Chiral hydroxymethyl-1H,3H-pyrrolo[1,2-c]thiazoles: the search for selective p53-activating agents for colorectal cancer therapy

Author:

Hendrikx Mees M.1,Pereira Adelino M. R.1ORCID,Pereira Ana B.1,Carvalho Carla S. C.2,Ribeiro João L. P.1ORCID,Soares Maria I. L.1ORCID,Saraiva Lucília2ORCID,Pinho e Melo Teresa M. V. D.1ORCID

Affiliation:

1. University of Coimbra, Coimbra Chemistry Centre – Institute of Molecular Sciences and Department of Chemistry, 3004-535 Coimbra, Portugal

2. LAQV/REQUIMTE, Laboratório de Microbiologia, Departamento de Ciências Biológicas, Faculdade de Farmácia, Universidade do Porto, Porto, Portugal

Abstract

Structural modulation of a lead p53-activating anticancer molecule was performed, leading to the synthesis of new bioactive molecules. Activity against human colorectal cancer cells with different p53 status provided in-depth SAR data.

Funder

Fundação para a Ciência e a Tecnologia

Publisher

Royal Society of Chemistry (RSC)

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