… | 10 mg | 19124-10 | More Info |
| JW 74 | An inhibitor of the catalytic PARP domain of TNKS1 / 2 that blocks canonic… | 5 mg | 19124-5 | More Info |
| JWH 007 | A potent CB receptor agonist that avidly binds to both CB1 and CB2 (Ki = 9… | 10 mg | 10266-10 | More Info |
| JWH 007 | A potent CB receptor agonist that avidly binds to both CB1 and CB2 (Ki = 9… | 25 mg | 10266-25 | More Info |
| JWH 007 | A potent CB receptor agonist that avidly binds to both CB1 and CB2 (Ki = 9… | 5 mg | 10266-5 | More Info |
| JWH 011 | A synthetic CB that is analogous to the N-hexyl JWH 004, which has high af… | 1 mg | 9001058-1 | More Info |
| JWH 011 | A synthetic CB that is analogous to the N-hexyl JWH 004, which has high af… | 10 mg | 9001058-10 | More Info |
| JWH 011 | A synthetic CB that is analogous to the N-hexyl JWH 004, which has high af… | 5 mg | 9001058-5 | More Info |
| JWH 016 | An analytical reference standard categorized as a synthetic cannabinoid; i… | 10 mg | 10849-10 | More Info |
| JWH 016 | An analytical reference standard categorized as a synthetic cannabinoid; i… | 25 mg | 10849-25 | More Info |
| JWH 016 | An analytical reference standard categorized as a synthetic cannabinoid; i… | 5 mg | 10849-5 | More Info |
| JWH 019 | A cannabimimetic indole that shows high-affinity for both CB1 (Ki = 9.8 nM… | 10 mg | 13633-10 | 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
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