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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AS-1842856 |
A potent FoxO1 inhibitor (IC50 = 33 nM in HepG2 cells); causes a dose-depe… |
5 mg |
16761-5 |
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AS-1892802 |
A potent ROCK inhibitor (IC50s = 122, 52, and 57 nM for human ROCK1, ROCK2… |
1 mg |
14978-1 |
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AS-1892802 |
A potent ROCK inhibitor (IC50s = 122, 52, and 57 nM for human ROCK1, ROCK2… |
10 mg |
14978-10 |
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AS-1892802 |
A potent ROCK inhibitor (IC50s = 122, 52, and 57 nM for human ROCK1, ROCK2… |
25 mg |
14978-25 |
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AS-1892802 |
A potent ROCK inhibitor (IC50s = 122, 52, and 57 nM for human ROCK1, ROCK2… |
5 mg |
14978-5 |
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AS-19 |
A 5-HT7 receptor agonist (IC50 = 0.83 nM); selective for 5-HT7 over 5-HT1A… |
1 mg |
20642-1 |
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AS-19 |
A 5-HT7 receptor agonist (IC50 = 0.83 nM); selective for 5-HT7 over 5-HT1A… |
10 mg |
20642-10 |
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AS-19 |
A 5-HT7 receptor agonist (IC50 = 0.83 nM); selective for 5-HT7 over 5-HT1A… |
5 mg |
20642-5 |
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AS-1949490 |
A selective inhibitor of SHIP2 (IC50s = 0.62 and 0.34 µM for human a… |
1 mg |
17627-1 |
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AS-1949490 |
A selective inhibitor of SHIP2 (IC50s = 0.62 and 0.34 µM for human a… |
10 mg |
17627-10 |
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AS-1949490 |
A selective inhibitor of SHIP2 (IC50s = 0.62 and 0.34 µM for human a… |
5 mg |
17627-5 |
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AS-1949490 |
A selective inhibitor of SHIP2 (IC50s = 0.62 and 0.34 µM for human a… |
50 mg |
17627-50 |
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AS-2077715 |
An inhibitor of fungal complex III (IC50 = 80 ng / ml for T. mentagrophyte… |
1 mg |
29775-1 |
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AS-252424 |
A potent inhibitor of PI3K with selectivity for the g isoform; inhibits hu… |
1 mg |
10009052-1 |
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AS-252424 |
A potent inhibitor of PI3K with selectivity for the g isoform; inhibits hu… |
10 mg |
10009052-10 |
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AS-252424 |
A potent inhibitor of PI3K with selectivity for the g isoform; inhibits hu… |
25 mg |
10009052-25 |
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AS-252424 |
A potent inhibitor of PI3K with selectivity for the g isoform; inhibits hu… |
5 mg |
10009052-5 |
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AS-2717638 |
An LPA5 antagonist (IC50 = 0.038 µM); selective for LPA5 over LPA1,… |
1 mg |
37787-1 |
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AS-2717638 |
An LPA5 antagonist (IC50 = 0.038 µM); selective for LPA5 over LPA1,… |
10 mg |
37787-10 |
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