Synthesis, Characterization and Biological Evaluation of Benzimidazole And Benzindazole Derivatives as Anti-Hypertensive Agents

被引:7
作者
Silky, Sethy [1 ,2 ]
Mandal, Sudip Kumar [3 ]
Ewies, Ewies Fawzy [4 ]
Neerupma, Dhiman [2 ]
Arun, Garg [1 ]
机构
[1] KR Mangalam Univ, Sch Med & Allied Sci, Gurgaon, Haryana, India
[2] Amity Univ AUUP, Amity Inst Pharm, Noida 201303, Uttar Pradesh, India
[3] Dr BC Roy Coll Pharm & AHS, Durgapur 713206, W Bengal, India
[4] Natl Res Ctr, Organometall & Organometalloid Chem Dept, 33 El Bohouth St,PO 12622, Giza, Egypt
来源
EGYPTIAN JOURNAL OF CHEMISTRY | 2021年 / 64卷 / 07期
关键词
Hypertension; Synthesis; Chracterisation; Non-peptide AT1 Receptor Antagonist; Renin-Angiotensin System; ANGIOTENSIN-II; DESIGN; ANTAGONISTS; BLOCKERS;
D O I
10.21608/EJCHEM.2021.79840.3931
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A substituted benzimidazole and benzindazole derivatives had been synthesized having antihypertensive activity through antagonizing the angiotensin II (Ang II) receptors. The in vivo antihypertensive activity of the compounds was done with acute renal hypertension model. Two compounds TG 1 and TG 3 were found to have antihypertensive activity comparable to Telmisartan which is a prototype for Angiotensin II receptor antagonists class of drugs. In an antihypertensive study the compounds TG 1, TG 2 and TG 3 had systolic blood pressures of 147.2 mm/Hg, 168.2 mm/Hg, and 126.3 mm/Hg, respectively. This systolic blood pressure was lower than the disease control vehicle-treated rodents, which had a systolic blood pressure of 167.2 mm/Hg. The diastolic blood pressure was 119.7 mm/Hg, 124.7 mm/Hg and 88.83 mm/Hg, respectively and that of the disease control vehicle-treated rodents was 122.3 mm/Hg. TG 3 had comparable decrease in the MABP to Telmisartan. These encouraging results make compound TG 3 effective anti-hypertensive drug candidate and worthy of further investigation.
引用
收藏
页码:3659 / 3664
页数:6
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