4.1.99.5	1,10-phenanthroline	0.1 mM; strong	62	
4.1.99.5	1,10-phenanthroline	strong	62	
4.1.99.5	1,10-phenanthroline	1 mM, complete inhibition, CuCl2 restores, CoCl2 and ZnCl2 partially restore activity; strong	62	
4.1.99.5	2-(2-tetradecylcyclopropyl)acetaldehyde	a cyclopropyl analogue of octadecanal in which the cyclopropyl group is positioned beta to the carbonyl group. The compound is partitioned between turnover and irreversible inhibition of the enzyme, mechanism of inactivation, overview. Formation of 1-octadecene at low level appears to be described by first-order kinetics might be involved in enzyme inhibition	194447	
4.1.99.5	8-hydroxyquinoline	strong	321	
4.1.99.5	ATP	6 mM	4	
4.1.99.5	coenzyme A	0.2 mM	534	
4.1.99.5	dithioerythritol	5 mM, complete inhibition	577	
4.1.99.5	EDTA	1 mM; strong	21	
4.1.99.5	EDTA	strong	21	
4.1.99.5	EDTA	10 mM, 58% inhibition	21	
4.1.99.5	ethyl acetate	-	2738	
4.1.99.5	metal ion chelators	strong	13460	
4.1.99.5	metal ion chelators	-	13460	
4.1.99.5	metal ion chelators	Cu2+ fully restores activity; strong	13460	
4.1.99.5	additional information	not inhibited by 1 mM imidazole	2	
4.1.99.5	additional information	not inhibited by KCN	2	
4.1.99.5	additional information	trans-3-nonyloxirane-2-carbaldehyde and trans-3-pentadecanyloxirane-2-carbaldehyde are no inhibitors of the enzyme	2	
4.1.99.5	additional information	substrate inhibition might occur with short aldehydes if a second substrate molecule is bound in the channel preventing product release	2	
4.1.99.5	NADH	0.2 mM	8	
4.1.99.5	NADH	presence causes 50% inhibition	8	
4.1.99.5	NADPH	presence causes 50% inhibition	5	
4.1.99.5	O2	-	9	
4.1.99.5	O2	complete inhibition	9