3,7-dihydroxyflavone (BioDeep_00000267058)
natural product PANOMIX_OTCML-2023
代谢物信息卡片
化学式: C15H10O4 (254.057906)
中文名称: 7-羟基黄烷醇
谱图信息:
最多检出来源 Viridiplantae(plant) 2.44%
分子结构信息
SMILES: c1(ccc2c(c1)oc(c(c2=O)O)c1ccccc1)O
InChI: InChI=1S/C15H10O4/c16-10-6-7-11-12(8-10)19-15(14(18)13(11)17)9-4-2-1-3-5-9/h1-8,16,18H
数据库引用编号
24 个数据库交叉引用编号
- ChEBI: CHEBI:109535
- PubChem: 5393152
- Metlin: METLIN44411
- ChEMBL: CHEMBL210276
- LipidMAPS: LMPK12111545
- KNApSAcK: C00004531
- CAS: 492-00-2
- MoNA: VF-NPL-QTOF003301
- MoNA: VF-NPL-QTOF003300
- MoNA: VF-NPL-QTOF003299
- MoNA: VF-NPL-QTOF003298
- MoNA: VF-NPL-QTOF003297
- MoNA: VF-NPL-QTOF003296
- MoNA: VF-NPL-LTQ007310
- MoNA: VF-NPL-LTQ007309
- MoNA: VF-NPL-LTQ007308
- MoNA: VF-NPL-LTQ007307
- MoNA: VF-NPL-QEHF014547
- MoNA: VF-NPL-QEHF014546
- MoNA: VF-NPL-QEHF014545
- MoNA: VF-NPL-QEHF014544
- MoNA: VF-NPL-QEHF014543
- MoNA: VF-NPL-QEHF014542
- LOTUS: LTS0164900
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)
10 个相关的物种来源信息
- 2759 - Eukaryota: LTS0164900
- 3803 - Fabaceae: LTS0164900
- 3398 - Magnoliopsida: LTS0164900
- 107372 - Platymiscium: LTS0164900
- 35493 - Streptophyta: LTS0164900
- 58023 - Tracheophyta: LTS0164900
- 33090 - Viridiplantae: LTS0164900
- 191957 - Zuccagnia: LTS0164900
- 191958 - Zuccagnia punctata: 10.1016/S0031-9422(00)80459-8
- 191958 - Zuccagnia punctata: LTS0164900
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
- Alberto Cassetta, Jure Stojan, Ivet Krastanova, Katja Kristan, Mojca Brunskole Švegelj, Doriano Lamba, Tea Lanišnik Rižner. Structural basis for inhibition of 17β-hydroxysteroid dehydrogenases by phytoestrogens: The case of fungal 17β-HSDcl.
The Journal of steroid biochemistry and molecular biology.
2017 07; 171(?):80-93. doi:
10.1016/j.jsbmb.2017.02.020
. [PMID: 28259640] - Ji Ma, Yuan Liu, Luan Chen, Yue Xie, Li-Yun Wang, Meng-Xia Xie. Spectroscopic investigation on the interaction of 3,7-dihydroxyflavone with different isomers of human serum albumin.
Food chemistry.
2012 May; 132(1):663-70. doi:
10.1016/j.foodchem.2011.11.023
. [PMID: 26434347] - I C Zampini, J Villena, S Salva, M Herrera, M I Isla, S Alvarez. Potentiality of standardized extract and isolated flavonoids from Zuccagnia punctata for the treatment of respiratory infections by Streptococcus pneumoniae: in vitro and in vivo studies.
Journal of ethnopharmacology.
2012 Mar; 140(2):287-92. doi:
10.1016/j.jep.2012.01.019
. [PMID: 22285202] - Teresa Tarragó, Nessim Kichik, Birgit Claasen, Roger Prades, Meritxell Teixidó, Ernest Giralt. Baicalin, a prodrug able to reach the CNS, is a prolyl oligopeptidase inhibitor.
Bioorganic & medicinal chemistry.
2008 Aug; 16(15):7516-24. doi:
10.1016/j.bmc.2008.04.067
. [PMID: 18650094] - Petra Brozic, Tina Smuc, Stanislav Gobec, Tea Lanisnik Rizner. Phytoestrogens as inhibitors of the human progesterone metabolizing enzyme AKR1C1.
Molecular and cellular endocrinology.
2006 Oct; 259(1-2):30-42. doi:
10.1016/j.mce.2006.08.001
. [PMID: 16962702] - Katja Kristan, Katja Krajnc, Janez Konc, Stanislav Gobec, Jure Stojan, Tea Lanisnik Rizner. Phytoestrogens as inhibitors of fungal 17beta-hydroxysteroid dehydrogenase.
Steroids.
2005 Sep; 70(10):694-703. doi:
10.1016/j.steroids.2005.02.023
. [PMID: 15936789] - Hideki Kanho, Sayaka Yaoya, Tomio Itani, Takahisa Nakane, Nobuo Kawahara, Yoichi Takase, Kazuo Masuda, Masanori Kuroyanagi. Glucosylation of phenolic compounds by Pharbitis nil hairy roots: I. Glucosylation of coumarin and flavone derivatives.
Bioscience, biotechnology, and biochemistry.
2004 Oct; 68(10):2032-9. doi:
10.1271/bbb.68.2032
. [PMID: 15502347] - . .
.
. doi:
. [PMID: 18487633]