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JP2023552793A |
The present invention provides RXFP1 modulators for the treatment of heart failure, heart failure with preserved ejection fraction, heart failure with mildly reduced ejection fraction, heart failure with reduced ejection fraction, chroni...
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JP2023179445A |
To provide new dihydroceramide desaturase (Des) inhibitor compounds and compositions, and their application as pharmaceuticals for the treatment of disease.For example, the following compound is illustrated.SELECTED DRAWING: None
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JP2023179389A |
To provide a compound for treating and preventing diseases and conditions including heart failure, heart failure with a maintained ejection fraction, heart failure with a mildly reduced ejection fraction, heart failure with a reduced eje...
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JP2023550751A |
[summary] The present invention provides a novel compound and an organic light emitting device containing the same.
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JP2023550831A |
The present invention relates to compounds of formula I that inhibit P2X purinergic receptor 3; in particular the present invention relates to compounds that are phthalazine derivatives, processes for the preparation of such compounds, p...
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JP2023550830A |
The present invention relates to compounds of formula I that inhibit P2X purinergic receptor 3; in particular the invention relates to compounds that are (aza)quinoline 4-amine derivatives, processes for the preparation of such compounds...
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JP7389786B2 |
Provided herein are compounds, compositions, and methods useful for modulating the integrated stress response (ISR) and for treating related diseases; disorders and conditions.
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JP7387818B2 |
This disclosure relates to the field of molecules having pesticidal utility against pests in Phyla Arthropoda, Mollusca, and Nematoda, processes to produce such molecules, intermediates used in such processes, pesticidal compositions con...
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JP2023548947A |
The present invention discloses compounds and their uses as sodium channel modulators, and compounds of this type have pronounced inhibitory and blocking effects on the activity of voltage-gated sodium ion channel subtype Nav1.8 ion chan...
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JP2023547770A |
The present disclosure provides compounds, pharmaceutical compositions comprising such compounds, and methods or treatments for the treatment of inflammatory diseases and certain neurological disorders associated with inflammatory signal...
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JP7379374B2 |
The present invention provides a heterocyclic compound having an orexin type 2 receptor agonist activity.A compound represented by the formula (I):wherein each symbol is as described in the description, or a salt thereof has an orexin ty...
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JP2023547381A |
The present disclosure describes a method for preparing pyridazinone derivatives, the method comprising contacting a compound of formula (I) or a salt thereof: (I) with a compound of formula (II) or a salt thereof: (II). , a compound of ...
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JP7375019B2 |
The present invention relates to novel hydrazone derivatives in which a terminal amine group is substituted with an aryl group or a heteroaryl group, and uses thereof.
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JP7369139B2 |
The present disclosure relates to tri-substituted aryl and heteroaryl derivatives, pharmaceutical compositions containing them, and methods of using them, including methods for modulating autophagy or preventing, reversing, slowing or in...
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JP7368365B2 |
Provided are compounds of Formula (I): and pharmaceutically acceptable salts and compositions thereof, which are useful for treating a variety of conditions associated with histone acetyltransferase (HAT).
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JP2023542843A |
The present specification relates to a compound represented by Chemical Formula 1 and an organic light-emitting device containing the same.
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JP2023145722A |
To provide molecules having pesticidal utility against pests in Phyla Arthropoda, Mollusca and Nematoda, processes to produce such molecules, intermediates used in such processes, pesticidal compositions containing such molecules, and pr...
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JP7357135B2 |
Substituted pyridazinone compounds, conjugates, and pharmaceutical compositions for use in the treatment of neuromuscular diseases, such as Duchenne Muscular Dystrophy (DMD), are disclosed herein. The disclosed compounds are useful, amon...
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JP2023542231A |
The present invention relates to novel compounds for use as inhibitors of NLRP3 inflammasome production, such compounds being as defined by compounds of formula (I), with the integer R1,R2and R3is defined herein and the compounds may be ...
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JP7352565B2 |
The present disclosure relates to chemical compounds that modulate pantothenate kinase (PanK) activity for the treatment of metabolic disorders (such as diabetes mellitus type II), neurologic disorders (such as pantothenate kinase-associ...
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JP2023134482A |
To provide methods and reagents useful for analyzing interfaces between target proteins.The present disclosure provides methods and reagents useful for analyzing protein-protein interfaces, such as interfaces between a presenter protein ...
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JP2023539526A |
Disclosed herein are compounds represented by formula (I), pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof. The compounds are useful as agonists of stimulator of interferon genes (STING), eg, in methods...
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JP2023539451A |
The invention inter alia provides a process for producing compounds of formula (I), wherein the substituents are as defined in claim 1. The invention further provides intermediate compounds used in the process and methods of producing th...
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JP2023538304A |
This disclosure generally describes small molecule modulators of the NLR family pyrin domain containing 3 (NLRP3) or pharmaceutically acceptable salts, isotopically enriched analogs, stereoisomers, mixtures of stereoisomers or prodrugs t...
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JP2023538022A |
The present invention relates inter alia to compounds of formula (I) wherein the substituents are as defined in claim 1. The invention further provides intermediate compounds utilized in said process and methods for producing said interm...
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JP7337790B2 |
Provided herein are compounds, compositions, and methods useful for modulating the integrated stress response (ISR) and for treating related diseases; disorders and conditions.
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JP7335241B2 |
Provided herein are compounds, compositions, and methods useful for modulating the integrated stress response (ISR) and for treating related diseases; disorders and conditions.
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JP7331067B2 |
A new crystalline form of 5-amino-2,3-dihydro-1,4-phthalazinedione (luminol) is provided. Advantageous uses for this crystalline form as a detecting agent or as an agent for forensic purposes are disclosed, as well a pharmaceutical compo...
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JP2023535957A |
Disclosed are compounds of Formula 1, stereoisomers, N-oxides, and salts thereof, [Chemical 1] where G is CONR5R.6or [Chemical 2] is selected from R.1~R18, Rfand G are as defined in this disclosure. Also disclosed is a composition contai...
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JP2023116627A |
To provide compounds, pharmaceutical compositions and methods of use that are useful for inhibiting the maturation of cytokines of the IL-1 family by inhibiting inflammasomes, and useful in treatment of disorders in which inflammasome ac...
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JP2023533496A |
[Chemical 1] P2X4 antagonists for the treatment of dry eye syndrome, more particularly for use in the treatment or prevention of dry eye syndrome, particularly dry eye, ocular neuropathic pain, ocular trauma and post-operative eye pain, ...
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JP2023533388A |
Disclosed herein are for the treatment of cancers such as glioblastoma, gastric cancer, colorectal cancer, pancreatic ductal adenocarcinoma (PDAC), and malignant pleural mesothelioma (MPM) Synthesis and use of covalent inhibitors that ar...
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JP2023532298A |
The present disclosure generally provides small molecule modulators of NLR family pyrin domain-containing 3 (NLRP3) or pharmaceutically acceptable salts, isotopically enriched analogs, stereoisomers, mixtures of stereoisomers or prodrugs...
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JP7313492B2 |
Disclosed in the present invention are a compound as represented by formula (I), and an isomer or pharmaceutically acceptable salt thereof, and disclosed is an application thereof in preparing drugs for treating DNA-PK inhibitor-related ...
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JP2023531283A |
Substituted N-phenylacetamide compounds of general formula (I), processes for preparing said compounds, intermediate compounds useful in preparing said compounds, pharmaceutical compositions and combinations comprising said compounds, an...
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JP2023100613A |
To provide a compound library having structural diversity, and a method of producing the same and a screening method.A library includes a compound of 1×102-1×108. The compound includes a structure of (first CB)-(first L)-(second CB), i...
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JP2023530761A |
The present invention provides 1,4-disubstituted pyridazine compounds such as 5-(1H-pyrazol-4-yl)-2-(6-((2,2,6,6-tetramethylpiperidin-4-yl
) New processes, new process steps, and new intermediates useful for the preparation of oxy)pyrida...
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JP2023530708A |
The compounds provided herein function as thyroid mimetic agents and have utility for treating diseases such as neurodegenerative disorders and fibrotic diseases. Pharmaceutical compositions containing such compounds are also provided, a...
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JP2023530343A |
The present invention relates to carbonohydrazonoyl dicyanide compounds containing at least two aryl or heteroaryl linked via a novel linker and uses thereof.
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JP2023530231A |
Provided herein are compounds of Formula (I''), Formula (I'), Formula (I), Formula (II'), and Formula (II), and pharmaceutically acceptable salts, solvates, hydrates, polymorphs, co-crystals, tautomers, stereoisomers, isotopically labele...
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JP2023530314A |
The present invention relates to novel oxopyridazinyl-phenyl-carbonohydrazonoyl dicyanide compounds and uses thereof.
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JP2023529475A |
The present disclosure provides formula (I): [Chemical 1] (In the formula, A1, A2, m, R3, R4, R5, L, R6, T, ring Y, p, R7, and Q have the meanings defined herein), compositions comprising such compounds, processes and intermediates for t...
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JP2023529294A |
The present invention relates to azabicyclic (thio)amide compounds and their use for controlling phytopathogenic microorganisms such as phytopathogenic fungi. It also relates to processes and intermediates for preparing these compounds.
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JP2023529022A |
This application relates to the use of phthalazinediones in the prevention or treatment of coronavirus infections. Pharmaceutical compositions, combinations and advantageous formulation techniques are disclosed.
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JP7301758B2 |
Fused bicyclic compounds are inhibitors of GPR91. The compounds, their stereoisomers, tautomers, prodrugs, polymorphs, solvates, pharmaceutically acceptable salts, and pharmaceutical compositions containing them are useful in the treatme...
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JP7301861B2 |
The present invention relates to polycyclic compounds of formula (I) and pharmaceutically acceptable salts thereof, wherein R1 to R4, R7 to R10, Y and A are as defined herein. The invention also relates to pharmaceutical compositions com...
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JP2023527498A |
Provided herein are compounds useful for inhibiting signaling and activators of transcription 5a and 5b (STAT5), and pharmaceutical compositions comprising the compounds. Additionally, the compounds and compositions are useful for treati...
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JP2023527379A |
Provided are compounds of formula (I): (I), and pharmaceutically acceptable salts and compositions thereof, that are useful for the treatment of various conditions associated with TREX1.
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JP2023527010A |
The present invention relates to novel compounds for use as inhibitors of NLRP3 inflammasome production, such compounds as defined by the compounds of formula (I) [Chemical 1] and the integer R1, R2and R3is defined herein and the compoun...
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JP2023526247A |
Disclosed herein are substituted pyridazinone compounds, conjugates, and pharmaceutical compositions for use in treating neuromuscular diseases such as Duchenne muscular dystrophy (DMD). The disclosed compounds are useful, inter alia, fo...
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