Carbamoyl compounds as dgat1 inhibitors 190

DGAT-1 inhibitor compounds of formula (1), pharmaceutically-acceptable salts and pro-drugs thereof are described, together with pharmaceutical compositions, processes for making them and their use in treating, for example, obesity wherein, for example, Ring A is optionally substituted 2,6-pyrazindiy...

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Main Authors JOHANNESSON PETRA, GREEN CLIVE, BIRCH ALAN MARTIN, BARLIND JONAS GUNNAR, BAUER UDO ANDREAS, BUTLIN ROGER JOHN, HOVLAND RAGNAR, PETERSSON ANNIKA ULRIKA, JOHANSSON JAN MAGNUS, LEACH ANDREW, NOESKE ALEXANDER TOBIAS
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LanguageChinese
English
Published 12.06.2013
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Abstract DGAT-1 inhibitor compounds of formula (1), pharmaceutically-acceptable salts and pro-drugs thereof are described, together with pharmaceutical compositions, processes for making them and their use in treating, for example, obesity wherein, for example, Ring A is optionally substituted 2,6-pyrazindiyl; X is 0; Ring B is optionally substituted 1,4-phenylene; Y1 is a direct bond or -O-; Y2 is -(CH2)r- wherein r is 2 or 3; n is 0 or n is 1 when Y1 is a direct bond between Ring B and Ring C and when Ring B is 1,4-phenylene and Ring C is (4-6C)cycloalkane; Ring C is optionally substituted (4-6C)cycloalkane, (7-10C)bicycloalkane, (8-12C)tricycloalkane, phenylene or pryidindiyl; L is a direct bond or -O-; p is 0, 1 or 2 and when p is 1 or 2 RA1 and RA2 are each independently hydrogen or (1-4C)alkyl; Z is carboxy or a mimic or bioisostere thereof.
AbstractList DGAT-1 inhibitor compounds of formula (1), pharmaceutically-acceptable salts and pro-drugs thereof are described, together with pharmaceutical compositions, processes for making them and their use in treating, for example, obesity wherein, for example, Ring A is optionally substituted 2,6-pyrazindiyl; X is 0; Ring B is optionally substituted 1,4-phenylene; Y1 is a direct bond or -O-; Y2 is -(CH2)r- wherein r is 2 or 3; n is 0 or n is 1 when Y1 is a direct bond between Ring B and Ring C and when Ring B is 1,4-phenylene and Ring C is (4-6C)cycloalkane; Ring C is optionally substituted (4-6C)cycloalkane, (7-10C)bicycloalkane, (8-12C)tricycloalkane, phenylene or pryidindiyl; L is a direct bond or -O-; p is 0, 1 or 2 and when p is 1 or 2 RA1 and RA2 are each independently hydrogen or (1-4C)alkyl; Z is carboxy or a mimic or bioisostere thereof.
Author HOVLAND RAGNAR
LEACH ANDREW
JOHANSSON JAN MAGNUS
BAUER UDO ANDREAS
BIRCH ALAN MARTIN
BUTLIN ROGER JOHN
GREEN CLIVE
NOESKE ALEXANDER TOBIAS
PETERSSON ANNIKA ULRIKA
BARLIND JONAS GUNNAR
JOHANNESSON PETRA
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– fullname: BUTLIN ROGER JOHN
– fullname: HOVLAND RAGNAR
– fullname: PETERSSON ANNIKA ULRIKA
– fullname: JOHANSSON JAN MAGNUS
– fullname: LEACH ANDREW
– fullname: NOESKE ALEXANDER TOBIAS
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Snippet DGAT-1 inhibitor compounds of formula (1), pharmaceutically-acceptable salts and pro-drugs thereof are described, together with pharmaceutical compositions,...
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HETEROCYCLIC COMPOUNDS
HUMAN NECESSITIES
HYGIENE
MEDICAL OR VETERINARY SCIENCE
METALLURGY
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PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
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Title Carbamoyl compounds as dgat1 inhibitors 190
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