Methods for preparing 2,3,5,6-substituted 3h-pyrimidin-4-ones
申请人:Shcherbakova Irina
公开号:US20070161792A1
公开(公告)日:2007-07-12
Pyrimidinone compounds are disclosed. Methods of preparing the pyrimidinone compounds are also disclosed.
本发明公开了嘧啶酮化合物。同时,本发明还公开了制备嘧啶酮化合物的方法。
Pyrimidinone Compounds As Calcilytics
申请人:Shcherbakova V. Irina
公开号:US20070197555A1
公开(公告)日:2007-08-23
The pyrimidinone compounds are disclosed. Methods of preparing the pyrimidinone compounds are also disclosed.
本发明公开了嘧啶酮化合物。本发明还公开了制备嘧啶酮化合物的方法。
Pyrimidinone compounds as calcilytics
申请人:SmithKline Beecham Corp.
公开号:US07491728B2
公开(公告)日:2009-02-17
The pyrimidinone compounds are disclosed. Methods of preparing the pyrimidinone compounds are also disclosed.
本文披露了嘧啶酮化合物。同时也披露了制备嘧啶酮化合物的方法。
PYRIMIDINONE DERIVATIVES AS FATTY ACID SYNTHASE INHIBITORS
申请人:Adams Nicholas D.
公开号:US20130303551A1
公开(公告)日:2013-11-14
This invention relates to the use of pyrimidinone derivatives for the modulation, notably the inhibition of the activity or function of fatty acid synthase (FAS). Suitably, the present invention relates to the use of pyrimidinones in the treatment of cancer.
Design, new synthesis, and calcilytic activity of substituted 3H-pyrimidin-4-ones
作者:Irina Shcherbakova、Guangfei Huang、Otto J. Geoffroy、Satheesh K. Nair、Krzysztof Swierczek、Manuel F. Balandrin、John Fox、William L. Heaton、Rebecca L. Conklin
DOI:10.1016/j.bmcl.2005.03.054
日期:2005.5
Design, new synthesis, structure-activity relationship studies and calcium receptor antagonist (calcilytic) properties of novel 3H-pyrimidin-4-ones are described. (c) 2005 Elsevier Ltd. All rights reserved.