3,4-Benzphenanthrene (BioDeep_00000012681)
Secondary id: BioDeep_00001868544
代谢物信息卡片
化学式: C18H12 (228.0939)
中文名称: 苯并-3,4-菲
谱图信息:
最多检出来源 Homo sapiens(not specific) 50%
分子结构信息
SMILES: C1=CC=C2C(=C1)C=CC3=C2C4=CC=CC=C4C=C3
InChI: InChI=1S/C18H12/c1-3-7-16-13(5-1)9-11-15-12-10-14-6-2-4-8-17(14)18(15)16/h1-12H
描述信息
D009676 - Noxae > D009153 - Mutagens
同义名列表
数据库引用编号
8 个数据库交叉引用编号
- ChEBI: CHEBI:82292
- KEGG: C19197
- PubChem: 9136
- Metlin: METLIN72925
- CAS: 195-19-7
- PMhub: MS000027006
- PubChem: 124489869
- KNApSAcK: 82292
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)
0 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。
亚细胞结构定位 | 关联基因列表 |
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文献列表
- Zheng Li, Courtney D Sandau, Lovisa C Romanoff, Samuel P Caudill, Andreas Sjodin, Larry L Needham, Donald G Patterson. Concentration and profile of 22 urinary polycyclic aromatic hydrocarbon metabolites in the US population.
Environmental research.
2008 Jul; 107(3):320-31. doi:
10.1016/j.envres.2008.01.013
. [PMID: 18313659] - James Grainger, Wenlin Huang, Donald G Patterson, Wayman E Turner, James Pirkle, Samuel P Caudill, Richard Y Wang, Larry L Needham, Eric J Sampson. Reference range levels of polycyclic aromatic hydrocarbons in the US population by measurement of urinary monohydroxy metabolites.
Environmental research.
2006 Mar; 100(3):394-423. doi:
10.1016/j.envres.2005.06.004
. [PMID: 16225859] - Xu Xu, Junfeng Zhang, Lin Zhang, Weili Liu, Clifford P Weisel. Selective detection of monohydroxy metabolites of polycyclic aromatic hydrocarbons in urine using liquid chromatography/triple quadrupole tandem mass spectrometry.
Rapid communications in mass spectrometry : RCM.
2004; 18(19):2299-308. doi:
10.1002/rcm.1625
. [PMID: 15384151] - Haruhiko Yagi, Andagar R Ramesha, Govind Kalena, Jane M Sayer, Subodh Kumar, Donald M Jerina. Novel stereoselective control over cis vs trans opening of benzo[c]phenanthrene 3,4-diol 1,2-epoxides by the exocyclic N(2)-amino group of deoxyguanosine in the presence of hexafluoropropan-2-ol.
The Journal of organic chemistry.
2002 Sep; 67(19):6678-89. doi:
10.1021/jo020418a
. [PMID: 12227797] - Donghui Li, Mianying Wang, Pervez Firoz Firozi, Ping Chang, Weiqing Zhang, Wanda Baer-Dubowska, Bhagavatula Moorthy, Suryanarayana V Vulimiri, Regine Goth-Goldstein, Eric H Weyand, John DiGiovanni. Characterization of a major aromatic DNA adduct detected in human breast tissues.
Environmental and molecular mutagenesis.
2002; 39(2-3):193-200. doi:
10.1002/em.10063
. [PMID: 11921189] - Christopher J Smith, Wenlin Huang, Charisse J Walcott, Wayman Turner, James Grainger, Donald G Patterson. Quantification of monohydroxy-PAH metabolites in urine by solid-phase extraction with isotope dilution-GC-MS.
Analytical and bioanalytical chemistry.
2002 Jan; 372(1):216-20. doi:
10.1007/s00216-001-1123-8
. [PMID: 11939197] - P Ilankumaran, L K Pannell, P Gebreselassie, A S Pilcher, H Yagi, J M Sayer, D M Jerina. Patterns of resistance to exonuclease digestion of oligonucleotides containing polycyclic aromatic hydrocarbon diol epoxide adducts at N6 of deoxyadenosine.
Chemical research in toxicology.
2001 Sep; 14(9):1330-8. doi:
10.1021/tx010092l
. [PMID: 11559050] - S R Vepachedu, N Ya, H Yagi, J M Sayer, D M Jerina. Marked differences in base selectivity between DNA and the free nucleotides upon adduct formation from Bay- and Fjord-region diol epoxides.
Chemical research in toxicology.
2000 Sep; 13(9):883-90. doi:
10.1021/tx000073w
. [PMID: 10995261] - V M Runge, J A Clanton, W A Herzer, S J Gibbs, A C Price, C L Partain, A E James. Intravascular contrast agents suitable for magnetic resonance imaging.
Radiology.
1984 Oct; 153(1):171-6. doi:
10.1148/radiology.153.1.6433402
. [PMID: 6433402]