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filingDate 2004-05-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6f4eb506c5a4d8aec3e61683df472bb9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7d4e7fdaace09837d732f1c6ccff1df5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_14fe86de53a0ead74baf450a1b5f4164
publicationDate 2013-04-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-2517718-A3
titleOfInvention Treatment of T-cell mediated diseases
abstract The invention provides an effective amount of a diketopiperazine having the following formula for use in the treatment of a T-cell mediated pulmonary disease or an autoimmune disease:n nwherein: nR 1 and R 2 , which may be the same or different, each is: n(a) a side chain of an amino acid, wherein the amino acid is glycine, alanine, valine, norvaline, α-aminoisobutyric acid, 2,4-diaminobutyric acid, 2,3-diaminobutyric acid, leucine, isoleucine, norleucine, serine, homoserine, threonine, aspartic acid, asparagine, glutamic acid, glutamine, lysine, hydroxylysine, histidine, arginine, homoarginine, citrulline, phenylalanine, p-aminophenylalanine, tyrosine, tryptophan, thyroxine, cysteine, homocysteine, methionine, penicillamine or ornithine; provided, however, that when R 1 is the side chain of asparagine or glutamine, then R 2 cannot be the side chain of lysine or ornithine, and when R 1 is the side chain of lysine or ornithine, then R 2 cannot be the side chain of asparagine or glutamine; n(b) a derivative of a side chain of an amino acid, wherein the amino acid is one of those recited in (a), and the derivatized side chain has: n(i) an -NH 2 group replaced by an -NHR 3 or -N(R 3 ) 2 group, wherein each R 3 may independently be a substituted or unsubstituted alkyl, cycloalkyl, heterocycloalkyl, aryl, alkylaryl, arylalkyl or heteroaryl; n(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; n(iii) a -COOH group replaced by a -COOR 3 group, wherein each R 3 may independently be a substituted or unsubstituted alkyl, cycloalkyl, heterocycloalkyl, aryl, alkylaryl, arylalkyl or heteroaryl; n(iv) a -COOH group replaced by a -CON(R 4 ) 2 group, wherein each R 4 may independently be H or a substituted or unsubstituted alkyl, cycloalkyl, heterocycloalkyl, aryl, alkylaryl, arylalkyl or heteroaryl; n(v) an -SH group replaced by -S-S-CH 2 -CH(NH 2 )-COOH or -S-S-CH 2 -CH 2 -CH(NH 2 )-COOH ; n(vi) a -CH 2 - group replaced by a -CH(NH 2 )- or a -CH(OH)- group; n(vii) a -CH 3 group replaced by a -CH 2 -NH 2 or a -CH 2 -OH group; and/or n(viii) an H which is attached to a carbon atom replaced by a halogen; or a physiologically-acceptable salt thereof.
priorityDate 2003-05-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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