8-Anilino-1-naphthalene sulfonate (BioDeep_00000001607)
human metabolite
代谢物信息卡片
1-Anilino-8-naphthalenesulfonate, monoammonium salt, hemihydrate
化学式: C16H13NO3S (299.0616)
中文名称: 8-苯胺-1-萘磺酸
谱图信息:
最多检出来源 Mus musculus(not specific) 10.08%
分子结构信息
SMILES: c(c3)ccc(c3)Nc(c2)c(c(cc2)1)c(ccc1)S(O)(=O)=O
InChI: InChI=1S/C16H13NO3S/c18-21(19,20)15-11-5-7-12-6-4-10-14(16(12)15)17-13-8-2-1-3-9-13/h1-11,17H,(H,18,19,20)
描述信息
8-Anilino-1-naphthalene sulfonate belongs to the class of organic compounds known as 1-naphthalene sulfonic acids and derivatives. These are organic aromatic compounds that contain a naphthalene moiety that carries a sulfonic acid group (or a derivative thereof) at the 1-position. Naphthalene is a bicyclic compound that is made up of two fused benzene ring.
KEIO_ID A177
同义名列表
34 个代谢物同义名
1-Anilino-8-naphthalenesulfonate, monoammonium salt, hemihydrate; 1-Anilino-8-naphthalenesulfonate, monoammonium salt; 1-Anilino-8-naphthalenesulfonate, magnesium (2:1); 1-Anilino-8-naphthalenesulfonate, monosodium salt; 1-Anilino-8-naphthalenesulfonate, 3H-labeled; 1-(Phenylamino)-8-naphthalenesulphonic acid; 8-(phenylamino)-1-naphthalenesulfonic acid; 8-(phenylamino)naphthalene-1-sulfonic acid; 1-(Phenylamino)-8-naphthalenesulfonic acid; 1-Anilino-8-naphthalenesulfonate, ion(1-); 1-(Phenylamino)-8-naphthalenesulphonate; 1-ANILINO-8-naphthalene sulphonic acid; 8-Anilino-1-naphthalene sulphonic acid; 1-(Phenylamino)-8-naphthalenesulfonate; 8-Anilinonaphthalene-1-sulphonic acid; 8-Anilino-1-naphthalene sulfonic acid; 1-Anilino-8-naphthalenesulphonic acid; 1-ANILINO-8-naphthalene sulfonic acid; 1-Anilinonaphthalene-8-sulfonic acid; 1-Anilino-8-naphthalenesulfonic acid; 8-Anilino-1-naphthalenesulfonic acid; 8-Anilinonaphthalene-1-sulfonic acid; 1-ANILINO-8-naphthalene sulphonate; 8-Anilino-1-naphthalene sulphonate; 1-ANILINO-8-naphthalene sulfonATE; 1-Anilino-8-naphthalenesulphonate; 8-Anilino-1-naphthalene sulfonate; 8-Anilinonaphthalene-1-sulphonate; 8-Anilinonaphthalene-1-sulfonate; 1-Anilino-8-naphthalenesulfonate; phenyl-peri acid; 1,8-ANS; ANS; 8-Anilino-1-naphthalene sulfonic acid
数据库引用编号
21 个数据库交叉引用编号
- ChEBI: CHEBI:39708
- KEGG: C11326
- PubChem: 1369
- HMDB: HMDB0061854
- Metlin: METLIN64696
- DrugBank: DB04474
- ChEMBL: CHEMBL285527
- Wikipedia: 8-Anilinonaphthalene-1-sulfonic_acid
- CAS: 82-76-8
- MoNA: KO000276
- MoNA: KO000274
- MoNA: KO000275
- MoNA: KO000273
- MoNA: KO000277
- PMhub: MS000000846
- PubChem: 13501
- PDB-CCD: 2AN
- NIKKAJI: J4.618C
- KNApSAcK: 39708
- LOTUS: LTS0262153
- wikidata: Q4644260
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)
2 个相关的物种来源信息
- 9606 - Homo sapiens: -
- 9606 - Homo sapiens: 10.1007/S11306-012-0464-Y
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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Molecules (Basel, Switzerland).
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Acta crystallographica. Section D, Structural biology.
2020 Jul; 76(Pt 7):653-667. doi:
10.1107/s2059798320006841. [PMID: 32627738] - Stephen Boulton, Rajeevan Selvaratnam, Rashik Ahmed, Katherine Van, Xiaodong Cheng, Giuseppe Melacini. Mechanisms of Specific versus Nonspecific Interactions of Aggregation-Prone Inhibitors and Attenuators.
Journal of medicinal chemistry.
2019 05; 62(10):5063-5079. doi:
10.1021/acs.jmedchem.9b00258. [PMID: 31074269] - Priya Singh, Susobhan Choudhury, V K Sharma, S Mitra, R Mukhopadhyay, Ranjan Das, Samir Kumar Pal. Modulation of Solvation and Molecular Recognition of a Lipid Bilayer under Dynamical Phase Transition.
Chemphyschem : a European journal of chemical physics and physical chemistry.
2018 10; 19(20):2709-2716. doi:
10.1002/cphc.201800522. [PMID: 30030893] - Maithili Deshpande, S K Sathe. Interactions with 8-Anilinonaphthalene-1-sulfonic Acid (ANS) and Surface Hydrophobicity of Black Gram (Vigna mungo) Phaseolin.
Journal of food science.
2018 Jul; 83(7):1847-1855. doi:
10.1111/1750-3841.14204. [PMID: 29928765] - Jie-Hua Shi, Yan-Yue Lou, Kai-Li Zhou, Dong-Qi Pan. Elucidation of intermolecular interaction of bovine serum albumin with Fenhexamid: A biophysical prospect.
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Journal of biomedical science.
2011 Jan; 18(?):4. doi:
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PloS one.
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Nutrients.
2011 01; 3(1):152-63. doi:
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Journal of environmental sciences (China).
2011; 23(2):315-21. doi:
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Journal of lipid research.
2011 Jan; 52(1):35-44. doi:
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PloS one.
2011; 6(11):e27037. doi:
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Protein science : a publication of the Protein Society.
2011 Jan; 20(1):42-50. doi:
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PloS one.
2011; 6(12):e28982. doi:
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Biochemistry research international.
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PloS one.
2011; 6(12):e29576. doi:
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Journal of lipids.
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Biochimica et biophysica acta.
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Journal of photochemistry and photobiology. B, Biology.
2010 Jul; 100(1):30-7. doi:
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Archives of biochemistry and biophysics.
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Journal of experimental botany.
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Analytical biochemistry.
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International journal of radiation biology.
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Journal of experimental botany.
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Archives of pharmacal research.
2010 May; 33(5):737-44. doi:
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Protein and peptide letters.
2010 May; 17(5):660-6. doi:
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Biochemistry.
2010 Mar; 49(10):2256-68. doi:
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Biochemistry. Biokhimiia.
2010 Mar; 75(3):367-74. doi:
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Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy.
2010 Mar; 75(3):1088-94. doi:
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Journal of fluorescence.
2010 Mar; 20(2):441-52. doi:
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Nutrients.
2010 02; 2(2):181-97. doi:
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PloS one.
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Biophysical journal.
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International journal of biological macromolecules.
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Organic & biomolecular chemistry.
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Drug metabolism and disposition: the biological fate of chemicals.
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Biochimie.
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Physical chemistry chemical physics : PCCP.
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Human molecular genetics.
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