Capsaicinoid prodrug compounds and their use in treating medical conditions
The invention provides capsaicinoid prodrug compounds (e.g., prodrugs of resiniferatoxin, tinyatoxin, iodoresiniferatoxin, and related compounds), pharmaceutical compositions, and their use in the treatment of medical conditions, such as pain, and in agonizing TRPV1 activity.
1. A compound of Formula I or Formula II, wherein Formula I is represented by:
or a pharmaceutically acceptable salt thereof; wherein:
R 1 represents independently for each occurrence hydrogen, C 1-6 alkyl, C 1-6 haloalkyl, C 3-7 cycloalkyl, C 6 aryl, or 3-8 membered heterocycloalkyl; or two occurrences of R 1 are taken together with the carbon atom to which they are attached to form a 3-6 membered saturated carbocyclic or heterocyclic ring;
R 2 represents independently for each occurrence hydrogen, C 1-6 alkyl, C 1-6 haloalkyl, C 3-7 cycloalkyl, C 6 aryl, or 3-8 membered heterocycloalkyl; or two occurrences of R 2 attached to the same carbon atom are taken together to represent an oxo group; or two occurrences of R 2 attached to the same carbon atom are taken together with the carbon atom to which they are attached to form a 3-6 membered saturated carbocyclic or heterocyclic ring;
R 3 is hydrogen, C 1-6 alkyl, C 1-6 haloalkyl, C 3-7 cycloalkyl, 4-8 membered heterocycloalkyl, or —C(═NH)—NH 2 ; wherein C 1-6 alkyl, C 3-7 cycloalkyl, and 4-8 membered heterocycloalkyl are each optionally substituted with 1, 2, or 3 substituents independently selected from the group consisting of halogen, hydroxyl, oxo, C 1-4 alkyl, C 1-4 haloalkyl, C 3-7 cycloalkyl, and C 1-4 alkoxyl; provided that if R 3 is hydrogen, methyl, or ethyl, then at least one of R 1 and R 2 is not hydrogen; and
R 4 represents independently for each occurrence hydrogen, halogen, C 1-4 alkyl, C 1-4 haloalkyl, C 1-4 alkoxyl, or C 1-4 haloalkoxyl;
m is 0, 1, 2, or 3; and
n is 0, 1, or 2; and
Formula II is represented by:
or a pharmaceutically acceptable salt thereof; wherein:
R 1 is hydrogen, C 1-6 alkyl, C 1-6 haloalkyl, C 3-7 cycloalkyl, C 6 aryl, or 4-8 membered heterocycloalkyl;
R 2 represents independently for each occurrence hydrogen, C 1-6 alkyl, C 1-6 haloalkyl, C 3-7 cycloalkyl, C 6 aryl, or 3-8 membered heterocycloalkyl; or two occurrences of R 2 are taken together to represent an oxo group; or two occurrences of R 2 are taken together with the carbon atom to which they are attached to form a 3-6 membered saturated carbocyclic or heterocyclic ring;
R 3 is hydrogen, C 1-6 alkyl, C 1-6 haloalkyl, C 3-7 cycloalkyl, 4-8 membered heterocycloalkyl, or —C(═NH)—NH 2 ; wherein C 1-6 alkyl, C 3-7 cycloalkyl, and 4-8 membered heterocycloalkyl are each optionally substituted with 1, 2, or 3 substituents independently selected from the group consisting of halogen, hydroxyl, oxo, C 1-4 alkyl, C 1-4 haloalkyl, C 3-7 cycloalkyl, and C 1-4 alkoxyl;
R 4 represents independently for each occurrence hydrogen, halogen, C 1-4 alkyl, C 1-4 haloalkyl, C 1-4 alkoxyl, or C 1-4 haloalkoxyl;
Ring A is one of the following:
a 3-8 membered heterocyclic ring or a C 3-8 saturated or partially unsaturated carbocyclic ring, each of which is optionally substituted with 1, 2, or 3 substituents independently selected from the group consisting of halogen, hydroxyl, C 1-6 alkyl, C 1-6 haloalkyl, C 3-7 cycloalkyl, C 1-4 alkoxyl, oxo, and C 1-4 haloalkoxyl; or
a 6-membered carbocyclic aromatic ring substituted with 1, 2, or 3 substituents independently selected from the group consisting of halogen, hydroxyl, C 1-6 alkyl, C 1-6 haloalkyl, C 3-7 cycloalkyl, C 1-4 alkoxyl, and C 1-4 haloalkoxyl; and
n is 0 or 1.
2. The compound of claim 1 , wherein the compound is a compound of Formula I or a pharmaceutically acceptable salt thereof.
3. The compound of claim 2 , wherein at least one R 1 represents C 1-6 alkyl, C 1-6 haloalkyl, C 3-7 cycloalkyl, C 6 aryl, or 3-8 membered heterocycloalkyl; or two occurrences of R 1 are taken together with the carbon atom to which they are attached to form a 3-6 membered saturated carbocyclic or heterocyclic ring.
4. The compound of claim 2 , wherein R 1 represents independently for each occurrence C 1-6 alkyl or C 3-7 cycloalkyl.
5. The compound of claim 2 , wherein two occurrences of R 1 are taken together with the carbon atom to which they are attached to form a 3-6 membered saturated carbocyclic or heterocyclic ring.
6. The compound of claim 2 , wherein at least one R 2 represents C 1-6 alkyl, C 1-6 haloalkyl, C 3-7 cycloalkyl, C 6 aryl, or 3-8 membered heterocycloalkyl; or two occurrences of R 2 attached to the same carbon atom are taken together to represent an oxo group; or two occurrences of R 2 attached to the same carbon atom are taken together with the carbon atom to which they are attached to form a 3-6 membered saturated carbocyclic or heterocyclic ring.
7. The compound of claim 2 , wherein two occurrences of R 2 attached to the same carbon atom are taken together with the carbon atom to which they are attached to form a 3-6 membered saturated carbocyclic or heterocyclic ring.
8. The compound of claim 1 , wherein the compound is a compound of Formula II or a pharmaceutically acceptable salt thereof.
9. The compound of claim 8 , wherein R 2 is hydrogen.
10. The compound of claim 8 , wherein at least one R 2 represents independently for each occurrence C 1-6 alkyl or C 3-7 cycloalkyl; or two occurrences of R 2 are taken together with the carbon atom to which they are attached to form a 3-6 membered saturated carbocyclic or heterocyclic ring.
11. The compound of claim 8 , wherein Ring A is a 3-8 membered heterocyclic ring optionally substituted with 1, 2, or 3 substituents independently selected from the group consisting of halogen, hydroxyl, C 1-6 alkyl, C 1-6 haloalkyl, C 3-7 cycloalkyl, C 1-4 alkoxyl, oxo, and C 1-4 haloalkoxyl.
12. The compound of claim 8 , wherein Ring A is a 5-6 membered heteroaromatic ring optionally substituted with 1, 2, or 3 substituents independently selected from the group consisting of halogen, hydroxyl, C 1-6 alkyl, C 1-6 haloalkyl, C 3-7 cycloalkyl, C 1-4 alkoxyl, and C 1-4 haloalkoxyl.
13. The compound of claim 8 , wherein Ring A is a C 3-8 saturated or partially unsaturated carbocyclic ring optionally substituted with 1, 2, or 3 substituents independently selected from the group consisting of halogen, hydroxyl, C 1-6 alkyl, C 1-6 haloalkyl, C 3-7 cycloalkyl, C 1-4 alkoxyl, oxo, and C 1-4 haloalkoxyl.
14. The compound of claim 8 , wherein Ring A is a 6-membered carbocyclic aromatic ring substituted with 1, 2, or 3 substituents independently selected from the group consisting of halogen, hydroxyl, C 1-6 alkyl, C 1-6 haloalkyl, C 3-7 cycloalkyl, C 1-4 alkoxyl, and C 1-4 haloalkoxyl.
15. The compound of claim 8 , wherein n is 1.
16. A compound represented by Formula III:
or a pharmaceutically acceptable salt thereof; wherein:
X is —C(R 1 ) 2 —, a bond, or —O—;
Y is —C(R 2 ) 2 — or a bond; provided X and Y are not both a bond;
R 1 represents independently for each occurrence hydrogen, halogen, C 1-6 alkyl, C 1-6 haloalkyl, C 3-7 cycloalkyl, C 6 aryl, or 3-8 membered heterocycloalkyl; or two occurrences of R 1 are taken together with the carbon atom to which they are attached to form a 3-6 membered saturated carbocyclic or heterocyclic ring;
R 2 represents independently for each occurrence hydrogen, C 1-6 alkyl, C 1-6 haloalkyl, C 3-7 cycloalkyl, C 6 aryl, or 3-8 membered heterocycloalkyl; or two occurrences of R 2 are taken together to represent an oxo group; or two occurrences of R 2 are taken together with the carbon atom to which they are attached to form a 3-6 membered saturated carbocyclic or heterocyclic ring;
R 3 is hydrogen, C 1-6 alkyl, C 1-6 haloalkyl, C 3-7 cycloalkyl, 4-8 membered heterocycloalkyl, or —C(═NH)—NH 2 ; wherein C 1-6 alkyl, C 3-7 cycloalkyl, and 4-8 membered heterocycloalkyl are each optionally substituted with 1, 2, or 3 substituents independently selected from the group consisting of halogen, hydroxyl, oxo, C 1-4 alkyl, C 1-4 haloalkyl, C 3-7 cycloalkyl, and C 1-4 alkoxyl;
R 4 represents independently for each occurrence hydrogen, halogen, C 1-4 alkyl, C 1-4 haloalkyl, C 1-4 alkoxyl, or C 1-4 haloalkoxyl; and
Ring A is one of the following:
a 6-membered carbocyclic aromatic ring or a 5-6 membered heteroaromatic ring, each of which is optionally substituted with 1, 2, or 3 substitutents independently selected from the group consisting of halogen, hydroxyl, C 1-6 alkyl, C 1-6 haloalkyl, C 3-7 cycloalkyl, C 1-4 alkoxyl, and C 1-4 haloalkoxyl; or
a C 3-8 saturated or partially unsaturated carbocyclic ring or a 3-8 membered saturated or partially unsaturated heterocylic ring, each of which is optionally substituted with 1, 2, or 3 substitutents independently selected from the group consisting of halogen, hydroxyl, oxo, C 1-6 alkyl, C 1-6 haloalkyl, C 3-7 cycloalkyl, C 1-4 alkoxyl, and C 1-4 haloalkoxyl.
17. A compound of Formula IV or V, wherein Formula IV is represented by:
or a pharmaceutically acceptable salt thereof; wherein:
R 1 is hydrogen, C 1-6 alkyl, C 1-6 haloalkyl, C 3-7 cycloalkyl, C 6 aryl, or 4-8 membered heterocycloalkyl; or R 1 and an occurrence of R 2A are taken together with the atoms to which they are attached to form a 3-8 membered saturated heterocyclic ring optionally substituted with 1, 2, or 3 substituents independently selected from the group consisting of halogen, hydroxyl, oxo, C 1-4 alkyl, C 1-4 haloalkyl, C 3-7 cycloalkyl, and C 1-4 alkoxyl;
R 2A represents independently for each occurrence hydrogen, C 1-6 alkyl, C 1-6 haloalkyl, C 3-7 cycloalkyl, C 6 aryl, or 3-8 membered heterocyclyl; or two occurrences of R 2A are taken together to represent an oxo group; or two occurrences of R 2A are taken together with the carbon atom to which they are attached to form a 3-6 membered saturated carbocyclic or heterocyclic ring; or an occurrence of R 2A and an occurrence of R 2B are taken together with the carbon atoms to which they are attached to form a 3-6 membered saturated carbocyclic or heterocyclic ring;
R 2B represents independently for each occurrence hydrogen, C 1-6 alkyl, C 1-6 haloalkyl, C 3-7 cycloalkyl, C 6 aryl, or 3-8 membered heterocyclyl; or two occurrences of R 2B are taken together to represent an oxo group; or two occurrences of R 2B are taken together with the carbon atom to which they are attached to form a 3-6 membered saturated carbocyclic or heterocyclic ring;
R 3 is hydrogen, C 1-6 alkyl, C 1-6 haloalkyl, C 3-7 cycloalkyl, 4-8 membered heterocycloalkyl, or —C(═NH)—NH 2 ; wherein C 1-6 alkyl, C 3-7 cycloalkyl, and 4-8 membered heterocycloalkyl are each optionally substituted with 1, 2, or 3 substituents independently selected from the group consisting of halogen, hydroxyl, oxo, C 1-4 alkyl, C 1-4 haloalkyl, C 3-7 cycloalkyl, and C 1-4 alkoxyl; and
R 4 represents independently for each occurrence hydrogen, halogen, C 1-4 alkyl, C 1-4 haloalkyl, C 1-4 alkoxyl, or C 1-4 haloalkoxyl; and
Formula V is represented by:
or a pharmaceutically acceptable salt thereof; wherein:
R 1 is hydrogen, C 1-6 alkyl, C 1-6 haloalkyl, C 3-7 cycloalkyl, C 6 aryl, or 4-8 membered heterocycloalkyl; or R 1 and an occurrence of R 2A are taken together with the atoms to which they are attached to form a 3-8 membered saturated heterocyclic ring optionally substituted with 1, 2, or 3 substituents independently selected from the group consisting of halogen, hydroxyl, oxo, C 1-4 alkyl, C 1-4 haloalkyl, C 3-7 cycloalkyl, and C 1-4 alkoxyl;
R 2A represents independently for each occurrence hydrogen, C 1-6 alkyl, C 1-6 haloalkyl, C 3-7 cycloalkyl, C 6 aryl, or 3-8 membered heterocyclyl; or two occurrences of R 2A are taken together to represent an oxo group; or two occurrences of R 2A are taken together with the carbon atom to which they are attached to form a 3-6 membered saturated carbocyclic or heterocyclic ring; or an occurrence of R 2A and an occurrence of R 2B are taken together with the carbon atoms to which they are attached to form a 3-6 membered saturated carbocyclic or heterocyclic ring;
R 2B represents independently for each occurrence hydrogen, C 1-6 alkyl, C 1-6 haloalkyl, C 3-7 cycloalkyl, C 6 aryl, or 3-8 membered heterocyclyl; or two occurrences of R 2B are taken together to represent an oxo group; or two occurrences of R 2B are taken together with the carbon atom to which they are attached to form a 3-6 membered saturated carbocyclic or heterocyclic ring:
R 3 is hydrogen, C 1-6 alkyl, C 1-6 haloalkyl, C 3-7 cycloalkyl, 4-8 membered heterocycloalkyl, or —C(═NH)—NH 2 ; wherein C 1-6 alkyl, C 3-7 cycloalkyl, and 4-8 membered heterocycloalkyl are each optionally substituted with 1, 2, or 3 substituents independently selected from the group consisting of halogen, hydroxyl, oxo, C 1-4 alkyl, C 1-4 haloalkyl, C 3-7 cycloalkyl, and C 1-4 alkoxyl;
R 4 represents independently for each occurrence hydrogen, halogen, C 1-4 alkyl, C 1-4 haloalkyl, C 1-4 alkoxyl, or C 1-4 haloalkoxyl; and
R 5 is hydrogen, C 1-6 alkyl, C 1-6 haloalkyl, C 3-7 cycloalkyl, C 6 aryl, or 3-8 membered heterocyclyl.
18. A pharmaceutical composition comprising a compound of claim 1 and a pharmaceutically acceptable carrier.
19. A method of treating pain in a subject, comprising administering a therapeutically effective amount of a compound of claim 1 to a subject in need thereof to treat the pain.
20. A method of agonizing the activity of TRPV1, comprising exposing a TRPV1 to an effective amount of a compound of claim 1 to agonize the activity of said TRPV1.