Exploring biological activities of novel Schiff bases derived from amlodipine and <i>in silico</i> molecular modeling studies

<b>Aim:</b> Calcium channel antagonists are of considerable interest in treating elevated blood pressure and its pathologies.<b>Materials & methods:</b> Schiff base derivatives of amlodipine were produced to check its urease inhibition potentials as well antibacterial and antioxidant activities. Structural illustration along with chemical characterization were achieved by spectral techniques (<sup>1</sup>H NMR, FTIR, <sup>13</sup>C NMR) and docking studies also performed.<b>Results & conclusion:</b> 3g displayed remarkable anti-hypertensive activity compared with parent drug. 3b, 3f and 3g showed urease inhibition potentials. These compounds can aid as lead for further investigations since they exhibited comparable or superior interactions.

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Journal
Future Medicinal Chemistry
Published
2024-09-20
DOI
https://doi.org/10.1080/17568919.2024.2401313
Primary Topic
Synthesis and biological activity
Type
article
Field-Weighted Citation Impact
0.00

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article

Exploring biological activities of novel Schiff bases derived from amlodipine and in silico molecular modeling studies

M. A. Bhat, Breena Awan, Farhat Ullah, Anum Masood et al.
Future Medicinal Chemistry
Synthesis and biological activity
article

Exploring biological activities of novel Schiff bases derived from amlodipine and in silico molecular modeling studies

M. A. Bhat, Breena Awan, Farhat Ullah, Anum Masood, Mohsin Abbas Khan, Asim Raza, Saharish Khaliq, Javaid Ahmed, Ramsha Hanif
article en

Abstract

<b>Aim:</b> Calcium channel antagonists are of considerable interest in treating elevated blood pressure and its pathologies.<b>Materials & methods:</b> Schiff base derivatives of amlodipine were produced to check its urease inhibition potentials as well antibacterial and antioxidant activities. Structural illustration along with chemical characterization were achieved by spectral techniques (<sup>1</sup>H NMR, FTIR, <sup>13</sup>C NMR) and docking studies also performed.<b>Results & conclusion:</b> 3g displayed remarkable anti-hypertensive activity compared with parent drug. 3b, 3f and 3g showed urease inhibition potentials. These compounds can aid as lead for further investigations since they exhibited comparable or superior interactions.

Future Medicinal ChemistryVol. 16(22)
University of the Punjab (PK), Islamia University of Bahawalpur (PK), King's College London (GB), King Saud University (SA)
King Saud University
Openalex Percentile: Top 89%
Synthesis and biological activity
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