IP Library Granted Patent US 8,163,919
Granted Patent B2
US 8,163,919 · App. 12/350,114 · Granted Apr 24, 2012

Imidazopyridinyl benzamide mitotic kinesin inhibitors

Assignee: Cytokinetics, Incorporated
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Quick Facts
Patent No.
US 8,163,919
App. No.
12/350,114
Granted
Apr 24, 2012
Kind
B2
Abstract

Compounds useful for treating cellular proliferative diseases and disorders by modulating the activity of one or more mitotic kinesins are disclosed.

Claims (24)

1. A compound that is N-(2-(2-dimethylamino-acetylamino)-1-{4-[8-(1-hydroxy-ethyl)-imidazo[1,2-a]pyridin-2-yl]-benzyl}-ethyl)-3-chloro-4-isopropoxy-benzamide.

2. A composition comprising at least one pharmaceutical excipient and a compound according to claim 1 .

3. The composition of claim 2 wherein the composition is formulated for administration by a route chosen from oral, subcutaneous, intravenous, intranasal, transdermal, intraperitoneal, intramuscular, intrapulmonary, vaginal, rectal, and intraocular.

4. The composition of claim 3 wherein the composition is formulated for oral administration.

5. The composition of claim 4 wherein the composition is formulated as a tablet, capsule, or liquid.

6. The composition of claim 4 wherein the at least one pharmaceutical excipient is selected from diluents, binders, glidants, lubricants, disintegrants, colors, flavors, sweetening agents, polymers, waxes and other solubility-retarding materials.

7. The composition of claim 3 wherein the composition is formulated for intravenous administration.

8. The composition of claim 7 wherein the at least one pharmaceutical excipient comprises a sterile solution of sugars, amino acids or electrolytes.

9. The composition of claim 7 wherein the at least one pharmaceutical excipient is water for injection USP.

10. The composition of claim 2 wherein the composition is formulated for parenteral administration.

11. The composition of claim 10 wherein the at least one pharmaceutical excipient comprises a sterile solution of sugars, amino acids or electrolytes.

12. The composition of claim 10 wherein the at least one pharmaceutical excipient is water for injection USP.

13. A compound of the formula

14. A composition comprising at least one pharmaceutical excipient and a compound according to claim 13 .

15. The composition of claim 14 wherein the composition is formulated for administration by a route chosen from oral, subcutaneous, intravenous, intranasal, transdermal, intraperitoneal, intramuscular, intrapulmonary, vaginal, rectal, and intraocular.

16. The composition of claim 15 wherein the composition is formulated for oral administration.

17. The composition of claim 16 wherein the composition is formulated as a tablet, capsule, or liquid.

18. The composition of claim 16 wherein the at least one pharmaceutical excipient is selected from diluents, binders, glidants, lubricants, disintegrants, colors, flavors, sweetening agents, polymers, waxes and other solubility-retarding materials.

19. The composition of claim 15 wherein the composition is formulated for intravenous administration.

20. The composition of claim 19 wherein the at least one pharmaceutical excipient comprises a sterile solution of sugars, amino acids or electrolytes.

21. The composition of claim 19 wherein the at least one pharmaceutical excipient is water for injection USP.

22. The composition of claim 14 wherein the composition is formulated for parenteral administration.

23. The composition of claim 22 wherein the at least one pharmaceutical excipient comprises a sterile solution of sugars, amino acids or electrolytes.

24. The composition of claim 22 wherein the at least one pharmaceutical excipient is water for injection USP.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 16, 2010
From: GLAXOSMITHKLINE LLC
To: CYTOKINETICS, INCORPORATED
Reel/Frame 024245/0345 →
Continuity (5)
Continuation 11271147 · Nov 9, 2005
Continuation In Part 11124608 · May 6, 2005
Continuation In Part 11121709 · May 3, 2005
Provisional Application 60569510 · May 6, 2004
Related Publication 20090306127A1 · Dec 10, 2009