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Privileged Structures Revisited.Biological Significance of Marine Actinobacteria of East Coast of Andhra Pradesh, India.Identification of Neuroprotective Spoxazomicin and Oxachelin Glycosides via Chemoenzymatic Glycosyl-Scanning.Matrix-based Molecular Descriptors for Prospective Virtual Compound Screening.High-Affinity α-Conotoxin PnIA Analogs Designed on the Basis of the Protein Surface Topography Method.Immunosuppressive Effects of Natural α,β-Unsaturated Carbonyl-Based Compounds, and Their Analogs and Derivatives, on Immune Cells: A Review.Systems Pharmacology-Based Discovery of Natural Products for Precision Oncology Through Targeting Cancer Mutated Genes.Profiling of Microbial Colonies for High-Throughput Engineering of Multistep Enzymatic Reactions via Optically Guided Matrix-Assisted Laser Desorption/Ionization Mass Spectrometry.The potential role of in silico approaches to identify novel bioactive molecules from natural resources.Dual inhibitors of cholinesterases and monoamine oxidases for Alzheimer's disease.Ligand Dependent Switch from RXR Homo- to RXR-NURR1 Heterodimerization.Design of a Mestranol 2-N-Piperazino-Substituted Derivative Showing Potent and Selective in vitro and in vivo Activities in MCF-7 Breast Cancer Models.Effects of Dihydrophaseic Acid 3'-O-β-d-Glucopyranoside Isolated from Lycii radicis Cortex on Osteoblast Differentiation.Deorphaning the Macromolecular Targets of the Natural Anticancer Compound Doliculide.Applications of visible light photoredox catalysis to the synthesis of natural products and related compounds.Induction of Cell Death by Betulinic Acid through Induction of Apoptosis and Inhibition of Autophagic Flux in Microglia BV-2 Cells.Quebrachitol: Global Status and Basic Research.Molecular insights into cancer therapeutic effects of the dietary medicinal phytochemical withaferin A.Total Synthesis and Functional Evaluation of Fourteen Derivatives of Lysocin E: Importance of Cationic, Hydrophobic, and Aromatic Moieties for Antibacterial Activity.Dietary Intervention by Phytochemicals and Their Role in Modulating Coding and Non-Coding Genes in Cancer.Natural product analogues: towards a blueprint for analogue-focused synthesis.C-H Activation and Alkyne Annulation via Automatic or Intrinsic Directing Groups: Towards High Step Economy.Unveiling (-)-Englerin A as a Modulator of L-Type Calcium Channels.Wound Healing Potential of Chlorogenic Acid and Myricetin-3-O-β-Rhamnoside Isolated from Parrotia persica.Evidence-Based TAM Classic Herbal Formula: From Myth to Science.Computer-Aided Drug Design Applied to Marine Drug Discovery: Meridianins as Alzheimer's Disease Therapeutic Agents.NPASS: natural product activity and species source database for natural product research, discovery and tool development.Himatanthus drasticus Leaves: Chemical Characterization and Evaluation of Their Antimicrobial, Antibiofilm, Antiproliferative Activities.Synthesis and Demonstration of the Biological Relevance of sp3 -rich Scaffolds Distantly Related to Natural Product Frameworks.Frontiers in Medicinal Chemistry 2017 in Bern, Switzerland.Hippeastrum reticulatum (Amaryllidaceae): Alkaloid Profiling, Biological Activities and Molecular Docking.Analysing and Navigating Natural Products Space for Generating Small, Diverse, But Representative Chemical Libraries.Harnessing the potential of natural products in drug discovery from a cheminformatics vantage point.Quantitative and Systems Pharmacology. 1. In Silico Prediction of Drug-Target Interactions of Natural Products Enables New Targeted Cancer Therapy.Synthesis of deoxyelephantopin analogues.Strategies to diversify natural products for drug discovery.Recent developments with rhodanine as a scaffold for drug discovery.Direct assembly of multiply oxygenated carbon chains by decarbonylative radical-radical coupling reactions.De-orphaning the marine natural product (±)-marinopyrrole A by computational target prediction and biochemical validation.A diversity oriented synthesis of natural product inspired molecular libraries.
P2860
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P2860
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
Counting on natural products for drug design.
@en
type
label
Counting on natural products for drug design.
@en
prefLabel
Counting on natural products for drug design.
@en
P50
P356
P1433
P1476
Counting on natural products for drug design.
@en
P2093
Petra Schneider
P2888
P304
P356
10.1038/NCHEM.2479
P577
2016-04-25T00:00:00Z
P6179
1015387138