Novel analgesic and immunomodulatory cannabinoids
AssigneeUniversity of Connecticut
InventorsAlexandros Makriyannis, Dai Lu, Atmaram Khanolkar
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AssigneeUniversity of Connecticut
InventorsAlexandros Makriyannis, Dai Lu, Atmaram Khanolkar
Estimating the term…
Disclosed are novel compounds represented by the following structural formula: R—X—Y; and physiologically acceptable salts thereof. R is a tricyclic core of a cannabinoid or substituted cannabinoid. X is a covalent bond, —CH2— or —CHR1—, wherein R1 a C1 to C3 substituted or unsubstituted alkyl group. Y is a heterocyclic ring, a substituted heterocyclic ring, a carbocyclic ring, a substituted carbocyclic ring, a fused bicyclic ring system, a substituted fused bicyclic ring system, a bridged bicyclic ring system, a substituted bridged bicyclic ring system, a bridged tricyclic ring system or a substituted bridged tricyclic ring system. Also disclosed is a method of stimulating a CB1 and/or CB2 receptor in a subject. The method comprises administering to the subject a therapeutically effective amount of R—X—Y.
A compound represented by the following structural formula:
A method of stimulating a CB1 or CB2 receptor in a subject, comprising administering to the subject a therapeutically effective amount of a compound represented by the following structural formula:
A substituted or unsubstituted cannabinoid having substituted at C-3 with a heterocyclic ring, a substituted heterocyclic ring, a carbocyclic ring, a substituted carbocyclic ring, a fused bicyclic ring, a substituted fused bicyclic ring, a bridged bicyclic ring, a substituted bridged bicyclic ring, a bridged tricyclic ring or a substituted bridged tricyclic ring, and physiologically acceptable salts thereof.
Dependencies are inferred from the claim text.