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Electrochemical Behavior of Biologically Important Indole Derivatives
Published 2011-01-01“…Use of electrochemistry is an important approach in drug discovery and research as well as quality control, drug stability, and determination of physiological activity. …”
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AiGPro: a multi-tasks model for profiling of GPCRs for agonist and antagonist
Published 2025-01-01“…Abstract G protein-coupled receptors (GPCRs) play vital roles in various physiological processes, making them attractive drug discovery targets. Meanwhile, deep learning techniques have revolutionized drug discovery by facilitating efficient tools for expediting the identification and optimization of ligands. …”
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Slow Metabolism–Driven Amplification of Hepatic PPARγ Agonism Mediates Benzbromarone‐Induced Obesity‐Specific Liver Injury
Published 2025-01-01“…Given the significance of BBR and its analogs in anti‐gout/hyperuricemia drug discovery, elucidating the mechanism by which BBR exacerbates obesity‐specific DILI warrants further investigation. …”
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Bioactive compounds and probiotics–a ray of hope in COVID-19 management
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A microscale thermophoresis-based enzymatic RNA methyltransferase assay enables the discovery of DNMT2 inhibitors
Published 2025-02-01“…Abstract RNA methyltransferases (MTases) have recently become increasingly important in drug discovery. Yet, most frequently utilized RNA MTase assays are limited in their throughput and hamper this rapidly evolving field of medicinal chemistry. …”
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Fully automated CFD simulation system research based on design scheme tree
Published 2025-02-01“…Abstract Compared with the remarkable achievements of computer-aided drug discovery systems for drug discovery, the role of computational fluid dynamics (CFD) in flow channel design requires further development. …”
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Isolation of MDCK cells with low expression of mdr1 gene and their use in membrane permeability screening
Published 2022-06-01“…The Madin-Darby canine kidney (MDCK) cell line is frequently used for permeability screening in drug discovery. It contains endogenous transporters, most prominently canine multidrug resistance P-glycoprotein (Mdr1), which can interfere with studies of P-glycoprotein substrate assessment and permeability measurements. …”
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