Document Detail


A molecular shape analysis and quantitative structure-activity relationship investigation of some triazine-antifolate inhibitors of Leishmania dihydrofolate reductase.
MedLine Citation:
PMID:  3178219     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Molecular shape analysis (MSA) is used to develop quantitative structure-activity relationships (QSARs) for a set of 45 4,6-diamino-1,2-dihydro-2,2-dimethyl-1-(3-substituted-phenyl)-s-triazine inhibitors of Leishmania major dihydrofolate reductase (DHFR). The MSA-QSARs are equally significant to a QSAR developed by R. G. Booth et al. [1987) J. Med. Chem. 30, 1218) using linear free energy descriptors. However, the MSA-QSARs have the same general form as all other QSARs developed for DHFR inhibitors using MSA. Molecular shape, as represented by common overlap steric volume of each inhibitor with a shape reference standard triazine from the set of 45 compounds, and relative lipophilicity account for the large majority of the variance in inhibition potency as a function of substituent choice. A general method of evaluating the impact of different conformational states of flexible substituents upon the form and significance of MSA-QSARs is developed. The results of applying this method to the 45 triazines indicate that the MSA-QSARs are relatively independent of the type of conformation assigned to the large flexible substituents. It is important to note, however, that the types of substituent conformations used in this analysis cannot necessarily be related to an "active" substituent conformation.
Authors:
M G Koehler; K Rowberg-Schaefer; A J Hopfinger
Related Documents :
12532299 - Substituent effects on o--h bond dissociation enthalpies and ionization potentials of c...
23909839 - A discrete three-layer stack aggregate of a linear porphyrin tetramer: solution-phase s...
24205889 - Selective hg(2+) sensing behaviors of rhodamine derivatives with extended conjugation b...
20524689 - Computational study on the interaction of n1 substituted pyrazole derivatives with b-ra...
24273039 - Increased halide recognition strength by enhanced intercomponent preorganisation in tri...
23169239 - Ultrathin silica films on metals: the long and winding road to understanding the atomic...
17985019 - Molecular tectonics: on the formation of 1-d silver coordination networks by thiacalixa...
16690859 - Formation and subdivision of deformation structures during plastic deformation.
19346599 - A unique two-dimensional coordination network of 1-benzofuran-2,3-dicarboxylate with la...
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Archives of biochemistry and biophysics     Volume:  266     ISSN:  0003-9861     ISO Abbreviation:  Arch. Biochem. Biophys.     Publication Date:  1988 Oct 
Date Detail:
Created Date:  1988-11-17     Completed Date:  1988-11-17     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  0372430     Medline TA:  Arch Biochem Biophys     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  152-61     Citation Subset:  IM    
Affiliation:
Department of Medicinal Chemistry, University of Illinois, Chicago 60680.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Animals
Folic Acid Antagonists*
Leishmania tropica / enzymology*
Molecular Conformation
Structure-Activity Relationship
Triazines / pharmacology*
Chemical
Reg. No./Substance:
0/Folic Acid Antagonists; 0/Triazines

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Botulinum neurotoxin type A: cleavage of the heavy chain into two halves and their partial sequences...
Next Document:  Acylation of gelatin-agarose and the enhancement by heparin of fibronectin binding.