Synthesis of Novel Pyrido[3,2-e][1,2,4]triazolo[1,5-c]pyrimidine Derivatives: Potent and Selective Adenosine A3 Receptor Antagonists

被引:10
作者
Banda, Veeraswamy [1 ]
Chandrasekaran, Balakumar [2 ,3 ]
Koese, Meryem [4 ]
Vielmuth, Christin [4 ]
Mueller, Christa E. [4 ]
Chavva, Kurumurthy [1 ]
Gautham, Santhosh Kumar [1 ]
Pillalamarri, Sambasivarao [1 ]
Mylavaram, Raghuprasad [5 ]
Akkinepally, Raghuramarao [6 ]
Pamulaparthy, Shanthanrao [1 ]
Banda, Narsaiah [1 ]
机构
[1] Indian Inst Chem Technol, Fluoroorgan Div, Hyderabad 500007, Andhra Pradesh, India
[2] Panjab Univ, Univ Inst Pharmaceut Sci, Chandigarh 160014, Punjab, India
[3] Panjab Univ, UGC Ctr Adv Study Pharmaceut Sci UGC CAS, Chandigarh 160014, Punjab, India
[4] Univ Bonn, Inst Pharmaceut, PharmaCtr Bonn, Bonn, Germany
[5] Vishnu Coll Pharm, West Godavari, Andhra Pradesh, India
[6] Univ Coll Pharmaceut Sci, Warangal, Andhra Pradesh, India
关键词
Adenosine receptors; 2-Aminonicotinonitrile; Aroyl hydrazide; Orthoacetate; Orthoformate; RADIOLIGAND; MEMBRANES; AFFINITY;
D O I
10.1002/ardp.201300003
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of novel pyrido[3,2-e][1,2,4]triazolo[1,5-c]pyrimidine derivatives 5 was prepared from 2-amino-3-cyano-4-trifluoromethyl-6-phenylpyridine 1 in two steps via formation of iminoether 3 followed by reaction with different aroylhydrazides 4. Representative products 5 were evaluated for their affinity towards all four subtypes of human adenosine receptors. Compounds 2-(3-fluorophenyl)-8-phenyl-10-(trifluoromethyl)pyrido[3,2-e][1,2,4]triazolo[1,5-c]pyrimidine (5b), 2-(furan-2-yl)-8-phenyl-10-(trifluoromethyl)pyrido[3,2-e][1,2,4]triazolo[1,5-c]pyrimidine (5d), and 2-(furan-2-yl)-5-methyl-8-phenyl-10-(trifluoromethyl)pyrido[3,2-e][1,2,4]triazolo[1,5-c]pyrimidine (5j) showed high affinity for the A(3) receptors, with K-i values of 8.1, 10.4, and 12.1nM, respectively, and were >1000-fold selective versus all other adenosine receptor subtypes.
引用
收藏
页码:699 / 707
页数:9
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