IP Library › Granted Patent US 9,040,714
Granted Patent B2
US 9,040,714 · App. 13/639,734 · Granted May 26, 2015

IRE-1α inhibitors

Inventors: Qingping Zeng (Thousand Oaks, CA); Andras Toro (Oxnard, CA); John Bruce Patterson (Ventura, CA); Warren Stanfield Wade (San Diego, CA); Zoltan Zubovics (Budapest, HU); Yun Yang (Tianjin, CN); Zhipeng Wu (Tianjin, CN)
Assignee: MannKind Corporation
A61K31/366C07D311/16A61K31/343A61K31/352A61K31/37A61K31/381A61K31/4025A61K31/404A61K31/4045A61K31/415A61K31/4155A61K31/4172A61K31/4184A61K31/423A61K31/427A61K31/4433A61K31/4439A61K31/452A61K31/453A61K31/454A61K31/4545A61K31/496A61K31/5377A61K45/06C07D311/20C07D311/94C07D401/04C07D405/04C07D405/10C07D409/04C07D417/04
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,040,714
App. No.
13/639,734
Granted
May 26, 2015
Kind
B2
Abstract

Compounds which directly inhibit IRE-1α activity in vitro, prodrugs, and pharmaceutically acceptable salts there-of. Such compounds and prodrugs are useful for treating diseases associated with the unfolded protein response or with regulated IRE1-dependent decay (RIDD) and can be used as single agents or in combination therapies.

Claims (30)

1. A compound, or a pharmaceutically acceptable salt or prodrug thereof, where the compound directly inhibits IRE-1αactivity in vitro and is represented by structural formula (A-1):

wherein

R3 is halogen; alkoxyl or alkylamino, each optionally substituted with (1) a C1-C6 hydrocarbon chain containing an N or O atom and optionally substituted with a C1-C3 perfluoroalkyl, or (2) a cycloalkyl which may contain 1 or 2 heteroatoms selected from N, O, and S, and which is optionally substituted with a C1-C3 perfluoroalkyl;

R4 is hydrogen; halogen; alkyl, alkoxyl, or alkylamino, each optionally substituted with (1) a C1-C6 ydrocarbon chain containing an N or O atom and optionally substituted with a C1-C3 perfluoroalkyl, or (2) a cycloalkyl which may contain 1 or 2 heteroatoms selected from N, O, and S, and which is optionally substituted with a C1-C3 perfluoroalkyl;

R5 is R21;

 alkenyl, alkynyl, or phenyl, each optionally substituted with 1, 2, or 3 substituents independently selected from the group consisting of halogen, —CN, alkyl, perfluoroalkyl, alkoxy, hydroxylalkyl, alkoxylalkyl, perfluoroalkoxy,

 a 5- or 6-membered heteroaryl that is substituted with 1, 2, or 3 substituents independently selected from the group consisting of halogen, —CN, alkyl, perfluoroalkyl, alkoxy, hydroxylalkyl, alkoxylalkyl, perfluoroalkoxyl,

 wherein n is 0 , 1, or 2;

R6is R21; alkenyl, alkynyl, or phenyl, each optionally substituted with 1 , 2, or 3substituents independently selected from the group consisting of halogen, —CN, alkyl, perfluoroalkyl, alkoxy, hydroxylalkyl, alkoxylalkyl, perfluoroalkoxy,

 a 5- or 6-membered heteroaryl that is substituted with 1 , 2, or 3 substituents independently selected from the group consisting of halogen, —CN, alkyl, perfluoroalkyl, alkoxy, hydroxylalkyl, alkoxylalkyl, perfluoroalkoxyl,

 wherein n is 0, 1, or 2;

 or R5 and R6, together with the carbon atoms to which they are attached, form a 5-membered cycloalkyl;

R9 and R10 are independently hydrogen; alkyl; alkoxylalkyl; perfluoroalkoxylalkyl; aryl, optionally substituted with 1, 2, or 3 substituents independently selected from members of R21; a 5- or 6-membered heterocycle, optionally substituted with 1 , 2, or 3 substituents independently selected from members of R21; a 5- or 6-membered heteroaryl, optionally substituted with 1 , 2 , or 3 substituents independently selected from members of R21; or

 wherein n is 0, 1, 2, or 3; or

R9 and R10, together with the nitrogen atom to which they are attached, form a heterocycle containing 1, 2, 3, or 4 heteroatoms selected from N, O, and S, optionally substituted with 1, 2, or 3 substituents selected independently from members of R11;

R11 is hydrogen; alkyl; aryl; heteroaryl containing 1 or 2 heteroatoms selected from N, O, and S; arylalkyl; heteroarylalkyl in which the heteroaryl contains 1 or 2 heteroatoms selected from N, O, and S;

R12 is amino; alkoxy; aryl, optionally substituted with 1, 2, or 3 substitutents selected independently from members of R11; a 5- or 6-membered heterocycle having 1, 2, or 3 heteroatoms selected from N, O, and S and optionally substituted with 1, 2, or 3 substitutents selected independently from members of R11; or a 5- or 6-membered heteroaryl having 1, 2, or 3 heteroatoms selected from N, O, and S and optionally substituted with 1, 2, or 3; substitutents selected independently from members of R11;

R13 is alkyl; alkoxylalkyl; perfluoroalkoxylalkyl; aryl, optionally substituted with 1, 2, or 3 substituents independently selected from members of R21; a 5- or 6-membered heterocycle, optionally substituted with 1, 2, or 3 substituents independently selected from members of R21; a 5- or 6-membered heteroaryl, optionally substituted with 1, 2, or 3 substituents independently selected from members of R21; or

 wherein n is 0, 1, 2, or 3; and R14 is hydrogen or R13; or

R13 and R14, together with the nitrogen to which they are attached, form a heterocycle containing 1, 2, or 3 heteroatoms selected independently from N, O, and S, optionally substituted with 1, 2, or 3 substitutents selected independently from R16;

R15 is amino; alkoxy; aryl, optionally substituted with 1, 2, or 3 substitutents selected independently from members of R21; a 5- or 6-membered heterocycle having 1, 2, or 3 heteroatoms selected from N, O, and S and optionally substituted with 1, 2, or 3 substitutents selected from members of R21; or a 5- or 6-membered heteroaryl having 1, 2, or 3 heteroatoms selected from N, O, and S and optionally substituted with 1, 2, or 3 substitutents selected from members of R21;

R16 is hydrogen; alkyl; aryl; heteroaryl containing 1 or 2 heteroatoms selected from N, O, and S; arylalkyl; heteroarylalkyl in which the heteroaryl contains 1 or 2 heteroatoms selected from N, O, and S;

 amino, or

R17 is alkyl; alkoxylalkyl; perfluoroalkoxylalkyl; aryl, optionally substituted with 1, 2, or 3 substituents independently selected from members of R21; a 5- or 6-membered heterocycle, optionally substituted with 1, 2, or 3 substituents independently selected from members of R21; a 5- or 6-membered heteroaryl, optionally substituted with 1, 2, or 3 substituents independently selected from members of or R21; or

 wherein n is 0, 1, 2, or 3; and R18 is hydrogen or R17; or

R17 and R18, together with the nitrogen to which they are attached, form a heterocycle containing 1, 2, 3, or 4 heteroatoms selected independently from N, O, and S, optionally substituted with 1, 2, or 3 substituents selected independently from members of R20;

R19 is alkoxy; aryl, optionally substituted with 1, 2, or 3 substitutents selected independently from members of R21; a 5- or 6-membered heterocycle, optionally substituted with 1, 2, or 3 substituents independently selected from members of R21; or a 5- or 6-membered heteroaryl, optionally substituted with 1, 2, or 3 substituents independently selected from members of R21;

R20 is a 5- or 6-membered heterocycle having 1 or 2 heteroatoms selected from N, O, and S and optionally substituted with 1, 2, or 3 substituents selected independently from members of R21; a 5- or 6-membered heteroaryl, optionally substituted with 1, 2, or 3 substituents selected independently from members of R21; or R21; and

R21 is perfluoroalkyl, perfluoroalkoxy, —CN, —CONH 2 , —CON(CH 3 ) 2 , alkyl, hydroxylalkyl, or alkoxylalkyl.

2. A pharmaceutical composition comprising the compound of claim 1 , or a pharmaceutically acceptable salt or prodrug thereof; and a pharmaceutically acceptable vehicle.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 22, 2018
From: SHANGHAI FOSUN PHARMACEUTICAL INDUSTRIAL DEVELOPMENT CO. LTD.
To: FOSUN ORINOVE PHARMATECH, INC.
Reel/Frame 045320/0357 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 23, 2017
From: MANNKIND CORPORATION
To: SHANGHAI FOSUN PHARMACEUTICAL INDUSTRIAL DEVELOPMENT CO. LTD.
Reel/Frame 042483/0622 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 1, 2012
From: ZENG, QINGPING; TORO, ANDRAS; PATTERSON, JOHN BRUCE; WADE, WARREN S.; ZUBOVICS, ZOLTAN; YANG, YUN; WU, ZHIPENG
To: MANNKIND CORPORATION
Reel/Frame 029226/0410 →
Continuity (2)
Provisional Application 61320975 · Apr 5, 2010
Related Publication 20130116247A1 · May 9, 2013