The present invention provides tetrahydrocannabinol glycoside and cannabidiol glycoside prodrugs and pharmaceutical compositions comprising these compounds, and their use for the site specific delivery of tetrahydrocannabinol or cannabidiol. Also provided are processes for the preparation of purified tetrahydrocannabinol glycoside and cannabidiol glycoside prodrugs.

The present invention provides tetrahydrocannabinol glycoside and cannabidiol glycoside prodrugs and pharmaceutical compositions comprising these compounds, and their use for the site specific delivery of tetrahydrocannabinol or cannabidiol. Also provided are processes for the preparation of purified tetrahydrocannabinol glycoside and cannabidiol glycoside prodrugs.

The present invention relates to compounds which are suitable for use in electronic devices, and to electronic devices, in particular organic electroluminescent devices, comprising these compounds. The compounds have a dibenzofuran, dibenzothiophene or a fluorene group substituted in the 1-position, either directly or through a linking group, to a carbon atom of a heteroaromatic group with one or two nitrogen atoms in a bicyclic 6/6 core, or to a carbon or nitrogen atom of a heteroaromatic group with two nitrogen atoms in a bicyclic 5/6 core and is further substituted with a group selected from dibenzofuran, dibenzothiophene, fluorene or carbazole.

The present invention relates to compounds which are suitable for use in electronic devices, and to electronic devices, in particular organic electroluminescent devices, comprising these compounds. The compounds have a dibenzofuran, dibenzothiophene or a fluorene group substituted in the 1-position, either directly or through a linking group, to a carbon atom of a heteroaromatic group with one or two nitrogen atoms in a bicyclic 6/6 core, or to a carbon or nitrogen atom of a heteroaromatic group with two nitrogen atoms in a bicyclic 5/6 core and is further substituted with a group selected from dibenzofuran, dibenzothiophene, fluorene or carbazole.

A condensed cyclic compound and an organic light-emitting device including the same. The a condensed cyclic compound represented by Formula 1: ##STR00001##

A condensed cyclic compound and an organic light-emitting device including the same. The a condensed cyclic compound represented by Formula 1: ##STR00001##

The present disclosure relates to fungicidal active compounds, more specifically to pyridylphenylaminoquinolines and analogues thereof, processes and, intermediates for their preparation and use thereof as fungicidal active compound, particularly in the form of fungicide compositions. The present disclosure also relates to methods for the control of phytopathogenic fungi of plants using these compounds or compositions comprising thereof.

The present invention provides a method for obtaining a specifically-shaped crystal (specifically, spherocrystal) of a compound with good reproducibility. This method for producing a specifically-shaped crystal (specifically spherocrystal) of a compound comprises: (1) a step for preparing a supersaturated solution of a compound having a degree of supersaturation equal to or higher than a critical degree of supersaturation; and (2) a step for precipitating a specifically-shaped crystal (specifically spherocrystal) of a compound from the supersaturated solution.

The present invention aims to provide a compound that may be useful for the prophylaxis or treatment of constipation and the like. The present invention provides a compound represented by the formula (I):

##STR00001##

wherein R.sup.1 is a hydrogen atom, a halogen atom, an optionally substituted C.sub.1-6 alkyl group, or an optionally substituted C.sub.1-6 alkoxy group; and ring A is an optionally further substituted ring, or a salt thereof.

The present invention aims to provide a compound that may be useful for the prophylaxis or treatment of constipation and the like. The present invention provides a compound represented by the formula (I):

##STR00001##

wherein R.sup.1 is a hydrogen atom, a halogen atom, an optionally substituted C.sub.1-6 alkyl group, or an optionally substituted C.sub.1-6 alkoxy group; and ring A is an optionally further substituted ring, or a salt thereof.