WWL70 |
A selective inhibitor of ABHD6 (IC50 = 70 nM); increases Ucp1 expression a… |
5 mg |
10011213-5 |
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Wy 14643 |
An agonist of PPARα; selectively transactivates PPARα over PPA… |
10 mg |
70730-10 |
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Wy 14643 |
An agonist of PPARα; selectively transactivates PPARα over PPA… |
250 mg |
70730-250 |
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Wy 14643 |
An agonist of PPARα; selectively transactivates PPARα over PPA… |
5 mg |
70730-5 |
More Info
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Wy 14643 |
An agonist of PPARα; selectively transactivates PPARα over PPA… |
50 mg |
70730-50 |
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WYE-125132 |
An ATP-competitive inhibitor of mTOR (IC50 = 0.19 nM) that inhibits signal… |
1 mg |
18372-1 |
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WYE-125132 |
An ATP-competitive inhibitor of mTOR (IC50 = 0.19 nM) that inhibits signal… |
10 mg |
18372-10 |
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WYE-125132 |
An ATP-competitive inhibitor of mTOR (IC50 = 0.19 nM) that inhibits signal… |
5 mg |
18372-5 |
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WYE-125132 |
An ATP-competitive inhibitor of mTOR (IC50 = 0.19 nM) that inhibits signal… |
500 µg |
18372-500 |
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WYE-23 |
An inhibitor of mTOR (IC50 = 0.45 nM); selective for mTOR over PI3Kα… |
1 mg |
21199-1 |
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WYE-23 |
An inhibitor of mTOR (IC50 = 0.45 nM); selective for mTOR over PI3Kα… |
10 mg |
21199-10 |
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WYE-23 |
An inhibitor of mTOR (IC50 = 0.45 nM); selective for mTOR over PI3Kα… |
5 mg |
21199-5 |
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WYE-23 |
An inhibitor of mTOR (IC50 = 0.45 nM); selective for mTOR over PI3Kα… |
500 µg |
21199-500 |
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WYE-28 |
An inhibitor of mTOR (IC50 = 0.08 nM); selective for mTOR over PI3Kα… |
1 mg |
21200-1 |
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WYE-28 |
An inhibitor of mTOR (IC50 = 0.08 nM); selective for mTOR over PI3Kα… |
10 mg |
21200-10 |
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WYE-28 |
An inhibitor of mTOR (IC50 = 0.08 nM); selective for mTOR over PI3Kα… |
5 mg |
21200-5 |
More Info
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WYE-28 |
An inhibitor of mTOR (IC50 = 0.08 nM); selective for mTOR over PI3Kα… |
500 µg |
21200-500 |
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WYE-354 |
A selective, potent, and cell-permeable inhibitor of mTOR (IC50 = 4.3 nM)… |
10 mg |
13604-10 |
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WYE-354 |
A selective, potent, and cell-permeable inhibitor of mTOR (IC50 = 4.3 nM)… |
25 mg |
13604-25 |
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WYE-354 |
A selective, potent, and cell-permeable inhibitor of mTOR (IC50 = 4.3 nM)… |
5 mg |
13604-5 |
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WYE-354 |
A selective, potent, and cell-permeable inhibitor of mTOR (IC50 = 4.3 nM)… |
50 mg |
13604-50 |
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WYE-687 |
An mTOR inhibitor (IC50 = 0.007 µM); selective for mTOR over PI3K&al… |
1 mg |
29977-1 |
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WYE-687 |
An mTOR inhibitor (IC50 = 0.007 µM); selective for mTOR over PI3K&al… |
10 mg |
29977-10 |
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WYE-687 |
An mTOR inhibitor (IC50 = 0.007 µM); selective for mTOR over PI3K&al… |
25 mg |
29977-25 |
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WYE-687 |
An mTOR inhibitor (IC50 = 0.007 µM); selective for mTOR over PI3K&al… |
5 mg |
29977-5 |
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WZ3146 |
An inhibitor of mutant EGFRs (IC50s = 2-2,740 nM); selective for EGFR muta… |
1 mg |
23440-1 |
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WZ3146 |
An inhibitor of mutant EGFRs (IC50s = 2-2,740 nM); selective for EGFR muta… |
10 mg |
23440-10 |
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WZ3146 |
An inhibitor of mutant EGFRs (IC50s = 2-2,740 nM); selective for EGFR muta… |
5 mg |
23440-5 |
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WZ3146 |
An inhibitor of mutant EGFRs (IC50s = 2-2,740 nM); selective for EGFR muta… |
50 mg |
23440-50 |
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WZ4002 |
An irreversible EGFR tyrosine kinase inhibitor that blocks ATP-dependent a… |
10 mg |
16297-10 |
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WZ4002 |
An irreversible EGFR tyrosine kinase inhibitor that blocks ATP-dependent a… |
100 mg |
16297-100 |
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WZ4002 |
An irreversible EGFR tyrosine kinase inhibitor that blocks ATP-dependent a… |
5 mg |
16297-5 |
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WZ4002 |
An irreversible EGFR tyrosine kinase inhibitor that blocks ATP-dependent a… |
50 mg |
16297-50 |
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WZ4003 |
A selective inhibitor of NUAK1 and NUAK2 (IC50s = 20 and 100 nM, respectiv… |
1 mg |
19177-1 |
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WZ4003 |
A selective inhibitor of NUAK1 and NUAK2 (IC50s = 20 and 100 nM, respectiv… |
10 mg |
19177-10 |
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WZ4003 |
A selective inhibitor of NUAK1 and NUAK2 (IC50s = 20 and 100 nM, respectiv… |
25 mg |
19177-25 |
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WZ4003 |
A selective inhibitor of NUAK1 and NUAK2 (IC50s = 20 and 100 nM, respectiv… |
5 mg |
19177-5 |
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WZ8040 |
An inhibitor of mutant EGFR (IC50s = 2-306 in Ba / F3 cells); selective fo… |
10 mg |
30062-10 |
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WZ8040 |
An inhibitor of mutant EGFR (IC50s = 2-306 in Ba / F3 cells); selective fo… |
25 mg |
30062-25 |
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WZ8040 |
An inhibitor of mutant EGFR (IC50s = 2-306 in Ba / F3 cells); selective fo… |
5 mg |
30062-5 |
More Info
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WZ8040 |
An inhibitor of mutant EGFR (IC50s = 2-306 in Ba / F3 cells); selective fo… |
50 mg |
30062-50 |
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WZ811 |
A potent inhibitor of binding of an SDF-1 peptide mimic to CXCR4 (EC50 = 0… |
1 mg |
13639-1 |
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WZ811 |
A potent inhibitor of binding of an SDF-1 peptide mimic to CXCR4 (EC50 = 0… |
10 mg |
13639-10 |
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WZ811 |
A potent inhibitor of binding of an SDF-1 peptide mimic to CXCR4 (EC50 = 0… |
25 mg |
13639-25 |
More Info
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WZ811 |
A potent inhibitor of binding of an SDF-1 peptide mimic to CXCR4 (EC50 = 0… |
5 mg |
13639-5 |
More Info
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WZB117 |
An irreversible inhibitor of Glut1 that blocks glucose transport in divers… |
10 mg |
19900-10 |
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WZB117 |
An irreversible inhibitor of Glut1 that blocks glucose transport in divers… |
25 mg |
19900-25 |
More Info
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WZB117 |
An irreversible inhibitor of Glut1 that blocks glucose transport in divers… |
5 mg |
19900-5 |
More Info
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WZB117 |
An irreversible inhibitor of Glut1 that blocks glucose transport in divers… |
50 mg |
19900-50 |
More Info
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X-82 |
A multi-kinase inhibitor; inhibits VEGFR2, PDGFRβ, FLT3, and c-Kit (I… |
1 mg |
38765-1 |
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