5-CHLORO-2-DIFLUOROMETHOXYPHENYL PYRAZOLOPYRIMIDINE COMPOUNDS, COMPOSITIONS AND METHODS OF USE THEREOF
申请人:Genentech, Inc.
公开号:US20150336962A1
公开(公告)日:2015-11-26
Compounds of Formula (00A) and methods of use as Janus kinase inhibitors are described herein.
这里描述了化合物的公式(00A)及其作为Janus激酶抑制剂的使用方法。
Compounds with activity on muscarinic receptors
申请人:Acadia Pharmaceuticals Inc.
公开号:US06528529B1
公开(公告)日:2003-03-04
Compounds and methods are provided for the alleviation or treatment of diseases or conditions in which modification of muscarinic m1 receptor activity has a beneficial effect. In the method, a therapeutically effective amount of a selective muscarinic m1 agonist compound is administered to a patient in need of such treatment.
FUSED HETEROCYCLIC COMPOUND AND MEDICINAL USE THEREOF
申请人:Mitsubishi Pharma Corporation
公开号:EP1396488A1
公开(公告)日:2004-03-10
The fused heterocyclic compound of the present invention, which is represented by the formula (I):
wherein each symbol is as defined in the specification, an optically active form thereof, a pharmaceutically acceptable salt thereof, a hydrate thereof and a water adduct thereof show poly(ADP-ribose) synthase inhibitory action and are useful as therapeutic drugs for cerebral infarction.
POLYMERS FUNCTIONALIZED WITH NITRILE COMPOUNDS COMTAINING A PROTECTED AMINO GROUP
申请人:Luo Steven
公开号:US20120059112A1
公开(公告)日:2012-03-08
A method for preparing a functionalized polymer, the method comprising the steps of (i) polymerizing monomer with a coordination catalyst to form a reactive polymer; and (ii) reacting the reactive polymer with a nitrile compound containing a protected amino group.
POLYMERS FUNCTIONALIZED WITH NITRILE COMPOUNDS CONTAINING A PROTECTED AMINO GROUP
申请人:Luo Steven
公开号:US20120296041A1
公开(公告)日:2012-11-22
A method for preparing a functionalized polymer, the method comprising the steps of: (i) polymerizing monomer with an anionic initiator to form a reactive polymer; and (ii) reacting the reactive polymer with a nitrile compound containing a protected amino group, where the protected amino group is directly attached to a moiety selected from the group consisting of acyclic moieties, heterocyclic moieties, and non-aromatic cyclic moieties.