Abstract
Several N-hydroxyalkyl desloratadines and N-methoxyl ethyl desloratadine were prepared and evaluated for H1 antihistamine activity. The effects on isolated ileum smooth muscle tension in guinea pigs in vitro and asthma-relieving effects on the histamine-induced asthmatic reaction in guinea-pigs in vivo were examined. Most of them exhibited satisfactory H1 antihistamine activity and were obviously more potent than loratadine. Among these, Compound 3, N-(3- hydroxy)propyl desloratadine was the most active one. And it was chosen as a candidate for evaluation of acute toxicity (LD50= 0.876(0.784-0.980) g/kg), significantly superior to that of desloratadine (LD50=0.353 g/kg). Meanwhile, the experimental results demonstrated that the oxygen atom in the side carbon chain is crucial for enhancing the antihistamine activities.
Keywords: Acute toxicity, Antiallergic activity, Antihistamine, Asthma-relieving effect, Desloratadine analogues, Ileum contraction effect
Medicinal Chemistry
Title:Design, Synthesis and Antihistamine Evaluations of Several N-hydroxyalkyl Desloratadine Analogues
Volume: 8 Issue: 6
Author(s): Yan Lin, Yue Wang, Li-feng Sima, Dong-hua Wang, Li-gong Chen and Lei Li
Affiliation:
Keywords: Acute toxicity, Antiallergic activity, Antihistamine, Asthma-relieving effect, Desloratadine analogues, Ileum contraction effect
Abstract: Several N-hydroxyalkyl desloratadines and N-methoxyl ethyl desloratadine were prepared and evaluated for H1 antihistamine activity. The effects on isolated ileum smooth muscle tension in guinea pigs in vitro and asthma-relieving effects on the histamine-induced asthmatic reaction in guinea-pigs in vivo were examined. Most of them exhibited satisfactory H1 antihistamine activity and were obviously more potent than loratadine. Among these, Compound 3, N-(3- hydroxy)propyl desloratadine was the most active one. And it was chosen as a candidate for evaluation of acute toxicity (LD50= 0.876(0.784-0.980) g/kg), significantly superior to that of desloratadine (LD50=0.353 g/kg). Meanwhile, the experimental results demonstrated that the oxygen atom in the side carbon chain is crucial for enhancing the antihistamine activities.
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Cite this article as:
Lin Yan, Wang Yue, Sima Li-feng, Wang Dong-hua, Chen Li-gong and Li Lei, Design, Synthesis and Antihistamine Evaluations of Several N-hydroxyalkyl Desloratadine Analogues, Medicinal Chemistry 2012; 8 (6) . https://dx.doi.org/10.2174/1573406411208061126
DOI https://dx.doi.org/10.2174/1573406411208061126 |
Print ISSN 1573-4064 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6638 |
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