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1.
Molecules ; 25(12)2020 Jun 18.
Article in English | MEDLINE | ID: mdl-32570872

ABSTRACT

The emergence of Plasmodium falciparum parasites, responsible for malaria disease, resistant to antiplasmodial drugs including the artemisinins, represents a major threat to public health. Therefore, the development of new antimalarial drugs or combinations is urgently required. In this context, several hybrid molecules combining a dihydroartemisinin derivative and gold(I) N-heterocyclic carbene (NHC) complexes have been synthesized based on the different modes of action of the two compounds. The antiplasmodial activity of these molecules was assessed in vitro as well as their cytotoxicity against mammalian cells. All the hybrid molecules tested showed efficacy against P. falciparum, in a nanomolar range for the most active, associated with a low cytotoxicity. However, cross-resistance between artemisinin and these hybrid molecules was evidenced. These results underline a fear about the risk of cross-resistance between artemisinins and new antimalarial drugs based on an endoperoxide part. This study thus raises concerns about the use of such molecules in future therapeutic malaria policies.


Subject(s)
Antimalarials , Artemether , Gold , Organogold Compounds , Plasmodium falciparum/growth & development , Antimalarials/chemical synthesis , Antimalarials/chemistry , Antimalarials/pharmacology , Artemether/chemistry , Artemether/pharmacology , Gold/chemistry , Gold/pharmacology , Humans , Organogold Compounds/chemical synthesis , Organogold Compounds/chemistry , Organogold Compounds/pharmacology
2.
Angew Chem Int Ed Engl ; 59(29): 12062-12068, 2020 07 13.
Article in English | MEDLINE | ID: mdl-32304346

ABSTRACT

A family of hybrid complexes combining two biologically active motifs, an artemisinin derivative and a cationic bis(NHC)-gold(I) unit, has been synthesized. One of these complexes, 2 a, has been analyzed by single-crystal X-ray diffraction. 2 a shows strong anticancer activities on a large panel of human cancer cell models (prostate, breast, lung, liver, bladder, bone, acute and chronic myeloid leukemias) with GI50 values in the nm range, together with a high selectivity. An original and distinctive mechanism of action, that is, through inhibition of the redox antioxidant NRF2 transcription factor (strongly associated with aggressiveness and resistance to cancer therapies) has been evidenced. 2 a could remarkably sensitize to sorafenib in HepG2 liver cells, in which dysregulated NRF2 signaling is linked to primary and acquired drug resistance. 2 a also inhibited NF-κB and HIF transcriptional activities, which are also associated with progression and resistance in cancer. Our findings provide evidence that hybrid (NHC)gold(I) compounds represent a new class of organometallic hybrid molecules that may yield new therapeutic agents.


Subject(s)
Antineoplastic Agents/chemical synthesis , Antineoplastic Agents/pharmacology , Artemisinins/chemistry , Gold/chemistry , NF-E2-Related Factor 2/antagonists & inhibitors , Cell Line, Tumor , Drug Resistance, Neoplasm/drug effects , Drug Screening Assays, Antitumor , Hep G2 Cells , Humans , NF-E2-Related Factor 2/biosynthesis , Sorafenib/pharmacology
3.
Eur J Med Chem ; 143: 1635-1643, 2018 Jan 01.
Article in English | MEDLINE | ID: mdl-29133045

ABSTRACT

A series of five new mononuclear neutral gold(I) complexes containing N-heterocyclic carbenes (NHCs) was synthesized and fully characterized by spectroscopic methods. The X-ray structures of four complexes are presented. These gold(I) complexes together with four other neutral gold(I)-NHC complexes previously described were evaluated in vitro against Leishmania infantum promastigotes and axenic amastigotes. Moreover, their cytotoxicity was assessed on the murine macrophages J774A.1. Except one complex (10), eight gold(I)-NHC-Cl complexes show potent activity against the pathological relevant form of L. infantum amastigote with IC50 in the low micromolar and submicromolar range and five of them exhibit a SI close to 10. The lead-complex 11 displays a very high and selective activity (IC50 = 190 nM, SI = 40.29) and constitutes the best promising gold(I)-based drug of this series.


Subject(s)
Antiprotozoal Agents/pharmacology , Heterocyclic Compounds/pharmacology , Leishmania infantum/drug effects , Methane/analogs & derivatives , Organogold Compounds/pharmacology , Animals , Antiprotozoal Agents/chemical synthesis , Antiprotozoal Agents/chemistry , Cell Line , Dose-Response Relationship, Drug , Heterocyclic Compounds/chemistry , Macrophages/drug effects , Methane/chemistry , Methane/pharmacology , Mice , Molecular Structure , Organogold Compounds/chemical synthesis , Organogold Compounds/chemistry , Parasitic Sensitivity Tests , Structure-Activity Relationship
4.
Bioorg Med Chem ; 24(13): 3075-3082, 2016 07 01.
Article in English | MEDLINE | ID: mdl-27240469

ABSTRACT

A series of twenty five molecules, including imidazolium salts functionalized by N-, O- or S-containing groups and their corresponding cationic, neutral or anionic gold(I) complexes were evaluated on Plasmodium falciparum in vitro and then on Vero cells to determine their selectivity. Among them, eight new compounds were synthesized and fully characterized by spectroscopic methods. The X-ray structures of three gold(I) complexes are presented. Except one complex (18), all the cationic gold(I) complexes show potent antiplasmodial activity with IC50 in the micro- and submicromolar range, correlated with their lipophilicity. Structure-activity relationships enable to evidence a lead-complex (21) displaying a good activity (IC50=210nM) close to the value obtained with chloroquine (IC50=514nM) and a weak cytotoxicity.


Subject(s)
Antimalarials/pharmacology , Gold/pharmacology , Methane/analogs & derivatives , Organometallic Compounds/chemical synthesis , Plasmodium falciparum/drug effects , Animals , Antimalarials/chemical synthesis , Antimalarials/chemistry , Antimalarials/toxicity , Cell Survival/drug effects , Chlorocebus aethiops , Chloroquine/chemistry , Chloroquine/pharmacology , Crystallography, X-Ray , Gold/chemistry , Inhibitory Concentration 50 , Methane/chemistry , Methane/pharmacology , Molecular Structure , Organometallic Compounds/chemistry , Organometallic Compounds/pharmacology , Organometallic Compounds/toxicity , Structure-Activity Relationship , Vero Cells
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