A QSAR Study of Quinolones Based on Electrotopological State Index for Atoms

This publication has 17 references indexed in Scilit:

• Synthesis and Structure-Activity Relationships of 7-(3'-Amino-4'-methoxypyrrolidin-1'-yl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic Acids.
  CHEMICAL & PHARMACEUTICAL BULLETIN, 1993
• Quantitative Structure-Activity Relationships of Antibacterial Agents, 7-Heterocyclic Amine Substituted 1-Cyclopropyl-6,8-difluoro-4-oxoquinoline-3-carboxylic Acids.
  CHEMICAL & PHARMACEUTICAL BULLETIN, 1993
• Fluoronaphthyridines as antibacterial agents. 4. Synthesis and structure-activity relationships of 5-substituted 6-fluoro-7-(cycloalkylamino)-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acids
  Journal of Medicinal Chemistry, 1992
• Synthesis and biological activity of 5-amino- and 5-hydroxyquinolones, and the overwhelming influence of the remote N1-substituent in determining the structure-activity relationship
  Journal of Medicinal Chemistry, 1991
• The electrotopological state: structure information at the atomic level for molecular graphs
  Journal of Chemical Information and Computer Sciences, 1991
• The Electrotopological State: An Atom Index for QSAR
  Quantitative Structure-Activity Relationships, 1991
• Three-dimensional structure-activity relationships and receptor mapping of N1-substituents of quinolone antibacterials
  Journal of Medicinal Chemistry, 1991
• Crossvalidation, Bootstrapping, and Partial Least Squares Compared with Multiple Regression in Conventional QSAR Studies
  Quantitative Structure-Activity Relationships, 1988
• New structure-activity relationships of the quinolone antibacterials using the target enzyme. The development and application of a DNA gyrase assay
  Journal of Medicinal Chemistry, 1986
• Development and use of quantum mechanical molecular models. 76. AM1: a new general purpose quantum mechanical molecular model
  Journal of the American Chemical Society, 1985