Nick A. Paras - San Francisco CA, US Yuan Cheng - Newbury Park CA, US Timothy Powers - Malibu CA, US James Brown - Moorpark CA, US Stephen A. Hitchcock - Jupiter FL, US Ted Judd - Simi Valley CA, US Patricia Lopez - West Hills CA, US Qiufen Xue - Newbury Park CA, US Bryant Yang - Simi Valley CA, US
The present invention comprises a new class of compounds useful for the modulation of Beta-secretase enzyme activity and for the treatment of Beta-secretase mediated diseases, including Alzheimer's disease (AD) and related conditions. In one embodiment, the compounds have a general Formula I, wherein ring A, B, B, B, L, R, R, ring Z, m and p of Formula I are defined herein. The invention also includes use of these compounds in pharmaceutical compositions for treatment, prophylactic or therapeutic, of disorders and conditions related to the activity of beta-secretase protein. Such disorders include, for example, Alzheimer's Disease (AD), cognitive deficits, cognitive impairment, schizophrenia and other central nervous system conditions related to and/or caused by the formation and/or deposition of plaque on the brain. The invention also comprises further embodiments of Formula I, intermediates and processes useful for the preparation of compounds of Formula I.
Amino Heteroaryl Compounds As Beta-Secretase Modulators And Methods Of Use
Nick A. Paras - San Francisco CA, US James Brown - Moorpark CA, US Yuan Cheng - Newbury Park CA, US Stephen A. Hitchcock - Jupiter FL, US Ted Judd - Granada Hills CA, US Patricia Lopez - West Hills CA, US Ana Elena Minatti - Santa Monica CA, US Thomas Nixey - Newbury Park CA, US Timothy Powers - Malibu CA, US Christopher M. Tegley - Thousand Oaks CA, US Qiufen Xue - Newbury Park CA, US Bryant Yang - Simi Valley CA, US Wenge Zhong - Thousands Oaks CA, US
The present invention comprises a new class of compounds useful for the modulation of Beta-secretase enzyme activity and for the treatment of Beta-secretase mediated diseases, including Alzheimer's disease (AD) and related conditions. In one embodiment, the compounds have a general Formula (I); wherein ring A, B, B, B, L, R, R, ring Z, m and n of Formula I are defined herein. The invention also includes use of these compounds in pharmaceutical compositions for treatment, prophylactic or therapeutic, of disorders and conditions related to the activity of beta-secretase protein. Such disorders include, for example, Alzheimer's Disease (AD), cognitive deficits, cognitive impairment, schizophrenia and other central nervous system conditions related to and/or caused by the formation and/or deposition of plaque on the brain. The invention also comprises further embodiments of Formula (I), intermediates and processes useful for the preparation of compounds of Formula (I).
Rnai Constructs And Methods For Inhibiting Lpa Expression
- Thousand Oaks CA, US Michael OLLMANN - San Carlos CA, US Oliver HOMANN - Berkeley CA, US Yuan CHENG - Newbury Park CA, US
Assignee:
AMGEN INC. - Thousand Oaks CA
International Classification:
C12N 15/113 A61P 9/10
Abstract:
The present invention relates to RNAi constructs for reducing expression of the LPA gene, which encodes apolipoprotein(a), a component of lipoprotein(a) (Lp(a)) particles. Methods of using such RNAi constructs to treat or prevent cardiovascular disease, such as coronary artery disease, peripheral artery disease, stroke, and myocardial infarction, and to reduce serum Lp(a) levels are also described.
Yuan Cheng (1996-2000), Tee Tee (1999-2003), Paul Edwards (1989-1993), Gobind Nandwani (1989-1993), Gilbert Richardson (1989-1993), Erik Sealander (1992-1996)