Synthesis and biological evaluation of novel potent angiotensin II receptor antagonists with anti-hypertension effect

被引:16
作者
Nie, Yong-yan [1 ]
Da, Ya-jing [1 ]
Zheng, Hao [1 ]
Yang, Xiao-xia [1 ]
Jia, Lin [1 ]
Wen, Cai-hong [1 ]
Liang, Li-sha [1 ]
Tian, Juan [1 ]
Chen, Zhi-long [1 ]
机构
[1] Donghua Univ, Dept Pharmaceut Sci & Technol, Coll Chem & Biol, Shanghai 201600, Peoples R China
关键词
Angiotensin II receptor antagonists; Hypertension; Synthesis; Acute toxicity; PHARMACOLOGY;
D O I
10.1016/j.bmc.2012.02.003
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
A series of novel angiotensin II type 1 receptor antagonists were prepared. Radioligand binding assay suggested that compounds 1b and 1c could be recognized by the AT(1) receptor with an IC50 value of 1.6 +/- 0.09 nM and 2.64 +/- 0.7 nM, respectively. In vivo anti-hypertension experiments showed that compounds (1a, 1b, 1c, 1e) elicited a significant decrease in SBP and DBP of spontaneous hypertensive rats (SHRs). The antihypertensive effects maintained for 10 h, which indicated that these compounds had a favorable blood pressure-lowering effect. Acute toxicity testing suggested that the LD50 value of compound 1b was 2316.8 mg/kg which was lower than valsartan (LD50 = 307.50 mg/kg) but higher than losartan (LD50 = 2248 mg/kg). So they could be considered as novel anti-hypertension candidates and deserved for further investigation. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2747 / 2761
页数:15
相关论文
共 16 条
[1]  
Andrea C., 2008, J MED CHEM, V51, P2137
[2]   The Comparative Effects of Azilsartan Medoxomil and Olmesartan on Ambulatory and Clinic Blood Pressure [J].
Bakris, George L. ;
Sica, Domenic ;
Weber, Michael ;
White, William B. ;
Roberts, Andrew ;
Perez, Alfonso ;
Cao, Charlie ;
Kupfer, Stuart .
JOURNAL OF CLINICAL HYPERTENSION, 2011, 13 (02) :81-88
[3]   VALSARTAN, A POTENT, ORALLY-ACTIVE ANGIOTENSIN-II ANTAGONIST DEVELOPED FROM THE STRUCTURALLY NEW AMINO-ACID SERIES [J].
BUHLMAYER, P ;
FURET, P ;
CRISCIONE, L ;
DEGASPARO, M ;
WHITEBREAD, S ;
SCHMIDLIN, T ;
LATTMANN, R ;
WOOD, J .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1994, 4 (01) :29-34
[4]  
Chung O, 1998, BASIC RES CARDIOL, V93, P15
[5]  
de Gasparo M, 2000, PHARMACOL REV, V52, P415
[6]  
Eric N., 1994, J MED CHEM, V37, P2371
[7]   DEVELOPMENT OF TETRAZOLE BIOISOSTERES IN ANGIOTENSIN-II ANTAGONISTS [J].
FERRARI, B ;
TAILLADES, J ;
PERREAUT, P ;
BERNHART, C ;
GOUGAT, J ;
GUIRAUDOU, P ;
CAZAUBON, C ;
ROCCON, A ;
NISATO, D ;
LEFUR, G ;
BRELIERE, JC .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1994, 4 (01) :45-50
[8]   EVALUATION OF HETEROCYCLIC ACID EQUIVALENTS AS TETRAZOLE REPLACEMENTS IN IMIDAZOPYRIDINE-BASED NONPEPTIDE ANGIOTENSIN-II RECEPTOR ANTAGONISTS [J].
KIM, D ;
MANTLO, NB ;
CHANG, RSL ;
KIVLIGHN, SD ;
GREENLEE, WJ .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1994, 4 (01) :41-44
[9]   Comparison of angiotensin II receptor antagonists [J].
Kirch, W ;
Horn, B ;
Schweizer, J .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 2001, 31 (08) :698-706
[10]   A NEW CLASS OF ANGIOTENSIN-II RECEPTOR ANTAGONISTS WITH A NOVEL ACIDIC BIOISOSTERE [J].
KOHARA, Y ;
IMAMIYA, E ;
KUBO, K ;
WADA, T ;
INADA, Y ;
NAKA, T .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1995, 5 (17) :1903-1908