2015
DOI: 10.17344/acsi.2015.1418
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Synthesis, crystal structure and biological activity screening of novel N-(α-bromoacyl)-α-amino esters containing valyl moiety

Abstract: Three novel N-(α-bromoacyl)-α-amino esters: methyl 2-(2-bromo-3-methylbutanamido)pentanoate (1), methyl 2-(2-bromo-3-methylbutanamido)-2-phenylacetate (2) and methyl 2-(2-bromo-3-methylbutanamido)-3-phenylpropanoate (3) were synthesized. Single crystal X-ray diffraction data are reported for compounds 1 and 2. The cytotoxicity, antiinflammatory and antibacterial activity of compounds 1-3 were investigated. Additionally, the physico-chemical properties of studied compounds were calculated and an in silico toxic… Show more

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Cited by 5 publications
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“…Taking in consideration predicted in silico properties and estimated drug likeness score, pharmacological and toxicological profile, thymyl esters might be used as prodrugs. Among the chemical bonds used to link parental drug and carrier, esters have already proven to be promising due to their amenability to hydrolysis in vivo and are most frequently used in order to enhance the lipophilicity 52 and passive membrane transport.…”
Section: Resultsmentioning
confidence: 99%
“…Taking in consideration predicted in silico properties and estimated drug likeness score, pharmacological and toxicological profile, thymyl esters might be used as prodrugs. Among the chemical bonds used to link parental drug and carrier, esters have already proven to be promising due to their amenability to hydrolysis in vivo and are most frequently used in order to enhance the lipophilicity 52 and passive membrane transport.…”
Section: Resultsmentioning
confidence: 99%
“…Taking in consideration predicted in silico properties and estimated drug likeness score, pharmacological and toxicological profile, eugenyl esters might be used as prodrugs of eugenol due to an expected enhanced lipophilicity 53 and passive membrane transport.…”
Section: Resultsmentioning
confidence: 99%