IP Library Granted Patent US 10,653,603
Granted Patent B2
US 10,653,603 · App. 15/407,474 · Granted May 19, 2020

N-acyldipeptide derivatives and their uses

Inventors: Ruey J. Yu (Chalfont, PA); Eugene J. Van Scott (Abington, PA)
Assignee: NEOSTRATA COMPANY, INC.
A61K8/64A61K8/671A61K9/0014A61K31/07A61K38/05A61Q19/00A61Q19/06A61Q19/08C07K5/0202C07K5/0205C07K5/0207C07K5/0606C07K5/06026C07K5/06034C07K5/06043C07K5/06052C07K5/06069C07K5/06078C07K5/06113C07K5/06147C07K5/06156C07K5/06165C07K5/06191A61K2800/10A61K2800/92A61Q5/00A61Q19/007A61Q19/008A61Q19/02Y02A50/463
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Quick Facts
Patent No.
US 10,653,603
App. No.
15/407,474
Granted
May 19, 2020
Kind
B2
Abstract

Methods of treating aging related skin changes and of increasing skin thickness with topical administration of N-acyldipeptide derivatives are described. Compositions comprising N-acyldipeptide derivatives, are therapeutically effective for increasing skin thickness, and for treating extrinsic and intrinsic aging and aging related skin changes, such as fine lines, wrinkles, photoaging, hyperpigmentation, laxity, age spots, lentigines, mottled skin, and cellulite.

Claims (27)

1. A method of treating skin, comprising topically administering to skin in need of increased thickness or treatment for abnormal or diminished synthesis of collagen, glycosaminoglycans, proteoglycans, or elastin a composition comprising a therapeutically effective amount of a dipeptide derivative of formula (I):

R 1 -AAB-AAC-R 2    Formula (I)

or an isomer or salt thereof, and optionally a pharmaceutically or cosmetically acceptable carrier, wherein R 1 is an acyl radical having up to 19 carbon atoms; AAB is Tyr and AAC is Tyr, or AAB is Val and AAC is Ala; R 2 is OR 3 , NHR 4 , or NHNHR 5 ; R 3 is H, an alkyl, aralkyl, or aryl radical having up to 19 carbon atoms; and R 4 or R 5 is independently H, OH, an alkyl, aralkyl, or aryl radical having up to 19 carbon atoms, thereby increasing skin thickness or treating abnormal or diminished synthesis of collagen, glycosaminoglycans, proteoglycans, or elastin.

2. The method of claim 1 , wherein AAB is Tyr and AAC is Tyr.

3. The method of claim 1 , wherein AAB is Val and AAC is Ala.

4. The method of claim 1 , wherein the dipeptide derivative is selected from the group consisting of N—Ac-Tyr-Tyr-NH2, N—Ac-Tyr-Tyr-OH, N—Ac-Tyr-Tyr-OEt, N—Ac-Tyr-Tyr-NHNH 2 , N—Ac-Tyr-Tyr-NHNHAc, N—Ac-Tyr-Tyr-NHOH, N—Pr-Tyr-Tyr-NH 2 , N—Pr-Tyr-Tyr-OH, N—Pr-Tyr-Tyr-OEt, N—Pr-Tyr-Tyr-NHNH 2 , and N—Pr-Tyr-Tyr-NHNHPr.

5. The method of claim 1 , wherein the dipeptide derivative is selected from the group consisting of N—Ac-Val-Ala-NH2, N—Ac—Val-Ala-OH, N—Ac—Val-Ala-NHOH, N—Pr—Val-Ala-NH2, and N—Pr-Val-Ala-OH.

6. The method of claim 1 , wherein the dipeptide derivative is selected from the group consisting of N—Ac-Tyr-Tyr-NH 2 and N—Ac-Val-Ala-NH 2 .

7. The method of claim 1 , being a method of treating skin in need of increased skin thickness.

8. The method of claim 1 , being a method of treating skin in need of treatment for abnormal or diminished synthesis of collagen, glycosaminoglycans, proteoglycans, or elastin.

9. The method of claim 8 , being a method of treating skin in need of treatment for abnormal or diminished synthesis of elastin.

10. A method of increasing skin thickness in a subject in need thereof, comprising topically administering to the skin of the subject a therapeutically effective amount of a dipeptide derivative of formula (I):

R 1 -AAB-AAC-R 2    Formula (I)

or an isomer or salt thereof, and optionally a pharmaceutically or cosmetically acceptable carrier, wherein R 1 is an acyl radical having up to 19 carbon atoms; AAB is Tyr and AAC is Tyr, or AAB is Val and AAC is Ala; R 2 is OR 3 , NHR 4 , or NHNHR 5 ; R 3 is H, an alkyl, aralkyl, or aryl radical having up to 19 carbon atoms; and R 4 or R 5 is independently H, OH, an alkyl, aralkyl, or aryl radical having up to 19 carbon atoms.

11. The method of claim 10 , wherein AAB is Tyr and AAC is Tyr.

12. The method of claim 10 , wherein AAB is Val and AAC is Ala.

13. The method of claim 10 , wherein the dipeptide derivative is selected from the group consisting of N—Ac-Tyr-Tyr-NH2, N—Ac-Tyr-Tyr-OH, N—Ac-Tyr-Tyr-OEt, N—Ac-Tyr-Tyr-NHNH 2 , N—Ac-Tyr-Tyr-NHNHAc, N—Ac-Tyr-Tyr-NHOH, N—Pr-Tyr-Tyr-NH 2 , N—Pr-Tyr-Tyr-OH, N—Pr-Tyr-Tyr-OEt, N—Pr-Tyr-Tyr-NHNH 2 , and N—Pr-Tyr-Tyr-NHNHPr.

14. The method of claim 10 , wherein the dipeptide derivative is selected from the group consisting of N—Ac-Val-Ala-NH2, N—Ac—Val-Ala-OH, N—Ac—Val-Ala-NHOH, N—Pr—Val-Ala-NH2, and N—Pr-Val-Ala-OH.

15. The method of claim 10 , wherein the dipeptide derivative is selected from the group consisting of N—Ac-Tyr-Tyr-NH2 and N—Ac-Val-Ala-NH2.

16. A method of reducing wrinkles in a subject in need thereof, comprising topically administering to the skin of the subject a therapeutically effective amount of a dipeptide derivative of formula (I):

R 1 -AAB-AAC-R 2    Formula (I)

or an isomer or salt thereof, and optionally a pharmaceutically or cosmetically acceptable carrier, wherein R 1 is an acyl radical having up to 19 carbon atoms; AAB is Tyr and AAC is Tyr, or AAB is Val and AAC is Ala; R 2 is OR 3 , NHR 4 , or NHNHR 5 ; R 3 is H, an alkyl, aralkyl, or aryl radical having up to 19 carbon atoms; and R 4 or R 5 is independently H, OH, an alkyl, aralkyl, or aryl radical having up to 19 carbon atoms.

17. The method of claim 16 , wherein AAB is Tyr and AAC is Tyr.

18. The method of claim 16 , wherein AAB is Val and AAC is Ala.

19. The method of claim 16 , wherein the dipeptide derivative is selected from the group consisting of N—Ac-Tyr-Tyr-NH2, N—Ac-Tyr-Tyr-OH, N—Ac-Tyr-Tyr-OEt, N—Ac-Tyr-Tyr-NHNH 2 , N—Ac-Tyr-Tyr-NHNHAc, N—Ac-Tyr-Tyr-NHOH, N—Pr-Tyr-Tyr-NH 2 , N—Pr-Tyr-Tyr-OH, N—Pr-Tyr-Tyr-OEt, N—Pr-Tyr-Tyr-NHNH 2 , and N—Pr-Tyr-Tyr-NHNHPr.

20. The method of claim 16 , wherein the dipeptide derivative is selected from the group consisting of N—Ac-Val-Ala-NH2, N—Ac—Val-Ala-OH, N—Ac—Val-Ala-NHOH, N—Pr—Val-Ala-NH2, and N—Pr-Val-Ala-OH.

21. The method of claim 16 , wherein the dipeptide derivative is selected from the group consisting of N—Ac-Tyr-Tyr-NH 2 and N—Ac-Val-Ala-NH 2 .

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 21, 2017
From: YU, RUEY J., PHD; VAN SCOTT, EUGENE J.
To: NEOSTRATA COMPANY, INC.
Reel/Frame 041319/0625 →
Continuity (7)
Continuation 15171601 · Jun 2, 2016
Continuation 14718317 · May 21, 2015
Division 14354711
Provisional Application 61582675 · Jan 3, 2012
Provisional Application 61554724 · Nov 2, 2011
Provisional Application 61552751 · Oct 28, 2011
Related Publication 20170119646A1 · May 4, 2017