Patent classifications
C07D215/60
NITROCATECHOL DERIVATIVES AS COMT INHIBITORS
New compounds of formula I are described:
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The compounds have potentially valuable pharmaceutical properties in the treatment of some central and peripheral nervous system disorders.
NITROCATECHOL DERIVATIVES AS COMT INHIBITORS
New compounds of formula I are described:
##STR00001##
The compounds have potentially valuable pharmaceutical properties in the treatment of some central and peripheral nervous system disorders.
BETA ADRENERGIC AGONIST AND METHODS OF USING THE SAME
The present disclosure is directed to chemical compounds and to the use of such compounds in the treatment of diseases associated with an adrenergic receptor.
Crystal form of compound used as mineralocorticoid receptor antagonist and preparation method therefor
The present invention belongs to the technical field of medicines, and relates to a crystal form of a compound used as a mineralocorticoid receptor antagonist and a preparation method therefor, and in particular, to a method for preparing a compound 2-chloro-4-[(3S,3aR)-3-cyclopentyl-7-(4-hydroxypiperidin-1-carbonyl)-3,3a,4,5-tetrahydro-2H-pyrazolo[3,4-f]quinolin-2-yl]benzonitrile of formula (1); a crystal form thereof, a preparation method for the crystal form, and the use of the crystal form in the preparation of drugs for the treatment and/or prevention of renal injury or cardiovascular diseases. ##STR00001##
Crystal form of compound used as mineralocorticoid receptor antagonist and preparation method therefor
The present invention belongs to the technical field of medicines, and relates to a crystal form of a compound used as a mineralocorticoid receptor antagonist and a preparation method therefor, and in particular, to a method for preparing a compound 2-chloro-4-[(3S,3aR)-3-cyclopentyl-7-(4-hydroxypiperidin-1-carbonyl)-3,3a,4,5-tetrahydro-2H-pyrazolo[3,4-f]quinolin-2-yl]benzonitrile of formula (1); a crystal form thereof, a preparation method for the crystal form, and the use of the crystal form in the preparation of drugs for the treatment and/or prevention of renal injury or cardiovascular diseases. ##STR00001##
SUBSTITUTED N,2-DIARYLQUINOLINE-4-CARBOXAMIDES AND THE USE THEREOF AS ANTI-INFLAMMATORY AGENTS
The present application relates to novel substituted N,2-diarylquinoline-4-carboxamide derivatives, to processes for preparation thereof, to the use thereof alone or in combinations for treatment and/or prevention of diseases, and to the use thereof for production of medicaments for treatment and/or prevention of diseases, especially for treatment and/or prevention of fibrotic and/or inflammatory disorders.
SUBSTITUTED N,2-DIARYLQUINOLINE-4-CARBOXAMIDES AND THE USE THEREOF AS ANTI-INFLAMMATORY AGENTS
The present application relates to novel substituted N,2-diarylquinoline-4-carboxamide derivatives, to processes for preparation thereof, to the use thereof alone or in combinations for treatment and/or prevention of diseases, and to the use thereof for production of medicaments for treatment and/or prevention of diseases, especially for treatment and/or prevention of fibrotic and/or inflammatory disorders.
HETEROARYL COMPOUNDS FOR THE TREATMENT OF PAIN
- Mark Thomas MILLER ,
- Dennis James HURLEY ,
- Timothy Donald Neubert ,
- Elamprakash Nesan Savariar ,
- Urvi Patel ,
- Sara Sabina Hadida Ruah ,
- Jason McCartney ,
- Jinglan Zhou ,
- Robert Martin Demoret ,
- Roman Askatovich Valiulin ,
- Alexander Frederik Kintzer ,
- Peter Webb ,
- David Robert Slochower ,
- Kathleen Aertgeerts ,
- Elizabeth Mary Beck ,
- Ronald Marcellus Alphonsus Knegtel ,
- Ewa Iwona Chudyk ,
- Joanne Louise Pinder
Compounds, and pharmaceutically acceptable salts thereof, useful as inhibitors of sodium channels are provided. Also provided are pharmaceutical compositions comprising the compounds or pharmaceutically acceptable salts and methods of using the compounds, pharmaceutically acceptable salts, and pharmaceutical compositions in the treatment of various disorders, including pain.
HETEROARYL COMPOUNDS FOR THE TREATMENT OF PAIN
- Mark Thomas MILLER ,
- Dennis James HURLEY ,
- Timothy Donald Neubert ,
- Elamprakash Nesan Savariar ,
- Urvi Patel ,
- Sara Sabina Hadida Ruah ,
- Jason McCartney ,
- Jinglan Zhou ,
- Robert Martin Demoret ,
- Roman Askatovich Valiulin ,
- Alexander Frederik Kintzer ,
- Peter Webb ,
- David Robert Slochower ,
- Kathleen Aertgeerts ,
- Elizabeth Mary Beck ,
- Ronald Marcellus Alphonsus Knegtel ,
- Ewa Iwona Chudyk ,
- Joanne Louise Pinder
Compounds, and pharmaceutically acceptable salts thereof, useful as inhibitors of sodium channels are provided. Also provided are pharmaceutical compositions comprising the compounds or pharmaceutically acceptable salts and methods of using the compounds, pharmaceutically acceptable salts, and pharmaceutical compositions in the treatment of various disorders, including pain.
Metabolites of N-(4-{[6,7-Bis(methyloxy)quinolin-4-yl]oxy}phenyl)-N'-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide
The invention relates to metabolites of cabozantinib (I) as well as uses thereof.
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