(2R,3R)-2,3-Butanediol (BioDeep_00000003073)
Main id: BioDeep_00000018434
human metabolite PANOMIX_OTCML-2023 BioNovoGene_Lab2019
代谢物信息卡片
化学式: C4H10O2 (90.0681)
中文名称: 2,3-丁二醇 (立体异构体的混合物), (2R,3R)-(-)-2,3-丁二醇, 2,3-丁二醇, （R，R）-2,3-丁二醇
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: CC(C(C)O)O
InChI: InChI=1S/C4H10O2/c1-3(5)4(2)6/h3-6H,1-2H3/t3-,4-/m1/s1
描述信息
(2R,3R)-2,3-Butanediol is found in cocoa and cocoa products. (2R,3R)-2,3-Butanediol is isolated from cocoa butter and roots of Ruta graveolens (rue).2,3-Butanediol is one of the constitutional isomers of butanediol. The 2R,3R stereoisomer of 2,3-butanediol is produced by a variety of microorganisms, in a process known as butanediol fermentation. It is found in cocoa butter and in the roots of Ruta graveolens. (Wikipedia).
(2R,3R)-Butane-2,3-diol is an endogenous metabolite.
(2R,3R)-Butane-2,3-diol is an endogenous metabolite.
2,3-Butanediol is a butanediol derived from the bioconversion of natural resources[1].
2,3-Butanediol is a butanediol derived from the bioconversion of natural resources[1].
同义名列表
18 个代谢物同义名
(2R,3R)-(-)-2,3-Butanediol; (R,R)-(-)-Butane-2,3-diol; (R,R)-2,3-Butylene glycol; (2R,3R)-Butane-2,3-diol; (-)-(2R,3R)-Butanediol; (2R,3R)-2,3-Butanediol; (R,R)-butane-2,3-diol; (R,R)-2,3-Butanediol; L-(-)-2,3-Butanediol; levo-2,3-Butanediol; 2,3-Butylene glycol; (-)-2,3-Butanediol; (±)-2,3-Butanediol; 2,3-butanediol; (R,R)-Butane-2,3-diol; (R,R)-2,3-butanediol; (R,R)-2,3-butanediol; 2,3-Butanediol
数据库引用编号
21 个数据库交叉引用编号
- ChEBI: CHEBI:16982
- KEGG: C03044
- KEGG: C91323
- PubChem: 225936
- HMDB: HMDB0033007
- Metlin: METLIN64614
- Metlin: METLIN104
- chemspider: 196452
- CAS: 24347-58-8
- CAS: 6982-25-8
- CAS: 513-85-9
- PubChem: 5947
- PDB-CCD: BU3
- 3DMET: B01625
- NIKKAJI: J9.308D
- medchemexpress: HY-W015954
- medchemexpress: HY-128387
- BioNovoGene_Lab2019: BioNovoGene_Lab2019-363
- KNApSAcK: 16982
- LOTUS: LTS0083517
- wikidata: Q27093418
分类词条
相关代谢途径
Reactome(0)
BioCyc(10)
- superpathway of pterocarpan biosynthesis (via daidzein)
- superpathway of pterocarpan biosynthesis (via formononetin)
- superpathway of (R,R)-butanediol biosynthesis
- superpathway of 2,3-butanediol biosynthesis
- isoflavonoid biosynthesis I
- formononetin biosynthesis
- (R,R)-butanediol degradation
- (R,R)-butanediol biosynthesis
- superpathway of acetoin and butanediol biosynthesis
- butanediol biosynthesis
PlantCyc(4)
代谢反应
19 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(19)
- (R,R)-butanediol degradation:
(R,R)-2,3-butanediol + NAD+ ⟶ (R)-acetoin + H+ + NADH - superpathway of (R,R)-butanediol biosynthesis:
(S)-2-acetolactate + H+ ⟶ (R)-acetoin + CO2 - (R,R)-butanediol biosynthesis:
(R,R)-2,3-butanediol + NAD+ ⟶ (R)-acetoin + H+ + NADH - superpathway of 2,3-butanediol biosynthesis:
(S)-2-acetolactate + H+ ⟶ (R)-acetoin + CO2 - (R,R)-butanediol biosynthesis:
(R,R)-2,3-butanediol + NAD+ ⟶ (R)-acetoin + H+ + NADH - superpathway of acetoin and butanediol biosynthesis:
H+ + acetaldehyde + pyruvate ⟶ CO2 + acetoin - butanediol biosynthesis:
(R,R)-2,3-butanediol + NAD+ ⟶ (R)-acetoin + H+ + NADH - (R,R)-butanediol degradation:
(R,R)-2,3-butanediol + NAD+ ⟶ (R)-acetoin + H+ + NADH - superpathway of (R,R)-butanediol biosynthesis:
H+ + pyruvate ⟶ (S)-2-acetolactate + CO2 - (R,R)-butanediol biosynthesis:
(R,R)-2,3-butanediol + NAD+ ⟶ (R)-acetoin + H+ + NADH - (R,R)-butanediol biosynthesis:
(R,R)-2,3-butanediol + NAD+ ⟶ (R)-acetoin + H+ + NADH - superpathway of (R,R)-butanediol biosynthesis:
H+ + pyruvate ⟶ (S)-2-acetolactate + CO2 - (R,R)-butanediol biosynthesis:
(R,R)-2,3-butanediol + NAD+ ⟶ (R)-acetoin + H+ + NADH - (R,R)-butanediol degradation:
(R,R)-2,3-butanediol + NAD+ ⟶ (R)-acetoin + H+ + NADH - (R,R)-butanediol degradation:
(R,R)-2,3-butanediol + NAD+ ⟶ (R)-acetoin + H+ + NADH - superpathway of (R,R)-butanediol biosynthesis:
H+ + pyruvate ⟶ (S)-2-acetolactate + CO2 - (R,R)-butanediol biosynthesis:
(R,R)-2,3-butanediol + NAD+ ⟶ (R)-acetoin + H+ + NADH - (R,R)-butanediol biosynthesis:
(R,R)-2,3-butanediol + NAD+ ⟶ (R)-acetoin + H+ + NADH - (R,R)-butanediol degradation:
(R,R)-2,3-butanediol + NAD+ ⟶ (R)-acetoin + H+ + NADH
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(0)
COVID-19 Disease Map(0)
PathBank(0)
PharmGKB(0)
4 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
- Safiyh Taghavi, Daniel van der Lelie, Adam Hoffman, Yian-Biao Zhang, Michael D Walla, Jaco Vangronsveld, Lee Newman, Sébastien Monchy. Genome sequence of the plant growth promoting endophytic bacterium Enterobacter sp. 638.
PLoS genetics.
2010 May; 6(5):e1000943. doi:
10.1371/journal.pgen.1000943. [PMID: 20485560] - Song Mi Cho, Beom Ryong Kang, Song Hee Han, Anne J Anderson, Ju-Young Park, Yong-Hwan Lee, Baik Ho Cho, Kwang-Yeol Yang, Choong-Min Ryu, Young Cheol Kim. 2R,3R-butanediol, a bacterial volatile produced by Pseudomonas chlororaphis O6, is involved in induction of systemic tolerance to drought in Arabidopsis thaliana.
Molecular plant-microbe interactions : MPMI.
2008 Aug; 21(8):1067-75. doi:
10.1094/mpmi-21-8-1067. [PMID: 18616403] - Song Hee Han, Seung Je Lee, Jae Hak Moon, Keun Hyung Park, Kwang Yeol Yang, Balk Ho Cho, Kil Yong Kim, Yong Whan Kim, Myung Chul Lee, Anne J Anderson, Young Cheol Kim. GacS-dependent production of 2R, 3R-butanediol by Pseudomonas chlororaphis O6 is a major determinant for eliciting systemic resistance against Erwinia carotovora but not against Pseudomonas syringae pv. tabaci in tobacco.
Molecular plant-microbe interactions : MPMI.
2006 Aug; 19(8):924-30. doi:
10.1094/mpmi-19-0924. [PMID: 16903358]
