IP Library Patent Application 15098362
Patent Application
App. No. 15/098,362

HEPCIDIN MIMETIC PEPTIDES AND USES THEREOF

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Quick Facts
Patent No.
US None
App. No.
15/098,362
Abstract

Compounds and methods are described herein that can be used to treat subjects for conditions related to hepcidin activity, such as but not limited diseases of iron metabolism, beta thalassemia, hemochromatosis, iron-loading anemias, alcoholic liver disease, or chronic hepatitis C.

Claims (167)

1 - 15 . (canceled)

16 . A compound, or a pharmaceutically acceptable salt thereof, of Formula II:

wherein:

R 1 is, H, —S—Z 1 ; —Z 2 , —SH, —C(═O)—Z 3 , or —S—C(═O)—Z 3 ,

R 2 and R 3 are each, independently, optionally substituted C 4 -C 7 alkyl,

D-Arg, D-Ile, Leu, D-Leu, Thr, D-Thr, Lys, D-Lys, Val, D-Val, D-Nω,ω-dimethyl-arginine, L-Nω,ω-dimethyl-arginine, D-homoarginine, L-homoarginine, D-norarginine, L-norarginine, citrulline, a modified Arg wherein the guanidinium group is modified or substituted, norleucine, norvaline, beta homo-Ile, Ach, N-Me-Arg, N-Me-Ile;

R 4 is Ida, Asp, Acetyl-Asp, N-MeAsp, Acetyl-Gly-Ida, or Acetyl-Gly-Asp or a derivative thereof to remove its negative charge above pH 4;

R 5 is CR 6 R 7 , aryl or heteroaryl;

B is absent or forms a 5-7 membered ring; and

q is 0-6, wherein when R 5 aryl or heteroaryl q is 1 and B is absent;

Z 1 is substituted or unsubstituted C 1 -C 18 alkyl, wherein the C 1 -C 18 alkyl is branched or unbranched;

Z 2 is substituted or unsubstituted C 1 -C 18 alkyl, wherein the C 1 -C 18 alkyl is branched or unbranched;

Z 3 is substituted or unsubstituted C 1 -C 18 alkyl, wherein the C 1 -C 18 alkyl is branched or unbranched;

R 6 and R 7 are each, independently, H, halo, optionally substituted C 1 -C 3 alkyl, or haloalkyl, provided that when R 1 is H, the compound is not Compound 1.

17 . The compound, or a pharmaceutically acceptable salt thereof, of claim 16 , wherein the compound is a compound of Formula II-A, II-B, or II-C:

18 . The compound, or a pharmaceutically acceptable salt thereof, of claim 16 , wherein R 1 is, H, —S—Z 1 or —C(═O)—Z 3 .

19 - 20 . (canceled)

21 . A compound, or a pharmaceutically acceptable salt thereof, of Formula III:

wherein:

R 1 is H, —S—Z 1 , —Z 2 , —SH, —S—C(═O)—Z 3 , or —C(═O)—Z 3

R 2 and R 3 are each, independently, optionally substituted C 4 -C 7 alkyl,

D-Arg, D-Ile, Leu, D-Leu, Thr, D-Thr, Lys, D-Lys, Val, D-Val, D-Nω,ω-dimethyl-arginine, L-Nω,ω-dimethyl-arginine, D-homoarginine, L-homoarginine, D-norarginine, L-norarginine, citrulline, a modified Arg wherein the guanidinium group is modified or substituted, norleucine, norvaline, beta homo-Ile, Ach, N-Me-Arg, N-Me-Ile;

R 4 is Ida, Asp, Acetyl-Asp, N-MeAsp, Acetyl-Gly-Ida, or Acetyl-Gly-Asp or a derivative thereof to remove its negative charge above pH 4;

B is absent or forms a 5-7 membered ring; and

Z 1 is substituted or unsubstituted C 1 -C 18 alkyl, wherein the C 1 -C 18 alkyl is branched or unbranched;

Z 2 is substituted or unsubstituted C 1 -C 18 alkyl, wherein the C 1 -C 18 alkyl is branched or unbranched;

Z 3 is substituted or unsubstituted C 1 -C 18 alkyl, wherein the C 1 -C 18 alkyl is branched or unbranched;

provided that when R 1 is H, the compound is not Compound 1.

22 . The compound, or a pharmaceutically acceptable salt thereof, of claim 21 , wherein the compound, or a pharmaceutically acceptable salt thereof, has a formula of Formula III-A.

23 . The compound, or a pharmaceutically acceptable salt thereof, of claim 16 , wherein R 5 is CR 6 R 7 .

24 . The compound, or a pharmaceutically acceptable salt thereof, of claim 23 , wherein R 6 and R 7 are H.

25 . The compound, or a pharmaceutically acceptable salt thereof, of claim 23 , wherein R 6 is H and R 7 is halo, optionally substituted C 1 -C 3 alkyl, or haloalkyl.

26 . The compound, or a pharmaceutically acceptable salt thereof, of claim 16 , wherein R 5 is aryl or heteroaryl.

27 . (canceled)

28 . The compound, or a pharmaceutically acceptable salt thereof, of claim 16 , wherein R 2 and R 3 are

29 . The compound, or a pharmaceutically acceptable salt thereof, of claim 16 , wherein R 2 and R 3 are

30 . The compound, or a pharmaceutically acceptable salt thereof, of claim 16 , wherein one of R 2 and R 3 is

and the other is

31 - 33 . (canceled)

34 . The compound, or a pharmaceutically acceptable salt thereof, of claim 16 , wherein

is modified to reduce the charge.

35 - 51 . (canceled)

52 . The compound, or a pharmaceutically acceptable salt thereof, of claim 16 , wherein the compound is a compound of Formula IV, or a pharmaceutically acceptable salt thereof:

wherein the carbonyl forms a bond with the 6-membered ring at C a , C b , or C c .

53 - 55 . (canceled)

56 . The compound, or a pharmaceutically acceptable salt thereof, of claim 16 , wherein the compound is a compound of Formula V, or a pharmaceutically acceptable salt thereof,

wherein the carbonyl forms a bond with the 5-membered ring at C d or C e .

57 . The compound, or a pharmaceutically acceptable salt thereof, of claim 16 , wherein the compound is a compound of Formula VI, or a pharmaceutically acceptable salt thereof,

wherein the bond from the carbonyl forms a bond with the 7-membered ring at C f , C g , C h , or C i .

58 - 60 . (canceled)

61 . A compound, or a pharmaceutically acceptable salt thereof, selected from the group consisting of: Compound 2, Compound 3, Compound 4, Compound 5, Compound 6, Compound 7, Compound 8, Compound 9, and Compound 10, or a pharmaceutically acceptable salt thereof.

62 . A compound, or a pharmaceutically acceptable salt thereof, of the formula:

P 1 -P 2 -P 3 -P 4 -P 5 -P 6 -P 7 -P 8 -P 9 -P 10 or P 10 -P 9 -P 8 -P 7 -P 6 -P 5 -P 4 -P 3 -P 2 -P 1 , wherein P 1 to P 10 are as defined in the following table:

Compound #

P 1

P 2

P 3

P 4

P 5

P 6

P 7

P 8

P 9

P 10

2

Ida

Thr

His

Dpa

bhPro

Arg

Cys-S—CH 3

Arg

Trp

X 3

3

Ida

Thr

His

Dpa

bhPro

Arg

Cys-C(═O)CH 3

Arg

Trp

X 3

4

Ida

Thr

His

Dpa

bhPro

Arg

Cys-CH 2 —CH 3

Arg

Trp

X 3

5

Ida

Thr

His

Dpa

Npc

Arg

Cys-S—CH 3

Arg

Trp

X 3

6

Ida

Thr

His

Dpa

Npc

Arg

Cys

Arg

Trp

X 3

7

Ida

Thr

His

Dpa

D-Npc

Arg

Cys-S—CH 3

Arg

Trp

X 3

8

Ida

Thr

His

Dpa

isoNpc

Arg

Cys-S—CH 3

Arg

Trp

X 3

9

Acetyl-Gly-Ida

Thr

His

Dpa

bhPro

Arg

Cys-S—CH 3

Arg

Trp

X 3

10

Ida

Thr

His

Dpa

bAla

Ara

Cys-S—CH 3

Arg

Trp

X 3

wherein: X 3 is Ahx-Ida(NH-PAL)-NH 2 , Ida is Iminodiacetic acid; bhPro is beta-homoproline, Npc is L-nipecotic acid; isoNpc is isonipecotic acid and bAla is beta-alanine.

63 . A pharmaceutical composition comprising the compound, or a pharmaceutically acceptable salt thereof, of claim 16 and a pharmaceutically acceptable carrier.

64 . A method of treating a subject or a subject in need thereof a disease of iron metabolism, beta thalassemia, hemochromatosis, iron-loading anemias, alcoholic liver disease, or chronic hepatitis C, comprising administering to the subject a compound, or a pharmaceutically acceptable salt thereof, of claim 16 .

65 - 82 . (canceled)

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 13, 2016
From: MERGANSER BIOTECH, INC.
To: LA JOLLA PHARMACEUTICAL COMPANY
Reel/Frame 040721/0617 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 3, 2016
From: MERUTKA, GENE SCOTT
To: MERGANSER BIOTECH, INC.
Reel/Frame 040209/0080 →