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

Citation
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
ISSN journal
10426507 → ACNP
Volume
156
Year of publication
2000
Pages
21 - 33
Database
ISI
SICI code
1042-6507(2000)156:<21:SAAAEO>2.0.ZU;2-9
Abstract
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.