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Pharmacophore Assessment Through 3-D QSAR: Evaluation of the Predictive Ability on New Derivatives by the Application on a Series of Antitubercular Agents

https://doi.org/10.1021/ci400132q
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Synthesis, biological evaluation and SAR study of novel pyrazole analogues as inhibitors of Mycobacterium tuberculosis
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1,5-Diaryl-2-ethyl pyrrole derivatives as antimycobacterial agents: Design, synthesis, and microbiological evaluation
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Electrogenerated acetonitrile anion induced selective N-alkylation of bifunctional compounds
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Building a pharmacophore model for a novel class of antitubercular compounds
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4Tuberculosis Chemotherapy: Recent Developments and Future Perspectives
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Antimycobacterial pyrroles: synthesis, anti-Mycobacterium tuberculosis activity and QSAR studies
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Importance of the thiomorpholine introduction in new pyrrole derivatives as antimycobacterial agents analogues of BM 212
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3-D QSAutogrid/R: An Alternative Procedure To Build 3-D QSAR Models. Methodologies and Applications
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Antimycobacterial Agents. Novel Diarylpyrrole Derivatives of BM212 Endowed with High Activity toward Mycobacterium tuberculosis and Low Cytotoxicity
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1,5-Diphenylpyrrole Derivatives as Antimycobacterial Agents. Probing the Influence on Antimycobacterial Activity of Lipophilic Substituents at the Phenyl Rings
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What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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SERS Spectra and MD Simulations of a Bioactive Diiodobenzaldehyde Derivative: Experimental and Theoretical Investigations
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Vascular endothelial growth factor receptor-2 (VEGFR-2) inhibitors: development and validation of predictive 3-D QSAR models through extensive ligand- and structure-based approaches
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QSAR based therapeutic management of M. tuberculosis
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Investigating the regio-, stereo-, and enantio-selectivities of the [3 + 2] cycloaddition reaction of C, N-diarylnitrone derivatives with N-propadienylindole derivatives. A DFT study
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Mannich bases in medicinal chemistry and drug design
inferred← citeshttps://doi.org/10.1016/j.ejmech.2017.05.026openalex-snapshot
QSAR-driven design, synthesis and discovery of potent chalcone derivatives with antitubercular activity
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Insights into development of Decaprenyl-phosphoryl-β-D-ribose 2′-epimerase (DprE1) inhibitors as antitubercular agents: A state of the art review
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Understanding the Molecular Determinant of Reversible Human Monoamine Oxidase B Inhibitors Containing 2H-Chromen-2-One Core: Structure-Based and Ligand-Based Derived Three-Dimensional Quantitative Structure–Activity Relationships Predictive Models
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In Memory of Maurizio Botta: His Contribution to the Development of Computer-Aided Drug Design
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Hsp90 Inhibitors, Part 1: Definition of 3-D QSAutogrid/R Models as a Tool for Virtual Screening
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