Synthesis, characterization and anti-inflammatory activity of novel pyrazolyl ketoamides

被引:0
作者
Mahaveer, P. [1 ]
Kulkarni, R. G. [2 ]
Radakrishna, P. [3 ]
Chandrashekar, V. M. [4 ]
Achaiah, G. [5 ]
机构
[1] Natl Inst Pharmaceut Educ & Res, Hyderabad 500037, Andhra Pradesh, India
[2] SVERIs Coll Pharm, Gopalpur 413304, Pandharpur, India
[3] CSIR, Indian Inst Chem Technol, Hyderabad 500007, Andhra Pradesh, India
[4] Coll Pharm, BVVS Kumareshwar, Bagalkot 587101, India
[5] Kakatiya Univ, Univ Coll Pharmaceut Sci, Warangal 506009, Andhra Pradesh, India
来源
INDIAN JOURNAL OF CHEMISTRY SECTION B-ORGANIC CHEMISTRY INCLUDING MEDICINAL CHEMISTRY | 2013年 / 52卷 / 06期
关键词
Inflammation; p38; kinase; ketoamides; carageenan; KINASE; INHIBITORS; MECHANISM; POTENT;
D O I
暂无
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Compounds containing pyrazolylurea group are known to possess potent anti-inflammatory activity by inhibiting cell signalling system. One of the potent compounds has demonstrated CNS related adverse effects in human studies which has further intensified the quest to search potent but safe antiinflammatory agents. In the present study, an attempt has been made to modify the urea group into alpha-ketoamide group. The synthesis involved the coupling of 5-aminopyrazole with substituted alpha-keto acids in presence of a coupling agent to afford the desired compounds and the structures of the synthesized compounds have been confirmed by spectral data. Compounds have been screened for antiinflammatory activity by carrageenan induced rat paw method. Compounds 6c,.6e and 6f demonstrate greater than 70% paw oedema protection when compared with indomethacin. The preliminary structure activity relationship suggests that the electron withdrawing groups are essential for potent antiinflammatory activity of compounds.
引用
收藏
页码:818 / 823
页数:6
相关论文
共 26 条
[21]   The inflammatory reflex [J].
Tracey, KJ .
NATURE, 2002, 420 (6917) :853-859
[22]   INFLAMMATION AND THE MECHANISM OF ACTION OF ANTIINFLAMMATORY DRUGS [J].
VANE, J ;
BOTTING, R .
FASEB JOURNAL, 1987, 1 (02) :89-96
[23]   INHIBITION OF PROSTAGLANDIN SYNTHESIS AS A MECHANISM OF ACTION FOR ASPIRIN-LIKE DRUGS [J].
VANE, JR .
NATURE-NEW BIOLOGY, 1971, 231 (25) :232-&
[24]  
WINTER CA, 1962, P SOC EXP BIOL MED, V111, P544
[25]   Activation and signaling of the p38 MAP kinase pathway [J].
Zarubin, T ;
Han, JH .
CELL RESEARCH, 2005, 15 (01) :11-18
[26]  
Zhang J, 2006, JAMA, V296