¼±Åà - È­»ìǥŰ/¿£ÅÍŰ ´Ý±â - ESC

 
"carbonyl"¿¡ ´ëÇÑ ¿µ¿µ ÀÇÇлçÀü ¼¼ºÎ °Ë»ö °á°úÀÔ´Ï´Ù
À̰ÍÀ» ¿øÇϼ̽À´Ï±î?
CancerWEB ¿µ¿µ ÀÇÇлçÀü ¸ÂÃã °Ë»ö °á°ú : 4 ÆäÀÌÁö: 1
carbonyl The characteristic group, -CO-, of the ketones, aldehydes, and organic acids.
(05 Mar 2000)
carbonyl cyanide m-chlorophenyl hydrazone <chemical> A proton ionophore. It is commonly used as an uncoupling agent and inhibitor of photosynthesis because of its effects on mitochondrial and chloroplast membranes.
Pharmacological action: uncoupling agents, ionophores.
Chemical name: Propanedinitrile, ((3-chlorophenyl)hydrazono)-
(12 Dec 1998)
carbonyl cyanide p-trifluoromethoxyphenylhydrazone <chemical> A proton ionophore that is commonly used as an uncoupling agent in biochemical studies.
Pharmacological action: ionophores, uncoupling agents.
Chemical name: Propanedinitrile, ((4-(trifluoromethoxy)phenyl)hydrazono)-
(12 Dec 1998)
carbonyl group A group in which an oxygen atom is double-bonded to a carbon atom: O=C. The carbon atom then has two additional bonds to attach to the rest of the molecule. Organic molecules containing a carbonyl group are a very important, major group of compounds studied in the field of organic chemistry.
(09 Oct 1997)
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
pig lung carbonyl reductase <enzyme> Tetrameric carbonyl reductase; mw 24 kD; properties distinct from monomeric cr; it is mainly distributed in the mitochondria of the pig lung; exhibits very low substrate specificity for aromatic and aliphatic carbonyl compounds and catalyses the oxidation of secondary alcohols and aldehydes; activated 2-5 fold by fatty acids ddbj/embl/genbank d16511
Registry number: EC 1.1.1.-
(26 Jun 1999)
ÅëÇÕ°Ë»ö ¿Ï·á