IP Library Granted Patent US 10,183,922
Granted Patent B2
US 10,183,922 · App. 15/425,739 · Granted Jan 22, 2019

Methods and compositions for wound healing

Inventors: Paul Warren Reddell (Yungaburra, AU); Victoria Anne Gordon (Yungaburra, AU); Ryan Moseley (Bridgend, GB); Robert Steadman (Caerphilly, GB); Rachael Louise Moses (Milton Keynes, GB); Glen Mathew Boyle (Taringa, AU); Peter Gordon Parsons (St. Lucia, AU)
Assignee: QBiotics Limited
C07D303/40A61K8/4973A61K9/0014A61K9/0019A61K9/06A61K31/122A61K31/336A61K36/47A61K47/10A61Q19/00C07D303/32A61K2236/15A61K2236/33A61K2800/74
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Quick Facts
Patent No.
US 10,183,922
App. No.
15/425,739
Granted
Jan 22, 2019
Kind
B2
Abstract

The present invention relates to epoxy-tigliane compounds and their use in promoting wound healing. In particular embodiments, the epoxy-tigliane compounds are epoxy-tigliaen-3-one compounds. Methods of inducing or promoting wound healing as well as methods of reducing scarring and improving cosmetic outcomes upon healing of a wound are described. Compounds and compositions for use in wound healing are also described.

Claims (31)

1. A compound selected from the group consisting of:

12-hexanoyl-13-(2-methylbutanoyl)-6,7-epoxy-4,5,9,12,13,20-hexahydroxy-1-tigliaen-3-one (Compound 5);

12-(3-butenoyl)-13-nonanoyl-6,7-epoxy-4,5,9,12,13,20-hexahydroxy-1-tigliaen-3-one (Compound 22);

12,13-di-nonoyl-6,7-epoxy-4,5,9,12,13,20-hexahydroxy-1-tigliaen-3-one (Compound 41);

12,13-di-hexanoyl-6,7-epoxy-4,5,9,12,13,20-hexahydroxy-1-tigliaen-3-one (Compound 42);

12,13-di-pentanoyl-6,7-epoxy-4,5,9,12,13,20-hexahydroxy-1-tigliaen-3-one (Compound 43);

12-hexanoyl-13-[2-(N-methylanthraniloyl)]-6,7-epoxy-4,5,9,12,13,20-hexahydroxy-1-tigliaen-3-one (Compound 47)

12,13-di-heptanoyl-6,7-epoxy-4,5,9,12,13,20-hexahydroxy-1-tigliaen-3-one (Compound 49);

12-myristoyl-13-acetyl-6,7-epoxy-4,5,9,12,13,20-hexahydroxy-1-tigliaen-3-one (Compound 50);

12-myristoyl-13-(2-methylbutanoyl)-6,7-epoxy-4,5,9,12,13,20-hexahydroxy-1-tigliaen-3-one (Compound 51);

and

12-hydroxy-13-hexanoyl-6,7-epoxy-4,5,9,12,13,20-hexahydroxy-1-tigliaen-3-one (Compound 53);

or a pharmaceutically acceptable salt thereof.

2. A pharmaceutical composition comprising a compound of claim 1 or pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier, diluent or excipient.

3. The pharmaceutical composition of claim 2 , wherein the compound is selected from the group consisting of:

12-(3-butenoyl)-13-nonanoyl-6,7-epoxy-4,5,9,12,13,20-hexahydroxy-1-tigliaen-3-one (Compound 22);

12,13-di-nonoyl-6,7-epoxy-4,5,9,12,13,20-hexahydroxy-1-tigliaen-3-one (Compound 41);

12,13-di-hexanoyl-6,7-epoxy-4,5,9,12,13,20-hexahydroxy-1-tigliaen-3-one (Compound 42);

12,13-di-pentanoyl-6,7-epoxy-4,5,9,12,13,20-hexahydroxy-1-tigliaen-3-one (Compound 43);

12-hexanoyl-13-[2-(N-methylanthraniloyl)]-6,7-epoxy-4,5,9,12,13,20-hexahydroxy-1-tigliaen-3-one (Compound 47);

12,13-di-heptanoyl-6,7-epoxy-4,5,9,12,13,20-hexahydroxy-1-tigliaen-3-one (Compound 49);

12-myristoyl-13-acetyl-6,7-epoxy-4,5,9,12,13,20-hexahydroxy-1-tigliaen-3-one (Compound 50);

12-myristoyl-13 (2-methylbutanoyl)-6,7-epoxy-4,5,9,12,13,20-hexahydroxy-1-tigliaen-3-one (Compound 51);

and

12-hydroxy-13-hexanoyl-6,7-epoxy-4,5,9,12,13,20-hexahydroxy-1-tigliaen-3-one (Compound 53);

or a pharmaceutically acceptable salt thereof.

4. A pharmaceutical composition comprising a compound selected from the group consisting of:

12-hexanoyl-13-(2-methylbutanoyl)-6,7-epoxy-4,5,9,12,13,20-hexahydroxy-1-tigliaen-3-one (Compound 5);

or pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier, diluent or excipient, wherein the carrier, diluent or excipient is selected from the group consisting of sugars, starches, cellulose and its derivatives, malt, gelatine, talc, calcium sulphate, vegetable oils, synthetic oils, alcohols and/or polyols, alginic acid, phosphate buffered solutions, emulsifiers, and isotonic saline.

5. The pharmaceutical composition according to claim 4 wherein the pharmaceutically acceptable carrier, diluent or excipient comprises an alcohol and/or a polyol.

6. A pharmaceutical composition according to any one of claims 2 - 5 formulated for topical administration.

Assignments (9)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 18, 2020
From: GORDON, VICTORIA ANNE
To: QBIOTICS LIMITED
Reel/Frame 054694/0186 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 18, 2020
From: BOYLE, GLEN MATHEW; PARSONS, PETER GORDON
To: THE COUNCIL OF THE QUEENSLAND INSTITUTE OF MEDICAL RESEARCH
Reel/Frame 054694/0261 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 18, 2020
From: THE COUNCIL OF THE QUEENSLAND INSTITUTE OF MEDICAL RESEARCH
To: ECOBIOTICS LIMITED
Reel/Frame 054694/0301 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 18, 2020
From: ECOBIOTICS LIMITED
To: QBIOTICS LIMITED
Reel/Frame 054694/0598 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 18, 2020
From: REDDELL, PAUL WARREN
To: QBIOTICS LIMITED
Reel/Frame 054694/0741 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 18, 2020
From: MOSES, RACHAEL LOUISE
To: QBIOTICS LIMITED
Reel/Frame 054694/0810 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 18, 2020
From: CARDIFF UNIVERSITY
To: QBIOTICS LIMITED
Reel/Frame 054808/0295 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 18, 2020
From: MOSELEY, RYAN; STEADMAN, ROBERT
To: CARDIFF UNIVERSITY
Reel/Frame 054808/0321 →
CHANGE OF NAME Recorded Dec 18, 2020
From: QBIOTICS LIMITED
To: QBIOTICS PTY LTD
Reel/Frame 054808/0416 →
Priority Claims (1)
AU 2013901359 · Apr 18, 2013 · national
Continuity (2)
Division 14785127
Related Publication 20170144981A1 · May 25, 2017