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Cat. No. Product Name Information
PC-45735

3PO

PFKFB3 inhibitor

PFKFB3 inhibitor 3PO is a small-molecule, competitive inhibitor of PFKFB3 isozyme with IC50 of 23 uM.
PC-45384

Amcasertib

Cancer stem cells inhibitor

Amcasertib (BBI503) is a small-molecule inhibitor that inhibits Nanog and other CSC (cancer stem cells) pathways by targeting kinases.
PC-45557

RR6

Vanin inhibitor

RR6 is a selective, reversible, and competitive Vanin inhibitor with IC50 of 0.54 uM for hVVN1 pantetheinase (vanin-1).
PC-45331

Bromethalin

Bromethalin is a rodenticide that poisons the central nervous system by uncoupling mitochondrial oxidative phosphorylation, which causes a decrease in adenosine triphosphate (ATP) synthesis.
PC-42291

Conduritol B epoxide

β-glucosidase inhibitor

Conduritol B epoxide is a potent, specific, irreversible glucocerebrosidase (acid β-glucosidase) inhibitor with Ki of 53 uM.
PC-42264

Rbin-1

Midasin inhibitor

Rbin-1 (Ribozinoindole-1) is a potent, specific and reversible inhibitor of eukaryotic ribosome biogenesis that targets the AAA+ protein Midasin (IC40=1 uM).
PC-42268

TN1

HbF inducer

TN1 is a potent, small molecule fetal hemoglobin (HbF) inducer with EC50 of 100 nM.
PC-42279

PF-1355

MPO inhibitor

PF-1355 (PF-06281355) is a potent, selective, orally active Myeloperoxidase (MPO) inhibitor with EC50 of 1.47 uM.
PC-45669

GSK2256294A

sEH inhibitor

GSK2256294A is a potent, selective soluble epoxide hydrolase (sEH, EPHX2) inhibitor with IC50 of 27/61/189 pM for recombinant human/rat/mouse sEH, respectively.
PC-45486

DZ2002

SAHH inhibitor

DZ2002 is a potent, reversible type III inhibitor of SAHH (S-adenosyl-L-homocysteine hydrolase) with Ki of 17.9 nM.
PC-45053

CH-5450

Chymase inhibitor

CH-5450 is a potent, peptide-inhibitor of human chymase with Ki of 1 nM.
PC-45604

PF-06282999

MPO inhibitor

PF-06282999 is a potent, highly selective and irreversible inhibitor of myeloperoxidase (MPO) with Kinact/KI of 116000 M-1s-1.

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