IP Library Granted Patent US 10,189,827
Granted Patent B2
US 10,189,827 · App. 15/866,613 · Granted Jan 29, 2019

Retinoic acid receptor antagonists as chaperone-mediated autophagy modulators and uses thereof

Inventors: Ana Maria Cuervo (Bronx, NY); Evripidis Gavathiotis (Flushing, NY); Qisheng Xin (Bronx, NY); Bhaskar C. Das (Kansas City, KS)
Assignee: ALBERT EINSTEIN COLLEGE OF MEDICINE OF YESHIVA UNIVERSITY
C07D413/10C07C279/22C07D265/36C07B2200/11C07C2601/16G01N2500/04G01N2800/7009
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Quick Facts
Patent No.
US 10,189,827
App. No.
15/866,613
Granted
Jan 29, 2019
Kind
B2
Abstract

Compounds, compositions and methods are provided for selectively activating chaperone-mediated autophagy (CMA), protecting cells from oxidative stress, proteotoxicity and lipotoxicity, and/or antagonizing activity of retinoic acid receptor alpha (RARα) in subjects in need thereof.

Claims (37)

1. A pharmaceutical composition comprising a pharmaceutically acceptable carrier or diluent, and a compound of formula (II), wherein formula (II) is

wherein

R1, R2, R3, R4, R5, R6, R8 and R9 of formula (II) are independently H, hydroxyl, halogen, SH, NO 2 , CF 3 , COOH, COOR10, CHO, CN, NH 2 , NHR10, NHCONH 2 , NHCONHR10, NHCOR10, NHSO 2 R10, OCR10, COR10, CH 2 R10, CON(R10,R11), CH═N-OR10, CH═NR10, OR10, SR10, SOR10, SO 2 R10, COOR10, CH 2 N(R10,R11), N(R10,R11), or optionally substituted lower alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, aralkyl, or heteroaralkyl; wherein the optional substituent is one or more of F, Cl, Br, I, OH, SH, NO 2 , COOH, COOR10, R10, CHO, CN, NH 2 , NHR10, NHCONH 2 , NHCONHR10, NHCOR10, NHSO 2 R10, HOCR10, COR10, CH 2 R10, CON(R10, R11), CH═N-OR10, CH═NR10, OR10, SR10, SOR10, SO 2 R10, COOR10, CH 2 N(R10, R11), N(R10, R11);

R7 of formula (II) is H, hydroxyl, halogen, CF 3 , CN, OCF 3 , COOH, COOCH 3 , COOR10, COO(CH 2 ) 2 Si(CH 3 ) 3 , COOR10Si(CH 3 ) 3 , NHCOCH 3 , C≡C—CH 2 OH, C≡C-R10-OH or optionally substituted alkyl, aryl, heteroaryl, aralkyl, heteroaralkyl, cyclic or heterocyclic; wherein the optional substituent is one or more of F, Cl, Br, I, OH, SH, NO 2 , CH 3 , R10, COOH, COOR10, CHO, CN, NH 2 , NHR10, NHCONH 2 , NHCONHR10, NHCOR10, NHSO 2 R10, HOCR10, COR10, CH 2 R10, CON(R10, R11), CH═N-OR10, CH═NR10, OR10, SR10, SOR10, SO 2 R10, COOR10, CH 2 N(R10, R11), N(R10, R11);

R10 and R11 are independently H or C1-C6 alkyl; and

X is CH 2 , C═O, NH, O, S or S═O; and Y is N or C;

or a pharmaceutically acceptable salt thereof.

2. The pharmaceutical composition of claim 1 , wherein the compound has the structure

or a pharmaceutically acceptable salt thereof.

3. The pharmaceutical composition of claim 1 , wherein the optionally substituted aryl or heteroaryl is

where the wavy line indicates the point of attachment of the optionally substituted aryl or heteroaryl to the main structure.

4. The pharmaceutical composition of claim 1 , wherein

X is O,

Y is N,

R1 is Cl,

R2, R3, R4, R5, R6, R8 and R9 are H, and

R7 is NHCOCH 3 ; or

a pharmaceutically acceptable salt thereof.

5. The pharmaceutical composition of claim 1 , wherein

X is NH and Y is N,

R1 is Cl,

R2, R3, R4, R5, R6, R8 and R9 are H, and

R7 is NHCOCH 3 ; or

a pharmaceutically acceptable salt thereof.

6. The pharmaceutical composition of claim 1 , wherein

X is O,

Y is N,

R1 is Cl,

R2, R3, R4, R5, R6, R8 and R9 are H, and

R7 is phenyl; or

a pharmaceutically acceptable salt thereof.

7. The pharmaceutical composition of claim 1 , wherein

X is NH and Y is N,

R1 is Cl,

R2, R3, R4, R5, R6, R8 and R9 are H, and

R7 is phenyl; or

a pharmaceutically acceptable salt thereof.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 18, 2018
From: CUERVO, ANA MARIA; GAVATHIOTIS, EVRIPIDIS; XIN, QISHENG; DAS, BHASKAR C.
To: ALBERT EINSTEIN COLLEGE OF MEDICINE OF YESHIVA UNIVERSITY
Reel/Frame 046895/0632 →
Continuity (4)
Continuation 15298280 · Oct 20, 2016
Division 14566762 · Dec 11, 2014
Provisional Application 61915063 · Dec 12, 2013
Related Publication 20180141937A1 · May 24, 2018