3.4.24.59	1,10-phenanthroline	total inhibition at 10 mM	62	
3.4.24.59	amastatin	-	625	
3.4.24.59	bestatin	significant inhibition	225	
3.4.24.59	captopril	-	469	
3.4.24.59	Co2+	1 mM	23	
3.4.24.59	Co2+	specific strong inhibition	23	
3.4.24.59	DTT	inhibits enzymatic activity above to 0.1 mM	177	
3.4.24.59	EDTA	-	21	
3.4.24.59	EDTA	90% inhibitiond by EDTA (10 mM)	21	
3.4.24.59	Fe2+	1 mM	25	
3.4.24.59	iodoacetamide	-	67	
3.4.24.59	iodoacetic acid	-	213	
3.4.24.59	JA-2	-	11665	
3.4.24.59	leupeptin	-	217	
3.4.24.59	additional information	no inhibition by peptides lacking the amino-terminal hydrophobic residue, while substitution of such a residue by a polar amino acid causes a 10fold reduction in the efficiency of MIP inhibition	2	
3.4.24.59	additional information	no inhibition by NaCl or KCl at concentrations up to 200 mM	2	
3.4.24.59	additional information	not inhibited by thiorphan, captopril, and JA-2	2	
3.4.24.59	N-ethylmaleimide	-	49	
3.4.24.59	NEM	-	89	
3.4.24.59	p-hydroxymercuribenzoate	-	98	
3.4.24.59	pepstatin	-	396	
3.4.24.59	Synthetic peptides	corresponding to the intermediate octapeptides of human ornithine transcarbamoylase and of Neurospora cytochrome c reductase Fe/S subunit	8292	
3.4.24.59	Synthetic peptides	-	8292	
3.4.24.59	thiol-blocking agent	-	132614	
3.4.24.59	Thiol-blocking reagents	-	20934	
3.4.24.59	thiorphan	-	1128	
3.4.24.59	Zn2+	1 mM	14