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Pharmacology and drug discovery research

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facet applications:Pharmacology and drug discovery research
facet content type:Technical Article
表示中 1-30 of 32 結果
標的タンパク質分解のための分解物ビルディングブロック
タンパク質分解誘導化合物ビルディングブロックは、標的リガンドと共有結合するペンダント基を持つクロスリンカー-E3リガンド複合体です。
ヒトiPS細胞由来腸オルガノイドを用いた薬物の細胞毒性スクリーニング
ヒト上皮性結腸オルガノイドは、Caco-2細胞の薬物透過性アッセイの代わりに、薬物スクリーニングおよび化合物毒性試験に使用できます。
3Dオルガノイド培養:発生と疾患の新しいin vitroモデル
オルガノイド培養用製品により、組織または幹細胞に由来する3Dの脳、腸、肺および腫瘍のオルガノイドモデルを作成できます。
3D細胞培養ツールおよび技術
3D細胞培養の概要2D細胞培養と3D細胞培養の比較、3D細胞培養の利点、3D細胞培養技術について紹介します。
薬物間相互作用における肝トランスポーターの役割
経口薬の送達には、小腸での溶解、腸細胞のバリアを超えた門脈への吸収、それに続く肝臓を介した体循環への送達が関わっています。
腸管排出系トランスポーターと薬物吸収
腸管排出系トランスポーターと薬物吸収に関する論文を報告しました。
薬物吸収がより予測的な Caco-2 腸管薬物トランスポーターモデル
臨床試験や規制当局への申請の前に、低分子薬物化合物をスクリーニングするために、Caco-2 細胞ベースのアッセイツールを活用します。
Human Renal Proximal Tubule Epithelial Cells (RPTEC) as an Essential Advanced Model to Express Kidney Drug Transporters and Toxicity
Human renal proximal tubule epithelial cells (RPTECs) are commonly used to predict human renal drug permeability and to investigate drug efflux. We have generated transporter knockout (KO) cell lines using CompoZr® Zinc Finger Nuclease (ZFN) technology in a proprietary renal
Inhibition of Nucleic Acid Synthesis by Antibiotics
Quinolones are a key group of antibiotics that interfere with DNA synthesis by inhibiting topoisomerase, most frequently topoisomerase II (DNA gyrase), an enzyme involved in DNA replication.
Membrane Integrity Test for Lipid-PAMPA Artificial Membranes
This is a protocol for a Membrane Integrity test for Lipid-PAMPA Artificial Membranes
Evaluation of the reproducibility of Parallel Artificial Membrane Permeation Assays (PAMPA)
This is a white paper on the Evaluation of the reproducibility of Parallel Artificial Membrane Permeation Assays (PAMPA) using MultiScreen® Filter Plates.
Using Human iPS Cell-derived Colon Organoids for Cytotoxicity Screening of Drug Compounds
Human epithelial intestinal colonic organoids can be used as an alternative to Caco-2 drug permeability assays for drug screening and compound toxicity testing.
Chromatography Profile Analysis of Phosphorothioate Oligonucleotides
Understand the impact of phosphorothioate internucleotide linkage addition to oligonucleotide chromatography profiles.
The Role of Intestinal Efflux Transporters In Drug Absorption
We presents an article on The Role of Intestinal Efflux Transporters In Drug Absorption.
Caco-2 Intestinal Drug Transporter Models for More Predictive Drug Absorption
Utilize these Caco-2 cell based assay tools for screening small molecule drug compounds prior to clinical studies and submission to regulatory agencies.
Famciclovir Tablets USP Monograph Method Using a Purospher™ STAR RP-8 endcapped HPLC Column and UV Detection
Following the new USP monograph for Famciclovir Tablets, Purospher™ STAR RP-8 endcapped HPLC columns can be used to monitor organic impurities in Famciclovir tablet formulations. Famciclovir is an antiviral drug indicated for the treatment of herpes zoster, herpes simplex virus
3D Cell Culture Tools and Techniques
3D cell culture overview. Learn about 2D vs 3D cell culture, advantages of 3D cell culture, and techniques available to develop 3D cell models
Discover Bioactive Small Molecules for Gene Regulation
We offer a variety of small molecule research tools, such as transcription factor modulators, inhibitors of chromatin modifying enzymes, and agonists/antagonists for target identification and validation in gene regulation research; a selection of these research tools is shown below.
Primary Cell Culture Basics
Overview of primary cells and media usage in biomedical culture applications highlights differences from cell lines.
3D Organoid Culture: New In Vitro Models of Development and Disease
Organoid culture products to generate tissue and stem cell derived 3D brain, intestinal, gut, lung and cancer tumor organoid models.
Phase I Drug Metabolism
Phase I biotransformation reactions increase drug compound polarity, mainly occurring in hepatic circulation.
Antimicrobial Peptides
Ribosomally synthesized antimicrobial peptides are a promising focus in antibiotic research amidst bacterial resistance and emerging infectious diseases.
Comparing Quantitative Viability Bioassays: An Evaluation of MTT, alamarBlue™, and Guava® ViaCount® Methods
This article shows a comparison of the quantitative viability bioassays MTT, alamarBlue™, and Guava® ViaCount®.
The Role of Liver Transporters in Drug-Drug Interactions
Oral drug delivery involves dissolution in the small intestine and absorption across the enterocyte barrier into the portal vein followed by subsequent delivery through the liver into the systemic circulation.
Drug transport assays in a 96-well system: reproducibility and correlation to human absorption
Application note on Drug transport assays in a 96-well system using Millicell-96 System from Millipore.
ADCC Assay Using BioIVT Cryopreserved NK Cells
ADCC assay performance and reproducibility using ready-to-use, cryopreserved NK effector cells, A549 target cells expressing a luciferase reporter gene, and anti-EGFR antibody.
Unnatural Amino Acids for Peptide Synthesis
Unnatural amino acids, the non-proteinogenic amino acids that either occur naturally or are chemically synthesized, are becoming more and more important as tools for modern drug discovery research.
Degrader Building Blocks for Targeted Protein Degradation
Protein Degrader Building Blocks are a collection of crosslinker-E3 ligand conjugates with a pendant functional group for covalent linkage to a target ligand.
Hit Discovery & Confirmation for Early Drug Discovery
Hit discovery and confirmation allows identification of molecules acting against the target. It requires compound screening assays, depending on the drug target.
Protein Binding Determination - Comparison Study of Techniques & Devices
Comparative analysis of Supel™ BioSPME 96-Pin device with a rapid equilibrium dialysis technique for accuracy of measured values, sample cleanliness, and workflow time in drug protein binding.
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