Abstract:
The present invention relates to TP receptor antagonists, which have the ability to bind to TP receptor and optionally cross the blood brain barrier. The invention also provides compositions and methods for treating a disorder wherein activation of TP receptor is detrimental.
Abstract:
The present invention relates to TP receptor antagonists, which have the ability to bind to TP receptor and optionally cross the blood brain barrier. The invention also provides compositions and methods for treating a disorder wherein activation of TP receptor is detrimental.
Abstract:
The present invention relates to TP receptor antagonists, which have the ability to bind to TP receptor and optionally cross the blood brain barrier. The invention also provides compositions and methods for treating a disorder wherein activation of TP receptor is detrimental.
Abstract:
The present invention is directed to methods of inhibiting a tauopathy in a patient by administration of a compound of formula (I): Novel aminothienopyridazine compounds are also described.
Abstract:
Disclosed herein are novel cycloalka[b]heteroaryl compounds having CX3CR1/ fractalkine receptor (CX3CR1) agonistic properties, pharmaceutical compositions comprising these compounds, chemical processes for preparing these compounds and their use in the treatment or prophylaxis of diseases associated with CX3CR1 receptor activity in animals, in particular humans.
Abstract:
The present invention is directed to methods of inhibiting a tauopathy in a patient by administration of a compound of formula (I): Novel aminothienopyridazine compounds are also described.
Abstract:
The invention concerns the use of beta -dicarbonyl or aromatic ortho-hydroxycarbonyl compounds to mark hydrocarbons, as well as hydrocarbons containing beta -dicarbonyl or aromatic ortho-hydroxycarbonyl compounds as markers and a method of assaying beta -dicarbonyl or aromatic ortho-hydroxycarbonyl compounds in hydrocarbons.