دورية أكاديمية
Molecular modeling of inhibitors against fructose bisphosphate aldolase from Candida albicans .
| العنوان: | Molecular modeling of inhibitors against fructose bisphosphate aldolase from Candida albicans . |
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| المؤلفون: | de Amorim AL; 1Grupo de Biocatálise e Biotransformação de Compostos Orgânicos, Universidade Federal do Amapá, Macapá, Amapá Brazil., de Lima AVM; 2Laboratório de Química Farmacêutica e Medicinal (PharMedChem), Universidade Federal do Amapá, Macapá, Amapá Brazil., Rosário ACAD; 2Laboratório de Química Farmacêutica e Medicinal (PharMedChem), Universidade Federal do Amapá, Macapá, Amapá Brazil., Souza ÉTDS; 2Laboratório de Química Farmacêutica e Medicinal (PharMedChem), Universidade Federal do Amapá, Macapá, Amapá Brazil., Ferreira JV; 2Laboratório de Química Farmacêutica e Medicinal (PharMedChem), Universidade Federal do Amapá, Macapá, Amapá Brazil., Hage-Melim LIDS; 2Laboratório de Química Farmacêutica e Medicinal (PharMedChem), Universidade Federal do Amapá, Macapá, Amapá Brazil. |
| المصدر: | In silico pharmacology [In Silico Pharmacol] 2018 Mar 09; Vol. 6 (1), pp. 2. Date of Electronic Publication: 2018 Mar 09 (Print Publication: 2018). |
| نوع المنشور: | Journal Article |
| اللغة: | English |
| بيانات الدورية: | Publisher: Springer-Verlag, GmbH Country of Publication: Germany NLM ID: 101623954 Publication Model: eCollection Cited Medium: Print ISSN: 2193-9616 (Print) Linking ISSN: 21939616 NLM ISO Abbreviation: In Silico Pharmacol Subsets: PubMed not MEDLINE |
| أسماء مطبوعة: | Original Publication: Heidelberg : Springer-Verlag, GmbH |
| مستخلص: | Candida albicans is an opportunistic pathogen that causes from vulvovaginal and oropharyngeal candidiasis to systemic infections. The enzyme 1,6-fructose bisphosphate aldolase class II (FBA II), is a macromolecule existing only in lower organisms, being essential for the survival of the pathogen due to its function of maintaining the glycolysis process. The aim of this paper was to evaluate the inhibitors of FBA II regarding their physicochemical, pharmacokinetic and toxicological properties and apply concepts of rational drug development to propose new compounds for the treatment of fungal infections of C. albicans. Physicochemical (HyperChem software and the webserver cactus) and ADME/Tox (PreADMET webserver) properties were calculated to four inhibitors described in the literature and three analogues. None of the compounds presented in this study violated RO5, however all inhibitors demonstrated low or moderate human intestinal absorption (HIA), as well as low or moderate permeability in Caco-2 and MDCK, poor plasma proteins binding (PPB) and low permeability of the blood-brain barrier (BBB); however, Compound 4 is the exception for BBB permeability, being also the only non-mutagenic compound, and therefore, used as a lead compound. Analogues B and C presented high HIA, weak PPB and low BBB permeability, as well as a positive prediction for carcinogenicity in rats and mouse and non-mutagenicity in the Ames test. Through the evaluations carried out, it was concluded that the analogues B and C have proved to be promising candidates for oral administration drugs in the treatment of fungal infections of the genus Candida. |
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| فهرسة مساهمة: | Keywords: Aldolase; Candida albicans; Fructose bisphosphate; Molecular modeling; Treatment |
| تواريخ الأحداث: | Date Created: 20190105 Latest Revision: 20240512 |
| رمز التحديث: | 20240512 |
| مُعرف محوري في PubMed: | PMC6314639 |
| DOI: | 10.1007/s40203-018-0040-x |
| PMID: | 30607315 |
| قاعدة البيانات: | MEDLINE |
Find this article in full text from Springer Verlag. 
Full Text Finder | تدمد: | 2193-9616 |
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| DOI: | 10.1007/s40203-018-0040-x |