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   <dc:title>Synthesis, solubility and antitumor activity of maslinic acid derivatives.</dc:title>
   <dc:creator>Fuentes-Ríos, David</dc:creator>
   <dc:creator>Cepero, Ana</dc:creator>
   <dc:creator>García-Castro, Miguel</dc:creator>
   <dc:creator>Contreras-Cáceres, Rafael</dc:creator>
   <dc:creator>López-Romero, Juan Manuel</dc:creator>
   <dc:creator>Luque, Cristina</dc:creator>
   <dc:creator>Cabeza, Laura</dc:creator>
   <dc:creator>Melguizo, Consolación</dc:creator>
   <dc:creator>Prados, José</dc:creator>
   <dc:subject>Triterpenos</dc:subject>
   <dc:subject>Enlaces químicos</dc:subject>
   <dc:subject>Neurotransmisores</dc:subject>
   <dc:subject>Cáncer</dc:subject>
   <dc:subject>Citotoxicidad por mediación celular</dc:subject>
   <dcterms:abstract>Maslinic acid (MA), a pentacyclic triterpenoid obtained from olives that is characterized by its antiproliferative&#xd;
activity in tumor cells, has become a promising molecule that could be modi ed to improve cancer treatment. In&#xd;
this work we have synthesized in good yields several new MA conjugates, including glycerin, oligo(ethylene&#xd;
glycol), and amino acid derivatives (compounds 3a-f). The synthesis offers the possibility of recovering unreacted&#xd;
MA, and thus the scaling up of the process. For the tyramine-MA conjugate, compound 3f or TMA, the preparation&#xd;
has been optimized to a one-pot reaction. Solubility of conjugates in polar solvents has been measured, showing a&#xd;
marked increase of solubility with respect to MA. Moreover, we selected the tyramidyl maslinic acid conjugate (3f&#xd;
or TMA) to determine antitumor capacity over a wide range of cancer cell lines, including glioblastoma, mela-&#xd;
noma, breast, lung, colorectal and pancreatic cancer. Our results clearly demonstrated that TMA induced higher&#xd;
cytotoxicity in all cancer cell types compared to MA. TMA was more effective than MA, especially in breast cancer&#xd;
cells (MCF-7) and melanoma cells (B16–F10) where IC50 reductions of 4.12 and 4.72, respectively, was detected.&#xd;
Interestingly, TMA showed a remarkable antitumor ability against the resistant HCT-15 colon cancer cell line.&#xd;
Furthermore, we demonstrated for the rst time a relevant effect of a MA derivative against glioblastoma cells&#xd;
(A172 and SF-268). These results suggest that TMA is able to improve the antitumor characteristics of MA in a&#xd;
wide range of cancers and that it may be a promising compound for various tumor types, including resistant&#xd;
cancer.</dcterms:abstract>
   <dcterms:dateAccepted>2025-10-28T11:25:14Z</dcterms:dateAccepted>
   <dcterms:available>2025-10-28T11:25:14Z</dcterms:available>
   <dcterms:created>2025-10-28T11:25:14Z</dcterms:created>
   <dcterms:issued>2022-02-05</dcterms:issued>
   <dc:type>journal article</dc:type>
   <dc:identifier>European Journal of Medicinal Chemistry Reports 4 (2022) 100032</dc:identifier>
   <dc:identifier>https://hdl.handle.net/10630/40476</dc:identifier>
   <dc:identifier>10.1016/j.ejmcr.2022.100032</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:rights>open access</dc:rights>
   <dc:publisher>Elsevier</dc:publisher>
</qdc:qualifieddc>
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