Compounds > baicalin
Page last updated: 2024-08-24

baicalin and hyperoside

baicalin has been researched along with hyperoside in 7 studies

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (14.29)29.6817
2010's3 (42.86)24.3611
2020's3 (42.86)2.80

Authors

AuthorsStudies
Saeki, K; Sunaga, S; Takahashi, S; Takasawa, R; Tanuma, S; Yoshimori, A1
Amić, D; Lucić, B1
Jin, YS1
Dranchak, PK; Huang, R; Inglese, J; Lamy, L; Oliphant, E; Queme, B; Tao, D; Wang, Y; Xia, M1
Ismail, NA; Jusoh, SA1
Ge, G; Lu, D; Shi, T; Tian, S; Tu, D; Xu, X; Yang, J; Yang, Y; Zeng, H; Zhang, F; Zhang, W; Zhao, J; Zhao, S; Zheng, Y1
Cai, W; Du, W; Ge, G; Hu, J; Liang, J; Liu, B; Liu, Y; Ma, G; Wu, X; Yang, P; Yang, Q; Yang, X; Zhang, Y; Zhu, G1

Reviews

1 review(s) available for baicalin and hyperoside

ArticleYear
Recent advances in natural antifungal flavonoids and their derivatives.
    Bioorganic & medicinal chemistry letters, 2019, 10-01, Volume: 29, Issue:19

    Topics: Antifungal Agents; Biological Products; Flavonoids; Fungi; Humans; Mycoses

2019

Other Studies

6 other study(ies) available for baicalin and hyperoside

ArticleYear
Structure-activity relationship of human GLO I inhibitory natural flavonoids and their growth inhibitory effects.
    Bioorganic & medicinal chemistry, 2008, Apr-01, Volume: 16, Issue:7

    Topics: Animals; Biological Products; Cell Line; Cell Proliferation; Enzyme Inhibitors; Flavonoids; Humans; Hydroxylation; Ketones; Lactoylglutathione Lyase; Molecular Structure; Spodoptera; Structure-Activity Relationship

2008
Reliability of bond dissociation enthalpy calculated by the PM6 method and experimental TEAC values in antiradical QSAR of flavonoids.
    Bioorganic & medicinal chemistry, 2010, Jan-01, Volume: 18, Issue:1

    Topics: Flavonoids; Free Radical Scavengers; Models, Biological; Quantitative Structure-Activity Relationship; Quantum Theory; Software; Thermodynamics

2010
In vivo quantitative high-throughput screening for drug discovery and comparative toxicology.
    Disease models & mechanisms, 2023, 03-01, Volume: 16, Issue:3

    Topics: Animals; Caenorhabditis elegans; Drug Discovery; High-Throughput Screening Assays; Humans; Proteomics; Small Molecule Libraries

2023
Molecular Docking and Molecular Dynamics Simulation Studies to Predict Flavonoid Binding on the Surface of DENV2 E Protein.
    Interdisciplinary sciences, computational life sciences, 2017, Volume: 9, Issue:4

    Topics: Dengue Virus; Flavanones; Flavones; Flavonoids; Molecular Dynamics Simulation; Quercetin; Viral Envelope Proteins

2017
Systems pharmacological study illustrates the immune regulation, anti-infection, anti-inflammation, and multi-organ protection mechanism of Qing-Fei-Pai-Du decoction in the treatment of COVID-19.
    Phytomedicine : international journal of phytotherapy and phytopharmacology, 2021, Volume: 85

    Topics: Animals; Anti-Inflammatory Agents; Antiviral Agents; Computational Biology; COVID-19 Drug Treatment; Drugs, Chinese Herbal; Flavonoids; Glycyrrhizic Acid; Hesperidin; Humans; Male; Medicine, Chinese Traditional; Mice; Molecular Docking Simulation; Quercetin; Rabbits; RAW 264.7 Cells; SARS-CoV-2; Signal Transduction

2021
Inhibition of Human UDP-Glucuronosyltransferases1A1-Mediated Bilirubin Glucuronidation by the Popular Flavonoids Baicalein, Baicalin, and Hyperoside Is Responsible for Herb (Shuang-Huang-Lian)-Induced Jaundice.
    Drug metabolism and disposition: the biological fate of chemicals, 2022, Volume: 50, Issue:5

    Topics: Bilirubin; Coptis chinensis; Flavanones; Flavonoids; Glucuronides; Glucuronosyltransferase; Humans; Jaundice; Molecular Docking Simulation; Quercetin; Uridine Diphosphate

2022