Synthesis and in Silico Docking Studies of Ethyl 2‐(2‐Arylidene‐1‐alkylhydrazinyl)thiazole‐4‐carboxylates as Antiglycating Agents

Author:

Shahzadi Kiran1,Haroon Muhammad12ORCID,Khalid Muhammad3,Akhtar Tashfeen1ORCID,Ghous Tahseen1,Alam Mohammed Mujahid4,Imran Muhammad4

Affiliation:

1. Department of Chemistry Mirpur University of Science and Technology (MUST) 10250- Mirpur (AJK) Pakistan

2. Department of Chemistry, Government Major Muhammad Afzal Khan (Shaheed), Boys Degree College Afzalpur Mirpur (Affiliated with Mirpur University of Science and Technology (MUST) 10250- Mirpur (AJK) Pakistan

3. Department of Chemistry Khwaja Fareed University of Engineering & Information Technology Rahim Yar Khan 64200 Pakistan

4. Department of Chemistry Faculty of Science King Khalid University P.O. Box 9004 Abha 61413 Saudi Arabia

Funder

Department of Chemistry, University of York

Publisher

Wiley

Subject

Molecular Biology,Molecular Medicine,General Chemistry,Biochemistry,General Medicine,Bioengineering

Reference44 articles.

1. ‘Dehydrated Foods, Chemistry of Browning Reactions in Model Systems’;Hodge J. E.;J. Agric. Food Chem.,1953

2. ‘Dietary advanced glycation end-product restriction for the attenuation of insulin resistance, oxidative stress and endothelialdysfunction: a systematic review’;Kellow N. J.;Euro. J. Clin. Nutr.,2013

3. ‘Antiglycation potential of commercially available extracts of two Indian medicinal plants: Pterocarpus marsupium and Artocarpus lakoocha using advanced glycation end products (AGE) competitive fluorescence assay’;Pande A.;Cogent Food Agric.,2021

4. ‘Advanced glycation end products: sparking the development of diabetic vascular injury’;Goldin A.;Circulation,2006

5. ‘Formation of crossline as a fluorescent advanced glycation end product in vitro and in vivo’;Obayashia H.;Biochem. Biophys. Res. Commun.,1996

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