Synthesis and in vitro antikinetoplastid activity of polyamine-hydroxybenzotriazole conjugates
Thirteen new polyamine derivatives coupled to hydroxybenzotriazole have been synthesized and evaluated for their in vitro antikinetoplastid activity. Trypanosoma Trypanothione reductase (TryR) was envisioned as a potential target. Among all tested molecules, only one compound, a N3-spermidine-benzot...
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| Hauptverfasser: | , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
2017
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| In: |
Bioorganic & medicinal chemistry
Year: 2016, Jahrgang: 25, Heft: 1, Pages: 84-90 |
| ISSN: | 1464-3391 |
| DOI: | 10.1016/j.bmc.2016.10.013 |
| Online-Zugang: | Verlag, Volltext: http://dx.doi.org/10.1016/j.bmc.2016.10.013 Verlag, Volltext: http://www.sciencedirect.com/science/article/pii/S0968089616309427 
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| Verfasserangaben: | Elodie Jagu, Sébastien Pomel, Alba Diez-Martinez, Florence Ramiandrasoa, R. Luise Krauth-Siegel, Stéphanie Pethe, Casimir Blonski, Raphaël Labruère, Philippe M. Loiseau |
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| 245 | 1 | 0 | |a Synthesis and in vitro antikinetoplastid activity of polyamine-hydroxybenzotriazole conjugates |c Elodie Jagu, Sébastien Pomel, Alba Diez-Martinez, Florence Ramiandrasoa, R. Luise Krauth-Siegel, Stéphanie Pethe, Casimir Blonski, Raphaël Labruère, Philippe M. Loiseau |
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| 520 | |a Thirteen new polyamine derivatives coupled to hydroxybenzotriazole have been synthesized and evaluated for their in vitro antikinetoplastid activity. Trypanosoma Trypanothione reductase (TryR) was envisioned as a potential target. Among all tested molecules, only one compound, a N3-spermidine-benzotriazole derivative, displayed relevant inhibitory activity on this enzyme but was not active on parasites. The corresponding Boc-protected spermidine-benzotriazole was however trypanocidal against Trypanosoma brucei gambiense with an IC50 value of 1μM and was completely devoid of cytotoxicity. On the intramacrophage amastigotes of Leishmania donovani, a N2-spermidine conjugate of this series, exhibited an interesting IC50 value of 3μM associated with both low cytotoxicity against axenic Leishmania donovani. These new compounds are promising leads for the development of antikinetoplastid agents and their targets have to be deciphered. | ||
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| 650 | 4 | |a Antikinetoplastids | |
| 650 | 4 | |a Benzotriazole | |
| 650 | 4 | |a Polyamines | |
| 650 | 4 | |a Trypanothione reductase | |
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