Synthesis of novel inhibitors of isoprenoid biosynthesis
Antibacterial IspF inhibitor compounds and compositions are described. Methods include administering described compounds and compositions to treat bacterial or parasitic infections and to inhibit or parasite or bacterial growth.
1. A compound of Formula II:
or a compound of Formula III:
or a pharmaceutically acceptable salt thereof, wherein
R 1 is H or lower alkyl;
R 2 is H or lower alkyl; and
R 3 is biphenyl, pyridine, pyrimidine, oxazine, oxathiazine,
or
each of which may be optionally substituted or R 3 is substituted alkylaryl;
wherein the alkyl of the alkylaryl is comprised of 2 to 8 carbon atoms.
2. The compound of claim 1 of Formula II:
or a pharmaceutically acceptable salt thereof, wherein
R 1 is H or lower alkyl;
R 2 is H or lower alkyl; and
R 3 is substituted alkylaryl or optionally substituted biphenyl, pyridine, pyrimidine, oxazine, or oxathiazine;
wherein the alkyl of the alkylaryl is comprised of 2 to 8 carbon atoms.
3. The compound of claim 1 of Formula III:
or a pharmaceutically acceptable salt thereof, wherein
R 1 is H or lower alkyl;
R 2 is H or lower alkyl; and
R 3 is substituted alkylaryl, or optionally substituted biphenyl, pyridine, pyrimidine, oxazine, or oxathiazine;
wherein the alkyl of the alkylaryl is comprised of 2 to 8 carbon atoms.
4. The pharmaceutically acceptable salt of claim 2 which is
5. A pharmaceutical composition comprising a therapeutically effective amount of at least one compound according to claim 1 and a pharmaceutically acceptable carrier.
6. A method of treating a bacterial infection, the method comprising administering a therapeutically effective amount of the compound according to claim 1 , wherein the bacterial infection is a Burkholderia infection.
7. A method of treating a bacterial infection, the method comprising administering a therapeutically effective amount of the compound according to claim 1 , wherein the bacterial infection is a Mycobacterium infection.
8. A method of treating tuberculosis, the method comprising administering a therapeutically effective amount of the compound, of claim 1 .
9. A method of treating malaria the method comprising administering a therapeutically effective amount of the compound of claim 1 .
10. The compound of claim 1 or a pharmaceutically acceptable salt thereof, wherein R 1 is hydrogen.
11. The compound of claim 1 or a pharmaceutically acceptable salt thereof, wherein R 2 is hydrogen.
12. The compound of claim 1 of Formula II:
or a compound of Formula III:
or a pharmaceutically acceptable salt thereof, wherein
R 3 is substituted alkylaryl, or optionally substituted pyridine, pyrimidine, oxazine, or oxathiazine, and
wherein the alkyl of the alkylaryl is comprised of 2 to 8 carbon atoms.
13. The compound of claim 1 or a pharmaceutically acceptable salt thereof, wherein R 3 is a substituted ethylaryl.
14. The compound of claim 1 or a pharmaceutically acceptable salt thereof, wherein
R 1 and R 2 are hydrogen, and
R 3 is a substituted ethylaryl.