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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AS-2717638 |
An LPA5 antagonist (IC50 = 0.038 µM); selective for LPA5 over LPA1,… |
25 mg |
37787-25 |
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AS-2717638 |
An LPA5 antagonist (IC50 = 0.038 µM); selective for LPA5 over LPA1,… |
5 mg |
37787-5 |
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AS-2863619 |
A dual inhibitor of Cdk8 and Cdk19 (IC50s = 0.6 and 4.3 nM, respectively);… |
1 mg |
30976-1 |
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AS-2863619 |
A dual inhibitor of Cdk8 and Cdk19 (IC50s = 0.6 and 4.3 nM, respectively);… |
5 mg |
30976-5 |
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AS-2863619 |
A dual inhibitor of Cdk8 and Cdk19 (IC50s = 0.6 and 4.3 nM, respectively);… |
500 µg |
30976-500 |
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AS-604850 |
AS-604850 is a selective, ATP-competitive inhibitor of PI3Kγ with IC… |
1 mg |
10010175-1 |
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AS-604850 |
AS-604850 is a selective, ATP-competitive inhibitor of PI3Kγ with IC… |
10 mg |
10010175-10 |
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AS-604850 |
AS-604850 is a selective, ATP-competitive inhibitor of PI3Kγ with IC… |
25 mg |
10010175-25 |
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AS-604850 |
AS-604850 is a selective, ATP-competitive inhibitor of PI3Kγ with IC… |
5 mg |
10010175-5 |
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AS-605240 |
A potent inhibitor of PI3Kγ; inhibits human recombinant PI3Kγ,… |
1 mg |
10007707-1 |
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AS-605240 |
A potent inhibitor of PI3Kγ; inhibits human recombinant PI3Kγ,… |
10 mg |
10007707-10 |
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AS-605240 |
A potent inhibitor of PI3Kγ; inhibits human recombinant PI3Kγ,… |
25 mg |
10007707-25 |
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AS-605240 |
A potent inhibitor of PI3Kγ; inhibits human recombinant PI3Kγ,… |
5 mg |
10007707-5 |
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AS-703026 |
Selectively inhibits MEK1 / 2; potently inhibits growth and survival of hu… |
1 mg |
11226-1 |
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