134439-96-6Relevant articles and documents
Synthesis and biological evaluation of enantiomerically pure pyrrolyloxazolidinones as a new class of potent and selective monoamine oxidase type A inhibitors
Mai,Artico, Marino,Esposito,Ragno,Sbardella,Massa
, p. 231 - 241 (2007/10/03)
Due to the key role played by monoamine oxidases (MAOs) in the metabolism of neurotransmitters, MAO inhibitors (MAOIs) represent an useful tool for the treatment of several neurological diseases. Among selective MAOIs, MAO-A inhibitors (e.g. clorgyline) are used as antidepressant and antianxiety drugs and are claimed to protect neuronal cells against apoptosis, and selective MAO-B inhibitors (e.g. L-deprenyl) can be used in the treatment of Parkinson's disease either alone or in combination with L-DOPA. However, they engender covalent bonds with the active site of the enzyme and induce irreversible inhibition; moreover, they tend to lose their initial selectivity at high dosages or with repeated administrations. Phenyloxazolidinones belong to third-generation-MAOIs, characterized by a selective and reversible inhibition of the enzyme. Among these molecules, the most representative are toloxatone and befloxatone, two selective and reversible MAO-A inhibitors used in therapy as antidepressant drugs. Going on our searches on CNS potentially active compounds containing a pyrrole moiety we prepared 3-(1H-pyrrol-1-yl)-2-oxazolidinones (1) and isomeric 3-(1H-pyrrol-2-and -3-yl)-2-oxazolidinones (2 and 3) as anti-MAO agents. Such derivatives resulted selective and reversible MAO-A inhibitors. The most potent compound is (R)-5-methoxymethyl-3-(1H-pyrrol-1-yl)-2-oxazolidinone (1b), endowed with very high potency (KiMAO-A=4.9 nM) and A-selectivity (A-selectivity=10,200, about 116-fold greater than that of befloxatone).
Vinyl Polymers Bearing Pyrrole Ring: I. Syntheses of Pyrroles Having 3-Substituent Bearing Vinyl Group
Kamogawa, Hiroyoshi,Nakata, Takuharu,Ohori, Shin,Komatsu, Sei
, p. 1066 - 1068 (2007/10/02)
Pyrroles having 3-substituent bearing the vinyl group with an ester or amide spacer were synthesized starting with 1-(phenylsulfonyl)pyrrole.Homopolymerization of the vinyl monomers thus synthesized provided crosslinked insoluble polymers, but their copolymers with 1-vinyl-2-pyrrolidone were soluble in common solvents.
