6-Chloro-3-nitro-2-[(phenylsulfonyl)methyl]imidazo[1,2-b]pyridazine

Author:

Paoli-Lombardo Romain1,Primas Nicolas12ORCID,Hutter Sébastien3,Bourgeade-Delmas Sandra4,Boudot Clotilde5,Castera-Ducros Caroline12,Jacquet Inès1,Courtioux Bertrand5ORCID,Azas Nadine3,Rathelot Pascal12ORCID,Vanelle Patrice12ORCID

Affiliation:

1. CNRS, ICR UMR 7273, Team Pharmaco-Chimie Radicalaire, Faculty of Pharmacy, Aix Marseille University, 27 Boulevard Jean Moulin, CS30064, CEDEX 05, 13385 Marseille, France

2. Central Service for Pharmaceutical Quality and Information SCQIP, Pharmacy Department, Hospital Conception, AP-HM, 13005 Marseille, France

3. IHU Méditerranée Infection, UMR VITROME—Tropical Eukaryotic Pathogens, Aix Marseille University, 19–21 Boulevard Jean Moulin, 13005 Marseille, France

4. UMR 152 PHARMA-DEV, University of Toulouse, IRD, UPS, 31062 Toulouse, France

5. Faculty of Pharmacy, Institute of Neuroepidemiology and Tropical Neurology, University of Limoges, INSERM U1094, 87025 Limoges, France

Abstract

As part of our ongoing scaffold-hopping work on an antikinetoplastid 3-nitroimidazo[1,2-a]pyridine scaffold, we explored 3-nitroimidazo[1,2-b]pyridazine as a potential new antikinetoplastid series. Using conditions previously described by our lab, we obtained 6-chloro-3-nitro-2-[(phenylsulfonyl)methyl]imidazo[1,2-b]pyridazine with 54% yield. In vitro activity of this compound was evaluated against both the promastigote form of Leishmania donovani, the axenic amastigote form of Leishmania infantum and the trypomastigote blood stream form of Trypanosomabrucei brucei, and its influence on cell viability was assessed on the HepG2 cell line. However, despite good activity against the trypomastigote blood stream form of T. b. brucei (EC50 = 0.38 µM), it showed poor solubility in both HepG2 (CC50 > 7.8 µM) and L. infantum axenic amastigotes (EC50 > 1.6 µM) culture media, associated with a loss of activity against the promastigote form of L. infantum (EC50 > 15.6 µM).

Funder

Aix-Marseille Université

Centre national de la recherche scientifique

Assistance publique—Hôpitaux de Marseille

Publisher

MDPI AG

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Reference14 articles.

1. Taming Parasites by Tailoring Them;Ren;Front. Cell. Infect. Microbiol.,2017

2. Bruschi, F., and Gradoni, L. (2018). The Leishmaniases: Old Neglected Tropical Diseases, Springer International Publishing.

3. World Health Organization (WHO) (2023, January 13). Trypanosomiasis, Human African (Sleeping Sickness). Available online: https://www.who.int/news-room/fact-sheets/detail/trypanosomiasis-human-african-(sleeping-sickness).

4. World Health Organization (WHO) (2022, January 13). Leishmaniasis. Available online: https://www.who.int/news-room/fact-sheets/detail/leishmaniasis.

5. Leishmaniasis;Burza;Lancet,2018

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