A new Suzuki synthesis of triphenylethylenes that inhibit aromatase and bind to estrogen receptors α and β-Reference-Cited by-同舟云学术

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A new Suzuki synthesis of triphenylethylenes that inhibit aromatase and bind to estrogen receptors α and β

Published:2016-11 Issue:21 Volume:24 Page:5400-5409
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Zhao Li-Ming,Jin Hai-Shan,Liu Jinzhong,Skaar Todd C.,Ipe Joseph,Lv Wei,Flockhart David A.,Cushman Mark

Funder

Purdue University Center for Cancer Research

Indiana University Center Joint Funding Award

Purdue Center for Cancer Research

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference39 articles.

1. Assessing Women at High Risk of Breast Cancer: A Review of Risk Assessment Models

2. Breast Cancer, Estrogen Receptor and Ligands

3. The evolution of nonsteroidal antiestrogens to become selective estrogen receptor modulators

4. An overview of current and emerging SERMs

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1. Dual-target inhibitors based on ERα: Novel therapeutic approaches for endocrine resistant breast cancer;European Journal of Medicinal Chemistry;2024-04

2. Aromatase Inhibitors as a Promising Direction for the Search for New Anticancer Drugs;Molecules;2024-01-10

3. Effectiveness of Selective Estrogen Receptor Modulators in Breast Cancer Therapy: An Update;Current Medicinal Chemistry;2023-09

4. An Exemestane Derivative, Oxymestane-D1, as a New Multi-Target Steroidal Aromatase Inhibitor for Estrogen Receptor-Positive (ER+) Breast Cancer: Effects on Sensitive and Resistant Cell Lines;Molecules;2023-01-12

5. A review on diverse heterocyclic compounds as the privileged scaffolds in non-steroidal aromatase inhibitors;Bioorganic Chemistry;2021-08

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