Iridium(iii)–Cp*-(imidazo[4,5-f][1,10]phenanthrolin-2-yl)phenol analogues as hypoxia active, GSH-resistant cancer cytoselective and mitochondria-targeting cancer stem cell therapeutic agents

Author:

Kar Binoy1ORCID,Shanavas Shanooja2ORCID,Nagendra Apoorva H.2,Das Utpal1ORCID,Roy Nilmadhab1ORCID,Pete Sudhindra1ORCID,Sharma S Ajay1ORCID,De Sourav1ORCID,Kumar S K Ashok1ORCID,Vardhan Seshu3ORCID,Sahoo Suban K.3ORCID,Panda Debashis4ORCID,Shenoy Sudheer2ORCID,Bose Bipasha2ORCID,Paira Priyankar1ORCID

Affiliation:

1. Department of Chemistry, School of Advanced Sciences, Vellore Institute of Technology, Vellore-632014, Tamilnadu, India

2. Department Stem Cells and Regenerative Medicine Centre, Institution Yenepoya Research Centre, Yenepoya University, University Road, Derlakatte, Mangalore 575018, Karnataka, India

3. Department of Applied Chemistry, S. V. National Institute of Technology (SVNIT), Ichchanath, Surat, Gujrat-395007, India

4. Department of Basic Sciences and Humanities, Rajiv Gandhi Institute of Petroleum Technology, An Institution of National Importance, Jais, Amethi-229304, Uttar Pradesh, India

Abstract

GSH-resistant, hypoxia active iridium(iii)–Cp*-(imidazo[4,5-f][1,10]phenanthrolin-2-yl)phenol complexes were developed as highly cytoselective anticancer agents and mitochondria-targeting CSC therapeutic agents.

Funder

Department of Science and Technology, Ministry of Science and Technology, India

VIT University

Science and Engineering Research Board

Publisher

Royal Society of Chemistry (RSC)

Subject

Inorganic Chemistry

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