IP Library › Patent Application 18435744

Patent Application

App. No. 18/435,744

COMPOSITION AND METHODS OF USE OF NOVEL PHENYLALANINE SMALL ORGANIC COMPOUNDS TO DIRECTLY MODULATE PCSK9 PROTEIN ACTIVITY

Loading inventors, assignments & file history…

Monitor This Case

Get email alerts when status or documents change.

Order Certified Copies

Most orders are placed with the USPTO same day — all within 24 business hours.

Order via The Patent Place →

Pre-filled with this patent's details

Quick Facts

Patent No.: US None
App. No.: 18/435,744

External Links

USPTO Patent Center↗ Full Patent PDF↗

Abstract

This invention is related to the field of PCSK9 biology and the composition and methods of use of small organic compounds as ligands for modulation of PCSK9 biological activity. In particular, the invention provides compositions of small organic compounds that modulate circulating levels of low density lipoproteins by altering the conformation of the protein PCSK9. Binding these small organic compound ligands to PCSK9 alters the conformation of the protein, modifying the interaction between PCSK9 and an endogenous low density lipoprotein receptor, and can lead to reduced or increased levels of circulating LDL-cholesterol. High LDL-cholesterol levels are associated with increased risk for heart disease. Low LDL-cholesterol levels may be problematic in other conditions, such as liver dysfunction; thus, there is also utility for small organic compound ligands that can raise LDL levels.

Claims (79)

1 .- 12 . (canceled)

13 . A compound of Formula I, or a pharmaceutically acceptable salt, hydrate, solvate, or tautomeric form thereof:

wherein

R 3 is selected from the group consisting of H, lower alkyl, halo, haloalkyl, hydroxyalkyl, alkoxyl, and nitrile;

R 4 is selected from the group consisting of H and —OH;

R 5 is selected from the group consisting of alkyl, lower alkyl, branched alkyl, aryl substituted alkyl, cycloalkyl, hydroxyalkyl, haloalkyl, and an amino acid, wherein the amino acid is an L- or D-isomer of the formula —CHR 6 —CON—R 7 ;

wherein i) R 6 is selected from the group consisting of natural or unnatural peptide side chains; ii) R 7 is selected from the group consisting of alkyl, lower alkyl, branched alkyl, cycloalkyl, and heterocyclyl;

X 1 through X 5 are selected independently from the group of CH, CR 1 , CR 2 , and N, wherein at most one of X 1 to X 5 is CR 1 and at most one of X 1 to X 5 is CR 2 , and wherein X 1 to X 5 are part of an aromatic or heteroaryl ring;

R 1 and R 2 are independently selected from the group consisting of lower alkyl, halo, —OH, and amino; and

W is C, CH, or N, wherein when W is C then the dashed bonds are single bonds, and W and Y join together, along with the atoms to which they are attached, to form a 5 membered ring in which Y is CH 2 , and wherein when W is CH or N, then the dashed bonds are absent and Y is absent.

14 . A pharmaceutical composition comprising a compound of claim 13 , or a pharmaceutically acceptable salt, hydrate, solvate, or tautomeric form thereof, and a pharmaceutically acceptable carrier or excipient.

15 . The pharmaceutical composition of claim 14 , wherein said pharmaceutical composition further comprises a pharmaceutical drug.

16 . The pharmaceutical composition of claim 15 , wherein said pharmaceutical drug is selected from the group consisting of a statin, a cardiovascular drug, a metabolic drug, and an antihypertensive drug.

17 . The compound of claim 13 , wherein the compound is selected from:

(S)-3-([1,1′-biphenyl]-4-yl)-2-amino-N-isopropylpropanamide;

(S)-3-([1,1′-biphenyl]-4-yl)-2-amino-N-butylpropanamide;

(S)-2-amino-3-(3-fluoro-4-(pyridin-4-yl)phenyl)-N-isopropylpropanamide;

(S)-2-amino-N-isopropyl-3-(3-methyl-4-(2-oxo-1,2-dihydropyridin-4-yl)phenyl)propanamide;

(S)-2-amino-3-(3′-hydroxy-2-methyl-[1,1′-biphenyl]-4-yl)-N-isopropylpropanamide;

(2S,3R)-2-amino-3-hydroxy-3-(5-(3-hydroxyphenyl)-4-methylpyridin-2-yl)-N-isopropylpropanamide;

(S)-2-amino-3-(5-(3-hydroxyphenyl)pyridin-2-yl)-N-isopropylpropanamide;

(S)-2-amino-3-(5-(3-hydroxyphenyl)-4-methylpyridin-2-yl)-N-isopropylpropanamide;

(S)-2-amino-3-(2′-fluoro-5′-hydroxy-2-methyl-[1,1′-biphenyl]-4-yl)-N-isopropylpropanamide;

(R)-2-amino-N-isopropyl-5-phenyl-2,3-dihydro-1H-indene-2-carboxamide;

(S)-3-([1,1′-biphenyl]-4-yl)-2-amino-N—((S)-1-(isopropylamino)-1-oxopropan-2-yl)propanamide;

(S)-3-([1,1′-biphenyl]-4-yl)-2-amino-N—((R)-1-(isopropylamino)-1-oxopropan-2-yl)propanamide;

(R)-2-((S)-3-([1,1′-biphenyl]-4-yl)-2-aminopropanamido)-N-ethyl-3-methylbutanamide;

(S)-2-amino-3-(3′-hydroxy-[1,1′-biphenyl]-4-yl)-N—((S)-1-(isopropylamino)-1-oxopropan-2-yl)propanamide;

(R)-2-amino-5-(3-hydroxyphenyl)-N-isopropyl-6-methyl-2,3-dihydro-1H-indene-2-carboxamide;

(S)-2-amino-N-isopropyl-3-(4-(2-oxo-1,2-dihydropyridin-4-yl)phenyl)propanamide;

(S)-2-amino-3-(3′-hydroxy-[1,1′-biphenyl]-4-yl)-N-isopropylpropanamide;

(S)-3-([1,1′-biphenyl]-4-yl)-2-amino-N-cyclopentylpropanamide;

(S)-3-([1,1′-biphenyl]-4-yl)-2-amino-N—((R)-1-phenylpropan-2-yl)propanamide;

(S)-3-([1,1′-biphenyl]-4-yl)-2-amino-N—((S)-1-phenylpropan-2-yl)propanamide;

(S)-2-amino-3-(2-cyano-[1,1′-biphenyl]-4-yl)-N-isopropylpropanamide;

(S)-2-amino-N-isopropyl-3-(2-methoxy-[1,1′-biphenyl]-4-yl)propanamide;

(S)-2-amino-N-isopropyl-3-(2-(trifluoromethyl)-[1,1′-biphenyl]-4-yl)propanamide;

(S)-2-amino-3-(2′,3′-difluoro-[1,1′-biphenyl]-4-yl)-N-isopropylpropanamide; and

(S)-2-amino-3-(2-ethyl-[1,1′-biphenyl]-4-yl)-N-isopropylpropanamide;

or a pharmaceutically acceptable salt thereof.

18 . A method for treating hypercholesterolemia, dyslipidemia, liver disease, or for reducing circulating LDL cholesterol levels in a mammal, comprising administering to said mammal a compound of Formula I, or a pharmaceutically acceptable salt, hydrate, solvate, or tautomeric form thereof:

wherein

R 3 is selected from the group consisting of H, lower alkyl, halo, haloalkyl, hydroxyalkyl, alkoxyl, and nitrile;

R 4 is selected from the group consisting of H and —OH;

R 1 and R 2 are independently selected from the group consisting of lower alkyl, halo, —OH, and amino; and

W is C, CH, or N, wherein when W is C then the dashed bonds are single bonds, and W and Y join together, along with the atoms to which they are attached, to form a 5 membered ring in which Y is CH2, and wherein when W is CH or N, then the dashed bonds are absent and Y is absent.

19 . The method of claim 18 , wherein said compound is formulated as a pharmaceutical composition.

20 . The method of claim 19 , wherein said pharmaceutical composition further comprises a pharmaceutical drug.

21 . The method of claim 18 , wherein said compound is selected from: