Synthesis and In Silico Drug-Likeness Modeling of 5-FU/ASA Hybrids
A series of 5-FU-ASA hybrids were synthesized with good yields using click chemistry as the key step. The structures of these compounds were elucidated by spectroscopic analysis. Finally, an optimal pharmacokinetic profile was also estimated for each synthetized hybrid. Taken together, hybrids <b...
Ausführliche Beschreibung
Autor*in: |
Wilson Castrillón-López [verfasserIn] Andrés F. Yepes [verfasserIn] Wilson Cardona-Galeano [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2023 |
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Übergeordnetes Werk: |
In: Molbank - MDPI AG, 2004, (2023), 4, p M1745 |
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Übergeordnetes Werk: |
year:2023 ; number:4, p M1745 |
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DOI / URN: |
10.3390/M1745 |
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Katalog-ID: |
DOAJ09882290X |
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10.3390/M1745 doi (DE-627)DOAJ09882290X (DE-599)DOAJe6b922e985364b4a845dbf1a841405f6 DE-627 ger DE-627 rakwb eng QD146-197 Wilson Castrillón-López verfasserin aut Synthesis and In Silico Drug-Likeness Modeling of 5-FU/ASA Hybrids 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier A series of 5-FU-ASA hybrids were synthesized with good yields using click chemistry as the key step. The structures of these compounds were elucidated by spectroscopic analysis. Finally, an optimal pharmacokinetic profile was also estimated for each synthetized hybrid. Taken together, hybrids <b<4a</b<–<b<h</b< could be used as starting points for further pharmacological studies concerning therapeutic cancer intervention. 5-FU ASA hybrid compounds click chemistry drug-likeness modeling Inorganic chemistry Andrés F. Yepes verfasserin aut Wilson Cardona-Galeano verfasserin aut In Molbank MDPI AG, 2004 (2023), 4, p M1745 (DE-627)474385426 (DE-600)2170280-9 14228599 nnns year:2023 number:4, p M1745 https://doi.org/10.3390/M1745 kostenfrei https://doaj.org/article/e6b922e985364b4a845dbf1a841405f6 kostenfrei https://www.mdpi.com/1422-8599/2023/4/M1745 kostenfrei https://doaj.org/toc/1422-8599 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 2023 4, p M1745 |
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A series of 5-FU-ASA hybrids were synthesized with good yields using click chemistry as the key step. The structures of these compounds were elucidated by spectroscopic analysis. Finally, an optimal pharmacokinetic profile was also estimated for each synthetized hybrid. Taken together, hybrids <b<4a</b<–<b<h</b< could be used as starting points for further pharmacological studies concerning therapeutic cancer intervention. |
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A series of 5-FU-ASA hybrids were synthesized with good yields using click chemistry as the key step. The structures of these compounds were elucidated by spectroscopic analysis. Finally, an optimal pharmacokinetic profile was also estimated for each synthetized hybrid. Taken together, hybrids <b<4a</b<–<b<h</b< could be used as starting points for further pharmacological studies concerning therapeutic cancer intervention. |
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A series of 5-FU-ASA hybrids were synthesized with good yields using click chemistry as the key step. The structures of these compounds were elucidated by spectroscopic analysis. Finally, an optimal pharmacokinetic profile was also estimated for each synthetized hybrid. Taken together, hybrids <b<4a</b<–<b<h</b< could be used as starting points for further pharmacological studies concerning therapeutic cancer intervention. |
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