Bavachalcone (BioDeep_00000266832)
PANOMIX_OTCML-2023 natural product
代谢物信息卡片
化学式: C21H22O4 (338.1518012)
中文名称: 4-O-甲基补骨脂查尔酮
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: C1=CC(O)=CC=C1/C=C/C(=O)C1C(O)=CC(OC)=C(C/C=C(\C)/C)C=1
InChI: InChI=1S/C21H22O4/c1-14(2)4-8-16-12-18(20(24)13-21(16)25-3)19(23)11-7-15-5-9-17(22)10-6-15/h4-7,9-13,22,24H,8H2,1-3H3/b11-7+
描述信息
4'-O-Methylbavachalcone is a chalcone isolated from Psoralea corylifolia, inhibits severe acute respiratory syndrome coronavirus (SARS-CoV) papain-like protease (PLpro) activity, with an IC50 of 10.1 μM[1].
4'-O-Methylbavachalcone is a chalcone isolated from Psoralea corylifolia, inhibits severe acute respiratory syndrome coronavirus (SARS-CoV) papain-like protease (PLpro) activity, with an IC50 of 10.1 μM[1].
同义名列表
数据库引用编号
8 个数据库交叉引用编号
- PubChem: 5321765
- Metlin: METLIN51852
- LipidMAPS: LMPK12120046
- KNApSAcK: C00007070
- CAS: 20784-60-5
- Flavonoid: FL1C1ANI0009
- medchemexpress: HY-N1910
- LOTUS: LTS0192027
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)
15 个相关的物种来源信息
- 109218 - Cullen: LTS0192027
- 429560 - Cullen corylifolium: 10.1002/CHIN.200548207
- 429560 - Cullen corylifolium: 10.1016/J.BMC.2004.06.014
- 429560 - Cullen corylifolium: 10.1248/BPB.28.2253
- 429560 - Cullen corylifolium: LTS0192027
- 2759 - Eukaryota: LTS0192027
- 3803 - Fabaceae: LTS0192027
- 3398 - Magnoliopsida: LTS0192027
- 33090 - Plants: -
- 3896 - Sophora: LTS0192027
- 76398 - Sophora prostrata: 10.1016/0031-9422(94)00721-5
- 76398 - Sophora prostrata: LTS0192027
- 35493 - Streptophyta: LTS0192027
- 58023 - Tracheophyta: LTS0192027
- 33090 - Viridiplantae: LTS0192027
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
- Ziying Liu, Changshui Wang, Yali Wang, Lei Wang, Yueyuan Zhang, Genquan Yan. 4'-O-Methylbroussochalcone B as a novel tubulin polymerization inhibitor suppressed the proliferation and migration of acute myeloid leukaemia cells.
BMC cancer.
2021 Jan; 21(1):91. doi:
10.1186/s12885-020-07759-4
. [PMID: 33482772] - Namrta Choudhry, Xin Zhao, Dan Xu, Mark Zanin, Weisan Chen, Zifeng Yang, Jianxin Chen. Chinese Therapeutic Strategy for Fighting COVID-19 and Potential Small-Molecule Inhibitors against Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2).
Journal of medicinal chemistry.
2020 11; 63(22):13205-13227. doi:
10.1021/acs.jmedchem.0c00626
. [PMID: 32845145] - Atieh Hajirahimkhan, Obinna Mbachu, Charlotte Simmler, Sarah G Ellis, Huali Dong, Dejan Nikolic, David C Lankin, Richard B van Breemen, Shao-Nong Chen, Guido F Pauli, Birgit M Dietz, Judy L Bolton. Estrogen Receptor (ER) Subtype Selectivity Identifies 8-Prenylapigenin as an ERβ Agonist from Glycyrrhiza inflata and Highlights the Importance of Chemical and Biological Authentication.
Journal of natural products.
2018 04; 81(4):966-975. doi:
10.1021/acs.jnatprod.7b01070
. [PMID: 29641206] - Nidhi Gupta, Arem Qayum, Arun Raina, Ravi Shankar, Sumeet Gairola, Shashank Singh, Payare L Sangwan. Synthesis and biological evaluation of novel bavachinin analogs as anticancer agents.
European journal of medicinal chemistry.
2018 Feb; 145(?):511-523. doi:
10.1016/j.ejmech.2018.01.006
. [PMID: 29335212]