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Synthesis of 2-methyl-3-indolylacetic derivatives as anti-inflammatory agents that inhibit preferentially cyclooxygenase 1 without gastric damage

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Fiorino,  F.
Moroder, Luis / Bioorganic Chemistry, Max Planck Institute of Biochemistry, Max Planck Society;

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Renner,  C.
Moroder, Luis / Bioorganic Chemistry, Max Planck Institute of Biochemistry, Max Planck Society;

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Perissutti, E., Fiorino, F., Renner, C., Severino, B., Roviezzo, F., Sautebin, L., et al. (2006). Synthesis of 2-methyl-3-indolylacetic derivatives as anti-inflammatory agents that inhibit preferentially cyclooxygenase 1 without gastric damage. Journal of Medicinal Chemistry, 49(26), 7774-7780.


Cite as: http://hdl.handle.net/11858/00-001M-0000-0010-615A-C
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