About: Quantitative structure-activity relationship studies of [(biphenyloxy)propyl]isoxazole derivatives. Inhibitors of human rhinovirus 2 replication

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About: Quantitative structure-activity relationship studies of [(biphenyloxy)propyl]isoxazole derivatives. Inhibitors of human rhinovirus 2 replication Goto Sponge NotDistinct Permalink

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scientific article published on 01 August 2007

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rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в серпні 2007 (uk) article scientifique publié en 2007 (fr) artículu científicu espublizáu n'agostu de 2007 (ast) scientific article published on 01 August 2007 (en)
publication date	wds:Q80708498-5106B128-AF14-40BC-B9D1-DAE0996C2B5E
publication date	2007-08-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q80708498-03FECC71-6C8A-47A7-8F20-E0B4F0E4BA98 wds:Q80708498-2263E90A-8C55-48DA-BF39-CE1B5251A3B7 wds:Q80708498-38874D86-8629-444E-BB6E-9147BE675787 wds:Q80708498-58978EE5-521E-4956-9AC2-1A5DEC7BE625 wds:Q80708498-67762E69-7C12-46F5-871A-2AF4AD5115F8 wds:Q80708498-8880D3C2-ED97-430B-BDF8-F1E66137AAC8 wds:Q80708498-AC9F9C09-961E-44C1-849A-FE2FC8E036A7 wds:Q80708498-E381779E-7861-4402-8FA0-23E3B5675C20
author name string	Peter Wutzler Michaela Schmidtke Eugene N Muratov Olga B Riabova Vadim A Makarov Victor E Kuz'min Anatoly G Artemenko Ingrid L Volineckaya
rdfs:label	Quantitative structure-activity relationship studies of [(biphenyloxy)propyl]isoxazole derivatives. Inhibitors of human rhinovirus 2 replication (en) Quantitative structure-activity relationship studies of [(biphenyloxy)propyl]isoxazole derivatives. Inhibitors of human rhinovirus 2 replication (nl)
skos:prefLabel	Quantitative structure-activity relationship studies of [(biphenyloxy)propyl]isoxazole derivatives. Inhibitors of human rhinovirus 2 replication (en) Quantitative structure-activity relationship studies of [(biphenyloxy)propyl]isoxazole derivatives. Inhibitors of human rhinovirus 2 replication (nl)
name	Quantitative structure-activity relationship studies of [(biphenyloxy)propyl]isoxazole derivatives. Inhibitors of human rhinovirus 2 replication (en) Quantitative structure-activity relationship studies of [(biphenyloxy)propyl]isoxazole derivatives. Inhibitors of human rhinovirus 2 replication (nl)
title	wds:Q80708498-92CC6286-28C8-4E30-91C4-CCAC08D21D9A
title	Quantitative structure-activity relationship studies of [(biphenyloxy)propyl]isoxazole derivatives. Inhibitors of human rhinovirus 2 replication (en)
page(s)	wds:Q80708498-5D3B2630-E428-46AA-93AF-0024CE762188
page(s)	4205-4213
instance of	wds:Q80708498-874802B8-9E8E-449F-8964-BE3716E57DD6
instance of	scholarly article
main subject	wds:Q80708498-3933F3F1-F689-4DA3-AADF-4886BBDA1AEF
main subject	quantitative structure-activity relationship
PubMed ID	wds:Q80708498-B0EC010E-89C1-4472-86AB-7ED070D30F49
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/17665898
PubMed ID	17665898
published in	wds:Q80708498-7F7BC94E-AD09-4A2F-9BA3-B76DEA19B648
published in	Journal of Medicinal Chemistry
issue	wds:Q80708498-CE5879BE-ADD4-43F4-8583-D7C907DC319F
volume	wds:Q80708498-C06D7886-1448-4893-99DD-8B8EBAFD6585
issue	17
volume	50
DOI	wds:Q80708498-24D736CB-E858-4970-AC32-2D5D371E2115
DOI	http://dx.doi.org/10.1021/JM0704806
DOI	10.1021/JM0704806
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q80708498
is cites work of	QSAR modeling: where have you been? Where are you going to? Applicability Domains for Classification Problems: Benchmarking of Distance to Models for Ames Mutagenicity Set Trust, but verify: on the importance of chemical structure curation in cheminformatics and QSAR modeling research The human rhinovirus: human-pathological impact, mechanisms of antirhinoviral agents, and strategies for their discovery. Crystal structure of 3-benzyl-sulfanyl-6-(5-methyl-1,2-oxazol-3-yl)-1,2,4-triazolo[3,4-b][1,3,4]thia-diazole Universal Approach for Structural Interpretation of QSAR/QSPR Models. Hierarchical QSAR technology based on the Simplex representation of molecular structure Unexpected heterocyclization of electrophilic alkenes by tetranitromethane in the presence of triethylamine. Synthesis of 3-nitroisoxazoles Predicting chemically-induced skin reactions. Part I: QSAR models of skin sensitization and their application to identify potentially hazardous compounds Predicting chemically-induced skin reactions. Part II: QSAR models of skin permeability and the relationships between skin permeability and skin sensitization QSAR analysis of the toxicity of nitroaromatics in Tetrahymena pyriformis: structural factors and possible modes of action Predicting binding affinity of CSAR ligands using both structure-based and ligand-based approaches Existing and Developing Approaches for QSAR Analysis of Mixtures. The effects of characteristics of substituents on toxicity of the nitroaromatics: HiT QSAR study Alarms about structural alerts Discovery of New Anti-Schistosomal Hits by Integration of QSAR-Based Virtual Screening and High Content Screening QSPR Approach to Predict Nonadditive Properties of Mixtures. Application to Bubble Point Temperatures of Binary Mixtures of Liquids Cheminformatics-driven discovery of polymeric micelle formulations for poorly soluble drugs. Synergistic effect of dual-frequency ultrasound irradiation in the one-pot synthesis of 3,5-disubstituted isoxazoles Telodendrimer-Based Macromolecular Drug Design using 1,3-Dipolar Cycloaddition for Applications in Biology
is cites work of	wds:Q36280549-88CCC1F6-67EF-4D52-AAD6-7AAC7A69D1BC wds:Q35533343-EF4DFCD6-BE58-4189-9EF0-91FC25E041B2 wds:Q80642889-3E04A0CD-B7F9-4A04-921E-61D4C7C52AE2 wds:Q43103167-E0FABF33-E1F6-4F93-9BB9-99EA5FC1EC64 wds:Q28386501-E14EC37B-5FC6-4493-8AC1-D9C611F226BB wds:Q38914231-24C08AD3-62A8-450C-9F57-26B08779D04A wds:Q54376695-E0A229DC-83E6-47E2-BD3E-A45CBBFDF9B6 wds:Q86955691-45C38456-E1F4-426C-8181-BC68BE832E48 wds:Q28222668-04A6114F-84FD-4423-ADE3-460F48E9F676 wds:Q39537117-76639FF3-B9C3-4C7D-96F8-82C587DE0A9D wds:Q41881422-F5D2FCFE-407E-4255-BDCB-37932CC11492 wds:Q39300204-10AEFF06-134C-4793-A462-192EB897B553 wds:Q42649336-87B406CF-4C24-4CFE-8150-0DFF6E72040C wds:Q64971130-D73A542F-C9D1-4969-89B6-A5E22D0C6DF9 wds:Q36233484-044B7971-46B7-4D3F-A2AC-BAFD6C130244 wds:Q39540069-AF47E665-9BB0-42CE-8F36-786CA1AF2161 wds:Q89783023-438D6A15-4145-43F7-81C8-5397E39FEB1D wds:Q28748220-FA0AD2D7-3EAF-47AF-A676-681417DF4308 wds:Q37588593-B6DEA01A-F8F7-4E7D-B9ED-0B1C6931A424 wds:Q46666631-FBBE4969-0EF4-4264-BA1C-67DA3B114F5C

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