2006
DOI: 10.1016/j.molstruc.2005.09.004
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Conformational analysis of the potential anticancer agent ethyl trihydroxycinnamate—A combined raman spectroscopy and ab initio study

Abstract: A conformational analysis of ethyl 3-(3,4,5-trihydroxyphenyl)-2-propenoate (ethyl 3,4,5-trihydroxycinnamate, ETHPPE), a polyphenolic cinnamic ester which displays antiproliferative activity towards human adenocarcinoma cells, was carried out by Raman spectroscopy coupled to ab initio MO calculations. Apart from the optimised geometrical parameters for the most stable conformations of this compound (both for the trans and cis isomers), the corresponding harmonic vibrational frequencies were obtained. Eighteen d… Show more

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Cited by 19 publications
(33 citation statements)
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References 42 publications
(65 reference statements)
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“…The present results are in perfect agreement with the ones obtained for cinnamic acid [43] and its analogues, such as hydroxycinnamic acid and its ester or amide derivatives [44][45][46][47][48][49]. In particular, the conformational preferences of naturally occurring hydroxycinnamic acids differing in the ring substitution pattern is strongly dependent on the number, type and relative orientation of these substituents (hydroxyl and/or methoxyl groups).…”
Section: Discussionsupporting
confidence: 90%
See 1 more Smart Citation
“…The present results are in perfect agreement with the ones obtained for cinnamic acid [43] and its analogues, such as hydroxycinnamic acid and its ester or amide derivatives [44][45][46][47][48][49]. In particular, the conformational preferences of naturally occurring hydroxycinnamic acids differing in the ring substitution pattern is strongly dependent on the number, type and relative orientation of these substituents (hydroxyl and/or methoxyl groups).…”
Section: Discussionsupporting
confidence: 90%
“…However, both geometries should be taken into consideration for structural, chemical and biological studies regarding hydroxycinnamic acids since they are the most populated ones at room temperature. In di-and tri substituted compounds a stabilising intramolecular H-bond is formed, which is known to be energetically favourable in this kind of phenolic systems [44][45][46][47][48][49]57], and is therefore essential for the interpretation of their structure-activity relationships (SAR's).…”
Section: Discussionmentioning
confidence: 99%
“…pH, temperature, ionic strength or exposure to drugs). 22,27,28 Following previous studies by the authors on dietary polyphenolic compounds -both regarding their structural and conformational preferences 17,[29][30][31][32][33][34][35][36][37][38][39][40] and their chemopreventive and/or chemotherapeutic properties towards several cancer cells -the present work reports the effect of daidzein on the biochemical profile of two human breast cancer cell lines: MCF-7 (estrogendependent, ER + ) and MDA-MB-231 (estrogen-independent, ER -). The results thus obtained are expected to help establishing an accurate balance between DAID´s antioxidant and prooxidant capacities, aiming at a prospective use against breast cancer: either as a chemopreventive agent (sole or in combination with other flavones) or as an adjuvant in chemotherapy (coupled with conventional drugs such as tamoxifen, paclitaxel, docetaxel, methotrexate, gemcitabine or doxorubicin 41,42 and cisplatin.…”
Section: A Introductionmentioning
confidence: 89%
“…In fact, numerous studies have been carried out in order to obtain new lead compounds for the design of cancer preventive or therapeutic agents. 10,18 Nevertheless, even though there is a wealth of data on the relevance of phenolic compounds as growth-inhibiting compounds, the correlation between anti-tumour activity and chemical structure is far from clear.…”
Section: Introductionmentioning
confidence: 99%