Oroxindin (BioDeep_00000230971)
Secondary id: BioDeep_00000231519
natural product PANOMIX_OTCML-2023
代谢物信息卡片
化学式: C22H20O11 (460.100557)
中文名称: 汉黄芩甙, 汉黄芩苷, 汉黄芩苷
谱图信息:
最多检出来源 Homo sapiens(natural_products) 4.68%
分子结构信息
SMILES: C1(O[C@H]2[C@H](O)[C@@H](O)[C@H](O)[C@@H](C(=O)O)O2)=C(OC)C2OC(C3C=CC=CC=3)=CC(=O)C=2C(O)=C1
InChI: InChI=1S/C22H20O11/c1-30-18-13(32-22-17(27)15(25)16(26)20(33-22)21(28)29)8-11(24)14-10(23)7-12(31-19(14)18)9-5-3-2-4-6-9/h2-8,15-17,20,22,24-27H,1H3,(H,28,29)/t15-,16-,17+,20-,22+/m0/s1
描述信息
Wogonin 7-O-beta-D-glucuronide is the glycosyloxyflavone which is the 7-O-glucuronide of wogonin. It is a glycosyloxyflavone, a monomethoxyflavone, a monohydroxyflavone, a monosaccharide derivative and a beta-D-glucosiduronic acid. It is functionally related to a wogonin. It is a conjugate acid of a wogonin 7-O-beta-D-glucuronate.
Oroxindin is a natural product found in Scutellaria discolor, Scutellaria indica, and other organisms with data available.
See also: Glycyrrhiza Glabra (part of).
The glycosyloxyflavone which is the 7-O-glucuronide of wogonin.
Wogonoside, a flavonoid glycoside isolated from Huangqin, possesses anti-inflammatory effects. Wogonoside induces autophagy in breast cancer cells by regulating MAPK-mTOR pathway[1][2].
Wogonoside, a flavonoid glycoside isolated from Huangqin, possesses anti-inflammatory effects. Wogonoside induces autophagy in breast cancer cells by regulating MAPK-mTOR pathway[1][2].
同义名列表
25 个代谢物同义名
(2S,3S,4S,5R,6S)-3,4,5-Trihydroxy-6-((5-hydroxy-8-methoxy-4-oxo-2-phenyl-4H-chromen-7-yl)oxy)tetrahydro-2H-pyran-2-carboxylic acid; (2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(5-hydroxy-8-methoxy-4-oxo-2-phenylchromen-7-yl)oxyoxane-2-carboxylic acid; .BETA.-D-GLUCOPYRANOSIDURONIC ACID, 5-HYDROXY-8-METHOXY-4-OXO-2-PHENYL-4H-1-BENZOPYRAN-7-YL; 5-hydroxy-8-methoxy-4-oxo-2-phenyl-4H-chromen-7-yl beta-D-glucopyranosiduronic acid; 5,7-dihydroxy-8-methoxyflavone 7-O-beta-D-glucuronide; wogonin 7-O-beta-glucuronine methyl ester; WOGONIN 7-O-.BETA.-D-GLUCURONOPYRANOSIDE; WOGONIN 7-O-beta-D-GLUCURONOPYRANOSIDE; WOGONIN 7-O-.BETA.-D-GLUCURONIDE; Wogonoside, >=95\\% (LC/MS-ELSD); wogonin 7-O-beta-D-glucuronide; WOGONIN 7-.BETA.-D-GLUCURONIDE; WOGONIN 7-beta-D-GLUCURONIDE; Wogonin 7-O-glucuronide; Wogonin 7-glucuronide; MEGxp0_000537; Glychionide B; ACon1_000851; Wogonoside; Oroxindin; (2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(5-hydroxy-4-keto-8-methoxy-2-phenyl-chromen-7-yl)oxy-tetrahydropyran-2-carboxylic acid; (2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[(5-hydroxy-8-methoxy-4-oxo-2-phenyl-7-chromenyl)oxy]-2-tetrahydropyrancarboxylic acid; (2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(5-hydroxy-8-methoxy-4-oxo-2-phenyl-chromen-7-yl)oxy-tetrahydropyran-2-carboxylic acid; (2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(5-hydroxy-8-methoxy-4-oxo-2-phenyl-chromen-7-yl)oxy-oxane-2-carboxylic acid; 51059-44-0
数据库引用编号
28 个数据库交叉引用编号
- ChEBI: CHEBI:61282
- PubChem: 3084961
- ChEMBL: CHEMBL464732
- Wikipedia: Oroxindin
- LipidMAPS: LMPK12111323
- MeSH: oroxindin
- ChemIDplus: 0051059440
- chemspider: 23089624
- CAS: 51059-44-0
- MoNA: VF-NPL-QTOF009189
- MoNA: VF-NPL-QTOF009188
- MoNA: VF-NPL-QTOF009187
- MoNA: VF-NPL-QTOF009186
- MoNA: VF-NPL-QTOF009185
- MoNA: VF-NPL-QTOF009184
- MoNA: VF-NPL-QTOF009183
- MoNA: VF-NPL-QTOF009182
- MoNA: VF-NPL-LTQ003682
- MoNA: VF-NPL-LTQ003680
- MoNA: VF-NPL-QEHF013278
- MoNA: VF-NPL-QEHF013277
- MoNA: VF-NPL-QEHF013276
- MoNA: VF-NPL-QEHF013275
- MoNA: VF-NPL-QEHF013274
- MoNA: VF-NPL-QEHF013273
- medchemexpress: HY-N0399
- MetaboLights: MTBLC61282
- RefMet: Oroxindin
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)
9 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。
文献列表
- Xuan Li, Ke Ding, Dang Yang, Meng-Hua Jiang, Chao Li, Fa-Gen Zhu, Jian-Guo Shao, E Sun, Liang Feng, Xiao-Bin Jia. [Optimization and evaluation of Xiaoer Pudilan Xiaoyan Syrup based on characterization of material properties].
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica.
2022 Nov; 47(21):5746-5756. doi:
10.19540/j.cnki.cjcmm.20220609.302
. [PMID: 36471992] - Qi Liu, Rui Zuo, Kai Wang, Fei-Fei Nong, Ya-Jun Fu, Shao-Wei Huang, Zeng-Feng Pan, Yi Zhang, Xia Luo, Xiang-Liang Deng, Xiao-Xue Zhang, Lian Zhou, Yang Chen. Oroxindin inhibits macrophage NLRP3 inflammasome activation in DSS-induced ulcerative colitis in mice via suppressing TXNIP-dependent NF-κB pathway.
Acta pharmacologica Sinica.
2020 Jun; 41(6):771-781. doi:
10.1038/s41401-019-0335-4
. [PMID: 31937929] - Harminder, V Singh, A K Chaudhary. A Review on the Taxonomy, Ethnobotany, Chemistry and Pharmacology of Oroxylum indicum Vent.
Indian journal of pharmaceutical sciences.
2011 Sep; 73(5):483-90. doi:
10.4103/0250-474x.98981
. [PMID: 22923859] - P K Chaudhuri, Rashmi Srivastava, Sunil Kumar, Sushil Kumar. Phytotoxic and antimicrobial constituents of Bacopa monnieri and Holmskioldia sanguinea.
Phytotherapy research : PTR.
2004 Feb; 18(2):114-7. doi:
10.1002/ptr.1278
. [PMID: 15022161]