메뉴 건너뛰기




Volumn 18, Issue 4, 2008, Pages 1364-1367

Syntheses of N3-substituted thymine acyclic nucleoside phosphonates and a comparison of their inhibitory effect towards thymidine phosphorylase

Author keywords

Acyclic nucleoside phosphonates; Alkylation; Fluorination; Pyrimidine; Thymidine phosphorylase

Indexed keywords

1 [2 (PHOSPHONOMETHOXY)ETHYL]THYMINE; 1 [3 FLUORO 2 (PHOSPHONOMETHOXY)PROPYL]THYMINE; 1 [3 HYDROXY 2 (PHOSPHONOMETHOXY)PROPYL]THYMINE; ALKYL GROUP; ANTINEOPLASTIC AGENT; THYMIDINE PHOSPHORYLASE; THYMINE ACYCLIC NUCLEOSIDE PHOSPHONATE; UNCLASSIFIED DRUG; DRUG DERIVATIVE; ENZYME INHIBITOR; PHOSPHONIC ACID DERIVATIVE; PYRIMIDINE NUCLEOSIDE; THYMINE;

EID: 39049090517     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2008.01.006     Document Type: Article
Times cited : (9)

References (23)
  • 17
    • 0004053611 scopus 로고
    • John Wiley & sons Inc 809
    • Voet D., and Voet J.G. Biochemistry (1990), John Wiley & sons Inc 795 809
    • (1990) Biochemistry , pp. 795
    • Voet, D.1    Voet, J.G.2
  • 19
    • 39049103891 scopus 로고    scopus 로고
    • note
    • 7P 433.2103: Found 433.2099.
  • 20
    • 39049096760 scopus 로고    scopus 로고
    • note
    • 6P 277.0753: Found 277.0762.
  • 21
    • 39049168639 scopus 로고    scopus 로고
    • note
    • Ref.6 The reaction was carried out at 37 °C for 10 min and stopped by spotting a 2 μl aliquot onto Silica gel 60 F254 plate that had been prespotted with 0.01 μmol of each thymine and thymidine. The plate was developed in the non-aquaeous phase of the solvent system ethyl acetate/water/formic acid (60:35:5). The spots were visualised under UV light (254 nm) and cut out for radioactivity determination in the toluene-based scintillation cocktail.
  • 22
    • 39049098165 scopus 로고    scopus 로고
    • note
    • Cytostatic activity assays. L1210 cells, CCRF-CEM cells, and HL-60 cells were cultivated in RPMI 1640 medium supplemented with calf foetal serum using 24-well tissue culture plates. The endpoint of the cell growth was 72 h following the drug addition. Cells were then counted in Celtac MEK 5208 (NIHON KOHDEN) haematological analyzer. HeLa S3 cells were seeded to 24-well dishes in RPMI 1640 HEPES modification with foetal calf serum. 48 h following the drug addition the cultivation was stopped and the cell growth was evaluated after methylene blue addition.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.