JQAD1 |
A PROTAC that drives p300 degradation; selectively induces the degradation… |
10 mg |
39566-10 |
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JQAD1 |
A PROTAC that drives p300 degradation; selectively induces the degradation… |
5 mg |
39566-5 |
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JQEZ5 |
An EZH2 inhibitor (IC50 = 11.1 nM); colony formation of primary human CD34… |
10 mg |
27457-10 |
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JQEZ5 |
An EZH2 inhibitor (IC50 = 11.1 nM); colony formation of primary human CD34… |
25 mg |
27457-25 |
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JQEZ5 |
An EZH2 inhibitor (IC50 = 11.1 nM); colony formation of primary human CD34… |
5 mg |
27457-5 |
More Info
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JQEZ5 |
An EZH2 inhibitor (IC50 = 11.1 nM); colony formation of primary human CD34… |
50 mg |
27457-50 |
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(+)-JQ1 (free acid) |
An inhibitor of BET family proteins; binds to BRD4 bromodomains 1 and 2 wi… |
1 mg |
9002910-1 |
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(+)-JQ1 (free acid) |
An inhibitor of BET family proteins; binds to BRD4 bromodomains 1 and 2 wi… |
10 mg |
9002910-10 |
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(+)-JQ1 (free acid) |
An inhibitor of BET family proteins; binds to BRD4 bromodomains 1 and 2 wi… |
25 mg |
9002910-25 |
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(+)-JQ1 (free acid) |
An inhibitor of BET family proteins; binds to BRD4 bromodomains 1 and 2 wi… |
5 mg |
9002910-5 |
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(+)-JQ1 PA |
A clickable form of (+)-JQ1; binds to BRD4 and displaces it from Myc in a… |
1 mg |
30414-1 |
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(+)-JQ1 PA |
A clickable form of (+)-JQ1; binds to BRD4 and displaces it from Myc in a… |
10 mg |
30414-10 |
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(+)-JQ1 PA |
A clickable form of (+)-JQ1; binds to BRD4 and displaces it from Myc in a… |
25 mg |
30414-25 |
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(+)-JQ1 PA |
A clickable form of (+)-JQ1; binds to BRD4 and displaces it from Myc in a… |
5 mg |
30414-5 |
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JSH-23 |
An inhibitor of NF-κB, blocking its translocation into the nucleus (… |
1 mg |
15036-1 |
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JSH-23 |
An inhibitor of NF-κB, blocking its translocation into the nucleus (… |
10 mg |
15036-10 |
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JSH-23 |
An inhibitor of NF-κB, blocking its translocation into the nucleus (… |
25 mg |
15036-25 |
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JSH-23 |
An inhibitor of NF-κB, blocking its translocation into the nucleus (… |
5 mg |
15036-5 |
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JS-K |
A nitric oxide donor; inhibits proliferation of HL-60 cells (IC50 = 0.5 &m… |
1 mg |
21225-1 |
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JS-K |
A nitric oxide donor; inhibits proliferation of HL-60 cells (IC50 = 0.5 &m… |
5 mg |
21225-5 |
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JT010 |
A TRPA1 agonist (EC50 = 0.65 nM in a calcium influx assay); selective for… |
1 mg |
29732-1 |
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JT010 |
A TRPA1 agonist (EC50 = 0.65 nM in a calcium influx assay); selective for… |
10 mg |
29732-10 |
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JT010 |
A TRPA1 agonist (EC50 = 0.65 nM in a calcium influx assay); selective for… |
5 mg |
29732-5 |
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JTC 801 |
A selective nociceptin receptor antagonist (ORL1; Ki = 44.5 nM; IC50 = 94… |
10 mg |
21254-10 |
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JTC 801 |
A selective nociceptin receptor antagonist (ORL1; Ki = 44.5 nM; IC50 = 94… |
25 mg |
21254-25 |
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JTC 801 |
A selective nociceptin receptor antagonist (ORL1; Ki = 44.5 nM; IC50 = 94… |
5 mg |
21254-5 |
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JTC 801 |
A selective nociceptin receptor antagonist (ORL1; Ki = 44.5 nM; IC50 = 94… |
50 mg |
21254-50 |
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JTE-013 |
An S1P2 and S1P4 receptor antagonist (IC50 = 17 and 237 nM, respectively);… |
1 mg |
10009458-1 |
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JTE-013 |
An S1P2 and S1P4 receptor antagonist (IC50 = 17 and 237 nM, respectively);… |
10 mg |
10009458-10 |
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JTE-013 |
An S1P2 and S1P4 receptor antagonist (IC50 = 17 and 237 nM, respectively);… |
5 mg |
10009458-5 |
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JTE-013 |
An S1P2 and S1P4 receptor antagonist (IC50 = 17 and 237 nM, respectively);… |
50 mg |
10009458-50 |
More Info
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JTE-607 |
A cytokine synthesis inhibitor; inhibits the production of TNF-α, IL… |
10 mg |
36942-10 |
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JTE-607 |
A cytokine synthesis inhibitor; inhibits the production of TNF-α, IL… |
25 mg |
36942-25 |
More Info
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JTE-607 |
A cytokine synthesis inhibitor; inhibits the production of TNF-α, IL… |
5 mg |
36942-5 |
More Info
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JTE-607 |
A cytokine synthesis inhibitor; inhibits the production of TNF-α, IL… |
50 mg |
36942-50 |
More Info
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JTE-907 |
A CB2 receptor inverse agonist; selective for CB2 over CB1 receptors (Kis… |
1 mg |
10009857-1 |
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JTE-907 |
A CB2 receptor inverse agonist; selective for CB2 over CB1 receptors (Kis… |
5 mg |
10009857-5 |
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Juglanin |
A flavonol with diverse biological activities; reduces OSS-induced increas… |
1 mg |
39824-1 |
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Juglanin |
A flavonol with diverse biological activities; reduces OSS-induced increas… |
10 mg |
39824-10 |
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Juglanin |
A flavonol with diverse biological activities; reduces OSS-induced increas… |
25 mg |
39824-25 |
More Info
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Juglanin |
A flavonol with diverse biological activities; reduces OSS-induced increas… |
5 mg |
39824-5 |
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Juglone |
A natural naphthoquinone that has allelopathic actions, suppressing growth… |
1 g |
16216-1 |
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Juglone |
A natural naphthoquinone that has allelopathic actions, suppressing growth… |
500 mg |
16216-500 |
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Jun9-72-2 |
A SARS-CoV-2 PLpro inhibitor (IC50 = 0.67 µM); inhibits viral replic… |
1 mg |
37195-1 |
More Info
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Jun9-72-2 |
A SARS-CoV-2 PLpro inhibitor (IC50 = 0.67 µM); inhibits viral replic… |
10 mg |
37195-10 |
More Info
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Jun9-72-2 |
A SARS-CoV-2 PLpro inhibitor (IC50 = 0.67 µM); inhibits viral replic… |
5 mg |
37195-5 |
More Info
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Juvenile Hormone III |
An acyclic sesquiterpenoid that regulates diverse processes in insects; ac… |
1 mg |
19646-1 |
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Juvenile Hormone III |
An acyclic sesquiterpenoid that regulates diverse processes in insects; ac… |
10 mg |
19646-10 |
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Juvenile Hormone III |
An acyclic sesquiterpenoid that regulates diverse processes in insects; ac… |
5 mg |
19646-5 |
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JW 480 |
A potent, selective inhibitor of KIAA1361 (IC50s = 20 nM in mouse brain me… |
10 mg |
10879-10 |
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JW 480 |
A potent, selective inhibitor of KIAA1361 (IC50s = 20 nM in mouse brain me… |
25 mg |
10879-25 |
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JW 480 |
A potent, selective inhibitor of KIAA1361 (IC50s = 20 nM in mouse brain me… |
5 mg |
10879-5 |
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JW 480 |
A potent, selective inhibitor of KIAA1361 (IC50s = 20 nM in mouse brain me… |
50 mg |
10879-50 |
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JW 55 |
An inhibitor of the PARP domain of TNKS1 and TNKS2 (IC50s = 1.9 and 0.83 &… |
10 mg |
16260-10 |
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JW 55 |
An inhibitor of the PARP domain of TNKS1 and TNKS2 (IC50s = 1.9 and 0.83 &… |
25 mg |
16260-25 |
More Info
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JW 55 |
An inhibitor of the PARP domain of TNKS1 and TNKS2 (IC50s = 1.9 and 0.83 &… |
5 mg |
16260-5 |
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JW 618 |
A potent, selective inhibitor of MAGL that displays IC50 values of 123, 38… |
10 mg |
11790-10 |
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JW 618 |
A potent, selective inhibitor of MAGL that displays IC50 values of 123, 38… |
25 mg |
11790-25 |
More Info
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JW 618 |
A potent, selective inhibitor of MAGL that displays IC50 values of 123, 38… |
5 mg |
11790-5 |
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JW 618 |
A potent, selective inhibitor of MAGL that displays IC50 values of 123, 38… |
50 mg |
11790-50 |
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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
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JW 642 |
An inhibitor of MAGL (IC50s = 3.7, 7.6, and 14 nM for the human, mouse, an… |
5 mg |
11789-5 |
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JW 74 |
An inhibitor of the catalytic PARP domain of TNKS1 / 2 that blocks canonic… |
1 mg |
19124-1 |
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JW 74 |
An inhibitor of the catalytic PARP domain of TNKS1 / 2 that blocks canonic… |
10 mg |
19124-10 |
More Info
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JW 74 |
An inhibitor of the catalytic PARP domain of TNKS1 / 2 that blocks canonic… |
5 mg |
19124-5 |
More Info
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JWH 007 |
A potent CB receptor agonist that avidly binds to both CB1 and CB2 (Ki = 9… |
10 mg |
10266-10 |
More Info
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JWH 007 |
A potent CB receptor agonist that avidly binds to both CB1 and CB2 (Ki = 9… |
25 mg |
10266-25 |
More Info
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JWH 007 |
A potent CB receptor agonist that avidly binds to both CB1 and CB2 (Ki = 9… |
5 mg |
10266-5 |
More Info
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JWH 011 |
A synthetic CB that is analogous to the N-hexyl JWH 004, which has high af… |
1 mg |
9001058-1 |
More Info
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JWH 011 |
A synthetic CB that is analogous to the N-hexyl JWH 004, which has high af… |
10 mg |
9001058-10 |
More Info
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JWH 011 |
A synthetic CB that is analogous to the N-hexyl JWH 004, which has high af… |
5 mg |
9001058-5 |
More Info
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JWH 016 |
An analytical reference standard categorized as a synthetic cannabinoid; i… |
10 mg |
10849-10 |
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JWH 016 |
An analytical reference standard categorized as a synthetic cannabinoid; i… |
25 mg |
10849-25 |
More Info
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JWH 016 |
An analytical reference standard categorized as a synthetic cannabinoid; i… |
5 mg |
10849-5 |
More Info
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JWH 019 |
A cannabimimetic indole that shows high-affinity for both CB1 (Ki = 9.8 nM… |
10 mg |
13633-10 |
More Info
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