4.6 Article

Fulvestrant-3-Boronic Acid (ZB716) Demonstrates Oral Bioavailability and Favorable Pharmacokinetic Profile in Preclinical ADME Studies

相关参考文献

注意:仅列出部分参考文献,下载原文获取全部文献信息。
Review Chemistry, Multidisciplinary

From Pure Antagonists to Pure Degraders of the Estrogen Receptor: Evolving Strategies for the Same Target

Madhusoodanan Mottamal et al.

Summary: Research has been ongoing to find orally bioavailable SERDs for the treatment of advanced breast cancer, with the currently FDA-approved pure antiestrogen fulvestrant limited in efficacy due to its low bioavailability. Early oral SERDs have not shown significant improvement in clinical trials, but hope lies in the new generation of basic SERD molecules and PROTAC ER degraders with improved oral bioavailability, low toxicity, and superior efficacy in receptor degradation.

ACS OMEGA (2021)

Article Chemistry, Medicinal

Fulvestrant-3 Boronic Acid (ZB716): An Orally Bioavailable Selective Estrogen Receptor Downregulator (SERD)

Jiawang Liu et al.

JOURNAL OF MEDICINAL CHEMISTRY (2016)

Review Oncology

A Good Drug Made Better: The Fulvestrant Dose-Response Story

John F. R. Robertson et al.

CLINICAL BREAST CANCER (2014)

Article Oncology

Final Overall Survival: Fulvestrant 500 mg vs 250 mg in the Randomized CONFIRM Trial

Angelo Di Leo et al.

JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE (2014)

Article Chemistry, Medicinal

Boron-Based 4-Hydroxytamoxifen Bioisosteres for Treatment of de Novo Tamoxifen Resistant Breast Cancer

Quan Jiang et al.

ACS MEDICINAL CHEMISTRY LETTERS (2012)

Article Oncology

Fulvestrant: pharmacokinetics and pharmacology

JFR Robertson et al.

BRITISH JOURNAL OF CANCER (2004)

Article Oncology

FDA drug approval summaries: Fulvestrant

PF Bross et al.

ONCOLOGIST (2002)