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Free Radical Research Volume 38, 2004 - Issue 5
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Original Article

2-Substituted-3H-indol-3-one-1-oxides: Preparation and Radical Trapping Properties

Jeremie Boyer Laboratoire Pharmacochimie des Substances Naturelles et Pharmacophores Redox, UMR-IRD-UPS 152, Faculté de Pharmacie, Université Paul Sabatier, cedex 4, 31062, Toulouse, FranceCorrespondence[email protected]
,
Vania Bernardes-Genisson Laboratoire Pharmacochimie des Substances Naturelles et Pharmacophores Redox, UMR-IRD-UPS 152, Faculté de Pharmacie, Université Paul Sabatier, cedex 4, 31062, Toulouse, France
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Vincent Farines Laboratoire Pharmacochimie des Substances Naturelles et Pharmacophores Redox, UMR-IRD-UPS 152, Faculté de Pharmacie, Université Paul Sabatier, cedex 4, 31062, Toulouse, France
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Jean-Pierre Souchard Laboratoire Pharmacochimie des Substances Naturelles et Pharmacophores Redox, UMR-IRD-UPS 152, Faculté de Pharmacie, Université Paul Sabatier, cedex 4, 31062, Toulouse, France
&
Francoise Nepveu Laboratoire Pharmacochimie des Substances Naturelles et Pharmacophores Redox, UMR-IRD-UPS 152, Faculté de Pharmacie, Université Paul Sabatier, cedex 4, 31062, Toulouse, France
Pages 459-471 | Received 04 Aug 2003, Published online: 07 Jul 2009

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Nicholas S. Kirk, Geraud N. Sansom, Pichit Sudta, Sunit Suksamrarn, Anthony C. Willis, John B. Bremner & Michael J. Kelso. (2017) Unexpected synthesis of 3-imino-2-(pyrrol-2-yl) isatogen derivatives affords facile access to a 2-pyrrolyl isatogen. Synthetic Communications 47:1, pages 62-67.
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Articles from other publishers (9)

Nehal Ibrahim, Hany Ibrahim, Jerome Dormoi, Sébastien Briolant, Bruno Pradines, Alicia Moreno, Dominique Mazier, Philippe Legrand & Françoise Nepveu. (2014) Albumin-bound nanoparticles of practically water-insoluble antimalarial lead greatly enhance its efficacy. International Journal of Pharmaceutics 464:1-2, pages 214-224.
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Tina M. Bott, Bren Jordan Atienza & F. G. West. (2014) Azide trapping of metallocarbenes: generation of reactive C-acylimines and domino trapping with nucleophiles. RSC Adv. 4:60, pages 31955-31959.
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Nguyen Thi Hoang Yen, Hany Ibrahim, Karine Reybier, Pierre Perio, Florence Souard, Ennaji Najahi, Paul-Louis Fabre & Francoise Nepveu. (2013) Pro-oxidant properties of indolone-N-oxides in relation to their antimalarial properties. Journal of Inorganic Biochemistry 126, pages 7-16.
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Karine Reybier, Thi Hoang Yen Nguyen, Hany Ibrahim, Pierre Perio, Armelle Montrose, Paul-Louis Fabre & Françoise Nepveu. (2012) Electrochemical behavior of indolone-N-oxides: Relationship to structure and antiplasmodial activity. Bioelectrochemistry 88, pages 57-64.
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Hany Ibrahim, Aurelie Furiga, Ennaji Najahi, Christel Pigasse Hénocq, Jean-Pierre Nallet, Christine Roques, Agnes Aubouy, Michel Sauvain, Patricia Constant, Mamadou Daffé & Françoise Nepveu. (2012) Antibacterial, antifungal and antileishmanial activities of indolone-N-oxide derivatives. The Journal of Antibiotics 65:10, pages 499-504.
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Chepuri V. Ramana, Pitambar Patel, Kumar Vanka, Benchun Miao & Alexei Degterev. (2010) A Combined Experimental and Density Functional Theory Study on the Pd-Mediated Cycloisomerization of o-Alkynylnitrobenzenes - Synthesis of Isatogens and Their Evaluation as Modulators of ROS-Mediated Cell Death. European Journal of Organic Chemistry 2010:31, pages 5955-5966.
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Françoise Nepveu, Sothea Kim, Jeremie Boyer, Olivier Chatriant, Hany Ibrahim, Karine Reybier, Marie-Carmen Monje, Severine Chevalley, Pierre Perio, Barbora H. Lajoie, Jalloul Bouajila, Eric Deharo, Michel Sauvain, Rachida Tahar, Leonardo Basco, Antonella Pantaleo, Francesco Turini, Paolo Arese, Alexis Valentin, Eloise Thompson, Livia Vivas, Serge Petit & Jean-Pierre Nallet. (2009) Synthesis and Antiplasmodial Activity of New Indolone N -Oxide Derivatives . Journal of Medicinal Chemistry 53:2, pages 699-714.
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Inas El Hassan, Laurence Charles, Robert Lauricella & Béatrice Tuccio. (2008) Detection and identification of various carbon-centred free radicals using N-arylketonitrones: a spin trapping/EPR/MS study. New J. Chem. 32:4, pages 680-688.
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Sibel Süzen. 2007. Bioactive Heterocycles V. Bioactive Heterocycles V 145 178 .

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