3.5.99.7	1-amino-2,2-difluorocyclopropane-1-carboxylic acid	rac-DFACC, chemical synthesis, overview. Mechanism of decomposition and inhibition of 1-aminocyclopropane-1-carboxylic acid deaminase, and Michaelis-Menten kinetics. DFACC is unstable under near-physiological conditions where it primarily decomposes via specific-base catalysis to 3-fluoro-2-oxobut-3-enoic acid. Different decomposotion mechanisms are described. Upon incubation with ACC deaminase, DFACC is a slow-dissociating inhibitor of ACC deaminase with submicromolar affinity	247567	
3.5.99.7	1-amino-2-methylenecyclopopropane-1-carboxylic acid	irreversible	114736	
3.5.99.7	1-aminocyclopropanephosphonate	-	90470	
3.5.99.7	5,5'-dithiobis(2-nitrobenzoic acid)	-	221	
3.5.99.7	aminooxyacetic acid	0.005-1 mM, enzymatic activity is progressively inhibited as the aminooxyacetic acid concentration is increased	1554	
3.5.99.7	beta-chloro-Ala	-	16065	
3.5.99.7	beta-chloro-Ala	mechanism-based inhibition	16065	
3.5.99.7	beta-fluoro-D-Ala	-	96220	
3.5.99.7	cyclohexylhydrazine	-	96308	
3.5.99.7	D-Ala	-	291	
3.5.99.7	D-Ser	slow inactivation	972	
3.5.99.7	D-Ser	-	972	
3.5.99.7	homoserine	-	5553	
3.5.99.7	KCN	-	161	
3.5.99.7	L-2-aminobutanoate	-	1471	
3.5.99.7	L-Ala	-	251	
3.5.99.7	L-Ser	competitive	262	
3.5.99.7	L-Ser	-	262	
3.5.99.7	L-serine	5 mM L-serine results in at least a 50% decrease of measurable ACD activity	95	
3.5.99.7	Monoiodoacetamide	-	30193	
3.5.99.7	NaBH4	-	616	
3.5.99.7	NEM	-	89	
3.5.99.7	NH2CONH-NH2	-	98137	
3.5.99.7	NH2OH	-	1109	
3.5.99.7	O-acetyl-D-Ser	-	45778