[EN] USE OF 1,2,4-OXADIAZOLE DERIVATIVES AS LIVER X RECEPTOR AGONISTS [FR] UTILISATION DE DÉRIVÉS DE 1,2,4-OXADIAZOLE EN TANT QU'AGONISTES DU RÉCEPTEUR X DU FOIE
[EN] INHIBITORS OF ALPHA-AMINO-BETA-CARBOXYMUCONIC ACID SEMIALDEHYDE DECARBOXYLASE<br/>[FR] INHIBITEURS DE LA SEMIALDÉHYDE DÉCARBOXYLASE DE L'ACIDE ALPHA-AMINO-BÊTA-CARBOXYMUCONIQUE
申请人:TES PHARMA S R L
公开号:WO2018069532A1
公开(公告)日:2018-04-19
The present disclosure discloses compounds capable of modulating the activity of α- amino-β-carboxymuconic acid semialdehyde decarboxylase (ACMSD), which are useful for the prevention and/or the treatment of diseases and disorders associated with defects in NAD+ biosynthesis, e.g., metabolic disorders, neurodegenerative diseases, chronic inflammatory diseases, kidney diseases, and diseases associated with ageing. The present application also discloses pharmaceutical compositions comprising said compounds and the use of such compounds as a medicament.
[EN] 1,2,4-OXADIAZOLE DERIVATIVES AS LIVER X RECEPTOR AGONISTS<br/>[FR] DÉRIVÉS DE 1,2,4-OXADIAZOLE EN TANT QU'AGONISTES DU RÉCEPTEUR X DU FOIE
申请人:NOVARTIS AG
公开号:WO2021105857A1
公开(公告)日:2021-06-03
Provided herein are compounds and pharmaceutical compositions useful for treating meibomian gland dysfunction (MGD), comprising administering to a subject in need thereof a therapeutically effective amount of a compound of Formula (I) or a compound of Formula (I'), or pharmaceutical composition described herein.
[EN] FORMULATIONS OF 3-((3-(4-(2-(ISOBUTYLSULFONYL)PHENOXY)-3-(TRIFLUOROMETHYL)PHENYL)-1,2,4-OXADIAZOL-5-YL)METHYL)-5,5-DIMETHYL-1-(2-MORPHOLINOETHYL)IMIDAZOLIDINE-2,4-DIONE<br/>[FR] FORMULATIONS DE 3-((3-(4-(2-(ISOBUTYLSULFONYL)PHÉNOXY)-3-(TRIFLUOROMÉTHYL)PHÉNYL)-1,2,4-OXADIAZOL-5-YL)MÉTHYL)-5,5-DIMÉTHYL-1-(2-MORPHOLINOÉTHYL)IMIDAZOLIDINE-2,4-DIONE
申请人:NOVARTIS AG
公开号:WO2022243907A1
公开(公告)日:2022-11-24
Formulations of 3-((3-(4-(2-(isobutylsulfonyl)phenoxy)-3-(trifluoromethyl)phenyl)-1,2,4-oxadiazol-5-yl)methyl)-5,5-dimethyl-1-(2-morpholinoethyl)imidazolidine-2,4-dione and pharmaceutically acceptable salts thereof, processes for their production, and uses thereof, including in the treatment of ocular diseases and disorders such as dry eye disease and Meibomian gland dysfunction (MGD).
INHIBITORS OF ALPHA-AMINO-BETA-CARBOXYMUCONIC ACID SEMIALDEHYDE DECARBOXYLASE
申请人:TES Pharma S.r.I.
公开号:US20180134667A1
公开(公告)日:2018-05-17
The present disclosure discloses compounds capable of modulating the activity of α-amino-β-carboxymuconic acid semialdehyde decarboxylase (ACMSD), which are useful for the prevention and/or the treatment of diseases and disorders associated with defects in NAD
+
biosynthesis, e.g., metabolic disorders, neurodegenerative diseases, chronic inflammatory diseases, kidney diseases, and diseases associated with ageing. The present application also discloses pharmaceutical compositions comprising said compounds and the use of such compounds as a medicament.
o-Hydroxyphenyl alkyl sulphides, -sulphoxides, and -sulphones
compounds have been synthesized and studied by means of NMR, IR, and UV spectra with special attention to H-bonding. These compounds appeared to exist in the chelated form. Furthermore, a detailed investigation of the electron-impact mass-spectra has been carried out,-in the case of sulphoxides, by means of a computer-monitored mixture analysis.