SYNTHESIS OF NEW 10-SUBSTITUTED PHENOTHIAZINES AS ANTIINFLAMMATORY AND ANALGESIC AGENTS.

Authors

  • Upendra Kumar Kushwaha Department of Chemistry, D.N College, Meerut,(U.P) India.
  • Yashovardhan Department of Chemistry, D.N College, Meerut,(U.P) India.
  • Sudhir Kumar Bhati Department of Pharmacology, L.L.R.M Medical College, Meerut,(U.P) India.
  • Ashok Kumar Department of Pharmacology, L.L.R.M Medical College, Meerut,(U.P) India.

Keywords:

Methylene amino phenothiazines/ Azetidinyl phenothiazines/ Antiinflammatory activity/Analgesic activity/Acute toxicity studies.

Abstract

Some new 2-chloro-10-[2-{3'-chloro-2'-oxo-4'-(substitutedphenyl)1'-azetidinyl} thiazol-4-yl] phenothiazines (4a-4g) and 2-chloro-10-[2-{3'-chloro-2'-oxo-4'-(substitutedphenyl)1'azetidinyl}oxazol-4-yl] phenothiazines (4a'-4g') have been synthesized from 2-chloro-10-[2(substitutedphenyl) methylene aminothiazol-4-yl] phenothiazines (3a-3g) and 2-chloro-10-[2(substituted phenyl) methylene aminooxazol -4-yl] phenothiazines (3a'-3g') respectively. The structures of all these compounds were established on the basis of elemental (C,H,N) and spectral (IR, 1H-NMR and mass spectral data) analysis. All these compounds have also been tested for their antiinflammatory, analgesic activity and acute toxicity. Compound 4a' i.e. 2-chloro-10-[2-{3'-chloro-2'-oxo-4'-(2,6-dichloro phenyl)1'-azetidinyl} oxazol-4-yl] phenothiazine was found to possess most potent antiinflammatory activity and compound 4a i.e. 2-chloro-10-[2-{3'-chloro-2'-oxo-4'-(2, 6-dichlorophenyl) 1'-azetidinyl} thiazol-4-yl] phenothiazine showed good analgesic activity. Furthermore, these two compounds (4a and 4a') were also screened for their ulcerogenic liability. 

Published

30.09.2010

How to Cite

Upendra Kumar Kushwaha, Yashovardhan, Sudhir Kumar Bhati, & Ashok Kumar. (2010). SYNTHESIS OF NEW 10-SUBSTITUTED PHENOTHIAZINES AS ANTIINFLAMMATORY AND ANALGESIC AGENTS. International Journal of Pharma and Bio Sciences, 1(3), 1–10. Retrieved from https://ijpbs.net/index.php/journal/article/view/125

Issue

Section

Research Articles