Pinocembrinchalcone (BioDeep_00000396972)
Secondary id: BioDeep_00000011167
PANOMIX_OTCML-2023
代谢物信息卡片
化学式: C15H12O4 (256.0736)
中文名称: 2,4,6-三羟基查耳酮, 2',4',6'-三羟基查耳酮
谱图信息:
最多检出来源 Homo sapiens(plant) 20.41%
分子结构信息
SMILES: c1(cc(c(c(c1)O)C(=O)/C=C/c1ccccc1)O)O
InChI: InChI=1S/C15H12O4/c16-11-8-13(18)15(14(19)9-11)12(17)7-6-10-4-2-1-3-5-10/h1-9,16,18-19H/b7-6+
描述信息
Pinocembrin chalcone is a member of the class of chalcones that is trans-chalcone substituted by hydroxy groups at positions 2, 4 and 6 respectively. It has a role as a plant metabolite and an antifungal agent. It is functionally related to a trans-chalcone.
Pinocembrin chalcone is a natural product found in Populus koreana, Populus laurifolia, and other organisms with data available.
A member of the class of chalcones that is trans-chalcone substituted by hydroxy groups at positions 2, 4 and 6 respectively.
同义名列表
12 个代谢物同义名
2-Propen-1-one, 3-phenyl-1-(2,4,6-trihydroxyphenyl)-, (E)-; (2E)-3-phenyl-1-(2,4,6-trihydroxyphenyl)prop-2-en-1-one; (E)-3-phenyl-1-(2,4,6-trihydroxyphenyl)prop-2-en-1-one; 3-phenyl-1-(2,4,6-trihydroxyphenyl)prop-2-en-1-one; (E)-3-Phenyl-1-(2,4,6-trihydroxy-phenyl)-propenone; 3-Phenyl-1-(2,4,6-trihydroxy-phenyl)-propenone; 2;,4;,6;-TRIHYDROXYCHALCONE; 2,4,6-trihydroxychalcone; Pinocembrin chalcone; Pinocenbrin chalcone; Pinocembrinchalcone; Spectrum5_001768
数据库引用编号
13 个数据库交叉引用编号
- ChEBI: CHEBI:80484
- KEGG: C16404
- PubChem: 6474295
- ChEMBL: CHEMBL129371
- LipidMAPS: LMPK12120243
- MeSH: pinocembrin chalcone
- KNApSAcK: C00006933
- CAS: 82451-30-7
- CAS: 4197-97-1
- medchemexpress: HY-N7515
- MetaboLights: MTBLC80484
- PubChem: 47205702
- NIKKAJI: J258.619C
分类词条
相关代谢途径
Reactome(0)
BioCyc(0)
代谢反应
4 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(0)
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(3)
- pinobanksin biosynthesis:
(2S)-pinocembrin + SAM ⟶ SAH + pinostrobin
- pinobanksin biosynthesis:
(2S)-pinocembrin + 2-oxoglutarate + O2 ⟶ (+)-pinobanksin + CO2 + succinate
- pinobanksin biosynthesis:
(2S)-pinocembrin + 2-oxoglutarate + O2 ⟶ (+)-pinobanksin + CO2 + succinate
COVID-19 Disease Map(0)
PharmGKB(0)
0 个相关的物种来源信息
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。
亚细胞结构定位 | 关联基因列表 |
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文献列表
- Mosaab Yahyaa, Samah Ali, Rachel Davidovich-Rikanati, Muhammad Ibdah, Alona Shachtier, Yoram Eyal, Efraim Lewinsohn, Mwafaq Ibdah. Characterization of three chalcone synthase-like genes from apple (Malus x domestica Borkh.).
Phytochemistry.
2017 Aug; 140(?):125-133. doi:
10.1016/j.phytochem.2017.04.022
. [PMID: 28482241] - Mohamed A Zaki, N P Dhammika Nanayakkara, Mona H Hetta, Melissa R Jacob, Shabana I Khan, Rabab Mohammed, Mohamed A Ibrahim, Volodymyr Samoylenko, Christina Coleman, Frank R Fronczek, Daneel Ferreira, Ilias Muhammad. Bioactive Formylated Flavonoids from Eugenia rigida: Isolation, Synthesis, and X-ray Crystallography.
Journal of natural products.
2016 09; 79(9):2341-9. doi:
10.1021/acs.jnatprod.6b00474
. [PMID: 27618204] - Patrick S Ruddock, Marijo Charland, Sandra Ramirez, Andres López, G H Neil Towers, John T Arnason, Mingmin Liao, Jo-Anne R Dillon. Antimicrobial activity of flavonoids from Piper lanceaefolium and other Colombian medicinal plants against antibiotic susceptible and resistant strains of Neisseria gonorrhoeae.
Sexually transmitted diseases.
2011 Feb; 38(2):82-8. doi:
10.1097/olq.0b013e3181f0bdbd
. [PMID: 20921932] - S Sogawa, Y Nihro, H Ueda, A Izumi, T Miki, H Matsumoto, T Satoh. 3,4-Dihydroxychalcones as potent 5-lipoxygenase and cyclooxygenase inhibitors.
Journal of medicinal chemistry.
1993 Nov; 36(24):3904-9. doi:
10.1021/jm00076a019
. [PMID: 8254620]