Synthesis of 5′-deoxy-5′-[18F]fluoro-adenosine by radiofluorination of 5′-deoxy-5′-haloadenosine derivatives

被引:13
作者
Lehel, S
Horváth, G
Boros, I
Mikecz, P
Márián, T
Trón, L
机构
[1] Univ Debrecen, Sch Med, Positron Emiss Tomog Ctr, H-4012 Debrecen, Hungary
[2] Hungarian Acad Sci, PET Study Grp, H-1051 Budapest, Hungary
关键词
D O I
10.1023/A:1006791211919
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
5'-Deoxy-5`-[F-18]fluoro-adenosine was synthesised by nucleophilic radiofluorination reactions of 5'-deoxy-5'-haloadenosines. The homogeneous isotope exchange in 5'-deoxy-5'-fluoro-adenosine was also investigated. The conversion of these reactions was found to be rather low and depends on the strength of the halogen-carbon bond: 0.248% for chloride-, 0.488% for bromide- and 1.070% for iodide-derivative; there was no reaction observed in the case of fluoro-compound.
引用
收藏
页码:399 / 401
页数:3
相关论文
共 10 条
  • [1] BERGMAN J, 1994, J LABEL COMPDS RADIO, V34, P174
  • [2] [11C]-labeling of some caffeine derivatives for mapping adenosine A2a receptors by PET technique
    Boros, I
    Horváth, G
    Lehel, S
    Márián, T
    Kovács, Z
    Szentmiklósi, J
    Tóth, G
    Trón, L
    [J]. JOURNAL OF RADIOANALYTICAL AND NUCLEAR CHEMISTRY, 1999, 242 (02) : 309 - 312
  • [3] HAMACHER K, 1986, J NUCL MED, V27, P235
  • [4] A1 adenosine receptor antagonists as ligands for positron emission tomography (PET) and single-photon emission tomography (SPET)
    Holschbach, MH
    Fein, T
    Krummeich, C
    Lewis, RG
    Wutz, W
    Schwabe, U
    Unterlugauer, D
    Olsson, RA
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1998, 41 (04) : 555 - 563
  • [5] ADENOSINE RECEPTORS - PHARMACOLOGY, STRUCTURE-ACTIVITY-RELATIONSHIPS, AND THERAPEUTIC POTENTIAL
    JACOBSON, KA
    VANGALEN, PJM
    WILLIAMS, M
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1992, 35 (03) : 407 - 422
  • [6] 5-DEOXY-5-FLUORO-D-RIBOFURANOSYL DERIVATIVES OF CERTAIN PURINES, PYRIMIDINES AND 5,6-DIMETHYLBENZIMIDAZOLE
    KISSMAN, HM
    WEISS, MJ
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1958, 80 (20) : 5559 - 5564
  • [7] Preparation and primary evaluation of [11C]CSC as a possible tracer for mapping adenosine A2A receptors by PET
    Márián, T
    Boros, I
    Lengyel, Z
    Balkay, L
    Horváth, G
    Emri, M
    Sarkadi, É
    Szentmiklósi, AJ
    Fekete, I
    Trón, L
    [J]. APPLIED RADIATION AND ISOTOPES, 1999, 50 (05) : 887 - 893
  • [8] Adenosine receptors: New opportunities for future drugs
    Poulsen, SA
    Quinn, RJ
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY, 1998, 6 (06) : 619 - 641
  • [9] NUCLEIC-ACID RELATED-COMPOUNDS .66. IMPROVED SYNTHESES OF 5'-CHLORO-5'-DEOXYNUCLEOSIDES AND 5'-S-ARYL(OR ALKYL)-5'-THIONUCLEOSIDES
    ROBINS, MJ
    HANSSKE, F
    WNUK, SF
    KANAI, T
    [J]. CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1991, 69 (09): : 1468 - 1474
  • [10] FACILE 5'-HALOGENATION OF UNPROTECTED NUCLEOSIDES
    TSUJI, T
    TAKENAKA, K
    [J]. NUCLEOSIDES & NUCLEOTIDES, 1987, 6 (03): : 575 - 580