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Flexible docking of pyridinone derivatives into the non-nucleoside inhibitor binding site of HIV-1 reverse transcriptase.
Bioorg Med Chem. 2004 Dec 1;12(23):6085-95. doi: 10.1016/j.bmc.2004.09.008.
Bioorg Med Chem. 2004.
PMID: 15519154
Docking-based CoMFA and CoMSIA studies of non-nucleoside reverse transcriptase inhibitors of the pyridinone derivative type.
Medina-Franco JL, Rodríguez-Morales S, Juárez-Gordiano C, Hernández-Campos A, Castillo R.
Medina-Franco JL, et al. Among authors: juarez gordiano c.
J Comput Aided Mol Des. 2004 May;18(5):345-60. doi: 10.1023/b:jcam.0000047816.15514.ab.
J Comput Aided Mol Des. 2004.
PMID: 15595461
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Pyridin-2(1H)-ones: a promising class of HIV-1 non-nucleoside reverse transcriptase inhibitors.
Medina-Franco JL, Martínez-Mayorga K, Juárez-Gordiano C, Castillo R.
Medina-Franco JL, et al. Among authors: juarez gordiano c.
ChemMedChem. 2007 Aug;2(8):1141-7. doi: 10.1002/cmdc.200700054.
ChemMedChem. 2007.
PMID: 17477343
Review.
No abstract available.
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New fragmentation processes of pyridin-2(1H)-ones upon electron impact ionization.
Medina-Franco JL, Juárez-Gordiano C, Hernández-Campos A, Duarte-Lisci G, Guzmán M, Castillo R.
Medina-Franco JL, et al. Among authors: juarez gordiano c.
Rapid Commun Mass Spectrom. 2005;19(16):2350-4. doi: 10.1002/rcm.2059.
Rapid Commun Mass Spectrom. 2005.
PMID: 16041820
No abstract available.
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