Treatment of T-cell mediated diseases
View Patent ↗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.
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 .