Literature DB >> 9420020

Antifolates in clinical development.

C H Takimoto1.   

Abstract

Many novel antifolate compounds with unique pharmacologic properties are currently in clinical development. These newer antifolates differ from methotrexate, the most widely used and studied drug in this class, in terms of their lipid solubility and cellular transport affinity, their level of polyglutamation, and their specificity for inhibiting folate-dependent enzymes, such as dihydrofolate reductase, thymidylate synthase, or glycinamide ribonucleotide formyltransferase. The current status (ie, mechanism of action, clinical response rates, and toxicity) of some of the newer antifolate compounds presently in clinical testing, including edatrexate, piritrexim, raltritrexed, LY 231514, AG337, AG331, 1843U89, ZD 9331, and lometrexol, is reviewed.

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Year:  1997        PMID: 9420020

Source DB:  PubMed          Journal:  Semin Oncol        ISSN: 0093-7754            Impact factor:   4.929


  9 in total

1.  Synthesis and biological activity of substituted 2,4-diaminopyrimidines that inhibit Bacillus anthracis.

Authors:  Baskar Nammalwar; Richard A Bunce; K Darrell Berlin; Christina R Bourne; Philip C Bourne; Esther W Barrow; William W Barrow
Journal:  Eur J Med Chem       Date:  2012-05-22       Impact factor: 6.514

2.  Synthesis and evaluation of a classical 2,4-diamino-5-substituted-furo[2,3-d]pyrimidine and a 2-amino-4-oxo-6-substituted-pyrrolo[2,3-d]pyrimidine as antifolates.

Authors:  Aleem Gangjee; Jie Yang; John J McGuire; Roy L Kisliuk
Journal:  Bioorg Med Chem       Date:  2006-09-20       Impact factor: 3.641

3.  Dual inhibitors of thymidylate synthase and dihydrofolate reductase as antitumor agents: design, synthesis, and biological evaluation of classical and nonclassical pyrrolo[2,3-d]pyrimidine antifolates(1).

Authors:  Aleem Gangjee; Hiteshkumar D Jain; Jaclyn Phan; Xin Lin; Xiaohong Song; John J McGuire; Roy L Kisliuk
Journal:  J Med Chem       Date:  2006-02-09       Impact factor: 7.446

Review 4.  Novel antifolate drugs.

Authors:  W Thomas Purcell; David S Ettinger
Journal:  Curr Oncol Rep       Date:  2003-03       Impact factor: 5.075

5.  Biological and structural evaluation of 10R- and 10S-methylthio-DDACTHF reveals a new role for sulfur in inhibition of glycinamide ribonucleotide transformylase.

Authors:  Stephen Connelly; Jessica K DeMartino; Dale L Boger; Ian A Wilson
Journal:  Biochemistry       Date:  2013-07-19       Impact factor: 3.162

6.  Asymmetric synthesis of inhibitors of glycinamide ribonucleotide transformylase.

Authors:  Jessica K DeMartino; Inkyu Hwang; Stephen Connelly; Ian A Wilson; Dale L Boger
Journal:  J Med Chem       Date:  2008-08-08       Impact factor: 7.446

7.  The effect of 5-alkyl modification on the biological activity of pyrrolo[2,3-d]pyrimidine containing classical and nonclassical antifolates as inhibitors of dihydrofolate reductase and as antitumor and/or antiopportunistic infection agents.

Authors:  Aleem Gangjee; Hiteshkumar D Jain; Sherry F Queener; Roy L Kisliuk
Journal:  J Med Chem       Date:  2008-07-08       Impact factor: 7.446

8.  Pharmacokinetics of the perioperative use of cancer chemotherapy in peritoneal surface malignancy patients.

Authors:  K Van der Speeten; K Govaerts; O A Stuart; P H Sugarbaker
Journal:  Gastroenterol Res Pract       Date:  2012-06-13       Impact factor: 2.260

9.  Molecular docking studies on DMDP derivatives as human DHFR inhibitors.

Authors:  Vivek Srivastava; Ashutosh Kumar; Bhartendu Nath Mishra; Mohammad Imran Siddiqi
Journal:  Bioinformation       Date:  2008-12-06
  9 in total

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