3,7,4-Trihydroxyflavone (BioDeep_00000398537)

Secondary id: BioDeep_00000003595, BioDeep_00000395491

PANOMIX_OTCML-2023

代谢物信息卡片

3,7,4-Trihydroxyflavone

化学式: C15H10O5 (270.052821)
中文名称: 5-脱氧莰非醇, 5-脱氧莰非醇
谱图信息: 最多检出来源 Viridiplantae(plant) 4.88%

分子结构信息

SMILES: C1=CC(=CC=C1C2=C(C(=O)C3=C(O2)C=C(C=C3)O)O)O
InChI: InChI=1S/C15H10O5/c16-9-3-1-8(2-4-9)15-14(19)13(18)11-6-5-10(17)7-12(11)20-15/h1-7,16-17,19H

描述信息

relative retention time with respect to 9-anthracene Carboxylic Acid is 0.962
relative retention time with respect to 9-anthracene Carboxylic Acid is 0.958
relative retention time with respect to 9-anthracene Carboxylic Acid is 0.954
relative retention time with respect to 9-anthracene Carboxylic Acid is 0.955
3,7,4'-Trihydroxyflavone, isolated from Rhus javanica var. roxburghiana, is a flavonoid with DNA strand-scission activity[1].
3,7,4'-Trihydroxyflavone, isolated from Rhus javanica var. roxburghiana, is a flavonoid with DNA strand-scission activity[1].

同义名列表

3 个代谢物同义名

3,7,4-Trihydroxyflavone; 5-Deoxykampferol; 3,7,4'-Trihydroxyflavone

数据库引用编号

19 个数据库交叉引用编号

ChEBI: CHEBI:196244
PubChem: 5281611
ChEMBL: CHEMBL242383
CAS: 2034-65-3
MoNA: MetaboBASE0733
MoNA: MetaboBASE0732
MoNA: MetaboBASE0731
MoNA: MetaboBASE0730
MoNA: MetaboBASE0729
MoNA: BML80343
MoNA: BML80342
MoNA: BML80341
MoNA: BML80340
MoNA: BML00342
MoNA: BML00337
MoNA: BML00332
MoNA: BML00322
MoNA: BML00317
medchemexpress: HY-111806

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)

41 个相关的物种来源信息

118891 Anthyllis vulneraria: 10.1016/S0031-9422(00)88397-1
181254 Lotus dorycnium:
118937 Lotus maritimus: 10.1016/S0031-9422(00)94254-7
47247 Lotus corniculatus: 10.1016/S0031-9422(00)94254-7
149639 Dermatophyllum secundiflorum: 10.1016/0031-9422(95)93530-S
3827 Cicer arietinum: 10.1016/S0031-9422(00)86150-6
65409 Scutellaria baicalensis: 10.1111/J.1600-0609.2009.01365.X
1969222 Baptisia lecontei:
1969224 Baptisia simplicifolia:
1969220 Baptisia calycosa:
556509 Erythrina fusca: 10.1016/J.FITOTE.2010.01.009
174171 Clematis hexapetala: 10.1515/ZNB-2007-0615
595347 Leontopodium nanum: 10.1002/JCCS.200200040
1071187 Pterocarpus marsupium:
3808 Acacia: 10.1042/BJ0820324
35938 Robinia pseudoacacia: 10.1042/BJ0820324
254779 Lathyrus pratensis: 10.1016/0031-9422(81)84073-3
191885 Biancaea decapetala: 10.1016/S1875-5364(09)60015-7
210348 Brucea javanica: 10.1016/J.FITOTE.2007.07.008
3864 Lens culinaris: 10.1016/S0031-9422(00)94253-5
118891 Anthyllis vulneraria: 10.1016/S0031-9422(00)88397-1
181254 Lotus dorycnium:
118937 Lotus maritimus: 10.1016/S0031-9422(00)94254-7
47247 Lotus corniculatus: 10.1016/S0031-9422(00)94254-7
149639 Dermatophyllum secundiflorum: 10.1016/0031-9422(95)93530-S
3827 Cicer arietinum: 10.1016/S0031-9422(00)86150-6
65409 Scutellaria baicalensis: 10.1111/J.1600-0609.2009.01365.X
1969222 Baptisia lecontei:
1969224 Baptisia simplicifolia:
1969220 Baptisia calycosa:
556509 Erythrina fusca: 10.1016/J.FITOTE.2010.01.009
174171 Clematis hexapetala: 10.1515/ZNB-2007-0615
595347 Leontopodium nanum: 10.1002/JCCS.200200040
1071187 Pterocarpus marsupium:
3808 Acacia: 10.1042/BJ0820324
35938 Robinia pseudoacacia: 10.1042/BJ0820324
254779 Lathyrus pratensis: 10.1016/0031-9422(81)84073-3
191885 Biancaea decapetala: 10.1016/S1875-5364(09)60015-7
210348 Brucea javanica: 10.1016/J.FITOTE.2007.07.008
3864 Lens culinaris: 10.1016/S0031-9422(00)94253-5
33090 Plants: -

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

Myeong Hyeon Park, In Sook Kim, Sun-A Kim, Chun-Soo Na, Cheol Yi Hong, Mi-Sook Dong, Hye Hyun Yoo. Inhibitory effect of Rhus verniciflua Stokes extract on human aromatase activity; butin is its major bioactive component. Bioorganic & medicinal chemistry letters. 2014 Apr; 24(7):1730-3. doi: 10.1016/j.bmcl.2014.02.039. [PMID: 24630560]
S Saponara, E Carosati, P Mugnai, G Sgaragli, F Fusi. The flavonoid scaffold as a template for the design of modulators of the vascular Ca(v) 1.2 channels. British journal of pharmacology. 2011 Nov; 164(6):1684-97. doi: 10.1111/j.1476-5381.2011.01476.x. [PMID: 21557738]
Phongsak Innok, Thitima Rukachaisirikul, Souwalak Phongpaichit, Apichart Suksamrarn. Fuscacarpans A-C, new pterocarpans from the stems of Erythrina fusca. Fitoterapia. 2010 Sep; 81(6):518-23. doi: 10.1016/j.fitote.2010.01.009. [PMID: 20079815]
Chun-Nan Lin, Hui-Ling Chen, Ming-Hong Yen. Flavonoids with DNA strand-scission activity from Rhus javanica var. roxburghiana. Fitoterapia. 2008 Jan; 79(1):32-6. doi: 10.1016/j.fitote.2007.07.008. [PMID: 17855017]
M Abou-Shoer, G E Ma, X H Li, N M Koonchanok, R L Geahlen, C J Chang. Flavonoids from Koelreuteria henryi and other sources as protein-tyrosine kinase inhibitors. Journal of natural products. 1993 Jun; 56(6):967-9. doi: 10.1021/np50096a027. [PMID: 8350096]