Composition and synthesis of new reagents for inhibition of HIV replication
The present invention provides compounds and compositions for inhibiting Vif and methods for treating viral infection, e.g., HIV infection.
1. A method for treating a Human Immunodeficiency Virus (HIV) infection in a subject, the method comprising administering to the subject a therapeutically effective amount of a pharmaceutical composition comprising a therapeutically effective amount of a compound having the following formula:
or pharmaceutically acceptable salt thereof.
2. The method of claim 1 , further comprising identifying in the subject HIV-infected cells comprising both Virion Infectivity Factor (Vif) and APOBEC3G protein; and then administering the pharmaceutical composition to the subject.
3. The method of claim 1 , further comprising identifying in the subject HIV-infected cells comprising at least one compound selected from the group consisting of Virion Infectivity Factor (Vif), APOBEC3G protein and APBEC3F protein; and then administering the pharmaceutical composition to the subject.
4. A method of inhibiting Human Immunodeficiency Virus (HIV) replication in a HIV-infected cell population of HIV-infected human lymphocyte cells, the method comprising contacting the HIV-infected cell population with a compound having the formula:
or pharmaceutically acceptable salt thereof.
5. The method of claim 4 , wherein the HIV-infected cell population comprises non-permissive cells, and the method further comprises identifying the cell population comprising the HIV-infected non-permissive cells.
6. The method of claim 4 , wherein the HIV-infected cell population includes cells comprising Virion Infectivity Factor (Vif), and the method further comprises identifying the cell population comprising the HIV-infected cells comprising Virion Infectivity Factor (Vif).
7. The method of claim 4 , wherein the HIV-infected cell population includes cells comprising APOBEC3G protein.
8. The method of claim 4 , wherein the HIV-infected cell population includes cells comprising both Virion Infectivity Factor (Vif) and APOBEC3G protein.
9. The method of claim 4 , wherein the cell population is selected from one or more cells in the group consisting of H9 cells, MT4 cells, and HUT78 cells.
10. The method of claim 8 , wherein the cell population comprises H9 cells.
11. A method of reducing the infectivity of a Human Immunodeficiency Virus (HIV)-infected cell population, the method comprising contacting the HIV-infected cell population with a compound having the formula:
or pharmaceutically acceptable salt thereof.
12. The method of claim 11 , wherein the cell population comprises non-permissive cells.
13. The method of claim 11 , wherein the cell population is a HIV-infected lymphocytic cell population where at least a portion of the cells in the cell population comprises Virion Infectivity Factor (Vif).
14. The method of claim 11 , wherein the cells in the cell population comprise both Virion Infectivity Factor (Vif) and APOBEC3G protein.
15. A method for treating a Human Immunodeficiency Virus (HIV) infection in a subject, the method comprising administering to the subject a therapeutically effective amount of a pharmaceutical composition comprising a therapeutically effective amount of a compound having the following formula:
or pharmaceutically acceptable salt thereof.
16. The method of claim 15 , further comprising identifying in the subject HIV-infected cells comprising both Virion Infectivity Factor (Vif) and APOBEC3G protein; and then administering the pharmaceutical composition to the subject.
17. The method of claim 15 , further comprising identifying in the subject HIV-infected cells comprising at least one compound selected from the group consisting of Virion Infectivity Factor (Vif), APOBEC3G protein and APBEC3F protein; and then administering the pharmaceutical composition to the subject.