XAP044 |
An antagonist of mGluR7, inhibiting lateral amygdala long term potentiatio… |
10 mg |
19095-10 |
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XAP044 |
An antagonist of mGluR7, inhibiting lateral amygdala long term potentiatio… |
5 mg |
19095-5 |
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XAV939 |
A small molecule inhibitor of tankyrase 1 and 2 (IC50 = 11 and 4 nM, respe… |
1 mg |
13596-1 |
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XAV939 |
A small molecule inhibitor of tankyrase 1 and 2 (IC50 = 11 and 4 nM, respe… |
10 mg |
13596-10 |
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XAV939 |
A small molecule inhibitor of tankyrase 1 and 2 (IC50 = 11 and 4 nM, respe… |
25 mg |
13596-25 |
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XAV939 |
A small molecule inhibitor of tankyrase 1 and 2 (IC50 = 11 and 4 nM, respe… |
5 mg |
13596-5 |
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XCT790 |
A selective inverse agonist of ERRα (IC50 = ~300-500 nM); blocks ERR… |
1 mg |
16035-1 |
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XCT790 |
A selective inverse agonist of ERRα (IC50 = ~300-500 nM); blocks ERR… |
10 mg |
16035-10 |
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XCT790 |
A selective inverse agonist of ERRα (IC50 = ~300-500 nM); blocks ERR… |
5 mg |
16035-5 |
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XD14 |
A BRD inhibitor; binds to BRD2, -3, and 4 (Kds = 170, 380, and 160 nM); in… |
10 mg |
30740-10 |
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XD14 |
A BRD inhibitor; binds to BRD2, -3, and 4 (Kds = 170, 380, and 160 nM); in… |
25 mg |
30740-25 |
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XD14 |
A BRD inhibitor; binds to BRD2, -3, and 4 (Kds = 170, 380, and 160 nM); in… |
5 mg |
30740-5 |
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XD14 |
A BRD inhibitor; binds to BRD2, -3, and 4 (Kds = 170, 380, and 160 nM); in… |
50 mg |
30740-50 |
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XE 991 (hydrochloride) |
A blocker of KCNQ channels that potently inhibits KCNQ1 and 2 homomeric ch… |
10 mg |
14582-10 |
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XE 991 (hydrochloride) |
A blocker of KCNQ channels that potently inhibits KCNQ1 and 2 homomeric ch… |
5 mg |
14582-5 |
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XE 991 (hydrochloride) |
A blocker of KCNQ channels that potently inhibits KCNQ1 and 2 homomeric ch… |
50 mg |
14582-50 |
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XEN445 |
A selective endothelial lipase inhibitor (IC50 = 237 nM); an oral dose of… |
1 mg |
19144-1 |
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XEN445 |
A selective endothelial lipase inhibitor (IC50 = 237 nM); an oral dose of… |
10 mg |
19144-10 |
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XEN445 |
A selective endothelial lipase inhibitor (IC50 = 237 nM); an oral dose of… |
5 mg |
19144-5 |
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Xenopsin |
A neurotensin-like octapeptide; inhibits neurotensin binding to rat brain… |
1 mg |
29968-1 |
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Xenopsin |
A neurotensin-like octapeptide; inhibits neurotensin binding to rat brain… |
10 mg |
29968-10 |
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Xenopsin |
A neurotensin-like octapeptide; inhibits neurotensin binding to rat brain… |
5 mg |
29968-5 |
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Xestospongin C |
An inositol-1,4,5-trisphosphate receptor antagonist; completely blocks the… |
10 µg |
64950-10 |
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Xestospongin C |
An inositol-1,4,5-trisphosphate receptor antagonist; completely blocks the… |
100 µg |
64950-100 |
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Xestospongin C |
An inositol-1,4,5-trisphosphate receptor antagonist; completely blocks the… |
250 µg |
64950-250 |
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Xestospongin C |
An inositol-1,4,5-trisphosphate receptor antagonist; completely blocks the… |
50 µg |
64950-50 |
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X-Gal |
A chromogenic substrate for β-galactosidase; upon cleavage, a blue pi… |
1 g |
16495-1 |
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X-Gal |
A chromogenic substrate for β-galactosidase; upon cleavage, a blue pi… |
5 g |
16495-5 |
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X-Gal |
A chromogenic substrate for β-galactosidase; upon cleavage, a blue pi… |
500 mg |
16495-500 |
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XIE62-1004 |
An inducer of autophagy; increases the number of p62 aggregates, as well a… |
1 mg |
40446-1 |
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XIE62-1004 |
An inducer of autophagy; increases the number of p62 aggregates, as well a… |
10 mg |
40446-10 |
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XIE62-1004 |
An inducer of autophagy; increases the number of p62 aggregates, as well a… |
25 mg |
40446-25 |
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XIE62-1004 |
An inducer of autophagy; increases the number of p62 aggregates, as well a… |
5 mg |
40446-5 |
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Ximelagatran |
An ester prodrug of melagatran, a potent, direct, and reversible thrombin… |
1 mg |
16862-1 |
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Ximelagatran |
An ester prodrug of melagatran, a potent, direct, and reversible thrombin… |
10 mg |
16862-10 |
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Ximelagatran |
An ester prodrug of melagatran, a potent, direct, and reversible thrombin… |
5 mg |
16862-5 |
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XL019 |
A potent, bioavailable JAK inhibitor with preference for JAK2 (IC50 = 2 nM… |
1 mg |
16298-1 |
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XL019 |
A potent, bioavailable JAK inhibitor with preference for JAK2 (IC50 = 2 nM… |
10 mg |
16298-10 |
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XL019 |
A potent, bioavailable JAK inhibitor with preference for JAK2 (IC50 = 2 nM… |
25 mg |
16298-25 |
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XL019 |
A potent, bioavailable JAK inhibitor with preference for JAK2 (IC50 = 2 nM… |
5 mg |
16298-5 |
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XL092 |
A multi-kinase inhibitor; selectively inhibits MET, VEGFR2, Axl, and Mer (… |
10 mg |
37749-10 |
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XL092 |
A multi-kinase inhibitor; selectively inhibits MET, VEGFR2, Axl, and Mer (… |
25 mg |
37749-25 |
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XL092 |
A multi-kinase inhibitor; selectively inhibits MET, VEGFR2, Axl, and Mer (… |
5 mg |
37749-5 |
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XL147 |
A class I PI3K inhibitor (IC50s = 0.039, 0.036, 0.023, and 0.383 µM… |
10 mg |
18011-10 |
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XL147 |
A class I PI3K inhibitor (IC50s = 0.039, 0.036, 0.023, and 0.383 µM… |
25 mg |
18011-25 |
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XL147 |
A class I PI3K inhibitor (IC50s = 0.039, 0.036, 0.023, and 0.383 µM… |
5 mg |
18011-5 |
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XL184 |
A VEGFR2 inhibitor (IC50 = 0.035 nM); selective for VEGFR2 over Ron, EGFR,… |
1 mg |
18464-1 |
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XL184 |
A VEGFR2 inhibitor (IC50 = 0.035 nM); selective for VEGFR2 over Ron, EGFR,… |
10 mg |
18464-10 |
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XL184 |
A VEGFR2 inhibitor (IC50 = 0.035 nM); selective for VEGFR2 over Ron, EGFR,… |
5 mg |
18464-5 |
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XL184 |
A VEGFR2 inhibitor (IC50 = 0.035 nM); selective for VEGFR2 over Ron, EGFR,… |
50 mg |
18464-50 |
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