Nifurtimox
Vue d'ensemble
Description
Le nifurtimox est un dérivé du nitrofurane utilisé principalement comme médicament antiparasitaire. Il est commercialisé sous le nom de marque Lampit et est utilisé pour traiter la maladie de Chagas (trypanosomiase américaine) et la trypanosomiase africaine (maladie du sommeil) . Le this compound a été développé par Bayer et est utilisé depuis 1965 . Il est inclus dans la Liste des médicaments essentiels de l'Organisation mondiale de la santé .
Mécanisme D'action
Target of Action
Nifurtimox primarily targets the parasite Trypanosoma cruzi , which causes Chagas disease . The drug exerts its trypanosomal activity against this parasite .
Mode of Action
It is believed to occur through the activation of nitroreductase enzymes that produce reactive metabolites . These metabolites have a series of deleterious effects on Trypanosoma cruzi . Nitro reductase activity results in the formation of nitro anion radicals, causing the formation of oxygen radicals that result in decreased protein and nucleic acid synthesis, breakage of DNA, and inhibition of parasite growth .
Biochemical Pathways
This compound and other benzofuran derivatives are known to reduce parasite dehydrogenase activity . This action affects the biochemical pathways of the parasite, leading to its death .
Pharmacokinetics
This compound exhibits low bioavailability . It is metabolized in the liver, with cytochrome P450 oxidase (CYP) involved in the process . The elimination half-life of this compound is approximately 2.95 ± 1.19 hours . Excretion is primarily through the kidneys, although the rate of renal excretion is very low . The pharmacokinetic analysis suggests that the low serum concentration of this compound is probably the result of a marked first-pass effect .
Result of Action
The result of this compound’s action is the reduction of the Trypanosoma cruzi population in the host. A significant number of patients with acute or chronic Chagas disease treated with this compound were found to be immunoglobulin G (IgG) antibody negative and demonstrated at least a 20% decrease in optical density on two IgG antibody tests for T. cruzi antigens .
Méthodes De Préparation
Voies de synthèse et conditions réactionnelles
Le nifurtimox est synthétisé par un processus en plusieurs étapes impliquant la réaction du 5-nitro-2-furfuraldéhyde avec le 3-méthyl-4-thiomorpholine-1,1-dioxyde . Les conditions réactionnelles impliquent généralement l'utilisation de solvants tels que l'éthanol et de catalyseurs pour faciliter la formation du produit final .
Méthodes de production industrielle
La production industrielle du this compound implique une synthèse à grande échelle utilisant des conditions réactionnelles similaires à celles de la synthèse en laboratoire. Le procédé est optimisé pour le rendement et la pureté, avec des mesures de contrôle qualité strictes pour garantir la constance du produit final .
Analyse Des Réactions Chimiques
Types de réactions
Le nifurtimox subit plusieurs types de réactions chimiques, notamment :
Oxydation : Le groupe nitro du this compound peut être réduit pour former des radicaux anions nitro.
Réduction : Le groupe nitro peut également subir une réduction pour former des amines.
Substitution : Le this compound peut participer à des réactions de substitution nucléophile.
Réactifs et conditions communes
Les réactifs courants utilisés dans les réactions du this compound comprennent des agents réducteurs tels que le borohydrure de sodium et des agents oxydants comme le peroxyde d'hydrogène . Les réactions sont généralement réalisées à température et pH contrôlés pour garantir la formation du produit souhaité .
Principaux produits formés
Les principaux produits formés à partir des réactions du this compound comprennent des amines réduites et des dérivés substitués, en fonction des conditions réactionnelles et des réactifs spécifiques utilisés .
Applications de la recherche scientifique
Le this compound a un large éventail d'applications de recherche scientifique, notamment :
Chimie : Utilisé comme composé modèle pour étudier les dérivés du nitrofurane et leur réactivité.
Biologie : Etudié pour ses effets sur les processus cellulaires et son potentiel en tant qu'agent antiparasitaire.
Médecine : Utilisé dans le traitement de la maladie de Chagas et de la maladie du sommeil.
Industrie : Employé dans le développement de nouveaux médicaments et formulations antiparasitaires.
Mécanisme d'action
Le mécanisme d'action exact du this compound n'est pas entièrement compris, mais il est considéré comme impliquant la bioréduction du groupe nitro pour former des radicaux anions nitro . Ces radicaux subissent un cycle redox avec l'oxygène moléculaire, ce qui conduit à la production d'espèces réactives de l'oxygène (ROS) . Les ROS endommagent les composants cellulaires, notamment l'ADN, les protéines et les lipides, ce qui conduit finalement à la mort du parasite .
Applications De Recherche Scientifique
Nifurtimox has a wide range of scientific research applications, including:
Chemistry: Used as a model compound to study nitrofuran derivatives and their reactivity.
Biology: Investigated for its effects on cellular processes and its potential as an antiparasitic agent.
Medicine: Used in the treatment of Chagas disease and sleeping sickness.
Industry: Employed in the development of new antiparasitic drugs and formulations.
Comparaison Avec Des Composés Similaires
Composés similaires
Benznidazole : Un autre dérivé du nitrofurane utilisé pour traiter la maladie de Chagas.
Pentamidine : Utilisé pour traiter la trypanosomiase africaine et d'autres infections parasitaires.
Unicité du nifurtimox
Le this compound est unique en sa capacité à générer des espèces réactives de l'oxygène par un cycle redox, ce qui contribue à son activité antiparasitaire . Il est également remarquable pour son inclusion dans les traitements combinés, tels que le traitement combiné this compound-éflornithine de la maladie du sommeil .
Propriétés
| The mechanism of action of nifurtimox has not been fully elucidated, however, is believed to occur by the activation of nitroreductase enzymes that produce reactive metabolites with a series of deleterious effects on Trypanosoma cruzi, the parasite causing Chagas disease. The antiprotozoal actions of nifurtimox occur both intracellularly and extracellularly. Inhibition of parasite dehydrogenase activity is another purported mode of action of nifurtimox that warrants further research. | |
Numéro CAS |
23256-30-6 |
Formule moléculaire |
C10H13N3O5S |
Poids moléculaire |
287.29 g/mol |
Nom IUPAC |
(Z)-N-(3-methyl-1,1-dioxo-1,4-thiazinan-4-yl)-1-(5-nitrofuran-2-yl)methanimine |
InChI |
InChI=1S/C10H13N3O5S/c1-8-7-19(16,17)5-4-12(8)11-6-9-2-3-10(18-9)13(14)15/h2-3,6,8H,4-5,7H2,1H3/b11-6- |
Clé InChI |
ARFHIAQFJWUCFH-WDZFZDKYSA-N |
SMILES |
CC1CS(=O)(=O)CCN1N=CC2=CC=C(O2)[N+](=O)[O-] |
SMILES isomérique |
CC1CS(=O)(=O)CCN1/N=C\C2=CC=C(O2)[N+](=O)[O-] |
SMILES canonique |
CC1CS(=O)(=O)CCN1N=CC2=CC=C(O2)[N+](=O)[O-] |
Apparence |
Solid powder |
Point d'ébullition |
550.3±50.0 |
melting_point |
177-183 |
| 23256-30-6 | |
Pictogrammes |
Health Hazard |
Pureté |
>98% (or refer to the Certificate of Analysis) |
Durée de conservation |
>5 years if stored properly |
Solubilité |
Soluble in DMSO, not in water |
Stockage |
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years). |
Synonymes |
Bayer 2502 Lampit Nifurtimox |
Origine du produit |
United States |
Retrosynthesis Analysis
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Strategy Settings
| Precursor scoring | Relevance Heuristic |
|---|---|
| Min. plausibility | 0.01 |
| Model | Template_relevance |
| Template Set | Pistachio/Bkms_metabolic/Pistachio_ringbreaker/Reaxys/Reaxys_biocatalysis |
| Top-N result to add to graph | 6 |
Feasible Synthetic Routes
Q1: What is the primary mechanism of action of Nifurtimox against trypanosomes?
A1: this compound is a prodrug that requires activation within the parasite. The key activation step is catalyzed by a trypanosomal type I nitroreductase (NTR). This enzyme reduces this compound, leading to the formation of an unsaturated open-chain nitrile metabolite. This metabolite is highly cytotoxic to trypanosomes and is considered the primary effector molecule. [] []
Q2: Does this compound's mechanism involve oxidative stress?
A2: While earlier studies suggested oxidative stress as the primary mechanism, recent research points to the crucial role of type I NTR-mediated activation and the formation of a cytotoxic nitrile metabolite. [] [] Although this compound can induce oxidative stress, this appears less critical for its selective toxicity towards trypanosomes.
Q3: What is the molecular formula and weight of this compound?
A3: this compound has a molecular formula of C11H13N3O5S and a molecular weight of 287.3 g/mol.
Q4: Is there any spectroscopic data available for this compound?
A5: Yes, studies utilize techniques like high-performance liquid chromatography (HPLC) coupled with high-resolution mass spectrometry (HRMS) and HRMS/MS, alongside offline liquid scintillation counting of radiolabeled samples, to analyze this compound and its metabolites. Nuclear magnetic resonance (NMR) spectroscopy is also employed for structural confirmation. []
Q5: Are there studies exploring this compound stability under different conditions?
A6: Yes, research indicates that food intake significantly enhances this compound bioavailability, suggesting its absorption is influenced by food intake. [] This highlights the importance of administration conditions for optimal drug exposure.
Q6: Does this compound possess any catalytic properties itself?
A7: this compound itself is not known to exhibit catalytic properties. It acts as a prodrug, relying on enzymatic activation by the trypanosomal type I NTR for its anti-parasitic activity. [] []
Q7: Have there been any computational studies on this compound?
A7: There is limited information available regarding specific computational studies or QSAR models developed for this compound in the provided abstracts.
Q8: How do structural modifications of this compound affect its trypanocidal activity?
A9: Research on 5-nitrofurans, a class of compounds similar to this compound, reveals that even minor structural modifications significantly impact their interaction with TbNTR. Some modifications resulted in compounds with a 50-fold higher affinity for TbNTR than this compound. [] These derivatives also exhibited enhanced trypanocidal activity with lower IC50 values. [] Further research is necessary to fully understand the SAR of this compound and optimize its efficacy.
Q9: Are there any 5-nitrofurans with improved activity against this compound-resistant trypanosomes?
A10: Yes, pentacyclic nitrofurans, structurally distinct from this compound, demonstrated potent activity against both drug-susceptible and this compound-resistant trypanosome strains. [] This suggests a different activation mechanism for these compounds, making them promising candidates for overcoming this compound resistance.
Q10: Are there any formulation strategies to improve this compound's bioavailability?
A11: Recent studies have focused on developing new formulations of this compound, particularly for pediatric use. The development of divisible and dispersible tablets (30 mg and 120 mg) has been shown to improve dose accuracy. [] Additionally, administration with food significantly enhances this compound bioavailability. []
Q11: Is there information on the environmental impact of this compound?
A11: The provided abstracts do not offer specific details about the environmental impact or degradation pathways of this compound. Further investigation is needed to assess its potential ecotoxicological effects and appropriate waste management strategies.
Q12: How is this compound metabolized in the body?
A13: this compound undergoes extensive metabolism, primarily through reduction and nucleophilic attack, with some evidence of oxidation. More than 30 metabolites have been identified in the urine of rats administered this compound. [] Interestingly, typical hepatic and renal drug-metabolizing enzymes do not appear to play a major role in this compound's metabolism. []
Q13: What is the efficacy of this compound in treating Chagas disease in children?
A15: A recent study (CHICO) demonstrated that this compound administered for 60 days, with age- and weight-adjusted dosing, was superior to historical placebo controls in achieving a serological response at 12 months post-treatment in children with Chagas disease. [] The study also confirmed a favorable safety profile for the drug in this population. [] Further long-term follow-up is needed to evaluate the durability of the response and the potential for cure.
Q14: Has this compound shown any efficacy against other parasitic diseases?
A16: Studies have explored this compound's potential against Toxoplasma gondii, the parasite responsible for toxoplasmosis. While this compound alone showed limited efficacy, combining it with pyrimethamine significantly reduced mortality in infected mice compared to either drug alone. [] This suggests a possible synergistic effect and warrants further investigation.
Q15: Does this compound demonstrate activity against tumor cells?
A17: In vitro and in vivo studies have revealed that this compound exhibits cytotoxic activity against various tumor cell lines, including neuroblastoma and medulloblastoma. [] [] The drug induces apoptosis in these cells, potentially through mechanisms involving oxidative stress and modulation of signaling pathways like AKT-GSK3β. [] []
Q16: Are there any clinical trials investigating this compound for cancer treatment?
A18: Yes, a phase 1 dose-escalation trial in pediatric patients with relapsed/refractory neuroblastoma has been conducted. [] The study determined the maximum tolerated dose (MTD) and demonstrated that this compound was generally well-tolerated. Notably, some tumor responses were observed, both with this compound as a single agent and in combination with chemotherapy. []
Q17: What are the known mechanisms of resistance to this compound in trypanosomes?
A19: Resistance to this compound in Trypanosoma brucei has been linked to alterations in the type I NTR. Studies identified resistant parasites with either a loss of one NTR gene copy or a significant decrease in NTR transcription. [] This highlights the crucial role of this enzyme in this compound activation and the emergence of resistance.
Q18: Does cross-resistance exist between this compound and other nitro drugs?
A20: Yes, significant cross-resistance has been observed between this compound and other nitro drugs, particularly fexinidazole, another nitroaromatic compound under investigation for trypanosomiasis. [] [] This cross-resistance is likely due to their shared reliance on the type I NTR for activation. [] []
Q19: Are there efforts to improve this compound delivery to specific targets?
A22: While the provided abstracts don't detail specific drug delivery strategies, one study explored encapsulating this compound in ethylcyanoacrylate nanoparticles. [] This formulation showed promising results in vitro, demonstrating enhanced trypanocidal activity against both trypomastigotes and intracellular amastigotes with reduced cytotoxicity compared to free this compound. [] This highlights the potential of nanoformulations for improving this compound delivery and therapeutic index.
Q20: What analytical methods are used to quantify this compound and its metabolites?
A24: High-performance liquid chromatography (HPLC) coupled with various detection methods, including high-resolution mass spectrometry (HRMS) and tandem mass spectrometry (MS/MS), is widely used for the identification and quantification of this compound and its metabolites in biological samples. []
Q21: How is the in vitro susceptibility of Trypanosoma cruzi to this compound determined?
A25: The MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay is a common method to assess the in vitro susceptibility of T. cruzi to this compound. This colorimetric assay measures cell viability and allows for the determination of the drug concentration that inhibits parasite growth by 50% (IC50). [] []
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