IP Library › Granted Patent US 10,730,835
Granted Patent B2
US 10,730,835 · App. 15/764,193 · Granted Aug 4, 2020

Thalidomide analogs and methods of use

Inventors: Nigel H. Greig (Phoenix, MD); Weiming Luo (Lutherville, MD); David Tweedie (Joppa, MD); Neil Vargesson (Aberdeen, GB); Shaunna Beedie (Aberdeen, GB); William Douglas Figg (Fairfax, VA)
Assignees: The United States of America, as represented by the Secretary, Health and Human Services; University Court of the University of Aberdeen
C07D209/44A61K31/4035A61K31/428A61K31/431A61K31/454A61K31/4545A61K31/536A61K45/06A61P29/00A61P35/00C07D209/46C07D209/48C07D209/52C07D401/04C07D401/12C07D401/14C07D413/04C07D417/04C07D471/04C07D499/80
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Quick Facts
Patent No.
US 10,730,835
App. No.
15/764,193
Granted
Aug 4, 2020
Kind
B2
Abstract

Thalidomide analogs and methods of using the thalidomide analogs are disclosed. Some embodiments of the disclosed compounds exhibit anti-angiogenic and/or anti-inflammatory activity. Certain embodiments of the disclosed compounds are non-teratogenic.

Claims (32)

1. A thalidomide analog or pharmaceutically acceptable salt thereof, wherein the thalidomide analog is a compound according to general formula I, wherein general formula I is

where Y 1 is a bond, —CH 2 —, or —CH(CH 3 )—;

A is general formula II or A is —NH 3 X where X is an anion with a −1 charge, wherein general formula II is

where bonds represented by “-----” are optional bonds, and each bond represented by “-----” is a single or double bond as needed to satisfy valence requirements,

R 1 is —H, —NO 2 , —NH 2 , or —OC(O)CH 3 ,

R 2 is —H, —NH 2 , or —N(H)CH(CH 3 ) 2 ,

Z 1 is CH 2 , or CH, and

Z 2 is C═O, CH 2 , C═S,

Ring B is:

where

R 3 is —H or —OH;

wherein:

if ring B is

 and R 1 -R 3 are H, then Y 1 is —CH 2 —, or —CH(CH 3 )—, or if ring B is

 R 1 is —H, —NH 2 or —NO 2 , R 2 and R 3 are —H, Z 1 is CH 2 , and Z 2 is C═O, then Y 1 is not a bond.

2. The thalidomide analog according to claim 1 , wherein the thalidomide analog is a compound in Group IV:

3. The thalidomide analog according to claim 1 , wherein the thalidomide analog is non-teratogenic in a zebrafish embryo assay and/or a chicken embryo assay at a concentration within a range of 10-200 μg/mL.

4. The thalidomide analog according to claim 1 , wherein the thalidomide analog possesses anti-inflammatory properties, but does not possess anti-angiogenic properties.

5. A thalidomide analog, wherein the thalidomide analog is:

6. A pharmaceutical composition comprising a thalidomide analog or pharmaceutically acceptable salt thereof according to claim 1 and at least one pharmaceutically acceptable carrier.

7. A method for inhibiting TNF-α activity, TNF-α synthesis, angiogenesis, inflammation, or a combination thereof, comprising contacting a cell with an effective amount of a thalidomide analog according to claim 1 or a pharmaceutically acceptable salt thereof.

8. The method according to claim 7 , wherein the thalidomide analog is non-teratogenic.

9. The method according to claim 7 wherein the thalidomide analog is:

10. A method for inhibiting TNF-α activity, TNF-α synthesis, angiogenesis, inflammation, or a combination thereof, comprising contacting a cell with an effective amount of a thalidomide analog according to claim 5 .

11. The method according to claim 7 , wherein contacting the cell with an effective amount of the thalidomide analog comprises administering to a subject a therapeutically effective amount of the thalidomide analog or a pharmaceutically acceptable salt thereof or a therapeutically effective amount of a pharmaceutical composition comprising the thalidomide analog or a pharmaceutically acceptable salt thereof.

12. The method according to claim 11 , wherein the subject has an inflammatory disorder or an autoimmune disorder.

13. The method according to claim 11 , wherein the thalidomide analog is non-teratogenic and possesses anti-inflammatory properties, and administering the therapeutically effective amount of the thalidomide analog or pharmaceutically acceptable salt thereof or the therapeutically effective amount of the pharmaceutical composition inhibits inflammation in the subject.

14. The method according to claim 11 , wherein the subject has an inflammatory disorder, the thalidomide analog is non-teratogenic and possesses anti-inflammatory properties, and administering the therapeutically effective amount of the thalidomide analog or pharmaceutically acceptable salt thereof or the therapeutically effective amount of the pharmaceutical composition to the subject treats the inflammatory disorder.

15. The method according to claim 11 , wherein the thalidomide analog is non-teratogenic, and administering the therapeutically effective amount of the thalidomide analog or pharmaceutically acceptable salt thereof or the therapeutically effective amount of the pharmaceutical composition to the subject inhibits TNF-α activity, TNF-α synthesis, or a combination thereof in the subject.

16. The method according to claim 11 , wherein the thalidomide analog is non-teratogenic and possesses anti-angiogenic properties, and administering the therapeutically effective amount of the thalidomide analog or pharmaceutically acceptable salt thereof or the therapeutically effective amount of the pharmaceutical composition to the subject inhibits angiogenesis in the subject.

17. The method according to claim 11 , wherein the thalidomide analog or pharmaceutically acceptable salt thereof or the pharmaceutical composition is administered orally, parenterally, rectally, nasally, buccally, vaginally, topically, optically, by inhalation spray, or via an implanted reservoir.

18. The method according to claim 11 , further comprising administering to the subject a second therapeutic agent.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 29, 2018
From: VARGESSON, NEIL; BEEDIE, SHAUNNA
To: UNIVERSITY COURT OF THE UNIVERSITY OF ABERDEEN
Reel/Frame 045383/0677 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 29, 2018
From: GREIG, NIGEL H.; LUO, WEIMING; TWEEDIE, DAVID; FIGG, WILLIAM DOUGLAS
To: THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES
Reel/Frame 045763/0141 →
Continuity (2)
Provisional Application 62235105 · Sep 30, 2015
Related Publication 20180273472A1 · Sep 27, 2018