New octahydroquinazoline derivatives: Synthesis and hypotensive activity

被引:32
作者
El-Sabbagh, O. I. [1 ]
Shabaan, Mohamed A. [2 ]
Kadry, Hanan H. [2 ]
Al-Din, Ehab Saad [3 ]
机构
[1] Zagazig Univ, Fac Pharm, Dept Med Chem, Zagazig, Egypt
[2] Cairo Univ, Fac Pharm, Dept Organ Pharmaceut Chem, Cairo, Egypt
[3] Al Azhar Univ, Fac Pharm, Dept Organ Pharmaceut Chem, Assiut, Egypt
关键词
Synthesis; Octahydroquinazoline derivatives; Hypotensive activity; ANTIHYPERTENSIVE ACTIVITY; ANTAGONISTS; PRESSURE; ANALOGS; AGENTS;
D O I
10.1016/j.ejmech.2010.08.064
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Several novel 1-(4-chlorophenyl)-7,7-dimethyl-1,2,3,4,5,6,7,8-octahydro-5-oxo-3-(substitutedphenyl) quinazoline derivatives (2-21) structurally similar to prazosin, were prepared using Mannich reaction of 3-(4-chlorophenylamino)-5,5-dimethyl-2-cyclohexenone (1) with different aromatic amines in the presence of formaline. The structures of the quinazoline derivatives were established using elemental and spectral analyses. Compounds 18, 20 and 21 were found to possess a high hypotensive effect through their expected alpha(1)-blocking activity like the clinically used drug prazosin but with advantageous of being did not cause reflex tachycardia and having prolonged duration of action when tested in adrenaline-induced hypertension in anaesthetized rats. (C) 2010 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:5390 / 5396
页数:7
相关论文
共 17 条
[1]   Synthesis and antihypertensive activity of novel 3-benzyl-2-substituted-3H-[1,2,4]triazolo[5,1-b]quinazolin-9-ones [J].
Alagarsamy, Veerachamy ;
Pathak, Urvishbhai S. .
BIOORGANIC & MEDICINAL CHEMISTRY, 2007, 15 (10) :3457-3462
[2]   Analogues of prazosin that bear a benextramine-related polyamine backbone exhibit different antagonism toward α-adrenoreceptor subtypes [J].
Bolognesi, ML ;
Marucci, G ;
Angeli, P ;
Buccioni, M ;
Minarini, A ;
Rosini, M ;
Tumiatti, V ;
Melchiorre, C .
JOURNAL OF MEDICINAL CHEMISTRY, 2001, 44 (03) :362-371
[3]   SIMPLE METHOD FOR RECORDING LEFT-VENTRICULAR PRESSURE DP-DT AND HEART-RATE IN THE CONSCIOUS CAT [J].
BURDEN, DT ;
BLABER, LC ;
NATOFF, IL .
PHARMACOLOGY & THERAPEUTICS, 1979, 5 (1-3) :99-102
[4]   Synthesis and vasodilator effects of rutaecarpine analogues which might be involved transient receptor potential vanilloid subfamily, member 1 (TRPV1) [J].
Chen, Zhuo ;
Hu, Gaoyun ;
Li, Dai ;
Chen, Jun ;
Li, Yuanjian ;
Zhou, Huayong ;
Xie, Ye .
BIOORGANIC & MEDICINAL CHEMISTRY, 2009, 17 (06) :2351-2359
[5]   Human epididymal and prostatic tracts of vas deferens: Different contraction response to noradrenaline stimulation in isolated organ bath assay [J].
Colabufo, Nicola A. ;
Pagliarulo, Vincenzo ;
Berardi, Francesco ;
Contino, Marialessandra ;
Perrone, Roberto ;
Niso, Mauro ;
Albo, Giancarlo ;
de Rienzo, Gaetano ;
Pagliarulo, Arcangelo .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2007, 577 (1-3) :150-155
[6]   SYNTHESIS AND ANTICONVULSANT ACTIVITY OF ENAMINONES [J].
EDAFIOGHO, IO ;
HINKO, CN ;
CHANG, HJ ;
MOORE, JA ;
MULZAC, D ;
NICHOLSON, JM ;
SCOTT, KR .
JOURNAL OF MEDICINAL CHEMISTRY, 1992, 35 (15) :2798-2805
[7]   Synthesis of hexahydro-1H-pyrido[3,2-c]azepines as hypotensive agents of expected calcium-channel blocking activity [J].
El-Sadek, Mohamed E. ;
Aboukull, Mansour ;
El-Sabbagh, Osama I. ;
Shallal, Hassan M. .
MONATSHEFTE FUR CHEMIE, 2007, 138 (03) :219-225
[8]  
Geleijnse JM, 2008, VASC HEALTH RISK MAN, V4, P963
[9]  
GHOSH MN, 1971, FUNDAMENTALS EXPT PH, P116
[10]   Recent advances in selective α1-adrenoreceptor antagonists as antihypertensive agents [J].
Jain, Kishor S. ;
Bariwal, Jitender B. ;
Kathiravan, Muthu K. ;
Phoujdar, Manisha S. ;
Sahne, Rajkumari S. ;
Chauhan, Bishram S. ;
Shah, Anamik K. ;
Yadav, Mange Ram .
BIOORGANIC & MEDICINAL CHEMISTRY, 2008, 16 (09) :4759-4800