Methods of using [3.2.0] heterocyclic compounds and analogs thereof
Disclosed are methods of treating cancer, inflammatory conditions, and/or infectious disease in an animal comprising: administering to the animal, a therapeutically effective amount of a heterocyclic compound. The animal is a mammal, preferably a human or a rodent.
1. A method of treating a neoplastic disease in an animal, the method consisting essentially of administering alone to the animal, a therapeutically effective amount of a compound, and pharmaceutically acceptable salts and pro-drug esters thereof, wherein the compound has the structure:
wherein:
the neoplastic disease is a cancer selected from the group consisting of angiosarcoma; sinus cancer; esophageal cancer; uretal cancer; liver cancer; and angioma.
2. The method of claim 1 , wherein the animal is a mammal.
3. The method of claim 1 , wherein the animal is a human.
4. The method of claim 1 , wherein the animal is a rodent.
5. The method of claim 1 , further comprising
identifying an animal that would benefit from administration of the compound, and pharmaceutically acceptable salts and pro-drug esters thereof.
6. A method of inhibiting the growth of a cancer cell, consisting essentially of contacting a cancer cell alone with a compound, and pharmaceutically acceptable salts and pro-drug esters thereof, wherein the compound has the structure:
wherein:
the cancer cell is selected from the group consisting of angiosarcoma cell; sinus cancer cell; esophageal cancer cell; uretal cancer cell; liver cancer cell; and angioma cell.
7. A method of inhibiting proteasome activity consisting essentially of the step contacting a cell alone with a compound, and pharmaceutically acceptable salts and pro-drug esters thereof, wherein the compound has the structure:
wherein:
the cell is a cancer cell selected from the group consisting of angiosarcoma cell; sinus cancer cell; esophageal cancer cell; uretal cancer cell; liver cancer cell; and angioma cell.
8. A method of inhibiting NF-κB activation consisting essentially of the step contacting a cell alone with a compound, and pharmaceutically acceptable salts and pro-drug esters thereof, wherein the compound the structure:
wherein:
the cell is a cancer cell selected from the group consisting of angiosarcoma cell; sinus cancer cell; esophageal cancer cell; uretal cancer cell; liver cancer cell; and angioma cell.
9. A method for treating an inflammatory condition, comprising administering an effective amount of a compound to a patient in need thereof, wherein the compound has the structure:
wherein:
the inflammatory condition is selected from the group consisting of ischemia, septic shock, autoimmune diseases, rheumatoid arthritis, inflammatory bowel disease, systemic lupus eythematosus, multiple sclerosis, asthma, osteoarthritis, osteoporosis, fibrotic diseases, dermatosis, psoriasis, atopic dermatitis, ultraviolet radiation (UV)-induced skin damage, psoriatic arthritis, alkylosing spondylitis, tissue rejection, organ rejection, Alzheimer's disease, stroke, atherosclerosis, restenosis, diabetes, glomerulonephritis, cachexia, inflammation associated with an infection, inflammation associated with acquired immune deficiency syndrome (AIDS), inflammation associated with adult respiratory distress syndrome and inflammation associated with Ataxia Telangiestasia.
10. The method of claim 9 , wherein the inflammatory condition is selected from the group consisting of rheumatoid arthritis, asthma, multiple sclerosis, psoriasis, stroke, tissue rejection, and organ rejection.
11. A method for treating a microbial illness comprising administering an effective amount of a compound to a patient in need thereof, wherein the compound has the structure:
wherein:
the microbial illness is caused by a microbe selected from the group consisting of B. anthracis, Plasmodium, Leishmania , and Trypanosoma.
12. The method of claim 9 , wherein the inflammatory condition is selected from tissue rejection and organ rejection.