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Cat. No. Product Name Information
PC-22222

Leflunomide

DHODH inhibitor

Leflunomide is a potent dihydroorotate dehydrogenase (DHODH) and pyrimidine synthesis inhibitor with IC50 of 208.5 nM in cell-free human DHODH enzyme inhibition assays.
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-22206

UNC-CA2-103

TLK2 inhibitor

UNC-CA2-103 is a potent, selective tousled like kinase 2 (TLK2) inhibitor with enzyme IC50 of 18 nM, exhibit excellent selectivity over TLK1 (16% inhibition at 0.5 μM).
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-22176

SMS121

CD36 inhibitor

SMS121 (SMS-121) is a drug-like small molecule inhibitor of the very long/long chain fatty acid transporter CD36 (FAT, scavenger receptor class B member 3/SCARB3) with binding Kd of 5.57 uM.
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.

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