Benzosulfonyl compounds

1. A compound of Formula (I) or a pharmaceutically acceptable salt thereof:

wherein,

is substituted or unsubstituted pyrrolyl, substituted or unsubstituted imidazolyl, substituted or unsubstituted pyrazolyl, substituted or unsubstituted oxazolyl, substituted or unsubstituted isoxazolyl, substituted or unsubstituted thiazolyl, substituted or unsubstituted isothiazolyl, substituted or unsubstituted triazolyl, substituted or unsubstituted tetrazolyl, substituted or unsubstituted oxadiazolyl, or substituted or unsubstituted thiadiazolyl;

each R z is independently H, halogen, —CN, substituted or unsubstituted C 1 -C 6 alkyl, substituted or unsubstituted C 1 -C 6 haloalkyl, substituted or unsubstituted C 1 -C 6 heteroalkyl, substituted or unsubstituted C 3 -C 10 cycloalkyl, substituted or unsubstituted C 2 -C 10 heterocycloalkyl, substituted or unsubstituted aralkyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, -L 1 -Y 1 , or -L 2 -L 3 -Y 2 ;

m is 0, 1, 2, 3, or 4;

L 1 is substituted or unsubstituted C 1 -C 6 alkylene, substituted or unsubstituted C 2 -C 10 cyclolkylene, or substituted or unsubstituted C 2 -C 10 heterocycloalkylene;

Y 1 is substituted or unsubstituted C 3 -C 10 cycloalkyl, substituted or unsubstituted C 2 -C 10 heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl;

L 2 is absent, substituted or unsubstituted C 1 -C 6 alkylene, substituted or unsubstituted C 2 -C 10 cyclolkylene, or substituted or unsubstituted C 2 -C 10 heterocycloalkylene;

L 3 is —O—, —S—, —(S═O)—, —(SO 2 )—, —NR 3 —, —(C═O)—, —(C═O)O—, —(C═O)—, —(C═O)NR 3 —, —(C═O)NR 3 —O—, —O—NR 3 (C═O)—, —NR 3 (C═O)—, —NR 3 (C═O)NR 3 —, —O(C═O)NR 3 —, —NR 3 (C═O)O—, —NR 3 (SO 2 )NR 3 —, —NR 3 (SO 2 )—, —(SO 2 )NR 3 —, —(SO 2 )NR 3 —(C═O)—, —(C═O)—NR 3 (SO 2 )—, —(SO 2 )NR 3 —(C═O)O—, —O(C═O)—NR 3 (SO 2 )—, —NR 3 (SO 2 )NR 3 —(C═O)—, —(C═O)—NR 3 (SO 2 )NR 3 —, —O(C═O)—NR 3 (SO 2 )—NR 3 —, or —NR 3 (SO 2 )NR 3 —(C═O)O—;

each R 3 is independently H or substituted or unsubstituted C 1 -C 6 alkyl;

Y 2 is H, substituted or unsubstituted C 1 -C 6 alkyl, substituted or unsubstituted C 1 -C 6 haloalkyl, substituted or unsubstituted C 1 -C 6 heteroalkyl, substituted or unsubstituted C 3 -C 10 cycloalkyl, substituted or unsubstituted C 2 -C 10 heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl;

or R 3 and Y 2 on the same N atom are taken together with the N atom to which they are attached to form a substituted or unsubstituted N-containing heterocycle;

R is NHR 1 or R 1 ;

R 1 is substituted or unsubstituted C 1 -C 6 alkyl, substituted or unsubstituted C 1 -C 6 haloalkyl, substituted or unsubstituted C 1 -C 6 heteroalkyl, substituted or unsubstituted C 3 -C 10 cycloalkyl, substituted or unsubstituted C 2 -C 10 heterocycloalkyl, substituted or unsubstituted aralkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl;

each R 2 is independently H, halogen, —N 3 , —CN, —OR 4 , —SR 4 , —(SO 2 )R 4 , —N(R 4 ) 2 , —CO 2 R 4 , substituted or unsubstituted C 1 -C 6 alkyl, substituted or unsubstituted C 1 -C 6 haloalkyl, substituted or unsubstituted C 1 -C 6 heteroalkyl, substituted or unsubstituted C 3 -C 10 cycloalkyl substituted or unsubstituted C 2 -C 10 heterocycloalkyl, substituted or unsubstituted aralkyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, or

n is 0, 1, 2, 3, 4, or 5; and

each R 4 is independently H, substituted or unsubstituted C 1 -C 6 alkyl, substituted or unsubstituted C 1 -C 6 haloalkyl, substituted or unsubstituted C 1 -C 6 heteroalkyl, substituted or unsubstituted C 3 -C 10 cycloalkyl, substituted or unsubstituted C 2 -C 10 heterocycloalkyl, substituted or unsubstituted aralkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl.

2. The compound or pharmaceutically acceptable salt thereof of claim 1 , wherein:

3. The compound or pharmaceutically acceptable salt thereof of claim 1 , wherein:

each R z is independently H, halogen, substituted or unsubstituted C 1 -C 6 alkyl, substituted or unsubstituted C 1 -C 6 haloalkyl, substituted or unsubstituted C 3 -C 10 cycloalkyl, substituted or unsubstituted C 2 -C 10 heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl.

4. The compound or pharmaceutically acceptable salt thereof of claim 3 , wherein:

each R z is independently H, P, —Cl, —Br, —I, methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, tert-butyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or phenyl.

5. The compound or pharmaceutically acceptable salt thereof of claim 1 , wherein:

6. The compound or pharmaceutically acceptable salt thereof of claim 1 , wherein:

R is NHR 1 ; and

R 1 is substituted or unsubstituted C 1 -C 6 alkyl, substituted or unsubstituted C 1 -C 6 haloalkyl, substituted or unsubstituted C 1 -C 6 heteroalkyl, substituted or unsubstituted C 3 -C 10 cycloalkyl, substituted or unsubstituted C 2 -C 10 heterocycloalkyl, substituted or unsubstituted aralkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl.

7. The compound or pharmaceutically acceptable salt thereof of claim 6 , wherein:

R 1 is methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, tert-butyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or phenyl.

8. The compound or pharmaceutically acceptable salt thereof of claim 1 , wherein:

9. The compound or pharmaceutically acceptable salt thereof of claim 8 , wherein:

10. The compound or pharmaceutically acceptable salt thereof of claim 1 , wherein:

each R 2 is independently H, halogen, —N 3 , —CN, —OR 4 , —SR 4 , —(SO 2 )R 4 , —N(R 4 ) 2 , —CH 2 R 4 , substituted or unsubstituted C 1 -C 6 alkyl, substituted or unsubstituted C 1 -C 6 haloalkyl, substituted or unsubstituted C 1 -C 6 heteroalkyl, substituted or unsubstituted C 3 -C 10 cycloakyl, substituted or unsubstituted C 2 -C 10 heterocycloalkyl, substituted or unsubstituted aralkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl.

11. The compound or pharmaceutically acceptable salt thereof of claim 1 , wherein the compound has the structure of Formula (Id), or a pharmaceutically acceptable salt thereof:

12. The compound or pharmaceutically acceptable salt thereof of claim 1 , wherein the compound has the structure of Formula (Ie), or a pharmaceutically acceptable salt thereof:

13. The compound or pharmaceutically acceptable salt thereof of claim 1 , wherein each R 2 is —CF 3 .

14. A pharmaceutical composition comprising a pharmaceutically acceptable excipient and a compound of claim 1 or a pharmaceutically acceptable salt thereof.

15. A method for treating a cancer in a subject in need thereof comprising administering a therapeutically effective amount of a compound of claim 1 or a pharmaceutically acceptable salt thereof.

16. The method of claim 15 , wherein the cancer is selected from mesothelioma, hepatocellular carcinoma, meningioma, malignant peripheral nerve sheath tumor, lung cancer, prostate cancer, pancreatic cancer, adenosquamous carcinoma, thyroid cancer, gastric cancer, esophageal cancer, ovarian cancer, melanoma, and breast cancer.

17. A method of inhibiting one or more of proteins encompassed by, or related to, the Hippo pathway in a subject, comprising administering to a subject a compound of claim 1 , or a pharmaceutically acceptable salt thereof.

18. A method of inhibiting transcriptional coactivator with PDZ binding motif/Yes-associated protein transcriptional coactivator (TAZ/YAP) in a subject comprising administering to a subject a compound of claim 1 , or a pharmaceutically acceptable salt thereof.

19. A compound that has one of the following structures: