2-Hydroxybutyric acid (BioDeep_00000003495)
Secondary id: BioDeep_00000229680, BioDeep_00000265237, BioDeep_00001868300
natural product human metabolite PANOMIX_OTCML-2023 Endogenous blood metabolite
代谢物信息卡片
化学式: C4H8O3 (104.0473)
中文名称: 2-羟基丁酸, (S)-2-羟基丁酸, S-2-羟基丁酸
谱图信息:
最多检出来源 Homo sapiens(blood) 27.03%
Last reviewed on 2024-07-16.
Cite this Page
2-Hydroxybutyric acid. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China.
https://query.biodeep.cn/s/2-hydroxybutyric_acid (retrieved
2024-12-22) (BioDeep RN: BioDeep_00000003495). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
分子结构信息
SMILES: CCC(C(=O)O)O
InChI: InChI=1S/C4H8O3/c1-2-3(5)4(6)7/h3,5H,2H2,1H3,(H,6,7)
描述信息
2-Hydroxybutyric acid (CAS: 600-15-7), also known as alpha-hydroxybutyrate, is an organic acid derived from alpha-ketobutyrate. alpha-Ketobutyrate is produced by amino acid catabolism (threonine and methionine) and glutathione anabolism (cysteine formation pathway) and is metabolized into propionyl-CoA and carbon dioxide (PMID: 20526369). 2-Hydroxybutyric acid is formed as a byproduct from the formation of alpha-ketobutyrate via a reaction catalyzed by lactate dehydrogenase (LDH) or alpha-hydroxybutyrate dehydrogenase (alphaHBDH). alpha-Hydroxybutyric acid is primarily produced in mammalian hepatic tissues that catabolize L-threonine or synthesize glutathione. Oxidative stress or detoxification of xenobiotics in the liver can dramatically increase the rate of hepatic glutathione synthesis. Under such metabolic stress conditions, supplies of L-cysteine for glutathione synthesis become limiting, so homocysteine is diverted from the transmethylation pathway (which forms methionine) into the transsulfuration pathway (which forms cystathionine). alpha-Ketobutyrate is released as a byproduct when cystathionine is cleaved into cysteine that is incorporated into glutathione. Chronic shifts in the rate of glutathione synthesis may be reflected by urinary excretion of 2-hydroxybutyrate. 2-Hydroxybutyrate is an early marker for both insulin resistance and impaired glucose regulation that appears to arise due to increased lipid oxidation and oxidative stress (PMID: 20526369). 2-Hydroxybutyric acid is often found in the urine of patients suffering from lactic acidosis and ketoacidosis. 2-Hydroxybutyric acid generally appears at high concentrations in situations related to deficient energy metabolism (e.g. birth asphyxia) and also in inherited metabolic diseases affecting the central nervous system during neonatal development, such as "cerebral" lactic acidosis, glutaric aciduria type II, dihydrolipoyl dehydrogenase (E3) deficiency, and propionic acidemia. More recently it has been noted that elevated levels of alpha-hydroxybutyrate in the plasma is a good marker for early-stage type II diabetes (PMID: 19166731). It was concluded from studies done in the mid-1970s that an increased NADH2/NAD ratio was the most important factor for the production of 2-hydroxybutyric acid (PMID: 168632).
2-Hydroxybutyric acid is an organic acid that is involved in propanoate metabolism. It is produced in mammalian tissues (principaly hepatic) that catabolize L-threonine or synthesize glutathione. Oxidative stress or detoxification demands can dramatically increase the rate of hepatic glutathione synthesis. Under such metabolic stress conditions, supplies of L-cysteine for glutathione synthesis become limiting, so homocysteine is diverted from the transmethylation pathway forming methionine into the transsulfuration pathway forming cystathionine. 2-Hydroxybutyrate is released as a by-product when cystathionine is cleaved to cysteine that is incorporated into glutathione. 2-Hydroxybutyric acid is often found in the urine of patients suffering from lactic acidosis and ketoacidosis. 2-Hydroxybutyric acid generally appears at high concentrations in situations related to deficient energy metabolism (e.g., birth asphyxia) and also in inherited metabolic diseases affecting the central nervous system during neonatal development, such as "cerebral" lactic acidosis, glutaric aciduria type II, dihydrolipoyl dehydrogenase (E3) deficiency, and propionic acidemia. More recently it has been noted that elevated levels of alpha-hydroxybutyrate in the plasma is a good marker for early stage type II diabetes (PMID: 19166731). It was concluded from studies done in the mid 1970s that an increased NADH2/NAD ratio was the most important factor for the production of 2-hydorxybutyric acid (PMID: 168632) [HMDB]
2-Hydroxybutyric acid. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=565-70-8 (retrieved 2024-07-16) (CAS RN: 600-15-7). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
(S)-2-Hydroxybutanoic acid is the S-enantiomer of?2-Hydroxybutanoic acid. 2-Hydroxybutanoic acid, a coproduct of protein metabolism, is an insulin resistance (IR) biomarker[1].
同义名列表
41 个代谢物同义名
DL-alpha-Hydroxybutyric acid barium salt; (S)-(+)-2-Hydroxybutanoic acid; (+)-alpha-Hydroxybutyric acid; (+)-2-Hydroxy-n-butyric acid; alpha-Hydroxy-n-butyric acid; L-alpha-Hydroxybutanoic acid; L-alpha-Hydroxybutyric acid; (2S)-2-Hydroxybutanoic acid; (+)-2-Hydroxybutanoic acid; (S)-2-Hydroxybutanoic acid; alpha-Hydroxybutanoic acid; (+)-α-Hydroxybutyric acid; alpha-Hydroxybutyric acid; (±)-2-hydroxybutyric acid; (S)-2-Hydroxybutyric acid; (+)-2-Hydroxybutyric acid; L-alpha-Hydroxybutanoate; L-a-Hydroxybutanoic acid; α-Hydroxy-n-butyric acid; L-Α-hydroxybutanoic acid; L-2-Hydroxybutanoic acid; L-2-Hydroxybutyric acid; L-alpha-Hydroxybutyrate; L-a-Hydroxybutyric acid; 2-hydroxy-butanoic acid; L-Α-hydroxybutyric acid; (S)-2-Hydroxybutanoate; α-Hydroxybutanoic acid; 2-Hydroxybutanoic acid; (S)-2-Hydroxybutyrate; α-Hydroxybutyric acid; 2-Hydroxybutyric acid; L-2-Hydroxybutanoate; L-a-Hydroxybutanoate; L-Α-hydroxybutanoate; L-a-Hydroxybutyrate; L-Α-hydroxybutyrate; L-2-Hydroxybutyrate; 2-Hydroxybutanoate; 2-Hydroxybutyrate; 2-Hydroxybutyric acid
数据库引用编号
21 个数据库交叉引用编号
- ChEBI: CHEBI:50613
- ChEBI: CHEBI:1148
- KEGG: C05984
- PubChem: 440864
- PubChem: 11266
- HMDB: HMDB0000008
- Metlin: METLIN35690
- ChEMBL: CHEMBL567588
- Wikipedia: 2-Hydroxybutyric_acid
- MetaCyc: CPD-3564
- foodb: FDB021867
- chemspider: 389701
- CAS: 3347-90-8
- MoNA: PS021901
- MoNA: PS021907
- PMhub: MS000009771
- LipidMAPS: LMFA01050342
- 3DMET: B01942
- NIKKAJI: J57.683B
- RefMet: 2-Hydroxybutyric acid
- medchemexpress: HY-W018499
分类词条
相关代谢途径
Reactome(0)
BioCyc(0)
PlantCyc(0)
代谢反应
17 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(0)
WikiPathways(0)
Plant Reactome(0)
INOH(2)
- Propanoate metabolism ( Propanoate metabolism ):
ATP + CoA + Propanoic acid ⟶ AMP + Propanoyl-CoA + Pyrophosphate
- NAD+ + 2-Hydroxy-butanoic acid = NADH + 2-Oxo-butanoic acid ( Propanoate metabolism ):
2-Hydroxy-butanoic acid + NAD+ ⟶ 2-Oxo-butanoic acid + NADH
PlantCyc(0)
COVID-19 Disease Map(0)
PathBank(15)
- Propanoate Metabolism:
2-Ketobutyric acid + Coenzyme A + NAD ⟶ NADH + Propionyl-CoA
- Malonic Aciduria:
2-Ketobutyric acid + Coenzyme A + NAD ⟶ NADH + Propionyl-CoA
- Methylmalonic Aciduria Due to Cobalamin-Related Disorders:
2-Ketobutyric acid + Coenzyme A + NAD ⟶ NADH + Propionyl-CoA
- Malonyl-CoA Decarboxylase Deficiency:
2-Ketobutyric acid + Coenzyme A + NAD ⟶ NADH + Propionyl-CoA
- Propanoate Metabolism:
2-Ketobutyric acid + Coenzyme A + NAD ⟶ NADH + Propionyl-CoA
- Malonic Aciduria:
2-Ketobutyric acid + Coenzyme A + NAD ⟶ NADH + Propionyl-CoA
- Methylmalonic Aciduria Due to Cobalamin-Related Disorders:
2-Ketobutyric acid + Coenzyme A + NAD ⟶ NADH + Propionyl-CoA
- Malonyl-CoA Decarboxylase Deficiency:
2-Ketobutyric acid + Coenzyme A + NAD ⟶ NADH + Propionyl-CoA
- Propanoate Metabolism:
2-Ketobutyric acid + Coenzyme A + NAD ⟶ NADH + Propionyl-CoA
- Propanoate Metabolism:
2-Ketobutyric acid + Coenzyme A + NAD ⟶ NADH + Propionyl-CoA
- Propanoate Metabolism:
2-Ketobutyric acid + Coenzyme A + NAD ⟶ NADH + Propionyl-CoA
- Propanoate Metabolism:
2-Ketobutyric acid + Coenzyme A + NAD ⟶ NADH + Propionyl-CoA
- Malonic Aciduria:
2-Ketobutyric acid + Coenzyme A + NAD ⟶ NADH + Propionyl-CoA
- Methylmalonic Aciduria Due to Cobalamin-Related Disorders:
2-Ketobutyric acid + Coenzyme A + NAD ⟶ NADH + Propionyl-CoA
- Malonyl-CoA Decarboxylase Deficiency:
2-Ketobutyric acid + Coenzyme A + NAD ⟶ NADH + Propionyl-CoA
PharmGKB(0)
8 个相关的物种来源信息
- 1080010 - Aloe africana: 10.1021/JF071110T
- 593583 - Carteriospongia: 10.1055/S-2006-960851
- 3055 - Chlamydomonas reinhardtii: 10.1111/TPJ.12747
- 9606 - Homo sapiens:
- 9606 - Homo sapiens: -
- 159736 - Macrobrachium nipponense: 10.3389/FPHYS.2018.00076
- 279624 - Phyllospongia: 10.1055/S-2006-960851
- 569774 - 金线莲: -
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
- Seyed Ali Rasooli, Rozita Fathi, Farhad Ahmadi-Kani Golzar, Masoumeh Baghersalimi. The effect of circuit resistance training on plasma levels of amino acids, alpha-hydroxybutyrate, mannose, and urinary levels of glycine conjugated adducts in obese adolescent boys.
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