Répertoire des ingrédients

The univalent carboacyl group formed by loss of -OH from the carboxy group of (2 E )-3-[3-(trifluoromethyl)phenyl]prop-2-enoic acid.

A 3-[(5 R ,6 S )-5,6-dihydroxycyclohexa-1,3-dienyl]acrylate where the acrylic double bond has ( E )-configuration.

A 3-[(5 R ,6 S )-5,6-dihydroxycyclohexa-1,3-dienyl]acrylic acid where the acrylic double bond has ( E )-configuration.

The ( E )-isomer of 3-[(5 S ,6 R )-5,6-dihydroxycyclohexa-1,3-dienyl]acrylate.

The ( E )-isomer of 3-[(5 S ,6 R )-5,6-dihydroxycyclohexa-1,3-dienyl]acrylic acid.

Major microspecies at pH 7.3.

Major microspecies at pH 7.3.

A 3-dodecene in which the double bond adopts a trans -configuration.

A 3-methylglutaconate anion obtained by deprotonation of at least one of the carboxyl groups of ( E )-3-methylglutaconic acid.

A dicarboxylic acid comprising ( E )-glutaconic acid carrying a 3-methyl substituent.

A 3-octene in which the double bond adopts a trans -configuration.

A 3-penten-1-yne in which the double bond adopts a trans -configuration.

A nitrile that is acrylonitrile in which the hydrogen located β, trans to the cyano group is replaced by a tosyl group. It is an inhibitor of cytokine-induced IκB-α phosphorylation in cells.

A member of the class of chalcones that is trans -chalcone substituted by hydroxy groups at positions 4, 2' and 4', a methoxy group at position 6' and methyl groups at positions 3' and 5'. Isolated from the buds of Cleistocalyx operculatus , it has been shown to exhibit inhibitory effects on the viral neuraminidases from two influenza viral strains, H1N1 and H9N2.

An alkatriene consisting of 4,8-dimethylnonane having the three double bonds in the 1-, 3- and 7-positions.

Major species at pH 7.3.

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

The univalent carboacyl group formed by loss of -OH from the carboxy group of ( E )-4-(trifluoromethyl)cinnamic acid.

A 4-(trimethylammonio)but-2-enoic acid with a ( E )-configuration at the double bond.

An acyl-CoA that results from the formal condensation of the thiol group of coenzyme A with the carboxy group of ( E )-4-(trimethylammonio)but-2-enoic acid.

An acyl-CoA oxoanion obtained via deprotonation of the phosphate and diphosphate OH groups of ( E )-4-(trimethylammonio)but-2-enoyl-CoA; major species at pH 7.3.