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Volumn 4, Issue 4, 2004, Pages 383-394

"Lock-in"-cycloSal-pronucleotides - A new generation of chemical Trojan horses?

Author keywords

[No Author keywords available]

Indexed keywords

2',3' DIDEHYDRO 2',3' DIDEOXYADENOSINE; 2',3' DIDEOXY 2' FLUOROADENOSINE; 2',3' DIDEOXYADENOSINE; 5 (2 BROMOVINYL) 2' DEOXYURIDINE; ABACAVIR; ACICLOVIR; AMPHOLYTE; BENZYL DERIVATIVE; BUTYL HYDROPEROXIDE; CARBOVIR; CYCLIC NUCLEOTIDE; ESTER DERIVATIVE; FLOXURIDINE; HYDROXYL GROUP; NUCLEOSIDE ANALOG; PRODRUG; SALIGENIN; SODIUM DIHYDROGEN PHOSPHATE; STAVUDINE; ZIDOVUDINE;

EID: 3042561444     PISSN: 13895575     EISSN: None     Source Type: Journal    
DOI: 10.2174/1389557043403972     Document Type: Review
Times cited : (30)

References (62)
  • 16
    • 25944467251 scopus 로고    scopus 로고
    • unpublished results
    • Müller, C.; Meier, C. 2003, unpublished results.
    • (2003)
    • Müller, C.1    Meier, C.2
  • 17
    • 3042607271 scopus 로고    scopus 로고
    • unpublished results
    • Naesens, L.; Meier, C. 1998, unpublished results.
    • (1998)
    • Naesens, L.1    Meier, C.2
  • 18
    • 3042518175 scopus 로고    scopus 로고
    • unpublished results. It should be added that salicyl alcohol (saligenin) is used as part of the antirheumatic and analgetic drug Salicin (2-[hydroxymethyl]phenyl-β-D-glucopyranoside; Assalix®). β-Glucosidase hydrolyzes Salicin to D-glucose and saligenin and the latter is then slowly oxidized by cytochrome P450 to salicylic acid in the blood and in the liver:
    • Balzarini, J. 2000, unpublished results. It should be added that salicyl alcohol (saligenin) is used as part of the antirheumatic and analgetic drug Salicin (2-[hydroxymethyl]phenyl-β-D-glucopyranoside; Assalix®). β-Glucosidase hydrolyzes Salicin to D-glucose and saligenin and the latter is then slowly oxidized by cytochrome P450 to salicylic acid in the blood and in the liver:
    • (2000)
    • Balzarini, J.1
  • 33
    • 3042564444 scopus 로고    scopus 로고
    • Different names for the nucleoside analogues 17 and 18 could be found. Terms as F-up- and F-down-ddA, F-ara- and F-ribo-ddA, as well as 2′,3′-dideoxy-2′-fluoroarabinosyladenine and 2′,3′-dideoxy-2′-fluororibosyladenine have been used. Here we use the abbreviation F-β- and F-α-ddA. The correct names are 9-(2′,3′-dideoxy-2′-fluoro-β -D-threo-pentofuranosyl)adenine (17) and 9-(2′,3′ -dideoxy-2′-fluoro-β-D-erythro-pentofuranosyl)adenine (18)
    • Different names for the nucleoside analogues 17 and 18 could be found. Terms as F-up- and F-down-ddA, F-ara- and F-ribo-ddA, as well as 2′,3′-dideoxy-2′-fluoroarabinosyladenine and 2′,3′-dideoxy-2′-fluororibosyladenine have been used. Here we use the abbreviation F-β- and F-α-ddA. The correct names are 9-(2′,3′-dideoxy-2′-fluoro-β -D-threo-pentofuranosyl)adenine (17) and 9-(2′,3′ -dideoxy-2′-fluoro-β-D-erythro-pentofuranosyl)adenine (18)
  • 45
    • 3543126803 scopus 로고
    • 2nd edition, Raven Press, New York
    • Fields, B.N. Virology, (Vol. 1) 2nd edition, Raven Press, New York, 1990, 450.
    • (1990) Virology , vol.1 , pp. 450
    • Fields, B.N.1
  • 49


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.