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Exploring biological activities of novel Schiff bases derived from amlodipine and in silico molecular modeling studies.
Masood, Anum; Khan, Mohsin Abbas; Bhat, Mashooq A; Awan, Breena; Hanif, Ramsha; Raza, Asim; Khaliq, Saharish; Ahmed, Javaid; Ullah, Farhat.
Afiliación
  • Masood A; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, The islamia University of Bahawalpur, P.O Box 63100, Pakistan.
  • Khan MA; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, The islamia University of Bahawalpur, P.O Box 63100, Pakistan.
  • Bhat MA; Institute of Pharmaceutical Science, Faculty of Life Science and Medicine, King's College, London, SE1 9NH, UK.
  • Awan B; Department of Pharmaceutical Chemistry, College of Pharmacy, King Saud University Riyadh, P.O Box 11451, Saudi Arabia.
  • Hanif R; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, The islamia University of Bahawalpur, P.O Box 63100, Pakistan.
  • Raza A; Department of Pharmaceutical Chemistry, College of Pharmacy, University of Punjab, Lahore, P.O Box 05422, Pakistan.
  • Khaliq S; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, The islamia University of Bahawalpur, P.O Box 63100, Pakistan.
  • Ahmed J; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, The islamia University of Bahawalpur, P.O Box 63100, Pakistan.
  • Ullah F; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, The islamia University of Bahawalpur, P.O Box 63100, Pakistan.
Future Med Chem ; : 1-12, 2024 Sep 20.
Article en En | MEDLINE | ID: mdl-39303045
ABSTRACT

Aim:

Calcium channel antagonists are of considerable interest in treating elevated blood pressure and its pathologies.Materials &

methods:

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 (1H NMR, FTIR, 13C NMR) and docking studies also performed.Results &

conclusion:

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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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Future Med Chem Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Future Med Chem Año: 2024 Tipo del documento: Article
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