메뉴 건너뛰기




Volumn 45, Issue 5, 2000, Pages 423-427

Phase I study of AG2034, a targeted GARFT inhibitor, administered once every 3 weeks

Author keywords

AG2034; Glycinamide ribonucleotide transformylase inhibitor; Phase I study

Indexed keywords

ANTINEOPLASTIC AGENT; N [[5 [2 (2 AMINO 4,6,7,8 TETRAHYDRO 4 OXO 1H PYRIMIDO[5,4 B][1,4]THIAZIN 6 YL)ETHYL] 2 THIENYL]CARBONYL]GLUTAMIC ACID; PHOSPHORIBOSYLGLYCINAMIDE FORMYLTRANSFERASE;

EID: 0034007649     PISSN: 03445704     EISSN: None     Source Type: Journal    
DOI: 10.1007/s002800051012     Document Type: Article
Times cited : (12)

References (16)
  • 1
    • 0001981191 scopus 로고
    • The contributions of the de novo and salvage pathways of nucleotide biosynthesis in normal and malignant cells
    • Tattersall MHN, Fox RM (eds). Academic Press, Sydney
    • 1. Jackson RC, Harkrader RJ (1981) The contributions of the de novo and salvage pathways of nucleotide biosynthesis in normal and malignant cells. In: Tattersall MHN, Fox RM (eds) Nucleosides and cancer treatment. Academic Press, Sydney, pp 18-31
    • (1981) Nucleosides and Cancer Treatment , pp. 18-31
    • Jackson, R.C.1    Harkrader, R.J.2
  • 2
    • 0024499104 scopus 로고
    • A new folate antimetabolite, 5,10-dideaza-5,6,7,8-tetrahydrofolate, is a potent inhibitor of de novo purine synthesis
    • 2. Beardsley GP, Moroson BA, Taylor EC, Moran RG (1989) A new folate antimetabolite, 5,10-dideaza-5,6,7,8-tetrahydrofolate, is a potent inhibitor of de novo purine synthesis. J Biol Chem 264: 328-333
    • (1989) J Biol Chem , vol.264 , pp. 328-333
    • Beardsley, G.P.1    Moroson, B.A.2    Taylor, E.C.3    Moran, R.G.4
  • 3
    • 0002696866 scopus 로고
    • In vivo antitumor activity of 5,10-dideazatetrahydrofolic acid (DDATHF) and its diastereomeric isomers
    • 3. Shih C, Grindey GB, Houghton PJ, Houghton JA (1980) In vivo antitumor activity of 5,10-dideazatetrahydrofolic acid (DDATHF) and its diastereomeric isomers. Proc Am Assoc Cancer Res 29: 283
    • (1980) Proc Am Assoc Cancer Res , vol.29 , pp. 283
    • Shih, C.1    Grindey, G.B.2    Houghton, P.J.3    Houghton, J.A.4
  • 4
    • 0025328483 scopus 로고
    • New pathways from pteridines. Design and synthesis of a new class of potent and selective antitumor agents
    • 4. Taylor EC (1990) New pathways from pteridines. Design and synthesis of a new class of potent and selective antitumor agents. J Heterocycl Chem 27: 11
    • (1990) J Heterocycl Chem , vol.27 , pp. 11
    • Taylor, E.C.1
  • 6
    • 0027179429 scopus 로고
    • Phase I study of (6R)-5,10-Dideazatetrahydrofolate: A folate antimetabolite inhibitory to de novo purine synthesis
    • 6. Ray MS, Muggia FM, Leichman CG, Grunberg SM, Nelson RL, Dyke RW (1993) Phase I study of (6R)-5,10-Dideazatetrahydrofolate: a folate antimetabolite inhibitory to de novo purine synthesis. J Natl Cancer Inst 85: 1154-1159
    • (1993) J Natl Cancer Inst , vol.85 , pp. 1154-1159
    • Ray, M.S.1    Muggia, F.M.2    Leichman, C.G.3    Grunberg, S.M.4    Nelson, R.L.5    Dyke, R.W.6
  • 8
    • 0030007680 scopus 로고    scopus 로고
    • Phase I study of the antipurine antifolate lometrexol (DDATHF) with folinic acid rescue
    • 8. Sessa C, Jong J de, D'Incalci M, Hatty S, Pagani O, Cavilli F (1996) Phase I study of the antipurine antifolate lometrexol (DDATHF) with folinic acid rescue. Clin Cancer Res 2: 1123-1127
    • (1996) Clin Cancer Res , vol.2 , pp. 1123-1127
    • Sessa, C.1    De Jong, J.2    D'Incalci, M.3    Hatty, S.4    Pagani, O.5    Cavilli, F.6
  • 10
    • 0029883293 scopus 로고    scopus 로고
    • Augmentation of the therapeutic activity of lometrexol [(6-R)5,10-dideazatetrahydrofolate] by oral folic acid
    • 10. Alati T, Worzalla JF, Shih C, Bewley JR, Lewis S, Moran RG, Grindey GB (1996) Augmentation of the therapeutic activity of lometrexol [(6-R)5,10-dideazatetrahydrofolate] by oral folic acid. Cancer Res 56: 2331-2335
    • (1996) Cancer Res , vol.56 , pp. 2331-2335
    • Alati, T.1    Worzalla, J.F.2    Shih, C.3    Bewley, J.R.4    Lewis, S.5    Moran, R.G.6    Grindey, G.B.7
  • 11
    • 0026668340 scopus 로고
    • Structure of Apo and complexed Escherichia coli glycinamide ribonucleotide transformylase
    • 11. Almassy RJ, Janson CA, Kan CC, Hostomaska Z (1992) Structure of Apo and complexed Escherichia coli glycinamide ribonucleotide transformylase. Proc Natl Acad Sci USA 89: 6114-6118
    • (1992) Proc Natl Acad Sci USA , vol.89 , pp. 6114-6118
    • Almassy, R.J.1    Janson, C.A.2    Kan, C.C.3    Hostomaska, Z.4
  • 12
    • 0021871375 scopus 로고
    • A computational procedure for determining energetically favorable binding sites on biologically important macromolecules
    • 12. Goodford PJ (1985) A computational procedure for determining energetically favorable binding sites on biologically important macromolecules. J Med Chem 28: 849-857
    • (1985) J Med Chem , vol.28 , pp. 849-857
    • Goodford, P.J.1
  • 16
    • 0029560236 scopus 로고
    • Clinical pharmacokinetics of the antipurine antifolate (6R)-5,10-dideaza-5,6,7,8-tetrahydrofolic acid (lometrexol) administered with an oral folic acid supplement
    • 16. Wedge SR, Laohavnjj S, Taylor GA, Boddy A, Calvert AH, Newell DR (1995) Clinical pharmacokinetics of the antipurine antifolate (6R)-5,10-dideaza-5,6,7,8-tetrahydrofolic acid (lometrexol) administered with an oral folic acid supplement. Clin Cancer Res 1: 1479-1486
    • (1995) Clin Cancer Res , vol.1 , pp. 1479-1486
    • Wedge, S.R.1    Laohavnjj, S.2    Taylor, G.A.3    Boddy, A.4    Calvert, A.H.5    Newell, D.R.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.