1-palmitoyl-dihydroxyacetone-phosphate (BioDeep_00000004610)
Secondary id: BioDeep_00000634115
human metabolite
代谢物信息卡片
化学式: C19H37O7P (408.2276782)
中文名称:
谱图信息:
最多检出来源 Viridiplantae(plant) 0.06%
分子结构信息
SMILES: CCCCCCCCCCCCCCCC(=O)OCC(=O)COP(=O)(O)O
InChI: InChI=1S/C19H37O7P/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-19(21)25-16-18(20)17-26-27(22,23)24/h2-17H2,1H3,(H2,22,23,24)
描述信息
1-palmitoyl-dihydroxyacetone-phosphate is also known as Palmitoyl glycerone phosphate or Hexadecanoate 2-oxo-3-(phosphonooxy)propyl ester. 1-palmitoyl-dihydroxyacetone-phosphate is considered to be practically insoluble (in water) and acidic. 1-palmitoyl-dihydroxyacetone-phosphate is an other glycerophospholipid lipid molecule
同义名列表
15 个代谢物同义名
Hexadecanoic acid 2-oxo-3-(phosphonooxy)propyl ester; [3-(hexadecanoyloxy)-2-oxopropoxy]phosphonic acid; Hexadecanoate 2-oxo-3-(phosphonooxy)propyl ester; Hexadecanoyl dihydroxyacetone phosphoric acid; 1-Palmitoyl-dihydroxyacetone-phosphoric acid; Palmitoyl dihydroxyacetone phosphoric acid; Hexadecanoyl dihydroxyacetone phosphate; 1-Palmitoylglycerone 3-phosphoric acid; 1-palmitoyl-dihydroxyacetone-phosphate; Palmitoyl dihydroxyacetone phosphate; Palmitoyl glycerone phosphoric acid; Palmitoylglycerone phosphoric acid; 1-palmitoylglycerone 3-phosphate; Palmitoyl glycerone phosphate; Palmitoylglycerone phosphate
数据库引用编号
12 个数据库交叉引用编号
- ChEBI: CHEBI:17868
- KEGG: C01192
- PubChem: 167650
- HMDB: HMDB0062190
- Metlin: METLIN65568
- chemspider: 146664
- CAS: 17378-38-0
- PMhub: MS000017145
- PubChem: 4418
- LipidMAPS: LMGP00000063
- 3DMET: B00257
- NIKKAJI: J1.063.182C
分类词条
相关代谢途径
Reactome(0)
BioCyc(0)
PlantCyc(0)
代谢反应
5 个相关的代谢反应过程信息。
Reactome(3)
- Metabolism:
1-3-oxo-THA-CoA + CoA-SH ⟶ DHA-CoA + propionyl CoA
- Metabolism of lipids:
1-3-oxo-THA-CoA + CoA-SH ⟶ DHA-CoA + propionyl CoA
- Plasmalogen biosynthesis:
HXOL + Palmitoylglycerone phosphate ⟶ GO3P + PALM
BioCyc(0)
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(0)
COVID-19 Disease Map(0)
PathBank(2)
- Glycerophospholipid Metabolism:
Adenosine triphosphate + Ethanolamine ⟶ Adenosine diphosphate + Hydrogen Ion + O-Phosphoethanolamine
- Choline Metabolism:
PC(16:0/16:0) + Water ⟶ Choline + Hydrogen Ion + PA(16:0/16:0)
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
- E C de Vet, Y H Hilkes, M W Fraaije, H van den Bosch. Alkyl-dihydroxyacetonephosphate synthase. Presence and role of flavin adenine dinucleotide.
The Journal of biological chemistry.
2000 Mar; 275(9):6276-83. doi:
10.1074/jbc.275.9.6276
. [PMID: 10692424] - A K Hajra. Glycerolipid biosynthesis in peroxisomes (microbodies).
Progress in lipid research.
1995; 34(4):343-64. doi:
10.1016/0163-7827(95)00013-5
. [PMID: 8685243] - A K Das, S Horie, A K Hajra. Biosynthesis of glycerolipid precursors in rat liver peroxisomes and their transport and conversion to phosphatidate in the endoplasmic reticulum.
The Journal of biological chemistry.
1992 May; 267(14):9724-30. doi:
. [PMID: 1577808]
- D M Peterson, R A Martinez, N Satsangi, S T Weintraub, P L Stotter, S J Friedberg. Synthesis of regiospecifically labeled [18O]glycolic acid and [18O]acyldihydroxyacetone phosphate.
Journal of lipid research.
1988 Jan; 29(1):94-101. doi:
10.1016/s0022-2275(20)38569-2
. [PMID: 3408514] - A K Das, A K Hajra. Estimation of acyldihydroxyacetone phosphate and lysophosphatidate in animal tissues.
Biochimica et biophysica acta.
1984 Nov; 796(2):178-89. doi:
10.1016/0005-2760(84)90346-1
. [PMID: 6388643] - S J Friedberg, S T Weintraub, M R Singer, R C Greene. The mechanism of ether bond formation in O-alkyl lipid synthesis in Ehrlich ascites tumor. Unusual cleavage of the fatty acid moiety of acyl dihydroxyacetone phosphate.
The Journal of biological chemistry.
1983 Jan; 258(1):136-42. doi:
10.1016/s0021-9258(18)33231-9
. [PMID: 6848491]