Catechin C (BioDeep_00000621567)
Main id: BioDeep_00000000763
PANOMIX_OTCML-2023
代谢物信息卡片
化学式: C15H14O6 (290.079)
中文名称: (+)-表儿茶素
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O
InChI: InChI=1S/C15H14O6/c16-8-4-11(18)9-6-13(20)15(21-14(9)5-8)7-1-2-10(17)12(19)3-7/h1-5,13,15-20H,6H2/t13-,15-/m0/s1
描述信息
C26170 - Protective Agent > C275 - Antioxidant
同义名列表
11 个代谢物同义名
(2S-cis)-2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-Benzopyran-3,5,7-triol; (2S,3S)-2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol; (2S,3S)-3,3',4',5,7-Pentahydroxyflavan; (+)-cis-3,3',4',5,7-Pentahydroxyflavan; (2S,3S)-(+)-Epicatechin; ent-Epicatechin; (+)-Epicatechin; (+)-epicatechol; d-Epicatechin; Catechin C; (+)-Epicatechin
数据库引用编号
13 个数据库交叉引用编号
- ChEBI: CHEBI:76125
- KEGG: C09728
- PubChem: 182232
- Metlin: METLIN92746
- ChEMBL: CHEMBL129482
- CAS: 35323-91-2
- PubChem: 11916
- KNApSAcK: C00000957
- 3DMET: B03227
- NIKKAJI: J21.709C
- LOTUS: LTS0265245
- wikidata: Q23050136
- KNApSAcK: 76125
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)
9 个相关的物种来源信息
- 97723 - Alpinia zerumbet: 10.1021/JF991294E
- 28974 - Averrhoa carambola: 10.1007/S11418-008-0239-Y
- 4270 - Byrsonima crassifolia: 10.1016/0031-9422(94)00934-L
- 233676 - Gambeya perpulchra: 10.3390/MOLECULES15096386
- 392747 - Paullinia cupana: 10.3390/12081950
- 2708928 - Pavetta owariensis: 10.1016/0031-9422(91)84150-Q
- 356281 - Pseudocedrela kotschyi: 10.1021/NP0680230
- 74652 - Rosa laevigata: 10.1271/BBB.80897
- 32250 - Vauquelinia corymbosa: 10.3390/MOLECULES200815330
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
- Yongzhen Pang, I Sarath B Abeysinghe, Ji He, Xianzhi He, David Huhman, K Mudith Mewan, Lloyd W Sumner, Jianfei Yun, Richard A Dixon. Functional characterization of proanthocyanidin pathway enzymes from tea and their application for metabolic engineering.
Plant physiology.
2013 Mar; 161(3):1103-16. doi:
10.1104/pp.112.212050. [PMID: 23288883] - Hassiba Aoudia, Nikoletta Ntalli, Nadhem Aissani, R Yahiaoui-Zaidi, Pierluigi Caboni. Nematotoxic phenolic compounds from Melia azedarach against Meloidogyne incognita.
Journal of agricultural and food chemistry.
2012 Nov; 60(47):11675-80. doi:
10.1021/jf3038874. [PMID: 23136941] - He Zhong Jiang, Xiao Fang Quan, Wei Xi Tian, Jiang Miao Hu, Peng Cheng Wang, Sheng Zhuo Huang, Zhong Quan Cheng, Wen Juan Liang, Jun Zhou, Xiao Feng Ma, You Xing Zhao. Fatty acid synthase inhibitors of phenolic constituents isolated from Garcinia mangostana.
Bioorganic & medicinal chemistry letters.
2010 Oct; 20(20):6045-7. doi:
10.1016/j.bmcl.2010.08.061. [PMID: 20817450] - Ai-Lin Liu, Hai-Di Wang, Simon MingYuen Lee, Yi-Tao Wang, Guan-Hua Du. Structure-activity relationship of flavonoids as influenza virus neuraminidase inhibitors and their in vitro anti-viral activities.
Bioorganic & medicinal chemistry.
2008 Aug; 16(15):7141-7. doi:
10.1016/j.bmc.2008.06.049. [PMID: 18640042] - Peter L Katavic, Kenneth Lamb, Hernan Navarro, Thomas E Prisinzano. Flavonoids as opioid receptor ligands: identification and preliminary structure-activity relationships.
Journal of natural products.
2007 Aug; 70(8):1278-82. doi:
10.1021/np070194x. [PMID: 17685652] - Harsh Pal Bais, Travis S Walker, Alan J Kennan, Frank R Stermitz, Jorge M Vivanco. Structure-dependent phytotoxicity of catechins and other flavonoids: flavonoid conversions by cell-free protein extracts of Centaurea maculosa (spotted knapweed) roots.
Journal of agricultural and food chemistry.
2003 Feb; 51(4):897-901. doi:
10.1021/jf020978a. [PMID: 12568546]
