IP Library Granted Patent US 9,085,528
Granted Patent B2
US 9,085,528 · App. 12/806,474 · Granted Jul 21, 2015

Nitric oxide amino acid ester compound, composition for increasing nitric oxide levels and method of use

Inventor: Michael Farber (Livingston, NJ)
Assignee: Oral Delivery Technology Ltd.
C07D207/16A23L1/3051A61K31/215A61K31/401A61K31/405A61K31/4164C07C229/02C07C229/08C07D209/20C07D233/64
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Quick Facts
Patent No.
US 9,085,528
App. No.
12/806,474
Granted
Jul 21, 2015
Kind
B2
Abstract

There is provided novel amino acid ester compounds comprising at least one nitric oxide releasing group and pharmaceutically acceptable salts thereof, and novel compositions comprising at least one amino acid ester compound comprising at least one nitric oxide releasing group, and, optionally, at least one nitric oxide donor and/or at least one therapeutic agent. Also provided are compositions for increasing nitric oxide physiological levels in a subject, methods for increasing nitric oxide physiological levels in a subject, methods for improving a subject's muscle strength, athletic performances and/or lean body mass gain and or performance in a subject.

Claims (12)

1. A compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein the compound of Formula (I) is:

wherein,

n=2 and

R 1 is

2. A composition for increasing nitric oxide physiological levels in a subject, which comprises a therapeutically effective amount of the compound of claim 1 in combination with a pharmaceutically acceptable carrier.

3. The composition according to claim 2 , wherein said pharmaceutically acceptable carrier is selected from the group consisting of polyethylene glycol MOL WT 330, polyethylene glycol MOL WT 300, propylene glycol monocaprylate, propylene glycol, water, sodium lauryl sulfate, salt solutions, alcohol, vegetable oils, polyethylene glycols, gelatin, lactose, amylose, magnesium stearate, talc, surfactants, silicic acid, viscous paraffin, perfume oil, fatty acid monoglycerides and diglycerides, petroethral fatty acid esters, hydroxymethyl-cellulose and polyvinylpyrrolidon.

4. The composition according to claim 2 , wherein said pharmaceutically acceptable carrier is saliva-absorbing microcrystalline cellulose.

5. The composition according to claim 2 formulated as a liquid formulation, a liquid dosage form, an enteric-coated soft-gel capsule, a capsule, a sustained-release capsule, a tablet, a sustained release tablet, a chewable tablet, a sublingual tablet, an effervescent tablet, a pill, a powder, a granule, a gel or a suppository.

6. The composition according to claim 2 further comprising creatine.

7. The composition according to claim 2 , wherein said increase in nitric oxide levels increases vasodilatation.

8. The composition according to claim 7 , further comprising a vasodilatory compound chosen from L-arginine, norvaline, and citrulline.

9. The composition according to claim 2 further comprising 17α-hydroxy-yohimban-16α-carboxylic acid methyl ester.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 17, 2015
From: BENOÎT & CÓTÉ, INC.
To: NITROGENIX, INC.; ORAL DELIVERY TECHNOLOGY, LTD.
Reel/Frame 036122/0959 →
SECURITY AGREEMENT Recorded Jul 26, 2013
From: NITROGENIX INC.; ORAL DELIVERY TECHNOLOGY LTD.
To: BENOIT & COTE
Reel/Frame 030900/0861 →
Continuity (3)
Continuation 12565347 · Sep 23, 2009
Provisional Application 61099621 · Sep 24, 2008
Related Publication 20100311780A1 · Dec 9, 2010