Synthesis, biological evaluation, and docking study of indole aryl sulfonamides as aromatase inhibitors
- 1 January 2020
- journal article
- research article
- Published by Elsevier in European Journal of Medicinal Chemistry
- Vol. 185, 111815
Abstract
No abstract availableKeywords
Funding Information
- Università degli Studi G. d'Annunzio Chieti - Pescara
This publication has 36 references indexed in Scilit:
- Breast Cancer TreatmentJAMA, 2019
- Polyphenolic natural products and natural product–inspired steroidal mimics as aromatase inhibitorsMedicinal Research Reviews, 2018
- Synthesis and biological characterization of 3-(imidazol-1-ylmethyl)piperidine sulfonamides as aromatase inhibitorsBioorganic & Medicinal Chemistry Letters, 2016
- Recent developments in steroidal and nonsteroidal aromatase inhibitors for the chemoprevention of estrogen-dependent breast cancerEuropean Journal of Medicinal Chemistry, 2015
- Synthesis and molecular docking of 1,2,3-triazole-based sulfonamides as aromatase inhibitorsBioorganic & Medicinal Chemistry, 2015
- Design, synthesis, and biological evaluation of resveratrol analogues as aromatase and quinone reductase 2 inhibitors for chemoprevention of cancerBioorganic & Medicinal Chemistry, 2010
- Combining Computational and Biochemical Studies for a Rationale on the Anti‐Aromatase Activity of Natural PolyphenolsChemMedChem, 2007
- Aromatase Inhibitors in Breast CancerNew England Journal of Medicine, 2003
- Aromatase—A Brief OverviewAnnual Review of Physiology, 2002
- Mechanisms of Estrogen ActionPhysiological Reviews, 2001