L-Canaline (BioDeep_00000000700)
Secondary id: BioDeep_00000871969
human metabolite PANOMIX_OTCML-2023 Endogenous
代谢物信息卡片
化学式: C4H10N2O3 (134.0691)
中文名称: 6-硝基-2-氨苯酚-4-磺酸
谱图信息:
最多检出来源 Viridiplantae(plant) 66.56%
分子结构信息
SMILES: C(CON)C(C(=O)O)N
InChI: InChI=1S/C4H10N2O3/c5-3(4(7)8)1-2-9-6/h3H,1-2,5-6H2,(H,7,8)/t3-/m0/s1
描述信息
L-canaline, also known as L-2-amino-4-(aminooxy)butyric acid, is a member of the class of compounds known as L-alpha-amino acids. L-alpha-amino acids are alpha amino acids which have the L-configuration of the alpha-carbon atom. L-canaline is soluble (in water) and a moderately acidic compound (based on its pKa). L-canaline can be found in a number of food items such as mulberry, rape, grape, and black chokeberry, which makes L-canaline a potential biomarker for the consumption of these food products. L-canaline is a substrate for ornithine aminotransferase resulting in the synthesis of L-ureidohomoserine (the corresponding analog of L-citrulline). In turn, the latter forms L-canavaninosuccinic acid in a reaction mediated by argininosuccinic acid synthetase. L-Canavaninosuccinic acid is cleaved to form L-canavanine by argininosuccinic acid synthetase. By these sequential reactions, the canaline-urea cycle (analogous to the ornithine-urea cycle) is formed. Every time a canavanine molecule runs through the canaline-urea cycle, the two terminal nitrogen atoms are released as urea. Urea is an important by-product of this reaction sequence because it makes ammonicial ammonia (urease-mediated) that is available to support intermediary nitrogen metabolism. L-canaline can by reductively cleaved to L-homoserine, a non-protein amino acid of great importance in the formation of a host of essential amino acids. In this way, the third nitrogen atom of canavanine enters into the reactions of nitrogen metabolism of the plant. As homoserine, its carbon skeleton also finds an important use .
L-canaline is a non-proteinogenic L-alpha-amino acid that is L-homoserine in which the hydroxy group at position 4 is substituted by an aminooxy group. It has been isolated from legumes and plays an essential role in lugume chemical defense against insects. It has a role as a plant metabolite, an antineoplastic agent, an antimetabolite and a phytogenic insecticide. It is functionally related to a L-homoserine. It is a tautomer of a L-canaline zwitterion.
Canavanine reacts with water to produce L-canaline and urea. The reaction is catalyzed by arginase. L-canaline reacts with carbamoyl-phosphate to produce O-ureidohomoserine and phosphate. The reaction is catalyzed by ornithine carbamoyltransferase.
A non-proteinogenic L-alpha-amino acid that is L-homoserine in which the hydroxy group at position 4 is substituted by an aminooxy group. It has been isolated from legumes and plays an essential role in lugume chemical defense against insects.
同义名列表
24 个代谢物同义名
L-alpha-amino-gamma-(aminooxy)-n-butyric acid; .GAMMA.-(AMINOOXY)-.ALPHA.-AMINOBUTYRIC ACID; (2S)-2-amino-4-(aminooxy)butanoic acid; (2S)-2-Amino-4-(aminooxy)butyric acid; (S)-2-Amino-4-(aminooxy)butanoic acid; L-a-amino-g-(aminooxy)-n-butyric acid; (2S)-2-amino-4-aminooxybutanoic acid; (S)-2-Amino-4-(aminooxy)butanoicacid; (2S)-2-Amino-4-(aminooxy)butanoate; L-2-amino-4-(aminooxy)butyric acid; (2S)-2-Amino-4-(aminooxy)butyrate; 2-Amino-4-(aminooxy)butyric acid; 1-amino-3-amino-oxybutyric acid; L-2-Amino-4-(aminooxy)butyrate; FQPGMQABJNQLLF-VKHMYHEASA-N; L-Homoserine, O-amino-; O-Amino-L-homoserine; UNII-T7H2XP1ZNS; L-Canaline base; T7H2XP1ZNS; L-Canaline; Canaline; 2-amino-4-aminooxybutanoic acid; L-Canaline
数据库引用编号
26 个数据库交叉引用编号
- ChEBI: CHEBI:41401
- KEGG: C08270
- PubChem: 441443
- PubChem: 4391006
- HMDB: HMDB0012251
- Metlin: METLIN62888
- DrugBank: DB02821
- ChEMBL: CHEMBL1231652
- Wikipedia: Canaline
- MeSH: canaline
- ChemIDplus: 0000496935
- MetaCyc: L-CANALINE
- KNApSAcK: C00001346
- foodb: FDB030959
- chemspider: 390176
- CAS: 496-93-5
- medchemexpress: HY-129476
- PMhub: MS000019794
- MetaboLights: MTBLC41401
- PubChem: 10469
- PDB-CCD: CAN
- NIKKAJI: J12.573C
- RefMet: L-Canaline
- KNApSAcK: 41401
- LOTUS: LTS0053367
- wikidata: Q5031083
分类词条
相关代谢途径
Reactome(0)
BioCyc(0)
代谢反应
2 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(0)
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(2)
- canavanine degradation:
H+ + L-canaline + NADPH ⟶ L-homoserine + NADP+ + ammonium
- canavanine biosynthesis:
L-canaline + carbamoyl phosphate ⟶ O-ureido-L-homoserine + phosphate
COVID-19 Disease Map(0)
PathBank(0)
PharmGKB(0)
1 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。
文献列表
- J F Risso, J J Montilla. [Flour from seeds of Canavalia ensiformis L (DC), raw, stored in an alkaline medium, autoclaved or extracted, in diets for growing pigs].
Archivos latinoamericanos de nutricion.
1992 Sep; 42(3):268-74. doi:
"
. [PMID: 1342160] - F N Bolkenius, B Knödgen, N Seiler. DL-canaline and 5-fluoromethylornithine. Comparison of two inactivators of ornithine aminotransferase.
The Biochemical journal.
1990 Jun; 268(2):409-14. doi:
10.1042/bj2680409
. [PMID: 2363680] - J N van Balgooy. Separation of canavanine and canaline by high performance liquid chromatography.
Experientia.
1987 Sep; 43(9):1034-7. doi:
10.1007/bf01952232
. [PMID: 3653341] - T K Prasad, M G Cline. Shoot inversion-induced ethylene in Pharbitis nil induces the release of apical dominance by restricting shoot elongation.
Plant science : an international journal of experimental plant biology.
1985; 38(?):163-72. doi:
10.1016/0168-9452(85)90034-2
. [PMID: 11539699] - M Sugii, H Miura, K Nagata. A new radiometric determination of L-canaline.
Analytical biochemistry.
1979 Jan; 92(2):265-9. doi:
10.1016/0003-2697(79)90657-2
. [PMID: 443525]