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Design, Synthesis, Antiproliferative Evaluation, and Molecular Docking Studies of <i>N</i>-(3-Hydroxyindole)-Appended β-Carbolines/Tetrahydro-β-Carbolines Targeting Triple-Negative and Non-Triple-Negative Breast Cancer

Bharvi Sharma, Sourav Saha, Shanen Perumal, Liang Gu, Oluwakemi Ebenezer, Parvesh Singh, Mandeep Kaur, Vipan Kumar

2020ACS Omega11 citationsDOIOpen Access PDF

Abstract

values of 13.61 and 22.76 μM against MCF-7 (ER+) and MDA-MB-231 (ER-) cells, respectively. The docking studies were found to be consistent with experimental results owing to the stronger binding affinity of the synthesized conjugates via hydrophobic and H-bonding interactions.

Topics & Concepts

Triple-negative breast cancerTriple bondBreast cancerCancer researchChemistryCancerComputational biologyCombinatorial chemistryBiologyGeneticsOrganic chemistryDouble bondSynthesis and bioactivity of alkaloidsMulticomponent Synthesis of HeterocyclesSynthesis and Biological Evaluation
Design, Synthesis, Antiproliferative Evaluation, and Molecular Docking Studies of <i>N</i>-(3-Hydroxyindole)-Appended β-Carbolines/Tetrahydro-β-Carbolines Targeting Triple-Negative and Non-Triple-Negative Breast Cancer | Litcius