Inhibitors of long and very long chain fatty acid metabolism as broad spectrum anti-virals
AssigneeThe Trustees of Princeton University
InventorsEmre Koyuncu, Joshua D. Rabinowitz, Thomas Shenk
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Abstract
The present invention provides methods and compounds for treating viral infections using modulators of host cell enzymes relating to long chain fatty acid and lipid droplet metabolism. It includes a method of treating viral infections using triacsin C and its relatives, analogs and derivatives as well as other inhibitors of long chain fatty acid metabolism and lipid droplet metabolism.
Claims4
A method of treating or preventing viral infection in a mammal, comprising administering to the mammalian subject in need thereof a therapeutically effective amount of an agent that inhibits a long chain fatty acid synthesis enzyme, wherein the virus is human cytomegalovirus (HCMV) and the agent is a compound of Formula VIII
- wherein R1 is selected from H, unsubstituted phenyl;
- substituted phenyl where substitutents are selected from F, Me, Et, Cl, OMe, OCF3 and CF3;
- C1-6 alkyl;
- and C3-6 cycloalkyl;
- wherein R3 and R4 are independently selected from H;
- C1-3 alkyl;
- and phenyl;
- or R3 and R4 taken together form a cycloalkyl of formula —(CH2)n— where n=2, 3, 4 and 5;
- wherein R5 is selected from methyl;
- CF3;
- cyclopropyl;
- unsubstituted phenyl;
- mono- and disubstituted phenyl where substitutents are selected from F, Me, Et, CN, iPr, Cl, OMe, OPh, OCF3, and CF3;
- unsubstituted heteroaromatic group;
- and imidazole;
- or prodrug thereof, or pharmaceutically acceptable salt or ester of said compound or prodrug thereof.
Dependencies are inferred from the claim text.