US2006004093A1PendingUtilityA1
Ligands of adenine nucleotide translocase (ANT) and compositions and methods related thereto
Est. expiryDec 20, 2022(expired)· nominal 20-yr term from priority
A61P 9/00A61P 43/00A61P 3/10A61P 3/04A61P 25/16A61P 25/00A61P 25/28A61P 25/14A61P 27/16A61P 25/06A61P 35/00A61P 25/18C07C 65/30C07C 65/40A61P 19/02A61K 31/185C07C 69/94C07D 333/16C07D 333/24C07D 307/80C07D 333/60C07D 263/57C07C 65/24A61P 19/04C07D 277/66C07D 333/56A61P 17/06
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Claims
Abstract
Compounds which have utility in the treatment of conditions associated with altered mitochondrial function. The compounds have the following structure (I): including stereoisomers, prodrugs, and pharmaceutically acceptable salts thereof, wherein R 1 , R 2 , R 3 , R 4 , R 5 and R 6 are as defined herein. Pharmaceutical compositions containing a compound of structure (I), as well as methods relating to the use thereof, are also disclosed.
Claims
exact text as granted — not AI-modified1 . A compound having the following structure:
or a stereoisomer, prodrug or pharmaceutically acceptable salt thereof, wherein:
R 1 is hydrogen, halogen, nitro, cyano, alkyl, substituted alkyl, alkoxy, hydroxy, aryl, substituted aryl, —NHC(═O)R′, heteroaryl or substituted heteroaryl;
R 2 , R 3 , R 5 and R 6 are the same or different and independently hydrogen, halogen, nitro, cyano, alkyl, substituted alkyl, alkoxy, hydroxy, aryl, substituted aryl, heteroaryl or substituted heteroaryl;
R 4 is hydrogen, halogen, nitro, cyano, alkyl, substituted alkyl, aryl, substituted aryl, arylalkyl, substituted arylalkyl, heteroaryl, substituted heteroaryl, heteroarylalkyl, substituted heteroarylalkyl, —O—R 7 , —C(═O)—R 7 , —C(═O)O—R 7 , —C(═O)—NH—R 7 or —NHC(═O)R″;
R 7 is hydrogen, alkyl, substituted alkyl, aryl, substituted aryl, arylalkyl or substituted arylalkyl;
R′ and R″ are the same or different and independently alkyl, substituted alkyl, aryl, substituted aryl, heteroaryl or substituted heteroaryl; and
R 4 and R 5 or R 5 and R 6 , taken together with the carbon atoms to which they are attached, optionally form a substituted or unsubstituted homocycle.
2 . The compound of claim 1 wherein R 1 is hydrogen
3 . The compound of claim 1 wherein R 1 is alkyl.
4 . The compound of claim 3 wherein alkyl is methyl.
5 . The compound of claim 3 wherein alkyl is —C(CH 3 ) 2 —CH 2 —C(CH 3 ) 2 —CH 3 .
6 . The compound of claim 1 wherein R 2 is hydrogen.
7 . The compound of claim 1 wherein R 3 is hydrogen.
8 . The compound of claim 1 wherein R 4 is hydrogen.
9 . The compound of claim 1 wherein R 4 is halogen.
10 . The compound of claim 1 wherein R 4 is alkyl.
11 . The compound of claim 10 wherein alkyl is tert-butyl.
12 . The compound of claim 1 wherein R 4 is heteroaryl.
13 . The compound of claim 12 wherein heteroaryl is thiophenyl.
14 . The compound of claim 1 wherein R 5 is hydrogen.
15 . The compound of claim 1 wherein R 5 is halogen.
16 . The compound of claim 1 wherein R 6 is hydrogen.
17 . The compound of claim 1 wherein R 6 is halogen.
18 . A composition comprising a compound of claim 1 in combination with a pharmaceutically acceptable carrier.
19 . A method for treating or preventing a condition in a mammal associated with altered mitochondrial function, comprising administering to a mammal in need thereof an effective amount of a composition of claim 18 .
20 . The method of claim 19 wherein the condition is: Alzheimer's Disease; diabetes mellitus; obesity; Parkinson's Disease; Huntington's disease; dystonia; Leber's hereditary optic neuropathy; schizophrenia; mitochondrial encephalopathy, lactic acidosis, and stroke (MELAS); cancer; psoriasis; hyperproliferative disorders; mitochondrial diabetes and deafness (MIDD); myoclonic epilepsy ragged red fiber syndrome; osteoarthritis; or Friedrich's ataxia.Cited by (0)
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