SYNTHESIS AND EVALUATION OF ANALGESIC, ANTI-INFLAMMATORY AND ANTI-BACTERIAL ACTIVITY OF SYNTHETIC PORPHYRIN DERIVATIVES

被引:0
作者
Naveed Umar, Muhammad [1 ]
Ur Rashid, Haroon [2 ,4 ]
Gul Sayed, Mian [1 ]
Karim, Nasiara [3 ]
Ghaffar, Rukhsana [3 ]
Antonio Utrera Martines, Marco [4 ]
Shoaib, Mohammad [5 ]
机构
[1] Univ Malakand, Dept Chem, Lower Dir, Khyber Pakhtunk, Pakistan
[2] Sarhad Univ Sci & Informat Technol, Dept Chem, Peshawar, Khyber Pakhtunk, Pakistan
[3] Univ Malakand, Dept Pharm, Chakdara, Khyber Pakhtunk, Pakistan
[4] Fed Univ Mato Grosso de Sul, Inst Chem, BR-CAMPO GR Campo Grande, Mato Grosso De, Brazil
[5] Univ Makaland, Dept Pharm, Khyber, Pakhtunkhwa, Pakistan
关键词
porphyrin; analgesic activity; analgesic; anti-inflammatory; INDUCED EDEMA; DRUGS;
D O I
暂无
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this work porphyrins compounds (N1-N4) were synthesized from monohydroxy tetraphenylporphyrin, and then characterized on the basis of their chemical properties and spectral data. They were further tested for their potential analgesic and anti-inflammatory activities in acetic acid induced writhing test in mice and carrageenan induced paw edema in rats. The compounds were also evaluated for antibacterial activity in disc diffusion method. Compounds N1, N2 and N4 showed significant analgesic and anti-inflammatory activity at 10 and 30 mg/kg (b.w), comparable to the standard reference drugs. Furthermore, all the tested compounds possessed significant anti-bacterial activity against both gram positive and gram negative bacteria. The analgesic, anti-inflammatory and anti-bacterial activities of the tested compounds were found comparable to reference drugs. These compounds can serve as precursors for the development of clinically useful analgesics, anti-inflammatory and anti-bacterial agents.
引用
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页码:861 / 866
页数:6
相关论文
共 12 条
[1]  
Aydin S, 1999, PHYTOTHER RES, V13, P20, DOI 10.1002/(SICI)1099-1573(199902)13:1<20::AID-PTR380>3.0.CO
[2]  
2-J
[3]   STUDIES ON CRYPTOLEPINE .2. INHIBITION OF CARRAGEENAN INDUCED EDEMA BY CRYPTOLEPINE [J].
BAMGBOSE, SOA ;
NOAMESI, BK .
PLANTA MEDICA, 1981, 41 (04) :392-396
[4]  
BAUER AW, 1966, AM J CLIN PATHOL, V45, P493
[5]   Design, synthesis and biological testing of a novel series of anti-inflammatory drugs [J].
Duffy, JC ;
Dearden, JC ;
Rostron, C .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 2001, 53 (11) :1505-1514
[6]   Acetic acid induced painful endogenous infliction in writhing test on mice [J].
Gawade, Shivaji P. .
JOURNAL OF PHARMACOLOGY & PHARMACOTHERAPEUTICS, 2012, 3 (04) :348-348
[7]   Porphyrins as new endogenous anti-inflammatory agents [J].
Jelic, Dubravko ;
Tatic, Iva ;
Trzun, Marija ;
Hrvacic, Boska ;
Brajsa, Karmen ;
Verbanac, Donatella ;
Tomaskovic, Marija ;
Culic, Ognjen ;
Antolovic, Roberto ;
Glojnaric, Ines ;
Weygand-Durasevic, Ivana ;
Vladimir-Knezevic, Sanda ;
Mildner, Boris .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2012, 691 (1-3) :251-260
[8]   Antinociceptive components of Ganoderma lucidum [J].
Koyama, K ;
Imaizumi, T ;
Akiba, M ;
Kinoshita, K ;
Takahashi, L ;
Suzuki, A ;
Yano, S ;
Horie, S ;
Watanabe, K ;
Naoi, Y .
PLANTA MEDICA, 1997, 63 (03) :224-227
[9]  
Nanthakumar R., 2011, ARABIAN J C IN PRESS
[10]   The phototoxicity of phenothiazinium derivatives against Escherichia coli and Staphylococcus aureus [J].
Phoenix, DA ;
Sayed, Z ;
Hussain, S ;
Harris, F ;
Wainwright, M .
FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY, 2003, 39 (01) :17-22