Patent classifications
C07D277/60
HUMAN PROTEIN TYROSINE PHOSPHATASE INHIBITORS AND METHODS OF USE
The present disclosure relates to compounds effective as human protein tyrosine phosphatase beta (HPTP-β) inhibitors thereby regulating angiogenesis. The present disclosure further relates to compositions comprising said human protein tyrosine phosphatase beta (HPTP-β) inhibitors, and to methods for regulating angiogenesis.
HETEROCYCLE AMINES AND USES THEREOF
Compounds and methods in the fields of chemistry and medicine are disclosed. Some of the disclosed embodiments include compounds, compositions and methods of using heterocycle amines. Some of the disclosed embodiments include heterocycle amines useful to treat inflammatory disorders.
HETEROCYCLE AMINES AND USES THEREOF
Compounds and methods in the fields of chemistry and medicine are disclosed. Some of the disclosed embodiments include compounds, compositions and methods of using heterocycle amines. Some of the disclosed embodiments include heterocycle amines useful to treat inflammatory disorders.
HETEROCYCLIC COMPOUND
- Yuichi KAJITA ,
- Yuhei MIYANOHANA ,
- 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 ,
- 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.
SUBSTITUTED AMINOTHIAZOLES AS INHIBITORS OF NUCLEASES
Compounds represented by the structural formula (1) R1, R2, R3, R4, R5, R6 are inhibitors of nucleases, and are useful in particular in a method of treatment and/or prevention of proliferative diseases, neurodegenerative diseases, and other genomic instability associated diseases.
SUBSTITUTED AMINOTHIAZOLES AS INHIBITORS OF NUCLEASES
Compounds represented by the structural formula (1) R1, R2, R3, R4, R5, R6 are inhibitors of nucleases, and are useful in particular in a method of treatment and/or prevention of proliferative diseases, neurodegenerative diseases, and other genomic instability associated diseases.
Heterocycle amines and uses thereof
Compounds and methods in the fields of chemistry and medicine are disclosed. Some of the disclosed embodiments include compounds, compositions and methods of using heterocycle amines. Some of the disclosed embodiments include heterocycle amines useful to treat inflammatory disorders.
Heterocycle amines and uses thereof
Compounds and methods in the fields of chemistry and medicine are disclosed. Some of the disclosed embodiments include compounds, compositions and methods of using heterocycle amines. Some of the disclosed embodiments include heterocycle amines useful to treat inflammatory disorders.
Heterocycle amines and uses thereof
Compounds and methods in the fields of chemistry and medicine are disclosed. Some of the disclosed embodiments include compounds, compositions and methods of using heterocycle amines. Some of the disclosed embodiments include heterocycle amines useful to treat inflammatory disorders.
Heterocycle amines and uses thereof
Compounds and methods in the fields of chemistry and medicine are disclosed. Some of the disclosed embodiments include compounds, compositions and methods of using heterocycle amines. Some of the disclosed embodiments include heterocycle amines useful to treat inflammatory disorders.