Literature DB >> 20167484

The synthesis and angiotensin converting enzyme (ACE) inhibitory activity of chalcones and their pyrazole derivatives.

Marco Bonesi1, Monica R Loizzo, Giancarlo A Statti, Sylvie Michel, François Tillequin, Francesco Menichini.   

Abstract

A series of chalcones (1-9) and pyrazoles (10-18) was prepared to investigate their potential activity as Angiotensin I-Converting Enzyme (ACE) inhibitors. Their structures were verified by elemental analysis, UV, IR, MS, (1)H NMR, (13)C NMR, and 2D NMR experiments. Among tested compounds, chalcone 7 exerted the highest activity with an IC(50) value of 0.219 mM, while the most potent pyrazole was 15 (IC(50) value of 0.213 mM). Copyright 2010 Elsevier Ltd. All rights reserved.

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Year:  2010        PMID: 20167484     DOI: 10.1016/j.bmcl.2010.01.113

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  3 in total

1.  TfOH mediated intermolecular electrocyclization for the synthesis of pyrazolines and its application in alkaloid synthesis.

Authors:  Sesuraj Babiola Annes; Pothiappan Vairaprakash; Subburethinam Ramesh
Journal:  RSC Adv       Date:  2018-08-24       Impact factor: 4.036

2.  Antimicrobial screening and one-pot synthesis of 4-(substituted-anilinomethyl)-3-(2-naphthyl)-1-phenyl-1H-pyrazole derivatives.

Authors:  Neelima Goel; Sushma Drabu; Obaid Afzal; Sandhya Bawa
Journal:  J Pharm Bioallied Sci       Date:  2014-10

Review 3.  Current status of pyrazole and its biological activities.

Authors:  Mohd Javed Naim; Ozair Alam; Farah Nawaz; Md Jahangir Alam; Perwaiz Alam
Journal:  J Pharm Bioallied Sci       Date:  2016 Jan-Mar
  3 in total

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