C07H5/10

Ruthenium carbon monoxide releasing molecules and uses thereof

The present invention provides novel ruthenium compounds of Formula (I): ##STR00001##
or salts, isomers, hydrates, or solvates thereof, or combinations thereof; wherein E, R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, X.sub.1, and X.sub.2 are as defined herein, and pharmaceutical compositions thereof. Also provided are methods of use and treatment. Such compounds have been found useful in the treatment of malaria infection. Such compounds may also be useful in the treatment of inflammatory conditions, such as acute lung injury and acute resipiratory distress syndrome, which optionally may be associated with a malaria infection.

Ruthenium carbon monoxide releasing molecules and uses thereof

The present invention provides novel ruthenium compounds of Formula (I): ##STR00001##
or salts, isomers, hydrates, or solvates thereof, or combinations thereof; wherein E, R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, X.sub.1, and X.sub.2 are as defined herein, and pharmaceutical compositions thereof. Also provided are methods of use and treatment. Such compounds have been found useful in the treatment of malaria infection. Such compounds may also be useful in the treatment of inflammatory conditions, such as acute lung injury and acute resipiratory distress syndrome, which optionally may be associated with a malaria infection.

DITHIOLSACCHARIDE MUCOLYTIC AGENTS AND USES THEREOF

There are provided, inter alia, methods for decreasing mucus elasticity or decreasing mucus viscosity in a subject in need thereof, the methods including administering to the subject an effective amount of a dithiolsaccharide mucolytic agent, and compounds and pharmaceutical compositions useful for the methods.

DITHIOLSACCHARIDE MUCOLYTIC AGENTS AND USES THEREOF

There are provided, inter alia, methods for decreasing mucus elasticity or decreasing mucus viscosity in a subject in need thereof, the methods including administering to the subject an effective amount of a dithiolsaccharide mucolytic agent, and compounds and pharmaceutical compositions useful for the methods.

DITHIOLSACCHARIDE MUCOLYTIC AGENTS AND USES THEREOF

There are provided, inter alia, methods for decreasing mucus elasticity or decreasing mucus viscosity in a subject in need thereof, the methods including administering to the subject an effective amount of a dithiolsaccharide mucolytic agent, and compounds and pharmaceutical compositions useful for the methods.

DITHIOLSACCHARIDE MUCOLYTIC AGENTS AND USES THEREOF

There are provided, inter alia, methods for decreasing mucus elasticity or decreasing mucus viscosity in a subject in need thereof, the methods including administering to the subject an effective amount of a dithiolsaccharide mucolytic agent, and compounds and pharmaceutical compositions useful for the methods.

Galactoside inhibitor of galectin-3 and its use for treating pulmonary fibrosis

The present invention relates to a compound of the general formula (I) for pulmonary administration. The compound of formula (I) is suitable for treating pulmonary fibrosis, such as Idiopathic pulmonary fibrosis in a mammal. Furthermore the present invention concerns a method for treatment of pulmonary fibrosis, such as Idiopathic pulmonary fibrosis in a human subject. ##STR00001##

Galactoside inhibitor of galectin-3 and its use for treating pulmonary fibrosis

The present invention relates to a compound of the general formula (I) for pulmonary administration. The compound of formula (I) is suitable for treating pulmonary fibrosis, such as Idiopathic pulmonary fibrosis in a mammal. Furthermore the present invention concerns a method for treatment of pulmonary fibrosis, such as Idiopathic pulmonary fibrosis in a human subject. ##STR00001##

REAGENT-CONTROLLED STEREOSELECTIVE GLYCOSYLATION
20170051003 · 2017-02-23 ·

Provided are methods for the efficient stereoselective formation of glycosidic bonds, without recourse to prosthetic or directing groups.

REAGENT-CONTROLLED STEREOSELECTIVE GLYCOSYLATION
20170051003 · 2017-02-23 ·

Provided are methods for the efficient stereoselective formation of glycosidic bonds, without recourse to prosthetic or directing groups.