22915-30-6Relevant academic research and scientific papers
Synthesis and in vitro evaluation of some isatin-thiazolidinone hybrid analogues as anti-proliferative agents
Ramshid,Jagadeeshan, Sankar,Krishnan, Anand,Mathew, Mary,Nair, S. Asha,Pillai, M. Radhakrishna
, p. 306 - 312 (2011/09/13)
A range of isatin-thiazolidinone hybrid analogues were synthesized and their cytotoxicity was evaluated against several cancer cell lines in vitro. The acute toxicity studies in mice models revealed that these analogues possess low systemic toxicity and are safe up to 1600mg/Kg. Among the compounds synthesized, 5-(2-nitrobenzylidene)-2-(isatin-3- azino)-thiazolidin-4-one (CI) has been shown to be the most active, highly promising compound which induced S phase arrest in cell cycle in a time dependent manner. Our initial analysis indicate that incorporation of electron withdrawing group at ortho position of the ring favors over the meta and para positions for eliciting its cytostatic effect. Overall, the in vitro biological evaluation suggests that the growth inhibitory effect of CI is promising and can be studied further.
Synthesis of Some New Thiazolidinone and 2-Thiohydantoin Derivatives Bearing an Isatin Moiety
Mahmoud, A.M.,Abdel-Rahman, A.E.,El-Naggar, G.M.,El-Sherief, H.A.
, p. 379 - 381 (2007/10/02)
2-(Isatin-3-azino)-4-thiazolidinone (I) and 1-(isatin-3-imino)-2-thiohydantoin (III) have been obtained by condensation of isatin-3-thiosemicarbazone with chloroacetic acid under different conditions.Compounds I and III on interaction with aromatic or heterocyclic aldehydes afford 5-arylidene-2-(isatin-3-azino)thiazolidinones (II) and 5-arylidene-3-(isatin-3-imino)-2-thiohydantoins (IV) respectively.These compounds (II, IV) have been screened for their antimicrobial activities.
