PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
9048894-7	1997	The inhibition of glucokinase enzyme activity was reversed by dithiothreitol with an EC50 value of 9 microM for alloxan and of 50 microM for ninhydrin.	Ninhydrin	141-150	glucokinase	Homo sapiens	18-29	
3419426-8	1988	Like alloxan, other dithiol reagents such as ninhydrin, N-ethylmaleimide, and maleimide inhibited glucokinase.	Ninhydrin	45-54	glucokinase	Homo sapiens	98-109	
3207996-0	1988	Structural requirements of alloxan and ninhydrin for glucokinase inhibition and of glucose for protection against inhibition.	Ninhydrin	39-48	glucokinase	Homo sapiens	53-64	
3207996-8	1988	Ninhydrin also inhibited glucokinase with a half-maximal inhibitory concentration of 5 microM.	Ninhydrin	0-9	glucokinase	Homo sapiens	25-36	
3207996-16	1988	Thus the mechanism of glucokinase inhibition by alloxan and other inhibitors, such as uramil and ninhydrin, is an oxidation of functionally essential SH groups of the enzyme, where the most reactive keto group of the inhibitor acts as the hydrogen acceptor.	Ninhydrin	97-106	glucokinase	Homo sapiens	22-33