C07C215/42

Adamantylmethylamine derivative and use thereof as pharmaceutical

The present invention provides a pharmaceutical composition for treating or preventing a cognitive disease or disorder, comprising a compound represented by Formula (I), an enantiomer thereof a diastereomer thereof, or a pharmaceutically acceptable salt thereof.

SUBSTITUTED BICYCLIC COMPOUNDS

Disclosed are compounds of Formulas (I), (II), (III), (IV), and (V):

##STR00001##

and/or a salt thereof, wherein R.sub.1 is —OH or —OP(O)(OH).sub.2, and X.sub.1, X.sub.2, X.sub.3, R.sub.2, R.sub.2a, R.sub.a, R.sub.b, and R.sub.c are defined herein. Also disclosed are methods of using such compounds as selective agonists for G protein-coupled receptor S1P.sub.1, and pharmaceutical compositions comprising such compounds. These compounds are useful in treating, preventing, or slowing the progression of diseases or disorders in a variety of therapeutic areas, such as autoimmune diseases and vascular disease.

SUBSTITUTED BICYCLIC COMPOUNDS

Disclosed are compounds of Formulas (I), (II), (III), (IV), and (V):

##STR00001##

and/or a salt thereof, wherein R.sub.1 is —OH or —OP(O)(OH).sub.2, and X.sub.1, X.sub.2, X.sub.3, R.sub.2, R.sub.2a, R.sub.a, R.sub.b, and R.sub.c are defined herein. Also disclosed are methods of using such compounds as selective agonists for G protein-coupled receptor S1P.sub.1, and pharmaceutical compositions comprising such compounds. These compounds are useful in treating, preventing, or slowing the progression of diseases or disorders in a variety of therapeutic areas, such as autoimmune diseases and vascular disease.

Fluorophenyl beta-hydroxyethylamines and their use in the treatment of hyperglycaemia
11648216 · 2023-05-16 · ·

There is herein provided a compound of formula (I). ##STR00001##

Fluorophenyl beta-hydroxyethylamines and their use in the treatment of hyperglycaemia
11648216 · 2023-05-16 · ·

There is herein provided a compound of formula (I). ##STR00001##

TRNA synthetase inhibitors

Disclosed herein are secondary amine compounds that inhibit tRNA synthetase. The compounds of the invention are useful in inhibiting tRNA synthetase in Gram-negative bacteria and are useful in killing Gram-negative bacteria. The secondary amine compounds of the invention are also useful in the treatment of tuberculosis.

Compounds Which Have a Protective Activity with Respect to the Action of Toxins and of Viruses with an Intracellular Mode of Action

The subject matter of the present invention is novel families of compounds which are aromatic amine, imine, aminoadamantane and benzodiazepine derivatives, medicaments comprising same and the use thereof as inhibitors of the toxic effects of toxins with intracellular activity, such as, for example, ricin, and of viruses that use the internalization pathway for infecting cells.

Acid gas absorbent, acid gas removal device, and acid gas removal method

An acid gas absorbent includes at least one kind of secondary amine compound represented by formula (1): ##STR00001##
where R.sup.1 is a cyclopentyl group or a cyclohexyl group which may be substituted by a substituted or non-substituted alkyl group having 1 to 3 carbon atoms, R.sup.2 and R.sup.3 each indicate an alkylene group having 2 to 4 carbon atoms, and R.sup.2 and R.sup.3 may each be the same or different, and be a straight chain or have a side chain.

Process for producing substituted amino alcohols

A process for producing a compound of the formula (I) ##STR00001##
involves at least reacting a compound of the formula (II) ##STR00002##
with hydrogen and water in the presence of at least one homogeneous transition metal catalyst TMC 1.

Process for producing substituted amino alcohols

A process for producing a compound of the formula (I) ##STR00001##
involves at least reacting a compound of the formula (II) ##STR00002##
with hydrogen and water in the presence of at least one homogeneous transition metal catalyst TMC 1.