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Prediction of the rodent carcinogenicity of organic compounds from their chemical structures using the FALS method.
Fuzzy adaptive least-squares (FALS), a pattern recognition method recently developed in our laboratory for correlating structure with activity rating, was used to generate quantitative structure-activity relationship (QSAR) models on the carcinogenicity of organic compounds of several chemical class...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
1996
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1469684/ https://www.ncbi.nlm.nih.gov/pubmed/8933054 |
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author | Moriguchi, I Hirano, H Hirono, S |
author_facet | Moriguchi, I Hirano, H Hirono, S |
author_sort | Moriguchi, I |
collection | PubMed |
description | Fuzzy adaptive least-squares (FALS), a pattern recognition method recently developed in our laboratory for correlating structure with activity rating, was used to generate quantitative structure-activity relationship (QSAR) models on the carcinogenicity of organic compounds of several chemical classes. Using the predictive models obtained from the chemical class-based FALS QSAR approach, the rodent carcinogenicity or noncarcinogenicity of a group of organic chemicals currently being tested by the U.S. National Toxicology Program was estimated from their chemical structures. |
format | Text |
id | pubmed-1469684 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1996 |
record_format | MEDLINE/PubMed |
spelling | pubmed-14696842006-06-01 Prediction of the rodent carcinogenicity of organic compounds from their chemical structures using the FALS method. Moriguchi, I Hirano, H Hirono, S Environ Health Perspect Research Article Fuzzy adaptive least-squares (FALS), a pattern recognition method recently developed in our laboratory for correlating structure with activity rating, was used to generate quantitative structure-activity relationship (QSAR) models on the carcinogenicity of organic compounds of several chemical classes. Using the predictive models obtained from the chemical class-based FALS QSAR approach, the rodent carcinogenicity or noncarcinogenicity of a group of organic chemicals currently being tested by the U.S. National Toxicology Program was estimated from their chemical structures. 1996-10 /pmc/articles/PMC1469684/ /pubmed/8933054 Text en |
spellingShingle | Research Article Moriguchi, I Hirano, H Hirono, S Prediction of the rodent carcinogenicity of organic compounds from their chemical structures using the FALS method. |
title | Prediction of the rodent carcinogenicity of organic compounds from their chemical structures using the FALS method. |
title_full | Prediction of the rodent carcinogenicity of organic compounds from their chemical structures using the FALS method. |
title_fullStr | Prediction of the rodent carcinogenicity of organic compounds from their chemical structures using the FALS method. |
title_full_unstemmed | Prediction of the rodent carcinogenicity of organic compounds from their chemical structures using the FALS method. |
title_short | Prediction of the rodent carcinogenicity of organic compounds from their chemical structures using the FALS method. |
title_sort | prediction of the rodent carcinogenicity of organic compounds from their chemical structures using the fals method. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1469684/ https://www.ncbi.nlm.nih.gov/pubmed/8933054 |
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