2-Aminomuconic semialdehyde: Difference between revisions

Revision as of 08:40, 6 August 2011 editCheMoBot (talk \| contribs)Bots141,565 edits Updating {{chembox}} (no changed fields - added verified revid - updated 'DrugBank_Ref', 'UNII_Ref', 'ChEMBL_Ref', 'ChEBI_Ref', 'KEGG_Ref') per Chem/Drugbox validation (report [[Wikipedia_talk:Wi← Previous edit		Revision as of 11:02, 22 October 2012 edit undoPlasmic Physics (talk \| contribs)Extended confirmed users, Rollbackers19,174 editsNo edit summaryNext edit →
Line 51:		Line 51:
	]		]

			{{alkene-stub}}

	{{organic-compound-stub}}		{{organic-compound-stub}}

Revision as of 11:02, 22 October 2012

2-Aminomuconic semialdehyde
Names


IUPAC name 2-Amino-6-oxohexa-2,4-dienoic acid
Identifiers
CAS Number	150994-59-5
3D model (JSmol)	Interactive image Interactive image
ChEBI	CHEBI:15745
ChemSpider	4444230
PubChem CID	30
InChI InChI=1S/C6H7NO3/c7-5(6(9)10)3-1-2-4-8/h1-4H,7H2,(H,9,10)/b2-1-,5-3+Key: QCGTZPZKJPTAEP-REDYYMJGSA-N InChI=1/C6H7NO3/c7-5(6(9)10)3-1-2-4-8/h1-4H,7H2,(H,9,10)/b2-1-,5-3+Key: QCGTZPZKJPTAEP-REDYYMJGBN
SMILES C(=CC=O)C=C(C(=O)O)N O=C\C=C\C=C(/N)C(=O)O
Properties
Chemical formula	C₆H₇NO₃
Molar mass	141.12 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Y verify (what is ?) Infobox references

Chemical compound

2-Aminomuconic semialdehyde is a metabolite of tryptophan.

lysine→	Saccharopine Allysine α-Aminoadipic acid 2-Oxoadipic acid Glutaryl-CoA Glutaconyl-CoA Crotonyl-CoA β-Hydroxybutyryl-CoA
leucine→	β-Hydroxy β-methylbutyric acid β-Hydroxy β-methylbutyryl-CoA Isovaleryl-CoA α-Ketoisocaproic acid β-Ketoisocaproic acid β-Ketoisocaproyl-CoA β-Leucine β-Methylcrotonyl-CoA β-Methylglutaconyl-CoA β-Hydroxy β-methylglutaryl-CoA
tryptophan→alanine→	N′-Formylkynurenine Kynurenine Anthranilic acid 3-Hydroxykynurenine 3-Hydroxyanthranilic acid 2-Amino-3-carboxymuconic semialdehyde 2-Aminomuconic semialdehyde 2-Aminomuconic acid Glutaryl-CoA

histidine→	Urocanic acid Imidazol-4-one-5-propionic acid Formiminoglutamic acid Glutamate-1-semialdehyde
proline→	1-Pyrroline-5-carboxylic acid
arginine→	Agmatine Ornithine Citrulline Cadaverine Putrescine
other	cysteine+glutamate→glutathione: γ-Glutamylcysteine

valine→	α-Ketoisovaleric acid Isobutyryl-CoA Methacrylyl-CoA 3-Hydroxyisobutyryl-CoA 3-Hydroxyisobutyric acid 2-Methyl-3-oxopropanoic acid
isoleucine→	2,3-Dihydroxy-3-methylpentanoic acid 2-Methylbutyryl-CoA Tiglyl-CoA 2-Methylacetoacetyl-CoA
methionine→	generation of homocysteine: S-Adenosyl methionine S-Adenosyl-L-homocysteine Homocysteine conversion to cysteine: Cystathionine α-Ketobutyric acid + Cysteine
threonine→	α-Ketobutyric acid
propionyl-CoA→	Methylmalonyl-CoA

phenylalanine→tyrosine→	4-Hydroxyphenylpyruvic acid Homogentisic acid 4-Maleylacetoacetic acid

Other

Cysteine metabolism	Cysteine sulfinic acid

This article about an alkene is a stub. You can help Misplaced Pages by expanding it.

This article about an organic compound is a stub. You can help Misplaced Pages by expanding it.