- 3-hydroxyglutaric acid
Medical dictionary. 2011.
3-hydroxyglutaric acid
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hydroxyglutaric acid — hy·droxy·glu·tar·ic ac·id (hi drok″se gloo tarґik) any of several hydroxylated derivatives of glutaric acid; 2 hydroxyglutaric acid is accumulated and excreted in glutaricaciduria, type II, and 3 hydroxyglutaric acid in glutaricaciduria,… … Medical dictionary
hydroxyglutaric acid — noun Any hydroxy derivative of glutaric acid, but especially 2 hydroxyglutaric acid which has biological activity … Wiktionary
Alpha-Hydroxyglutaric acid — chembox new Name = alpha Hydroxyglutaric acid ImageFile=alpha hydroxyglutaric acid.png ImageSize=200px IUPACName=2 Hydroxypentanedioic acid OtherNames= Section1=Chembox Identifiers CASNo=2889 31 8 PubChem=43 SMILES=C(CC(=O)O)C(C(=O)O)O… … Wikipedia
2-Hydroxyglutaric aciduria — Classification and external resources Alpha Hydroxyglutaric acid OMIM 600721 … Wikipedia
L2HGDH — L 2 hydroxyglutarate dehydrogenase, also known as L2HGDH, is a human gene.cite web | title = Entrez Gene: L2HGDH L 2 hydroxyglutarate dehydrogenase| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=79944|… … Wikipedia
Glutaric aciduria type 1 — DiseaseDisorder infobox Name = Glutaric acidemia type 1 ICD10 = ICD10|E|72|3|e|70 ICD9 = ICDO = Caption = Glutaric acid OMIM = 231670 MedlinePlus = eMedicineSubj = eMedicineTopic = DiseasesDB = 29830 Glutaric acidemia type 1 (or Glutaric Aciduria … Wikipedia
Organic anion transporter 1 — Figure 1 Schematic representation of transmembrane proteins: 1. a membrane protein with one transmembrane domain 2. a membrane protein with three transmembrane domains 3. OAT1 is believed to have twelve transmembrane domains. [1] The membrane is… … Wikipedia
Statin development — The discovery of HMG CoA (3 hydroxy 3 methylglutaryl CoA) reductase inhibitors, called statins, was a breakthrough in the prevention of hypercholesterolemia and related diseases. Hypercholesterolemia is considered to be one of the major risk… … Wikipedia
Tetrahydromethanopterin — Identifiers PubChem 5459995 … Wikipedia
glutaricaciduria type I — a disorder caused by mutation in the GCDH gene (locus: 19p13.2), resulting in a deficiency of glutaryl CoA dehydrogenase; 3 hydroxyglutaric acid is excreted in addition to glutaric acid, and there are progressive dystonia and dyskinesia,… … Medical dictionary
