References
- Arranz, M. E., Vega, S., and Díaz, J. A., Synthesis of Hetero [ 1,2,4]thiadiazine 1,1-Dioxides. Heterocycles, 45, 1767-1774 (1997) https://doi.org/10.3987/COM-97-7882
- Arranz M. E., Diaz, J. A., Ingate, S. T., Witvrouw, M., Pannecouque, C., Balzarini, J., De Clercq, E., and Vega, S., Novel 1,1,3-trioxo-2H,4H-thieno[3,4-e][1,2,4]thiadiazine derivatives as non-nucleoside reverse transcriptase inhibitors that inhibit human immunodeficiency virus type 1 replication. J. Med. Chem., 41, 4109-4117 (1998) https://doi.org/10.1021/jm9802012
- Arranz, M. E., Díaz, J. A., Ingate, S. T., Witvrouw, M., Pannecouque, C., Balzarini, J., De Clerq, E., and Vega, S., Synthesis and anti-HIV activity of 1,1,3-trioxo-2H,4H-thieno [3,4-e] [1,2,4]thiadiazines (TTDs): a new family of HIV-1 specific non-nucleoside reverse transcriptase inhibitors. Bioorg. Med. Chem., 7, 2811-2822 (1999) https://doi.org/10.1016/S0968-0896(99)00221-7
- Arranz, M. E., Díaz, J. A., Vega, S., Campos-Toimil, M., Orallo, F., Cardelus, I., Llenas, J., and Fernandez, A. G., Synthesis and pharmacological evaluation of 2, 3-dihydro-3-oxo-4Hthieno [3, 4-e][1, 2, 4]thiadiazine 1, 1-dioxidesas voltagedependent calcium channel blockers. Eur. J. Med. Chem., 35, 751-759 (2000) https://doi.org/10.1016/S0223-5234(00)00188-4
- Das, K., Lewi, P. J., Hughes, S. H., and Arnold, E., Crystallography and the design of anti-AIDS drugs: conformational flexibility and positional adaptability are important in the design of non-nucleoside HIV-1 reverse transcriptase inhibitors. Prog. Biophys. Mol. Biol., 88, 209- 231 (2005) https://doi.org/10.1016/j.pbiomolbio.2004.07.001
- De Clercq, E., Recent highlights in the development of new antiviral drugs. Curr Opin Microbiol., 8, 552-560 (2005) https://doi.org/10.1016/j.mib.2005.08.010
- Joncckheere, H., Anne, J., and De Clercq, E., The HIV-1 reverse transcription (RT) process as target for RT inhibitors. Med. Res. Rev., 20, 129-154 (2000) https://doi.org/10.1002/(SICI)1098-1128(200003)20:2<129::AID-MED2>3.0.CO;2-A
- Martinez, A., Gil, C., Abasolo, M. I., Castro, A., Bruno, A. M., Perez, C., Prieto, C., and Otero, J., Benzothiadiazine dioxide dibenzyl derivatives as potent human cytomegalovirus inhibitors: Synthesis and comparative molecular field analysis. J. Med. Chem., 43, 3218-3225 (2000a) https://doi.org/10.1021/jm000033p
- Martinez, A., Gil, C., Perez, C., Castro, A., Prieto, C., Otero, J., Andrei, G., Snoeck, R., Balzarini, J., and De Clercq E., Nucleoside human cytomegalovirus inhibitors: Synthesis and antiviral evaluation of (chlorophenylmethyl)benzothiadiazine dioxide derivatives. J. Med. Chem., 43, 3267-3273 (2000b) https://doi.org/10.1021/jm000118q
- Patani, G. P. and LaVoie, E. J., Bioisosterism: A rational approach in drug design. Chem. Rev., 96, 3147-3176 (1996) https://doi.org/10.1021/cr950066q
- Pauwels, R., Balzarini, J., Baba, M., Snoeck, R., Schols, D., Herdewijn, P., Desmyter, J., and De Clercq, E., Rapid and automated tetrazolium-based colorimetric assay for the detection of anti-HIV compounds. J. Virol. Methods., 20,309- 321 (1988) https://doi.org/10.1016/0166-0934(88)90134-6
- Schaefer, W., Gunar Friebe, W., Leinert, H., Mertens, A., Poll, T., Vonder Saal, W., Zilch, H., Nuber, B., and L. Ziegler, M., Non-nucleoside inhibitors of HIV-1 reverse transcriptase: molecular modeling and x-ray structure investigations. J. Med. Chem., 36, 726-732 (1993) https://doi.org/10.1021/jm00058a009
- Witvrouw, M., Arranz, M. E., Pannecouque, C., Declerq, R., Jonckheere, H., Schmit, J. C., Vandamme, A. M., Dia, J. A., Ingate, S. E., Desmyter, J., Esnouf, E., Meervelt, L. V., Vega, S., Bazarni, J., and De Clercq, E., 1,1,3-Trioxo-2H,4H-thieno [e-3,4][1,2,4]thiadiazines (TTDs) derivatives: a new class of nonnucleoside human immunodeficiency virus type 1 (HIV-1) reverse transcriptase inhibitors with anti-HIV-1 activity. Antimicrob. Agents. Chemother., 42, 618 -623 (1998)