Flavokawain C (BioDeep_00000017321)
human metabolite PANOMIX_OTCML-2023 Endogenous Cytotoxicity Antitumor activity
代谢物信息卡片
化学式: C17H16O5 (300.0998)
中文名称: 2',4-二羟基-4',6'-二甲氧基查耳酮, 黄姜素C
谱图信息:
最多检出来源 Astragalus membranaceus(otcml) 27.08%
Last reviewed on 2024-10-09.
Cite this Page
Flavokawain C. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China.
https://query.biodeep.cn/s/flavokawain_c (retrieved
2025-02-19) (BioDeep RN: BioDeep_00000017321). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
分子结构信息
SMILES: C1(OC)=CC(OC)=C(C(=O)/C=C/C2C=CC(O)=CC=2)C(O)=C1
InChI: InChI=1S/C17H16O5/c1-21-13-9-15(20)17(16(10-13)22-2)14(19)8-5-11-3-6-12(18)7-4-11/h3-10,18,20H,1-2H3/b8-5+
描述信息
2,4-Dihydroxy-4,6-dimethoxychalcone is found in beverages. 2,4-Dihydroxy-4,6-dimethoxychalcone is found in kava (Piper methysticum). FDA advises against use of kava in food due to potential risk of severe liver damage (2002
Flavokawain C is a member of chalcones.
2,4-Dihydroxy-4,6-dimethoxychalcone is a natural product found in Argyrochosma dealbata, Piper methysticum, and other organisms with data available.
Flavokawain C is a natural chalcone found in Kava root. Flavokawain C exerts cytotoxicity against human cancer cell lines, with an IC50 of 12.75 μM for HCT 116 cells[1].
Flavokawain C is a natural chalcone found in Kava root. Flavokawain C exerts cytotoxicity against human cancer cell lines, with an IC50 of 12.75 μM for HCT 116 cells[1].
同义名列表
24 个代谢物同义名
(E)-1-(2-Hydroxy-4,6-dimethoxyphenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one (flavokawain C); 2-Propen-1-one, 1-(2-hydroxy-4,6-dimethoxyphenyl)-3-(4-hydroxyphenyl)-, (2E)-; 2-Propen-1-one, 1-(2-hydroxy-4,6-dimethoxyphenyl)-3-(4-hydroxyphenyl)-, (E)-; (2E)-1-(2-hydroxy-4,6-dimethoxyphenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one; (2E)-1-(2-Hydroxy-4,6-dimethoxyphenyl)-3-(4-hydroxyphenyl)-2-propen-1-one; (E)-1-(2-hydroxy-4,6-dimethoxyphenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one; 2-Propen-1-one, 1-(2-hydroxy-4,6-dimethoxyphenyl)-3-(4-hydroxyphenyl)-; 1-(2-hydroxy-4,6-dimethoxyphenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one; 1-(2-hydroxy-4,6-dimethoxyphenyl)-3-(4-hydroxyphenyl)-2-propen-1-one; 2,4-Dihydroxy-4,6-dimethoxy-trans-chalcone; 2,4-Dihydroxy-4,6-dimethoxychalcone; 2,4-DIHYDROXY-4,6-DIMETHOXYCHALCONE; 4,2-Dihydroxy-4,6-dimethoxychalcone; 4,2-DIHYDROXY-4,6-DIMETHYLCHALCONE; UXUFMIJZNYXWDX-VMPITWQZSA-N; 4-Hydroxyflavokawain B; flavokawain C; Flavokavain C; Flavokawin C; FLAVOKAWAINC; Flavokavin C; Flavokawain; 5LE8KTR6G2; flavokawin
数据库引用编号
17 个数据库交叉引用编号
- ChEBI: CHEBI:157718
- PubChem: 6293081
- HMDB: HMDB0030875
- ChEMBL: CHEMBL251958
- Wikipedia: Flavokavain_C
- LipidMAPS: LMPK12120320
- MeSH: flavokawain C
- KNApSAcK: C00006957
- foodb: FDB002836
- chemspider: 4874893
- CAS: 37308-75-1
- medchemexpress: HY-N2445
- PMhub: MS000225833
- LOTUS: LTS0123960
- wikidata: Q5458168
- LOTUS: LTS0204512
- wikidata: Q105281027
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)
11 个相关的物种来源信息
- 1055476 - Argyrochosma dealbata: 10.1515/ZNC-1991-5-601
- 97729 - Boesenbergia rotunda: 10.1021/NP070286M
- 9606 - Homo sapiens: -
- 3486 - Humulus lupulus: 10.1021/NP800188B
- 405306 - Macropiper latifolium:
- 405323 - Piper dilatatum: 10.1002/CHIN.199902259
- 130404 - Piper methysticum:
- 130409 - Piper peltatum:
- 33090 - Plants: -
- 318063 - Pseudognaphalium affine: 10.1021/JF990282Q
- 33090 - 卡瓦胡椒: -
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
- Chung-Weng Phang, Sri Nurestri Abd Malek, Saiful Anuar Karsani. Flavokawain C exhibits anti-tumor effects on in vivo HCT 116 xenograft and identification of its apoptosis-linked serum biomarkers via proteomic analysis.
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.
2021 May; 137(?):110846. doi:
10.1016/j.biopha.2020.110846
. [PMID: 33761587] - M Morimoto, S Kumeda, K Komai. Insect antifeedant flavonoids from Gnaphalium affine D. Don.
Journal of agricultural and food chemistry.
2000 May; 48(5):1888-91. doi:
10.1021/jf990282q
. [PMID: 10820110]