Synthesis and anti-inflammatory activity evaluation of some acridinyl amino antipyrine, acridinyl amino anthraquinone, acridino thiourea and thiazolino thiourea derivatives

被引:42
|
作者
Sondhi, SM [1 ]
Sharma, VK
Singhal, N
Verma, RP
Shukla, R
Raghubir, R
Dubey, MP
机构
[1] Univ Roorkee, Dept Chem, Roorkee 247667, Uttar Pradesh, India
[2] Cent Drug Res Inst, Div Pharmacol, Lucknow 226001, Uttar Pradesh, India
关键词
acridinyl derivatives; acridino thiourea; thiazolino thiourea; antiinflammatory activity; NMR; HRMS;
D O I
10.1080/10426500008044991
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
9-Chloro-2(subsrituted)-acridines (I) on condensation with 4-amino antipyrine, 1-amino anthraquinone and 2-amino anthraquinone gave corresponding condensed products II, III and IV. Phenyl isothiocyanate reacts with 9- amino - 2 or 4 (substituted)-acridines (V) and iminothiazolines (VII) to give corresponding N-phenyl-N'- substituted thioureas VI and VIII in good yield. Anti-inflammatory activity screening for IIa, b, III, IV, VIb and VIIIa-I was carried our at 100 mg/kg p.o. and compounds IV, VIIIa, VIIIb and VIIIg-k showed 12, 12,14,18,7,23,13 and 18% activity whereas all others were found to be inactive. Analgesic activity screening for IIb, III and IV was carried out at 100mg/kg p.o.Only compound III showed 25% activity whereas IIb and IV were found to be inactive.
引用
收藏
页码:21 / 33
页数:13
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