Synthesis of febrifugine derivatives and development of an effective and safe tetrahydroquinazoline-type antimalarial

被引:41
作者
Kikuchi, Haruhisa [1 ]
Horoiwa, Seiko [1 ]
Kasahara, Ryota [1 ]
Hariguchi, Norimitsu [2 ]
Matsumoto, Makoto [2 ]
Oshima, Yoshiteru [1 ]
机构
[1] Tohoku Univ, Grad Sch Pharmaceut Sci, Aoba Ku, Sendai, Miyagi 9808578, Japan
[2] Otsuka Pharmaceut Co Ltd, Microbiol Res Inst, Tokushima 7710192, Japan
关键词
Antimalarials; Quinazoline alkaloids; Plasmodium falciparum; Structure-activity relationship; PLASMODIUM MALARIA PARASITE; HALOFUGINONE; ANALOGS; GROWTH; AGENTS; DRUGS; ASSAY;
D O I
10.1016/j.ejmech.2014.01.036
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Febrifugine, a quinazoline alkaloid isolated from Dichroa febrifuga roots, shows powerful antimalarial activity against Plasmodium falciparum. Although the use of ferifugine as an antimalarial drug has been precluded because of its severe side effects, its potent antimalarial activity has stimulated medicinal chemists to pursue its derivatives instead, which may provide valuable leads for novel antimalarial drugs. In the present study, we synthesized new derivatives of febrifugine and evaluated their in vitro and in vivo antimalarial activities to develop antimalarials that are more effective and safer. As a result, we proposed tetrahydroquinazoline-type derivative as a safe and effective antimalarial candidate. (C) 2014 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:10 / 19
页数:10
相关论文
共 33 条
[1]   Chemoselective debenzylation of N-benzyl tertiary amines with ceric ammonium nitrate [J].
Bull, SD ;
Davies, SG ;
Fenton, G ;
Mulvaney, AW ;
Prasad, RS ;
Smith, AD .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 2000, (22) :3765-3774
[2]   STRUCTURAL MODIFICATION OF FEBRIFUGINE - SOME METHYLENEDIOXY ANALOGS [J].
CHIEN, PL ;
CHENG, CC .
JOURNAL OF MEDICINAL CHEMISTRY, 1970, 13 (05) :867-+
[3]   DIMETHYLOXOSULFONIUM METHYLIDE ((CH3)2SOCH2) AND DIMETHYLSULFONIUM METHYLIDE ((CH3)2SCH2) FORMATION AND APPLICATION TO ORGANIC SYNTHESIS [J].
COREY, EJ ;
CHAYKOVSKY, M .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1965, 87 (06) :1353-+
[4]   A NOVEL PYRIMIDINE SYNTHESIS .1. 4-AMINO-5-PHENYLPYRIMIDINE [J].
DAVIES, WH ;
PIGGOTT, HA .
JOURNAL OF THE CHEMICAL SOCIETY, 1945, (MAY) :347-351
[5]   The role of plant-derived drugs and herbal medicines in healthcare [J].
DeSmet, PAGM .
DRUGS, 1997, 54 (06) :801-840
[6]  
Elkin M, 1999, CANCER RES, V59, P4111
[7]   FEBRIFUGINE ANTIMALARIAL AGENTS .1. PYRIDINE ANOLOGS OF FEBRIFUGINE [J].
FISHMAN, M ;
CRUICKSHANK, PA .
JOURNAL OF MEDICINAL CHEMISTRY, 1970, 13 (01) :155-+
[8]   Inhibition of collagen type I synthesis by skin fibroblasts of graft versus host disease and scleroderma patients: Effect of halofuginone [J].
Halevy, O ;
Nagler, A ;
LeviSchaffer, F ;
Genina, O ;
Pines, M .
BIOCHEMICAL PHARMACOLOGY, 1996, 52 (07) :1057-1063
[9]   AN ANTIMALARIAL ALKALOID FROM HYDRANGEA .13. THE EFFECTS OF VARIOUS SYNTHETIC QUINAZOLONES AGAINST PLASMODIUM-LOPHURAE IN DUCKS [J].
HEWITT, RI ;
WALLACE, WS ;
GILL, ER ;
WILLIAMS, JH .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1952, 1 (05) :768-772
[10]   Metabolites of febrifugine and its synthetic analogue by mouse liver S9 and their antimalarial activity against Plasmodium malaria parasite [J].
Hirai, S ;
Kikuchi, H ;
Kim, HS ;
Begum, K ;
Wataya, Y ;
Tasaka, H ;
Miyazawa, Y ;
Yamamoto, K ;
Oshima, Y .
JOURNAL OF MEDICINAL CHEMISTRY, 2003, 46 (20) :4351-4359