Hawkinsin

Hawkinsin

chembox new
ImageFile=Hawkinsin.pngImageSize=200px
IUPACName= 2-Amino-3- [2-(carboxymethyl)-2,5-dihydroxy-1-cyclohex-3-enyl] sulfanyl] propanoic acid
OtherNames=(2-L-Cystein-"S"-yl-1,4-dihydroxycyclohex-5-en-1-yl)acetic acid
Section1=Chembox Identifiers
CASNo=63224-90-8
PubChem=173909
SMILES=C1C(C=CC(C1SCC(C(=O)O)N)(CC(=O)O)O)O
Section2=Chembox Properties
Formula=C11H17NO6S
MolarMass=291.32 g/mol
Appearance=
Density=
MeltingPt=
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Section3=Chembox Hazards
MainHazards=
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Hawkinsin is an amino acid.

It is found in elevated concentrations in the urine in hawkinsinuria.


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  • hawkinsin — haw·kin·sin (hawґkin sin) a cyclic amino acid metabolite of tyrosine excreted in hawkinsinuria, a rare aminoacidopathy. It is formed from an intermediate of the 4 hydroxyphenylpyruvate dioxygenase reaction combined with glutathione …   Medical dictionary

  • Hawkinsinuria — Infobox Disease Name = PAGENAME Caption = Hawkinsin DiseasesDB = 29836 ICD10 = ICD9 = ICDO = OMIM = 276710 OMIM mult = OMIM2|140350 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = D020176 Hawkinsinuria, also called 4 Alpha… …   Wikipedia

  • ТИРОЗИНЕМИЯ — мед. Тирозинемия повышенная концентрация тирозина в крови приводит к увеличению выделения с мочой соединений тирозина, гепатоспленомегалии, узловому циррозу печени, множественным дефектам почечной канальцевой реабсорбции и витамин D резистентному …   Справочник по болезням

  • hawkinsinuria — haw·kin·sin·u·ria (haw″kin sin uґre ə) a rare autosomal dominant disorder caused by heterozygous mutation in the HPD gene (locus: 12q24 qter), which encodes 4 hydroxyphenylpyruvate dioxygenase, an enzyme important in tyrosine… …   Medical dictionary

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