IP Library Granted Patent US 9,089,547
Granted Patent B2
US 9,089,547 · App. 13/903,748 · Granted Jul 28, 2015

Use of equol for treating androgen mediated diseases

Inventors: Edwin Douglas Lephard (Montgomery, TX); Trent D. Lund (Wheaton, IL); Robert J. Handa (Fort Collins, CO)
Assignees: Brigham Young University; Colorado State University Research Foundation
A61K31/352A61K31/35A61K31/353
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Quick Facts
Patent No.
US 9,089,547
App. No.
13/903,748
Granted
Jul 28, 2015
Kind
B2
Abstract

Equol (7-hydroxy-3(4′hydroxyphenyl)-chroman), the major metabolite of the phytoestrogen daidzein, specifically binds and blocks the hormonal action of 5α-dihydrotestosterone (DHT) in vitro and in vivo. Equol can bind circulating free DHT and sequester it from the androgen receptor, thus altering growth and physiological hormone responses that are regulated by androgens. These data suggest a novel model to explain equol's biological properties. The significance of equol's ability to specifically bind and sequester DHT from the androgen receptor have important ramifications in health and disease and may indicate a broad and important usage for equol in the treatment and prevention of androgen-mediated pathologies. Thus, equol can specifically bind DHT and prevent DHT's biological actions in physiological and pathophysiological processes.

Claims (6)

1. A method of modulating physiological and pathophysiological conditions of benign prostatic hyperplasia and prostate cancer and mediated by androgens in a mammal, comprising administering an effective amount of equol comprising a racemic mixture of R-equol and S-equol enantiomers to the mammal thereby modulating physiological and pathophysiological conditions of benign prostatic hyperplasia and prostate cancer and mediated by androgens in the mammal.

2. The method according to claim 1 , wherein the equol is administered as an oral composition comprising at least 1 mg of equol.

3. The method according to claim 1 , wherein the equol is administered as a topical composition comprising at least 0.1% of equol.

4. A method of treating and preventing an androgen-related disease of benign prostatic hyperplasia and prostate cancer in a mammal, comprising administering an effective amount of equol comprising a racemic mixture of R-equol and S-equol enantiomers to the mammal, wherein the equol can bind with free 5α-dihydrotestosterone, thereby inhibiting the binding of the 5α-dihydrotestosterone with the androgen receptors in the mammal.

5. The method according to claim 4 , wherein the equol is administered as an oral composition comprising at least 1 mg of equol.

6. The method according to claim 4 , wherein the equol is administered as a topical composition comprising at least 0.1% of equol.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 9, 2015
From: LEPHART, EDWIN DOUGLAS
To: BRIGHAM YOUNG UNIVERSITY
Reel/Frame 035808/0513 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 9, 2015
From: HANDA, ROBERT J.; LUND, TRENT D.
To: COLORADO STATE UNIVERSITY RESEARCH FOUNDATION
Reel/Frame 035866/0101 →
Continuity (5)
Continuation 13442466 · Apr 9, 2012
Continuation 12572791 · Oct 2, 2009
Continuation 10533045
Provisional Application 60422469 · Oct 29, 2002
Related Publication 20140135387A1 · May 15, 2014