US2014005400A1PendingUtilityA1
New azacyclic compounds
Est. expiryAug 13, 2030(~4 yrs left)· nominal 20-yr term from priority
Inventors:Jean AckermannAurelia ConteDaniel HunzikerWerner NeidhartMatthias NettekovenTanja Schulz-GaschStanley Wertheimer
A61P 9/00A61P 3/06A61P 3/10A61P 9/10A61P 43/00A61K 31/437C07D 471/10A61P 3/04A61P 3/00A61K 31/438
56
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
The invention provides novel compounds having the general formula (I) wherein R 1 , R 2 and n are as described herein, compositions including the compounds and methods of using the compounds. The compounds are useful as inhibitors of hormone sensitive lipase (HSL) for the treatment of diabetes, metabolic syndrome and obesity.
Claims
exact text as granted — not AI-modified1 - 12 . (canceled)
13 . A compound according to formula (I)
wherein:
R 1 is selected from the group consisting of: imidazolyl, pyrazolyl, triazolyl, phenyl, pyridinyl, pyrazinyl, pyrimidyl, pyridazinyl and 2-oxo-1,2-dihydro-pyridinyl,
and is optionally substituted with one to three substituents independently selected from the group consisting of alkyl, cycloalkyl, alkylcycloalkyl, cycloalkylalkyl, cycloalkylalkoxy, cycloalkylalkoxyalkyl, cycloalkoxy, cycloalkoxyalkyl, alkylcycloalkylalkyl, halocycloalkyl, halocycloalkylalkyl, halogen, haloalkyl, hydroxy, hydroxyalkyl, alkoxy, alkoxyalkyl, haloalkoxy, hydroxyalkoxy, alkoxyalkoxy, alkoxyalkoxyalkyl and hydroxyhaloalkyl;
R 2 is pyridinyl or 2-oxo-1,2-dihydro-pyridinyl,
and is optionally substituted with one to three substituents independently selected from alkyl and hydroxy; and
n is zero;
or a pharmaceutically acceptable salt thereof.Join the waitlist — get patent alerts
Track US2014005400A1 — get alerts on status changes and closely related new filings.
We store only your email — no account needed. See our privacy policy.