2-Deoxy-5-Guanylic Acid (BioDeep_00000398682)
Main id: BioDeep_00000001331
natural product PANOMIX_OTCML-2023 BioNovoGene_Lab2019
代谢物信息卡片
化学式: C10H14N5O7P (347.0631)
中文名称: 2-脱氧-5-鸟苷酸
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: C1C(C(OC1N2C=NC3=C2N=C(NC3=O)N)COP(=O)(O)O)O
InChI: InChI=1S/C10H14N5O7P/c11-10-13-8-7(9(17)14-10)12-3-15(8)6-1-4(16)5(22-6)2-21-23(18,19)20/h3-6,16H,1-2H2,(H2,18,19,20)(H3,11,13,14,17)
描述信息
COVID info from COVID-19 Disease Map
Corona-virus
Coronavirus
SARS-CoV-2
COVID-19
SARS-CoV
COVID19
SARS2
SARS
relative retention time with respect to 9-anthracene Carboxylic Acid is 0.057
relative retention time with respect to 9-anthracene Carboxylic Acid is 0.055
同义名列表
7 个代谢物同义名
[5-(2-amino-6-oxo-3H-purin-9-yl)-3-hydroxyoxolan-2-yl]methyl dihydrogen phosphate; 2-Deoxy-5-Guanylic Acid; 2-Deoxyguanosine 5-phosphate; [(2R,5R)-5-(2-Amino-6-oxo-1H-purin-9-yl)-3-hydroxyoxolan-2-yl]methyl dihydrogen phosphate; 2-Deoxyguanosine 5-monophosphate; 2-deoxyguanosine 5-monophosphate sodium salt hydrate; dGMP
数据库引用编号
22 个数据库交叉引用编号
- ChEBI: CHEBI:182849
- ChEBI: CHEBI:16192
- KEGG: C00362
- PubChem: 135402021
- PubChem: 135398597
- PubChem: 135925427
- DrugBank: DB04457
- ChEMBL: CHEMBL477487
- CAS: 902-04-5
- MoNA: HMDB0001044_ms_ms_1396
- MoNA: PT204800
- MoNA: PT104800
- MoNA: BML80266
- MoNA: BML80265
- PubChem: 3653
- KNApSAcK: C00019356
- PDB-CCD: DG
- PDB-CCD: DGP
- 3DMET: B01228
- NIKKAJI: J195.198J
- BioNovoGene_Lab2019: BioNovoGene_Lab2019-185
- KNApSAcK: 16192
分类词条
相关代谢途径
Reactome(0)
BioCyc(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)
2 个相关的物种来源信息
- 9606 - Homo sapiens: 10.1007/S11306-016-1051-4
- 5665 - Leishmania mexicana: 10.1016/J.IJPDDR.2019.05.003
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
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Inorganic chemistry.
2018 May; 57(10):6124-6134. doi:
10.1021/acs.inorgchem.8b00713
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Acta biomaterialia.
2015 May; 18(?):68-76. doi:
10.1016/j.actbio.2015.02.009
. [PMID: 25707922] - Michael Groessl, Christian G Hartinger, Kasia Połeć-Pawlak, Maciej Jarosz, Paul J Dyson, Bernhard K Keppler. Elucidation of the interactions of an anticancer ruthenium complex in clinical trials with biomolecules utilizing capillary electrophoresis hyphenated to inductively coupled plasma-mass spectrometry. Short communication.
Chemistry & biodiversity.
2008 Aug; 5(8):1609-1614. doi:
10.1002/cbdv.200890148
. [PMID: 18729095] - Michael Groessl, Christian G Hartinger, Paul J Dyson, Bernhard K Keppler. CZE-ICP-MS as a tool for studying the hydrolysis of ruthenium anticancer drug candidates and their reactivity towards the DNA model compound dGMP.
Journal of inorganic biochemistry.
2008 May; 102(5-6):1060-5. doi:
10.1016/j.jinorgbio.2007.11.018
. [PMID: 18222004] - Chun Hung Ma, Joannie Hui, Janet Tsui Ying Tang, Danny Tze Ming Leung, Yiu Loon Chui, Tai Fai Fok, Pak-Leong Lim. Antibodies to guanosine triphosphate misidentified as anti-double-stranded DNA antibodies in a patient with antinuclear antibody-negative lupus, due to buckling of insolubilized assay DNA.
Arthritis and rheumatism.
2004 May; 50(5):1533-8. doi:
10.1002/art.20188
. [PMID: 15146423] - S Obrecht-Pflumio, G Dirheimer. Horseradish peroxidase mediates DNA and deoxyguanosine 3'-monophosphate adduct formation in the presence of ochratoxin A.
Archives of toxicology.
2001 Dec; 75(10):583-90. doi:
10.1007/s00204-001-0289-3
. [PMID: 11808918] - Y M Li, Z H Han, S H Jiang, Y Jiang, S D Yao, D Y Zhu. Fast repairing of oxidized OH radical adducts of dAMP and dGMP by phenylpropanoid glycosides from Scrophularia ningpoensis Hemsl.
Acta pharmacologica Sinica.
2000 Dec; 21(12):1125-8. doi:
. [PMID: 11603287]
- S Obrecht-Pflumio, G Dirheimer. In vitro DNA and dGMP adducts formation caused by ochratoxin A.
Chemico-biological interactions.
2000 Jun; 127(1):29-44. doi:
10.1016/s0009-2797(00)00169-1
. [PMID: 10903417] - Q Cai, L Tian, H Wei. Age-dependent increase of indigenous DNA adducts in rat brain is associated with a lipid peroxidation product.
Experimental gerontology.
1996 May; 31(3):373-85. doi:
10.1016/0531-5565(95)02027-6
. [PMID: 9415120] - A C Povey, V L Wilson, J L Zweier, P Kuppusamy, I K O'Neill, C C Harris. Detection by 32P-postlabelling of DNA adducts induced by free radicals and unsaturated aldehydes formed during the aerobic decomposition of fecapentaene-12.
Carcinogenesis.
1992 Mar; 13(3):395-401. doi:
10.1093/carcin/13.3.395
. [PMID: 1547529] - S Y Shiue, J C Hsieh, J Ito. Mapping of the DNA linking tyrosine residue of the PRD1 terminal protein.
Nucleic acids research.
1991 Jul; 19(14):3805-10. doi:
10.1093/nar/19.14.3805
. [PMID: 1861973] - J G Liehr, B B DaGue, A M Ballatore. Reactivity of 4',4"-diethylstilbestrol quinone, a metabolic intermediate of diethylstilbestrol.
Carcinogenesis.
1985 Jun; 6(6):829-36. doi:
10.1093/carcin/6.6.829
. [PMID: 4006069]