메뉴 건너뛰기




Volumn 53, Issue 1, 1999, Pages 33-40

Glycosidopyrroles. Part 1. Acyclic derivatives: 1-(2-hydroxyethoxy) methylpyrroles as potential anti-viral agents

Author keywords

1 (2 Hydroxyethoxy) methylpyrroles; Acyclic glycosidopyrroles; Anti viral agents

Indexed keywords

1 (2 HYDROXYETHOXY)METHYLPYRROLE DERIVATIVE; ANTIVIRUS AGENT; PYRROLE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0345369592     PISSN: 0014827X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0014-827X(97)00002-5     Document Type: Article
Times cited : (49)

References (13)
  • 1
    • 0023771683 scopus 로고
    • Synthesis and antiviral activity of certain 4-and 4,5-disubstituted 7-[(2-hydroxyethoxy)methyl]pyrrolo[2,3-d]pyrimidine
    • [1] J.S. Pudlo, N.K. Saxena, M.R. Nassiri, S.R. Turk, J.C. Drach, L.B. Townsend, Synthesis and antiviral activity of certain 4-and 4,5-disubstituted 7-[(2-hydroxyethoxy)methyl]pyrrolo[2,3-d]pyrimidine, J. Med. Chem. 31 (1988) 2086-2092.
    • (1988) J. Med. Chem. , vol.31 , pp. 2086-2092
    • Pudlo, J.S.1    Saxena, N.K.2    Nassiri, M.R.3    Turk, S.R.4    Drach, J.C.5    Townsend, L.B.6
  • 2
    • 0026718161 scopus 로고
    • Improved synthesis and biological evaluation of an acyclic thiosangivamycin active against human cytomegalovirus
    • [2] T.E. Renau, M.R. Nassiri, E.E. Swayze, E.R. Kern, L.B. Townsend, Improved synthesis and biological evaluation of an acyclic thiosangivamycin active against human cytomegalovirus, Antiviral Res. 19 (1992) 15-28.
    • (1992) Antiviral Res. , vol.19 , pp. 15-28
    • Renau, T.E.1    Nassiri, M.R.2    Swayze, E.E.3    Kern, E.R.4    Townsend, L.B.5
  • 3
    • 0026675874 scopus 로고
    • Synthesis, antiproliferative, and antiviral evaluation of certain acyclic 6-substituted pyrrolo[2,3-d]pyrimidine nucleoside analogs related to sangivamycin and toyocamycin
    • [3] E.E. Swayze, W.M. Shannon, R.W. Buckheit, L.L. Wotring, J.C. Drach, L.B. Townsend, Synthesis, antiproliferative, and antiviral evaluation of certain acyclic 6-substituted pyrrolo[2,3-d]pyrimidine nucleoside analogs related to sangivamycin and toyocamycin, Nucleosides Nucleotides 11 (1992) 1507-1527.
    • (1992) Nucleosides Nucleotides , vol.11 , pp. 1507-1527
    • Swayze, E.E.1    Shannon, W.M.2    Buckheit, R.W.3    Wotring, L.L.4    Drach, J.C.5    Townsend, L.B.6
  • 4
    • 0025309042 scopus 로고
    • Synthesis and antiviral activity of some acyclic and C-cyclic pyrrolo[2,3-d]pyrimidine nucleoside analogues
    • [4] S.M. Bennet, N. Guyen-Ba, K.K. Ogilvie, Synthesis and antiviral activity of some acyclic and C-cyclic pyrrolo[2,3-d]pyrimidine nucleoside analogues, J. Med. Chem. 33 (1990) 2162-2173.
    • (1990) J. Med. Chem. , vol.33 , pp. 2162-2173
    • Bennet, S.M.1    Guyen-Ba, N.2    Ogilvie, K.K.3
  • 5
    • 0019975382 scopus 로고
    • Nucleic acid related compounds. 37. Convenient and high-yield synthesis of N-[(2-hydroxyethoxy)methyl]-heterocycles as 'acyclic nucleoside' analogues
    • [5] M.J. Robins, P.W. Hatfield. Nucleic acid related compounds. 37. Convenient and high-yield synthesis of N-[(2-hydroxyethoxy)methyl]-heterocycles as 'acyclic nucleoside' analogues, Can. J. Chem. 60 (1982) 547-553.
    • (1982) Can. J. Chem. , vol.60 , pp. 547-553
    • Robins, M.J.1    Hatfield, P.W.2
  • 8
    • 0344711134 scopus 로고
    • Reazioni con nitrito di amile. Nota III
    • [8] T. Aiello, Reazioni con nitrito di amile. Nota III, Gazz. Chim. Ital. 69 (1939) 315-322.
    • (1939) Gazz. Chim. Ital. , vol.69 , pp. 315-322
    • Aiello, T.1
  • 9
    • 0010505654 scopus 로고
    • Oxidative halogenation of substituted pyrroles with cu (II). Part II. Bromination of some ethyl 3-pyrrolecarboxylates and corresponding acids
    • [9] S. Petruso, S. Caronna, M. Sferlazzo, V. Sprio, Oxidative halogenation of substituted pyrroles with Cu (II). Part II. Bromination of some ethyl 3-pyrrolecarboxylates and corresponding acids. J. Heterocycl. Chem. 27 (1990) 1277-1280.
    • (1990) J. Heterocycl. Chem. , vol.27 , pp. 1277-1280
    • Petruso, S.1    Caronna, S.2    Sferlazzo, M.3    Sprio, V.4
  • 11
    • 0024716284 scopus 로고
    • Atomic physicochemical parameters for three dimensional structure directed quantitative structure-activity relationships. 4. Additional parameters for hydrophobic and dispersive interactions and their application for an automated superposition of certain naturally occurring nucleoside antibiotics
    • [11] V.N. Viswanadhan, A.K. Ghose, G.R. Revankar, R.K. Robin, Atomic physicochemical parameters for three dimensional structure directed quantitative structure-activity relationships. 4. Additional parameters for hydrophobic and dispersive interactions and their application for an automated superposition of certain naturally occurring nucleoside antibiotics, J. Chem. Inf. Comput. Sci. 29 (1989) 163-172.
    • (1989) J. Chem. Inf. Comput. Sci. , vol.29 , pp. 163-172
    • Viswanadhan, V.N.1    Ghose, A.K.2    Revankar, G.R.3    Robin, R.K.4
  • 13
    • 0017620356 scopus 로고
    • Relative potencies of anti-herpes compounds
    • [13] P. Collins, D.J. Bauer. Relative potencies of anti-herpes compounds. Ann. N.Y. Acad. Sci. 284 (1977) 49-59.
    • (1977) Ann. N.y. Acad. Sci. , vol.284 , pp. 49-59
    • Collins, P.1    Bauer, D.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.