Barbituric acid derivatives, their preparation and use thereof as leukocyte transmigration inhibitors and for treating inflammatory diseases, autoimmune diseases and cancer
Provided herein are novel barbituric acid derivatives, their synthesis and use thereof in blocking leukocyte transmigration. The novel barbituric acid derivatives are useful for the treatment of disorders associated with leukocyte transmigration, such as for example inflammatory diseases and disorders, autoimmune diseases and disorders, and cancers.
1. A compound of general Formula (Ib):
wherein
Z is absent; and
R 5 is hydrogen, linear alkyl, branched alkyl, linear alkenyl or branched alkenyl, wherein each of the alkyl and the alkenyl may be unsubstituted or substituted with one, two, or three substituents selected from the group consisting of halo, nitro, cyano and amino; and stereoisomers, enantiomers and tautomers thereof, pharmaceutically acceptable salts thereof and mixtures thereof,
wherein the bonds to the barbituric acid moiety and to the linking group —O—CH 2 —are located meta to each other.
2. The compound of claim 1 , wherein R 5 is a linear or branched alkyl having 1 to 6 carbon atoms (C 1-6 alkyl).
3. The compound of claim 1 , wherein, R 5 is unsubstituted.
4. The compound of claim 3 , wherein R 5 is selected from unsubstituted linear alkyl or unsubstituted branched alkyl, having 1 to 4 carbon atoms (C 1-4 alkyl), selected from methyl, ethyl, n-propyl, iso-propyl, butyl, iso-butyl, sec-butyl, tert-butyl.
5. The compound of claim 4 , wherein R 5 is methyl.
6. The compound of claim 1 , wherein the carboxylic group —CO(═O)R 5 is present at the para position to the linking group —O—CH 2 —; or wherein the carboxylic group —CO(═O)R 5 is present at the meta position to the linking group —O—CH 2 —; or wherein the carboxylic group —CO(═O)R 5 is present at the ortho position to the linking group —O—CH 2 —.
7. The compound of claim 1 , having the Formula 1:
or a pharmaceutically acceptable salt thereof.
8. The compound of claim 1 , having the Formula 9:
or a pharmaceutically acceptable salt thereof.
9. A pharmaceutical composition comprising one or more of the compounds of Formula (Ib) as defined in claim 1 or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier or diluent.
10. The pharmaceutical composition of claim 9 , further comprising one or more additional therapeutic agents.
11. The pharmaceutical composition of claim 9 , wherein the compound is of Formula 1:
or a pharmaceutically acceptable salt thereof.
12. The pharmaceutical composition of claim 9 , wherein the compound is of Formula 9:
or a pharmaceutically acceptable salt thereof.
13. A method for inhibiting leukocyte transmigration, comprising administering to a subject in need thereof a therapeutically effective amount of a compound of Formula (Ib) as defined claim 1 , thereby inhibiting leukocyte transmigration in the subject.
14. The method of claim 13 , wherein the compound is of Formula 1 as defined in claim 7 , or of Formula 9 as defined in claim 8 , or pharmaceutically acceptable salts thereof.
15. The method of claim 13 , wherein leukocyte transmigration inhibition is applied in the treatment of a disease or condition selected from the group consisting of an inflammatory disease or condition, and autoimmune disease or condition and cancer.