Dutasteride

"目錄號(hào): HY-13613

Metabolic Enzyme/Protease-

Dutasteride (GG745)是5α還原酶同工酶抑制劑损离,還可能因其結(jié)構(gòu)域DHT相似對(duì)雄激素受體(AR)產(chǎn)生脫靶效應(yīng)。

5 alpha Reductase

相關(guān)產(chǎn)品

Finasteride-CGP-53153-

生物活性

Description

Dutasteride (GG745) is a potent inhibitor of both 5 alpha-reductase isozymes. Dutasteride may possess off-target effects on the androgen receptor (AR) due to its structural similarity to DHT.IC50 Value:Target:? 5 alpha-reductasein vitro: Dutasteride inhibited (3)H-T conversion to (3)H-DHT and, as anticipated, inhibited T-induced secretion of PSA and proliferation. However the drug also inhibited DHT-induced PSA secretion and cell proliferation (IC(50) approximately 1 microM). Dutasteride competed for binding the LNCaP cell AR with an IC(50) approximately 1.5 microM. High concentrations of dutasteride (10-50 microM), but not finasteride, in steroid-free medium, resulted in enhanced cell death, possibly by apoptosis [1]. Dutasteride reduces cell viability and cell proliferation in both cell lines tested (androgen-responsive (LNCaP) and androgen-unresponsive (DU145) human prostate cancer (PCa)) [2].in vivo: GG745 has a terminal half-life of approximately 240 hr, and single doses of >10 mg decreased DHT levels significantly more than did single 5-mg doses of finasteride [3]. In placebo treated men without prostate cancer there was an 8.3% median increase in PSA at month 24 compared with -59.5% in those who received dutasteride, using doubled values to correct for dutasteride treatment [4].Toxicity: Dutasteride may affect male fertility and steroid hormone dynamics. Therefore, a 21-day reproduction study was conducted to determine the effects of dutasteride (10, 32 and 100 μg/L) on fish reproduction. Exposure to dutasteride significantly reduced fecundity of fish and affected several aspects of reproductive endocrine functions in both males and females [5].Clinical trial: Bioequivalence Study Of Dutasteride Five 0.1 mg And One 0.5 mg Soft Gelatin Capsules In Healthy Male Volunteers. Phase 1

Clinical Trial

NCT00802321

UConn Health-National Institutes of Health (NIH)-National Institute on Alcohol Abuse and Alcoholism (NIAAA)

Alcohol Related Disorders-Alcoholism-Alcohol Abuse

April 2006

NCT01004809

GlaxoSmithKline

Alopecia

April 2010

NCT00985738

University of Colorado, Denver-GlaxoSmithKline

Prostate Cancer

September 2009

Phase 2

NCT00706966

University of California, San Francisco

Nonmalignant Neoplasm-Prostate Cancer

June 2005

NCT01525914

Sunnybrook Health Sciences Centre-Toronto Sunnybrook Regional Cancer Centre

Prostate Cancer

May 2010

NCT01957189

GlaxoSmithKline

Prostatic Hyperplasia

October 25, 2013

Phase 1

NCT00382356

North Florida/South Georgia Veterans Health System

Benign Prostatic Hypertrophy

November 2004

NCT01262287

UConn Health-National Institute on Alcohol Abuse and Alcoholism (NIAAA)

Alcoholism-Alcohol Abuse-Alcohol Dependence

January 2011

Phase 4

NCT02578953

GlaxoSmithKline

Prostatic Hyperplasia

September 9, 2015

Phase 1

NCT00441116

GlaxoSmithKline

Alopecia

December 15, 2006

Phase 3

NCT00303446

National Institute of Neurological Disorders and Stroke (NINDS)-National Institutes of Health Clinical Center (CC)

Kennedy's Disease-Spinal and Bulbar Muscular Atrophy

March 2006

Phase 2

NCT01254071

GlaxoSmithKline

Prostatic Hyperplasia

September 10, 2010

Phase 1

NCT00363311

GlaxoSmithKline

Neoplasms, Prostate

July 2006

Phase 4

NCT00553878

Canadian Urology Research Consortium-GlaxoSmithKline

Prostate Cancer

March 2007

Phase 2-Phase 3

NCT00853697

Memorial Sloan Kettering Cancer Center-GlaxoSmithKline-University of Washington

Prostate Cancer-Castration-resistant, Metastatic

March 2009

Phase 2

NCT00673127

Beth Israel Deaconess Medical Center-Massachusetts General Hospital-Dana-Farber Cancer Institute-Sunnybrook Health Sciences Centre-Oregon Health and Science University-M.D. Anderson Cancer Center-Sidney Kimmel Comprehensive Cancer Center

Prostate Cancer

February 2005

Phase 2

NCT01471678

GlaxoSmithKline

Prostatic Hyperplasia

June 30, 2011

Phase 1

NCT01831791

GlaxoSmithKline

Alopecia

April 2013

Phase 3

NCT00194675

University of Washington-GlaxoSmithKline-Seattle Institute for Biomedical and Clinical Research-VA Office of Research and Development-Solvay Pharmaceuticals

Hypogonadism-Benign Prostatic Hyperplasia

March 2005

Phase 4

NCT00827814

Samsung Medical Center-GlaxoSmithKline

Benign Prostatic Hyperplasia

June 2006

Phase 4

NCT01299571

GlaxoSmithKline

Benign Prostatic Hyperplasia-Prostatic Hyperplasia

December 2004

NCT00400335

GlaxoSmithKline

Hypogonadism-Hypogonadism, Male

October 2006

Phase 1

NCT00090103

GlaxoSmithKline

Prostatic Hyperplasia

November 2003

Phase 3

NCT01758523

UConn Health-National Institute on Alcohol Abuse and Alcoholism (NIAAA)

Alcoholism-Alcohol Abuse-Alcohol Dependence

January 2013

Phase 4

NCT01673490

GlaxoSmithKline

Prostatic Hyperplasia

June 2012

Phase 4

NCT00668642

NorthShore University HealthSystem Research Institute-University of Chicago-Northwestern University

Prostate Cancer

March 2007

Phase 2

NCT00780754

Kaunas University of Medicine

Prostate Cancer

April 2007

Phase 3

NCT02014584

Stiefel, a GSK Company-GlaxoSmithKline

Alopecia

July 2014

Phase 3

NCT02509104

GlaxoSmithKline

Prostatic Hyperplasia

July 30, 2015

Phase 1

NCT02052713

GlaxoSmithKline

Urologic Diseases

February 19, 2014

Phase 1

NCT00062790

GlaxoSmithKline

Prostatic Hyperplasia

October 2003

Phase 4

NCT01657851

GlaxoSmithKline

Prostatic Hyperplasia

August 23, 2012

Phase 1

NCT02058576

GlaxoSmithKline

Urologic Diseases

February 11, 2014

Phase 1

NCT00880672

Seoul National University Hospital-The Korean Urological Association-GlaxoSmithKline

Benign Prostatic Hyperplasia

January 2008

Phase 4

NCT00866554

CHU de Quebec-Universite Laval-GlaxoSmithKline

Prostate Cancer-Erectile Dysfunction-Lower Urinary Tract Symptoms

March 2009

Phase 2

NCT02213107

University of Rochester

Prostate Cancer

September 2014

Phase 2

NCT00527605

GlaxoSmithKline

Benign Prostatic Hyperplasia-Prostatic Hyperplasia

October 2007

Phase 3

NCT01577693

GlaxoSmithKline

Prostatic Hyperplasia

May 12, 2011

Phase 1

NCT00368979

GlaxoSmithKline

Prostatic Hyperplasia

February 2006

Phase 3

NCT01393730

Mary-Ellen Taplin, MD-Dana-Farber Cancer Institute

Prostate Cancer

September 2011

Phase 2

NCT00398281

Sidney Kimmel Cancer Center at Thomas Jefferson University-National Cancer Institute (NCI)

Prostate Cancer

November 2006

Phase 3

NCT00398580

GlaxoSmithKline

Hypogonadism-Hypogonadism, Male

October 2006

Phase 2

NCT00939120

Siami, Paul F., M.D.-GlaxoSmithKline-Pfizer

Benign Prostatic Hyperplasia (BPH)

July 2009

Phase 4

NCT02839122

Yuyu Pharma, Inc.

Benign Prostate Hyperplasia

May 2016

Phase 1

NCT00431626

Northwestern University-GlaxoSmithKline

Benign Prostatic Hyperplasia

October 2006

Phase 3

NCT01368003

Toni Choueiri, MD-Dana-Farber Cancer Institute

Adenocarcinoma of the Prostate

April 2011

Phase 2

NCT01294592

GlaxoSmithKline

Prostatic Hyperplasia

December 2010

Phase 4

NCT01495026

GlaxoSmithKline

Prostatic Hyperplasia

November 2011

Phase 1

NCT00082043

National Institute of Mental Health (NIMH)-National Institutes of Health Clinical Center (CC)

Premenstrual Syndrome-PMS-Healthy-Depression

March 31, 2004

Phase 1

NCT00274417

Urology of Virginia-GlaxoSmithKline

Beni

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