IP Library Granted Patent US 8,796,456
Granted Patent B2
US 8,796,456 · App. 12/745,431 · Granted Aug 5, 2014

Naphthalene diimide compounds

Inventors: Mekala Gunaratnam (London, GB); Francisco Cuenca (Valencia, ES); Stephen Neidle (London, GB)
Assignee: University College London
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Quick Facts
Patent No.
US 8,796,456
App. No.
12/745,431
Granted
Aug 5, 2014
Kind
B2
Abstract

The invention relates to novel compounds which are naphthalene diimides of general formula (I). The compounds are used in therapy, particularly in cancer treatment.

Claims (47)

1. A pharmaceutical composition comprising a compound that is of general formula (I) or is a salt, solvate, or prodrug thereof,

wherein R 1 and R 2 are each independently divalent radicals selected from C 1-20 alkyl, C 2-20 alkenyl, C 7-20 alkaryl, C 2-10 alkynyl, C 7-20 aralkyl, C 2-20 heteroaralkyl, C 3-30 heterocyclylalkyl, C 3-30 alkylheterocyclyl, C 3-20 cycloalkyl, C 3-20 heterocyclyl, C 2-20 heteroaryl, C 5-20 aryl and C 1-10 alkoxy;

R is H or A 2 X 4 ;

wherein X 1 -X 4 are each independently selected from halo, OH, OR 3 , COH, NH 2 , NHR 3 , NR 3 R 4 , COOH, CONH 2 , COOR 3 , CONHR 3 , CONR 3 R 4 , SH, SR 3 , COR 3 and cyano, provided that at least one of groups X 1 -X 4 is a tertiary amine;

wherein R 3 and R 4 are independently selected from C 1-6 alkyl, C 6-20 aryl, and C 7-20 aralkyl or R 3 and R 4 together with the nitrogen atom to which they are attached form a 3-8 membered ring, which is optionally substituted and optionally comprises other hetero atoms;

A 1 and A 2 are each independently selected from NHR 5 ;

wherein R 5 is a divalent radical selected from C 1-20 alkyl, C 6-20 aryl, C 7-20 alkaryl and C 7-20 aralkyl;

wherein any of the groups R 1 -R 5 , A 1 and A 2 may be substituted with C 1-20 alkyl, C 2-20 alkenyl, C 7-20 alkaryl, C 2-10 alkynyl, C 7-20 aralkyl, C 2-20 heteroaralkyl, C 3-30 heterocyclylalkyl, C 3-30 alkylheterocyclyl, C 3-20 cycloalkyl, C 3-20 heterocyclyl, C 2-20 heteroaryl, C 5-20 aryl or C 1-10 alkoxy, halo, OH, OR 3 , COH, NH 2 , NHR 3 , NR 3 R 4 , COOH, CONH 2 , COOR 3 , CONHR 3 , CONR 3 R 4 , SH, SR 3 , COR 3 or cyano; and

wherein the pharmaceutical composition also comprises a pharmaceutically acceptable carrier.

2. The pharmaceutical composition according to claim 1 wherein R is H.

3. The pharmaceutical composition according to claim 1 wherein R is A 2 X 4 .

4. The pharmaceutical composition according to claim 1 wherein R 1 x 1 ═R 2 X 2 .

5. The pharmaceutical composition according to claim 3 wherein X 1 -X 4 are selected from NH 2 , NR 3 R 4 , OH, OR 3 and NHR 3 .

6. The pharmaceutical composition according to claim 5 wherein X 1 -X 4 are NR 3 R 4 , wherein R 3 and R 4 are independently methyl or ethyl.

7. The pharmaceutical composition according to claim 5 wherein X 1 -X 4 are NR 3 R 4 , wherein R 3 and R 4 together with the nitrogen-atom to which they are attached form a 5 or 6 membered ring.

8. The pharmaceutical composition according to claim 7 wherein the group NR 3 R 4 is pyrrolidine, piperidine or morpholine.

9. The pharmaceutical composition according to claim 1 comprising a prodrug of a compound of formula (I), wherein groups X 1 -X 4 of the prodrug are N-oxides or N + (—O − ) R 3 R 4 .

10. The pharmaceutical composition according to claim 1 wherein R 1 and R 2 are divalent radicals selected from C 1-10 alkyl.

11. The pharmaceutical composition according to claim 1 wherein R 5 is a divalent radical selected from C 1-10 alkyl.

12. The pharmaceutical composition according to claim 3 wherein at least one of A 1 X 3 and A 2 X 4 has the structure

wherein n is 1-4 and p is 2-6.

13. A compound that is of general formula (I) or is a salt, solvate, or prodrug thereof

wherein R 1 and R 2 are each independently divalent radicals selected from C 1-20 alkyl, C 2-20 alkenyl, C 7-20 alkaryl, C 2-10 alkynyl, C 7-20 aralkyl, C 2-20 heteroaralkyl, C 3-30 heterocyclylalkyl, C 3-30 alkylheterocyclyl, C 3-20 cycloalkyl, C 3-20 heterocyclyl, C 2-20 heteroaryl, C 5-20 aryl and C 1-10 alkoxy;

R is H or A 2 X 4 ;

wherein X 1 -X 4 are each independently selected from halo, OH, OR 3 , COH, NH 2 , NHR 3 , NR 3 R 4 , COOH, CONH 2 , COOR 3 , CONHR 3 , CONR 3 R 4 , SH, SR 3 , COR 3 and cyano, provided that at least one of groups X 1 -X 4 is a tertiary amine;

wherein R 3 and R 4 are independently selected from C 1-6 alkyl, C 6-20 aryl, and C 7-20 aralkyl or R 3 and R 4 together with the nitrogen atom to which they are attached form a 3-8 membered ring, which is optionally substituted and optionally comprises other hetero atoms;

A 1 and A 2 are each independently selected from NHR 5 ;

wherein R 5 is a divalent radical seleced from C 1-20 alkyl, C 6-20 aryl, C 7-20 alkaryl and C 7-20 aralkyl;

wherein any of the groups R 1 -R 5 , A l and A 2 may be substituted with C 1-20 alkyl, C 2-20 alkenyl, C 7-20 alkaryl, C 2-10 alkynyl, C 7-20 aralkyl, C 2-20 heteroaralkyl, C 3-30 heterocyclylalkyl, C 3-30 alkylheterocyclyl, C 3-20 cycloalkyl, C 3-20 heterocyclyl, C 2-20 heteroaryl, C 5-20 aryl or C 1-10 alkoxy, halo, OH, OR 3 , COH, NH 2 , NHR 3 , NR 3 R 4 , COOH, CONH 2 , COOR 3 , CONHR 3 , CONR 3 R 4 , SH, SR 3 , COR 3 or cyano.

14. A compound according to claim 13 wherein R is H.

15. A compound according to claim 13 wherein R is A 2 X 4 .

16. A compound according to claim 13 wherein R 1 X 1 ═R 2 X 2 .

17. A compound according to claim 15 wherein X 1 -X 4 are selected from NH 2 , NR 3 R 4 , OH, OR 3 and NHR 3 .

18. A compound according to claim 17 wherein X 1 -X 4 are NR 3 R 4 , wherein R 3 and R 4 are independently methyl or ethyl.

19. A compound according to claim 17 wherein X 1 -X 4 are NR 3 R 4 , wherein R 3 and R 4 together with the nitrogen-atom to which they are attached form a 5 or 6 membered ring.

20. A compound according to claim 19 wherein the group NR 3 R 4 is pyrrolidine, piperidine or morpholine.

21. A compound according to claim 13 which is a prodrug of a compound of formula (I), wherein groups X 1 -X 4 of the prodrug are N-oxides or N + (—O − ) R 3 R 4 .

22. A compound according to claim 13 wherein R 1 and R 2 are divalent radicals selected from C 1-10 alkyl.

23. A compound according to claim 13 wherein R 5 is a divalent radical selected from C 1-10 alkyl.

24. A compound according to claim 15 wherein at least one of A 1 X 3 and A 2 X 4 the structure

wherein n is 1-4 and p is 2-6.

25. The pharmaceutical composition according to claim 7 wherein the 5 or 6 membered ring contains an oxygen atom.

26. The pharmaceutical composition according to claim 10 wherein R 1 and R 2 are divalent radicals selected from C 2-4 alkyl.

27. The pharmaceutical composition according to claim 11 wherein R 5 is a divalent radical selected from C 2-4 alkyl.

28. A compound according to claim 19 wherein the 5 or 6 membered ring contains an oxygen atom.

29. A compound according to claim 22 wherein R 1 and R 2 are divalent radicals selected from C 2-4 alkyl.

30. A compound according to claim 23 wherein R 5 is a divalent radical selected from C 2-4 alkyl.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 8, 2012
From: THE SCHOOL OF PHARMACY, UNIVERSITY OF LONDON
To: UNIVERSITY COLLEGE LONDON
Reel/Frame 028174/0005 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 1, 2010
From: GUNARATNAM, MEKALA; CUENCA, FRANCISCO; NEIDLE, STEPHEN
To: SCHOOL OF PHARMACY, UNIVERSITY OF LONDON
Reel/Frame 024460/0758 →
Priority Claims (1)
GB 0723439.6 · Nov 29, 2007 · national
Continuity (1)
Related Publication 20100311739A1 · Dec 9, 2010