These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
6. Quinazoline antifolate thymidylate synthase inhibitors: replacement of glutamic acid in the C2-methyl series. Marsham PR; Jackman AL; Barker AJ; Boyle FT; Pegg SJ; Wardleworth JM; Kimbell R; O'Connor BM; Calvert AH; Hughes LR J Med Chem; 1995 Mar; 38(6):994-1004. PubMed ID: 7699716 [TBL] [Abstract][Full Text] [Related]
7. Novel 2-amino-4-oxo-5-arylthio-substituted-pyrrolo[2,3-d]pyrimidines as nonclassical antifolate inhibitors of thymidylate synthase. Gangjee A; Jain HD; Kisliuk RL Bioorg Med Chem Lett; 2005 May; 15(9):2225-30. PubMed ID: 15837298 [TBL] [Abstract][Full Text] [Related]
8. ICI D1694, a quinazoline antifolate thymidylate synthase inhibitor that is a potent inhibitor of L1210 tumor cell growth in vitro and in vivo: a new agent for clinical study. Jackman AL; Taylor GA; Gibson W; Kimbell R; Brown M; Calvert AH; Judson IR; Hughes LR Cancer Res; 1991 Oct; 51(20):5579-86. PubMed ID: 1913676 [TBL] [Abstract][Full Text] [Related]
9. Carrier- and receptor-mediated transport of folate antagonists targeting folate-dependent enzymes: correlates of molecular-structure and biological activity. Westerhof GR; Schornagel JH; Kathmann I; Jackman AL; Rosowsky A; Forsch RA; Hynes JB; Boyle FT; Peters GJ; Pinedo HM Mol Pharmacol; 1995 Sep; 48(3):459-71. PubMed ID: 7565626 [TBL] [Abstract][Full Text] [Related]
10. Synthesis of N-{4-[(2,4-diamino-5-methyl-4,7-dihydro-3H-pyrrolo[2,3-d]pyrimidin-6-yl)thio]benzoyl}-L-glutamic acid and N-{4-[(2-amino-4-oxo-5-methyl-4,7-dihydro-3H-pyrrolo[2,3-d]pyrimidin-6-yl)thio]benzoyl}-L-glutamic acid as dual inhibitors of dihydrofolate reductase and thymidylate synthase and as potential antitumor agents. Gangjee A; Lin X; Kisliuk RL; McGuire JJ J Med Chem; 2005 Nov; 48(23):7215-22. PubMed ID: 16279780 [TBL] [Abstract][Full Text] [Related]
11. Quinazoline antifolates inhibiting thymidylate synthase: computer modelling of the N10 substituent. Jones TR; Betteridge RF; Neidle S; Jackman AL; Calvert AH Anticancer Drug Des; 1989 Mar; 3(4):243-8. PubMed ID: 2930626 [TBL] [Abstract][Full Text] [Related]
12. Increased thymidylate synthase in L1210 cells possessing acquired resistance to N10-propargyl-5,8-dideazafolic acid (CB3717): development, characterization, and cross-resistance studies. Jackman AL; Alison DL; Calvert AH; Harrap KR Cancer Res; 1986 Jun; 46(6):2810-5. PubMed ID: 2938731 [TBL] [Abstract][Full Text] [Related]
13. Activity of the thymidylate synthase inhibitor 2-desamino-N10-propargyl-5,8-dideazafolic acid and related compounds in murine (L1210) and human (W1L2) systems in vitro and in L1210 in vivo. Jackman AL; Taylor GA; O'Connor BM; Bishop JA; Moran RG; Calvert AH Cancer Res; 1990 Sep; 50(17):5212-8. PubMed ID: 2386929 [TBL] [Abstract][Full Text] [Related]
14. Drug-resistant variants of Escherichia coli thymidylate synthase: effects of substitutions at Pro-254. Fantz C; Shaw D; Jennings W; Forsthoefel A; Kitchens M; Phan J; Minor W; Lebioda L; Berger FG; Spencer HT Mol Pharmacol; 2000 Feb; 57(2):359-66. PubMed ID: 10648646 [TBL] [Abstract][Full Text] [Related]
15. Quinazoline-based thymidylate synthase inhibitors: relationship between structural modifications and polyglutamation. Jackman AL; Kimbell R; Brown M; Brunton L; Bisset GM; Bavetsias V; Marsham P; Hughes LR; Boyle FT Anticancer Drug Des; 1995 Oct; 10(7):573-89. PubMed ID: 7495480 [TBL] [Abstract][Full Text] [Related]
16. Quinazoline antifolate thymidylate synthase inhibitors: alkyl, substituted alkyl, and aryl substituents in the C2 position. Hughes LR; Jackman AL; Oldfield J; Smith RC; Burrows KD; Marsham PR; Bishop JA; Jones TR; O'Connor BM; Calvert AH J Med Chem; 1990 Nov; 33(11):3060-7. PubMed ID: 2231606 [TBL] [Abstract][Full Text] [Related]
17. Potentiation of the cytotoxicity of thymidylate synthase (TS) inhibitors by dipyridamole analogues with reduced alpha1-acid glycoprotein binding. Curtin NJ; Bowman KJ; Turner RN; Huang B; Loughlin PJ; Calvert AH; Golding BT; Griffin RJ; Newell DR Br J Cancer; 1999 Aug; 80(11):1738-46. PubMed ID: 10468290 [TBL] [Abstract][Full Text] [Related]
18. Structure-based design and synthesis of lipophilic 2,4-diamino-6-substituted quinazolines and their evaluation as inhibitors of dihydrofolate reductases and potential antitumor agents. Gangjee A; Vidwans AP; Vasudevan A; Queener SF; Kisliuk RL; Cody V; Li R; Galitsky N; Luft JR; Pangborn W J Med Chem; 1998 Aug; 41(18):3426-34. PubMed ID: 9719595 [TBL] [Abstract][Full Text] [Related]
19. Folate-based inhibitors of thymidylate synthase: synthesis and antitumor activity of gamma-linked sterically hindered dipeptide analogues of 2-desamino-2-methyl-N10-propargyl-5,8-dideazafolic acid (ICI 198583). Bavetsias V; Jackman AL; Marriott JH; Kimbell R; Gibson W; Boyle FT; Bisset GM J Med Chem; 1997 May; 40(10):1495-510. PubMed ID: 9154971 [TBL] [Abstract][Full Text] [Related]
20. High-affinity inhibitors of dihydrofolate reductase: antimicrobial and anticancer activities of 7,8-dialkyl-1,3-diaminopyrrolo[3,2-f]quinazolines with small molecular size. Kuyper LF; Baccanari DP; Jones ML; Hunter RN; Tansik RL; Joyner SS; Boytos CM; Rudolph SK; Knick V; Wilson HR; Caddell JM; Friedman HS; Comley JC; Stables JN J Med Chem; 1996 Feb; 39(4):892-903. PubMed ID: 8632413 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]