Mifepristone

"目录号: HY-13683

OthersGPCR/G ProteinAutophagy-

Mifepristone 是一种孕激素受体 (progesterone receptorPR) 拮抗剂,T47D 细胞检测中,IC50为 0.2 nM,Mifepristone也是一种糖皮质激素受体(glucocorticoid receptorGR)拮抗剂,在 A549 细胞检测中,IC50为 2.6 nM。

Progesterone ReceptorGlucocorticoid ReceptorAutophagy

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生物活性

Description

Mifepristone is aprogesterone receptor(PR) antagonist (IC50=0.2 nM) in a T47D cell-based assay, also is aglucocorticoid receptor(GR) antagonist (IC50=2.6 nM) in an A549 cell-based assay.

IC50& Target

IC50: 0.2 nM (progesterone receptor, in T47D cells), 2.6 nM (glucocorticoid receptor, in A549 cells)[1]

In Vitro

The discovery of the first competitive progesterone antagonist, Mifepristone, has stimulated an intense search for more potent and more selective antiprogestins[1]. Cell growth is evaluated after 4 days of exposure to Mifepristone at 10 μM, a concentration close to the plasma concentration achievable in humans. The antiproliferative effect of Cisplatin is potentiated when administered in combination with Mifepristone in HeLa cells. The IC50of Cisplatin in combination with Mifepristone is lower (14.2 μM) than that of Cisplatin alone (34.2 μM) in HeLa cells with an approximately 2.5-fold difference. After treatment with Mifepristone, the accumulation of intracellular Cisplatin in HeLa cells is 2-fold greater, representing a significant difference (p=0.009), compare with Cisplatin alone from 0.79 to 1.52 μg/mg of protein[2].

In Vivo

The cervix tumor xenograft models are treated with Cisplatin alone, there is a tumor growth inhibition compare with control group. However, the tumor weight loss is even more significant (p<0.05) with the combination of Cisplatin and Mifepristone at the doses used, showing a decrease of ~50% compared with the treatments alone by the end of the study[2]. Adult male Sprague-Dawley rats are subjected to a 4-day binge-like EtOH administration regimen (3 to 5 g/kg/i.g. every 8 hours designed to produce peak blood EtOH levels (BELs) of <300 mg/dL). Subgroups of animals receive s.c. injection of Mifepristone (20 or 40 mg/kg in peanut oil). Although Mifepristone produces no significant changes in behavior of EtOH-na?ve animals, pretreatment with Mifepristone (40 mg/kg) significantly reducesthe severity of EtOH withdrawal. Asignificant interaction between diet and drug, F(5,55)=3.92, p<0.05, such that EtOH-treated animals receiving vehicle or 20 mg/kg of Mifepristone displayssignificantly more signs of EtOH withdrawal than does EtOH-na?ve animals receiving the same drug treatment. Importantly, treatment with 40 mg/kg of Mifepristone significantly reduces the severity of EtOH withdrawal, in a dose-dependent manner[3].

Clinical Trial

NCT01811056

Gynuity Health Projects

Termination of Pregnancy

April 2013

NCT00832871

New Mexico Cancer Care Alliance-The Feminist Majority Foundation

Cancer

November 2008

NCT01224509

University of Southern California

Cervical Prostaglandin EP3 Receptors-Pregnancy

September 2004

NCT00712595

Mediterranea Medica S. L.

Uterine Fibroids

January 2007

Phase 2-Phase 3

NCT00936741

Corcept Therapeutics

Cushing's Syndrome

July 2009

Phase 3

NCT01990560

Icahn School of Medicine at Mount Sinai

Mild Hypercortisolism

November 2013

Phase 4

NCT00140478

Dana-Farber Cancer Institute-Beth Israel Deaconess Medical Center-Massachusetts General Hospital-Brigham and Women's Hospital-Georgetown University

Prostate Cancer-Adenocarcinoma of Prostate

February 2005

Phase 2

NCT02642939

Check, Jerome H., M.D., Ph.D.-Corcept Therapeutics

Non-Small Cell Lung Cancer (NSCLC)

December 2015

Phase 2

NCT00886873

Mediterranea Medica S. L.

Uterine Fibroids

May 2008

Phase 2-Phase 3

NCT01636063

Boston University-Society of Family Planning

Induced Abortion-Abortion Techniques-Mifepristone-Misoprostol

June 2012

NCT01786226

Mediterranea Medica S. L.

Uterine Fibroids

March 2010

Phase 2-Phase 3

NCT01925092

Corcept Therapeutics-Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Cushing's Disease

August 2013

Phase 3

NCT02720991

Gynuity Health Projects-Hopital La Rabta

Abortion, 3 Months

July 2014

Phase 4

NCT00177372

University of Pittsburgh

Anembryonic Pregnancy-Gestation Abnormality-Intrauterine Fetal Demise Term

January 2005

Phase 4

NCT00133705

University of Rochester-Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Leiomyoma

July 2003

Phase 3

NCT00637494

Corcept Therapeutics

Psychotic Depression-Severe Major Depression With Psychotic Features-Psychosis

March 2008

Phase 3

NCT02651844

Hospital Provincial Magdalena V. de Martínez-Agencia Nacional de Promoción de Ciencia y Tecnología, MINCYT-Instituto de Biología y Medicina Experimental (IBYME-CONICET)

Breast Cancer

April 2016

NCT01134198

New York State Psychiatric Institute

Cocaine Dependence

May 2010

Phase 2-Phase 3

NCT00505739

M.D. Anderson Cancer Center

Endometrial Cancer

September 2001

Phase 2

NCT01798017

Gynuity Health Projects

Menstrual Regulation

November 2012

Phase 4

NCT01371565

Corcept Therapeutics

Cushing's Disease-Cushing's Syndrome

November 2010

Phase 3

NCT02620904

Montefiore Medical Center

Intrauterine Fetal Demise-Fetal Death

February 2016

Phase 4

NCT02014337

Corcept Therapeutics

Breast Cancer-Ovarian Epithelial Cancer Recurrent-Sarcoma-Non-small Cell Lung Cancer-Carcinoma, Transitional Cell-Prostate Cancer-Prostatic Neoplasms

January 2014

Phase 1

NCT00386282

Gynuity Health Projects

Abortion, First Trimester

September 2006

NCT00994734

Gynuity Health Projects

Termination of Pregnancy

May 2009

NCT00881140

BioPro Medical Ltd

Uterine Fibroid-Vaginal Bleeding.

April 2009

Phase 2

NCT03210324

China Resources Zizhu Pharmaceutical Co., Ltd.

Uterine Fibroid

June 1, 2017

Phase 4

NCT00285818

Stanford University

Depression

January 2003

NCT03052400

Charles Drew University of Medicine and Science

Type 2 Diabetes Mellitus-Insulin Resistance

February 3, 2017

Phase 2

NCT00186056

Stanford University

Depression

January 2003

NCT00752843

Corcept Therapeutics

Healthy Subjects

September 2008

Phase 1

NCT01768299

Gynuity Health Projects

Complete Uterine Evacuation After Use of Study Drugs

February 2013

Phase 4

NCT03015701

Southwest Oncology Group-National Cancer Institute (NCI)

Meningioma

August 1992

Phase 3

NCT01739335

VA Office of Research and Development

Stress Disorders, Post-Traumatic

November 19, 2012

Phase 2

NCT00208156

Corcept Therapeutics

Depressive Disorder, Major

May 2005

Phase 3

NCT00128505

Corcept Therapeutics

Major Depressive Disorder-Psychotic Disorders

August 2005

Phase 3

NCT01333098

Eric Lenze-Washington University School of Medicine

Anxiety Disorders

September 2012

Phase 1-Phase 2

NCT03225547

University of Chicago

Advanced HER2-negative Breast Cancer

September 2017

Phase 2

NCT00359125

University of British Columbia-Western Economic Diversification Canada-Stanley Medical Research Institute

Bipolar Depression

July 2006

Phase 2

NCT00957346

Gynuity Health Projects-University of Puerto Rico

Abortion, Induced

February 2011

Phase 3

NCT00969982

Gynuity Health Projects

Abortion, Induced

June 2009

NCT01138553

University of California, San Diego

Invasive Breast Cancer-Ductal Carcinoma in Situ

June 2010

Early Phase 1

NCT02342002

Gynuity Health Projects

Missed Abortion-Pregnancy

January 2015

Phase 4

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