Atom/fragment contribution method for estimating octanol-water partition coefficients.
about
Subcellular in vivo 1H MR spectroscopy of Xenopus laevis oocytes.Incorporation of potential for multimedia exposure into chemical hazard scores for pollution preventionData quality in predictive toxicology: identification of chemical structures and calculation of chemical propertiesExpanding frontiers in weight-control research explored by young investigatorsChemical Composition and Potential Environmental Impacts of Water-Soluble Polar Crude Oil Components Inferred from ESI FT-ICR MSSynthesis, structural characterization, and thermoresponsivity of hybrid supramolecular dendrimers bearing a polyoxometalate core.Typology of secondary cyanobacterial metabolites from minimum spanning tree analysis.European Chemicals Agency dossier submissions as an experimental data source: refinement of a fish toxicity model for predicting acute LC50 values.Global Model for Octanol-Water Partition Coefficients from Proton Nuclear Magnetic Resonance Spectra.Computer-assisted design of new drugs based on retrometabolic concepts.In silico techniques for the study and prediction of xenobiotic metabolism: a review.Detection of aqueous phase chemical warfare agent degradation products by negative mode ion mobility time-of-flight mass spectrometry [IM(tof)MS].The toxicity data landscape for environmental chemicals.Domain of EPI suite biotransformation models.Persistent binding of ligands to the aryl hydrocarbon receptor.Continuous steady-state method using tenax for delivering tetrachloroethene to chloro-respiring bacteria.Screening marine fungi for inhibitors of the C4 plant enzyme pyruvate phosphate dikinase: unguinol as a potential novel herbicide candidate.Measurement of drinking water contaminants by solid phase microextraction initially quantified in source water samples by the USGS.Determination of lipophilicity of γ-butyrolactone derivatives with anticonvulsant and analgesic activity using micellar electrokinetic chromatography.Ligand-Specific Transcriptional Mechanisms Underlie Aryl Hydrocarbon Receptor-Mediated Developmental Toxicity of Oxygenated PAHs.A NON-LINEAR STRUCTURE-PROPERTY MODEL FOR OCTANOL-WATER PARTITION COEFFICIENTHuman health risk on environmental exposure to Bisphenol-A: a review.Synthesis and pharmacological evaluation of novel 9- and 10-substituted cytisine derivatives. Nicotinic ligands of enhanced subtype selectivity.Kinetic analysis of intracellular concentrations of reactive nitrogen species.Polar 3-alkylidene-5-pivaloyloxymethyl-5'-hydroxymethyl-gamma-lactones as protein kinase C ligands and antitumor agentsTemporal integration in nasal lateralization of homologous propionates.In vitro and in vivo percutaneous absorption of seleno-L-methionine, an antioxidant agent, and other selenium species.Computational medicinal chemistry in fragment-based drug discovery: what, how and when.Prediction of the Fate of Organic Compounds in the Environment From Their Molecular Properties: A Review.Enhanced cellular uptake of nanoparticles by increasing the hydrophobicity of poly(lactic acid) through copolymerization with cell-membrane-lipid components.Synthesis of novel 2',3'-didehydro-2',3'-dideoxyinosine phosphoramidate prodrugs and evaluation of their anticancer activity.A Review of the Environmental Degradation, Ecotoxicity, and Bioaccumulation Potential of the Low Molecular Weight Polyether Polyol Substances.On the Use of Local and Global QSPRs for the Prediction of Physico-chemical Properties of Polybrominated Diphenyl Ethers.Increased Uptake of Chelated Copper Ions by Lolium perenne Attributed to Amplified Membrane and Endodermal Damage.Predicting the biodegradation products of perfluorinated chemicals using CATABOL.Classifying class I and class II compounds by hydrophobicity and hydrogen bonding descriptors.Quantitative prediction of biodegradability, metabolite distribution and toxicity of stable metabolites.Comparison of structure-activity relationships derived from two methods for estimating octanol-water partition coefficients.A check on rational drug design: molecular simulation of the allosteric inhibition of HIV-1 reverse transcriptase.Quantitative Property-Property Relationship for Screening-Level Prediction of Intrinsic Clearance of Volatile Organic Chemicals in Rats and Its Integration within PBPK Models to Predict Inhalation Pharmacokinetics in Humans.
P2860
Q22065138-894717C2-1FBE-41F3-B041-7CA179CB2B59Q23911639-0727DDF5-B444-466C-9E32-ADFE789814BAQ24811043-95C32279-42E4-4D75-8540-82A4E19BD618Q28077983-BDE7E3B0-9533-41FF-AB20-3CFC94C9E7B6Q28547673-EC9D9F8E-6479-4426-9DFC-0E15F0106955Q30652438-8663A80E-9CCC-44A2-97A5-092A376D54C1Q30763667-8EF5C545-8E10-426F-BD9C-106C1B2A3A42Q30874127-FBD208C8-C573-40BE-AC5D-A7197794F463Q31119234-F0F0001F-2598-4974-A760-C8749DF784E6Q32083850-5AAE2DB7-E44B-4C8F-97D3-898DAE10F0D5Q33230918-51D761EC-9C1C-4B81-A328-FF73D17425E3Q33231644-11AAF033-254B-449B-BF1D-5A19364FAEAFQ33455654-FDD87440-C2BC-4A55-B481-6C0107E53614Q33684808-674BC0F3-9967-40D2-8F43-9A8C8FB48757Q33803848-2D525EEF-5A33-4D38-9C68-18DAAE3A716CQ34050584-79348D7F-C160-4475-B566-6E6A464A36ACQ34601317-CA0E7C6E-7AE6-41C7-BA9D-B8352B760584Q34687615-32C0D454-D3A2-4727-B39C-3561B56E2C90Q34987697-8893F755-4E45-4F6D-86FB-330E1E487127Q36181367-6D140E52-DCF3-4F31-BDF9-36D130FC248CQ36419612-50BF863F-A5E4-4167-85B5-033E3F047E31Q36657409-46B26C5D-0DD5-49E3-8368-69E0ABD25C4AQ36825487-0F1005A5-B00E-4D3B-8378-80381CCBF601Q37043643-3C33AE68-0FBF-4BE3-BBB2-E4225A47B52EQ37050189-7EEB439D-E5A6-4A23-8AB7-EE8B35D114ACQ37294871-7E500A8B-E711-423C-B949-754EFD356053Q37729812-66C5765E-C298-4237-90B0-3536A8963F17Q37856296-85922029-D505-47CD-A135-33DCB81A173DQ38417877-FECB25BC-A783-4FBA-877F-5FACAF8DBC75Q38842597-420931B8-CB56-445E-B0E2-3B0A821ABFC1Q38976742-0909730C-1A00-4FA1-A0DC-6E50DC976380Q39279884-9C528049-1791-4A71-9867-07105A2A2A06Q39551466-946B8615-D4DE-4F6B-9FEE-4BDB544A62A6Q40381149-1AE51D68-68B8-4237-BF87-0E9D7E78335BQ40514304-A09E3695-7AD7-42EC-9C1B-77AB3FE16E3AQ40632636-DD1ADC25-3032-4314-867D-2DD7204549DAQ40638918-DBA50AE9-665B-4220-AEBD-4FE11A76CEA0Q41073634-D4EF4BC5-BCF7-4007-9367-AEB95643C07EQ41452204-C69F160E-153A-488B-B721-4D9665925263Q42182148-B92C4865-F77B-47AC-BFD6-5AEAC0ED6A7C
P2860
Atom/fragment contribution method for estimating octanol-water partition coefficients.
description
1995 nî lūn-bûn
@nan
1995年の論文
@ja
1995年学术文章
@wuu
1995年学术文章
@zh
1995年学术文章
@zh-cn
1995年学术文章
@zh-hans
1995年学术文章
@zh-my
1995年学术文章
@zh-sg
1995年學術文章
@yue
1995年學術文章
@zh-hant
name
Atom/fragment contribution method for estimating octanol-water partition coefficients.
@en
Atom/fragment contribution method for estimating octanol-water partition coefficients.
@nl
type
label
Atom/fragment contribution method for estimating octanol-water partition coefficients.
@en
Atom/fragment contribution method for estimating octanol-water partition coefficients.
@nl
prefLabel
Atom/fragment contribution method for estimating octanol-water partition coefficients.
@en
Atom/fragment contribution method for estimating octanol-water partition coefficients.
@nl
P356
P1476
Atom/fragment contribution method for estimating octanol-water partition coefficients.
@en
P2093
P H Howard
W M Meylan
P356
10.1002/JPS.2600840120
P407
P577
1995-01-01T00:00:00Z