Anticancer SAR establishment and α/β-tubulin isoform specific targeting: a detailed insight of the anticancer potential of 4H-chromene derivatives

Author:

Mayank 12ORCID,Singh Ashutosh3,Saumya Kumar Udit3,Joshi Mayank4ORCID,Kaur Navneet5ORCID,Garg Neha36ORCID,Singh Narinder1ORCID

Affiliation:

1. Department of Chemistry, Indian Institute of Technology Ropar, Punjab 140001, India

2. University College of Pharmacy, Guru Kashi University, Talwandi Sabo, India

3. School of Basic Sciences, Indian Institute of Technology Mandi, Himachal Pradesh 175005, India

4. M. M. College of Pharmacy, Maharishi Markandeshwar (Deemed to be University), Mullana, Ambala, Haryana, 133207, India

5. Department of Chemistry, Punjab University, Chandigarh, 160014, India

6. Department of Medicinal Chemistry, Faculty of Ayurveda, Institute of Medical Sciences, Banaras Hindu University, Varanasi, Uttar Pradesh-221005, India

Abstract

The anticancer activity of chromene derivatives was explored. MNC-1 showed the best anticancer potential and is expected to deliver the best activity against cancer cells with β1 and/or β8 over-expression.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

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