Ingredients directory

An acyl-CoA that results from the formal condensation of the thiol group of coenzyme A with the carboxy group of ( E )-2-benzylidenesuccinic acid.

Pentaanion of ( E )-2-benzylidenesuccinyl-CoA.

A 2-dodecene that is dodecane which has been dehydrogenated to introduce a trans double bond between positions 2 and 3.

A 2-ethyl-2-hexenal in which the double bond adopts a trans -configuration.

A member of the class of cinnamic acids that is trans -cinnamic acid carrying a methoxy substituent at position 2 on the benzene ring.

A 2-methylbutanal oxime in which the oxime double bond has E geometry.

An alkyl diphosphate where the alkyl group is specified as ( E )-2-methylgeranyl.

An organophosphate oxoanion resulting from deprotonation of the three diphosphate OH groups of ( E )-2-methylgeranyl diphosphate.

An unsaturated fatty acyl-CoA that results from the formal condensation of the thiol group of coenzyme A with the carboxy group of ( E )-2-methylpentadec-2-enoic acid.

A monounsaturated fatty acyl-CoA(4−) obtained by deprotonation of the phosphate and diphosphate OH groups of ( E )-2-methylpentadec-2-enoyl-CoA; major species at pH 7.3.

A 2-methylpropanal oxime in which the oxime double bond has E geometry.

A 2-octene in which the double bond adopts a trans -configuration.

A 2-penten-1-ol in which the double bond has ( E )-configuration. It is a volatile compound found in cooked mussels, olive oil, fermented cucumber brine and cashew apple juice.

A 2-pentenal in which the double bond has ( E )-configuration. It is found in cigarette smoke, virgin olive oil, and milk.

A 2-undecenal in which the C=C bond has E configuration.

The trianion of phytyl diphosphate.

A butan-4-olide that is dihydrofuran-2(3 H )-one substituted by a 3,4-dihydroxybenzylidene group at position 3 and a 3,4-dihydroxyphenyl group at position 5. It has been isolated from the roots of Scorzonera judaica .

An α,β-unsaturated monocarboxylic acid that is acrylic acid in which one of the hydrogens at position 3 is replaced by an indol-2-yl group.

A monocarboxylic acid anion that is the conjugate base of 3-indoleacrylic acid, obtained by deprotonation of the carboxy group; major species at pH 7.3.

An α,β-unsaturated monocarboxylic acid that is acrylic acid in which one of the hydrogens at position 3 is replaced by an indol-3-yl group.

A member of the class of (trifluoromethyl)benzenes consisting of trans -cinnamic acid having a trifluoromethyl substituent at the meta -position.