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Cat. No. Product Name Information
PC-62216

GSK199

PAD4 inhibitor

GSK199 is a potent, highly selective and reversible protein arginine deiminase PAD4 inhibitor with IC50 of 250 nM in FP binding assay (0.2 mM Ca), 200 nM in PAD4 NH3 release inhibition assay.
PC-62215

GSK484 hydrochloride

PAD4 inhibitor

GSK484 hydrochloride is a potent, highly selective and reversible protein arginine deiminase PAD4 inhibitor with IC50 of 80 nM in FP binding assay (0.2 mM Ca), 50 nM in PAD4 NH3 release inhibition assay.
PC-62214

GSK484

PAD4 inhibitor

GSK484 is a potent, highly selective and reversible protein arginine deiminase PAD4 inhibitor with IC50 of 80 nM in FP binding assay (0.2 mM Ca), 50 nM in PAD4 NH3 release inhibition assay.
PC-61919

Streptonigrin

PAD4 inhibitor, RAD54 inhibitor

Streptonigrin (Bruneomycin, NSC 45383) is a potent, selective, and irreversible PAD4 inactivator with IC50 of 1.87 uM, also binds directly to RAD54 with Kd of 9.1 uM, inhibits ATPase and DNA branch migration activity of RAD54.
PC-23180

PF-3166

PAD2 inhibitor

PF-3166 is a potent, selective, noncovalent, cell-active peptidyl arginine deiminase 2 (PAD2) inhibitor with IC50 of 150 nM in fluorescence quenching (FQ) assay.
PC-23134

YW4-03

PAD4 inhibitor

YW4-03 is a small molecule peptidylarginine deiminase (PAD) inhibitor with IC50 of 5 uM against PAD4, exhibits cell-killing efficacy in osteosarcoma U2OS cells with IC50 of 2.5-5 uM.
PC-22866

Cl-amidine TFA

PAD inhibitor

Cl-amidine TFA is a potent, irreversible, orall active inhibitor of protein arginine deiminases (PADs) with IC50 of 0.8, 6.2, and 5.9 µM for PAD1, PAD3, and PAD4, respectively.
PC-22865

Cl-amidine hydrochloride

PAD inhibitor

Cl-amidine hydrochloride is a potent, irreversible, orall active inhibitor of protein arginine deiminases (PADs) with IC50 of 0.8, 6.2, and 5.9 µM for PAD1, PAD3, and PAD4, respectively.

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