Quantum mechanical quantitative structure activity relationships to avoid mutagenicity in dental monomers-Reference-Cited by-同舟云学术

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Quantum mechanical quantitative structure activity relationships to avoid mutagenicity in dental monomers

Published:2001-01 Issue:1 Volume:12 Page:89-105
ISSN:0920-5063
Container-title:Journal of Biomaterials Science, Polymer Edition
language:en
Short-container-title:Journal of Biomaterials Science, Polymer Edition

Author:

Yourtee David,Holder Andrew J.,Smith Robert,Morrill Jason A.,Kostoryz Elisabet,Brockmann William,Glaros Alan,Chappelow Cecil,Eick David

Publisher

Informa UK Limited

Subject

Biomedical Engineering,Biomaterials,Bioengineering,Biophysics

Reference33 articles.

1. In Vitro Conversion of Environmental Estrogenic Chemical Bisphenol A to DNA Binding Metabolite(s)

2. Theoretical descriptors in quantitative structure–affinity and selectivity relationship study of potent N4-substituted arylpiperazine 5-HT1A receptor antagonists

3. Revised methods for the Salmonella mutagenicity test

4. Comparative mutagenicity of aliphatic epoxides in Salmonella

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1. Bioactive Peptides of Fermented Food Products Targeting the Structural Rigid Core of Amyloid Fibril Unravelled by Simulated Thermal Unfolding in Alzheimer’s Disorder;International Journal of Peptide Research and Therapeutics;2023-07-04

2. First multi-target QSAR model for predicting the cytotoxicity of acrylic acid-based dental monomers;Dental Materials;2022-02

3. 3,4-Epoxycyclohexylcarbonsäure-3,4-epoxycyclohexylmethylester [MAK Value Documentation in German Language, 2015];The MAK-Collection for Occupational Health and Safety;2015-07-06

4. QSAR models to predict mutagenicity of acrylates, methacrylates and α,β-unsaturated carbonyl compounds;Dental Materials;2010-05

5. A topological substructural molecular design approach for predicting mutagenesis end-points of α, β-unsaturated carbonyl compounds;Toxicology;2010-01

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