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Cat. No. Product Name Information
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.
PC-45514

BoNT-IN-1

BoNT inhibitor

BoNT-IN-1 is a potent inhibitor of Botulinum Neurotoxin A (BoNT) Light Chain with IC50 of 0.9 uM.
PC-45318

Amicarbazone

Photosystem II Inhibitor

Amicarbazone (BAY-314666) is a potent inhibitor of photosynthetic electron transport via binding to the Qb domain of photosystem II (PSII).
PC-45038

ISO-1

MIF inhibitor

ISO-1 is a potent inhibitor of Migration inhibitory factor (MIF) tautomerase activity with IC50 of 7 uM.
PC-42227

ML390

DHODH inhibitor

ML390 is a potent DHODH inhibitor that causes myeloid differentiation in murine (ER-HoxA9) and human (U937 and THP1) AML models (ED50=2 uM).
PC-42253

HTHQ

Anti-oxidative agent

HTHQ is a potent anti-oxidative agent that effectively scavenges t-butyl peroxyl radicals with IC50 of 0.31 mM (ROS inhibition).
PC-44643

HJC0350

EPAC2 antagonist

HJC0350 is a potent and specific EPAC2 antagonist with IC50 of 0.3 uM for competing with 8-NBD-cAMP in binding EPAC2, about 133-fold more potent than cAMP.
PC-42382

NIH-12848

PI5P4Kγ inhibitor

NIH-12848 is a potent and selective PI5P4Kγ inhibitor with IC50 of 1 uM, shows no significant inhibitory activity for PI5P4Kα and PI5P4Kβ (>100 uM).

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