1.14.11.26	(2S,4S,6R,7R)-1-aza-7-((5R)-5-carboxypentanamidol)-4-methyl-8-oxo-5-thiatricyclo-(4,2,0,0)octane-2-carboxylate	reversible, 0.04 mM, 90% inhibition	57516	
1.14.11.26	5,5'-dithiobis-2-nitrobenzoic acid	reactivation by dithiothreitol	5368	
1.14.11.26	5,5'-dithiobis-2-nitrobenzoic acid	1 mM, 100% inhibition of hydroxylation reaction, EC 1.14.11.26	5368	
1.14.11.26	5,5'-dithiobis-2-nitrobenzoic acid	1 mM, no residual activity	5368	
1.14.11.26	ammonium hydrogencarbonate	100-500 mM, complete inactivation	57637	
1.14.11.26	ampicillin	-	191	
1.14.11.26	bathophenanthroline	-	2722	
1.14.11.26	Ca2+	weak	15	
1.14.11.26	Co2+	inhibition in decreasing order, Zn2+, Co2+, Ni2+	23	
1.14.11.26	EDTA	-	21	
1.14.11.26	EDTA	0.6 mM, 83% inhibition of hydroxylation reaction, EC 1.14.11.26	21	
1.14.11.26	EDTA	0.5 mM, no residual activity	21	
1.14.11.26	iodoacetic acid	-	213	
1.14.11.26	iodoacetic acid	1 mM, 2% inhibition of hydroxylation reaction, EC 1.14.11.26	213	
1.14.11.26	iodoacetic acid	1 mM, 19% residual activity	213	
1.14.11.26	N-ethylmaleimide	-	49	
1.14.11.26	N-ethylmaleimide	1 mM, 97% inhibition of hydroxylation reaction, EC 1.14.11.26	49	
1.14.11.26	N-ethylmaleimide	1 mM, no residual activity	49	
1.14.11.26	Ni2+	inhibition in decreasing order, Zn2+, Co2+, Ni2+	38	
1.14.11.26	o-phenanthroline	-	239	
1.14.11.26	o-phenanthroline	0.6 mM, 100% inhibition of hydroxylation reaction, EC 1.14.11.26	239	
1.14.11.26	o-phenanthroline	0.5 mM, no residual activity	239	
1.14.11.26	p-hydroxymercuribenzoate	-	98	
1.14.11.26	p-hydroxymercuribenzoate	1 mM, 100% inhibition of hydroxylation reaction, EC 1.14.11.26	98	
1.14.11.26	p-hydroxymercuribenzoate	0.1 mM, no residual activity	98	
1.14.11.26	penicillin G	-	181	
1.14.11.26	Penicillin N	1 mM, 62% inhibition, competitive with deacetoxycephalosporin C	792	
1.14.11.26	Penicillin V	-	2755	
1.14.11.26	Zn2+	inhibition in decreasing order, Zn2+, Co2+, Ni2+	14	
1.14.11.26	Zn2+	strong	14