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US 10,118,896 B2Granted
Antagonists of the kappa opioid receptor
AssigneesUniversity of Kansas, The Scripps Research Institute
InventorsJeffrey Aube, Kevin Frankowski, Thomas Prisinzano, Laura Bohn
Life of this patent
Estimating the term…
Abstract
The present technology is directed to compounds, compositions, and methods related to non-morphinan-like kappa opioid receptor (KOR) antagonists. The technology is suited to treat addiction, diuresis, depression, post traumatic stress disorder, an eating disorder, panic disorder, social anxiety disorder, general anxiety disorder, obsessive compulsive disorders, excessive or unreasonable specific phobias, and/or other conditions related to anxiety or aversion-reward responses.
Claims18
A compound according to formula I
- or stereoisomers, tautomers, solvates, and/or salts thereof;
- wherein
- G1 and G2 are each independently C═O or S(O)2;
- R1, R2, R3, R4, R5, R7, R8, R9, R10, and R11 are each independently H, halo, hydroxy, amino, cyano, trifluoromethyl, thiol, alkylthio, sulfoxide, sulfone, nitro, pentafluorosulfanyl, carboxylate, amide, ester, or a substituted or unsubstituted C1-C6 alkyl, C1-C6 alkoxy, aryl, aryloxy, C1-C6 alkanoyl, C1-C8 alkanoyloxy, aryloyl, or aryloyloxy group, where any two adjacent R1, R2, R3, R4, R5, R7, R8, R9, R10, and R11 may join to form a 5-membered or 6-membered substituted or unsubstituted heteroalkyl group;
- R6 is a branched C1-C8 alkyl group or a substituted or unsubstituted cycloalkyl or aryl group;
- and
- R12 and R13 are each independently H or a substituted or unsubstituted C1-C8 alkyl or C5-C7 cycloalkyl group;
- and
- n is 0, 1, or 2;
- provided that when G1 is S(O)2, G2 is C═O, R1, R2, R4, R5, R7, R8, R9, R10, R11, R12, R13 are each H, R6 is isopropyl, and n is 1, then R3 is not methyl.
7 more elements
Dependencies are inferred from the claim text.