Hypolaetin (BioDeep_00000007862)

PANOMIX_OTCML-2023

代谢物信息卡片

2-(3,4-dihydroxyphenyl)-5,7,8-trihydroxy-4H-chromen-4-one

化学式: C15H10O7 (302.042651)
中文名称:
谱图信息: 最多检出来源 Astragalus membranaceus(plant) 40%

分子结构信息

SMILES: C1(O)=C(O)C2OC(C3C=CC(O)=C(O)C=3)=CC(=O)C=2C(O)=C1
InChI: InChI=1S/C15H10O7/c16-7-2-1-6(3-8(7)17)12-5-10(19)13-9(18)4-11(20)14(21)15(13)22-12/h1-5,16-18,20-21H

描述信息

A pentahydroxyflavone that consists of luteolin substituted by an additional hydroxy group at position 8.

同义名列表

11 个代谢物同义名

8-Hydroxyluteolin; Hypolaetin; 2-(3,4-dihydroxyphenyl)-5,7,8-trihydroxy-4H-chromen-4-one; 2-(3,4-dihydroxyphenyl)-5,7,8-trihydroxy-chromen-4-one; 2-(3,4-dihydroxyphenyl)-5,7,8-trihydroxychromen-4-one; 2-(3,4-dihydroxyphenyl)-5,7,8-trihydroxy-4-chromenone; 2-(3,4-dihydroxyphenyl)-5,7,8-trihydroxy-chromone; CHEBI:5837; 27696-41-9; C10078; 3,4,5,7,8-Pentahydroxyflavone

数据库引用编号

14 个数据库交叉引用编号

ChEBI: CHEBI:5837
KEGG: C10078
PubChem: 5281648
Metlin: METLIN49821
ChEMBL: CHEMBL1829395
LipidMAPS: LMPK12111397
KNApSAcK: C00001053
CAS: 27696-41-9
PMhub: MS000021368
Flavonoid: FL3FFCNS0001
MetaboLights: MTBLC5837
PubChem: 12264
3DMET: B03520
NIKKAJI: J53.100F

分类词条

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)

35 个相关的物种来源信息

33090 车前子: -
33128 Papaver rhoeas: 10.1055/S-2004-818956
1272984 Moquilea pyrifolia:
103975 Libocedrus yateensis: 10.1016/0031-9422(90)85105-O
103974 Libocedrus bidwillii: 10.1016/0031-9422(90)85105-O
13595 Libocedrus plumosa: 10.1016/0031-9422(90)85105-O
89193 Callitris pancheri: 10.1016/0031-9422(90)85105-O
2250722 Libocedrus chevalieri: 10.1016/0031-9422(90)85105-O
29719 Mentha spicata: 10.1016/S0367-326X(99)00062-3
38859 Mentha longifolia: 10.1016/S0367-326X(99)00062-3
155251 Sideritis incana: 10.1055/S-2007-969310
2820225 Veronica traversii: 10.1016/S0031-9422(00)00397-6
631204 Veronica stenophylla: 10.1016/S0031-9422(00)00397-6
1367250 Veronica strictissima: 10.1016/S0031-9422(00)00397-6
163752 Veronica parviflora: 10.1016/S0031-9422(00)00397-6
1391945 Sideritis leucantha: 10.1016/S0031-9422(00)85000-1
53027 Bucegia romanica: 10.1016/S0031-9422(00)80075-8
1125853 Hypolaena fastigiata: 10.1016/S0031-9422(00)88096-6
33128 Papaver rhoeas: 10.1055/S-2004-818956
1272984 Moquilea pyrifolia:
103975 Libocedrus yateensis: 10.1016/0031-9422(90)85105-O
103974 Libocedrus bidwillii: 10.1016/0031-9422(90)85105-O
13595 Libocedrus plumosa: 10.1016/0031-9422(90)85105-O
89193 Callitris pancheri: 10.1016/0031-9422(90)85105-O
2250722 Libocedrus chevalieri: 10.1016/0031-9422(90)85105-O
29719 Mentha spicata: 10.1016/S0367-326X(99)00062-3
38859 Mentha longifolia: 10.1016/S0367-326X(99)00062-3
155251 Sideritis incana: 10.1055/S-2007-969310
2820225 Veronica traversii: 10.1016/S0031-9422(00)00397-6
631204 Veronica stenophylla: 10.1016/S0031-9422(00)00397-6
1367250 Veronica strictissima: 10.1016/S0031-9422(00)00397-6
163752 Veronica parviflora: 10.1016/S0031-9422(00)00397-6
1391945 Sideritis leucantha: 10.1016/S0031-9422(00)85000-1
53027 Bucegia romanica: 10.1016/S0031-9422(00)80075-8
1125853 Hypolaena fastigiata: 10.1016/S0031-9422(00)88096-6

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

Nan Qin, Chun-Bao Li, Mei-Na Jin, Li-Huan Shi, Hong-Quan Duan, Wen-Yan Niu. Synthesis and biological activity of novel tiliroside derivants. European journal of medicinal chemistry. 2011 Oct; 46(10):5189-95. doi: 10.1016/j.ejmech.2011.07.059. [PMID: 21856048]
Wafa Marouane, Ahlem Soussi, Jean-Claude Murat, Sofiane Bezzine, Abdelfattah El Feki. The protective effect of Malva sylvestris on rat kidney damaged by vanadium. Lipids in health and disease. 2011 Apr; 10(?):65. doi: 10.1186/1476-511x-10-65. [PMID: 21513564]
Jie Feng, Xiu-Wei Yang, Ru-Feng Wang. Bio-assay guided isolation and identification of α-glucosidase inhibitors from the leaves of Aquilaria sinensis. Phytochemistry. 2011 Feb; 72(2-3):242-7. doi: 10.1016/j.phytochem.2010.11.025. [PMID: 21215978]
Elizabeth A Mazzio, Fran Close, Karam F A Soliman. The biochemical and cellular basis for nutraceutical strategies to attenuate neurodegeneration in Parkinson's disease. International journal of molecular sciences. 2011 Jan; 12(1):506-69. doi: 10.3390/ijms12010506. [PMID: 21340000]
Jasmina Petreska, Gjose Stefkov, Svetlana Kulevanova, Kalina Alipieva, Vassya Bankova, Marina Stefova. Phenolic compounds of mountain tea from the Balkans: LC/DAD/ESI/MSn profile and content. Natural product communications. 2011 Jan; 6(1):21-30. doi: . [PMID: 21366039]
Peng-Fei Xia, Zi-Ming Feng, Ya-Nan Yang, Pei-Cheng Zhang. Two flavonoid glycosides and a phenylpropanoid glucose ester from the leaves of Sterculia foetida. Journal of Asian natural products research. 2009 Aug; 11(8):766-71. doi: 10.1080/10286020903055103. [PMID: 20183322]
Bisera Janeska, Marina Stefova, Kalina Alipieva. Assay of flavonoid aglycones from the species of genus Sideritis (Lamiaceae) from Macedonia with HPLC-UV DAD. Acta pharmaceutica (Zagreb, Croatia). 2007 Sep; 57(3):371-7. doi: 10.2478/v10007-007-0030-8. [PMID: 17878116]
Marita Hillenbrand, Josef Zapp, Hans Becker. Depsides from the petals of Papaver rhoeas. Planta medica. 2004 Apr; 70(4):380-2. doi: 10.1055/s-2004-818956. [PMID: 15095160]
E A Aboutabl, M I Nassar, F M Elsakhawy, Y A Maklad, A F Osman, E A M El-Khrisy. Phytochemical and pharmacological studies on Sideritis taurica Stephan ex Wild. Journal of ethnopharmacology. 2002 Oct; 82(2-3):177-84. doi: 10.1016/s0378-8741(02)00172-1. [PMID: 12241993]