Synthesis and in vitro evaluation of some new pyrimidines and related condensed ring systems as potential anticancer agents

被引:22
作者
Badawey, ESAM
机构
[1] Dept. of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Alexandria, Alexandria
关键词
D O I
10.1002/jhet.5570330202
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Several new pyrimidines 6-11, 18-20, furo-, thieno-, and pyrrolo[2,3-d]pyrimidines 3, 8, 12, triazolo[4,3-a]pyrimidines 14, 15, 16 and tetrazolo[1,5-a]pyrimidine 17 were prepared from the known intermediate 5-(2-hydroxyethyl)-6-methyl-2-thiouracil (2). Compound 7 (4-chloro-5-(2-chloroethyl)-2-methylthio-6-methyl-pyrimidine) exhibited weak antitumor activity in vitro.
引用
收藏
页码:229 / 233
页数:5
相关论文
共 9 条
[1]   BENZIMIDAZOLE CONDENSED RING-SYSTEM .9. POTENTIAL ANTINEOPLASTICS - NEW SYNTHESIS OF SOME PYRIDO[1,2-A]BENZIMIDAZOLES AND RELATED DERIVATIVES [J].
BADAWEY, E ;
KAPPE, T .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 1995, 30 (04) :327-332
[2]   SYNTHESIS OF SOME NEW IMIDAZO[1,2-A]PYRIMIDIN-5(1H)-ONES AS POTENTIAL ANTINEOPLASTIC AGENTS [J].
BADAWEY, ES ;
KAPPE, T .
JOURNAL OF HETEROCYCLIC CHEMISTRY, 1995, 32 (03) :1003-1006
[3]   STUDIES ON THE SYNTHESIS OF FURO[3,2-D]PYRIMIDINE C-NUCLEOSIDES - NEW INOSINE ANALOGS WITH ANTIPROTOZOAN ACTIVITY [J].
BHATTACHARYA, BK ;
OTTER, BA ;
BERENS, RL ;
KLEIN, RS .
NUCLEOSIDES & NUCLEOTIDES, 1990, 9 (08) :1021-1043
[4]  
HITAKA T, 1991, J MED CHEM, V34, P555
[5]  
Kawanishi M., 1958, TANABE SEIYAKU KENKY, V3, P4
[6]  
KUWAYAMA Y, 1962, Yakugaku Zasshi, V82, P1028
[7]  
SURUKAWA S, 1981, J HETEROCYCLIC CHEM, V18, P581
[8]  
TAKEUCHI T, 1992, Patent No. 4217681
[9]   A DIDEAZATETRAHYDROFOLATE ANALOG LACKING A CHIRAL CENTER AT C-6, N-[4-[2-(2-AMINO-3,4-DIHYDRO-4-OXO-7H-PYRROLO[2,3-D]PYRIMIDIN-5-YL)ETHYL]BENZOYL]-L-GLUTAMIC ACID, IS AN INHIBITOR OF THYMIDYLATE SYNTHASE [J].
TAYLOR, EC ;
KUHNT, D ;
SHIH, C ;
RINZEL, SM ;
GRINDEY, GB ;
BARREDO, J ;
JANNATIPOUR, M ;
MORAN, RG .
JOURNAL OF MEDICINAL CHEMISTRY, 1992, 35 (23) :4450-4454