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Novel Antifungal Compounds Discovered in Medicines for Malaria Venture’s Malaria Box

机译:疟疾风险投资公司疟疾药盒在药物中发现的新型抗真菌化合物

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Similarities in fungal and animal cells make antifungal discovery efforts more difficult than those for other classes of antimicrobial drugs. Currently, there are only three major classes of antifungal drugs used for the treatment of systemic fungal diseases: polyenes, azoles, and echinocandins. Even in situations where the offending fungal organism is susceptible to the available drugs, treatment courses can be lengthy and unsatisfactory, since eradication of infection is often very difficult, especially in individuals with impaired immunity. Consequently, there is a need for new and more effective antifungal drugs. We have identified compounds with significant antifungal activity in the Malaria Box (Medicines for Malaria Ventures, Geneva, Switzerland) that have higher efficacy than some of the currently used antifungal drugs. Our best candidate, MMV665943 (IUPAC name 4-[6-[[2-(4-aminophenyl)-3H-benzimidazol-5-yl]methyl]-1H-benzimidazol-2-yl]aniline), here referred to as DM262, showed 16- to 32-fold-higher activity than fluconazole against Cryptococcus neoformans . There was also significant antifungal activity in other fungal species with known antifungal resistance, such as Lomentospora prolificans and Cryptococcus gattii . Antifungal activity was also observed against a common fungus, Candida albicans . These results are important because they offer a potentially new class of antifungal drugs and the repurposing of currently available therapeutics. IMPORTANCE Much like the recent increase in drug-resistant bacteria, there is a rise in antifungal-resistant strains of pathogenic fungi. There is a need for novel and more potent antifungal therapeutics. Consequently, we investigated a mixed library of drug-like and probe-like compounds with activity in Plasmodium spp. for activity against two common fungal pathogens, Cryptococcus neoformans and Candida albicans , along with two less common pathogenic species, Lomentospora prolificans and Cryptococcus gattii . We uncover a previously uncharacterized drug with higher broad-spectrum antifungal activity than some current treatments. Our findings may eventually lead to a compound added to the arsenal of antifungal therapeutics.
机译:真菌和动物细胞中的相似性使得抗真菌发现的努力比其他类型的抗微生物药物更加困难。当前,用于治疗系统性真菌病的抗真菌药只有三大类:多烯,唑类和棘球and素。即使在侵害性真菌有机体对可用药物敏感的情况下,治疗过程也可能漫长且不令人满意,因为根除感染通常非常困难,尤其是在免疫力受损的个体中。因此,需要新的和更有效的抗真菌药。我们在“疟疾药箱”(瑞士日内瓦的疟疾风险药物)中鉴定出具有显着抗真菌活性的化合物,其功效比某些目前使用的抗真菌药物高。我们最好的候选人,MMV665943(IUPAC名称为4- [6-[[2-(4-(4-氨基苯基)-3H-苯并咪唑-5-基]甲基] -1H-苯并咪唑-2-基]苯胺),此处称为DM262 ,对新生隐球菌的活性比氟康唑高16到32倍。在其他具有已知抗真菌耐药性的真菌物种中,例如多产黑门孢菌(Lomentospora prolificans)和加氏隐球菌(Cryptococcus gattii),也具有显着的抗真菌活性。还观察到了对普通真菌白色念珠菌的抗真菌活性。这些结果很重要,因为它们提供了潜在的新型抗真菌药物,并且重新定位了当前可用的治疗方法。重要事项就像最近耐药菌的增加一样,病原真菌的抗真菌菌株也有所增加。需要新颖和更有效的抗真菌治疗剂。因此,我们研究了在疟原虫属物种中具有活性的类药物和类探针化合物的混合文库。对两种常见的真菌病原体,新隐球菌和白色念珠菌,以及两种较不常见的致病菌,多产牙形孢子虫和加蒂隐球菌,具有活性。我们发现比以前的某些治疗方法具有更高广谱抗真菌活性的以前未表征的药物。我们的发现最终可能导致将某种化合物添加到抗真菌治疗药库中。

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