Isovalerylglucuronide (BioDeep_00000027762)
human metabolite Endogenous blood metabolite
代谢物信息卡片
化学式: C11H18O8 (278.1001628)
中文名称:
谱图信息:
最多检出来源 Homo sapiens(blood) 50%
分子结构信息
SMILES: CC(C)CC(=O)OC1C(C(C(C(O1)C(=O)O)O)O)O
InChI: InChI=1S/C11H18O8/c1-4(2)3-5(12)18-11-8(15)6(13)7(14)9(19-11)10(16)17/h4,6-9,11,13-15H,3H2,1-2H3,(H,16,17)/t6-,7-,8+,9-,11+/m0/s1
描述信息
Isovaleryl glucuronide has been identified in the urine of patients with isovaleric acidemia made possible by using gas chromatograph-mass spectrometry (GC-MS). Isovaleryl glucuronide is more likely to be excreted when the amount of urinary 3-hydroxyisovaleric acid excretion is high. Isovaleryl glucuronide is more likely to be excreted when the amount of urinary 3-hydroxyisovaleric acid excretion is high. (PMID: 6547525). Isovaleric acidemia is caused by mutation in the isovaleryl CoA dehydrogenase gene and is closely related to maple syrup urine disease. It presents in two forms: the acute neonatal form, leading to massive metabolic acidosis from the first days of life and rapid death and a chronic form in which periodic attacks of severe ketoacidosis occur with asymptomatic intervening periods. (OMIM 243500).
Isovaleryl glucuronide has been identified in the urine of patients with isovaleric acidemia made possible by using gas chromatograph-mass spectrometry (GC-MS). Isovaleryl glucuronide is more likely to be excreted when the amount of urinary 3-hydroxyisovaleric acid excretion is high. Isovaleryl glucuronide is more likely to be excreted when the amount of urinary 3-hydroxyisovaleric acid excretion is high. (PMID: 6547525)
同义名列表
数据库引用编号
6 个数据库交叉引用编号
- ChEBI: CHEBI:174651
- PubChem: 137383
- HMDB: HMDB0002091
- foodb: FDB022841
- chemspider: 121058
- CAS: 88070-93-3
分类词条
相关代谢途径
Reactome(0)
BioCyc(0)
PlantCyc(0)
代谢反应
22 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(0)
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(0)
COVID-19 Disease Map(0)
PathBank(22)
- Starch and Sucrose Metabolism:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Glycogen Synthetase Deficiency:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Glycogenosis, Type III. Cori Disease, Debrancher Glycogenosis:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Glycogenosis, Type IV. Amylopectinosis, Anderson Disease:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Glycogenosis, Type VI. Hers Disease:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Mucopolysaccharidosis VII. Sly Syndrome:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Sucrase-Isomaltase Deficiency:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Starch and Sucrose Metabolism:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Glycogen Synthetase Deficiency:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Glycogenosis, Type III. Cori Disease, Debrancher Glycogenosis:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Glycogenosis, Type IV. Amylopectinosis, Anderson Disease:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Glycogenosis, Type VI. Hers Disease:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Mucopolysaccharidosis VII. Sly Syndrome:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Sucrase-Isomaltase Deficiency:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Starch and Sucrose Metabolism:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Starch and Sucrose Metabolism:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Glycogen Synthetase Deficiency:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Glycogenosis, Type III. Cori Disease, Debrancher Glycogenosis:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Glycogenosis, Type IV. Amylopectinosis, Anderson Disease:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Glycogenosis, Type VI. Hers Disease:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Mucopolysaccharidosis VII. Sly Syndrome:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Sucrase-Isomaltase Deficiency:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
PharmGKB(0)
1 个相关的物种来源信息
在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有:
- PubMed: 来源于PubMed文献库中的文献信息,我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表,这个列表按照代谢物同时出现的文献数量降序排序,取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
- NCBI Taxonomy: 通过文献数据挖掘,得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序,取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
- Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
- Chemical Reaction: 在化学反应过程中,存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。
点击图上的相关代谢物的名称,可以跳转到相关代谢物的信息页面。
文献列表
- D G Hine, K Tanaka. Capillary gas chromatographic/mass spectrometric analysis of abnormal metabolites in hypoglycin-treated rat urine.
Biomedical mass spectrometry.
1984 Jul; 11(7):332-9. doi:
10.1002/bms.1200110704
. [PMID: 6478044] - D G Hine, K Tanaka. The identification and the excretion pattern of isovaleryl glucuronide in the urine of patients with isovaleric acidemia.
Pediatric research.
1984 Jun; 18(6):508-12. doi:
10.1203/00006450-198406000-00004
. [PMID: 6547525] - L Dorland, M Duran, S K Wadman, A Niederwieser, L Bruinvis, D Ketting. Isovalerylglucuronide, a new urinary metabolite in isovaleric acidemia. Identification problems due to rearrangement reactions.
Clinica chimica acta; international journal of clinical chemistry.
1983 Oct; 134(1-2):77-83. doi:
10.1016/0009-8981(83)90186-9
. [PMID: 6652913]