Hexanoyl-CoA (BioDeep_00001868782)
Main id: BioDeep_00000005768
PANOMIX_OTCML-2023
代谢物信息卡片
化学式: C27H46N7O17P3S (865.1884)
中文名称:
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: CCCCCC(=O)SCCNC(=O)CCNC(=O)C(C(C)(C)COP(=O)(O)OP(=O)(O)OCC1C(C(C(O1)N2C=NC3=C(N=CN=C32)N)O)OP(=O)(O)O)O
InChI: InChI=1S/C27H46N7O17P3S/c1-4-5-6-7-18(36)55-11-10-29-17(35)8-9-30-25(39)22(38)27(2,3)13-48-54(45,46)51-53(43,44)47-12-16-21(50-52(40,41)42)20(37)26(49-16)34-15-33-19-23(28)31-14-32-24(19)34/h14-16,20-22,26,37-38H,4-13H2,1-3H3,(H,29,35)(H,30,39)(H,43,44)(H,45,46)(H2,28,31,32)(H2,40,41,42)/t16-,20-,21-,22+,26-/m1/s1
描述信息
A medium-chain fatty acyl-CoA having hexanoyl as the S-acyl group.
同义名列表
2 个代谢物同义名
数据库引用编号
12 个数据库交叉引用编号
- ChEBI: CHEBI:27540
- KEGG: C05270
- PubChem: 449118
- DrugBank: DB02563
- CAS: 5060-32-2
- MetaboLights: MTBLC27540
- PubChem: 7657
- LipidMAPS: LMFA07050328
- PDB-CCD: HXC
- 3DMET: B04998
- NIKKAJI: J358.059H
- RefMet: Hexanoyl-CoA
分类词条
相关代谢途径
Reactome(0)
BioCyc(0)
PlantCyc(0)
代谢反应
0 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(0)
PharmGKB(0)
1 个相关的物种来源信息
- 9606 - Homo sapiens: 10.1007/S11306-016-1051-4
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
- Xiaozhou Luo, Michael A Reiter, Leo d'Espaux, Jeff Wong, Charles M Denby, Anna Lechner, Yunfeng Zhang, Adrian T Grzybowski, Simon Harth, Weiyin Lin, Hyunsu Lee, Changhua Yu, John Shin, Kai Deng, Veronica T Benites, George Wang, Edward E K Baidoo, Yan Chen, Ishaan Dev, Christopher J Petzold, Jay D Keasling. Complete biosynthesis of cannabinoids and their unnatural analogues in yeast.
Nature.
2019 03; 567(7746):123-126. doi:
10.1038/s41586-019-0978-9
. [PMID: 30814733] - Chitra Bhatia, Stephanie Oerum, James Bray, Kathryn L Kavanagh, Naeem Shafqat, Wyatt Yue, Udo Oppermann. Towards a systematic analysis of human short-chain dehydrogenases/reductases (SDR): Ligand identification and structure-activity relationships.
Chemico-biological interactions.
2015 Jun; 234(?):114-25. doi:
10.1016/j.cbi.2014.12.013
. [PMID: 25526675] - Randy W Purves, Stephen J Ambrose, Shawn M Clark, Jake M Stout, Jonathan E Page. Separation of isomeric short-chain acyl-CoAs in plant matrices using ultra-performance liquid chromatography coupled with tandem mass spectrometry.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.
2015 Feb; 980(?):1-7. doi:
10.1016/j.jchromb.2014.12.007
. [PMID: 25553535] - Luis Morales-Quintana, María Ximena Nuñez-Tobar, María Alejandra Moya-León, Raúl Herrera. Molecular dynamics simulation and site-directed mutagenesis of alcohol acyltransferase: a proposed mechanism of catalysis.
Journal of chemical information and modeling.
2013 Oct; 53(10):2689-700. doi:
10.1021/ci400409s
. [PMID: 24032548] - Jake M Stout, Zakia Boubakir, Stephen J Ambrose, Randy W Purves, Jonathan E Page. The hexanoyl-CoA precursor for cannabinoid biosynthesis is formed by an acyl-activating enzyme in Cannabis sativa trichomes.
The Plant journal : for cell and molecular biology.
2012 Aug; 71(3):353-65. doi:
10.1111/j.1365-313x.2012.04949.x
. [PMID: 22353623] - Raja Noor Zaliha Raja Abdul Rahman, Iffah Izzati Zakaria, Abu Bakar Salleh, Mahiran Basri. Enzymatic properties and mutational studies of chalcone synthase from Physcomitrella patens.
International journal of molecular sciences.
2012; 13(8):9673-9691. doi:
10.3390/ijms13089673
. [PMID: 22949824] - Hideki Katagiri, Tomoichiro Asano, Tetsuya Yamada, Toshifumi Aoyama, Yasushi Fukushima, Masatoshi Kikuchi, Tatsuhiko Kodama, Yoshitomo Oka. Acyl-coenzyme A dehydrogenases are localized on GLUT4-containing vesicles via association with insulin-regulated aminopeptidase in a manner dependent on its dileucine motif.
Molecular endocrinology (Baltimore, Md.).
2002 May; 16(5):1049-59. doi:
10.1210/mend.16.5.0831
. [PMID: 11981039] - . .
.
. doi:
. [PMID: 12139488]