Compounds to inhibit calcium/calmodulin dependent protein kinase II and applications thereof
Provided are novel benzenesulfonamide compounds that inhibit calcium/calmodulin-dependent protein kinase II (CaMKII) and pharmaceutical compositions containing the benzenesulfonamide compounds. Also provided are methods of using the benzenesulfonamide compounds to treat diseases or conditions that are associated with CaMKII activity, such as a flavivirus infection.
1. A compound which is represented by formula (I):
wherein R 1 is hydrogen, cycloalkyl having 3 to 7 carbon ring atoms, heterocycle having 2 to 8 carbon ring atoms and at least one heteroatom selected from the group consisting of nitrogen, oxygen, and sulfur, or aryl having 2 to 3 rings each with 4 to 6 ring atoms; or R 1 together with the phenyl ring to which R 1 is attached form a fused bicyclic carbocycle having 8 to 10 carbon ring atoms;
R 2 is cycloalkyl having 4 to 10 carbon ring atoms, or heterocycle selected from the group consisting of thiazole, imidazole, tetrazole, imidazolidine, imidazoline, isoxazole, and benzimidazole; and
n is 1, 2, 4, or 6.
2. The compound of claim 1 , wherein R 1 is hydrogen and n is 1.
3. The compound of claim 2 , which is represented by one of the following formulas:
4. The compound of claim 1 , wherein R 1 is hydrogen; R 2 is cycloheptyl; and n is 2, 4, or 6.
5. The compound of claim 1 , wherein R 2 is cycloheptyl and n is 1.
6. The compound of claim 5 , which is represented by one of the following formulas:
7. A pharmaceutical composition, comprising a compound of claim 1 and a pharmaceutically acceptable carrier.