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Target Separation and Potential Anticancer Activity of Withanolide-Based Glucose Transporter Protein 1 Inhibitors from 
J Nat Prod 87: 2-13 (2024)
China Pharmaceutical University
A Simple Chiral 
J Nat Prod 87: 77-84 (2024)
National and Kapodistrian University of Athens
Coriaceumins A-D, the First Nitrogen-Containing Crenulide Diterpenoids from the Brown Alga 
J Nat Prod 87: 121-131 (2024)
The Second Affiliated Hospital of Nanchang University
Diaporaustalides A-L, Austalide Meroterpenoids from a Plant Endophytic 
J Nat Prod 87: 141-151 (2024)
Huazhong University of Science and Technology
Synthesis and Evaluation of Natural and Unnatural Tetrahydrocannabiorcol for Its Potential Use in Neuropathologies.
J Nat Prod 87: 167-175 (2024)
Csir-Indian Institute of Integrative Medicine
Discovery of Anti-Hypercholesterolemia Agents Targeting LXRα from Marine Microorganism-Derived Natural Products.
J Nat Prod 87: 322-331 (2024)
Guangxi University of Chinese Medicine
Neopetrotaurines A-C, Isoquinoline Alkaloids with an Unprecedented Taurine Bridge from the Sponge 
J Nat Prod 87: 332-339 (2024)
National Cancer Institute
Norterpene Cyclic Peroxides from the Marine Sponge 
J Nat Prod 87: 358-364 (2024)
Korea Institute of Ocean Science and Technology
Chemical Analysis and Antidiabetic Potential of a Decoction from 
J Nat Prod 87: 501-513 (2024)
National Autonomous University of Mexico
Amide Alkaloids as Privileged Sources of Senomodulators for Therapeutic Purposes in Age-Related Diseases.
J Nat Prod 87: 617-628 (2024)
Sorbonne University
Sokotrasterol Sulfate Suppresses IFN-γ-Induced PD-L1 Expression by Inhibiting JAK Activity.
J Nat Prod 87: 713-721 (2024)
Fudan University
Phytochemical Characterization and TRPA1/TRPM8 Modulation Profile of the Cannabigerol-Rich 
J Nat Prod 87: 722-732 (2024)
University of Naples Federico Ii
Transient Receptor Potential Melastatin 7 (TRPM7) Ion Channel Inhibitors: Preliminary SAR and Conformational Studies of Xenicane Diterpenoids from the Hawaiian Soft Coral 
J Nat Prod 87: 783-797 (2024)
Huazhong University of Science and Technology
Microascones, Decahydrofluorene-Class Alkaloids from the Marine-Derived Fungus 
J Nat Prod 87: 810-819 (2024)
Chinese Academy of Sciences
Facile Synthesis and First Antifungal Exploration of Tetracyclic Meroterpenoids: (+)-Aureol, (-)-Pelorol, and Its Analogs.
J Nat Prod 87: 1092-1102 (2024)
Guizhou University
Total Synthesis, Structure Reassignment, and Biological Evaluation of the Anti-Inflammatory Macrolactone 13-Hydroxy-14-deoxyoxacyclododecindione.
J Nat Prod 87: 1131-1149 (2024)
Johannes Gutenberg-University
A Survey of Recently Discovered Naturally Occurring Organohalogen Compounds.
J Nat Prod 87: 1285-1305 (2024)
Dartmouth College
Terpenes and Terpenoids Conjugated with BODIPYs: An Overview of Biological and Chemical Properties.
J Nat Prod 87: 1306-1319 (2024)
Palacky University
Direct Inhibition of BK Channels by Cannabidiol, One of the Principal Therapeutic Cannabinoids Derived from Cannabis sativa.
J Nat Prod 87: 1368-1375 (0)
Universidad Nacional de La Plata - CICPBA - CONICET
Metabolomic Analysis and Antiviral Screening of a Marine Algae Library Yield Jobosic Acid (2,5-Dimethyltetradecanoic Acid) as a Selective Inhibitor of SARS-CoV-2.
J Nat Prod 87: 1513-1520 (0)
University of Puerto Rico-Medical Sciences Campus
Discovery of Oxidized p-Terphenyls as Phosphodiesterase 4 Inhibitors from Marine-Derived Fungi.
J Nat Prod 87: 1808-1816 (0)
Chinese Academy of Sciences
A Diterpenoid of the Medicinal Plant Andrographis paniculata Targets Cutaneous TRPV3 Channel and Relieves Itch.
J Nat Prod 87: 1852-1859 (0)
Russian Academy of Sciences
Undobolins A-L, Ophiobolin-Type Sesterterpenoids from Aspergillus undulatus.
J Nat Prod 87: 1965-1974 (0)
Huazhong University of Science and Technology
Identification of an m6A Natural Inhibitor, Lobeline, That Reverses Lenvatinib Resistance in Hepatocellular Tumors.
J Nat Prod 87: 1983-1993 (0)
The First Hospital of China Medical University
Acroamine A, a 2-Amino Adenine Alkaloid from the Marine Soft Coral Acrozoanthus australiae and Its Semisynthetic Derivatives That Inhibit cAMP-Dependent Protein Kinase A Catalytic Subunit Alpha.
J Nat Prod 87: 2014-2020 (0)
National Cancer Institute