Please use this identifier to cite or link to this item: http://scholarbank.nus.edu.sg/handle/10635/92355
Title: Study of synthesis and cardiovascular activity of some furoxan derivatives as potential NO-donors
Authors: Mu, L. 
Feng, S.-S. 
Go, M.L. 
Keywords: Furoxan derivatives
Hypertension
Nitric oxide
NO- donor
Synthesis
Vasodilation
Issue Date: Jun-2000
Source: Mu, L.,Feng, S.-S.,Go, M.L. (2000-06). Study of synthesis and cardiovascular activity of some furoxan derivatives as potential NO-donors. Chemical and Pharmaceutical Bulletin 48 (6) : 808-816. ScholarBank@NUS Repository.
Abstract: A series of hybrid molecules incorporating the furoxan and nicorandil moieties were designed as potential NO donors with cardiovascular and cerebrovascular activities. Thirty-six target molecules were successfully synthesized by conventional methods and characterized by infrared spectroscopy, 1H-NMR spectroscopy and high resolution mass spectra. The compounds were tested for their effects on KCl-induced contraction of rabbit thoracic aorta whose endothelium was denuded. Eight compounds were found to reduce KCl-induced contraction by more than 30% at 10 μM. All except one of these compounds are characterized by the presence of electron withdrawing groups in the phenyl ring attached via an amide or ester linkage to the furoxan moiety. The nature of the terminal carbonyl linkage (ester or amide) and the length or type of the alkyl chain bridging the two carbonyl functions have little effect on the activity. One of the active compounds, N-(4- methoxy-benzoyl)-N'-[3-methylfuroxanyl-4-carbonyl)piperazine (17i) was tested for hypotensive effects on anaesthetized rats at 1.5 mg/kg, and found to demonstrate a gradual and sustained hypotensive effect. The results suggest that the furoxannicorandil derivatives are a useful lead in the design of NO- donor compounds for hypertension.
Source Title: Chemical and Pharmaceutical Bulletin
URI: http://scholarbank.nus.edu.sg/handle/10635/92355
ISSN: 00092363
Appears in Collections:Staff Publications

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