Synthesis of novel pyrrolyl-indomethacin derivatives

…, D Agas, MG Sabbieti, M Di Magno, A Migliorini…

Index: Serra Moreno, Judith; Agas, Dimitrios; Sabbieti, Maria Giovanna; Di Magno, Matteo; Migliorini, Antonella; Loreto, M. Antonietta European Journal of Medicinal Chemistry, 2012 , vol. 57, p. 391 - 397

Full Text: HTML

Citation Number: 4

Abstract

In the present work, we report the synthesis of the novel esters of indomethacin (IDMC) and an ester of reduced IDMC. For this purpose, IDMC is covalently bound by using a spacer chain to the pyrrole (Py) in the 3-position. The innovative pyrrole-indomethacin (3-Py-IDMC) derivates show no cytotoxic effects in primary calvarial osteoblasts. The designed IDMC derivates have been studied because they could be injected locally as a component of ...

Related Articles:

Regioselective synthesis of acylpyrroles

[Kakushima, Masatoshi; Hamel, Pierre; Frenette, Richard; Rokach, Joshua Journal of Organic Chemistry, 1983 , vol. 48, # 19 p. 3214 - 3219]

Synthesis and polymerization of 2-(3-pyrrolyl) acetic acid derivatives from pyrrole

[Synthetic Communications, , vol. 26, # 7 p. 1289 - 1304]

Regioselective synthesis of acylpyrroles

[Journal of Organic Chemistry, , vol. 48, # 19 p. 3214 - 3219]

Design, Synthesis, and Evaluation of 3??Aryl??4??pyrrolyl??maleimides as Glycogen Synthase Kinase??3β Inhibitors

[Archiv der Pharmazie, , vol. 346, # 5 p. 349 - 358]

Design, Synthesis, and Evaluation of 3??Aryl??4??pyrrolyl??maleimides as Glycogen Synthase Kinase??3β Inhibitors

[Archiv der Pharmazie, , vol. 346, # 5 p. 349 - 358]

More Articles...