Cl-amidine hydrochloride is an orally active peptidylarginine deminase (PAD) inhibitor, with IC50 values of 0.8 µM, 6.2 µM and 5.9 µM for PAD1, PAD3, and PAD4, respectively. Cl-amidine hydrochloride induces apoptosis in cancer cells. Cl-amidine hydrochloride induces microRNA (miR)-16 (miRNA-16, microRNA-16) expression and causes cell cycle arrest. Cl-Amidine hydrochloride prevents histone 3 citrullination and neutrophil extracellular trap formation, and improves survival in a murine sepsis model[1][2][3][4][5].
Molekulargewicht:
347.25
Reinheit:
99.82
CAS Nummer:
[1373232-26-8]
Formel:
C14H20Cl2N4O2
Target-Kategorie:
Apoptosis,MicroRNA,Protein Arginine Deiminase
Anwendungsbeschreibung:
MCE Product type: Reference compound
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