Cernuine (BioDeep_00000001077)
Secondary id: BioDeep_00000641031
human metabolite PANOMIX_OTCML-2023
代谢物信息卡片
化学式: C15H10O6 (286.0477)
中文名称: 噢弄斯定, 金鱼草素
谱图信息:
最多检出来源 Viridiplantae(plant) 19.78%
分子结构信息
SMILES: C1=CC(=C(C=C1C=C2C(=O)C3=C(C=C(C=C3O2)O)O)O)O
InChI: InChI=1S/C15H10O6/c16-8-5-11(19)14-12(6-8)21-13(15(14)20)4-7-1-2-9(17)10(18)3-7/h1-6,16-19H/b13-4+
描述信息
Aureusidin is a hydroxyaurone that is aurone substituted by hydroxy groups at positions 4, 6, 3 and 4 respectively. It has a role as a plant metabolite. It is functionally related to an aurone. It is a conjugate acid of an aureusidin-6-olate.
Aureusidin is a natural product found in Eleocharis dulcis, Eleocharis pallens, and other organisms with data available.
Cernuine is found in citrus. Cernuine is isolated from Citrus medica (citron).
Isolated from Citrus medica (citron). Cernuine is found in lemon and citrus.
Aureusidin is an aurone with high antioxidant and lipoxygenase inhibitory activity. Aureusidin also shows anti-inflammatory effects[1].
Aureusidin is an aurone with high antioxidant and lipoxygenase inhibitory activity. Aureusidin also shows anti-inflammatory effects[1].
Aureusidin is an aurone with high antioxidant and lipoxygenase inhibitory activity. Aureusidin also shows anti-inflammatory effects[1].
同义名列表
23 个代谢物同义名
(2E)-2-[(3,4-dihydroxyphenyl)methylidene]-4,6-dihydroxy-2,3-dihydro-1-benzofuran-3-one; (2Z)-2-[(3,4-dihydroxyphenyl)methylidene]-4,6-dihydroxy-2,3-dihydro-1-benzofuran-3-one; (2Z)-2-((3,4-DIHYDROXYPHENYL)METHYLENE)-4,6-DIHYDROXY-3(2H)-BENZOFURANONE (ACI); (2Z)-2-[(3,4-dihydroxyphenyl)methylidene]-4,6-dihydroxy-1-benzofuran-3(2H)-one; 3(2H)-BENZOFURANONE, 2-((3,4-DIHYDROXYPHENYL)METHYLENE)-4,6-DIHYDROXY-, (Z)-; (2E)-2-[(3,4-dihydroxyphenyl)methylidene]-4,6-dihydroxy-1-benzofuran-3-one; (2Z)-2-[(3,4-dihydroxyphenyl)methylidene]-4,6-dihydroxy-1-benzofuran-3-one; (2Z)-2-[(3,4-dihydroxyphenyl)methylene]-4,6-dihydroxy-3(2H)-benzofuranone; 4,6-Dihydroxy-2-[(3,4-dihydroxyphenyl)methylene]-3(2H)-benzofuranone, 9ci; (2Z)-2-[(3,4-dihydroxyphenyl)methylene]-4,6-dihydroxy-benzofuran-3-one; 2-(3,4-Dihydroxybenzylidene)-4,6-dihydroxybenzofuran-3(2H)-one; (Z)-4,6,3,4-TETRAHYDROXYAURONE; WBEFUVAYFSOUEA-PQMHYQBVSA-N; 4,6,3,4-Tetrahydroxyaurone; UNII-U8B4XHN2DX; AUREUSIDIN(RG); LMPK12130041; Auresudidin; U8B4XHN2DX; Aureusidin; Cernuine; Cernuin; Aureusidin
数据库引用编号
23 个数据库交叉引用编号
- ChEBI: CHEBI:18149
- KEGG: C08576
- PubChem: 5281220
- PubChem: 6123196
- PubChem: 193757
- HMDB: HMDB0034150
- Metlin: METLIN52456
- ChEMBL: CHEMBL593229
- Wikipedia: Aureusidin
- MeSH: aureusidin
- ChemIDplus: 0038216545
- KNApSAcK: C00008027
- foodb: FDB012432
- chemspider: 11284214
- CAS: 38216-54-5
- CAS: 480-70-6
- medchemexpress: HY-N9834
- PMhub: MS000020027
- PubChem: 10769
- LipidMAPS: LMPK12130041
- 3DMET: B02234
- NIKKAJI: J37.389C
- KNApSAcK: 18149
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)
70 个相关的物种来源信息
- 76410 - Actinoscirpus grossus: 10.1016/S0031-9422(00)84889-X
- 2607214 - Anthelepis paludosa: 10.1016/S0031-9422(00)84889-X
- 2607223 - Anthelepis undulata: 10.1016/S0031-9422(00)84889-X
- 4151 - Antirrhinum majus: 10.1016/0003-9861(54)90206-4
- 4151 - Antirrhinum majus: 10.1016/S0168-9452(00)00385-X
- 269566 - Bulbostylis barbata: 10.1016/S0031-9422(00)84889-X
- 269567 - Bulbostylis densa: 10.1016/S0031-9422(00)84889-X
- 2759440 - Bulbostylis humilis: 10.1016/S0031-9422(00)84889-X
- 224677 - Carpha nivicola: 10.1016/S0031-9422(00)84889-X
- 1914789 - Caustis blakei: 10.1016/S0031-9422(00)84889-X
- 76426 - Caustis dioica: 10.1016/S0031-9422(00)84889-X
- 224684 - Cyathochaeta diandra: 10.1016/S0031-9422(00)84889-X
- 1287958 - Cyperus aristulatus: 10.1016/S0031-9422(00)84889-X
- 529428 - Cyperus capitatus: 10.1016/S0031-9422(97)00035-6
- 180965 - Cyperus congestus: 10.1016/S0031-9422(00)84889-X
- 388567 - Cyperus iria: 10.1016/S0031-9422(00)84889-X
- 76471 - Cyperus leptocarpus: 10.1016/S0031-9422(00)84889-X
- 679958 - Eleocharis brassii: 10.1016/S0031-9422(00)84889-X
- 269574 - Eleocharis cylindrostachys: 10.1016/S0031-9422(00)84889-X
- 110284 - Eleocharis dulcis: 10.1016/S0031-9422(00)84889-X
- 110296 - Eleocharis pallens: 10.1016/S0031-9422(00)84889-X
- 372386 - Eleocharis sphacelata: 10.1016/S0031-9422(00)84889-X
- 306622 - Evandra aristata: 10.1016/S0031-9422(00)84889-X
- 241637 - Exocarya sclerioides: 10.1016/S0031-9422(00)84889-X
- 372387 - Ficinia nodosa: 10.1016/S0031-9422(00)84889-X
- 269577 - Fimbristylis bisumbellata: 10.1016/S0031-9422(00)84889-X
- 269578 - Fimbristylis cephalophora: 10.1016/S0031-9422(00)84889-X
- 76444 - Fimbristylis dichotoma: 10.1016/S0031-9422(00)84889-X
- 269583 - Fimbristylis ferruginea: 10.1016/S0031-9422(00)84889-X
- 269589 - Fimbristylis nutans: 10.1016/S0031-9422(00)84889-X
- 269556 - Fimbristylis pachyptera: 10.1016/S0031-9422(00)84889-X
- 46329 - Gahnia deusta: 10.1016/S0031-9422(00)84889-X
- 1651857 - Gahnia radula: 10.1016/S0031-9422(00)84889-X
- 224686 - Gahnia sieberiana: 10.1016/S0031-9422(00)84889-X
- 9606 - Homo sapiens: -
- 35883 - Ipomoea nil: 10.1016/S0031-9422(00)90588-0
- 130947 - Isolepis humillima: 10.1016/S0031-9422(00)84889-X
- 130949 - Isolepis inundata: 10.1016/S0031-9422(00)84889-X
- 2814769 - Isolepis nigricans: 10.1016/S0031-9422(00)84889-X
- 130956 - Isolepis prolifera: 10.1016/S0031-9422(00)84889-X
- 372397 - Lepidosperma laterale: 10.1016/S0031-9422(00)84889-X
- 76469 - Lepironia articulata: 10.1016/S0031-9422(00)84889-X
- 2607219 - Mesomelaena graciliceps: 10.1016/S0031-9422(00)84889-X
- 76477 - Mesomelaena pseudostygia: 10.1016/S0031-9422(00)84889-X
- 224689 - Oreobolus distichus: 10.1016/S0031-9422(00)84889-X
- 224690 - Oreobolus pumilio: 10.1016/S0031-9422(00)84889-X
- 33090 - Plants: -
- 224702 - Ptilothrix deusta: 10.1016/S0031-9422(00)84889-X
- 140888 - Schoenoplectiella dissachantha: 10.1016/S0031-9422(00)84889-X
- 316505 - Schoenoplectiella mucronata: 10.1016/S0031-9422(00)84889-X
- 372400 - Schoenus apogon: 10.1016/S0031-9422(00)84889-X
- 2607220 - Schoenus brevisetis: 10.1016/S0031-9422(00)84889-X
- 882628 - Schoenus calostachyus: 10.1016/S0031-9422(00)84889-X
- 1914811 - Schoenus ericetorum: 10.1016/S0031-9422(00)84889-X
- 1914812 - Schoenus falcatus: 10.1016/S0031-9422(00)84889-X
- 372405 - Schoenus fluitans: 10.1016/S0031-9422(00)84889-X
- 224695 - Schoenus paludosus: 10.1016/S0031-9422(00)84889-X
- 1914834 - Schoenus scabripes: 10.1016/S0031-9422(00)84889-X
- 1914836 - Schoenus sesquispiculus: 10.1016/S0031-9422(00)84889-X
- 1914837 - Schoenus sparteus: 10.1016/S0031-9422(00)84889-X
- 1914838 - Schoenus subaphyllus: 10.1016/S0031-9422(00)84889-X
- 1914843 - Schoenus submicrostachyus: 10.1016/S0031-9422(00)84889-X
- 1914845 - Schoenus unispiculatus: 10.1016/S0031-9422(00)84889-X
- 1735510 - Scleria mackaviensis: 10.1016/S0031-9422(00)84889-X
- 1735542 - Scleria sphacelata: 10.1016/S0031-9422(00)84889-X
- 2812738 - Tricostularia compressa: 10.1016/S0031-9422(00)84889-X
- 1914849 - Tricostularia neesii: 10.1016/S0031-9422(00)84889-X
- 224700 - Tricostularia pauciflora: 10.1016/S0031-9422(00)84889-X
- 53742 - Zinnia angustifolia: 10.1016/S0031-9422(00)97685-4
- 34245 - Zinnia elegans: 10.1016/S0031-9422(00)97685-4
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
- Roshani Shakya, Jingsong Ye, Caius M Rommens. Altered leaf colour is associated with increased superoxide-scavenging activity in aureusidin-producing transgenic plants.
Plant biotechnology journal.
2012 Dec; 10(9):1046-55. doi:
10.1111/j.1467-7652.2012.00732.x
. [PMID: 22924954] - M Jiménez-Atiénzar, M Pérez-Gilabert, J Cabanes, J Escribano, F Gandía-Herrero, F García-Carmona. A continuous spectrophotometric assay for determination of the aureusidin synthase activity of tyrosinase.
Phytochemical analysis : PCA.
2010 May; 21(3):273-8. doi:
10.1002/pca.1197
. [PMID: 20029997] - Anastasia Detsi, Maya Majdalani, Christos A Kontogiorgis, Dimitra Hadjipavlou-Litina, Panagiotis Kefalas. Natural and synthetic 2'-hydroxy-chalcones and aurones: synthesis, characterization and evaluation of the antioxidant and soybean lipoxygenase inhibitory activity.
Bioorganic & medicinal chemistry.
2009 Dec; 17(23):8073-85. doi:
10.1016/j.bmc.2009.10.002
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