furoic acid (BioDeep_00001868700)
Main id: BioDeep_00000002914
BioNovoGene_Lab2019
代谢物信息卡片
L-Cysteic acid
化学式: C3H7NO5S (169.0045)
中文名称: 磺基丙氨酸, L-磺基丙氨酸 一水合物, L-磺基丙氨酸
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: C(C(C(=O)O)N)S(=O)(=O)O
InChI: InChI=1S/C3H7NO5S/c4-2(3(5)6)1-10(7,8)9/h2H,1,4H2,(H,5,6)(H,7,8,9)/t2-/m0/s1
描述信息
The L-enantiomer of cysteic acid.
同义名列表
4 个代谢物同义名
数据库引用编号
15 个数据库交叉引用编号
- ChEBI: CHEBI:17285
- KEGG: C00506
- KEGGdrug: D81957
- PubChem: 72886
- DrugBank: DB03661
- MeSH: Cysteic Acid
- CAS: 498-40-8
- MetaboLights: MTBLC17285
- PubChem: 3789
- CAS: 13100-82-8
- PDB-CCD: OCS
- 3DMET: B01274
- NIKKAJI: J8.084E
- BioNovoGene_Lab2019: BioNovoGene_Lab2019-190
- KNApSAcK: 17285
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)
16 个相关的物种来源信息
- 90345 - Abies balsamea: 10.1016/S0021-9673(01)97854-9
- 7461 - Apis cerana: 10.1371/JOURNAL.PONE.0175573
- 5111 - Claviceps purpurea: 10.1055/S-0028-1100051
- 3039 - Euglena gracilis: 10.3389/FBIOE.2021.662655
- 9606 - Homo sapiens: 10.1007/S11306-016-1051-4
- 244307 - Juniperus communis var. communis: 10.1016/S0021-9673(01)97854-9
- 466205 - Juniperus scopulorum: 10.1016/S0021-9673(01)97854-9
- 3330 - Picea glauca: 10.1016/S0021-9673(01)97854-9
- 3335 - Picea mariana: 10.1016/S0021-9673(01)97854-9
- 3331 - Picea pungens: 10.1016/S0021-9673(01)97854-9
- 3339 - Pinus contorta: 10.1016/S0021-9673(01)97854-9
- 55062 - Pinus ponderosa: 10.1016/S0021-9673(01)97854-9
- 3357 - Pseudotsuga menziesii: 10.1016/S0021-9673(01)97854-9
- 5297 - Puccinia graminis: 10.1139/V60-033
- 3359 - Tsuga heterophylla: 10.1016/S0021-9673(01)97854-9
- 29760 - Vitis vinifera: 10.1016/J.DIB.2020.106469
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
- Xiao-Lin Li, Jing Yu, Li Liu. Poly[bis-(μ(7)-3-sulfonato-l-alaninato)sodiumzinc].
Acta crystallographica. Section E, Structure reports online.
2012 Jun; 68(Pt 6):m849. doi:
10.1107/s160053681202394x. [PMID: 22719385] - Monika Janczarek, Jolanta Kutkowska, Tomasz Piersiak, Anna Skorupska. Rhizobium leguminosarum bv. trifolii rosR is required for interaction with clover, biofilm formation and adaptation to the environment.
BMC microbiology.
2010 Nov; 10(?):284. doi:
10.1186/1471-2180-10-284. [PMID: 21070666] - Sorin J Brull, Mohamed Naguib. Selective reversal of muscle relaxation in general anesthesia: focus on sugammadex.
Drug design, development and therapy.
2009 Sep; 3(?):119-29. doi:
10.2147/dddt.s3868. [PMID: 19920928] - Alessia Farinazzo, Elisa Fasoli, Alexander V Kravchuk, Giovanni Candiano, Giancarlo Aldini, Luca Regazzoni, Pier Giorgio Righetti. En bloc elution of proteomes from combinatorial peptide ligand libraries.
Journal of proteomics.
2009 May; 72(4):725-30. doi:
10.1016/j.jprot.2009.02.009. [PMID: 19269355] - Sarah T Pruett, Anatoliy Bushnev, Kerri Hagedorn, Madhura Adiga, Christopher A Haynes, M Cameron Sullards, Dennis C Liotta, Alfred H Merrill. Biodiversity of sphingoid bases ('sphingosines') and related amino alcohols.
Journal of lipid research.
2008 Aug; 49(8):1621-39. doi:
10.1194/jlr.r800012-jlr200. [PMID: 18499644] - Hiroto Tanamachi, Yoshimasa Okamoto, Natsumi Fujiwara, Hisashi Tsujimura, Junko Sonoda, Satoru Naito, Yoshiya Sugai. Prevention effects of lipid-related materials on human hair damage progress.
Journal of cosmetic science.
2004; 55 Suppl(?):S171-3. doi:
". [PMID: 15645093] - M J Croucher, L S Thomas, H Ahmadi, V Lawrence, J R Harris. Endogenous sulphur-containing amino acids: potent agonists at presynaptic metabotropic glutamate autoreceptors in the rat central nervous system.
British journal of pharmacology.
2001 Jul; 133(6):815-24. doi:
10.1038/sj.bjp.0704138. [PMID: 11454654] - C R Santhosh-Kumar, J C Deutsch, J C Kolhouse, K L Hassell, J F Kolhouse. Measurement of excitatory sulfur amino acids, cysteine sulfinic acid, cysteic acid, homocysteine sulfinic acid, and homocysteic acid in serum by stable isotope dilution gas chromatography-mass spectrometry and selected ion monitoring.
Analytical biochemistry.
1994 Aug; 220(2):249-56. doi:
10.1006/abio.1994.1335. [PMID: 7978266] - L Gorski, E R Leadbetter, W Godchaux. Temporal sequence of the recovery of traits during phenotypic curing of a Cytophaga johnsonae motility mutant.
Journal of bacteriology.
1991 Dec; 173(23):7534-9. doi:
10.1128/jb.173.23.7534-7539.1991. [PMID: 1938948] - S D Gupta, P S Sastry. The biosynthesis of sulfoquinovosyldiacylglycerol: studies with groundnut (Arachis hypogaea) leaves.
Archives of biochemistry and biophysics.
1988 Jan; 260(1):125-33. doi:
10.1016/0003-9861(88)90432-8. [PMID: 3341737] - R H White. Biosynthesis of the sulfonolipid 2-amino-3-hydroxy-15-methylhexadecane-1-sulfonic acid in the gliding bacterium Cytophaga johnsonae.
Journal of bacteriology.
1984 Jul; 159(1):42-6. doi:
10.1128/jb.159.1.42-46.1984. [PMID: 6330048] - D S Gilbert. Axoplasm chemical composition in Myxicola and solubility properties of its structural proteins.
The Journal of physiology.
1975 Dec; 253(1):303-19. doi:
10.1113/jphysiol.1975.sp011191. [PMID: 1260] - J L Harwood. Synthesis of sulphoquinovosyl diacylglycerol by higher plants.
Biochimica et biophysica acta.
1975 Aug; 398(2):224-30. doi:
10.1016/0005-2760(75)90138-1. [PMID: 1182135]
