(R)-5-Hydroxy-2-(4-hydroxyphenyl)-7-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)chroman-4-one (BioDeep_00000174807)

human metabolite PANOMIX_OTCML-2023 blood metabolite PANOMIX-Anthocyanidin

代谢物信息卡片

(R)-5-Hydroxy-2-(4-hydroxyphenyl)-7-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)chroman-4-one

化学式: C21H22O10 (434.1212912)
中文名称: 普鲁宁
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: c1(cc(c2c(c1)O[C@@H](CC2=O)c1ccc(cc1)O)O)O[C@H]1[C@@H]([C@H]([C@H]([C@H](O1)CO)O)O)O
InChI: InChI=1S/C21H22O10/c22-8-16-18(26)19(27)20(28)21(31-16)29-11-5-12(24)17-13(25)7-14(30-15(17)6-11)9-1-3-10(23)4-2-9/h1-6,14,16,18-24,26-28H,7-8H2

描述信息

Prunin, also known as pru du 6.01 protein, prunus, is a member of the class of compounds known as flavonoid-7-o-glycosides. Flavonoid-7-o-glycosides are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C7-position. Prunin is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Prunin is a bitter tasting compound found in almond, garden tomato (variety), peach, and pine nut, which makes prunin a potential biomarker for the consumption of these food products. Prunin is a flavanone glycoside found in immature citrus fruits and in tomatoes. Its aglycone form is called naringenin .
Prunin is a potent inhibitor of human enterovirus A71 (HEVA71). Prunin shows strong inhibitory activity against protein tyrosine phosphatase 1B (PTP1B), with an IC50 of 5.5 μM[1][2].
Prunin is a potent inhibitor of human enterovirus A71 (HEVA71). Prunin shows strong inhibitory activity against protein tyrosine phosphatase 1B (PTP1B), with an IC50 of 5.5 μM[1][2].

同义名列表

15 个代谢物同义名

(R)-5-Hydroxy-2-(4-hydroxyphenyl)-7-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)chroman-4-one; 5-hydroxy-2-(4-hydroxyphenyl)-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,4-dihydro-2H-1-benzopyran-4-one; 5-hydroxy-2-(4-hydroxyphenyl)-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,3-dihydro-1-benzopyran-4-one; 5-Hydroxy-2-(4-hydroxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one; 5,7,4-Trihydroxyflavanone 7-O-beta-D-glucopyranoside; Naringenin 7-O-beta-D-glucoside; Pru du 6.01 protein, Prunus; Pru du 6.02 protein, Prunus; Pru du 6 protein, Prunus; PRUNIN PROTEIN, PRUNUS; Pru2 protein, Prunus; Pru1 protein, Prunus; Prunin; Naringenin 7-0-glucoside; Naringenin 7-O-beta-D-glucoside

数据库引用编号

15 个数据库交叉引用编号

PubChem: 282013
HMDB: HMDB0246916
Wikipedia: Prunin
KNApSAcK: C00000998
foodb: FDB016683
chemspider: 248332
CAS: 529-55-5
RefMet: Naringenin 7-O-beta-D-glucoside
PubChem: 92794
medchemexpress: HY-N1549
KEGG: C09099
PubChem: 11291
KNApSAcK: 28327
LOTUS: LTS0207777
wikidata: Q104984380

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)

17 个相关的物种来源信息

204988 - Acacia adunca: 10.1016/J.JEP.2018.10.031
205042 - Acacia dealbata: 10.1016/J.JEP.2018.10.031
872542 - Aglaomorpha fortunei: 10.1248/CPB.56.46
4151 - Antirrhinum majus: 10.1021/JA01626A065
171251 - Citrus medica: 10.1021/NP060217S
558546 - Citrus sudachi: 10.1021/NP060217S
225592 - Gnetum latifolium: 10.1248/CPB.54.1053
261776 - Helichrysum arenarium:
9606 - Homo sapiens: -
884034 - Juniperus communis var. depressa: 10.1016/J.PHYTOCHEM.2003.10.025
586100 - Phyllanthus oligospermus: 10.1248/CPB.50.841
33090 - Plants: -
140311 - Prunus cerasus: 10.1021/JA01143A513
151430 - Prunus davidiana:
3760 - Prunus persica:
50172 - Viscum articulatum:
159976 - Viscum coloratum: 10.1248/CPB.52.858

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

LeAnna N Willison, Qian Zhang, Mengna Su, Suzanne S Teuber, Shridhar K Sathe, Kenneth H Roux. Conformational epitope mapping of Pru du 6, a major allergen from almond nut. Molecular immunology. 2013 Oct; 55(3-4):253-63. doi: 10.1016/j.molimm.2013.02.004. [PMID: 23498967]
Tengchuan Jin, Silvia M Albillos, Feng Guo, Andrew Howard, Tong-Jen Fu, Mahendra H Kothary, Yu-Zhu Zhang. Crystal structure of prunin-1, a major component of the almond (Prunus dulcis) allergen amandin. Journal of agricultural and food chemistry. 2009 Sep; 57(18):8643-51. doi: 10.1021/jf9017355. [PMID: 19694440]
Fernando Soria, Guillermo Ellenrieder. Thermal inactivation and product inhibition of Aspergillus terreus CECT 2663 alpha-L-rhamnosidase and their role on hydrolysis of naringin solutions. Bioscience, biotechnology, and biochemistry. 2002 Jul; 66(7):1442-9. doi: 10.1271/bbb.66.1442. [PMID: 12224626]
J Garcia-Mas, R Messeguer, P Arús, P Puigdomènech. Molecular characterization of cDNAs corresponding to genes expressed during almond (Prunus amygdalus Batsch) seed development. Plant molecular biology. 1995 Jan; 27(1):205-10. doi: 10.1007/bf00019192. [PMID: 7865791]
J S Choi, T Yokozawa, H Oura. Improvement of hyperglycemia and hyperlipemia in streptozotocin-diabetic rats by a methanolic extract of Prunus davidiana stems and its main component, prunin. Planta medica. 1991 Jun; 57(3):208-11. doi: 10.1055/s-2006-960075. [PMID: 1896517]
J S Choi, T Yokozawa, H Oura. Antihyperlipidemic effect of flavonoids from Prunus davidiana. Journal of natural products. 1991 Jan; 54(1):218-24. doi: 10.1021/np50073a022. [PMID: 2045817]
K Habelt, F Pittner. A rapid method for the determination of naringin, prunin, and naringenin applied to the assay of naringinase. Analytical biochemistry. 1983 Oct; 134(2):393-7. doi: 10.1016/0003-2697(83)90314-7. [PMID: 6418025]