NUCLEOSIDE ANALOGS AS CHEMOTHERAPEUTIC-AGENTS - A REVIEW

被引：289
作者：
PERIGAUD, C
GOSSELIN, G
IMBACH, JL
机构：
[1] UNIV MONTPELLIER 2, CHIM BIOORGAN LAB,CNRS,URA 488,CASE COURRIER 008, PL EUGENE BATAILLON, F-34095 MONTPELLIER 5, FRANCE
[2] UNIV MONTPELLIER 2, CNRS, UMR 112, F-34095 MONTPELLIER 5, FRANCE
来源：
NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS | 1992年 / 11卷 / 2-4期
关键词：
D O I：
10.1080/07328319208021748
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
The importance of nucleoside analogues in chemotherapy and in other potential therapeutic approaches as immunomodulation or regulation of gene expression, is reviewed.
引用
收藏
页码：903 / 945
页数：43
相关论文
共 217 条
[31]  
CHABNER BA, 1981, CANCER CHEMOTHERAPY, V3, P3
[32]   2'-O-NITRO-1-BETA-D-ARABINOFURANOSYLCYTOSINE - A NEW DERIVATIVE OF 1-BETA-D-ARABINOFURANOSYLCYTOSINE THAT RESISTS ENZYMATIC DEAMINATION AND HAS ANTI-LEUKEMIC ACTIVITY [J].
CHWANG, TL ;
FRIDLAND, A ;
AVERY, TL .
JOURNAL OF MEDICINAL CHEMISTRY, 1983, 26 (02) :280-283
[33]  
COHEN JS, 1989, TOPICS MOL STRUCTURA, V12
[34]  
CREASEY WA, 1974, ANTINEOPLASTIC IMM 2, P232
[35]  
CRETTON EM, 1991, MOL PHARMACOL, V39, P258
[36]  
DAHMUS ME, 1981, J BIOL CHEM, V256, P3332
[37]  
DAMBA MJ, 1991, TETRAHEDRON LETT, V32, P2573
[38]   SUGAR MODIFIED OLIGONUCLEOTIDES .2. SOLID-PHASE SYNTHESIS OF NUCLEASE RESISTANT ALPHA-ANOMERIC URIDYLATES AS POTENTIAL ANTISENSE AGENTS [J].
DEBART, F ;
RAYNER, B ;
IMBACH, JL .
TETRAHEDRON LETTERS, 1990, 31 (25) :3537-3540
[39]  
DECLERCQ E, 1987, ANTICANCER RES, V7, P1023
[40]   SYNTHESIS AND ANTIVIRAL PROPERTIES OF 5-VINYLPYRIMIDINE NUCLEOSIDE ANALOGS [J].
DECLERCQ, E ;
WALKER, RT .
PHARMACOLOGY & THERAPEUTICS, 1984, 26 (01) :1-44
12345678910