Crystalline ACAT inhibitor
View Patent ↗The invention is directed to the Form A polymorph of N-benzyl-N′-(2,6-diisopropyl-phenyl)-N-isopropyl-malonamide and its use as a therapeutic/cosmetic agent.
1. A method for decreasing sebum secretion in a patient in need thereof, comprises administering to said patient an effective amount of a pharmaceutical composition comprising Form A polymorph of N-benzyl-N′-(2,6-diisopropyl-phenyl)-N-isopropyl-malonamide.
2. The method of claim 1 , wherein the Form A polymorph is a crystalline polymorph that exhibits an X-ray powder diffraction pattern that has at least one characteristic peak expressed in degrees 2θ at approximately 16.0, 19.6, or 28.1.
3. The method of claim 2 , wherein the crystalline polymorph exhibits an X-ray powder diffraction pattern that has characteristic peaks expressed in degrees 2θ at approximately 16.0, 19.6, and 28.1.
4. The method of claim 2 , wherein the crystalline polymorph exhibits at least one additional peak, expressed in degrees 2θ, at approximately 7.3, 10.3, 16.5, 17.9, 19.1, 20.7, or 25.
5. The method of claim 2 , wherein the crystalline polymorph exhibits at least two additional peaks, expressed in degrees 2θ, at approximately 7.3, 10.3, 10.8, 11.3, 12.1, 14.6, 14.9, 16.5, 17.9, 18.1, 18.9, 19.1, 20.7, 21.8, 22.9, 23.2, 25.0, or 26.0.
6. The method of claim 1 , wherein the pharmaceutical composition is administered topically.
7. The method of claim 1 , wherein the patient is afflicted with or susceptible to seborrheic dermatitis or oily skin.
8. A method for treating acne in a patient in need thereof, comprises administering to said patient an effective amount of a pharmaceutical composition comprising Form A polymorph of N-benzyl-N′-(2,6-diisopropyl-phenyl)-N-isopropyl-malonamide.
9. A method of claim 8 , wherein the Form A polymorph is a crystalline polymorph that exhibits an X-ray powder diffraction pattern that has at least one characteristic peak expressed in degrees 2θ at approximately 16.0, 19.6, or 28.1.
10. The method of claim 9 , wherein the crystalline polymorph exhibits an X-ray powder diffraction pattern that has characteristic peaks expressed in degrees 2θ at approximately 16.0, 19.6, and 28.1.
11. The method of claim 9 , wherein the crystalline polymorph exhibits at least one additional peak, expressed in degrees 2θ, at approximately 7.3, 10.3, 16.5, 17.9, 19.1, 20.7, or 25.
12. The method of claim 9 , wherein the crystalline polymorph exhibits at least two additional peaks, expressed in degrees 2θ, at approximately 7.3, 10.3, 10.8, 11.3, 12.1, 14.6, 14.9, 16.5, 17.9, 18.1, 18.9, 19.1, 20.7, 21.8, 22.9, 23.2, 25.0, or 26.0.
13. The method of claim 8 , wherein the pharmaceutical composition is administered topically.
14. A method for reducing Acyl CoA cholesterol acyl transferase (ACAT) activity in a patient in need thereof, comprises administering to said patient an effective amount of a pharmaceutical composition comprising Form A polymorph of N-benzyl-N′-(2,6-diisopropyl-phenyl)-N-isopropyl-malonamide.
15. A method of claim 14 , wherein the Form A polymorph is a crystalline polymorph that exhibits an X-ray powder diffraction pattern that has at least one characteristic peak expressed in degrees 2θ at approximately 16.0, 19.6, or 28.1.
16. The method of claim 15 , wherein the crystalline polymorph exhibits an X-ray powder diffraction pattern that has characteristic peaks expressed in degrees 2θ at approximately 16.0, 19.6, and 28.1.
17. The method of claim 15 , wherein the crystalline polymorph exhibits at least one additional peak, expressed in degrees 2θ, at approximately 7.3, 10.3, 16.5, 17.9, 19.1, 20.7, or 25.
18. The method of claim 15 , wherein the crystalline polymorph exhibits at least two additional peaks, expressed in degrees 2θ, at approximately 7.3, 10.3, 10.8, 11.3, 12.1, 14.6, 14.9, 16.5, 17.9, 18.1, 18.9, 19.1, 20.7, 21.8, 22.9, 23.2, 25.0, or 26.0.
19. The method of claim 14 , wherein the pharmaceutical composition is administered topically.