IP Library Granted Patent US 8,207,171
Granted Patent B2
US 8,207,171 · App. 13/164,873 · Granted Jun 26, 2012

Cosmetic use of 1-Aroyl-N-(2-oxo-3-piperidinyl)-2-piperazine carboxamides and related compounds

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Quick Facts
Patent No.
US 8,207,171
App. No.
13/164,873
Granted
Jun 26, 2012
Kind
B2
Abstract

Cosmetic compositions comprising 1-aroyl-N-(2-oxo-3-piperidinyl)-2-piperazine carboxamides and methods of using such compositions to impart anti-aging benefits to the skin are disclosed. The 1-aroyl-N-(2-oxo-3-piperidinyl)-2-piperazine carboxamides are believed to have modulatory activity against one or more biochemical pathways implicated in skin aging.

Claims (40)

1. A method for providing a benefit to human skin comprising topically applying to the skin of an individual in need thereof an effective amount of a 1-aroyl-N-(2-oxo-3-piperidinyl)-2-piperazine carboxamide compound or a diastereomer or cosmetically acceptable salt thereof in a cosmetically acceptable vehicle, wherein said 1-aroyl-N-(2-oxo-3-piperidinyl)-2-piperazine carboxamide compound, or diastereomer or cosmetically acceptable salt thereof, has the structure of formula (Ia):

where R 3 and R 6 are independently hydrogen or a group —R 9 -R 10 ;

R 9 represents, independently at each occurrence, a bond; an aliphatic C 1 -C 20 hydrocarbon radical;

a C 1 -C 20 aromatic hydrocarbon radical; or a C 1 -C 20 heteroaryl radical;

R 10 is selected independently at each occurrence from hydrogen; —F; —Cl; —Br; —I; —OH;—OR; —NH 2 ; —NHR; —N(R) 2 ; —N(R) 3 + ; —N(R)—OH; —N(→O)(R) 2 ; —O—N(R) 2 ; —N(R)—O—R; —N(R)—N(R) 2 ; —C═N—R; —N═C(R) 2 ; —C═N—N(R) 2 ; —C(═NR)—N(R) 2 ; —SH; —SR; —CN; —NC; —CHO; —CO 2 H; —CO 2 − ; —CO 2 R; —(C═O)—S—R; —O—(C═O)—H; —O—(C═O)—R; —S—(C═O)—R; —(C═O)—NH 2 ; —(C═O)—N(R) 2 ; —(C═O)—NHNH 2 ; —O—(C═O)—NHNH 2 ; —(C═S)—NH 2 ; —(C═S)—N(R) 2 ; —N(R)—CHO; —N(R)—(C═O)—R; —(C═NR)—O—R; —O—(C═NR)—R; —SCN; —NCS; —NSO; —SSR; —N(R)—C(═O)—N(R) 2 ; —N(R)—C(═S)—N(R) 2 ; —SO 2 —R; —O—S(═O) 2 —R; —S(═O) 2 —OR; —N(R)—SO 2 —R; —SO 2 —N(R) 2 ; —O—SO 3 − ; —O—S(═O) 2 —OR; —O—S(═O)—OR; —O—S(═O)—R; —S(═O)—OR; —S(═O)—R; —NO; —NO 2 ; —NO 3 ; —O—NO; —O—NO 2 ; —N 3 ; —N 2 ; —N(C 2 H 4 ); —Si(—R) 3 ; —CF 3 ; —O—CF 3 ; —(C═O)—R; —PR 2 ; —O—P(═O)(OR) 2 ; —P(═O)(OR) 2 ; ═O; ═S; ═NR; an aliphatic C 1 -C 20 hydrocarbon radical; a C 1 -C 20 aromatic hydrocarbon radical; or a C 1 -C 20 heteroaryl radical;

where R is independently at each occurrence hydrogen or a saturated, partially saturated, or aromatic C 1 -C 20 hydrocarbon radical or halogenated derivative thereof.

2. The method according to claim 1 , where R 3 represents a group —OR.

3. The method according to claim 2 , where R 3 represents —OCH 3 .

4. The method according to claim 1 , where R 6 is a group —(C═O )—R, where R is selected from the group consisting of methyl, ethyl, propyl, butyl, pentyl, hexyl, phenyl, toluyl, or benzyl.

5. The method according to claim 4 , where R 6 is a group —(C═O)—(C 6 H 5 ).

6. The method according to claim 1 , where R 6 is a group —SO 2 —R, where R is selected from the group consisting of methyl, ethyl, propyl, butyl, pentyl, hexyl, phenyl, toluyl, or benzyl.

7. The method according to claim 6 , where R 6 is a group —SO 2 —CH 3 .

8. The method according to claim 1 , wherein said skin benefit is selected from the group consisting of:

(a) treatment and/or reduction of fine lines or wrinkles, and/or reduction of severity of existing fine lines or wrinkles and/or inhibition of formation of new fine lines or wrinkles,

(b) reduction of skin pore size,

(c) improvement in skin thickness, plumpness, and/or tautness;

(d) improvement in skin suppleness and/or softness;

(e) improvement in skin tone, radiance, and/or clarity;

(f) improvement in procollagen and/or collagen production;

(g) improvement in maintenance and remodeling of elastin;

(h) improvement in skin texture and/or promotion of retexturization;

(i) improvement in skin barrier repair and/or function;

(j) improvement in appearance of skin contours;

(k) restoration of skin luster and/or brightness;

(l) replenishment of essential nutrients and/or constituents in the skin;

(m) improvement of skin appearance decreased by menopause;

(n) improvement in skin moisturization;

(o) increase in skin elasticity and/or resiliency; or

(p) treatment and/or reduction of skin sagging.

9. The method according to claim 8 , wherein said skin benefit is the treatment and/or reduction of fine lines or wrinkles and/or reduction of severity of existing fine lines or wrinkles and/or inhibition of formation of new fine lines or wrinkles.

10. The method according to claim 8 , wherein said skin benefit is the treatment and/or reduction of skin sagging.

11. The method according to claim 1 , wherein said 1-aroyl-N-(2-oxo-3-piperidinyl)-2-piperazine carboxamide compound has the structure:

or a diastereomer or a cosmetically acceptable salt thereof.

12. The method according to claim 1 , wherein said 1-aroyl-N-(2-oxo-3-piperidinyl)-2-piperazine carboxamide compound has the structure:

or a diastereomer or a cosmetically acceptable salt thereof.

13. A method for treating wrinkles and/or fine lines comprising topically applying to said wrinkle and/or fine line on the skin of an individual in need thereof an effective amount of a 1-aroyl-N-(2-oxo-3-piperidinyl)-2-piperazine carboxamide compound or a diastereomer or a cosmetically acceptable salt thereof in a cosmetically acceptable vehicle for a time sufficient to reduce the severity of said wrinkles or fine lines.

14. The method according to claim 1 , wherein a (R,R) diastereomer comprises at least 95% by weight of the total weight of said compound having the structure of formula (Ia).

15. The method according to claim 1 , wherein a (R,S) diastereomer comprises at least 95% by weight of the total weight of said compound having the structure of formula (Ia).

16. The method according to claim 1 , wherein a (S,R) diastereomer comprises at least 95% by weight of the total weight of said compound having the structure of formula (Ia).

17. The method according to claim 1 , wherein a (S,S) diastereomer comprises at least 95% by weight of the total weight of said compound having the structure of formula (Ia).

Assignments (9)
RELEASE OF SECURITY INTEREST Recorded Jan 28, 2026
From: NATURA &CO LUXEMBOURG HOLDINGS S.À R.L., AS A SECURED PARTY; NATURA &CO UK HOLDINGS LIMITED, AS A SECURED PARTY
To: AVON PRODUCTS, INC.
Reel/Frame 074508/0281 →
RELEASE OF SECURITY INTEREST Recorded Dec 11, 2024
From: NATURA &CO HOLDING S.A.; NATURA COSMETICOS S.A.; NATURA &CO LUXEMBOURG HOLDINGS S.A R.L. - LUXEMBOURG; NATURA &CO UK HOLDINGS LIMITED - UK
To: AVON PRODUCTS, INC
Reel/Frame 069591/0494 →
PATENT SECURITY AGREEMENT Recorded Aug 16, 2024
From: AVON PRODUCTS, INC.
To: NATURA &CO HOLDING S.A.; NATURA &CO LUXEMBOURG HOLDINGS S.À R.L.; NATURA COSMÉTICOS S.A.; NATURA &CO UK HOLDINGS LIMITED
Reel/Frame 068659/0915 →
SECURITY INTEREST Recorded Apr 29, 2024
From: AVON PRODUCTS, INC.; MI HOLDINGS, INC.; AVON INTERNATIONAL OPERATIONS, INC.; AVON CAPITAL CORPORATION; AVON COSMETICS LIMITED; AVON BEAUTY LIMITED
To: NATURA &CO HOLDING S.A., AS SECURED PARTY; NATURA &CO LUXEMBOURG HOLDINGS S.À R.L., AS A SECURED PARTY; NATURA COSMÉTICOS S.A., AS A SECURED PARTY
Reel/Frame 067249/0491 →
SECURITY INTEREST Recorded Aug 11, 2023
From: AVON PRODUCTS, INC.
To: NATURA &CO LUXEMBOURG HOLDINGS S.À R.L., AS A SECURED PARTY; NATURA &CO UK HOLDINGS LIMITED, AS A SECURED PARTY
Reel/Frame 064566/0872 →
SECURITY INTEREST Recorded Nov 14, 2019
From: AVON PRODUCTS, INC.
To: CITIBANK, N.A., LONDON BRANCH
Reel/Frame 051032/0210 →
RELEASE OF SECURITY INTEREST IN PATENTS Recorded Aug 15, 2016
From: CITIBANK, N.A.
To: AVON PRODUCTS, INC.
Reel/Frame 039690/0331 →
SECURITY INTEREST Recorded Jun 12, 2015
From: AVON PRODUCTS, INC.
To: CITIBANK, N.A.
Reel/Frame 035899/0776 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 21, 2011
From: PTCHELINSEV, DMITRI S.; HU, HONG; MENON, GOPINATHAN K.; SCHMALENBERG, KRISTINE; LYGA, JOHN W.
To: AVON PRODUCTS, INC.
Reel/Frame 026469/0806 →