C07D221/04

TRNA SYNTHETASE INHIBITORS
20230102879 · 2023-03-30 ·

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.

TRNA SYNTHETASE INHIBITORS
20230102879 · 2023-03-30 ·

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.

HETEROCYCLIC COMPOUND AND USE THEREOF

Provided is a heterocyclic compound that can have an antagonistic action on an NMD A receptor containing the NR2B subunit and that is expected to be useful as a prophylactic or therapeutic agent for depression, bipolar disorder, migraine, pain, peripheral symptoms of dementia and the like. A compound represented by the formula (I), wherein each symbol is as defined in the DESCRIPTION, or a salt thereof.

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COMPOUNDS FOR THE TREATMENT OF CANCER AND INFLAMMATORY DISEASE

Provided herein are compounds that inhibit the phosphorylation of MAPK and thus are useful in compositions and methods for treating cancer and inflammatory disease.

COMPOUNDS FOR THE TREATMENT OF CANCER AND INFLAMMATORY DISEASE

Provided herein are compounds that inhibit the phosphorylation of MAPK and thus are useful in compositions and methods for treating cancer and inflammatory disease.

Acyl hydrazone derivative compounds for treating disease

The present invention relates to compounds that have zinc and/or iron ionophore activity and their use in treating diseases that are modulated by reducing zinc and/or iron. In particular embodiments, the compounds are compounds of formula (I): ##STR00001##

Acyl hydrazone derivative compounds for treating disease

The present invention relates to compounds that have zinc and/or iron ionophore activity and their use in treating diseases that are modulated by reducing zinc and/or iron. In particular embodiments, the compounds are compounds of formula (I): ##STR00001##

METAL COMPLEX, AND COMPOSITION AND LIGHT EMITTING DEVICE CONTAINING THE SAME
20230070277 · 2023-03-09 ·

A metal complex which is useful for production of a light emitting device showing improved luminance is provided. A composition containing the metal complex and a light emitting device containing the metal complex are also provided. The metal complex is represented by the following formula (0). The composition contains the metal complex and at least one material selected from the group consisting of a host material, a light emitting material other than the metal complex, an antioxidant and a solvent, and a light emitting device containing the metal complex.

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SUBSTITUTED BICYCLIC AND TRICYCLIC UREAS AND AMIDES, ANALOGUES THEREOF, AND METHODS USING SAME

The present disclosure includes in one aspect substituted arylmethyl ureas, substituted heteroarylmethyl ureas, or analogues thereof, and compositions comprising the same, that can be used to treat or prevent hepatitis B virus (HBV) and/or hepatitis D virus (HDV) infections in a patient.

BETA ADRENERGIC AGONIST AND METHODS OF USING THE SAME
20220315534 · 2022-10-06 ·

The present disclosure is directed to chemical compounds and to the use of such compounds in the treatment of diseases associated with an adrenergic receptor.