VU6036720 (hydrochloride) |
An inhibitor of heteromeric Kir4.1 / 5.1 channels (IC50 = 0.24 µM);… |
1 mg |
40286-1 |
More Info
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VU6036720 (hydrochloride) |
An inhibitor of heteromeric Kir4.1 / 5.1 channels (IC50 = 0.24 µM);… |
10 mg |
40286-10 |
More Info
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VU6036720 (hydrochloride) |
An inhibitor of heteromeric Kir4.1 / 5.1 channels (IC50 = 0.24 µM);… |
5 mg |
40286-5 |
More Info
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Vulpinic Acid |
A lichen metabolite with diverse biological activities; active against var… |
10 mg |
21685-10 |
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Vulpinic Acid |
A lichen metabolite with diverse biological activities; active against var… |
100 mg |
21685-100 |
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Vulpinic Acid |
A lichen metabolite with diverse biological activities; active against var… |
25 mg |
21685-25 |
More Info
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Vulpinic Acid |
A lichen metabolite with diverse biological activities; active against var… |
50 mg |
21685-50 |
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VU0155041 (sodium salt) |
A selective positive allosteric modulator of mGluR4 (EC50 = 2.5 µM i… |
10 mg |
21775-10 |
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VU0155041 (sodium salt) |
A selective positive allosteric modulator of mGluR4 (EC50 = 2.5 µM i… |
5 mg |
21775-5 |
More Info
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VU0155041 (sodium salt) |
A selective positive allosteric modulator of mGluR4 (EC50 = 2.5 µM i… |
50 mg |
21775-50 |
More Info
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VU0364572 (trifluoroacetate salt) |
A potent and selective agonist of M1 receptors (EC50 = 0.2 mM compared to… |
1 mg |
20466-1 |
More Info
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VU0364572 (trifluoroacetate salt) |
A potent and selective agonist of M1 receptors (EC50 = 0.2 mM compared to… |
10 mg |
20466-10 |
More Info
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VU0364572 (trifluoroacetate salt) |
A potent and selective agonist of M1 receptors (EC50 = 0.2 mM compared to… |
25 mg |
20466-25 |
More Info
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VU0364572 (trifluoroacetate salt) |
A potent and selective agonist of M1 receptors (EC50 = 0.2 mM compared to… |
5 mg |
20466-5 |
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VV116 |
An antiviral agent and a derivative of remdesivir; inhibits viral replicat… |
1 mg |
37745-1 |
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VV116 |
An antiviral agent and a derivative of remdesivir; inhibits viral replicat… |
10 mg |
37745-10 |
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VV116 |
An antiviral agent and a derivative of remdesivir; inhibits viral replicat… |
25 mg |
37745-25 |
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VV116 |
An antiviral agent and a derivative of remdesivir; inhibits viral replicat… |
5 mg |
37745-5 |
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VX-509 |
A selective JAK3 inhibitor (Ki = 2.5 nM; IC50 = 50-170 nM); reduces proinf… |
1 mg |
19513-1 |
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VX-509 |
A selective JAK3 inhibitor (Ki = 2.5 nM; IC50 = 50-170 nM); reduces proinf… |
10 mg |
19513-10 |
More Info
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VX-509 |
A selective JAK3 inhibitor (Ki = 2.5 nM; IC50 = 50-170 nM); reduces proinf… |
25 mg |
19513-25 |
More Info
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VX-509 |
A selective JAK3 inhibitor (Ki = 2.5 nM; IC50 = 50-170 nM); reduces proinf… |
5 mg |
19513-5 |
More Info
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VX-661 |
An investigational compound that promotes the maturation of Delta F508 mut… |
10 mg |
21480-10 |
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VX-661 |
An investigational compound that promotes the maturation of Delta F508 mut… |
25 mg |
21480-25 |
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VX-661 |
An investigational compound that promotes the maturation of Delta F508 mut… |
5 mg |
21480-5 |
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VX-661 |
An investigational compound that promotes the maturation of Delta F508 mut… |
50 mg |
21480-50 |
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VX-702 |
A third generation inhibitor of p38 MAP kinases, binding to both p38&alpha… |
10 mg |
13108-10 |
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VX-702 |
A third generation inhibitor of p38 MAP kinases, binding to both p38&alpha… |
25 mg |
13108-25 |
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VX-702 |
A third generation inhibitor of p38 MAP kinases, binding to both p38&alpha… |
5 mg |
13108-5 |
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VX-745 |
A p38α MAPK inhibitor (IC50 = 9 nM); selective for p38α over p… |
1 mg |
18075-1 |
More Info
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VX-745 |
A p38α MAPK inhibitor (IC50 = 9 nM); selective for p38α over p… |
10 mg |
18075-10 |
More Info
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VX-745 |
A p38α MAPK inhibitor (IC50 = 9 nM); selective for p38α over p… |
5 mg |
18075-5 |
More Info
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VX-745 |
A p38α MAPK inhibitor (IC50 = 9 nM); selective for p38α over p… |
50 mg |
18075-50 |
More Info
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VX-765 |
A prodrug form of VRT-043198; inhibits LPS-induced increases in serum IL-1… |
10 mg |
28825-10 |
More Info
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VX-765 |
A prodrug form of VRT-043198; inhibits LPS-induced increases in serum IL-1… |
25 mg |
28825-25 |
More Info
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VX-765 |
A prodrug form of VRT-043198; inhibits LPS-induced increases in serum IL-1… |
5 mg |
28825-5 |
More Info
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VX-765 |
A prodrug form of VRT-043198; inhibits LPS-induced increases in serum IL-1… |
50 mg |
28825-50 |
More Info
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VX-809 |
A F508del-CFTR corrector; enhances F508del-CFTR protein maturation and res… |
1 mg |
22196-1 |
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VX-809 |
A F508del-CFTR corrector; enhances F508del-CFTR protein maturation and res… |
10 mg |
22196-10 |
More Info
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VX-809 |
A F508del-CFTR corrector; enhances F508del-CFTR protein maturation and res… |
25 mg |
22196-25 |
More Info
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VX-809 |
A F508del-CFTR corrector; enhances F508del-CFTR protein maturation and res… |
5 mg |
22196-5 |
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W123 |
An analog of FTY720 that is a competitive antagonist of S1P1; has a Ki val… |
1 mg |
10010992-1 |
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W123 |
An analog of FTY720 that is a competitive antagonist of S1P1; has a Ki val… |
10 mg |
10010992-10 |
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W123 |
An analog of FTY720 that is a competitive antagonist of S1P1; has a Ki val… |
5 mg |
10010992-5 |
More Info
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W-54011 |
A selective C5aR antagonist (Ki = 2.2 nM); inhibitor of C5a-mediated Ca2+… |
1 mg |
21231-1 |
More Info
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W-54011 |
A selective C5aR antagonist (Ki = 2.2 nM); inhibitor of C5a-mediated Ca2+… |
10 mg |
21231-10 |
More Info
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W-54011 |
A selective C5aR antagonist (Ki = 2.2 nM); inhibitor of C5a-mediated Ca2+… |
25 mg |
21231-25 |
More Info
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W-54011 |
A selective C5aR antagonist (Ki = 2.2 nM); inhibitor of C5a-mediated Ca2+… |
5 mg |
21231-5 |
More Info
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Walrycin B |
An antibiotic that has activity against Gram-positive bacteria via inhibit… |
1 mg |
21566-1 |
More Info
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Walrycin B |
An antibiotic that has activity against Gram-positive bacteria via inhibit… |
10 mg |
21566-10 |
More Info
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Walrycin B |
An antibiotic that has activity against Gram-positive bacteria via inhibit… |
25 mg |
21566-25 |
More Info
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Walrycin B |
An antibiotic that has activity against Gram-positive bacteria via inhibit… |
5 mg |
21566-5 |
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(-)-Warfarin |
An anticoagulant; interferes with interconversion of vitamin K and vitamin… |
1 mg |
13531-1 |
More Info
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(-)-Warfarin |
An anticoagulant; interferes with interconversion of vitamin K and vitamin… |
10 mg |
13531-10 |
More Info
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(-)-Warfarin |
An anticoagulant; interferes with interconversion of vitamin K and vitamin… |
25 mg |
13531-25 |
More Info
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(-)-Warfarin |
An anticoagulant; interferes with interconversion of vitamin K and vitamin… |
5 mg |
13531-5 |
More Info
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(+)-Warfarin |
An anticoagulant; interferes with interconversion of vitamin K and vitamin… |
1 mg |
13526-1 |
More Info
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(+)-Warfarin |
An anticoagulant; interferes with interconversion of vitamin K and vitamin… |
10 mg |
13526-10 |
More Info
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(+)-Warfarin |
An anticoagulant; interferes with interconversion of vitamin K and vitamin… |
25 mg |
13526-25 |
More Info
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(+)-Warfarin |
An anticoagulant; interferes with interconversion of vitamin K and vitamin… |
5 mg |
13526-5 |
More Info
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WaTx (36-68) (scorpion) (trifluoroacetate salt) |
A cell-penetrating peptide and TRPA1 activator; selectively induces curren… |
1 mg |
37495-1 |
More Info
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WaTx (36-68) (scorpion) (trifluoroacetate salt) |
A cell-penetrating peptide and TRPA1 activator; selectively induces curren… |
10 mg |
37495-10 |
More Info
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WaTx (36-68) (scorpion) (trifluoroacetate salt) |
A cell-penetrating peptide and TRPA1 activator; selectively induces curren… |
5 mg |
37495-5 |
More Info
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WAY-161503 |
A full agonist of 5-HT2C receptors (Ki = 3.3 nM) that is ~6-fold less pote… |
1 mg |
17269-1 |
More Info
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WAY-161503 |
A full agonist of 5-HT2C receptors (Ki = 3.3 nM) that is ~6-fold less pote… |
10 mg |
17269-10 |
More Info
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WAY-161503 |
A full agonist of 5-HT2C receptors (Ki = 3.3 nM) that is ~6-fold less pote… |
5 mg |
17269-5 |
More Info
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WAY-161503 |
A full agonist of 5-HT2C receptors (Ki = 3.3 nM) that is ~6-fold less pote… |
50 mg |
17269-50 |
More Info
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WAY-169916 |
A pathway-selective estrogen receptor ligand; binds to human ERα and… |
10 mg |
35842-10 |
More Info
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WAY-169916 |
A pathway-selective estrogen receptor ligand; binds to human ERα and… |
25 mg |
35842-25 |
More Info
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WAY-169916 |
A pathway-selective estrogen receptor ligand; binds to human ERα and… |
5 mg |
35842-5 |
More Info
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WAY-169916 |
A pathway-selective estrogen receptor ligand; binds to human ERα and… |
50 mg |
35842-50 |
More Info
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WAY-200070 |
A potent and selective ERβ agonist (IC50s = 2 and 187 nM for human fu… |
10 mg |
23323-10 |
More Info
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WAY-200070 |
A potent and selective ERβ agonist (IC50s = 2 and 187 nM for human fu… |
25 mg |
23323-25 |
More Info
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WAY-200070 |
A potent and selective ERβ agonist (IC50s = 2 and 187 nM for human fu… |
5 mg |
23323-5 |
More Info
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WAY-200070 |
A potent and selective ERβ agonist (IC50s = 2 and 187 nM for human fu… |
50 mg |
23323-50 |
More Info
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