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Results 1 - 10 of 583

EC Number	Substrates	Commentary Substrates	Organism	Products	Commentary (Products)	Reversibility
1.11.2.1	(1E)-prop-1-en-1-ylbenzene + H2O2	-	Cyclocybe aegerita	2-methyl-3-phenyloxirane + H2O	71% conversion, 7% enantiomeric excess	?
1.11.2.1	(1Z)-prop-1-en-1-ylbenzene + H2O2	-	Cyclocybe aegerita	2-methyl-3-phenyloxirane + H2O	96% conversion, 29% enantiomeric excess	?
1.11.2.1	(prop-1-en-2-yl)benzene + H2O2	-	Thermothelomyces thermophilus	2-methyl-2-phenyloxirane + H2O	-	?
1.11.2.1	(R)-(+)-limonene + H2O2	-	Cyclocybe aegerita	? + H2O	76% epoxide products	?
1.11.2.1	(R)-2-phenoxypropionic acid + H2O2	-	Coprinellus radians	(R)-2-(4-hydroxyphenoxy)propionic acid + H2O	-	?
1.11.2.1	(R)-2-phenoxypropionic acid + H2O2	-	Cyclocybe aegerita	(R)-2-(4-hydroxyphenoxy)propionic acid + H2O	-	?
1.11.2.1	(R)-2-phenoxypropionic acid + H2O2	-	Marasmius rotula	(R)-2-(4-hydroxyphenoxy)propionic acid + H2O	-	?
1.11.2.1	(S)-(-)-limonene + H2O2	-	Cyclocybe aegerita	? + H2O	85% epoxide products	?
1.11.2.1	1,2,3,4-tetrahydronaphthalene + H2O2	-	Cyclocybe aegerita	(1R)-1,2,3,4-tetrahydronaphthalen-1-ol	85% conversion, 99% enantiomeric excess	?
1.11.2.1	1,2,3,4-tetrahydronaphthalene + H2O2	reaction is performed by mutant enzyme L60F (74% ee)	Thermothelomyces thermophilus	(1R)-1,2,3,4-tetrahydronaphthalen-1-ol + H2O	-	?

Results 1 - 10 of 583

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Release 2023.1 (January 2023)