Methionine sulfoximine (BioDeep_00000003408)
Secondary id: BioDeep_00000400075
human metabolite Endogenous natural product
代谢物信息卡片
化学式: C5H12N2O3S (180.0568602)
中文名称: L-蛋氨酸磺酸盐, 蛋氨酸磺酸, L-蛋氨酸砜亚胺
谱图信息:
最多检出来源 Astragalus membranaceus(plant) 75%
Last reviewed on 2024-09-13.
Cite this Page
Methionine sulfoximine. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China.
https://query.biodeep.cn/s/methionine_sulfoximine (retrieved
2024-11-24) (BioDeep RN: BioDeep_00000003408). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
分子结构信息
SMILES: CS(=N)(=O)CCC(C(=O)O)N
InChI: InChI=1S/C5H12N2O3S/c1-11(7,10)3-2-4(6)5(8)9/h4,7H,2-3,6H2,1H3,(H,8,9)
描述信息
Methionine sulfoximine is found in flours treated with NCl3 as a produced of NCl3 action on wheat protein
同义名列表
23 个代谢物同义名
Butanoic acid, 2-amino-4-(S-methylsulfonimidoyl)- (9ci); 2-amino-4-[imino(methyl)oxo-λ⁶-sulfanyl]butanoic acid; S-(3-Amino-3-carboxypropyl)-S-methylsulfoximine, 9ci; S-(3-Amino-3-carboxypropyl)-S-methyl-DL-sulfoximine; (2S)-2-Amino-4-(S-methylsufonimidoyl)-butanoic acid; L -S-(3-Amino-3-carboxypropyl)-S-methylsulfoximine; 2-Amino-4-(S-methylsulfonimidoyl)-butanoic acid; DL-(3-Amino-3-carboxypropyl) methyl sulfoximine; 2-Amino-4-(S-methylsulphonimidoyl)butyric acid; 2-Amino-4-(S-methylsulfonimidoyl)butanoic acid; 2-Amino-4-(S-methylsulfonimidoyl)butyric acid; 2-Amino-4-(S-methylsulphonimidoyl)butyrate; 2-Amino-4-(S-methylsulfonimidoyl)butyrate; DL-Methionine DL-sulfoximine; DL-Methionine-DL-sulfoximine; L-Methionine-DL-sulfoximine; L-Methionine-RS-sulfoximine; DL-Methionine sulfoximine; L-Methionine sulfoximine; Methionine sulphoximine; METHIONINE SULFOXIMINE; Methionine analog; Methionine sulfoximine
数据库引用编号
22 个数据库交叉引用编号
- ChEBI: CHEBI:28490
- ChEBI: CHEBI:47833
- KEGG: C03510
- PubChem: 16118
- PubChem: 89034
- HMDB: HMDB0029430
- Metlin: METLIN65992
- DrugBank: DB14103
- ChEMBL: CHEMBL1627202
- ChEMBL: CHEMBL1615096
- ChEMBL: CHEMBL143324
- Wikipedia: Methionine sulfoximine
- MeSH: Methionine Sulfoximine
- foodb: FDB000532
- chemspider: 15302
- CAS: 1982-67-8
- PMhub: MS000009626
- PubChem: 6320
- PDB-CCD: MSL
- NIKKAJI: J225.433F
- RefMet: Methionine sulfoximine
- LOTUS: LTS0193763
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)
13 个相关的物种来源信息
- 1237198 - Cnestis: LTS0193763
- 1237199 - Cnestis polyphylla: 10.1016/0378-8741(85)90023-6
- 1237199 - Cnestis polyphylla: LTS0193763
- 25889 - Connaraceae: LTS0193763
- 2759 - Eukaryota: LTS0193763
- 9606 - Homo sapiens: -
- 3398 - Magnoliopsida: LTS0193763
- 85260 - Rourea: LTS0193763
- 1237792 - Rourea orientalis: 10.1016/0378-8741(85)90023-6
- 1237792 - Rourea orientalis: LTS0193763
- 35493 - Streptophyta: LTS0193763
- 58023 - Tracheophyta: LTS0193763
- 33090 - Viridiplantae: LTS0193763
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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Toxicology and applied pharmacology.
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Proceedings of the National Academy of Sciences of the United States of America.
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Laboratory investigation; a journal of technical methods and pathology.
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The Journal of investigative dermatology.
1995 Jun; 104(6):964-9. doi:
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Molecular and biochemical parasitology.
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Comparative biochemistry and physiology. Part C, Pharmacology, toxicology & endocrinology.
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Toxicology.
1995 Apr; 98(1-3):67-72. doi:
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Plant physiology.
1995 Apr; 107(4):1059-66. doi:
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Archives of biochemistry and biophysics.
1995 Feb; 316(2):941-9. doi:
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Kidney international.
1995 Feb; 47(2):395-403. doi:
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Environmental health perspectives.
1995 Feb; 103 Suppl 1(?):85-8. doi:
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The Journal of pharmacology and experimental therapeutics.
1995 Feb; 272(2):484-8. doi:
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Teratogenesis, carcinogenesis, and mutagenesis.
1995; 15(1):33-42. doi:
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Methods in enzymology.
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Research communications in molecular pathology and pharmacology.
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Toxicology.
1994 Nov; 94(1-3):57-67. doi:
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Journal of applied physiology (Bethesda, Md. : 1985).
1994 Nov; 77(5):2177-87. doi:
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Environmental research.
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Drug metabolism and disposition: the biological fate of chemicals.
1994 Nov; 22(6):835-42. doi:
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Nihon Jinzo Gakkai shi.
1994 Oct; 36(10):1082-9. doi:
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Transplantation proceedings.
1994 Oct; 26(5):2912-4. doi:
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International journal of radiation oncology, biology, physics.
1994 Sep; 30(2):373-81. doi:
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Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.).
1994 Sep; 206(4):360-4. doi:
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The Journal of pharmacology and experimental therapeutics.
1994 Sep; 270(3):858-64. doi:
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International journal of pancreatology : official journal of the International Association of Pancreatology.
1994 Aug; 16(1):31-6. doi:
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Kidney international.
1994 Aug; 46(2):388-95. doi:
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Cancer research.
1994 Aug; 54(15):4077-83. doi:
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Pflugers Archiv : European journal of physiology.
1994 Jul; 427(5-6):524-32. doi:
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