Pyrrolidinone derivatives
AssigneeUcb, S.A.
InventorsDong Zou, Olivier Dasse, Janelle Evans, Paul Higgins, Jeremy Kintigh, Rama Kondru, Eric Schwartz, Laurent Knerr, Hai-Xiao Zhai
Life of this patent
Estimating the term…
Abstract
The present invention provides pharmaceutical compositions and novel compounds useful in the treatment of conditions mediated by CCR2, MCP-1 or the interaction thereof. The compounds of the present invention are pyrrolidinones and pyrrolidine-thiones.
Claims28
A pharmaceutical composition comprising a compound according to formula I
- 3
- wherein,
- Y is oxygen or sulfur;
- G and G′, together with the bond linking them, are HC—CH or C═C;
- V is aryl, heterocycle or cycloalkyl;
- Z is halogen, alkyl, alkenyl, alkynyl, hydroxyl, amino, alkoxy, aryloxy, nitro or cyano;
- R1 is hydrogen, halogen, alkyl, cycloalkyl, alkenyl, cycloalkenyl, alkynyl, aryl or heterocycle;
- R2 is hydrogen or hydroxy;
- R3 is —C(O)R3a, —C(O)OR3a, —C(O)N(R3a)(R3b), —S(O)2R3a, —S(O)R3a or —SR3a wherein R3a and R3b have independently the same meaning as R1;
- R4 is hydroxy, sulfanyl or amino;
- t is 0, 1, 2, 3, 4 or 5;
- or a pharmaceutically acceptable salt or metabolically cleavable derivative thereof, together with a pharmaceutically acceptable diluent or carrier.
A method of treating or preventing conditions mediated by CCR2, MCP-1 or the interaction thereof, the method comprising administering to a patient an amount of a CCR2 antagonist sufficient to prevent, reduce or eliminate the condition.
Dependencies are inferred from the claim text.