1. The overall reaction of catechol 1, 2-dioxygenase . 2. 1-Methyltryptophan inhibits indoleamine dioxygenase , but is also a very slow substrate. 3. The most prominent class of inhibitor of NO dioxygenase to date is imidazole antibiotics. 4. It is a synthetic 4-hydroxyphenylpyruvate dioxygenase . 5. Subsequent oxidation is followed by a proposed dioxygenase mechanism that leads to epoxide formation. 6. Examples include the non-heme dioxygenase enzymes and JmjC-family histone demethylases. 7. Structure based development of phenylimidazole-derived inhibitors of indoleamine 2, 3-dioxygenase . 8. This enzyme is also called "'4-hydroxyphenylpyruvate dioxygenase II " '. 9. This enzyme is also called "'linoleate dioxygenase , manganese lipoxygenase " '. 10. The latter reaction is a remnant activity of the more ancient nitric oxide dioxygenase function of globins.
