GSK1292263 |
A GPR119 agonist (EC50 = 43.9 nM in CHO-K1 cells expressing human GPR119);… |
50 mg |
26181-50 |
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GSK189254 |
A histamine H3 receptor antagonist (Kis = 0.13, 0.68, and 1.74 nM for the… |
10 mg |
36705-10 |
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GSK189254 |
A histamine H3 receptor antagonist (Kis = 0.13, 0.68, and 1.74 nM for the… |
25 mg |
36705-25 |
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GSK189254 |
A histamine H3 receptor antagonist (Kis = 0.13, 0.68, and 1.74 nM for the… |
5 mg |
36705-5 |
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GSK1940029 |
A stearoyl-CoA desaturase inhibitor; increases palmitate-induced phosphory… |
1 mg |
36704-1 |
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GSK1940029 |
A stearoyl-CoA desaturase inhibitor; increases palmitate-induced phosphory… |
10 mg |
36704-10 |
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GSK1940029 |
A stearoyl-CoA desaturase inhibitor; increases palmitate-induced phosphory… |
25 mg |
36704-25 |
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GSK1940029 |
A stearoyl-CoA desaturase inhibitor; increases palmitate-induced phosphory… |
5 mg |
36704-5 |
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GSK2018682 |
An S1P1 and S1P5 receptor agonist; selective for S1P1 and S1P5 over S1P2,… |
10 mg |
31437-10 |
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GSK2018682 |
An S1P1 and S1P5 receptor agonist; selective for S1P1 and S1P5 over S1P2,… |
25 mg |
31437-25 |
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GSK2018682 |
An S1P1 and S1P5 receptor agonist; selective for S1P1 and S1P5 over S1P2,… |
5 mg |
31437-5 |
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GSK2018682 |
An S1P1 and S1P5 receptor agonist; selective for S1P1 and S1P5 over S1P2,… |
50 mg |
31437-50 |
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GSK2033 |
An antagonist of LXRα and LXRβ (IC50s = 0.1 and 0.398 µM,… |
1 mg |
25443-1 |
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GSK2033 |
An antagonist of LXRα and LXRβ (IC50s = 0.1 and 0.398 µM,… |
10 mg |
25443-10 |
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GSK2033 |
An antagonist of LXRα and LXRβ (IC50s = 0.1 and 0.398 µM,… |
5 mg |
25443-5 |
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GSK2126458 |
A potent inhibitor of PI3K isoforms (Kis = 19, 130, 24, and 60 pM for p110… |
1 mg |
17377-1 |
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GSK2126458 |
A potent inhibitor of PI3K isoforms (Kis = 19, 130, 24, and 60 pM for p110… |
10 mg |
17377-10 |
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GSK2126458 |
A potent inhibitor of PI3K isoforms (Kis = 19, 130, 24, and 60 pM for p110… |
5 mg |
17377-5 |
More Info
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GSK2126458 |
A potent inhibitor of PI3K isoforms (Kis = 19, 130, 24, and 60 pM for p110… |
50 mg |
17377-50 |
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GSK2190915 |
A selective inhibitor of human FLAP (IC50 = 2.9 nM); selective for FLAP ov… |
1 mg |
28600-1 |
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GSK2193874 |
A potent, selective antagonist of TRPV4 channels, blocking the influx of c… |
1 mg |
17715-1 |
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GSK2193874 |
A potent, selective antagonist of TRPV4 channels, blocking the influx of c… |
10 mg |
17715-10 |
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GSK2193874 |
A potent, selective antagonist of TRPV4 channels, blocking the influx of c… |
25 mg |
17715-25 |
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GSK2193874 |
A potent, selective antagonist of TRPV4 channels, blocking the influx of c… |
5 mg |
17715-5 |
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GSK2194069 |
An inhibitor of fatty acid synthase (IC50 = 7.7 nM in an assay detecting r… |
1 mg |
20022-1 |
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