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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 
Chemical Compound Review

CHEMBL56170     5-[4-(benzyl-methyl-amino)-3- nitro-phenyl]...

Synonyms: AG-K-11597, SureCN8590014, ACMC-20ashh, CHEBI:186885, Neuro_000220, ...
 
 
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High impact information on NSC 382035

  • The compounds exhibited potent inhibitory activity against T. gondii (IC50 values 0.0018-0.14 microM) and rat liver (IC50 values 0.0029-0.27 microM) DHFR, with a 4-substituent invariably enhancing binding to both enzymes relative to the unsubstituted benzoprim (5) or methylbenzoprim (6) [1].
  • Structural studies on bio-active compounds. 20. Molecular modeling and crystallographic studies on methylbenzoprim, a potent inhibitor of dihydrofolate reductase [2].

References

  1. Nonclassical 2,4-diamino-5-aryl-6-ethylpyrimidine antifolates: activity as inhibitors of dihydrofolate reductase from Pneumocystis carinii and Toxoplasma gondii and as antitumor agents. Robson, C., Meek, M.A., Grunwaldt, J.D., Lambert, P.A., Queener, S.F., Schmidt, D., Griffin, R.J. J. Med. Chem. (1997) [Pubmed]
  2. Structural studies on bio-active compounds. 20. Molecular modeling and crystallographic studies on methylbenzoprim, a potent inhibitor of dihydrofolate reductase. Denny, B.J., Ringan, N.S., Schwalbe, C.H., Lambert, P.A., Meek, M.A., Griffin, R.J., Stevens, M.F. J. Med. Chem. (1992) [Pubmed]
 
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