ARUK3001185 |
An inhibitor of NOTUM (IC50 = 6.7 nM); selective for NOTUM over a panel of… |
5 mg |
37113-5 |
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Arundic Acid |
An inhibitor of astrocyte activation; reduces increases in brain GFAP and… |
1 mg |
29087-1 |
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Arundic Acid |
An inhibitor of astrocyte activation; reduces increases in brain GFAP and… |
10 mg |
29087-10 |
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Arundic Acid |
An inhibitor of astrocyte activation; reduces increases in brain GFAP and… |
25 mg |
29087-25 |
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Arundic Acid |
An inhibitor of astrocyte activation; reduces increases in brain GFAP and… |
5 mg |
29087-5 |
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ARV-110 |
A PROTAC that drives AR degradation; reduces androgen receptor levels in V… |
10 mg |
39662-10 |
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ARV-110 |
A PROTAC that drives AR degradation; reduces androgen receptor levels in V… |
25 mg |
39662-25 |
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ARV-110 |
A PROTAC that drives AR degradation; reduces androgen receptor levels in V… |
5 mg |
39662-5 |
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ARV-110 |
A PROTAC that drives AR degradation; reduces androgen receptor levels in V… |
50 mg |
39662-50 |
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ARV-771 |
A PROTAC that drives BET family protein degradation; induces degradation o… |
1 mg |
21299-1 |
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ARV-771 |
A PROTAC that drives BET family protein degradation; induces degradation o… |
10 mg |
21299-10 |
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ARV-771 |
A PROTAC that drives BET family protein degradation; induces degradation o… |
5 mg |
21299-5 |
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ARV-825 |
A hetero-bifunctional molecule composed of a BRD4 binding moiety joined to… |
1 mg |
21109-1 |
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ARV-825 |
A hetero-bifunctional molecule composed of a BRD4 binding moiety joined to… |
5 mg |
21109-5 |
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ARV-825 |
A hetero-bifunctional molecule composed of a BRD4 binding moiety joined to… |
500 µg |
21109-500 |
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Arvanil |
A structural analog of capsaicin with complex interactions in the CB syste… |
10 mg |
90052-10 |
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Arvanil |
A structural analog of capsaicin with complex interactions in the CB syste… |
100 mg |
90052-100 |
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Arvanil |
A structural analog of capsaicin with complex interactions in the CB syste… |
5 mg |
90052-5 |
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Arvanil |
A structural analog of capsaicin with complex interactions in the CB syste… |
50 mg |
90052-50 |
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Aryl Hydrocarbon Receptor Bioassay |
This assay kit provides the convenience of an all-inclusive cell-based rep… |
96 well |
41037-96 |
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Arylpiperazine 5k |
A FATP1 inhibitor (IC50 = 4.6 nM for the human protein); reduces neutral a… |
10 mg |
38135-10 |
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Arylpiperazine 5k |
A FATP1 inhibitor (IC50 = 4.6 nM for the human protein); reduces neutral a… |
25 mg |
38135-25 |
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Arylpiperazine 5k |
A FATP1 inhibitor (IC50 = 4.6 nM for the human protein); reduces neutral a… |
5 mg |
38135-5 |
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Arylpiperazine 5k |
A FATP1 inhibitor (IC50 = 4.6 nM for the human protein); reduces neutral a… |
50 mg |
38135-50 |
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Arylquin 1 |
A Par-4 secretagogue; binds to vimentin to displace Par-4 for secretion; i… |
1 mg |
16961-1 |
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Arylquin 1 |
A Par-4 secretagogue; binds to vimentin to displace Par-4 for secretion; i… |
10 mg |
16961-10 |
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Arylquin 1 |
A Par-4 secretagogue; binds to vimentin to displace Par-4 for secretion; i… |
5 mg |
16961-5 |
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(-)-AS 115 |
A single enantiomer of a potent and selective inactivator of KIAA1363, a M… |
1 mg |
13250-1 |
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(-)-AS 115 |
A single enantiomer of a potent and selective inactivator of KIAA1363, a M… |
100 µg |
13250-100 |
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(-)-AS 115 |
A single enantiomer of a potent and selective inactivator of KIAA1363, a M… |
500 µg |
13250-500 |
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(+)-AS 115 |
A single enantiomer of a potent and selective inactivator of KIAA1363, a M… |
1 mg |
10009650-1 |
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(+)-AS 115 |
A single enantiomer of a potent and selective inactivator of KIAA1363, a M… |
100 µg |
10009650-100 |
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(+)-AS 115 |
A single enantiomer of a potent and selective inactivator of KIAA1363, a M… |
500 µg |
10009650-500 |
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AS-041164 |
A potent inhibitor of PI3K with selectivity for the class IB isoform PI3K&… |
10 mg |
13622-10 |
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AS-041164 |
A potent inhibitor of PI3K with selectivity for the class IB isoform PI3K&… |
25 mg |
13622-25 |
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AS-041164 |
A potent inhibitor of PI3K with selectivity for the class IB isoform PI3K&… |
5 mg |
13622-5 |
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AS-041164 |
A potent inhibitor of PI3K with selectivity for the class IB isoform PI3K&… |
50 mg |
13622-50 |
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AS-101 |
An immunomodulator; inhibits IL-10 secretion from and cell proliferation o… |
1 mg |
21443-1 |
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AS-101 |
An immunomodulator; inhibits IL-10 secretion from and cell proliferation o… |
10 mg |
21443-10 |
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AS-101 |
An immunomodulator; inhibits IL-10 secretion from and cell proliferation o… |
5 mg |
21443-5 |
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AS-1269574 |
An agonist of GPR199 that is effective both in isolated cells and in vivo;… |
1 mg |
10626-1 |
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AS-1269574 |
An agonist of GPR199 that is effective both in isolated cells and in vivo;… |
10 mg |
10626-10 |
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AS-1269574 |
An agonist of GPR199 that is effective both in isolated cells and in vivo;… |
25 mg |
10626-25 |
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AS-1269574 |
An agonist of GPR199 that is effective both in isolated cells and in vivo;… |
5 mg |
10626-5 |
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AS1517499 |
A STAT6 inhibitor (IC50 = 21 nM in a reporter assay); inhibits IL-4-induce… |
1 mg |
29071-1 |
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AS1517499 |
A STAT6 inhibitor (IC50 = 21 nM in a reporter assay); inhibits IL-4-induce… |
10 mg |
29071-10 |
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AS1517499 |
A STAT6 inhibitor (IC50 = 21 nM in a reporter assay); inhibits IL-4-induce… |
25 mg |
29071-25 |
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AS1517499 |
A STAT6 inhibitor (IC50 = 21 nM in a reporter assay); inhibits IL-4-induce… |
5 mg |
29071-5 |
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AS-1842856 |
A potent FoxO1 inhibitor (IC50 = 33 nM in HepG2 cells); causes a dose-depe… |
1 mg |
16761-1 |
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AS-1842856 |
A potent FoxO1 inhibitor (IC50 = 33 nM in HepG2 cells); causes a dose-depe… |
10 mg |
16761-10 |
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