Liquiritigenin (BioDeep_00000000383)
Secondary id: BioDeep_00000228373, BioDeep_00000270165, BioDeep_00000860867
human metabolite PANOMIX_OTCML-2023 Endogenous Chemicals and Drugs BioNovoGene_Lab2019
代谢物信息卡片
化学式: C15H12O4 (256.0735552)
中文名称: 甘草素
谱图信息:
最多检出来源 Homo sapiens(blood) 2.75%
分子结构信息
SMILES: C1(O)C=C2O[C@]([H])(C3C=CC(O)=CC=3)CC(=O)C2=CC=1
InChI: InChI=1S/C15H12O4/c16-10-3-1-9(2-4-10)14-8-13(18)12-6-5-11(17)7-15(12)19-14/h1-7,14,16-17H,8H2
描述信息
Liquiritigenin is a dihydroxyflavanone compound having the two hydroxy substituents at the 4- and 7-positions. Isolated from the root of Glycyrrhizae uralensis, it is a selective agonist for oestrogen receptor beta. It has a role as a hormone agonist and a plant metabolite.
5-deoxyflavanone is a solid. This compound belongs to the flavanones. These are compounds containing a flavan-3-one moiety, whose structure is characterized by a 2-phenyl-3,4-dihydro-2H-1-benzopyran bearing a ketone at the carbon C3.
MF101 is a novel estrogen receptor beta (ERβ) selective agonist and unlike currently available hormone therapies, does not activate the estrogen receptor alpha (ERα), known to be implicated in tumor formation. MF101 is an oral drug designed for the treatment of hot flashes and night sweats in peri-menopausal and menopausal women.
Liquiritigenin is a natural product found in Dracaena draco, Pterocarpus marsupium, and other organisms with data available.
See also: Glycyrrhiza Glabra (part of); Glycyrrhiza uralensis Root (part of); Pterocarpus marsupium wood (part of).
Isolated from Glycyrrhiza, Medicago, Myroxylon, Cicer and all Leguminosae subspecies Several glycosides, particularly the rutinoside and neohesperidoside, are important in influencing citrus fruit flavour [DFC]. Liquiritigenin is found in many foods, some of which are sorrel, roselle, pepper (c. annuum), and black crowberry.
Liquiritigenin is found in alfalfa. Liquiritigenin is isolated from Glycyrrhiza, Medicago, Myroxylon, Cicer, and all Leguminosae species. Several glycosides, particularly rutinoside and neohesperidoside, are important in influencing citrus fruit flavour.
A dihydroxyflavanone compound having the two hydroxy substituents at the 4- and 7-positions. Isolated from the root of Glycyrrhizae uralensis, it is a selective agonist for oestrogen receptor beta.
Liquiritigenin, a flavanone isolated from Glycyrrhiza uralensis, is a highly selective estrogen receptor β (ERβ) agonist with an EC50 of 36.5 nM for activation of the ERE tk-Luc.
Liquiritigenin, a flavanone isolated from Glycyrrhiza uralensis, is a highly selective estrogen receptor β (ERβ) agonist with an EC50 of 36.5 nM for activation of the ERE tk-Luc.
同义名列表
35 个代谢物同义名
4H-1-Benzopyran-4-one, 2,3-dihydro-7-hydroxy-2-(4-hydroxyphenyl)-, (2S)-; 4H-1-Benzopyran-4-one, 2,3-dihydro-7-hydroxy-2-(4-hydroxyphenyl)-, (S)-; 4H-1-Benzopyran-4-one, 2,3-dihydro-7-hydroxy-2-(4-hydroxyphenyl)-,(2S)-; (2S)-7-hydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-one; (2S)-7-Hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-1-benzopyran-4-one; (2S)-2,3-Dihydro-7-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one; (S)-2,3-Dihydro-7-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one; (2S)-7-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one; (2S)-2-(4-hydroxyphenyl)-7-oxidanyl-2,3-dihydrochromen-4-one; (2S)-7-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one; (2S)-7-hydroxy-2-(4-hydroxyphenyl)chroman-4-one; (S)-7-Hydroxy-2-(4-hydroxyphenyl)chroman-4-one; 7-hydroxy-2-(4-hydroxy-phenyl)-chroman-4-one; (-)-(2S)-7,4’-Dihydroxyflavanone; (-)-(S)-4’,7-Dihydroxyflavanone; Liquiritigenin, >=97.0\\% (HPLC); (-)-(2s)-7,4-dihydroxyflavanone; (-)-(S)-4,7-Dihydroxyflavanone; FURUXTVZLHCCNA-AWEZNQCLSA-N; FLAVANONE, 4,7-DIHYDROXY-; 7,4’-Dihydroxyflavanone; 4’,7-Dihydroxyflavanone; 4,7-Dihydroxyflavanone; 7,4-dihydroxyflavanone; LIQUIRITIGENIN [INCI]; (2S)-liquiritigenin; (-)-liquiritigenin; (S)-liquiritigenin; 5-DEOXYFLAVANONE; Liquiritigenin; LIQUIRTIGENIN; Menerba; DFV; DL-Liquiritigenin; 4',7-Dihydroxyflavanone
数据库引用编号
28 个数据库交叉引用编号
- ChEBI: CHEBI:28777
- KEGG: C09762
- PubChem: 114829
- PubChem: 1889
- HMDB: HMDB0029519
- Metlin: METLIN52551
- DrugBank: DB03601
- ChEMBL: CHEMBL252642
- Wikipedia: Liquiritigenin
- LipidMAPS: LMPK12140061
- MeSH: liquiritigenin
- ChemIDplus: 0000578869
- MetaCyc: CPD-3061
- KNApSAcK: C00000977
- foodb: FDB000655
- chemspider: 102790
- CAS: 578-86-9
- medchemexpress: HY-N0377
- PMhub: MS000005051
- MetaboLights: MTBLC28777
- PubChem: 11950
- PDB-CCD: DFV
- 3DMET: B03260
- NIKKAJI: J22.604A
- RefMet: Liquiritigenin
- LOTUS: LTS0251224
- wikidata: Q6557526
- BioNovoGene_Lab2019: BioNovoGene_Lab2019-672
分类词条
相关代谢途径
Reactome(0)
代谢反应
29 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(3)
- 6,7,4'-trihydroxyisoflavone biosynthesis:
6,7,4'-trihydroxyflavanone + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ 2,6,7,4'-tetrahydroxyisoflavanone + H2O + an oxidized [NADPH-hemoprotein reductase]
- isoflavonoid biosynthesis I:
SAM + daidzein ⟶ H+ + SAH + isoformononetin
- echinatin biosynthesis:
isoliquiritigenin ⟶ (2S)-liquiritigenin
WikiPathways(0)
Plant Reactome(3)
- Metabolism and regulation:
ATP + CoA + propionate ⟶ AMP + PPi + PROP-CoA
- Secondary metabolism:
GPP + H2O ⟶ PPi + geraniol
- 6,7,4'-Trihydroxyisoflavone biosynthesis:
H+ + Oxygen + TPNH + liquiritigenin ⟶ 6,7,4'-trihydroxyflavanone + H2O + TPN
INOH(0)
PlantCyc(22)
- 6,7,4'-trihydroxyisoflavone biosynthesis:
(2S)-liquiritigenin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ 6,7,4'-trihydroxyflavanone + H2O + an oxidized [NADPH-hemoprotein reductase]
- 6,7,4'-trihydroxyisoflavone biosynthesis:
2,6,7,4'-tetrahydroxyisoflavanone ⟶ 6,7,4'-trihydroxyisoflavone + H2O
- 6,7,4'-trihydroxyisoflavone biosynthesis:
2,6,7,4'-tetrahydroxyisoflavanone ⟶ 6,7,4'-trihydroxyisoflavone + H2O
- 6,7,4'-trihydroxyisoflavone biosynthesis:
6,7,4'-trihydroxyflavanone + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ 2,6,7,4'-tetrahydroxyisoflavanone + H2O + an oxidized [NADPH-hemoprotein reductase]
- echinatin biosynthesis:
isoliquiritigenin ⟶ (2S)-liquiritigenin
- isoflavonoid biosynthesis I:
SAM + daidzein ⟶ H+ + SAH + isoformononetin
- isoflavonoid biosynthesis I:
2,4',7-trihydroxyisoflavanone ⟶ H2O + daidzein
- echinatin biosynthesis:
(2S)-liquiritigenin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ 2-hydroxyliquiritigenin + H2O + an oxidized [NADPH-hemoprotein reductase]
- isoflavonoid biosynthesis I:
2,4',7-trihydroxyisoflavanone ⟶ H2O + daidzein
- echinatin biosynthesis:
(2S)-liquiritigenin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ 2-hydroxyliquiritigenin + H2O + an oxidized [NADPH-hemoprotein reductase]
- isoflavonoid biosynthesis I:
2,4',7-trihydroxyisoflavanone ⟶ H2O + daidzein
- echinatin biosynthesis:
(2S)-liquiritigenin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ 2-hydroxyliquiritigenin + H2O + an oxidized [NADPH-hemoprotein reductase]
- echinatin biosynthesis:
SAM + licodione ⟶ 2'-O-methyllicodione + H+ + SAH
- isoflavonoid biosynthesis I:
2,4',7-trihydroxyisoflavanone ⟶ H2O + daidzein
- isoflavonoid biosynthesis I:
SAM + daidzein ⟶ H+ + SAH + isoformononetin
- echinatin biosynthesis:
isoliquiritigenin ⟶ (2S)-liquiritigenin
- echinatin biosynthesis:
(2S)-liquiritigenin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ 2-hydroxyliquiritigenin + H2O + an oxidized [NADPH-hemoprotein reductase]
- isoflavonoid biosynthesis I:
2,4',7-trihydroxyisoflavanone ⟶ H2O + daidzein
- echinatin biosynthesis:
(2S)-liquiritigenin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ 2-hydroxyliquiritigenin + H2O + an oxidized [NADPH-hemoprotein reductase]
- isoflavonoid biosynthesis I:
2,4',7-trihydroxyisoflavanone ⟶ H2O + daidzein
- echinatin biosynthesis:
SAM + licodione ⟶ 2'-O-methyllicodione + H+ + SAH
- isoflavonoid biosynthesis I:
SAM + daidzein ⟶ H+ + SAH + isoformononetin
COVID-19 Disease Map(0)
PharmGKB(0)
101 个相关的物种来源信息
- 217498 - Acalypha wilkesiana: 10.1002/CBDV.200890015
- 3702 - Arabidopsis thaliana: 10.1007/BF00392354
- 1960787 - Astragalus microcephalus: 10.1007/S10600-011-9800-0
- 1969222 - Baptisia lecontei: 10.1016/S0031-9422(00)84834-7
- 1835378 - Brosimum acutifolium:
- 1835378 - Brosimum acutifolium: 10.1021/NP010389J
- 56060 - Butea monosperma: 10.1248/CPB.57.428
- 30426 - Carpodacus: 10.3987/COM-03-9994
- 500180 - Centrolobium robustum: 10.1071/CH9841127
- 76958 - Clausena: 10.1016/S0031-9422(99)00220-4
- 76959 - Clausena excavata:
- 209086 - Crinum bulbispermum: 10.1016/S0031-9422(00)00184-9
- 450024 - Dalbergia ecastaphyllum:
- 450024 - Dalbergia ecastaphyllum: 10.1016/0031-9422(75)83053-6
- 1288010 - Dalbergia latifolia:
- 2805520 - Dalbergia louvelii: 10.1021/NP030008X
- 1265830 - Dalbergia nitidula: 10.1016/S0031-9422(01)00462-9
- 499988 - Dalbergia odorifera:
- 499988 - Dalbergia odorifera T.Chen: -
- 1353466 - Dalbergia parviflora:
- 2507847 - Dalbergia sissoides:
- 2507847 - Dalbergia sissoides: 10.4268/CJCMM20140916
- 1966414 - Dalbergia stevensonii:
- 149639 - Dermatophyllum secundiflorum:
- 64700 - Dioscorea nipponica: 10.1016/J.JEP.2014.06.043
- 100532 - Dracaena draco: 10.1021/NP000085H
- 556509 - Erythrina fusca:
- 556509 - Erythrina fusca: 10.1016/S0031-9422(98)00132-0
- 46348 - Glycyrrhiza echinata:
- 46348 - Glycyrrhiza echinata: 10.3987/COM-89-5304
- 49827 - Glycyrrhiza glabra:
- 49827 - Glycyrrhiza glabra L.: -
- 74614 - Glycyrrhiza inflata:
- 74614 - Glycyrrhiza inflata: 10.3987/COM-89-5304
- 74614 - Glycyrrhiza inflata Bat.: -
- 74859 - Glycyrrhiza pallidiflora:
- 74613 - Glycyrrhiza uralensis:
- 74613 - Glycyrrhiza uralensis: 10.3987/COM-89-5260
- 74613 - Glycyrrhiza uralensis Fisch.: -
- 119828 - Hedysarum polybotrys: 10.1248/CPB.32.3267
- 9606 - Homo sapiens: -
- 161756 - Isatis tinctoria: 10.4268/CJCMM20130812
- 701533 - Lespedeza cyrtobotrya: 10.1021/NP800395J
- 701533 - Lespedeza cyrtobotrya: 10.1021/NP800535G
- 486170 - Luxemburgia octandra: 10.1590/S0103-50532004000100023
- 37501 - Maackia amurensis: 10.1007/S10600-009-9195-3
- 47085 - Medicago lupulina: 10.1016/J.PHYTOCHEM.2006.10.023
- 3879 - Medicago sativa: 10.1016/J.PHYTOCHEM.2006.10.023
- 3880 - Medicago truncatula: 10.1016/J.PHYTOCHEM.2006.10.023
- 1155344 - Melilotus altissimus: 10.1515/ZNC-1977-5-625
- 1078768 - Melilotus dentatus: 10.1515/ZNC-1977-5-625
- 1632797 - Melilotus elegans: 10.1515/ZNC-1977-5-625
- 1632799 - Melilotus infestus: 10.1515/ZNC-1977-5-625
- 78528 - Melilotus italicus: 10.1515/ZNC-1977-5-625
- 1279044 - Melilotus messanensis: 10.1016/S0031-9422(98)00453-1
- 1279044 - Melilotus messanensis: 10.1515/ZNC-1977-5-625
- 1524233 - Melilotus neapolitanus: 10.1515/ZNC-1977-5-625
- 1632800 - Melilotus polonicus: 10.1515/ZNC-1977-5-625
- 861159 - Melilotus sulcatus: 10.1515/ZNC-1977-5-625
- 1632803 - Melilotus tauricus: 10.1515/ZNC-1977-5-625
- 1632804 - Melilotus wolgicus: 10.1515/ZNC-1977-5-625
- 3881 - Onobrychis: 10.1515/ZNC-1978-1-227
- 3882 - Onobrychis viciifolia: 10.1515/ZNC-1978-1-227
- 1479707 - Oxytropis falcata:
- 1479707 - Oxytropis falcata: 10.1021/NP100339U
- 2715301 - Oxytropis trichophysa: 10.1007/BF00630449
- 44586 - Panax Notoginseng (Burk.) F. H. Chen Ex C. Chow: -
- 644807 - Pancratium maritimum: 10.1016/S0031-9422(98)00429-4
- 162874 - Peltogyne: 10.1016/0031-9422(74)80331-6
- 327141 - Peltogyne paniculata: 10.1016/0031-9422(74)80331-6
- 327909 - Peltogyne venosa: 10.1016/0031-9422(74)80331-6
- 1079081 - Pericopsis elata: 10.1039/P19760000186
- 53917 - Pericopsis mooniana: 10.1039/P19760000186
- 337186 - Physochlaina physaloides: 10.1007/BF00633404
- 421375 - Pison: 10.1016/0031-9422(81)80130-6
- 3887 - Pisum: 10.1016/0031-9422(81)80130-6
- 3888 - Pisum sativum: 10.1016/0031-9422(81)80130-6
- 33090 - Plants: -
- 500185 - Platymiscium floribundum: 10.1021/NP049854D
- 557757 - Platymiscium yucatanum: 10.1515/HFSG.1998.52.5.459
- 56065 - Pongamia pinnata: 10.1055/A-0626-7356
- 182271 - Pterocarpus angolensis:
- 182271 - Pterocarpus angolensis: 10.1039/P19810000263
- 108278 - Pterocarpus macrocarpus:
- 108278 - Pterocarpus macrocarpus: 10.1055/S-2007-969163
- 1071187 - Pterocarpus marsupium:
- 1071199 - Pterocarpus santalinus: 10.1016/S0031-9422(99)00526-9
- 35938 - Robinia pseudoacacia: 10.1246/NIKKASHI1948.87.11_1201
- 508984 - Schnella guianensis: 10.1016/0031-9422(88)80455-2
- 3895 - Sesbania rostrata: 10.1094/MPMI-4-262
- 41786 - Sinofranchetia chinensis: 10.1007/PL00000710
- 3896 - Sophora: 10.1016/S0031-9422(97)00802-9
- 455371 - Spatholobus suberectus: 10.1016/J.PHYTOCHEM.2006.05.008
- 3900 - Trifolium subterraneum:
- 3900 - Trifolium subterraneum: 10.1016/S0031-9422(00)85667-8
- 58847 - Virgilia oroboides: 10.1016/0031-9422(90)80205-U
- 1592184 - Xanthorrhoea glauca: 10.1016/S0305-1978(97)00031-8
- 1592185 - Xanthorrhoea johnsonii: 10.1016/S0305-1978(97)00031-8
- 1592186 - Xanthorrhoea latifolia: 10.1016/S0305-1978(97)00031-8
- 49740 - Xanthorrhoea resinosa: 10.1016/S0305-1978(97)00031-8
- 33090 - 甘草: -
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
- Peijun Sun, Huixian Chen, Xiaoyu Fan, Jiayi Wang, Lujie Lu, Guangchao Yang, Jining Liu, Weifeng Yao, Feng Ding, Jie Ding, Jianmei Liu, Tulin Lu, Lihong Chen. Exploring the effective components of honey-processed licorice (Glycyrrhiza uralensis Fisch.) in attenuating Doxorubicin-induced myocardial cytotoxicity by combining network pharmacology and in vitro experiments.
Journal of ethnopharmacology.
2024 Jul; 329(?):118178. doi:
10.1016/j.jep.2024.118178
. [PMID: 38604511] - Lei Bao, Pei Hao, Meiju Jiang, Weijiang Chu. Liquiritigenin regulates insulin sensitivity and ameliorates inflammatory responses in the nonalcoholic fatty liver by activation PI3K/AKT pathway.
Chemical biology & drug design.
2023 Jul; ?(?):. doi:
10.1111/cbdd.14292
. [PMID: 37455324] - Atieh Hajirahimkhan, Caitlin Howell, Elizabeth T Bartom, Huali Dong, Daniel D Lantvit, Xiaoling Xuei, Shao-Nong Chen, Guido F Pauli, Judy L Bolton, Susan E Clare, Seema A Khan, Birgit M Dietz. Breast cancer prevention with liquiritigenin from licorice through the inhibition of aromatase and protein biosynthesis in high-risk women's breast tissue.
Scientific reports.
2023 05; 13(1):8734. doi:
10.1038/s41598-023-34762-z
. [PMID: 37253812] - Vineet Babu, Deepak Singh Kapkoti, Monika Binwal, Rajendra S Bhakuni, Karuna Shanker, Manju Singh, Sudeep Tandon, Madhav N Mugale, Narendra Kumar, Dnyaneshwar U Bawankule. Liquiritigenin, isoliquiritigenin rich extract of glycyrrhiza glabra roots attenuates inflammation in macrophages and collagen-induced arthritis in rats.
Inflammopharmacology.
2023 Mar; ?(?):. doi:
10.1007/s10787-023-01152-w
. [PMID: 36947299] - Qi Lu, Lin-Feng Zou, Yuan-Zhen Gao, Ting Ye, Meng-Jiao Li, Yu-Kun Zhang, Bing Liang, Wenshe Sun, Dong-Ming Xing. Liquiritigenin reverses skin aging by inhibiting UV-induced mitochondrial uncoupling and excessive energy consumption.
Journal of cosmetic dermatology.
2023 Mar; 22(3):1017-1030. doi:
10.1111/jocd.15506
. [PMID: 36575875] - Muqing Zhang, Jiaying Qi, Qianqian He, Donglai Ma, Jing Li, Xi Chu, Saijie Zuo, Yixin Zhang, Li Li, Li Chu. Liquiritigenin protects against myocardial ischemic by inhibiting oxidative stress, apoptosis, and L-type Ca2+ channels.
Phytotherapy research : PTR.
2022 Sep; 36(9):3619-3631. doi:
10.1002/ptr.7528
. [PMID: 35747908] - Meng Zhou, Yanpeng Dai, Yong Ma, Yi Yan, Min Hua, Qi Gao, Xue Geng, Qian Zhou. Protective Effects of Liquiritigenin against Cisplatin-Induced Nephrotoxicity via NRF2/SIRT3-Mediated Improvement of Mitochondrial Function.
Molecules (Basel, Switzerland).
2022 Jun; 27(12):. doi:
10.3390/molecules27123823
. [PMID: 35744945] - Hong Qin, Ziyu Song, Chunyu Zhao, Jinxin Yang, Fan Xia, Lewen Wang, Anwar Ali, Wenya Zheng. Liquiritigenin Inhibits Lipid Accumulation in 3T3-L1 Cells via mTOR-Mediated Regulation of the Autophagy Mechanism.
Nutrients.
2022 Mar; 14(6):. doi:
10.3390/nu14061287
. [PMID: 35334944] - Zhibing Xu, Zongde Hu, Hanchen Xu, Lifen Zhang, Liang Li, Yi Wang, Yuanqing Zhu, Limeng Yang, Dan Hu. Liquiritigenin alleviates doxorubicin-induced chronic heart failure via promoting ARHGAP18 and suppressing RhoA/ROCK1 pathway.
Experimental cell research.
2022 02; 411(2):113008. doi:
10.1016/j.yexcr.2022.113008
. [PMID: 34990617] - Zhanwei Zhang, Jie Lin, Jinhui Hu, Lifang Liu. Liquiritigenin Blocks Breast Cancer Progression by Inhibiting Connective Tissue Growth Factor Expression via Up-Regulating miR-383-5p.
International journal of toxicology.
2022 Jan; 41(1):5-15. doi:
10.1177/10915818211059470
. [PMID: 35045746] - Yingchen Ji, Weiwei Hu, Yan Jin, Huiming Yu, Jin Fang. Liquiritigenin exerts the anti-cancer role in oral cancer via inducing autophagy-related apoptosis through PI3K/AKT/mTOR pathway inhibition in vitro and in vivo.
Bioengineered.
2021 12; 12(1):6070-6082. doi:
10.1080/21655979.2021.1971501
. [PMID: 34488535] - Muqing Zhang, Yucong Xue, Bin Zheng, Li Li, Xi Chu, Yang Zhao, Yongchao Wu, Jianping Zhang, Xue Han, Zhonglin Wu, Li Chu. Liquiritigenin protects against arsenic trioxide-induced liver injury by inhibiting oxidative stress and enhancing mTOR-mediated autophagy.
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.
2021 Nov; 143(?):112167. doi:
10.1016/j.biopha.2021.112167
. [PMID: 34560535] - Li Li, Hui Fang, Yong-Hong Yu, Shan-Xin Liu, Zhi-Qiang Yang. Liquiritigenin attenuates isoprenaline‑induced myocardial fibrosis in mice through the TGF‑β1/Smad2 and AKT/ERK signaling pathways.
Molecular medicine reports.
2021 Oct; 24(4):. doi:
10.3892/mmr.2021.12326
. [PMID: 34328199] - Yexiang Du, Min Luo, Yehong Du, Mingliang Xu, Qiuhui Yao, Kejian Wang, Guiqiong He. Liquiritigenin Decreases Aβ Levels and Ameliorates Cognitive Decline by Regulating Microglia M1/M2 Transformation in AD Mice.
Neurotoxicity research.
2021 Apr; 39(2):349-358. doi:
10.1007/s12640-020-00284-z
. [PMID: 32990912] - Eun Ju Lee, Sibhghatulla Shaikh, Khurshid Ahmad, Syed Sayeed Ahmad, Jeong Ho Lim, Soyoung Park, Hye Jin Yang, Won-Kyung Cho, Sang-Joon Park, Yong-Ho Lee, So-Young Park, Jin-Yeul Ma, Inho Choi. Isolation and Characterization of Compounds from Glycyrrhiza uralensis as Therapeutic Agents for the Muscle Disorders.
International journal of molecular sciences.
2021 Jan; 22(2):. doi:
10.3390/ijms22020876
. [PMID: 33467209] - Mingming Qin, Aili Guo, Feng Li, Fuxiang Zhang, Meirong Bi, Yamin Zhang, Weiwei Zhu. Liquiritigenin enhances cyclic adenosine monophosphate production to mitigate inflammation in dendritic cells.
International journal of immunopathology and pharmacology.
2021 Jan; 35(?):20587384211038098. doi:
10.1177/20587384211038098
. [PMID: 34939873] - Chang-Can Shi, Kun-Ming Qin, Ke Xu, An Chen, Ting Cai, Bao-Chang Cai. Development of liquiritigenin-phospholipid complex with the enhanced oral bioavailability.
Chinese journal of natural medicines.
2020 Dec; 18(12):916-921. doi:
10.1016/s1875-5364(20)60035-8
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Phytomedicine : international journal of phytotherapy and phytopharmacology.
2020 Nov; 78(?):153313. doi:
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Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment.
2020 Sep; 37(9):1437-1448. doi:
10.1080/19440049.2020.1778187
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Journal of ethnopharmacology.
2020 Jul; 257(?):112892. doi:
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Molecules (Basel, Switzerland).
2020 Apr; 25(9):. doi:
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Biomedical chromatography : BMC.
2020 Apr; 34(4):e4788. doi:
10.1002/bmc.4788
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Journal of microbiology and biotechnology.
2020 Feb; 30(2):178-186. doi:
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Molecules (Basel, Switzerland).
2020 Jan; 25(2):. doi:
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International journal of nanomedicine.
2020; 15(?):1101-1115. doi:
10.2147/ijn.s235832
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Toxicology.
2019 12; 428(?):152307. doi:
10.1016/j.tox.2019.152307
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Molecules (Basel, Switzerland).
2019 Nov; 24(22):. doi:
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Natural product research.
2019 Nov; 33(22):3298-3302. doi:
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Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica.
2019 Oct; 44(19):4249-4256. doi:
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European journal of pharmacology.
2019 Aug; 856(?):172421. doi:
10.1016/j.ejphar.2019.172421
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Journal of separation science.
2019 Aug; 42(15):2534-2549. doi:
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Xenobiotica; the fate of foreign compounds in biological systems.
2019 Jun; 49(6):708-717. doi:
10.1080/00498254.2018.1493756
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Molecules (Basel, Switzerland).
2019 May; 24(9):. doi:
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Nutrients.
2019 May; 11(5):. doi:
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European journal of medicinal chemistry.
2019 Apr; 167(?):291-311. doi:
10.1016/j.ejmech.2019.01.044
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European journal of medicinal chemistry.
2019 Mar; 166(?):186-196. doi:
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Phytomedicine : international journal of phytotherapy and phytopharmacology.
2019 Mar; 55(?):119-124. doi:
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Food & function.
2018 Nov; 9(11):5528-5535. doi:
10.1039/c8fo01217b
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Toxicology and applied pharmacology.
2018 09; 355(?):18-27. doi:
10.1016/j.taap.2018.06.014
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Toxicology letters.
2018 Sep; 294(?):27-36. doi:
10.1016/j.toxlet.2018.05.008
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The Journal of membrane biology.
2018 08; 251(4):551-562. doi:
10.1007/s00232-018-0031-1
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BMC complementary and alternative medicine.
2018 May; 18(1):140. doi:
10.1186/s12906-018-2207-8
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Journal of natural products.
2018 04; 81(4):966-975. doi:
10.1021/acs.jnatprod.7b01070
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Drug testing and analysis.
2018 Feb; 10(2):262-271. doi:
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Bioorganic & medicinal chemistry.
2018 01; 26(1):278-284. doi:
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Bioorganic & medicinal chemistry letters.
2017 12; 27(24):5400-5403. doi:
10.1016/j.bmcl.2017.11.013
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Bioorganic & medicinal chemistry.
2017 10; 25(20):5522-5530. doi:
10.1016/j.bmc.2017.08.018
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Bioorganic & medicinal chemistry.
2017 07; 25(14):3706-3713. doi:
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Journal of experimental botany.
2017 06; 68(12):3231-3241. doi:
10.1093/jxb/erx059
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Journal of pharmaceutical and biomedical analysis.
2017 Apr; 137(?):23-32. doi:
10.1016/j.jpba.2017.01.021
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European journal of nutrition.
2017 Mar; 56(2):635-647. doi:
10.1007/s00394-015-1107-7
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Journal of natural products.
2017 02; 80(2):334-346. doi:
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Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.
2017 Feb; 86(?):694-704. doi:
10.1016/j.biopha.2016.12.066
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Yao xue xue bao = Acta pharmaceutica Sinica.
2017 Feb; 52(2):318-26. doi:
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Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.
2016 Dec; 84(?):1930-1936. doi:
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Phytotherapy research : PTR.
2016 Oct; 30(10):1708-1715. doi:
10.1002/ptr.5677
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Behavioural brain research.
2016 07; 308(?):177-86. doi:
10.1016/j.bbr.2016.04.039
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Psychiatry research.
2016 Jun; 240(?):131-136. doi:
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Journal of natural products.
2016 Feb; 79(2):281-92. doi:
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Molecular nutrition & food research.
2016 Feb; 60(2):369-80. doi:
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Steroids.
2016 Jan; 105(?):42-9. doi:
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Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials.
2016 Jan; 39(1):82-5. doi:
"
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Chemical research in toxicology.
2015 Nov; 28(11):2130-41. doi:
10.1021/acs.chemrestox.5b00310
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Phytotherapy research : PTR.
2015 Nov; 29(11):1714-21. doi:
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Chinese journal of natural medicines.
2015 Nov; 13(11):801-807. doi:
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Molecules (Basel, Switzerland).
2015 Sep; 20(10):18031-46. doi:
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Metabolic engineering.
2015 Sep; 31(?):84-93. doi:
10.1016/j.ymben.2015.07.002
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Molecules (Basel, Switzerland).
2015 Jul; 20(7):13041-54. doi:
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Phytotherapy research : PTR.
2015 Jul; 29(7):969-77. doi:
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Journal of ethnopharmacology.
2015 Jul; 169(?):1-7. doi:
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Applied microbiology and biotechnology.
2015 Jul; 99(14):6049-58. doi:
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Planta medica.
2015 May; 81(7):586-93. doi:
10.1055/s-0035-1545914
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Journal of ethnopharmacology.
2015 Mar; 162(?):134-9. doi:
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Planta medica.
2015 Mar; 81(5):357-62. doi:
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Asian Pacific journal of cancer prevention : APJCP.
2015; 16(10):4369-76. doi:
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International journal of cosmetic science.
2014 Dec; 36(6):553-60. doi:
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Food & function.
2014 Jul; 5(7):1432-40. doi:
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Scientific reports.
2014 Jul; 4(?):5676. doi:
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Journal of pharmaceutical and biomedical analysis.
2014 Jul; 95(?):76-84. doi:
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Journal of chromatographic science.
2014 Apr; 52(4):310-4. doi:
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Journal of natural products.
2014 Mar; 77(3):563-70. doi:
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Phytomedicine : international journal of phytotherapy and phytopharmacology.
2014 Mar; 21(4):415-22. doi:
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The Journal of pharmacy and pharmacology.
2014 Mar; 66(3):408-17. doi:
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Microbiology and immunology.
2014 Mar; 58(3):180-7. doi:
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Biological & pharmaceutical bulletin.
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