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Cat. No. Product Name Information
PC-22221

HOSU-53 sodium

DHODH inhibitor

HOSU-53 sodium is selective and potent dihydroorotate dehydrogenase (DHODH) inhibitor with IC50 of 0.95 nM in cell-free human DHODH enzyme inhibition assays.
PC-22220

HOSU-53

DHODH inhibitor

HOSU-53 is selective and potent dihydroorotate dehydrogenase (DHODH) inhibitor with IC50 of 0.95 nM in cell-free human DHODH enzyme inhibition assays.
PC-22201

NUDT5/NUDT14 inhibitor 9

NUDT5/NUDT14 inhibitor

NUDT5/NUDT14 inhibitor 9 is a potent dual cell-active NUDT5/NUDT14 inhibitor with SPR KD of 400 nM for purified human NUDT14 protein.
PC-22199

BAY R3401

Glycogen phosphorylase inhibitor

BAY R3401 is a potent, competive glycogen phosphorylase inhibitor, inhibits muscle glycogen phosphorylase a and b.
PC-22198

Bay W1807

Glycogen phosphorylase inhibitor

BAY W1807 is a potent, competive glycogen phosphorylase inhibitor with Ki of 1.6 nM for rabbit muscle glycogen phosphorylase b (GPb), inhibits muscle glycogen phosphorylase a and b.
PC-22184

Tacrolimus

FKBP ligand

Tacrolimus (FK506) is a macrocyclic lactone that binds to FK506 binding protein (FKBP) to form a complex, inhibits calcineurin phosphatase, which inhibits T-lymphocyte signal transduction and IL-2 transcription, shows immunosuppressive properties.
PC-22182

RSMI-29

Ricin inhibitor

RSMI-29 is a small molecule inhibitor of ricin toxin, specifically targeting ricin toxin A chain (RTA) with binding KD of 0.9 uM, inhibits cytotoxicity of RTA/ricin.
PC-22178

Trolox

Antioxidant agent

Trolox is a water-soluble vitamin E analogue and antioxidant agent, scavenges peroxyl radicals better than vitamin E in sodium dodecyl sulfate micelles and in liposomes.
PC-22173

Compound 797780-71-3

DJ-1/PARK7 inhibitor

Compound 797780-71-3 is a small molevcule, covalent inhibitor of DJ-1 (PARK7), effectively inhibits the proliferation of ACHN cells with IC50 of 12.18 uM, inhibits the Wnt signaling pathway.
PC-22172

UCP0054278

DJ-1/PARK7 inhibitor

DJ-1 inhibitor comp-23 is a small molecule binding to DJ-1 (PARK7) with binding Kd of 1.33 uM, inhibits oxidative stress-induced cell death of human dopaminergic neuroblastoma cell line SH-SY5Y cells at 1 uM.
PC-22171

DJ-1 inhibitor comp-23

DJ-1/PARK7 inhibitor

DJ-1 inhibitor comp-23 is a small molecule binding to DJ-1 (PARK7) with binding constant (Kd) of 0.1 uM, exerts a neuroprotective effect by reducing ROS-mediated neuronal injury.
PC-22163

MO-I-1151

ASPH inhibitor

MO-I-1151 is a second-generation small molecule inhibitor of aspartate β-hydroxylase (ASPH), inhibits cholangiocarcinoma (CCA) cell proliferation and migration.

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