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Revision as of 17:52, 16 February 2012 editBeetstra (talk | contribs)Edit filter managers, Administrators172,031 edits Saving copy of the {{chembox}} taken from revid 452198925 of page 3-Hydroxykynurenine for the Chem/Drugbox validation project (updated: 'CASNo').  Latest revision as of 02:17, 9 September 2024 edit 98.191.202.231 (talk) Cat. 
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{{ambox | text = This page contains a copy of the infobox ({{tl|chembox}}) taken from revid of page ] with values updated to verified values.}}
{{chembox {{chembox
| Verifiedfields = changed
| verifiedrevid = 443348502 | verifiedrevid = 477218877
|ImageFile=3-hydroxykynurenine.png | ImageFile=3-hydroxykynurenine.png
|ImageSize=200px | ImageSize=200px
|IUPACName=2-Amino-4-(2-amino-3-hydroxyphenyl)-4-oxobutanoic acid
| ImageAlt = Skeletal formula of 3-hydroxykynurenine
|OtherNames=
| ImageFile1 = 3-Hydroxy-L-kynurenine-zwitterion-3D-balls.png
| ImageAlt1 = Ball-and-stick model of the 3-hydroxykynurenine molecule as a zwitterion
| IUPACName=2-Amino-4-(2-amino-3-hydroxyphenyl)-4-oxobutanoic acid
| OtherNames=
|Section1={{Chembox Identifiers |Section1={{Chembox Identifiers
| KEGG_Ref = {{keggcite|correct|kegg}} | KEGG_Ref = {{keggcite|correct|kegg}}
| KEGG = C02794 | KEGG = C02794
| InChI = 1/C10H12N2O4/c11-6(10(15)16)4-8(14)5-2-1-3-7(13)9(5)12/h1-3,6,13H,4,11-12H2,(H,15,16) | InChI = 1/C10H12N2O4/c11-6(10(15)16)4-8(14)5-2-1-3-7(13)9(5)12/h1-3,6,13H,4,11-12H2,(H,15,16)
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| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = VCKPUUFAIGNJHC-UHFFFAOYSA-N | StdInChIKey = VCKPUUFAIGNJHC-UHFFFAOYSA-N
| CASNo_Ref = {{cascite|correct|CAS}}
| CASNo = <!-- blanked - oldvalue: 484-78-6 -->
| CASNo=484-78-6
| PubChem=89
| ChEBI_Ref = {{ebicite|correct|EBI}} | UNII_Ref = {{fdacite|correct|FDA}}
| UNII = 27723548JL
| PubChem=89
| ChEBI_Ref = {{ebicite|correct|EBI}}
| ChEBI = 1547 | ChEBI = 1547
| SMILES = O=C(O)C(N)CC(=O)c1cccc(O)c1N | SMILES = O=C(O)C(N)CC(=O)c1cccc(O)c1N
| MeSHName=3-hydroxykynurenine | MeSHName=3-hydroxykynurenine
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 87 | ChemSpiderID = 87
}} }}
|Section2={{Chembox Properties |Section2={{Chembox Properties
| Formula=C<sub>10</sub>H<sub>12</sub>N<sub>2</sub>O<sub>4</sub> | Formula=C<sub>10</sub>H<sub>12</sub>N<sub>2</sub>O<sub>4</sub>
| MolarMass=224.21 g/mol | MolarMass=224.21 g/mol
| Appearance= | Appearance=
| Density= | Density=
| MeltingPt= | MeltingPt=
| BoilingPt= | BoilingPt=
| Solubility= | Solubility=
}} }}
|Section3={{Chembox Hazards |Section3={{Chembox Hazards
| MainHazards= | MainHazards=
| FlashPt= | FlashPt=
| AutoignitionPt =
| Autoignition=
}} }}
}} }}

'''3-Hydroxykynurenine''' is a metabolite of ], which filters UV light in the human ].<ref>{{cite journal|last1=Malina|first1=HZ|last2=Martin |first2=XD|title=Deamination of 3-hydroxykynurenine in bovine lenses: a possible mechanism of cataract formation in general.|journal=Graefes Arch Clin Exp Ophthalmol|year=1995|volume=233|issue=1|pages=38–44|pmid=7721122|doi=10.1007/bf00177784|s2cid=25414197}}</ref> It is one of two pigments identified as responsible for the ]'s (''Misumena vatia)'' yellow coloration.
], which connects ] to tryptophan. The pathway is named for the first intermediate, ], which is a precursor to ] and 3-hydroxykynurenine.<ref name=Schwarcz>{{cite journal|last=Schwarcz|first=Robert |author2=John P. Bruno |author3=Paul J. Muchowski |author4=Hui-Qiu Wu|title=Kynurenines in the Mammalian Brain: When Physiology Meets Pathology|journal=Nature Reviews Neuroscience|date=July 2012|volume=13|pages=465–477|doi=10.1038/nrn3257|issue=7|pmid=22678511 |pmc=3681811}}</ref>]]

==References==
{{reflist}}

==See also==
* ]
* ]

{{Amino acid metabolism intermediates}}

{{DEFAULTSORT:Hydroxykynurenine, 3-}}

]
]
]


{{organic-compound-stub}}