메뉴 건너뛰기




Volumn 24, Issue 5-7, 2005, Pages 387-392

Design and evaluation of 5′-modified nucleoside analogs as prodrugs for an E. coli purine nucleoside phosphorylase mutant

Author keywords

[No Author keywords available]

Indexed keywords

5' METHYLTHIOADENOSINE PHOSPHORYLASE; 9 (6 DEOXY ALPHA DEXTRO TALOFURANOSYL) 2 ADENINE; 9 (6 DEOXY ALPHA DEXTRO TALOFURANOSYL) 6 METHYLPURINE; ADENINE DERIVATIVE; BACTERIAL ENZYME; NUCLEOSIDE PHOSPHORYLASE; PHOSPHORYLASE; PRODRUG; PURINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 26644451885     PISSN: 15257770     EISSN: 15322335     Source Type: Journal    
DOI: 10.1081/NCN-200059807     Document Type: Conference Paper
Times cited : (13)

References (12)
  • 2
    • 0016427543 scopus 로고
    • Purine nucleoside phosphorylase from Escherichia coli and Salmonella typhimurium. Purification and some properties
    • Jensen, K.F.; Nygaard, P. Purine nucleoside phosphorylase from Escherichia coli and Salmonella typhimurium. Purification and some properties. Eur. J. Biochem. 1975, 51, 253-265.
    • (1975) Eur. J. Biochem. , vol.51 , pp. 253-265
    • Jensen, K.F.1    Nygaard, P.2
  • 3
    • 0028465423 scopus 로고
    • Tumor cell bystander killing in colonic carcinoma utilizing the E. coli Deo D gene to generate toxic purines
    • Sorscher, E.J.; Peng, S.; Bebok, Z.; Allan, P.W.; Bennett, L.L., Jr.; Parker, W.B. Tumor cell bystander killing in colonic carcinoma utilizing the E. coli Deo D gene to generate toxic purines. Gene Ther. 1994, 1, 233-238.
    • (1994) Gene Ther. , vol.1 , pp. 233-238
    • Sorscher, E.J.1    Peng, S.2    Bebok, Z.3    Allan, P.W.4    Bennett Jr., L.L.5    Parker, W.B.6
  • 4
    • 0031914978 scopus 로고    scopus 로고
    • Cell to cell contact is not required for bystander cell killing by E. coli purine nucleoside phosphorylase
    • Hughes, B.W.; King, S.A.; Allan, P.W.; Parker, W.B.; Sorscher, E.J. Cell to cell contact is not required for bystander cell killing by E. coli purine nucleoside phosphorylase. J. Biol. Chem. 1998, 273, 2322-2328.
    • (1998) J. Biol. Chem. , vol.273 , pp. 2322-2328
    • Hughes, B.W.1    King, S.A.2    Allan, P.W.3    Parker, W.B.4    Sorscher, E.J.5
  • 6
    • 0033759371 scopus 로고    scopus 로고
    • In vivo sensitization of ovarian tumors to chemotherapy by expression of E. coli PNP in a small fraction of tumor cells
    • Gadi, V.K.; Alexander, S.D.; Kudlow, J.E.; Allan, P.W.; Parker, W.B.; Sorscher, E.J. In vivo sensitization of ovarian tumors to chemotherapy by expression of E. coli PNP in a small fraction of tumor cells. Gene Ther. 2000, 7, 1738-1743.
    • (2000) Gene Ther. , vol.7 , pp. 1738-1743
    • Gadi, V.K.1    Alexander, S.D.2    Kudlow, J.E.3    Allan, P.W.4    Parker, W.B.5    Sorscher, E.J.6
  • 7
    • 0037276433 scopus 로고    scopus 로고
    • Anti-tumor activity of 2-fluoro-2′-deoxyadenosine against tumors that express E. coli purine nucleoside phosphorylase
    • Parker, W.B.; Allan, P.W.; Hassan, A.E.A.; Secrist, J.A., III; Sorscher, E.J.; Waud, W.R. Anti-tumor activity of 2-fluoro-2′-deoxyadenosine against tumors that express E. coli purine nucleoside phosphorylase. Cancer Gene Ther. 2003, 10, 23-29.
    • (2003) Cancer Gene Ther. , vol.10 , pp. 23-29
    • Parker, W.B.1    Allan, P.W.2    Hassan, A.E.A.3    Secrist III, J.A.4    Sorscher, E.J.5    Waud, W.R.6
  • 10
    • 50549099444 scopus 로고
    • Structure-activity relationships and cross-resistance observed on evaluation of a series of purine analogs against experimental neoplasms
    • Skipper, H.E.; Montgomery, J.A.; Thomson, J.R.; Schabel, F.M., Jr. Structure-activity relationships and cross-resistance observed on evaluation of a series of purine analogs against experimental neoplasms. Cancer Res. 1959, 19, 287-308.
    • (1959) Cancer Res. , vol.19 , pp. 287-308
    • Skipper, H.E.1    Montgomery, J.A.2    Thomson, J.R.3    Schabel Jr., F.M.4
  • 11
    • 1542298120 scopus 로고    scopus 로고
    • Synthesis of a potent transition-state inhibitor of 5′-deoxy- 5′-methylthioadenosine phosphorylase
    • Kamath, V.P.; Ananth, S.; Bantia, S.; Morris, P.E., Jr. Synthesis of a potent transition-state inhibitor of 5′-deoxy-5′-methylthioadenosine phosphorylase. J. Med. Chem. 2004, 47, 1322-1324. The compound was obtained from Biocryst Pharmaceuticals, Birmingham, Alabama.
    • (2004) J. Med. Chem. , vol.47 , pp. 1322-1324
    • Kamath, V.P.1    Ananth, S.2    Bantia, S.3    Morris Jr., P.E.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.