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Tytuł pozycji:

The Chemical Property Position of Bedaquiline Construed by a Chemical Global Positioning System-Natural Product.

Tytuł:
The Chemical Property Position of Bedaquiline Construed by a Chemical Global Positioning System-Natural Product.
Autorzy:
Alajlani MM; Pharmacognosy, BMC-Biomedical Center, Department of Pharmaceutical Biosciences, Faculty of Pharmacy, Uppsala University, S-75123 Uppsala, Sweden.; Department of Pharmaceutical Biology/Pharmacognosy, Institute of Pharmacy, University of Halle-Wittenberg, D-06120 Halle (Saale), Germany.; Faculty of Pharmacy, Main Campus, Qasyoun Private University, Damascus build 131, Syria.
Źródło:
Molecules (Basel, Switzerland) [Molecules] 2022 Jan 24; Vol. 27 (3). Date of Electronic Publication: 2022 Jan 24.
Typ publikacji:
Journal Article
Język:
English
Imprint Name(s):
Original Publication: Basel, Switzerland : MDPI, c1995-
MeSH Terms:
Databases, Chemical*
Diarylquinolines*/chemistry
Diarylquinolines*/pharmacology
Principal Component Analysis*
Antitubercular Agents/chemistry ; Antitubercular Agents/pharmacology ; Antitubercular Agents/therapeutic use ; Biological Products/chemistry ; Biological Products/pharmacology ; Cluster Analysis ; Computational Biology ; Drug-Related Side Effects and Adverse Reactions/diagnosis ; Forecasting/methods ; Humans ; Models, Theoretical ; Quantitative Structure-Activity Relationship ; Tuberculosis, Multidrug-Resistant/drug therapy
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Contributed Indexing:
Keywords: ChemGPS-NP; antituberculosis agents; bedaquiline; chemical property space; data mining; screening; structural similarity
Substance Nomenclature:
0 (Antitubercular Agents)
0 (Biological Products)
0 (Diarylquinolines)
78846I289Y (bedaquiline)
Entry Date(s):
Date Created: 20220215 Date Completed: 20220228 Latest Revision: 20220228
Update Code:
20240105
PubMed Central ID:
PMC8838968
DOI:
10.3390/molecules27030753
PMID:
35164018
Czasopismo naukowe
Bedaquiline is a novel adenosine triphosphate synthase inhibitor anti-tuberculosis drug. Bedaquiline belongs to the class of diarylquinolines, which are antituberculosis drugs that are quite different mechanistically from quinolines and flouroquinolines. The fact that relatively similar chemical drugs produce different mechanisms of action is still not widely understood. To enhance discrimination in favor of bedaquiline, a new approach using eight-score principal component analysis (PCA), provided by a ChemGPS-NP model, is proposed. PCA scores were calculated based on 35 + 1 different physicochemical properties and demonstrated clear differences when compared with other quinolines. The ChemGPS-NP model provided an exceptional 100 compounds nearest to bedaquiline from antituberculosis screening sets (with a cumulative Euclidian distance of 196.83), compared with the different 2Dsimilarity provided by Tanimoto methods (extended connective fingerprints and the Molecular ACCess System, showing 30% and 182% increases in cumulative Euclidian distance, respectively). Potentially similar compounds from publicly available antituberculosis compounds and Maybridge sets, based on bedaquiline's eight-dimensional similarity and different filtrations, were identified too.
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