Patent classifications
C07D307/24
CXCR6 SULFONAMIDE COMPOUNDS
Provided are sulfonamide compounds having formula (I):
##STR00001##
or a pharmaceutically acceptable salt thereof, wherein R, R.sup.1, R.sup.2, R.sup.3, R.sup.4 and the subscripts n and m have the meanings provided in the specification. The compounds are useful for treating diseases and conditions associated with CXCR6 activity.
Treprostinil derivatives and compositions and uses thereof
The present disclosure provides treprostinil derivatives that can act as prodrugs of treprostinil. The treprostinil derivatives can be used to treat any conditions responsive to treatment with treprostinil, including pulmonary hypertension, such as pulmonary arterial hypertension.
Treprostinil derivatives and compositions and uses thereof
The present disclosure provides treprostinil derivatives that can act as prodrugs of treprostinil. The treprostinil derivatives can be used to treat any conditions responsive to treatment with treprostinil, including pulmonary hypertension, such as pulmonary arterial hypertension.
AMIDE DERIVATIVES, PROCESS FOR PREPARATION THEREOF AND USE THEREOF AS INSECTICIDE
A compound represented by Formula (1):
##STR00001##
The compound can be used as insecticides.
AMIDE DERIVATIVES, PROCESS FOR PREPARATION THEREOF AND USE THEREOF AS INSECTICIDE
A compound represented by Formula (1):
##STR00001##
The compound can be used as insecticides.
Fluorine-containing monomer, fluorine-containing polymer, pattern forming composition using same, and pattern forming method of same
Provided is a fluorine-containing polymer which has no perfluoroalkyl group of 4 or more carbon atoms and which, when formed together with a photoacid generator into a film, shows water repellency after film formation, but becomes hydrophilic by the action of an acid generated under light irradiation, and thus serves as a pattern forming material capable of forming a film with high sensitivity and resolution. A fluorine-containing polymer according to the present invention has a repeating unit of the formula (1) ##STR00001##
where R.sup.1 is a hydrogen atom, a fluorine atom or a C.sub.1-C.sub.10 alkyl group; R.sup.2 to R.sup.5 are each independently a hydrogen atom or a C.sub.1-C.sub.10 alkyl group; X is a single bond or a divalent group; Y is a C.sub.1-C.sub.3 fluoroalkyl or carboxylate (—COOR) group; R is a C.sub.1-C.sub.3 fluoroalkyl group; and seven or less of hydrogen atoms contained in the substituent group may be substituted with fluorine.
Substituted tetrahydrofurans as modulators of sodium channels
- Steven John Durrant ,
- Nadia Ahmad ,
- Elizabeth Mary Beck ,
- Lidio Marx Carvalho Meireles ,
- Ewa Iwona Chudyk ,
- Gorka Etxebarria Jardi ,
- Bhairavi Galan ,
- Sara S. Hadida Ruah ,
- Dennis James HURLEY ,
- Ronald Marcellus Knegtel ,
- Timothy Donald Neubert ,
- Joanne Louise Pinder ,
- Joseph PONTILLO ,
- Robert Pullin ,
- Yvonne Schmidt ,
- David Matthew Shaw ,
- Sarah Skerratt ,
- Dean Stamos ,
- Stephen Andrew Thomson ,
- Anisa Nizarali Virani ,
- Christopher Wray
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.
Substituted tetrahydrofurans as modulators of sodium channels
- Steven John Durrant ,
- Nadia Ahmad ,
- Elizabeth Mary Beck ,
- Lidio Marx Carvalho Meireles ,
- Ewa Iwona Chudyk ,
- Gorka Etxebarria Jardi ,
- Bhairavi Galan ,
- Sara S. Hadida Ruah ,
- Dennis James HURLEY ,
- Ronald Marcellus Knegtel ,
- Timothy Donald Neubert ,
- Joanne Louise Pinder ,
- Joseph PONTILLO ,
- Robert Pullin ,
- Yvonne Schmidt ,
- David Matthew Shaw ,
- Sarah Skerratt ,
- Dean Stamos ,
- Stephen Andrew Thomson ,
- Anisa Nizarali Virani ,
- Christopher Wray
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.
Triaryl compounds for treatment of PD-L1 diseases
Compounds are provided that are useful as immunomodulators. The compounds have the Formula (I) ##STR00001##
including stereoisomers and pharmaceutically acceptable salts thereof, wherein R.sup.1a, R.sup.1b, R.sup.1c, R.sup.1d, R.sup.2a, R.sup.2b, R.sup.3, R.sup.3a, R.sup.4, R.sup.6, R.sup.7, R.sup.8, A, Z, X.sup.1 and n are as defined herein. Methods associated with preparation and use of such compounds, as well as pharmaceutical compositions comprising such compounds, are also disclosed.
AMIDE DERIVATIVES, PROCESS FOR PREPARATION THEREOF AND USE THEREOF AS INSECTICIDE
A compound represented by Formula (1):
##STR00001##
The compound can be used as insecticides.