Patent classifications
C07H9/04
ASGPR-binding compounds for the degradation of extracellular proteins
Compounds and compositions that have an asialoglycoprotein receptor (ASGPR) binding ligand bound to an extracellular protein binding ligand for the selective degradation of the target extracellular protein in vivo to treat disorders mediated by the extracellular protein are described.
C-aryl glucoside derivative, preparation methods thereof, and medical applications thereof
C-aryl glucoside derivatives, preparation methods thereof, and medical applications thereof are described. Specifically, compounds represented by formula I, and, tautomers, enantiomers, diastereomers, racemates, and pharmaceutically acceptable salts of the compounds, preparation methods thereof, pharmaceutical compositions containing the compounds, and applications thereof are described. Compounds of formula (I) are useful as therapeutic agents, and particularly as sodium-dependent glucose contransporter protein (SGLT) inhibitors. ##STR00001##
C-aryl glucoside derivative, preparation methods thereof, and medical applications thereof
C-aryl glucoside derivatives, preparation methods thereof, and medical applications thereof are described. Specifically, compounds represented by formula I, and, tautomers, enantiomers, diastereomers, racemates, and pharmaceutically acceptable salts of the compounds, preparation methods thereof, pharmaceutical compositions containing the compounds, and applications thereof are described. Compounds of formula (I) are useful as therapeutic agents, and particularly as sodium-dependent glucose contransporter protein (SGLT) inhibitors. ##STR00001##
ERTUGLIFLOZIN CO-CRYSTALS AND PROCESS FOR THEIR PREPARATION
The present invention relates to processes for the preparation of an ertugliflozin-L-pyroglutamic acid (1:1) and co-crystal ertugliflozin-L-proline (1:1) co-crystal. The present invention further relates to an ertugliflozin-L-proline (1:2) co-crystal, processes for its preparation, and its use for the treatment of type 2 diabetes mellitus.
Reagent-controlled stereoselective glycosylation
Provided are methods for the efficient stereoselective formation of glycosidic bonds, without recourse to prosthetic or directing groups.
Reagent-controlled stereoselective glycosylation
Provided are methods for the efficient stereoselective formation of glycosidic bonds, without recourse to prosthetic or directing groups.
ASGPR-BINDING COMPOUNDS FOR THE DEGRADATION OF EXTRACELLULAR PROTEINS
Compounds and compositions that have an asialoglycoprotein receptor (ASGPR) binding ligand bound to an extracellular protein binding ligand for the selective degradation of the target extracellular protein in vivo to treat disorders mediated by the extracellular protein are described.
ASGPR-BINDING COMPOUNDS FOR THE DEGRADATION OF EXTRACELLULAR PROTEINS
Compounds and compositions that have an asialoglycoprotein receptor (ASGPR) binding ligand bound to an extracellular protein binding ligand for the selective degradation of the target extracellular protein in vivo to treat disorders mediated by the extracellular protein are described.
CATALYTIC METHOD FOR THE PRODUCTION OF DIFRUCTOSE ANHYDRIDE
Disclosed herein are methods, compositions, and reactor systems for producing difructose anhydride. The method comprises contacting a solution comprising fructose and gamma valerolactone with an acidic catalyst at an effective temperature for an effective contact time to produce difructose anhydride.
CATALYTIC METHOD FOR THE PRODUCTION OF DIFRUCTOSE ANHYDRIDE
Disclosed herein are methods, compositions, and reactor systems for producing difructose anhydride. The method comprises contacting a solution comprising fructose and gamma valerolactone with an acidic catalyst at an effective temperature for an effective contact time to produce difructose anhydride.