Abstract |
In order to find new molecules with cytotoxic activity against cancer cells, we prepared bis-akyne amides derived from propiolic acid. The bis- alkynes were then transformed in their mono-1,2,3-triazole analogs onto the amide side, due to its greater reactivity, using a catalyst-free Huisgen's reaction. The mono- triazoles were then subjected to the copper (I)-catalyzed version of the previous reaction (CuAAC), using a supported catalyst, to produce bis- triazoles. All products were obtained pure after simple trituration or filtration procedures. All synthetic compounds were tested in vitro for their cytotoxic activity using B16 melanoma cells. Four compounds (7, 23, 25 and 33) showed activities in the micromolar range (<21 μM) whereas three compounds (3, 22 and 38) presented activity at low micromolar concentrations (<10 μM), and two analogs (2 and 13) were active at nanomolar levels (<1 μM).
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Authors | Hichem Elamari, Riadh Slimi, Guy G Chabot, Lionel Quentin, Daniel Scherman, Christian Girard |
Journal | European journal of medicinal chemistry
(Eur J Med Chem)
Vol. 60
Pg. 360-4
(Feb 2013)
ISSN: 1768-3254 [Electronic] France |
PMID | 23314049
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2012 Elsevier Masson SAS. All rights reserved. |
Chemical References |
- Alkynes
- Amides
- Antineoplastic Agents
- Triazoles
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Topics |
- Alkynes
(chemical synthesis, chemistry, pharmacology)
- Amides
(chemical synthesis, chemistry, pharmacology)
- Animals
- Antineoplastic Agents
(chemical synthesis, chemistry, pharmacology)
- Cell Line, Tumor
- Cell Proliferation
(drug effects)
- Dose-Response Relationship, Drug
- Drug Screening Assays, Antitumor
- Molecular Structure
- Structure-Activity Relationship
- Triazoles
(chemical synthesis, chemistry, pharmacology)
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