Synthesis and anti-inflammatory activity evaluation of some acridinyl amino antipyrine, acridinyl amino anthraquinone, acridino thiourea and thiazolino thiourea derivatives
Sm. Sondhi et al., Synthesis and anti-inflammatory activity evaluation of some acridinyl amino antipyrine, acridinyl amino anthraquinone, acridino thiourea and thiazolino thiourea derivatives, PHOSPHOR SU, 156, 2000, pp. 21-33
Citations number
27
Categorie Soggetti
Inorganic & Nuclear Chemistry
Journal title
PHOSPHORUS SULFUR AND SILICON AND THE RELATED ELEMENTS
9-Chloro-2(subsrituted)-acridines (I) on condensation with 4-amino antipyri
ne, 1-amino anthraquinone and 2-amino anthraquinone gave corresponding cond
ensed products II, III and IV. Phenyl isothiocyanate reacts with 9- amino -
2 or 4 (substituted)-acridines (V) and iminothiazolines (VII) to give corr
esponding N-phenyl-N'- substituted thioureas VI and VIII in good yield. Ant
i-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 sh
owed 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 I
V were found to be inactive.