Multitarget Enzyme Inhibition and Anticancer Potential of 3‐Substituted Indole Derivatives Supported by Molecular Docking Studies
= 38.43 and 47.53 µM at 48 h). These indole-based derivatives are also subjected to a structure-activity relationship (SAR) study by the molecular docking method. Most indole derivatives showed enzyme inhibition results similar to, but below, those of the standard drug.
Authors
- Natalia Berdzik (ORCID: https://orcid.org/0000-0002-5113-6026)
- Ercan Oğuz (ORCID: https://orcid.org/0000-0002-8737-9986)
- Karolina Babijczuk (ORCID: https://orcid.org/0000-0002-5620-1800)
- Fikret Türkan (ORCID: https://orcid.org/0000-0002-0538-3157)
- Beata Jasiewicz (ORCID: https://orcid.org/0000-0002-6741-473X)
- Adnan Cetin
- Ceylan Kurgan
Institutions
- Van Yüzüncü Yıl Üniversitesi (TR)
- University of Turku (FI)
- Başkent University (TR)
- Department of Health Services (NP)
- Adam Mickiewicz University in Poznań (PL)
- Nakhchivan State University (AZ)
Publication Details
- Journal
- Biotechnology and Applied Biochemistry
- Published
- 2026-04-01
- DOI
- https://doi.org/10.1002/bab.70166
- Primary Topic
- Enzyme function and inhibition
- Type
- article
- Field-Weighted Citation Impact
- 0.00