IP Library Granted Patent US 10,934,256
Granted Patent B2
US 10,934,256 · App. 16/575,733 · Granted Mar 2, 2021

Compounds and methods for treating cancer

Inventors: James Bradner (Weston, MA); Michael Erb (Boston, MA); Jun Qi (Sharon, MA)
Assignee: DANA-FARBER CANCER INSTITUTE, INC.
C07D211/44A61P35/00C07D211/58C07D213/30C07D239/78C07D401/04C07D401/14C07D413/04C07D471/04
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Quick Facts
Patent No.
US 10,934,256
App. No.
16/575,733
Granted
Mar 2, 2021
Kind
B2
Abstract

The present application relates to compounds comprising an ester, a thioester, or a hydrazide moiety and methods of synthesizing these compounds. The present application also relates to pharmaceutical compositions containing the compounds and methods of treating cell proliferative disorders mediated by the Hh signaling pathway, such as cancer, by administering the compounds and pharmaceutical compositions to subjects in need thereof.

Claims (37)

1. A compound having formula II:

or a pharmaceutically acceptable salt thereof, wherein:

Z 1 -Z 2 is C(O)—O, O—C(O), C(O)—S, S—C(O), C(O)—NR—NR, or NR—NR—C(O);

Y 1 is N and Y 2 is N or CR 24 ;

each R 24 is independently H, halogen, cyano, unsubstituted or substituted C 1 -C 6 alkyl, or unsubstituted or substituted C 1 -C 6 alkoxy;

n2 is 0, 1, 2, 3, 4, or 5;

each R 21 is independently halogen, cyano, unsubstituted or substituted C 1 -C 6 alkyl, unsubstituted or substituted C 1 -C 6 alkoxy, S(O) o2 -(unsubstituted or substituted C 1 -C 6 alkyl), amino, di-C 1 -C 6 alkylamino, or unsubstituted or substituted C 6 -C 10 aryl;

o2 is 0, 1, or 2;

m2 is 0, 1, 2, 3, or 4;

each R 22 is independently halogen, unsubstituted or substituted C 1 -C 6 alkyl, or unsubstituted or substituted C 1 -C 6 alkoxy;

R 23 is R 25 , S(O) 2 R 25 , C(O)R 25 , OR 25 , or NR 26 R 27 ;

R 25 is unsubstituted or substituted C 3 -C 8 cycloalkyl, unsubstituted or substituted C 6 -C 10 aryl, unsubstituted or substituted heterocyclyl comprising one or two 5- to 8-membered rings and 1-4 heteroatoms selected from O, N, and S, or unsubstituted or substituted heteroaryl comprising one or two 5- to 8-membered rings and 1-4 heteroatoms selected from O, N, and S; and

R 26 and R 27 are each independently H or unsubstituted or substituted C 1 -C 6 alkyl.

2. The compound of claim 1 , having formula IIa:

or a pharmaceutically acceptable salt thereof, wherein:

Z 3 is O, S, or NR—NR;

p2 is 0, 1, 2, 3, or 4; and

each R 28 is independently unsubstituted or substituted C 1 -C 6 alkyl.

3. A pharmaceutical composition comprising the compound of claim 1 or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.

4. A method of modulating the SMO, comprising contacting the SMO with the compound of claim 1 or a pharmaceutically acceptable salt thereof.

5. A method of treating a disorder mediated by the Hedgehog (Hh) signaling pathway, comprising administering to a subject in need thereof, a therapeutically effective amount of the compound of claim 1 , or a pharmaceutically acceptable salt thereof.

6. The compound of claim 1 , wherein Y 2 is CR 24 .

7. The compound of claim 6 , wherein R 24 is H.

8. The compound of claim 1 , wherein n 2 is 1.

9. The compound of claim 1 , wherein R 21 is unsubstituted or substituted straight-chain C 1 -C 6 alkoxy.

10. The compound of claim 9 , wherein R 21 is trifluoromethoxy.

11. The compound of claim 1 , wherein m 2 is 1.

12. The compound of claim 1 , wherein R 22 is unsubstituted or substituted straight-chain C 1 -C 6 alkyl.

13. The compound of claim 12 , wherein R 22 is methyl.

14. The compound of claim 1 , wherein R 23 is heterocyclyl optionally substituted with one or more substituents independently selected from halogen, OH, cyano, nitro, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, and amino.

15. The compound of claim 14 , wherein R 23 is morpholinyl substituted with two substituents independently selected from methyl, ethyl, and propyl.

16. The compound of claim 1 , which is:

or a pharmaceutically acceptable salt thereof, wherein Z is O, S, or NH—NH.

17. The compound of claim 16 , which is:

or a pharmaceutically acceptable salt thereof, wherein Z is O.

18. The compound of claim 1 , which is:

or a pharmaceutically acceptable salt thereof, wherein Z is O, S, or NH—NH.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 19, 2019
From: BRADNER, JAMES; ERB, MICHAEL; QI, JUN
To: DANA-FARBER CANCER INSTITUTE, INC.
Reel/Frame 050431/0668 →
Continuity (3)
Division 15577845
Provisional Application 62171783 · Jun 5, 2015
Related Publication 20200010418A1 · Jan 9, 2020
Cited By (1)
US 12,441,685