IP Library › Granted Patent US 8,377,971
Granted Patent B2
US 8,377,971 · App. 12/376,238 · Granted Feb 19, 2013

Non-flushing niacin analogues, and methods of use thereof

Inventors: William W. Bachovchin (Cambridge, MA); Hung-Sen Lai (Andover, MA)
Assignee: Trustees of Tufts College
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 8,377,971
App. No.
12/376,238
Granted
Feb 19, 2013
Kind
B2
Abstract

One aspect of the present invention relates to substituted pyridines and pharmaceutically acceptable salts thereof that are active against a range of mammalian maladies. Another aspect of the invention relates to a pharmaceutical composition, comprising a compound of the present invention or a pharmaceutically acceptable salt thereof; and a pharmaceutically acceptable excipient. The present invention also relates to methods of treating a range of mammalian maladies or conditions, including but not limited to hyperlipidemia, hypercholesterolemia, atherosclerosis, coronary artery disease, congestive heart failure, cardiovascular disease, hypertension, coronary heart disease, angina, pellagra, Hartnup's syndrome, carcinoid syndrome, arterial occlusive disease, obesity, hypothyroidism, vasoconstriction, osteoarthritis, rheumatoid arthritis, diabetes, Alzheimer's disease, lipodystrophy, or dyslipidemia, raising serum high-density lipoprotein (HDL) levels, and lowering serum low-density lipoprotein (LDL) levels.

Claims (13)

1. A compound represented by structure A, or a pharmaceutically acceptable salt thereof:

wherein

R represents independently for each occurrence H, alkyl, alkenyl, alkynyl, aryl, heteroaryl, aralkyl, heteroaralkyl, fluoride, chloride, bromide, iodide, nitro, cyano, sulfonic acid, alkylsulfoxyl, arylsulfoxyl, heteroarylsulfoxyl, aralkylsulfoxyl, heteroaralkylsulfoxyl, alkenylsulfoxyl, alkynylsulfoxyl, alkylsulfonyl, arylsulfonyl, heteroarylsulfonyl, aralkylsulfonyl, heteroaralkylsulfonyl, alkenylsulfonyl, alkynylsulfonyl, hydroxyl, alkoxyl, aryloxyl, heteroaryloxyl, aralkyloxy, heteroaralkyloxy, alkenyloxy, alkynyloxy, thiol, alkylthio, arylthio, aralkylthio, heteroaralkylthio, alkenylthio, alkynylthio, formyl, acyl, formyloxy, acyloxy, formylthio, acylthio, amino, alkylamino, arylamino, heteroarylamino, aralkylamino, heteroaralkylamino, alkenylamino, alkynylamino, formylamino, acylamino, carboxylate, alkyloxycarbonyl, aryloxycarbonyl, heteroaryloxycarbonyl, aralkyloxycarbonyl, heteroaralkyloxycarbonyl, carboxamido, alkylaminocarbonyl, arylaminocarbonyl, heteroarylaminocarbonyl, aralkylaminocarbonyl, or heteroaralkylaminocarbonyl;

R′ represents independently for each occurrence alkenyl, alkynyl, aryl, heteroaryl, aralkyl, heteroaralkyl, alkylsulfonyl, arylsulfonyl, heteroarylsulfonyl, aralkylsulfonyl, heteroaralkylsulfonyl, alkenylsulfonyl, alkynylsulfonyl, hydroxyl, alkoxyl, aryloxyl, heteroaryloxyl, aralkyloxy, heteroaralkyloxy, alkenyloxy, alkynyloxy, formyl, acyl, amino, alkylamino, arylamino, heteroarylamino, aralkylamino, heteroaralkylamino, alkenylamino, alkynylamino, formylamino, acylamino, alkyloxycarbonyl, aryloxycarbonyl, heteroaryloxycarbonyl, aralkyloxycarbonyl, heteroaralkyloxycarbonyl, alkylaminocarbonyl, arylaminocarbonyl, heteroarylaminocarbonyl, aralkylaminocarbonyl, or heteroaralkylaminocarbonyl; or the two instances of R′ taken together represent —(CH 2 ) 2 —, —(CH 2 ) 3 —, or —(CH 2 ) 6 —;

R″ represents independently for each occurrence H, alkyl, alkenyl, alkynyl, aryl, heteroaryl, aralkyl, or heteroaralkyl; and

n is 1, 2, 3, or 4.

2. The compound of claim 1 , wherein R represents independently for each occurrence H, alkyl, fluoride, chloride, bromide, nitro, cyano, sulfonic acid, hydroxyl, alkoxyl, thiol, alkylthio, formyl, acyl, formyloxy, acyloxy, formylthio, acylthio, amino, alkylamino, formylamino, acylamino, or carboxylate.

3. The compound of claim 1 , wherein R′ represents independently for each occurrence alkenyl, alkynyl, aryl, heteroaryl, aralkyl, or heteroaralkyl; or the two instances of R′ taken together represent —(CH 2 ) 2 —, —(CH 2 ) 3 —, or —(CH 2 ) 6 —.

4. The compound of claim 1 , wherein R″ represents H or alkyl.

5. The compound of claim 1 , wherein n is 2.

6. The compound of claim 1 , wherein R represents independently for each occurrence H; and n is 2.

7. The compound of claim 1 , wherein R represents independently for each occurrence H; and R″ represents H or alkyl.

8. The compound of claim 1 , wherein R represents independently for each occurrence H; R″ represents H or alkyl; and n is 2.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 15, 2009
From: BACHOVCHIN, WILLIAM W.; LAI, HUNG-SEN
To: TRUSTEES OF TUFTS COLLEGE
Reel/Frame 023231/0172 →
Continuity (2)
Provisional Application 60835194 · Aug 3, 2006
Related Publication 20090312355A1 · Dec 17, 2009