Granted Patent B2

US 8,865,740 · App. 13/905,708 · Granted Oct 21, 2014

Abstract

Claims (42)

1. A method for improving the aesthetic appearance of human skin comprising topically applying to an area of the skin in need thereof an effective amount of an active agent that suppresses miR-29a, having the sequence UAGCACCAUCUGAAAUCGGUUA (SEQ. ID. No.: 1), and/or miR-29b, having the sequence UAGCACCAUUUGAAAUCAGUGUU (SEQ. ID No.: 2), in a cosmetically acceptable vehicle comprising caprylyl glycol, for a time sufficient to enhance the production of collagen, elastin, and/or fibrillin in the skin,

wherein said active agent is a compound having the structure of formula II:

wherein,

R 5 , when not hydrogen, is selected from hydrogen; —R or X 1 ; where “m” is an integer from 1 to 4, and, in the case where “m” is 2, 3 or 4, R 5 is independently selected at each occurrence; and

R 7 and R 8 are independently C 1-20 hydrocarbon radicals; wherein said C 1-20 hydrocarbon radicals may optionally be substituted with a group X 1 and/or with from one to six heteroatoms selected from oxygen, nitrogen, and sulfur;

R, R*, and R N are independently hydrogen or a C 1-20 hydrocarbon radical; wherein said C 1-20 hydrocarbon radical may optionally be substituted with a group X 1 and/or with from one to twelve heteroatoms selected from oxygen, nitrogen, and sulfur; and

X 1 is selected from the group consisting of —F; —Cl; —Br; —I; —OH; —C≡C—R*; —C≡N; —C(R)═N—R N ; —C═N—N(R N ) 2 ; —C(═NR N )—N(R N ) 2 ; —CH 2 OH; —CHO; —(C═O)—R*; —CO 2 H; —CO 2 − ; —CO 2 R*; —CS 2 R*; —(C═O)—S—R*; —S—(C═O)—R*; —(C═O)—NH 2 ; —(C═O)—NR N R N ; —(C═O)—NHNH 2 ; —O—(C═O)—NHNH 2 ; —(C═S)—NH 2 ; —(C═S)—N(R N ) 2 ; —O—(C═O)—H; —O—(C═O)—R*; —O—(C═O)—NH 2 ; —O—(C═O)—NR N R N ; —OR*; —SR*; —NH 2 ; —NHR N ; —NR N 2 ; —N(R N ) 3 + ; —N(R N )—OH; —N(→O)(R*) 2 ; —O—N(R N ) 2 ; —N(R N )—O—R*; —N(R N )—N(R N ) 2 ; —NR N —(C═O)—R*; —NR N C(═O)O—R*; —NR N —CHO; —NR N —(C═O)—R*; —NR N C(═O)NR N ; —N(R N )—C(═O)—N(R N ) 2 ; —N(R N )—C(═S)—N(R N ) 2 ; —N═C(R*) 2 ; —N═N—R N ; —SCN; —NCS; —NSO; —SS—R*; —SO—R*; —SO 2 —R*; —O—S(═O) 2 —R*; —S(═O) 2 —OR*; —N(R N )—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*; —P(R*) 2 ; —O—P(═O)(OR*) 2 ; and —P(═O)(OR*) 2 ;

and cosmetically acceptable salts thereof.

2. The method according to claim 1 , wherein said active agent suppresses miR-29a.

3. The method according to claim 1 , wherein said active agent suppresses miR-29b.

4. The method according to claim 1 , wherein said active agent suppresses miR-29a and miR-29b.

5. The method according to claim 1 , wherein R 5 , when not hydrogen, is alkyl, aryl, arylalkyl, or alkylaryl.

6. The method according to claim 5 , wherein R 5 is hydrogen.

7. The method according to claim 1 , wherein R N , R 7 and R 8 are independently a group —R, where R is selected from alkyl, aryl, arylalkyl, and alkylaryl, each being optionally substituted with 1-12 heteroatoms selected from halogen, O, N and S.

8. The method according to claim 1 , wherein R7 is a C 1 to C 4 alkyl.

9. The method of claim 5 , wherein R 7 and R 8 independently is a C1 to C4 alkyl or phenyl, and R N is hydrogen or a C 1 to C 4 alkyl.

10. The method according to claim 1 , wherein the compound (II) has the formula:

or a cosmetically acceptable salt thereof.

11. The method according to claim 1 , wherein said aesthetic improvement of said skin is selected from the group consisting of:

(a) treatment, reduction, and/or prevention of 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 maintenance and remodeling of elastin;

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

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

(i) improvement in appearance of skin contours;

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

(k) improvement of skin appearance decreased by menopause;

(l) improvement in skin moisturization;

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

(n) treatment, reduction, and/or prevention of skin sagging; or

(o) reduction of pigment spots.

12. A method of improving the appearance of aging skin by stimulating extracellular matrix proteins selected from the group consisting of collagen, elastin, fibrillin, and combinations thereof comprising topically applying to the skin in need of such stimulation a composition containing an effective amount of an active agent that suppresses miR-29a and/or miR-29b, in a topically acceptable vehicle comprising caprylyl glycol,

wherein said active agent is a compound having the structure of formula II:

wherein,

R 5 is selected from hydrogen; —R; or X 1 ; where “m” is an integer from 0 to 5, and, in the case where “m” is 2, 3 or 4, R 5 is independently selected at each occurrence; and

R 7 and R 8 are independently C 1-20 hydrocarbon radicals; wherein said C 1-20 hydrocarbon radicals may optionally be substituted with a group X 1 and/or with from one to six heteroatoms selected from oxygen, nitrogen, and sulfur;

R, R*, and R N are independently hydrogen or a C 1-20 hydrocarbon radical; wherein said C 1-20 hydrocarbon radical may optionally be substituted with a group X 1 and/or with from one to twelve heteroatoms selected from oxygen, nitrogen, and sulfur; and

X 1 is selected from the group consisting of —F; —Cl; —Br; —I; —OH; —C≡C—R*; —C≡N; —C(R)═N—R N ; —C═N—N(R N ) 2 ; —C(═NR N )—N(R N ) 2 ; —CH 2 OH; —CHO; —(C═O)—R*; —CO 2 H; —CO 2 − ; —CO 2 R*; —CS 2 R*; —(C═O)—S—R*; —S—(C═O)—R*; —(C═O)—NH 2 ; —(C═O)—NR N R N ; —(C═O)—NHNH 2 ; —O—(C═O)—NHNH 2 ; —(C═S)—NH 2 ; —(C═S)—N(R N ) 2 ; —O—(C═O)—H; —O—(C═O)—R*; —O—(C═O)—NH 2 ; —O—(C═O)—NR N R N ; —OR*; —SR*; —NH 2 ; —NHR N ; —NR N 2 ; —N(R N ) 3 + ; N(R N )—OH; —N(→O)(R*) 2 ; —O—N(R N ) 2 ; —N(R N )—O—R*; —N(R N )—N(R N ) 2 ; —NR N —(C═O)R*; —NR N C(═O)O—R*; —NR N —CHO; —NR N —(C═O)—R*; —NR N C(═O)NR N ; —N(R N )—C(═O)—N(R N ) 2 ; —N(R N )—C(═S)—N(R N ) 2 ; —N═C(R*) 2 ; —N═N—R N ; —SCN; —NCS; —NSO; —SS—R*; —SO—R*; —SO 2 —R*; —O—S(═O) 2 —R*; —S(═O) 2 —OR*; —N(R N )—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*; —P(R*) 2 ; —O—P(═O)(OR*) 2 ; and —P(═O)(OR*) 2 ;

and cosmetically acceptable salts thereof.

Assignments (8)