Document |
Document Title |
JP7384903B2 |
The present invention relates to fulvestrant prodrugs of formula II and process for the preparation thereof. The present disclosure also relates to pharmaceutical composition of fulvestrant prodrugs and method of treatment using the same.
|
JP7339677B2 |
Disclosed in the present invention were a fluorosulfonyl-containing compound, an intermediate thereof, a preparation method therefor and use thereof. The fluorosulfonyl-containing compound disclosed in the present invention comprises a c...
|
JP2023036004A |
To provide a salt that can produce a resist pattern having excellent CD uniformity (CDU) and a resist composition comprising the same.The present invention provides a salt represented by formula (I), an acid generator and a resist compos...
|
JP2023022187A |
To provide compositions and methods for treating CNS disorders.Described herein are neuroactive steroids of the formula (II) in the figure or pharmaceutically acceptable salts thereof. Such compounds are supposed, in certain embodiments,...
|
JP2023503898A |
Invention Name: Prodrug of Fulvestrant The present invention relates to fulvestrant prodrugs and processes for their preparation. The present disclosure also relates to pharmaceutical compositions of fulvestrant prodrugs and methods of t...
|
JP7190966B2 |
To provide a salt, an acid generator and a resist composition that make it possible to produce a resist pattern with excellent CD uniformity.The present invention provides a salt represented by formula (I), an acid generator and a resist...
|
JP2022533069A |
Described herein are methods and compositions for the inhibition of bile salt hydrolases (BSH), as well as their use. Provided herein are metabolic disorders (eg, diabetes, obesity), gastrointestinal disorders (eg, gastrointestinal infec...
|
JP7077165B2 |
To provide a method for producing a sulfate of a hydroxy compound capable of easily producing a sulfate without using special reagents, equipment or reaction conditions and suppressing the decomposition of the hydroxy compound compared w...
|
JP2022522670A |
A method for preparing fulvestrant 3-boronic acid, which comprises converting a compound of formula (IV) to a compound of formula (III), and an intermediate useful for preparing fulvestrant 3-boronic acid by the method are described. .. ...
|
JP7021080B2 |
The present application provides a compound of formula I:or a pharmaceutically acceptable salt, solvate, or amino acid conjugate thereof, wherein R1-R10, m, n, p, and - - - are as described herein. The present invention relates generally...
|
JP6984626B2 |
A resist composition comprising a base polymer and an onium salt of N-carbonylsulfonamide having iodized benzene ring offers a high sensitivity, minimal LWR and improved CDU, independent of whether it is of positive or negative tone.
|
JP6972255B2 |
The present invention further provides method of preparing nanocrystals of a hydrophobic therapeutic agent such as fluticasone or triamcinolone, pharmaceutical compositions (e.g., topical or intranasal compositions) thereof and methods f...
|
JP2021138713A |
To provide a compound for the prevention and treatment of lipid metabolic disorders and inflammatory disorders e.g. hyperlipidemia, diabetes, fatty liver diseases and atherosclerosis.The present disclosure provides 5-cholesten,-3β, 25-d...
|
JP6893173B2 |
Described herein are neuroactive steroids of the Formula (II):or a pharmaceutically acceptable salt thereof; wherein A, R1, R2a, R2b, R3a, R3b, R4a, R4b, R5, R6and------are as defined herein. Such compounds are envisioned, in certain emb...
|
JP2021080299A |
To provide new receptor specific ligand conjugated iRNA agents and methods for their preparation that address shortcomings of in vivo delivery of oligonucleotide therapeutics.The present invention provides iRNA agents comprising at least...
|
JP2021512909A |
The present invention relates to a steroidal derivative modulator, a method for producing the same, and an application thereof. The present invention particularly relates to a compound represented by the general formula (I), a method for...
|
JP6800748B2 |
The present disclosure is in relation to the field of nanotechnology and cancer therapeutics. In particular, the present disclosure relates to platinum based compounds comprising platinum moiety, linker moiety and lipid moiety and corres...
|
JP2020180161A |
To provide 19-nor neuroactive steroids and use methods thereof.The invention is based, in part, on the desire to provide novel 19-nor (i.e., C19 desmethyl) compounds, e.g., related to progesterone, deoxycorticosterone, and their metaboli...
|
JP6752940B2 |
The present invention further provides method of preparing nanocrystals of a hydrophobic therapeutic agent such as fluticasone or triamcinolone, pharmaceutical compositions (e.g., topical or intranasal compositions) thereof and methods f...
|
JP6725501B2 |
Boron-based prodrugs of phenol- or aromatic hydroxyl group -containing therapeutic molecules ("original drugs"), uses thereof, and methods of making the same, are provided for achieving, for example, improved bioavailability, prolonged r...
|
JP2020514339A |
The present invention relates to a method for catalytic aryl transfer to translocate the scaffold of an aromatic CX bond.
|
JP6646633B2 |
New methods are provided for synthesis of photoacid generator compounds ("PAGs"), new photoacid generator compounds and photoresist compositions that comprise such PAG compounds. In a particular aspect, sulfonium-containing (S+) photoaci...
|
JP6636031B2 |
and salts thereof and compositions and uses thereof. The compounds are useful as inhibitors of LSD1. Also included are pharmaceutical compositions comprising a compound of formula I or a pharmaceutically acceptable salt thereof, and meth...
|
JP6621217B2 |
Chemical compounds and the therapeutic use thereof, in particular for improving muscular quality in mammals. More particularly, a method of improving muscular quality in sarcopenic mammals and treating and/or preventing sarcopenia using ...
|
JP2019210297A |
To provide farnesoid X receptor modulators.The present application provides a compound of a formula I in the figure or a pharmaceutically acceptable salt, solvate or amino acid conjugate thereof, as described herein. The present inventio...
|
JP2019529481A |
The crystal form of the bile acid compound and its preparation and usage are described.
|
JP6564891B2 |
The present invention further provides method of preparing nanocrystals of a hydrophobic therapeutic agent such as fluticasone or triamcinolone, pharmaceutical compositions (e.g., topical or intranasal compositions) thereof and methods f...
|
JP2019089777A |
To provide a compound for prevention and treatment of lipid metabolic disorders, inflammatory disorders, hyperlipidemia, diabetes, fatty liver diseases and atherosclerosis.The compound is 5-cholesten-3,25-diol disulfate (25HCDS) represen...
|
JP2019511486A |
The present invention relates to prodrug forms of selective progesterone receptor modulators (SPRMs) and their application in treatment. (3α, 11β, 17β) -11- [4- (methylsulfonyl) phenyl] -17- (pentafluoroethyl) estra-4,9-diene-3,17-dio...
|
JP6437636B2 |
The present invention provides amphiphilic compounds with a tetradecahydrophenanthrene skeleton of formula (I), wherein R1-R5 are as defined herein, and their enantiomers, exhibiting neuroprotective effects, for use as medicaments for tr...
|
JP2018528230A |
Dual agonists targeting both FXR and TGR5 may be useful in the treatment of various liver and metabolic disorders, as well as renal and gastrointestinal disorders. The present invention relates to methods and novel intermediates useful i...
|
JP6366696B2 |
The present invention relates to methods of treatment of inflammatory conditions using S-[4-(3-fluoro-3-methylbutyryloxy)-but-2-ynyl]6α,9α-difluo
ro-17α-(furan-2-yl)carbonyloxy-11β-hydroxy-16α-methyl-3-o
xoandrosta-1,4-diene-17β-ca...
|
JP6285419B2 |
The present invention further provides method of preparing nanocrystals of a hydrophobic therapeutic agent such as fluticasone or triamcinolone, pharmaceutical compositions (e.g., topical or intranasal compositions) thereof and methods f...
|
JP2018503667A |
The present invention is S- [4- (3-fluoro-3-methylbutyryloxy) buta-2-inyl] 6α, 9α-difluoro-, which is an anti-inflammatory compound and an anti-allergic glucocorticoid compound. Regarding the crystal morphology of 17α- (furan-2-yl) ca...
|
JP6272888B2 |
or a pharmaceutically acceptable salt or solvate thereof.
|
JP2017535570A |
The present invention relates to compounds of formula (IA) and formula (IB) for treating TGR5-mediated diseases or conditions and pharmaceutically acceptable salts thereof (in formula, R).1, R2, R3, R4, R5, R6, R7, R8, R9And m are as def...
|
JP2017160213A |
To provide compounds for the prevention and treatment of lipid metabolic disorders and inflammatory diseases, e.g., hyperlipidemia, diabetes, fatty liver diseases and atherosclerosis.The invention provides compounds being 5-cholesten-3,2...
|
JP6125610B2 |
5-cholesten-3, 25-diol, disulfate (25HCDS) has been found to be an authentic PPAR ³ agonist and LXR antagonist, and is used for the therapy of lipid disorders and inflammatory diseases, including without limitation fatty liver, inflamma...
|
JP5990557B2 |
This invention describes compounds of Structures 1, 2, and 3 and their use as allosteric modulators of the GABA receptor chloride ionophore complex to alleviate stress, anxiety, mood disorders, seizures, depression, treatment of drug and...
|
JP2016505038A |
The present invention is a novel compound and composition of 11β-hydroxysteroids, as well as pharmaceuticals for preventing or reversing mitochondrial damage in human or animal subjects, for treating or preventing diseases associated wi...
|
JP5808830B2 |
A process for preparing crystalline particles of an active principal in the presence of ultrasonic irradiation that comprises contacting a solution of a solute in a solvent in a first flowing stream with an anti-solvent in a second flowi...
|
JP2014528485A |
The 3,3-disubstituted 19-nor-steroid compounds according to formulas (I) and (III) are provided herein: R1, R2, R3, R3', R4, R6a, R6a in the formulas. , R11a and R11b are as defined herein. The compounds of the present invention are inte...
|
JP5417562B2 |
The invention provides 17-alpha-substituted-11-beta-substituted-4-aryl and 21-substituted 19-norpregnadienediones as antiprogestational agents.
|
JP5274453B2 |
A new industrial process for the synthesis of solvate-free 17α-acetoxy-11β-[4-(N,N-dimethyl-amino)-phenyl]-19-norpreg
na-4,9-diene-3,20-dione [CDB-2914] of formula (I) which is a strong antiprogestogene and antiglucocorticoid agent. Th...
|
JP5230450B2 |
The present invention is directed to novel 17-phosphorous steroid derivatives, pharmaceutical compositions containing them and their use in the treatment of disorders and conditions modulated by a progesterone or glucocorticoid receptor.
|
JP5222846B2 |
The present invention relates to compounds of formula (I): wherein R is hydrogen or alpha-hydroxy, the hydroxyl group in position 7 is in the alpha or beta position; and pharmaceutically acceptable salts, solvates or amino acid conjugate...
|
JP5199667B2 |
A compound of formula (I): or a pharmaceutically-acceptable salt thereof, may be made by a process including a triflating step by which a ketone of formula (II) is converted into a triflate of formula (III): in the presence of a base com...
|
JP5191079B2 |
There is provided a compound of Formula I wherein X is a ring system; R 1 is any one of a sulphamate group, a phosphonate group, a thiophosphonate group, a sulphonate group or a sulphonamide group; R 2 is any one of a sulphamate group, a...
|
JP5150607B2 |
According to one aspect of the invention, there is provided a compound of formula (I) and solvates thereof. There are also provided compositions containing the compound, processes for preparing it, and its use in therapy.
|
JP5133937B2 |
A process for preparing an intermediate compound of formula (II) where X is as defined in the specification, R 1 is haloalkyl, alkyl, alkenyl, cycloalkyl, carboxyalkyl, alkoxycarbonylalkyl, aryl or arylalkyl; R 2 , R 3 , R 4 and R 5 are ...
|