IP Library Granted Patent US 9,707,227
Granted Patent B2
US 9,707,227 · App. 12/707,942 · Granted Jul 18, 2017

Treatment of T-cell mediated diseases

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Quick Facts
Patent No.
US 9,707,227
App. No.
12/707,942
Granted
Jul 18, 2017
Kind
B2
Abstract

The invention provides a method of treating T-cell mediated diseases and a method of inhibiting the activation of T-cells using certain diketopiperazines. The invention also provides methods of synthesizing diketopiperazines and pharmaceutical compositions comprising certain diketopiperazines. The invention further provides methods of making improved pharmaceutical compositions of proteins and peptides by either increasing or decreasing the content of diketopiperazines in the compositions and the resultant improved pharmaceutical compositions.

Claims (32)

1. A pharmaceutical composition having therapeutic activity, comprising a pharmaceutically-acceptable carrier and a diketopiperazine having the following formula:

wherein:

(a) R 5 and R 6 are each a different side chain of an amino acid, wherein,

the side chain of R 5 is isoleucine and the side chain of R 6 is a derivative of a side chain of isoleucine or a derivative of a side chain of homoserine, or

the side chain of R 5 is a derivative of a side chain of isoleucine or a derivative of a side chain of homoserine and the side chain of R 6 is isoleucine, or the side chains of R 5 and R 6 are each different derivatives of a side chain of isoleucine or homoserine,

and wherein the derivatized side chain has:

(i) an —OH group replaced by an —O—PO 3 H 2 or —OR 3 group, wherein each R 3 is independently a substituted or unsubstituted alkyl, cycloalkyl, heterocycloalkyl, aryl, alkylaryl, arylalkyl or heteroaryl;

(ii) a —CH 2 — group replaced by a —CH(NH 2 )— or a —CH(OH)— group;

(iii) a —CH 3 group replaced by a —CH 2 —NH 2 or a —CH 2 —OH group;

(iv) an H which is attached to a carbon atom replaced by a halogen; or

(v) a combination of the foregoing replacements; or

(b) R 5 and R 6 are each a different side chain of an amino acid, wherein the amino acid is 2,4-diaminobutyric acid, 2,3-diaminobutyric acid, or is a derivative of a side chain of 2,4-diaminobutyric acid or 2,3-diaminobutyric acid, wherein the derivatized side chain has:

(i) an —NH 2 group replaced by an —NHR 3 or —N(R 3 ) 2 group, wherein each R 3 is independently a substituted or unsubstituted alkyl, cycloalkyl, heterocycloalkyl, aryl, alkylaryl, arylalkyl or heteroaryl;

(ii) an —OH group replaced by an —O—PO 3 H 2 or —OR 3 group, wherein each R 3 may independently be a substituted or unsubstituted alkyl, cycloalkyl, heterocycloalkyl, aryl, alkylaryl, arylalkyl or heteroaryl;

(iii) a —CH 2 — group replaced by a —CH(NH 2 )— or a —CH(OH)— group;

(iv) an H which is attached to a carbon atom replaced by a halogen; or

(v) a combination of the foregoing replacements; or

(c) R 5 and R 6 are each a different side chain of an amino acid, wherein the amino acid is ornithine or a side chain of one of the amino acids or derivatives thereof as set forth in part (b); or

(d) R 5 and R 6 are each a different side chain of an amino acid, wherein the amino acid is hydroxylysine or a side chain of one of the amino acids or derivatives thereof as set forth in part (b); or

(e) R 5 and R 6 are each a different side chain of an amino acid, wherein the amino acid is citrulline or a side chain of one of the amino acids or derivatives thereof as set forth in part (b); or

a physiologically-acceptable salt thereof.

2. The composition according to claim 1 wherein:

R 5 and R 6 are each a different side chain of an amino acid, wherein

the side chain of R 5 is isoleucine and the side chain of R 6 is a derivative of a side chain of isoleucine or homoserine, or

the side chain of R 5 is a derivative of a side chain of isoleucine or homoserine and the side chain of R 6 is isoleucine, or

the side chains of R 5 and R 6 are each different derivatives of a side chain of isoleucine or homoserine,

and wherein the derivatized side chain is as defined in claim 1 .

3. The composition according to claim 1 wherein: R 5 and R 6 are defined as in section b of claim 1 .

4. The composition according to claim 1 wherein R 5 and R 6 are each a different side chain of 2,4-diaminobutyric acid, or 2,3-diaminobutyric acid.

5. The composition according to claim 1 wherein: R 5 and R 6 are defined as in section c of claim 1 .

6. The composition according to claim 1 wherein: R 5 and R 6 are defined as in section d of claim 1 .

7. The composition according to claim 1 wherein: R 5 and R 6 are defined as in section e of claim 1 .

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 9, 2013
From: DMI ACQUISITION CORP.
To: AMPIO PHARMACEUTICALS, INC.
Reel/Frame 031305/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 4, 2013
From: DMI BIOSCIENCES, INC.
To: DMI ACQUISITION CORP.
Reel/Frame 029565/0273 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 28, 2012
From: BAR-OR, DAVID; BAR-OR, RAPHAEL; SHIMONKEVITZ, RICHARD
To: DMI BIOSCIENCES, INC.
Reel/Frame 029543/0645 →