Inhibition of FGFR3 and treatment of multiple myeloma
Methods of inhibiting fibroblast growth factor receptor 3 and treating various conditions mediated by fibroblast growth factor receptor 3 are provided that include administering to a subject a compound of Structure I, a pharmaceutically acceptable salt thereof, a tautomer thereof, or a pharmaceutically acceptable salt of the tautomer. Compounds having the Structure I have the following structure where and have the variables described herein. Such compounds may be used to prepare medicaments for use in inhibiting fibroblast growth factor receptor 3 and for use in treating conditions mediated by fibroblast growth factor receptor 3 such as multiple myeloma.
1. A method of inhibiting fibroblast growth factor receptor 3 in a subject or treating a biological condition mediated by fibroblast growth factor receptor 3 in a subject, comprising: administering to the subject a compound, a tautomer of the compound, a pharmaceutically acceptable salt of the compound, a pharmaceutically acceptable salt of the tautomer, or a mixture thereof, wherein the biological condition is multiple myeloma, the subject is a multiple myeloma patient with a t(4;14) chromosomal translocation, and further wherein the compound has the following formula,
and fibroblast growth factor receptor 3 is inhibited in the subject after administration of the compound of, the tautomer of the compound, the pharmaceutically acceptable salt of the compound, the pharmaceutically acceptable salt of the tautomer, or the mixture thereof.
2. The method of claim 1 , wherein the lactate salt of the compound or the tautomer thereof is administered to the subject.
3. A method of treating multiple myeloma comprising administering an effective amount of a compound, a tautomer of the compound, a pharmaceutically acceptable salt of the compound, a pharmaceutically acceptable salt of the tautomer, or a mixture thereof, to a multiple myeloma patient, wherein the multiple myeloma expresses fibroblast growth factor receptor 3 and the compound is
4. The method of claim 3 , wherein the lactate salt of the compound or the tautomer thereof is administered to the multiple myeloma patient.
5. The method of claim 3 wherein the multiple myeloma patient is one with a t(4;14) chromosomal translocation.
6. The method of claim 3 , wherein the multiple myeloma patient has multiple myeloma cells, and further wherein apoptotic cell death is induced in the multiple myeloma cells after administration of the compound, the tautomer of the compound, the pharmaceutically acceptable salt of the compound, the pharmaceutically acceptable salt of the tautomer, or the mixture thereof to the multiple myeloma patient.
7. The method of claim 3 , wherein osteolytic bone loss is reduced in the multiple myeloma patient after administration of the compound, the tautomer of the compound, the pharmaceutically acceptable salt of the compound, the pharmaceutically acceptable salt of the tautomer, or the mixture thereof to the multiple myeloma patient.
8. A method of treating multiple myeloma comprising administering an effective amount of a compound, a tautomer of the compound, a pharmaceutically acceptable salt of the compound, a pharmaceutically acceptable salt of the tautomer, or a mixture thereof, to a multiple myeloma patient with a t(4;14) chromosomal translocation, wherein the compound is
9. The method of claim 8 , wherein the lactate salt of the compound or the tautomer thereof is administered to the multiple myeloma patient.