Patent classifications
C07D487/04
HETEROCYCLIC COMPOUND
- Yuhei MIYANOHANA ,
- Yuichi KAJITA ,
- Tatsuki KOIKE ,
- Yasutaka HOASHI ,
- Yasushi Hattori ,
- Norihito Tokunaga ,
- Tsuneo ODA ,
- Tohru Miyazaki ,
- Dilhumar UYGHUR ,
- Yoshiteru ITO ,
- Kohei TAKEUCHI ,
- Keisuke IMAMURA ,
- Takahiro SUGIMOTO ,
- Koichiro FUKUDA ,
- Yasuhisa KOHARA ,
- Rei OKAMOTO ,
- Taiichi OHRA ,
- Naoki MIYAMOTO ,
- Jun CHIBA ,
- Yoshito Terao ,
- Masanori KAWASAKI
The present invention provides a heterocyclic compound having an orexin type 2 receptor agonist activity.
A compound represented by the formula (I):
##STR00001## wherein each symbol is as described in the description, or a salt thereof has an orexin type 2 receptor agonist activity, and is useful as an agent for the prophylaxis or treatment of narcolepsy.
Compounds for the Treatment of Kinase-Dependent Disorders
Disclosed herein are compounds of Formula (I) which inhibit, regulate and/or modulate tyrosine kinase receptors, particularly Ax1 and Mer signal transduction pathways related to the changes in cellular activities, compositions containing the compounds, methods of using the compounds to treat kinase-dependent diseases and conditions, and methods for making the compounds.
##STR00001##
1H-PYRAZOLO[4,3-d]PYRIMIDINE COMPOUNDS AS TOLL-LIKE RECEPTOR 7 (TLR7) AGONISTS
Compounds according to formula I are useful as agonists of Toll-like receptor 7 (TLR7). (I) Such compounds can be used in cancer treatment, especially in combination with an anti-cancer immunotherapy agent, or as a vaccine adjuvant.
##STR00001##
1H-PYRAZOLO[4,3-d]PYRIMIDINE COMPOUNDS AS TOLL-LIKE RECEPTOR 7 (TLR7) AGONISTS
Compounds according to formula I are useful as agonists of Toll-like receptor 7 (TLR7). (I) Such compounds can be used in cancer treatment, especially in combination with an anti-cancer immunotherapy agent, or as a vaccine adjuvant.
##STR00001##
METHODS AND MATERIALS FOR INHIBITING NF-kB ACTIVITY
This document provides compounds that are inhibitors of NF-κB activity, as well as the methods of using such compounds for treating diseases and conditions such as cancer, inflammatory conditions, or autoimmune diseases.
METHODS AND MATERIALS FOR INHIBITING NF-kB ACTIVITY
This document provides compounds that are inhibitors of NF-κB activity, as well as the methods of using such compounds for treating diseases and conditions such as cancer, inflammatory conditions, or autoimmune diseases.
FLUORINE-CONTAINING HETEROCYCLIC DERIVATIVES WITH MACROCYCLIC STRUCTURE AND USE THEREOF
Disclosed are a macrocyclic fluorine-containing heterocyclic derivative of formula (I), a preparation method thereof, and a use thereof in treatment of TRK kinase-mediated diseases.
##STR00001##
POTENT AND SELECTIVE AZAINDOLE INHIBITORS OF CDK8 AND CDK19
Provided herein are compounds, pharmaceutical compositions comprising such compounds, and methods of using such compounds to treat diseases or disorders associated with CDK8 and/or CDK19.
POTENT AND SELECTIVE AZAINDOLE INHIBITORS OF CDK8 AND CDK19
Provided herein are compounds, pharmaceutical compositions comprising such compounds, and methods of using such compounds to treat diseases or disorders associated with CDK8 and/or CDK19.
ARYL HETEROBICYCLIC COMPOUNDS AS Kv1.3 POTASSIUM SHAKER CHANNEL BLOCKERS
A compound of Formula (I), or a pharmaceutically acceptable salt thereof, is described, where the substituents are as defined herein. Pharmaceutical compositions including the same and method of using the same are also described.
##STR00001##