Chimaphilin (BioDeep_00000008014)
natural product
代谢物信息卡片
化学式: C12H10O2 (186.0681)
中文名称: 2,7-二甲基-1,4-萘醌
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: CC1=CC(=O)c2ccc(C)cc2C1=O
InChI: InChI=1S/C12H10O2/c1-7-3-4-9-10(5-7)12(14)8(2)6-11(9)13/h3-6H,1-2H3
描述信息
同义名列表
14 个代谢物同义名
Chimaphilin; Chimaphylin; 1,4-Naphthalenedione, 2,7-dimethyl- (9CI); 1,4-Naphthoquinone, 2,7-dimethyl- (8CI); 1,4-Naphthalenedione, 2,7-dimethyl-; 2,7-dimethylnaphthalene-1,4-dione; 1,4-Naphthoquinone, 2,7-dimethyl-; 2,7-Dimethyl-1,4-naphthoquinone; NCI60_003733; NSC 400245; NSC400245; 482-70-2; C10310; Chimaphylin
数据库引用编号
13 个数据库交叉引用编号
- ChEBI: CHEBI:3595
- KEGG: C10310
- PubChem: 101211
- Metlin: METLIN68238
- ChEMBL: CHEMBL495277
- KNApSAcK: C00002802
- CAS: 482-70-2
- PMhub: MS000021544
- PubChem: 12496
- 3DMET: B03730
- NIKKAJI: J5.981A
- KNApSAcK: 3595
- LOTUS: LTS0209349
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)
42 个相关的物种来源信息
- 93812 - Chimaphila: 10.1111/J.1600-0536.1988.TB02890.X
- 93812 - Chimaphila: LTS0209349
- 93815 - Chimaphila umbellata:
- 93815 - Chimaphila umbellata: 10.1007/BF00602666
- 93815 - Chimaphila umbellata: 10.1007/BF00602667
- 93815 - Chimaphila umbellata: 10.1016/J.PHYTOCHEM.2007.09.007
- 93815 - Chimaphila umbellata: LTS0209349
- 4345 - Ericaceae: LTS0209349
- 2759 - Eukaryota: LTS0209349
- 3398 - Magnoliopsida: LTS0209349
- 93816 - Moneses: LTS0209349
- 93817 - Moneses uniflora:
- 93817 - Moneses uniflora: 10.1002/PCA.2800060303
- 93817 - Moneses uniflora: 10.1021/NP960006V
- 93817 - Moneses uniflora: LTS0209349
- 13650 - Pyrola: LTS0209349
- 93820 - Pyrola americana:
- 93820 - Pyrola americana: 10.1248/CPB.33.5355
- 93820 - Pyrola americana: 10.1248/CPB.40.2083
- 93820 - Pyrola americana: LTS0209349
- 93823 - Pyrola asarifolia: LTS0209349
- 642526 - Pyrola calliantha: 10.1248/CPB.52.714
- 642531 - Pyrola incarnata:
- 642531 - Pyrola incarnata: 10.1248/CPB.40.2083
- 642531 - Pyrola incarnata: LTS0209349
- 642532 - Pyrola japonica:
- 642532 - Pyrola japonica: 10.1007/BF02975157
- 642532 - Pyrola japonica: 10.1248/CPB.40.2083
- 642532 - Pyrola japonica: 10.1248/CPB.52.714
- 642532 - Pyrola japonica: LTS0209349
- 642534 - Pyrola media: 10.1039/J39680000857
- 642534 - Pyrola media: LTS0209349
- 642537 - Pyrola renifolia: 10.1248/CPB.12.533
- 642537 - Pyrola renifolia: LTS0209349
- 13651 - Pyrola rotundifolia:
- 13651 - Pyrola rotundifolia: 10.1248/CPB.33.5355
- 13651 - Pyrola rotundifolia: 10.1248/CPB.40.2083
- 13651 - Pyrola rotundifolia: LTS0209349
- 35493 - Streptophyta: LTS0209349
- 58023 - Tracheophyta: LTS0209349
- 33090 - Viridiplantae: LTS0209349
- 33090 - 鹿衔草: -
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
- Dong-Yang Zhang, Xiao-Hui Yao, Ming-Hui Duan, Meng Luo, Chun-Jian Zhao, Yuan-Gang Zu, Yu-Jie Fu. An effective homogenate-assisted negative pressure cavitation extraction for the determination of phenolic compounds in pyrola by LC-MS/MS and the evaluation of its antioxidant activity.
Food & function.
2015 Oct; 6(10):3323-33. doi:
10.1039/c5fo00727e. [PMID: 26256648] - Xiao-Hui Yao, Dong-Yang Zhang, Meng Luo, Shuang Jin, Yuan-Gang Zu, Thomas Efferth, Yu-Jie Fu. Negative pressure cavitation-microwave assisted preparation of extract of Pyrola incarnata Fisch. rich in hyperin, 2'-O-galloylhyperin and chimaphilin and evaluation of its antioxidant activity.
Food chemistry.
2015 Feb; 169(?):270-6. doi:
10.1016/j.foodchem.2014.07.115. [PMID: 25236226] - YuanYuan Zhang, XiaoHui Chen, ShengYing Qin, ChulSa Kim, Shin-ichi Tebayashi, KaiShun Bi. LC-MS method for determination and pharmacokinetic study of chimaphilin in rat plasma after oral administration of the traditional Chinese medicinal preparation Lu xian cao decoction.
Biological & pharmaceutical bulletin.
2006 Dec; 29(12):2523-7. doi:
10.1248/bpb.29.2523. [PMID: 17142995] - Jens A Pedersen. On the application of electron paramagnetic resonance in the study of naturally occurring quinones and quinols.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy.
2002 Apr; 58(6):1257-70. doi:
10.1016/s1386-1425(01)00715-6. [PMID: 11993473] - D L Garver, D M Davis, H Dekirmenjian, S Ericksen, L Gosenfeld, J Haraszti. Dystonic reactions following neuroleptics: time course and proposed mechanisms.
Psychopharmacologia.
1976 May; 47(2):199-201. doi:
10.1007/bf00735822. [PMID: 5743]
