Isosalipurposide (BioDeep_00000011169)

PANOMIX_OTCML-2023

代谢物信息卡片

(E) -3- (4-Hydroxyphenyl) -1- (2-beta-D-glucopyranosyloxy-4,6-dihydroxyphenyl) -2-propene-1-one

化学式: C21H22O10 (434.1212912)
中文名称:
谱图信息: 最多检出来源 Viridiplantae(plant) 0.34%

分子结构信息

SMILES: C1(O)C=C(O)C(C(=O)/C=C/C2C=CC(O)=CC=2)=C(OC2OC(CO)C(O)C(O)C2O)C=1
InChI: InChI=1S/C21H22O10/c22-9-16-18(27)19(28)20(29)21(31-16)30-15-8-12(24)7-14(26)17(15)13(25)6-3-10-1-4-11(23)5-2-10/h1-8,16,18-24,26-29H,9H2/b6-3+

描述信息

A monosaccharide derivative that is trans-chalcone substituted by hydroxy groups at positions 4, 4 and 6 and a beta-D-glucopyranosyloxy group at position 2 respectively.

同义名列表

4 个代谢物同义名

Chalcone 2-O-glucoside; Phlorizin chalcone; Isosalipurposide; (E) -3- (4-Hydroxyphenyl) -1- (2-beta-D-glucopyranosyloxy-4,6-dihydroxyphenyl) -2-propene-1-one

数据库引用编号

17 个数据库交叉引用编号

ChEBI: CHEBI:80486
KEGG: C16406
PubChem: 5318659
PubChem: 6526201
PubChem: 4398471
Metlin: METLIN52054
Metlin: METLIN64214
ChEMBL: CHEMBL2430461
LipidMAPS: LMPK12120250
MetaCyc: CPD-8062
KNApSAcK: C00007881
CAS: 4547-85-7
PMhub: MS000025128
Flavonoid: FL1CAAGS0004
MetaboLights: MTBLC80486
PubChem: 47205704
NIKKAJI: J107.406G

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)

11 个相关的物种来源信息

205042 - Acacia dealbata: 10.12980/APJTB.4.2014C1038
420411 - Acacia saligna: 10.12980/APJTB.4.2014C1038
87530 - Cyclamen persicum: 10.2503/JJSHS.60.409
261776 - Helichrysum arenarium:
261777 - Helichrysum armenium: 10.1021/NP50020A005
630307 - Helichrysum graveolens: 10.1007/S11418-007-0223-Y
630317 - Helichrysum maracandicum: 10.1007/S11418-007-0223-Y
4513 - Hordeum vulgare: 10.1034/J.1399-3054.1997.1010421.X
1616377 - Nymphaea nouchali var. caerulea: 10.1016/J.PHYTOCHEM.2008.04.009
35924 - Paeonia lactiflora: 10.1016/J.JPBA.2014.10.020
152196 - Xerochrysum bracteatum: 10.1007/S11418-007-0223-Y

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

Hongzhu Zou, Lulu Han, Meng Yuan, Mengjie Zhang, Lin Zhou, Yan Wang. Sequence Analysis and Functional Verification of the Effects of Three Key Structural Genes, PdTHC2'GT, PdCHS and PdCHI, on the Isosalipurposide Synthesis Pathway in Paeonia delavayi var. lutea. International journal of molecular sciences. 2022 May; 23(10):. doi: 10.3390/ijms23105696. [PMID: 35628506]
Rudi Hendra, Anthony Willis, Paul A Keller. Phytochemical studies on the Australian native plant species Acacia pycnantha and Jacaranda mimosifolia D.Don. Natural product research. 2019 Jul; 33(14):1997-2003. doi: 10.1080/14786419.2018.1483922. [PMID: 29888976]
Ji-Hye Seo, Jung-Eun Kim, Jung-Hyun Shim, Goo Yoon, Mi-Ae Bang, Chun-Sik Bae, Kyung-Jin Lee, Dae-Hun Park, Seung-Sik Cho. HPLC Analysis, Optimization of Extraction Conditions and Biological Evaluation of Corylopsis coreana Uyeki Flos. Molecules (Basel, Switzerland). 2016 Jan; 21(1):94. doi: 10.3390/molecules21010094. [PMID: 26784157]
Jae Yun Han, Seung Sik Cho, Ji Hye Yang, Kyu Min Kim, Chang Ho Jang, Da Eon Park, Joon Seok Bang, Young Suk Jung, Sung Hwan Ki. The chalcone compound isosalipurposide (ISPP) exerts a cytoprotective effect against oxidative injury via Nrf2 activation. Toxicology and applied pharmacology. 2015 Aug; 287(1):77-85. doi: 10.1016/j.taap.2015.05.015. [PMID: 26028482]
Robert Brkljača, Jonathan M White, Sylvia Urban. Phytochemical Investigation of the Constituents Derived from the Australian Plant Macropidia fuliginosa. Journal of natural products. 2015 Jul; 78(7):1600-8. doi: 10.1021/acs.jnatprod.5b00161. [PMID: 26151487]
Chonghui Li, Hui Du, Liangsheng Wang, Qingyan Shu, Yuanrun Zheng, Yanjun Xu, Jingjing Zhang, Jie Zhang, Ruizhen Yang, Yuxuan Ge. Flavonoid composition and antioxidant activity of tree peony (Paeonia section moutan) yellow flowers. Journal of agricultural and food chemistry. 2009 Sep; 57(18):8496-503. doi: 10.1021/jf902103b. [PMID: 19711909]
Toru Yagura, Tomoko Motomiya, Michiho Ito, Gisho Honda, Akira Iida, Fumiyuki Kiuchi, Harukuni Tokuda, Hoyoku Nishino. Anticarcinogenic compounds in the Uzbek medicinal plant, Helichrysum maracandicum. Journal of natural medicines. 2008 Apr; 62(2):174-8. doi: 10.1007/s11418-007-0223-y. [PMID: 18404319]
Bernd Kammerer, Rainer Kahlich, Claudia Biegert, Christoph H Gleiter, Lutz Heide. HPLC-MS/MS analysis of willow bark extracts contained in pharmaceutical preparations. Phytochemical analysis : PCA. 2005 Nov; 16(6):470-8. doi: 10.1002/pca.873. [PMID: 16315493]