Design, Synthesis, Antimicrobial Activity, and Molecular Docking of Novel Thiazoles, Pyrazoles, 1,3-Thiazepinones, and 1,2,4-Triazolopyrimidines Derived from Quinoline-Pyrido[2,3-d] Pyrimidinones

The SAR study confirmed a relationship between antimicrobial activity and the tested compounds. Molecular docking demonstrated that compounds <b>10</b>, <b>11</b>, <b>12</b>, <b>13</b>, and <b>14</b> exhibited significant binding energy, effectively interacting with the active sites of antimicrobial protein receptors. This consistent finding supports that these new compounds' practical and theoretical studies align regarding their antimicrobial activity.

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Publication Details

Journal
Pharmaceuticals
Published
2024-12-04
DOI
https://doi.org/10.3390/ph17121632
Citations
28
Primary Topic
Synthesis and biological activity
Type
article
Field-Weighted Citation Impact
7.00

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article

Design, Synthesis, Antimicrobial Activity, and Molecular Docking of Novel Thiazoles, Pyrazoles, 1,3-Thiazepinones, and 1,2,4-Triazolopyrimidines Derived from Quinoline-Pyrido[2,3-d] Pyrimidinones

Sami A. Al‐Hussain, Ameen A. Abu‐Hashem
28 citations
Pharmaceuticals
Synthesis and biological activity
7.00
article

Design, Synthesis, Antimicrobial Activity, and Molecular Docking of Novel Thiazoles, Pyrazoles, 1,3-Thiazepinones, and 1,2,4-Triazolopyrimidines Derived from Quinoline-Pyrido[2,3-d] Pyrimidinones

Sami A. Al‐Hussain, Ameen A. Abu‐Hashem
article en
28 citations

Abstract

The SAR study confirmed a relationship between antimicrobial activity and the tested compounds. Molecular docking demonstrated that compounds <b>10</b>, <b>11</b>, <b>12</b>, <b>13</b>, and <b>14</b> exhibited significant binding energy, effectively interacting with the active sites of antimicrobial protein receptors. This consistent finding supports that these new compounds' practical and theoretical studies align regarding their antimicrobial activity.

PharmaceuticalsVol. 17(12)
Imam Mohammad ibn Saud Islamic University (SA), Jazan University (SA)
National Research Centre
Openalex Percentile: Top 2%
Synthesis and biological activity
7.00
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