Linear relationships between lipophilic character and biological activity of drugs.
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Breaking the Meyer-Overton rule: predicted effects of varying stiffness and interfacial activity on the intrinsic potency of anesthetics.4D-QSAR analysis of a set of propofol analogues: mapping binding sites for an anesthetic phenol on the GABA(A) receptorActivity of phosphatidylinositol transfer protein is sensitive to ethanol and membrane curvature.Physicochemical and biological data for the development of predictive organophosphorus pesticide QSARs and PBPK/PD models for human risk assessment.Predicting Mouse Liver Microsomal Stability with "Pruned" Machine Learning Models and Public Data.Correlative and mechanistic QSAR models in toxicology.Interaction of dietary antioxidants in vivo: how fruit and vegetables prevent disease?Genetic activity spectra of some antischistosomal compounds, with particular emphasis on thioxanthenones and benzothiopyranoindazoles.Antitumor activity of kielmeyera coriacea leaf constituents in experimental melanoma, tested in vitro and in vivo in syngeneic mice.Back to the future: can physical models of passive membrane permeability help reduce drug candidate attrition and move us beyond QSPR?Parameter and structure-activity data bases: management for maximum utilityStructure-activity relationships in nitrosamine carcinogenesis.Purification and characterization of a secondary alcohol dehydrogenase from a pseudomonadA NON-LINEAR STRUCTURE-PROPERTY MODEL FOR OCTANOL-WATER PARTITION COEFFICIENTImproving metabolic stability by glycosylation: bifunctional peptide derivatives that are opioid receptor agonists and neurokinin 1 receptor antagonistsModeling kinetics of subcellular disposition of chemicals.Implication of membrane functions in toxicology.In vitro influences of alcohols on mouse synaptosomes, and structure-activity relationships.Toward a quantitative comparative toxicology of organic compounds.QSAR models of antiproliferative activity of imidazo[2,1-b][1,3,4]thiadiazoles in various cancer cell lines.(Q)SARs to predict environmental toxicities: current status and future needs.Partitioning and lipophilicity in quantitative structure-activity relationships.The QSAR paradigm in the design of less toxic molecules.Comparative QSAR in toxicology: examples from teratology and cancer chemotherapy of aniline mustards.The rationale for the development of improved hypoxic cell radiosensitizers.Structure-activity relationships in the development of hypoxic cell radiosensitizers. I. Sensitization efficiency.Ethical review in the pharmaceutical industryQuantitative structure-activity relationships of cytochrome P-450.Influence of derivation on the lipophilicity and inhibitory actions of cardiac glycosides on myocardial Na+-K+-ATPase.Further studies on the substrate specificity and inhibition of the stereospecific CS2 secondary alkylsulphohydrolase of Comamonas terrigena.Liposomes as carriers of poorly water-soluble substrates: linear modelling of membrane systems with catalytic or binding sites of different facedness. Significance of experimental membrane partition coefficients and of kinetic and equilibrium paramePurification and properties of the P2 primary alkylsulphohydrolase of the detergent-degrading bacterium pseudomonas C12B.Enhancement by terpenes of 5-fluorouracil permeation through the stratum corneum: model solvent approach.High-throughput microplate assay for the determination of drug partition coefficients.Multiple effects of short-chain alcohols on binding to rat heart muscarinic receptors.A framework for grouping nanoparticles based on their measurable characteristics.Metabolism of bisphenol A in isolated rat hepatocytes and oestrogenic activity of a hydroxylated metabolite in MCF-7 human breast cancer cells.Anti-Salmonella Activity of Volatile Compounds of Vietnam Coriander.Cytotoxicity and topoisomerase I/II inhibition activity of novel 4-aryl/alkyl-1-(piperidin-4-yl)-carbonylthiosemicarbazides and 4-benzoylthiosemicarbazides.Liposomes as a model for the biological membrane: studies on daunorubicin bilayer interaction.
P2860
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P2860
Linear relationships between lipophilic character and biological activity of drugs.
description
1972 nî lūn-bûn
@nan
1972年の論文
@ja
1972年学术文章
@wuu
1972年学术文章
@zh-cn
1972年学术文章
@zh-hans
1972年学术文章
@zh-my
1972年学术文章
@zh-sg
1972年學術文章
@yue
1972年學術文章
@zh
1972年學術文章
@zh-hant
name
Linear relationships between lipophilic character and biological activity of drugs.
@en
Linear relationships between lipophilic character and biological activity of drugs.
@nl
type
label
Linear relationships between lipophilic character and biological activity of drugs.
@en
Linear relationships between lipophilic character and biological activity of drugs.
@nl
prefLabel
Linear relationships between lipophilic character and biological activity of drugs.
@en
Linear relationships between lipophilic character and biological activity of drugs.
@nl
P356
P1476
Linear relationships between lipophilic character and biological activity of drugs.
@en
P2093
P356
10.1002/JPS.2600610102
P407
P577
1972-01-01T00:00:00Z