Literature DB >> 27485744

Chemoinformatic expedition of the chemical space of fungal products.

Mariana González-Medina1, Fernando D Prieto-Martínez1, J Jesús Naveja1, Oscar Méndez-Lucio1, Tamam El-Elimat2, Cedric J Pearce3, Nicholas H Oberlies4, Mario Figueroa1, José L Medina-Franco1.   

Abstract

AIM: Fungi are valuable resources for bioactive secondary metabolites. However, the chemical space of fungal secondary metabolites has been studied only on a limited basis. Herein, we report a comprehensive chemoinformatic analysis of a unique set of 207 fungal metabolites isolated and characterized in a USA National Cancer Institute funded drug discovery project.
RESULTS: Comparison of the molecular complexity of the 207 fungal metabolites with approved anticancer and nonanticancer drugs, compounds in clinical studies, general screening compounds and molecules Generally Recognized as Safe revealed that fungal metabolites have high degree of complexity. Molecular fingerprints showed that fungal metabolites are as structurally diverse as other natural products and have, in general, drug-like physicochemical properties.
CONCLUSION: Fungal products represent promising candidates to expand the medicinally relevant chemical space. This work is a significant expansion of an analysis reported years ago for a smaller set of compounds (less than half of the ones included in the present work) from filamentous fungi using different structural properties.

Entities:  

Keywords:  chemical space; chemoinformatics; fungal metabolites; master key compound; molecular complexity; molecular fingerprint

Mesh:

Substances:

Year:  2016        PMID: 27485744      PMCID: PMC5558535          DOI: 10.4155/fmc-2016-0079

Source DB:  PubMed          Journal:  Future Med Chem        ISSN: 1756-8919            Impact factor:   3.808


  41 in total

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4.  Cheminformatic comparison of approved drugs from natural product versus synthetic origins.

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5.  Peptaibols from two unidentified fungi of the order Hypocreales with cytotoxic, antibiotic, and anthelmintic activities.

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2.  Cheminformatic characterization of natural products from Panama.

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Review 7.  Screening and identification of novel biologically active natural compounds.

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9.  Cytotoxic Naphthoquinone Analogues, Including Heterodimers, and Their Structure Elucidation Using LR-HSQMBC NMR Experiments.

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