Oligomer-protease inhibitor conjugates
View Patent ↗The invention provides protease inhibitors that are chemically modified by covalent attachment of a water-soluble oligomer. A conjugate of the invention, when administered by any of a number of administration routes, exhibits characteristics that are different from the protease inhibitors not attached to the water-soluble oligomer.
1. A compound comprising a residue of a small molecule protease inhibitor covalently attached to a water-soluble, non-peptidic oligomer, wherein (i) the water-soluble, non-peptidic oligomer is a poly(alkylene oxide) and is made of between 1 and 30 monomers, covalently bound to a primary or secondary amine residue of the small molecule protease inhibitor.
2. The compound of claim 1 , wherein the small molecule protease inhibitor is from the amino acid derivative class of small molecule protease inhibitors.
3. The compound of claim 1 , wherein the small molecule protease inhibitor is selected from the group consisting of amprenavir, atazanavir, fosamprenavir, indinavir, lopinavir, saquinavir, nelfinavir, ritonavir, tipranovir, and darunavir.
4. The compound of claim 1 , wherein the poly(alkylene oxide) is a poly(ethylene oxide).
5. The compound of claim 1 , wherein the water-soluble, non-peptidic oligomer is made of between 1 and 10 monomers.
6. The compound of claim 1 , wherein the poly(alkylene oxide) includes an alkoxy or hydroxy end-capping moiety.
7. The compound of claim 1 , wherein a single water-soluble, non-peptidic oligomer is covalently attached to the residue of the small molecule protease inhibitor.
8. The compound of claim 1 , wherein more than one water-soluble, non-peptidic oligomer is covalently attached to the residue of the small molecule protease inhibitor.
9. The compound of claim 1 , wherein the residue of the small molecule protease inhibitor is covalently attached to the water-soluble, non-peptidic oligomer via an amide linkage.
10. A composition comprising a compound of claim 1 , and optionally, a pharmaceutically acceptable excipient.
11. A composition of matter comprising a compound of claim 1 , wherein the compound is present in a dosage form.
12. A method of inhibiting protease activity in a subject in need thereof comprising administering a compound of claim 1 .
13. A compound of the following formula, wherein each n is independently an integer from 0-30: