QSAR and Binding Model for Inhibition of Rat Liver Catechol-O-Methyl-Transferase by 1,5-Substituted-3,4-Dihydroxybenzenes
- 1 January 1989
- journal article
- research article
- Published by Wiley in Quantitative Structure-Activity Relationships
- Vol. 8 (3), 210-213
- https://doi.org/10.1002/qsar.19890080304
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Synthesis of some novel potent and selective catechol O-methyltransferase inhibitorsJournal of Medicinal Chemistry, 1989
- Crossvalidation, Bootstrapping, and Partial Least Squares Compared with Multiple Regression in Conventional QSAR StudiesQuantitative Structure-Activity Relationships, 1988
- Thermodynamics of proton transfer in phenol-acetate hydrogen bonds with large proton polarizability and the conversion of light energy into chemical energy in bacteriorhodopsinThe Journal of Physical Chemistry, 1986
- Development and use of quantum mechanical molecular models. 76. AM1: a new general purpose quantum mechanical molecular modelJournal of the American Chemical Society, 1985
- The chemistry and biology of ring‐fluorinated biogenic aminesMedicinal Research Reviews, 1984
- Catechol O-methyltransferase. 10. 5-Substituted, 3-hydroxy-4-methoxybenzoic acids (isovanillic acids) and 5-substituted, 3-hydroxy-4-methoxybenzaldehydes (isovanillins) as potential inhibitorsJournal of Medicinal Chemistry, 1982
- A genetic approach to the biosynthesis of the rifamycin-chromophore in Nocardia mediterranei. V. Studies on the biogenetic origin of 3-substituents.The Journal of Antibiotics, 1982
- pK a Prediction for Organic Acids and BasesPublished by Springer Nature ,1981
- Kinetic studies on catechol O-methyltransferase, Product inhibition and the nature of the catechol binding siteBiochemistry, 1973
- A New Substituent Constant, π, Derived from Partition CoefficientsJournal of the American Chemical Society, 1964