Literature DB >> 808614

Methotrexate analogs. 6. Replacement of glutamic acid by various amino acid esters and amines.

M Chaykovsky, B L Brown, E J Modest.   

Abstract

A series of methotrexate (MTX) analogs was prepared in which the glutamic acid moiety is replaced by various amino acid esters and amines. The synthetic method consisted of the reaction of 4-amino-4-deoxy-N10-methylpteroic acid with various reagents to form intermediate mixed anhydrides, which then reacted with amino acid esters or amines to give the MTX analogs. These compounds were tested for antibacterial activity against Streptococcus faecium and for antitumor activity against L1210 leukemia in mice. Several compounds showed significant antibacterial activity; the MTX homocysteinethiolactone and MTX aspartate analogs showed marginal in vivo antitumor activity.

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Year:  1975        PMID: 808614     DOI: 10.1021/jm00243a010

Source DB:  PubMed          Journal:  J Med Chem        ISSN: 0022-2623            Impact factor:   7.446


  3 in total

Review 1.  A "Double-Edged" Scaffold: Antitumor Power within the Antibacterial Quinolone.

Authors:  Gregory S Bisacchi; Michael R Hale
Journal:  Curr Med Chem       Date:  2016       Impact factor: 4.530

2.  Prodrug forms of N-[(4-deoxy-4-amino-10-methyl)pteroyl]glutamate-gamma-[psiP(O)(OH)]-glutarate, a potent inhibitor of folylpoly-gamma-glutamate synthetase: synthesis and hydrolytic stability.

Authors:  Yan Feng; James K Coward
Journal:  J Med Chem       Date:  2006-01-26       Impact factor: 7.446

3.  Efficacies of lipophilic inhibitors of dihydrofolate reductase against parasitic protozoa.

Authors:  H Lau; J T Ferlan; V H Brophy; A Rosowsky; C H Sibley
Journal:  Antimicrob Agents Chemother       Date:  2001-01       Impact factor: 5.191

  3 in total

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