Novel hybrid DHPM-fatty acids: synthesis and activity against glioma cell growth in vitro.
Eur J Med Chem
; 95: 552-62, 2015 May 05.
Article
in En
| MEDLINE
| ID: mdl-25863023
We described the first synthesis of fatty acid 3,4-dihydropyrimidinones (DHPM-fatty acids) using the Biginelli multicomponent reaction. Antiproliferative activity on two glioma cell lines (C6 rat and U-138-MG human) was also reported. The novel DHPM-fatty acids reduced glioma cell viability relative to temozolomide. Hybrid oxo-monastrol-palmitic acid was the most potent, reducing U-138-MG human cell viability by ca. 50% at 10 µM. In addition, the DHPM-fatty acids showed a large safety range to neural cells, represented by the organotypic hippocampal culture. These results suggest that the increased lipophilicity of DHPM-fatty acids offer a promising approach to overcoming resistance to chemotherapy and may play an important role in the development of new antitumor drugs.
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Uridine
/
Fatty Acids
/
Glioma
/
Antineoplastic Agents
Limits:
Animals
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Humans
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Male
Language:
En
Journal:
Eur J Med Chem
Year:
2015
Document type:
Article
Affiliation country:
Brazil
Country of publication:
France