Voglibose |
An α-glucosidase inhibitor (IC50s = 5.6, 0.11, 0.16, and 0.07 µ… |
10 mg |
14179-10 |
More Info
|
Voglibose |
An α-glucosidase inhibitor (IC50s = 5.6, 0.11, 0.16, and 0.07 µ… |
100 mg |
14179-100 |
More Info
|
Voglibose |
An α-glucosidase inhibitor (IC50s = 5.6, 0.11, 0.16, and 0.07 µ… |
50 mg |
14179-50 |
More Info
|
Voglibose |
An α-glucosidase inhibitor (IC50s = 5.6, 0.11, 0.16, and 0.07 µ… |
500 mg |
14179-500 |
More Info
|
Volinanserin |
A potent and selective antagonist of the serotonin receptor 5-HT2A (Ki = 0… |
1 mg |
15936-1 |
More Info
|
Volinanserin |
A potent and selective antagonist of the serotonin receptor 5-HT2A (Ki = 0… |
10 mg |
15936-10 |
More Info
|
Volinanserin |
A potent and selective antagonist of the serotonin receptor 5-HT2A (Ki = 0… |
5 mg |
15936-5 |
More Info
|
Vonoprazan (fumarate) |
A selective and reversible proton pump inhibitor; inhibits gastric H+/K+ A… |
1 g |
24200-1 |
More Info
|
Vonoprazan (fumarate) |
A selective and reversible proton pump inhibitor; inhibits gastric H+/K+ A… |
10 g |
24200-10 |
More Info
|
Vonoprazan (fumarate) |
A selective and reversible proton pump inhibitor; inhibits gastric H+/K+ A… |
5 g |
24200-5 |
More Info
|
Vonoprazan (fumarate) |
A selective and reversible proton pump inhibitor; inhibits gastric H+/K+ A… |
500 mg |
24200-500 |
More Info
|
VO-OHpic (hydrate) |
A specific inhibitor of PTEN (IC50 = 35 nM in vitro); increases cellular P… |
1 mg |
10009965-1 |
More Info
|
VO-OHpic (hydrate) |
A specific inhibitor of PTEN (IC50 = 35 nM in vitro); increases cellular P… |
10 mg |
10009965-10 |
More Info
|
VO-OHpic (hydrate) |
A specific inhibitor of PTEN (IC50 = 35 nM in vitro); increases cellular P… |
25 mg |
10009965-25 |
More Info
|
VO-OHpic (hydrate) |
A specific inhibitor of PTEN (IC50 = 35 nM in vitro); increases cellular P… |
5 mg |
10009965-5 |
More Info
|
Vorapaxar |
A PAR1 antagonist (Ki = 8.1 nM); selective for PAR1 over other PARs, as we… |
1 mg |
23119-1 |
More Info
|
Vorapaxar |
A PAR1 antagonist (Ki = 8.1 nM); selective for PAR1 over other PARs, as we… |
5 mg |
23119-5 |
More Info
|
Vorasidenib |
An inhibitor of mutant IDH (IC50s = 31.9 and 31.7 nM for IDH1R132H and IDH… |
1 mg |
28462-1 |
More Info
|
Vorasidenib |
An inhibitor of mutant IDH (IC50s = 31.9 and 31.7 nM for IDH1R132H and IDH… |
10 mg |
28462-10 |
More Info
|
Vorasidenib |
An inhibitor of mutant IDH (IC50s = 31.9 and 31.7 nM for IDH1R132H and IDH… |
5 mg |
28462-5 |
More Info
|
Voriconazole |
A triazole antifungal agent; active against a variety of yeast and fungi (… |
10 mg |
15633-10 |
More Info
|
Voriconazole |
A triazole antifungal agent; active against a variety of yeast and fungi (… |
25 mg |
15633-25 |
More Info
|
Voriconazole |
A triazole antifungal agent; active against a variety of yeast and fungi (… |
50 mg |
15633-50 |
More Info
|
Voriconazole-d3 |
An internal standard for the quantification of voriconazole by GC- or LC-MS |
1 mg |
17803-1 |
More Info
|
Voriconazole-d3 |
An internal standard for the quantification of voriconazole by GC- or LC-MS |
500 µg |
17803-500 |
More Info
|
Voriconazole-d3 N-oxide |
An internal standard for the quantification of voriconazole N-oxide by GC-… |
1 mg |
40332-1 |
More Info
|
Voriconazole-d3 N-oxide |
An internal standard for the quantification of voriconazole N-oxide by GC-… |
100 µg |
40332-100 |
More Info
|
Voriconazole-d3 N-oxide |
An internal standard for the quantification of voriconazole N-oxide by GC-… |
250 µg |
40332-250 |
More Info
|
Voriconazole N-oxide |
A major metabolite of voriconazole; formed via oxidation of voriconazole b… |
1 mg |
28047-1 |
More Info
|
Voriconazole N-oxide |
A major metabolite of voriconazole; formed via oxidation of voriconazole b… |
5 mg |
28047-5 |
More Info
|
Vortioxetine |
A multimodal serotonergic agent; inhibits 5-HT reuptake (Ki = 1.6 nM); bin… |
10 mg |
30183-10 |
More Info
|
Vortioxetine |
A multimodal serotonergic agent; inhibits 5-HT reuptake (Ki = 1.6 nM); bin… |
25 mg |
30183-25 |
More Info
|
Vortioxetine |
A multimodal serotonergic agent; inhibits 5-HT reuptake (Ki = 1.6 nM); bin… |
5 mg |
30183-5 |
More Info
|
Vortioxetine |
A multimodal serotonergic agent; inhibits 5-HT reuptake (Ki = 1.6 nM); bin… |
50 mg |
30183-50 |
More Info
|
Vortioxetine-d8 |
An internal standard for the quantification of vortioxetine by GC- or LC-MS |
1 mg |
28163-1 |
More Info
|
Vortioxetine (hydrobromide) |
A multimodal serotonergic agent; inhibits 5-HT reuptake (Ki = 1.6 nM); bin… |
1 mg |
23694-1 |
More Info
|
Vortioxetine (hydrobromide) |
A multimodal serotonergic agent; inhibits 5-HT reuptake (Ki = 1.6 nM); bin… |
10 mg |
23694-10 |
More Info
|
Vortioxetine (hydrobromide) |
A multimodal serotonergic agent; inhibits 5-HT reuptake (Ki = 1.6 nM); bin… |
5 mg |
23694-5 |
More Info
|
Voruciclib |
A pan-CDK inhibitor (Kis = 0.626-9.1 nM); selective for CDKs over MAK and… |
1 mg |
29085-1 |
More Info
|
Voruciclib |
A pan-CDK inhibitor (Kis = 0.626-9.1 nM); selective for CDKs over MAK and… |
10 mg |
29085-10 |
More Info
|
Voruciclib |
A pan-CDK inhibitor (Kis = 0.626-9.1 nM); selective for CDKs over MAK and… |
5 mg |
29085-5 |
More Info
|
Vosaroxin |
A topoisomerase II inhibitor; induces relaxation of supercoiled DNA (IC50… |
1 mg |
30614-1 |
More Info
|
Vosaroxin |
A topoisomerase II inhibitor; induces relaxation of supercoiled DNA (IC50… |
10 mg |
30614-10 |
More Info
|
Vosaroxin |
A topoisomerase II inhibitor; induces relaxation of supercoiled DNA (IC50… |
25 mg |
30614-25 |
More Info
|
Vosaroxin |
A topoisomerase II inhibitor; induces relaxation of supercoiled DNA (IC50… |
5 mg |
30614-5 |
More Info
|
Voxilaprevir |
A pan-genotypic HCV NS3 / 4A protease inhibitor; inhibits replication of w… |
1 mg |
33974-1 |
More Info
|
Voxilaprevir |
A pan-genotypic HCV NS3 / 4A protease inhibitor; inhibits replication of w… |
10 mg |
33974-10 |
More Info
|
Voxilaprevir |
A pan-genotypic HCV NS3 / 4A protease inhibitor; inhibits replication of w… |
5 mg |
33974-5 |
More Info
|
Voxtalisib |
A dual inhibitor of PI3K and mTORC (IC50s = 9, 110, 43, 9, 160, and 910 nM… |
10 mg |
30323-10 |
More Info
|
Voxtalisib |
A dual inhibitor of PI3K and mTORC (IC50s = 9, 110, 43, 9, 160, and 910 nM… |
25 mg |
30323-25 |
More Info
|
Voxtalisib |
A dual inhibitor of PI3K and mTORC (IC50s = 9, 110, 43, 9, 160, and 910 nM… |
5 mg |
30323-5 |
More Info
|
Voxtalisib |
A dual inhibitor of PI3K and mTORC (IC50s = 9, 110, 43, 9, 160, and 910 nM… |
50 mg |
30323-50 |
More Info
|
VP-14637 |
An RSV inhibitor that demonstrates antiviral activity with an EC50 value o… |
1 mg |
17805-1 |
More Info
|
VP-14637 |
An RSV inhibitor that demonstrates antiviral activity with an EC50 value o… |
10 mg |
17805-10 |
More Info
|
VP-14637 |
An RSV inhibitor that demonstrates antiviral activity with an EC50 value o… |
5 mg |
17805-5 |
More Info
|
VPC 23019 |
A competitive antagonist of S1P1 and S1P3 receptors (pKis = 7.86 and 5.93,… |
1 mg |
13240-1 |
More Info
|
VPC 23019 |
A competitive antagonist of S1P1 and S1P3 receptors (pKis = 7.86 and 5.93,… |
10 mg |
13240-10 |
More Info
|
VPC 23019 |
A competitive antagonist of S1P1 and S1P3 receptors (pKis = 7.86 and 5.93,… |
5 mg |
13240-5 |
More Info
|
VPC 23019 |
A competitive antagonist of S1P1 and S1P3 receptors (pKis = 7.86 and 5.93,… |
500 µg |
13240-500 |
More Info
|
VPM-p15 (trifluoroacetate salt) |
A peptide ADGRG2 agonist; induces cAMP accumulation in HEK293 cells expres… |
1 mg |
37470-1 |
More Info
|
VPM-p15 (trifluoroacetate salt) |
A peptide ADGRG2 agonist; induces cAMP accumulation in HEK293 cells expres… |
10 mg |
37470-10 |
More Info
|
VPM-p15 (trifluoroacetate salt) |
A peptide ADGRG2 agonist; induces cAMP accumulation in HEK293 cells expres… |
5 mg |
37470-5 |
More Info
|
Vps34-IN1 |
A potent and selective inhibitor of Vps34 (IC50 = 25 nM in vitro); dose-de… |
1 mg |
17392-1 |
More Info
|
Vps34-IN1 |
A potent and selective inhibitor of Vps34 (IC50 = 25 nM in vitro); dose-de… |
10 mg |
17392-10 |
More Info
|
Vps34-IN1 |
A potent and selective inhibitor of Vps34 (IC50 = 25 nM in vitro); dose-de… |
25 mg |
17392-25 |
More Info
|
Vps34-IN1 |
A potent and selective inhibitor of Vps34 (IC50 = 25 nM in vitro); dose-de… |
5 mg |
17392-5 |
More Info
|
V-PYRRO/NO |
V-PYRRO / NO is a NO donor in vivo. Following hepatic metabolism, it spont… |
10 mg |
82160-10 |
More Info
|
V-PYRRO/NO |
V-PYRRO / NO is a NO donor in vivo. Following hepatic metabolism, it spont… |
100 mg |
82160-100 |
More Info
|
V-PYRRO/NO |
V-PYRRO / NO is a NO donor in vivo. Following hepatic metabolism, it spont… |
5 mg |
82160-5 |
More Info
|
V-PYRRO/NO |
V-PYRRO / NO is a NO donor in vivo. Following hepatic metabolism, it spont… |
50 mg |
82160-50 |
More Info
|
VR23 |
A trypsin-like proteasome inhibitor (IC50 = 1 nM) that deregulates the act… |
1 mg |
19133-1 |
More Info
|
VR23 |
A trypsin-like proteasome inhibitor (IC50 = 1 nM) that deregulates the act… |
10 mg |
19133-10 |
More Info
|
VR23 |
A trypsin-like proteasome inhibitor (IC50 = 1 nM) that deregulates the act… |
25 mg |
19133-25 |
More Info
|
VR23 |
A trypsin-like proteasome inhibitor (IC50 = 1 nM) that deregulates the act… |
5 mg |
19133-5 |
More Info
|
VS-5584 |
A purine analog that inhibits mTOR (IC50 = 37 nM) and PI3K (IC50s = 16, 68… |
1 mg |
16294-1 |
More Info
|
VS-5584 |
A purine analog that inhibits mTOR (IC50 = 37 nM) and PI3K (IC50s = 16, 68… |
10 mg |
16294-10 |
More Info
|
VS-5584 |
A purine analog that inhibits mTOR (IC50 = 37 nM) and PI3K (IC50s = 16, 68… |
5 mg |
16294-5 |
More Info
|
VS-5584 analog |
A dual inhibitor of PI3Kα and mTOR (IC50s = 17 and 150 nM, respectiv… |
1 mg |
30324-1 |
More Info
|
VS-5584 analog |
A dual inhibitor of PI3Kα and mTOR (IC50s = 17 and 150 nM, respectiv… |
10 mg |
30324-10 |
More Info
|
VS-5584 analog |
A dual inhibitor of PI3Kα and mTOR (IC50s = 17 and 150 nM, respectiv… |
25 mg |
30324-25 |
More Info
|
VS-5584 analog |
A dual inhibitor of PI3Kα and mTOR (IC50s = 17 and 150 nM, respectiv… |
5 mg |
30324-5 |
More Info
|
VTP-50469 |
An inhibitor of the menin-MLL1 fusion protein interaction (Ki = 0.104 nM);… |
10 mg |
40759-10 |
More Info
|
VTP-50469 |
An inhibitor of the menin-MLL1 fusion protein interaction (Ki = 0.104 nM);… |
25 mg |
40759-25 |
More Info
|
VTP-50469 |
An inhibitor of the menin-MLL1 fusion protein interaction (Ki = 0.104 nM);… |
5 mg |
40759-5 |
More Info
|
VTP-50469 |
An inhibitor of the menin-MLL1 fusion protein interaction (Ki = 0.104 nM);… |
50 mg |
40759-50 |
More Info
|
VTP-27999 (trifluoroacetate salt) |
A renin inhibitor (IC50 = 0.47 nM for the recombinant human enzyme); selec… |
1 mg |
27689-1 |
More Info
|
VTP-27999 (trifluoroacetate salt) |
A renin inhibitor (IC50 = 0.47 nM for the recombinant human enzyme); selec… |
10 mg |
27689-10 |
More Info
|
VTP-27999 (trifluoroacetate salt) |
A renin inhibitor (IC50 = 0.47 nM for the recombinant human enzyme); selec… |
25 mg |
27689-25 |
More Info
|
VTP-27999 (trifluoroacetate salt) |
A renin inhibitor (IC50 = 0.47 nM for the recombinant human enzyme); selec… |
5 mg |
27689-5 |
More Info
|
VTX-27 |
A PKCθ inhibitor (Ki = 0.08 nM); selective for PKCθ over PKC&a… |
1 mg |
36938-1 |
More Info
|
VTX-27 |
A PKCθ inhibitor (Ki = 0.08 nM); selective for PKCθ over PKC&a… |
500 µg |
36938-500 |
More Info
|
VU0029251 |
A partial antagonist of mGluR5; inhibits calcium mobilization induced by g… |
1 mg |
21987-1 |
More Info
|
VU0029251 |
A partial antagonist of mGluR5; inhibits calcium mobilization induced by g… |
10 mg |
21987-10 |
More Info
|
VU0029251 |
A partial antagonist of mGluR5; inhibits calcium mobilization induced by g… |
25 mg |
21987-25 |
More Info
|
VU0029251 |
A partial antagonist of mGluR5; inhibits calcium mobilization induced by g… |
5 mg |
21987-5 |
More Info
|
VU0071063 |
A Kir6.2 / SUR1 activator (EC50 = 7 µM) |
1 mg |
21897-1 |
More Info
|
VU0071063 |
A Kir6.2 / SUR1 activator (EC50 = 7 µM) |
10 mg |
21897-10 |
More Info
|
VU0071063 |
A Kir6.2 / SUR1 activator (EC50 = 7 µM) |
25 mg |
21897-25 |
More Info
|
VU0071063 |
A Kir6.2 / SUR1 activator (EC50 = 7 µM) |
5 mg |
21897-5 |
More Info
|
VU0119498 |
An M1, M3, and M5 muscarinic receptor positive allosteric modulator (EC50s… |
100 mg |
36132-100 |
More Info
|