AS-1842856 |
A potent FoxO1 inhibitor (IC50 = 33 nM in HepG2 cells); causes a dose-depe… |
5 mg |
16761-5 |
More Info
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AS-1892802 |
A potent ROCK inhibitor (IC50s = 122, 52, and 57 nM for human ROCK1, ROCK2… |
1 mg |
14978-1 |
More Info
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AS-1892802 |
A potent ROCK inhibitor (IC50s = 122, 52, and 57 nM for human ROCK1, ROCK2… |
10 mg |
14978-10 |
More Info
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AS-1892802 |
A potent ROCK inhibitor (IC50s = 122, 52, and 57 nM for human ROCK1, ROCK2… |
25 mg |
14978-25 |
More Info
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AS-1892802 |
A potent ROCK inhibitor (IC50s = 122, 52, and 57 nM for human ROCK1, ROCK2… |
5 mg |
14978-5 |
More Info
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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 |
More Info
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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 |
More Info
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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 |
More Info
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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 |
More Info
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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 |
More Info
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AS-2077715 |
An inhibitor of fungal complex III (IC50 = 80 ng / ml for T. mentagrophyte… |
1 mg |
29775-1 |
More Info
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AS-252424 |
A potent inhibitor of PI3K with selectivity for the g isoform; inhibits hu… |
1 mg |
10009052-1 |
More Info
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AS-252424 |
A potent inhibitor of PI3K with selectivity for the g isoform; inhibits hu… |
10 mg |
10009052-10 |
More Info
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AS-252424 |
A potent inhibitor of PI3K with selectivity for the g isoform; inhibits hu… |
25 mg |
10009052-25 |
More Info
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AS-252424 |
A potent inhibitor of PI3K with selectivity for the g isoform; inhibits hu… |
5 mg |
10009052-5 |
More Info
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AS-2717638 |
An LPA5 antagonist (IC50 = 0.038 µM); selective for LPA5 over LPA1,… |
1 mg |
37787-1 |
More Info
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AS-2717638 |
An LPA5 antagonist (IC50 = 0.038 µM); selective for LPA5 over LPA1,… |
10 mg |
37787-10 |
More Info
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AS-2717638 |
An LPA5 antagonist (IC50 = 0.038 µM); selective for LPA5 over LPA1,… |
25 mg |
37787-25 |
More Info
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AS-2717638 |
An LPA5 antagonist (IC50 = 0.038 µM); selective for LPA5 over LPA1,… |
5 mg |
37787-5 |
More Info
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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 |
More Info
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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 |
More Info
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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 |
More Info
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AS-604850 |
AS-604850 is a selective, ATP-competitive inhibitor of PI3Kγ with IC… |
10 mg |
10010175-10 |
More Info
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AS-604850 |
AS-604850 is a selective, ATP-competitive inhibitor of PI3Kγ with IC… |
25 mg |
10010175-25 |
More Info
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AS-604850 |
AS-604850 is a selective, ATP-competitive inhibitor of PI3Kγ with IC… |
5 mg |
10010175-5 |
More Info
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AS-605240 |
A potent inhibitor of PI3Kγ; inhibits human recombinant PI3Kγ,… |
1 mg |
10007707-1 |
More Info
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AS-605240 |
A potent inhibitor of PI3Kγ; inhibits human recombinant PI3Kγ,… |
10 mg |
10007707-10 |
More Info
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AS-605240 |
A potent inhibitor of PI3Kγ; inhibits human recombinant PI3Kγ,… |
25 mg |
10007707-25 |
More Info
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AS-605240 |
A potent inhibitor of PI3Kγ; inhibits human recombinant PI3Kγ,… |
5 mg |
10007707-5 |
More Info
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AS-703026 |
Selectively inhibits MEK1 / 2; potently inhibits growth and survival of hu… |
1 mg |
11226-1 |
More Info
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AS-703026 |
Selectively inhibits MEK1 / 2; potently inhibits growth and survival of hu… |
10 mg |
11226-10 |
More Info
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AS-703026 |
Selectively inhibits MEK1 / 2; potently inhibits growth and survival of hu… |
25 mg |
11226-25 |
More Info
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AS-703026 |
Selectively inhibits MEK1 / 2; potently inhibits growth and survival of hu… |
5 mg |
11226-5 |
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AS-8351 |
A histone demethylase inhibitor that is used in combination with 8 other c… |
10 mg |
20811-10 |
More Info
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AS-8351 |
A histone demethylase inhibitor that is used in combination with 8 other c… |
25 mg |
20811-25 |
More Info
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AS-8351 |
A histone demethylase inhibitor that is used in combination with 8 other c… |
5 mg |
20811-5 |
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Asapiprant |
An antagonist of DP1 (Ki = 0.44 nM); selective for DP1 over DP2, as well a… |
1 mg |
30008-1 |
More Info
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Asapiprant |
An antagonist of DP1 (Ki = 0.44 nM); selective for DP1 over DP2, as well a… |
10 mg |
30008-10 |
More Info
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Asapiprant |
An antagonist of DP1 (Ki = 0.44 nM); selective for DP1 over DP2, as well a… |
25 mg |
30008-25 |
More Info
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Asapiprant |
An antagonist of DP1 (Ki = 0.44 nM); selective for DP1 over DP2, as well a… |
5 mg |
30008-5 |
More Info
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Asaraldehyde |
A plant metabolite with diverse biological activities; selectively inhibit… |
100 g |
36798-100 |
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Asaraldehyde |
A plant metabolite with diverse biological activities; selectively inhibit… |
25 g |
36798-25 |
More Info
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Asaraldehyde |
A plant metabolite with diverse biological activities; selectively inhibit… |
250 g |
36798-250 |
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Asaraldehyde |
A plant metabolite with diverse biological activities; selectively inhibit… |
50 g |
36798-50 |
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Asarinin |
A lignan; an inhibitor of Δ5-desaturase (Ki = 0.28 mM); selective fo… |
1 mg |
27456-1 |
More Info
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Asarinin |
A lignan; an inhibitor of Δ5-desaturase (Ki = 0.28 mM); selective fo… |
10 mg |
27456-10 |
More Info
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Asarinin |
A lignan; an inhibitor of Δ5-desaturase (Ki = 0.28 mM); selective fo… |
25 mg |
27456-25 |
More Info
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