2024-03-19T05:48:29Zhttp://digital.csic.es/dspace-oai/requestoai:digital.csic.es:10261/880832022-12-14T11:50:12Zcom_10261_81com_10261_5col_10261_334
DIGITAL.CSIC
author
Martínez, Ana
author
Gil, Carmen
author
Castro, Ana
author
Pérez, Concepción
author
Prieto, Carlos
author
Otero, Joaquín
2013-12-03T11:29:39Z
2013-12-03T11:29:39Z
2003
Bioorganic and Medicinal Chemistry 11: 2395- 2402 (2003)
http://hdl.handle.net/10261/88083
10.1016/S0968-0896(03)00148-2
Two new series of BTD derivatives have been synthesised allowing to explore the steric requirements for their biological activity. The N3-alkylBTD compounds have shown antiviral activity in the same order or lower than previously prepared compounds. However, the cytotoxicity values observed prevent this new series of BTD derivatives from its potential therapeutic application. Concerning BTD derivatives with the modified linker attached to N1 position, we have obtained new non-nucleoside anti-HCMV derivatives. The activity against HCMV is shown at concentrations that were 10-fold lower than the concentration that was toxic for the host cells, which confirm that these derivatives show a specific antiviral effect against HCMV. SAR conclusions derived from these last compounds have provided new knowledge about the structural requirements of BTD showing certain positions that could be modified for enhancing the anti-HCMV action. © 2003 Elsevier Science Ltd. All rights reserved.
eng
closedAccess
Benzothiadiazine dioxides (BTD) derivatives as non-nucleoside human cytomegalovirus (HCMV) inhibitors. Study of structural requirements for biological activity
artículo
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accesoRestringido.pdf.txt
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accesoRestringido.pdf.txt