Talk:Oxaloacetic acid

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Merge from Oxaloacetate

Latest comment: 19 years ago1 comment1 person in discussion

In line with normal naming conventions, oxaloacetate has been merged here, and now redirects to this page. At the time of the merge/redirect, the edit history of oxaloacetate was as follows:

14:51, 10 Mar 2005 131.251.0.7
07:24, 10 Mar 2005 RJFJR m (stub to chem-stub)
21:31, 8 Mar 2005 161.97.202.245 (Revert to version by Chris Edgemon [from vandalism])
20:39, 8 Mar 2005 Remuel m (sorted stub)
17:28, 8 Mar 2005 193.63.118.247
17:25, 8 Mar 2005 193.63.119.25
08:30, 28 Oct 2004 Chris Edgemon
10:55, 20 Jul 2004 132.66.16.12
20:15, 18 Jul 2004 132.66.16.12
20:06, 18 Jul 2004 132.66.16.34
04:04, 11 Mar 2004 Moink (wikify, msg:stub)
02:13, 11 Mar 2004 194.81.199.46

For copyright reasons, please do not remove this information. Physchim62 21:21, 24 May 2005 (UTC)Reply

Mitochondria

Oxaloacetate is converted into Malate or Phosphoenolpyruvate before it leaves the mitochondria, does that mean it cannot leave in oxaloacetate form?

Interconversion picture

Latest comment: 17 years ago1 comment1 person in discussion

The picture is misleading because it does not relate to any biological process - at pH7, carboxylic acids are deprotonated - dehydrogenation does not produce free H2, it is coupled to reduction of NAD+ - similarly, NH3 is not released as free ammonia, as shown - etc —Preceding unsigned comment added by 90.242.88.79 (talk) 16:32, 23 September 2007 (UTC)Reply

Enol form(s)

Latest comment: 8 years ago1 comment1 person in discussion

Properties section says "The enol forms of oxaloacetic acid are particularly stable, so much so that the two tautomer have different melting points (152 °C for the cis isoform and 184 °C for the trans isoform)." Does this mean the structure shown is the keto form and that there are two enol (iso)forms ? A diagram of at least one of the enol isoforms would be helpful ? - Rod57 (talk) 05:48, 29 March 2016 (UTC)Reply

Assessment comment

Latest comment: 17 years ago1 comment1 person in discussion

The comment(s) below were originally left at Talk:Oxaloacetic acid/Comments, and are posted here for posterity. Following several discussions in past years, these subpages are now deprecated. The comments may be irrelevant or outdated; if so, please feel free to remove this section.

Rated "high" because oxaloacetate redirects here and is highschool/SAT biology content. - tameeria 20:31, 28 April 2007 (UTC)Reply

Last edited at 20:31, 28 April 2007 (UTC). Substituted at 02:04, 30 April 2016 (UTC)

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