linoleate การใช้

• This enzyme is also called "'linoleate dioxygenase, manganese lipoxygenase " '.
• The systematic name of this enzyme class is "'linoleate : oxygen 11S-oxidoreductase " '.
• The systematic name of this enzyme class is "'linoleate : oxygen 7S, 8S-oxidoreductase " '.
• This could be cured by administration of ethyl linoleate ( the ethyl ester of linoleic acid ) with about 1 % of the energy intake.
• This enzyme belongs to the family of isomerases, specifically systematic name of this enzyme class is "'linoleate Delta12-cis-Delta11-trans-isomerase " '.
• The oil from the cultivar Carter had the highest mol percentage of linoleate ( 61.6 ), linolenate ( 5.97 % ), and palmitate ( 3.98 % ); the oil from the cultivar Baugh had the highest mol percentage of oleate ( 42.7 % ); the oil from the cultivar Ogden has the highest mol percentage of stearate ( 2.98 % ).
• Manos and Stone studied the composition of seed oils from several species of the Rhoipteleaceae and Juglandaceae and found the nut oils were generally more unsaturated from species which grow in the oleate; " J . neotropica " contained 3 % linolenate, 5 % palmitate, and 50 % linoleate; and " J . olanchana " contained only a trace of linolenate, 9 % palmitate, and 73 % linoleate;
• Manos and Stone studied the composition of seed oils from several species of the Rhoipteleaceae and Juglandaceae and found the nut oils were generally more unsaturated from species which grow in the oleate; " J . neotropica " contained 3 % linolenate, 5 % palmitate, and 50 % linoleate; and " J . olanchana " contained only a trace of linolenate, 9 % palmitate, and 73 % linoleate;
• Since the ?-n notation is used almost exclusively to indicate the positions of the double bonds close to the-CH 3 end in essential fatty acids, there is no necessity for an equivalent  ?-like notation-the use of the  ?-n notation always refers to the position of a double bond . | group = nb } } . ) Hence mammals cannot synthesize linoleate or linolenate ( which have double bonds at the C-12 ( = ? 12 ), or the C-12 and C-15 ( = ? 12 and ? 15 ) positions, respectively, as well as at the ? 9 position ), nor the polyunsaturated, 20-carbon arachidonic acid that is derived from linoleate.
• Since the ?-n notation is used almost exclusively to indicate the positions of the double bonds close to the-CH 3 end in essential fatty acids, there is no necessity for an equivalent  ?-like notation-the use of the  ?-n notation always refers to the position of a double bond . | group = nb } } . ) Hence mammals cannot synthesize linoleate or linolenate ( which have double bonds at the C-12 ( = ? 12 ), or the C-12 and C-15 ( = ? 12 and ? 15 ) positions, respectively, as well as at the ? 9 position ), nor the polyunsaturated, 20-carbon arachidonic acid that is derived from linoleate.