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Volumn 53, Issue 8-9, 1998, Pages 594-601

Quinoxaline chemistry. Part 12. 3-Carboxy-2[phenoxyl-6(7)substituted quinoxalines and N-[4-(6(7) substituted-3-carboxyquinoxalin- 2-yl)hydroxy]-benzoylglutamates. Synthesis and evaluation of in vitro anticancer activity

Author keywords

Anticancer agents; Phenoxyquinoxalines; Quinoxaline derivatives

Indexed keywords

GLUTAMIC ACID DERIVATIVE; QUINOXALINE DERIVATIVE;

EID: 0032464876     PISSN: 0014827X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0014-827X(98)00075-5     Document Type: Article
Times cited : (15)

References (6)
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    • M. Loriga, M. Fiore, P. Sanna, G. Paglietti, Quinoxaline chemistry. Part 4: 2-(R)-anilinoquinoxalines as non-classic antifolate agents. Synthesis, structure elucidation and evaluation of in vitro anticancer activity, Farmaco 50 (1997) 289-301.
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  • 2
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    • Quinoxaline chemistry. Part 7: 2-[Aminobenzoates] and 2-[aminobenzoylglutamate] quinoxalines as antifolate agents. Synthesis and evaluation of in vitro anticancer, anti HIV and antifungal activity
    • M. Loriga, S. Piras, P. Sanna, G. Paglietti, Quinoxaline chemistry. Part 7: 2-[Aminobenzoates] and 2-[aminobenzoylglutamate] quinoxalines as antifolate agents. Synthesis and evaluation of in vitro anticancer, anti HIV and antifungal activity, Farmaco 52 (1997) 157-166.
    • (1997) Farmaco , vol.52 , pp. 157-166
    • Loriga, M.1    Piras, S.2    Sanna, P.3    Paglietti, G.4
  • 3
    • 0032581439 scopus 로고    scopus 로고
    • Quinoxaline chemistry. Part 11 - 3-Phenyl-2[phenoxy- and phenoxymethyl]6(7) or 6,8-substituted quinoxalines and N[4-(6(7)substituted or 6,8-disubstituted-3-phenylquinoxalin-2-yl)hydroxy or hydroxymethyl]benzoylglutamates. Synthesis and evaluation of in vitro anticancer activity and enzymatic inhibitory activity against dihydrofolate reductase (DHFR) and thymidylate synthase (TS)
    • P. Corona, G. Vitale, M. Loriga, G. Paglietti, Quinoxaline chemistry. Part 11 - 3-Phenyl-2[phenoxy- and phenoxymethyl]6(7) or 6,8-substituted quinoxalines and N[4-(6(7)substituted or 6,8-disubstituted-3-phenylquinoxalin-2-yl)hydroxy or hydroxymethyl]benzoylglutamates. Synthesis and evaluation of in vitro anticancer activity and enzymatic inhibitory activity against dihydrofolate reductase (DHFR) and thymidylate synthase (TS), Farmaco 53 (1998) 480-493.
    • (1998) Farmaco , vol.53 , pp. 480-493
    • Corona, P.1    Vitale, G.2    Loriga, M.3    Paglietti, G.4
  • 5
    • 0000719887 scopus 로고
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    • New Soluble-Formazan assay for HIV-1 cytophathic effect: Application to high-flux screening of synthetic and natural products for AIDS antiviral activity
    • O.V. Weislow, R. Kiser, D. Fine, J. Bader, R.H. Shoemaker, M.R. Boyd, New Soluble-Formazan assay for HIV-1 cytophathic effect: application to high-flux screening of synthetic and natural products for AIDS antiviral activity, J. Natl. Cancer Inst. 81 (1989) 577-586.
    • (1989) J. Natl. Cancer Inst. , vol.81 , pp. 577-586
    • Weislow, O.V.1    Kiser, R.2    Fine, D.3    Bader, J.4    Shoemaker, R.H.5    Boyd, M.R.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.