[go: up one dir, main page]

MA39034B1 - Composés de quinoline sélectivement substitués - Google Patents

Composés de quinoline sélectivement substitués

Info

Publication number
MA39034B1
MA39034B1 MA39034A MA39034A MA39034B1 MA 39034 B1 MA39034 B1 MA 39034B1 MA 39034 A MA39034 A MA 39034A MA 39034 A MA39034 A MA 39034A MA 39034 B1 MA39034 B1 MA 39034B1
Authority
MA
Morocco
Prior art keywords
selectively substituted
substituted quinoline
quinoline compounds
compounds
toll
Prior art date
Application number
MA39034A
Other languages
English (en)
Other versions
MA39034A1 (fr
Inventor
Eric Carlson
Hans Hansen
Matthew Mackey
Shawn Schiller
Chikako Ogawa
Heather Davis
Atsushi Endo
Lynn Hawkins
Sally Ishizaka
Original Assignee
Eisai R&D Man Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Eisai R&D Man Co Ltd filed Critical Eisai R&D Man Co Ltd
Publication of MA39034A1 publication Critical patent/MA39034A1/fr
Publication of MA39034B1 publication Critical patent/MA39034B1/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/04Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/472Non-condensed isoquinolines, e.g. papaverine
    • A61K31/4725Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/553Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one oxygen as ring hetero atoms, e.g. loxapine, staurosporine
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D215/48Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/10Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D451/00Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
    • C07D451/02Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
    • C07D451/04Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof with hetero atoms directly attached in position 3 of the 8-azabicyclo [3.2.1] octane or in position 7 of the 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring system
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/10Spiro-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/10Spiro-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D493/00Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
    • C07D493/02Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
    • C07D493/10Spiro-condensed systems
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6897Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids involving reporter genes operably linked to promoters
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/5005Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells
    • G01N33/5008Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics
    • G01N33/502Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics for testing non-proliferative effects
    • G01N33/5023Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics for testing non-proliferative effects on expression patterns
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/5005Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells
    • G01N33/5008Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics
    • G01N33/5044Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics involving specific cell types
    • G01N33/5047Cells of the immune system
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/07Optical isomers

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Immunology (AREA)
  • General Health & Medical Sciences (AREA)
  • Biomedical Technology (AREA)
  • Medicinal Chemistry (AREA)
  • Molecular Biology (AREA)
  • Hematology (AREA)
  • Urology & Nephrology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • Analytical Chemistry (AREA)
  • Cell Biology (AREA)
  • Biochemistry (AREA)
  • Microbiology (AREA)
  • Biotechnology (AREA)
  • Physics & Mathematics (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Food Science & Technology (AREA)
  • General Physics & Mathematics (AREA)
  • Toxicology (AREA)
  • Genetics & Genomics (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Pathology (AREA)
  • Biophysics (AREA)
  • General Engineering & Computer Science (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Quinoline Compounds (AREA)

Abstract

La présente invention concerne, selon divers modes de réalisation, des composés de quinoline sélectivement substitués qui agissent en tant qu'antagonistes ou inhibiteurs des récepteurs 7 et/ou 8 de type toll, et leur utilisation dans des compositions pharmaceutiques se révélant efficaces en vue du traitement du lupus érythémateux disséminé et de la néphropathie lupique.
MA39034A 2013-10-14 2014-10-14 Composés de quinoline sélectivement substitués MA39034B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201361890718P 2013-10-14 2013-10-14
PCT/US2014/060418 WO2015057659A1 (fr) 2013-10-14 2014-10-14 Composés de quinoline sélectivement substitués

Publications (2)

Publication Number Publication Date
MA39034A1 MA39034A1 (fr) 2018-01-31
MA39034B1 true MA39034B1 (fr) 2018-09-28

Family

ID=51842881

Family Applications (1)

Application Number Title Priority Date Filing Date
MA39034A MA39034B1 (fr) 2013-10-14 2014-10-14 Composés de quinoline sélectivement substitués

Country Status (35)

Country Link
US (5) US9428495B2 (fr)
EP (3) EP3626717A1 (fr)
JP (3) JP6223563B2 (fr)
KR (2) KR102103256B1 (fr)
CN (2) CN106414432B (fr)
AR (1) AR098014A1 (fr)
AU (2) AU2014334554B2 (fr)
BR (1) BR112016008359B1 (fr)
CA (1) CA2927510C (fr)
CL (1) CL2016000662A1 (fr)
CY (1) CY1122776T1 (fr)
DK (1) DK3057964T3 (fr)
ES (1) ES2773303T3 (fr)
HR (1) HRP20200147T1 (fr)
HU (1) HUE048706T2 (fr)
IL (2) IL245131B (fr)
JO (1) JO3554B1 (fr)
LT (1) LT3057964T (fr)
MA (1) MA39034B1 (fr)
MD (1) MD4635C1 (fr)
MX (2) MX364657B (fr)
MY (1) MY192489A (fr)
PE (1) PE20160608A1 (fr)
PH (1) PH12016500642A1 (fr)
PL (1) PL3057964T3 (fr)
PT (1) PT3057964T (fr)
RS (1) RS59911B1 (fr)
RU (1) RU2679622C2 (fr)
SG (3) SG11201602818TA (fr)
SI (1) SI3057964T1 (fr)
SM (1) SMT202000076T1 (fr)
TW (2) TWI702218B (fr)
UA (1) UA120039C2 (fr)
WO (1) WO2015057659A1 (fr)
ZA (4) ZA201601882B (fr)

Families Citing this family (90)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9139568B2 (en) * 2011-12-22 2015-09-22 Merck Patent Gmbh Heterocyclic carboxamides as modulators of kinase activity
EP3626717A1 (fr) 2013-10-14 2020-03-25 Eisai R&D Management Co., Ltd. Composés de quinoline sélectivement substitués
KR102365952B1 (ko) 2013-10-14 2022-02-22 에자이 알앤드디 매니지먼트 가부시키가이샤 선택적으로 치환된 퀴놀린 화합물
SI3889145T1 (sl) 2015-12-17 2024-05-31 Merck Patent Gmbh 8-ciano-5-piperidino-kinolini kot antagonisti tlr7/8 in njihove uporabe za zdravljenje imunskih motenj
US10071079B2 (en) 2016-06-29 2018-09-11 Bristol-Myers Squibb Company [1,2,4]triazolo[1,5-a]pyridinyl substituted indole compounds
EA038972B1 (ru) 2016-07-30 2021-11-16 Бристол-Маерс Сквибб Компани Диметоксифенилзамещенные соединения индола в качестве ингибиторов tlr7, tlr8 или tlr9
SG11201900947RA (en) * 2016-08-08 2019-02-27 Merck Patent Gmbh Tlr7/8 antagonists and uses thereof
MA46188A (fr) 2016-09-09 2019-07-17 Bristol Myers Squibb Co Composés indole substitués par pyridyle
DK3510033T3 (da) * 2016-09-09 2022-02-28 Novartis Ag Forbindelser og sammensætninger som inhibitorer af endosomale toll-lignende receptorer
US10662416B2 (en) 2016-10-14 2020-05-26 Precision Biosciences, Inc. Engineered meganucleases specific for recognition sequences in the hepatitis B virus genome
EP4248968A3 (fr) 2017-07-18 2023-12-06 Merck Patent GmbH Antagonistes de tlr7/8 et leurs utilisations
ES2921020T3 (es) 2017-08-04 2022-08-16 Bristol Myers Squibb Co Compuestos de indol sustituidos con [1,2,4]triazolo[4,3-a]piridinilo
ES2909401T3 (es) 2017-08-04 2022-05-06 Bristol Myers Squibb Co Compuestos de indol sustituidos útiles como inhibidores de TLR7/8/9
US11466010B2 (en) 2017-10-30 2022-10-11 The Regents Of The University Of Colorado, A Body Corporate Toll-like receptor 8 (TLR8) specific antagonists and methods of making and uses thereof
US20210253593A1 (en) 2017-11-14 2021-08-19 Bristol-Myers Squibb Company Substituted indole compounds
MX2020006093A (es) 2017-12-15 2020-08-24 Bristol Myers Squibb Co Compuestos de indol eter sustituidos.
PE20210129A1 (es) 2017-12-18 2021-01-19 Bristol Myers Squibb Co Compuestos de 4-azaindol
ES2922174T3 (es) 2017-12-19 2022-09-09 Bristol Myers Squibb Co Compuestos de indol sustituidos con amida útiles como inhibidores de TLR
BR112020011788A2 (pt) 2017-12-19 2020-11-24 Bristol-Myers Squibb Company compostos 6-azaindóis
WO2019125849A1 (fr) * 2017-12-19 2019-06-27 Merck Patent Gmbh Antagonistes de tlr7/8 et leurs utilisations
CN111491930B (zh) 2017-12-19 2023-09-26 百时美施贵宝公司 可用作tlr抑制剂的经取代的吲哚化合物
KR102714788B1 (ko) 2017-12-20 2024-10-08 브리스톨-마이어스 스큅 컴퍼니 Tlr 억제제로서 유용한 아미노 인돌 화합물
US11299501B2 (en) 2017-12-20 2022-04-12 Bristol-Myers Squibb Company Diazaindole compounds
JP7291707B2 (ja) 2017-12-20 2023-06-15 ブリストル-マイヤーズ スクイブ カンパニー アリールおよびヘテロアリール置換されたインドール化合物
CN111566120B (zh) 2017-12-20 2023-09-29 捷克共和国有机化学与生物化学研究所 活化sting转接蛋白的具有膦酸酯键的3’3’环状二核苷酸
US11203610B2 (en) 2017-12-20 2021-12-21 Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. 2′3′ cyclic dinucleotides with phosphonate bond activating the sting adaptor protein
CN108101860B (zh) * 2018-02-08 2021-11-23 苏州敬业医药化工有限公司 顺式-2,6-二甲基吗啉的制备方法
EP3752505B1 (fr) 2018-02-12 2023-01-11 F. Hoffmann-La Roche AG Nouveaux composés et dérivés de sulfone pour le traitement et la prophylaxie d'une infection virale
US10836769B2 (en) 2018-02-26 2020-11-17 Gilead Sciences, Inc. Substituted pyrrolizine compounds and uses thereof
WO2019183145A1 (fr) 2018-03-20 2019-09-26 Plexxikon Inc. Composés et procédés de modulation d'ido et de tdo, et indications pour ceux-ci
US10870691B2 (en) 2018-04-05 2020-12-22 Gilead Sciences, Inc. Antibodies and fragments thereof that bind hepatitis B virus protein X
TWI818007B (zh) 2018-04-06 2023-10-11 捷克科學院有機化學與生物化學研究所 2'3'-環二核苷酸
TWI833744B (zh) 2018-04-06 2024-03-01 捷克科學院有機化學與生物化學研究所 3'3'-環二核苷酸
TW202005654A (zh) 2018-04-06 2020-02-01 捷克科學院有機化學與生物化學研究所 2,2,─環二核苷酸
TW201945388A (zh) 2018-04-12 2019-12-01 美商精密生物科學公司 對b型肝炎病毒基因體中之識別序列具有特異性之最佳化之經工程化巨核酸酶
WO2019211799A1 (fr) 2018-05-03 2019-11-07 Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. Analogue de dinucléotide 2'3'-cyclique comprenant un nucléotide modifié par cyclopentanyle
JP7374130B2 (ja) * 2018-06-05 2023-11-06 エフ. ホフマン-ラ ロシュ アーゲー 自己免疫疾患治療用の新規なテトラヒドロ-1H-ピラジノ[2,1-a]イソインドリルキノリン化合物
EP3805203A4 (fr) * 2018-06-07 2022-02-23 Daiichi Sankyo Company, Limited Dérivé d'azétidine, et promédicament de celui-ci
CN112313228A (zh) 2018-06-12 2021-02-02 豪夫迈·罗氏有限公司 用于治疗自身免疫性疾病的新型杂芳基杂环基化合物
WO2019238629A1 (fr) 2018-06-13 2019-12-19 F. Hoffmann-La Roche Ag Composés pyridinyles hétérocyclyles pour le traitement d'une maladie auto-immune
CA3103987C (fr) * 2018-07-06 2023-08-01 Gilead Sciences, Inc. Composes heterocycliques therapeutiques
CN112584903B (zh) 2018-07-23 2025-12-23 豪夫迈·罗氏有限公司 用于自身免疫性疾病治疗的哌嗪化合物
WO2020028097A1 (fr) 2018-08-01 2020-02-06 Gilead Sciences, Inc. Formes solides d'acide (r)-11-(méthoxyméthyl)-12-(3-méthoxypropoxy)-3,3-diméthyl-8-0 x0-2,3,8,13b-tétrahydro-1h-pyrido[2,1-a] pyrrolo[1,2-c]phtalazine-7-carboxylique
CN112638908A (zh) * 2018-09-04 2021-04-09 豪夫迈·罗氏有限公司 用于治疗自身免疫性疾病的苯并噻唑类化合物
WO2020048596A1 (fr) 2018-09-06 2020-03-12 F. Hoffmann-La Roche Ag Nouveaux composés de pyrazolopyridine pour le traitement d'une maladie auto-immune
EP3847170B1 (fr) * 2018-09-06 2022-06-22 F. Hoffmann-La Roche AG Nouveaux composés amidine cyclique pour le traitement d'une maladie auto-immune
WO2020048605A1 (fr) * 2018-09-07 2020-03-12 F. Hoffmann-La Roche Ag Nouveaux composés de pyrrolidine amine pour le traitement d'une maladie auto-immune
US20220112187A1 (en) * 2018-09-11 2022-04-14 Hoffmann-La Roche Inc. Pyrazolopyridine amine compounds for the treatment of autoimmune disease
EP3623369B1 (fr) 2018-09-12 2023-10-25 F. Hoffmann-La Roche AG Nouveaux composés de morpholinyle amine pour le traitement des maladies auto-immunes
WO2020064792A1 (fr) 2018-09-27 2020-04-02 F. Hoffmann-La Roche Ag Composés hétérocyclyles pour le traitement d'une maladie auto-immune
EP3870589B1 (fr) 2018-10-24 2023-09-06 Bristol-Myers Squibb Company Composés dimères d'indole substitués
KR102839382B1 (ko) 2018-10-24 2025-07-25 브리스톨-마이어스 스큅 컴퍼니 치환된 인돌 및 인다졸 화합물
KR102658602B1 (ko) 2018-10-31 2024-04-19 길리애드 사이언시즈, 인코포레이티드 Hpk1 억제 활성을 갖는 치환된 6-아자벤즈이미다졸 화합물
EP4371987B9 (fr) 2018-10-31 2025-11-26 Gilead Sciences, Inc. Composés de 6-azabenzimidazole substitués utilisés en tant qu'inhibiteurs de hpk1
JP2022506790A (ja) * 2018-11-09 2022-01-17 エフ.ホフマン-ラ ロシュ アーゲー 全身性エリテマトーデスを処置するためのTLR7~9アンタゴニストとしての、5-[6-[[3-(4,5,6,7-テトラヒドロピラゾロ[4,3-c]ピリジン-1-イル)アゼチジン-1-イル]メチル]モルホリン-4-イル]キノリン-8-カルボニトリル誘導体及び類似化合物
US11807622B2 (en) 2019-01-30 2023-11-07 Insilico Medicine Ip Limited TLR 9 inhibitors
EP3935065A1 (fr) 2019-03-07 2022-01-12 Institute of Organic Chemistry and Biochemistry ASCR, V.V.I. Analogue du dinucléotide 3'3'-cyclique comprenant un nucléotide modifié par cyclopentanyle utilisé en tant que modulateur de sting
US20220143061A1 (en) 2019-03-07 2022-05-12 Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. 3'3'-cyclic dinucleotides and prodrugs thereof
CN113543851B (zh) 2019-03-07 2025-03-18 捷克共和国有机化学与生物化学研究所 2’3’-环二核苷酸及其前药
TWI751517B (zh) 2019-04-17 2022-01-01 美商基利科學股份有限公司 類鐸受體調節劑之固體形式
TW202210480A (zh) 2019-04-17 2022-03-16 美商基利科學股份有限公司 類鐸受體調節劑之固體形式
EP3965888B1 (fr) 2019-05-09 2024-08-21 Bristol-Myers Squibb Company Composés de benzimidazolone substitués
WO2020237025A1 (fr) 2019-05-23 2020-11-26 Gilead Sciences, Inc. Exo-méthylène-oxindoles substitués qui sont des inhibiteurs de hpk1/map4k1
EP4017476A1 (fr) 2019-08-19 2022-06-29 Gilead Sciences, Inc. Formulations pharmaceutiques de ténofovir alafénamide
JP2022546863A (ja) 2019-09-10 2022-11-09 エフ.ホフマン-ラ ロシュ アーゲー 自己免疫疾患の処置のための新規キノリン化合物
EP3795570B1 (fr) * 2019-09-23 2022-02-23 Accutar Biotechnology Inc. Dérivés substitués de quinoline-8-carbonitrile ayant une activité de dégradation de récepteur d'androgène et leurs utilisations
CA3149557A1 (fr) 2019-09-30 2021-04-08 Scott J. Balsitis Vaccins contre le virus de l'hepatite b et methodes de traitement du vhb
WO2021067326A1 (fr) 2019-10-01 2021-04-08 Bristol-Myers Squibb Company Composés hétéroaryle bicycliques substitués
ES2965164T3 (es) 2019-10-04 2024-04-11 Bristol Myers Squibb Co Compuestos de carbazol sustituidos
EP4051387B1 (fr) 2019-10-31 2025-02-19 F. Hoffmann-La Roche AG Composés d'hydropyrazino[1,2-d][1,4]diazépine pour le traitement d'une maladie auto-immune
US12486273B2 (en) 2019-11-19 2025-12-02 Hoffmann-La Roche Inc. Hydro-1H-pyrrolo[1,2-a]pyrazine compounds for the treatment of autoimmune disease
WO2021099285A1 (fr) * 2019-11-19 2021-05-27 F. Hoffmann-La Roche Ag Composés triazatricycliques pour le traitement d'une maladie auto-immune
EP4061821B1 (fr) 2019-11-20 2025-08-06 F. Hoffmann-La Roche AG Composés de spiro(isobenzofurane azétidine) pour le traitement d'une maladie auto-immune
CN114761406B (zh) * 2019-12-03 2024-04-19 豪夫迈·罗氏有限公司 用于治疗自身免疫性疾病的氢吡啶并[1,2-a]吡嗪化合物
WO2021113765A1 (fr) 2019-12-06 2021-06-10 Precision Biosciences, Inc. Méganucléases modifiées optimisées ayant une spécificité pour une séquence de reconnaissance dans un génome du virus de l'hépatite b
JPWO2021112251A1 (fr) * 2019-12-06 2021-06-10
AR121620A1 (es) 2020-03-20 2022-06-22 Gilead Sciences Inc Profármacos de nucleósidos 4’-c-sustituidos-2-halo-2’-deoxiadenosina y métodos de preparación y uso de los mismos
JP2024502083A (ja) * 2020-12-31 2024-01-17 清華大学 ピリジン-2-アミン誘導体、その医薬組成物、及び使用
US11661431B2 (en) 2021-04-16 2023-05-30 Gilead Sciences, Inc. Thienopyrrole compounds
JP2024518558A (ja) 2021-05-13 2024-05-01 ギリアード サイエンシーズ, インコーポレイテッド TLR8調節化合物と抗HBV siRNA治療薬との組合せ
AU2022289728A1 (en) * 2021-06-11 2023-11-16 Neuronascent, Inc. Methods and compositions for lipid formulation of lipophilic small molecule therapies of the heterocyclic type
WO2022271659A1 (fr) 2021-06-23 2022-12-29 Gilead Sciences, Inc. Composés modulant les diacylglycérol kinases
EP4359413A1 (fr) 2021-06-23 2024-05-01 Gilead Sciences, Inc. Composés de modulation de la diacylglycérol kinase
US11932634B2 (en) 2021-06-23 2024-03-19 Gilead Sciences, Inc. Diacylglycerol kinase modulating compounds
US11976072B2 (en) 2021-06-23 2024-05-07 Gilead Sciences, Inc. Diacylglycerol kinase modulating compounds
TWI849499B (zh) 2021-09-10 2024-07-21 美商基利科學股份有限公司 噻吩并吡咯化合物
WO2025240242A1 (fr) 2024-05-13 2025-11-20 Gilead Sciences, Inc. Polythérapies avec ribavirine
US20250345390A1 (en) 2024-05-13 2025-11-13 Gilead Sciences, Inc. Combination therapies
US20250345389A1 (en) 2024-05-13 2025-11-13 Gilead Sciences, Inc. Combination therapies
WO2025240246A1 (fr) 2024-05-13 2025-11-20 Gilead Sciences, Inc. Polythérapies avec de la ribavirine

Family Cites Families (168)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NO156828C (no) 1980-11-10 1987-12-02 Otsuka Pharma Co Ltd Analogifremgangsm te for fremstilling av antibakterielt virksomme benzoheterocykliske forbindelser.
IL62783A (en) 1981-05-04 1987-01-30 Usv Pharma Corp Antihypertensive 1,4-thiazine,1,4-thiazepine and 1,4-thiazocine compounds,method for the preparation thereof and pharmaceutical compositions containing the same
JPS5890511A (ja) 1981-11-25 1983-05-30 Otsuka Pharmaceut Co Ltd 抗菌剤
US5358949A (en) 1986-03-05 1994-10-25 Otsuka Pharmaceutical Co., Ltd. Carbostyril derivatives and salts thereof and anti-arrhythmic agents containing the carbostyril derivatives
JPS6354363A (ja) 1986-08-26 1988-03-08 Ss Pharmaceut Co Ltd キノリン誘導体
AU639529B2 (en) 1987-03-04 1993-07-29 Higuchi, Yoshinari Carbostyril derivatives and salts thereof and anti-arrhythmic agents containing the carbostyril derivatives
US4933447A (en) 1987-09-24 1990-06-12 Ss Pharmaceutical Co., Ltd. Quinoline derivatives
JPH08295690A (ja) 1995-04-26 1996-11-12 Tokuyama Corp クロメン化合物
JP2000510865A (ja) * 1996-05-20 2000-08-22 ダーウィン・ディスカバリー・リミテッド Tnfとpde―ivのインヒビターとしてのキノリンカルボキサミド
AU4471497A (en) 1996-10-11 1998-05-11 Kowa Co. Ltd. Novel diamide compounds and drugs containing the same
DE19643048A1 (de) 1996-10-18 1998-04-23 Daimler Benz Ag Verbindungen und deren Verwendung sowie Verfahren zur Herstellung von flüssigkristallinen Polymeren daraus
GB9712761D0 (en) 1997-06-17 1997-08-20 Chiroscience Ltd Quinolines and their therapeutic use
US6933272B1 (en) 1998-09-22 2005-08-23 Erik Helmerhorst Use of non-peptidyl compounds for the treatment of insulin related ailments
CN1331862C (zh) 1999-04-28 2007-08-15 萨诺费-阿文蒂斯德国有限公司 作为ppar受体配体的二芳基酸衍生物
CZ20013834A3 (cs) 1999-04-28 2002-04-17 Aventis Pharma Deutschland Gmbh Deriváty kyselin se třemi arylovými zbytky jako ligandy receptorů PPAR a farmaceutické prostředky, které je obsahují
DE19936437A1 (de) 1999-08-03 2001-02-08 Aventis Cropscience Gmbh Kombinationen aus Herbiziden und Safenern
US6710205B2 (en) 2000-02-22 2004-03-23 Ono Pharmaceutical Co., Ltd. Benzoic acid derivatives, processes for producing the same and drugs containing the same as the active ingredient
IL151552A0 (en) 2000-03-17 2003-04-10 Bristol Myers Squibb Pharma Co Cyclic beta-amino acid derivatives as inhibitors of matrix metalloproteases and tnf-alpha
DE60102137T2 (de) 2000-03-17 2004-10-21 Bristol Myers Squibb Pharma Co Beta-aminsäure-derivate zur verwendung als matrix-metalloproteasen- und tna-alpha-inhibitoren
WO2002018335A1 (fr) 2000-08-28 2002-03-07 Yamanouchi Pharmaceutical Co., Ltd. Derives d'amine cyclique
US20030028018A1 (en) 2000-09-11 2003-02-06 Chiron Coporation Quinolinone derivatives
AP1666A (en) 2000-09-11 2006-09-29 Chiron Corp Quinolinone derivatives as tyrosine kinase inhibitors.
EP1217000A1 (fr) 2000-12-23 2002-06-26 Aventis Pharma Deutschland GmbH Inhibiteurs du factor Xa et factor VIIa
US20040116450A1 (en) 2001-03-19 2004-06-17 Tatsuya Oyama Antipruritics
US20030055263A1 (en) 2001-07-11 2003-03-20 Boehringer Ingelheim Pharma Kg Carboxylic acid derivatives, medicaments comprising these compounds, their use and processes for their production
KR20100107509A (ko) 2001-09-14 2010-10-05 9222-9129 퀘벡 인코포레이티드 히스톤 데아세틸라아제의 억제제
US7868204B2 (en) 2001-09-14 2011-01-11 Methylgene Inc. Inhibitors of histone deacetylase
US6897220B2 (en) 2001-09-14 2005-05-24 Methylgene, Inc. Inhibitors of histone deacetylase
DE10222166A1 (de) 2002-05-20 2003-12-11 Fraunhofer Ges Forschung Chirale Verbindungen und deren Verwendung
DE10229070A1 (de) 2002-06-28 2004-01-15 Merck Patent Gmbh Phenylderivate 5
DE60322920D1 (de) 2002-08-13 2008-09-25 Shionogi & Co Heterocyclische verbindungen mit hiv-integrase-hemmender wirkung
US7825132B2 (en) 2002-08-23 2010-11-02 Novartis Vaccines And Diagnostics, Inc. Inhibition of FGFR3 and treatment of multiple myeloma
US20050256157A1 (en) 2002-08-23 2005-11-17 Chiron Corporation Combination therapy with CHK1 inhibitors
CA2496164C (fr) 2002-08-23 2010-11-09 Chiron Corporation Quinolinones de benzimidazole et leurs utilisations
AU2003282920A1 (en) 2002-10-04 2004-05-04 Bristol-Myers Squibb Company Hydantoin derivatives as inhibitors of matrix metalloproteinases and/or tnf-alpha converting enzyme (tace)
AU2003284001A1 (en) 2002-10-07 2004-05-04 Bristol-Myers Squibb Company Triazolone and triazolethione derivatives
US20040072802A1 (en) 2002-10-09 2004-04-15 Jingwu Duan Beta-amino acid derivatives as inhibitors of matrix metalloproteases and TNF-alpha
GB2396154B (en) 2002-10-15 2007-02-28 Merck Patent Gmbh 4,5-Dicyanoimidazole derivatives and their use in liquid crystal media and liquid crystal devices
WO2004074253A1 (fr) 2003-02-22 2004-09-02 Merck Patent Gmbh Derives de cyanopyridone utilises sous forme de cristaux liquides
JP4960085B2 (ja) 2003-03-19 2012-06-27 エクセリクシス, インク. Tie−2モジュレータと使用方法
JP2006524688A (ja) 2003-03-25 2006-11-02 バーテックス ファーマシューティカルズ インコーポレイテッド プロテインキナーゼのインヒビターとして有用なチアゾール
WO2004087835A1 (fr) 2003-04-01 2004-10-14 Merck Patent Gmbh Composes polymerisables chiraux
US7410975B2 (en) 2003-06-20 2008-08-12 Coley Pharmaceutical Group, Inc. Small molecule toll-like receptor (TLR) antagonists
CN1809357B (zh) * 2003-06-20 2010-12-22 科勒制药有限公司 小分子Toll样受体(TLR)拮抗剂
WO2005028488A1 (fr) 2003-09-12 2005-03-31 Quatrx Pharmaceuticals Co. Composes heteroaryle phosphinyle et thiophosphinyle utiles dans la regulation des taux de glucose, triglycerides et ldl/hdl
US7211671B2 (en) 2003-10-01 2007-05-01 Bristol Myers Squibb Company Substituted 1,3-dihydro-imidazol-2-one and 1,3-dihydro-imidazol-2-thione derivatives as inhibitors of matrix metalloproteinases and/or TNF-α converting enzyme (TACE)
JP2005132834A (ja) 2003-10-09 2005-05-26 Kyowa Hakko Kogyo Co Ltd キノリン誘導体
CN1291977C (zh) * 2003-10-20 2006-12-27 复旦大学 多取代喹啉衍生物功能材料及其制备方法和应用
GB0325956D0 (en) 2003-11-06 2003-12-10 Addex Pharmaceuticals Sa Novel compounds
EP1682529A4 (fr) 2003-11-07 2010-06-30 Novartis Vaccines & Diagnostic Methodes de synthese de composes de quinolinone
KR101104100B1 (ko) 2003-11-19 2012-01-12 제이엔씨 석유 화학 주식회사 광 중합성 액정 조성물, 그의 중합체 또는 중합체 조성물및 광학보상 소자
CA2555311A1 (fr) 2004-02-04 2005-08-18 Neurosearch A/S Derives d'aryle diazabicyclique constituant des ligands du recepteur de l'acetylcholine nicotinique
RU2006127575A (ru) 2004-02-18 2008-03-27 Астразенека Аб (Se) Соединение триазола и их применение в качестве антагонистов метаботропного рецептора глутамата
CN1960731B (zh) 2004-02-20 2011-12-07 诺华疫苗和诊断公司 调节炎性和转移过程的方法
WO2005087217A1 (fr) 2004-03-05 2005-09-22 The General Hospital Corporation Compositions et procedes pour moduler l'interaction entre des polypeptides
JPWO2005108370A1 (ja) 2004-04-16 2008-03-21 味の素株式会社 ベンゼン化合物
CN101248069A (zh) 2004-05-17 2008-08-20 阿卡蒂亚药品公司 雄激素受体调节剂及用其治疗疾病的方法
US20070004679A1 (en) 2004-05-17 2007-01-04 Nathalie Schlienger Androgen receptor modulators and methods of treating disease using the same
JP2007538046A (ja) 2004-05-19 2007-12-27 ノイロサーチ アクティーゼルスカブ 新規なアザビシクロアリール誘導体
GB0418046D0 (en) 2004-08-12 2004-09-15 Prosidion Ltd Eantioselective process
DE102004039789A1 (de) 2004-08-16 2006-03-02 Sanofi-Aventis Deutschland Gmbh Arylsubstituierte polycyclische Amine, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel
GB0510143D0 (en) 2005-05-18 2005-06-22 Addex Pharmaceuticals Sa Novel compounds A1
EP1831194A4 (fr) 2004-12-21 2009-12-02 Astrazeneca Ab ANTAGONISTES HETEROCYCLIQUES DE MCHr1 ET LEURS APPLICATIONS THERAPEUTIQUES
WO2006071875A1 (fr) 2004-12-29 2006-07-06 Millennium Pharmaceuticals, Inc. Composes utilises comme antagonistes des recepteurs de la chemokine
US7317024B2 (en) 2005-01-13 2008-01-08 Bristol-Myers Squibb Co. Heterocyclic modulators of the glucocorticoid receptor, AP-1, and/or NF-κB activity and use thereof
WO2006110276A2 (fr) 2005-04-08 2006-10-19 Cropsolution, Inc. Thiosemicarbazides acyles utiles en tant qu'herbicides
GB0510139D0 (en) 2005-05-18 2005-06-22 Addex Pharmaceuticals Sa Novel compounds B1
ES2401441T3 (es) 2005-06-30 2013-04-19 Bionumerik Pharmaceuticals, Inc. Análogos de platino con ligandos de monoimina
JP2007045752A (ja) 2005-08-10 2007-02-22 Takeda Chem Ind Ltd 5員芳香族複素環誘導体、その製造法および用途
JP2007131765A (ja) 2005-11-11 2007-05-31 Fujifilm Corp 液晶性組成物
US7910595B2 (en) 2005-12-21 2011-03-22 Abbott Laboratories Anti-viral compounds
US20070254894A1 (en) 2006-01-10 2007-11-01 Kane John L Jr Novel small molecules with selective cytotoxicity against human microvascular endothelial cell proliferation
BRPI0707223A2 (pt) 2006-01-27 2011-04-26 Pfizer Prod Inc compostos de derivados de aminoftalazina
EP2044056B1 (fr) 2006-07-14 2012-08-22 Novartis AG Dérivés de la pyrimidine en tant qu'inhibiteurs d'alk-5
JP2010500365A (ja) 2006-08-07 2010-01-07 インサイト・コーポレイション キナーゼ阻害剤としてのトリアゾロトリアジン
EP1900731A1 (fr) 2006-09-07 2008-03-19 Bayer Schering Pharma Aktiengesellschaft N-(1-Phthalazin-1-yl-piperidin-4-yl)-amides comme modulateurs du récepteur EP2
WO2008063609A2 (fr) 2006-11-17 2008-05-29 Polyera Corporation Matériaux semi-conducteurs à base de diimide et procédés de préparation et d'utilisation de ceux-ci
MX2009010059A (es) * 2007-03-22 2009-10-12 Astrazeneca Ab Derivados de quinolina para el tratamiento de enfermedades inflamatorias.
DE102007015169A1 (de) 2007-03-27 2008-10-02 Universität des Saarlandes Campus Saarbrücken 17Beta-Hydroxysteroid-Dehydrogenase-Typ1-Inhibitoren zur Behandlung hormonabhängiger Erkrankungen
EP2137177B1 (fr) 2007-04-05 2014-05-07 Amgen, Inc Modulateurs de la kinase aurora et méthode d'utilisation
WO2008131779A1 (fr) 2007-04-26 2008-11-06 H. Lundbeck A/S Dérivés d'isoquinolinone utilisés en tant qu'antagonistes de nk3
US8173639B2 (en) 2007-04-26 2012-05-08 H. Lundbeck A/S Isoquinolinone derivatives as NK3 antagonists
EP2167058B1 (fr) 2007-06-18 2015-08-12 University Of Louisville Research Foundation, Inc. Famille d'inhibiteurs de pfkfb3 à activités anti-néoplasiques
US8557823B2 (en) 2007-06-18 2013-10-15 Advanced Cancer Therapeutics, Llc Family of PFKFB3 inhibitors with anti-neoplastic activities
CA2689575A1 (fr) 2007-06-20 2008-12-24 Merck Sharp & Dohme Corp. Inhibiteurs de cetp derives de benzoxazole arylamides
AU2008266956A1 (en) 2007-06-20 2008-12-24 Merck Sharp & Dohme Corp. CETP inhibitors derived from benzoxazole arylamides
JP5057056B2 (ja) 2007-08-03 2012-10-24 Jsr株式会社 液晶配向剤、液晶配向膜の製造方法、ポリアミック酸およびポリイミドならびにジアミン化合物
CN101910164A (zh) 2007-10-29 2010-12-08 先灵公司 作为蛋白质激酶抑制剂的二酰氨基噻唑衍生物
JP2009108152A (ja) 2007-10-29 2009-05-21 Sumitomo Chemical Co Ltd 重合性化合物および光学フィルム
CN101440062B (zh) 2007-11-23 2011-09-28 齐齐哈尔大学 N-酰基-8-氨基喹啉衍生物的合成及其作为荧光分子探针的应用
JP2009149754A (ja) 2007-12-20 2009-07-09 Sumitomo Chemical Co Ltd 重合性化合物および該重合性化合物を重合してなる光学フィルム
MX2010009403A (es) 2008-03-07 2010-09-24 Hoffmann La Roche Derivados de 2-aminoquinolina.
JP5219583B2 (ja) 2008-03-31 2013-06-26 住友化学株式会社 組成物、光学フィルムとその製造方法、光学部材及び表示装置
US8980877B2 (en) 2008-04-15 2015-03-17 Dac S.R.L. Spirocyclic derivatives as histone deacetylase inhibitors
US8703811B2 (en) 2008-05-07 2014-04-22 Genzyme Corporation Small molecule inhibitors of Plasmodium falciparum dihydroorotate dehydrogenase
WO2009139438A1 (fr) 2008-05-15 2009-11-19 田辺三菱製薬株式会社 Procédé de production d'un acide carboxylique optiquement actif
CA2726158A1 (fr) 2008-06-11 2009-12-17 Dana Farber Cancer Institute Composes et compositions utiles pour le traitement de la malaria
EP2300438A4 (fr) 2008-06-11 2012-06-27 Merck Sharp & Dohme Dérivés imidazole utiles comme inhibiteurs de la faah
AU2009257795A1 (en) 2008-06-11 2009-12-17 Merck Sharp & Dohme Corp. Pyrazole derivatives useful as inhibitors of FAAH
US8822513B2 (en) 2010-03-01 2014-09-02 Gtx, Inc. Compounds for treatment of cancer
ES2927660T3 (es) 2008-06-16 2022-11-10 Univ Tennessee Res Found Compuestos para el tratamiento del cáncer
WO2010010187A1 (fr) 2008-07-25 2010-01-28 Galapagos Nv Nouveaux composés utiles pour le traitement de maladies dégénératives et inflammatoires
BRPI0916713A2 (pt) 2008-07-28 2015-11-10 Gilead Science Inc compostos inibidores de histona desacetilase de cicloalquilideno e heterocicloalquilideno
CN102171196B (zh) 2008-08-04 2015-03-25 默沙东公司 用作脂肪酸酰胺水解酶的抑制剂的*唑衍生物
UY32045A (es) 2008-08-12 2010-03-26 Takeda Pharmaceutical Compuesto amida
JP5443720B2 (ja) 2008-09-05 2014-03-19 住友化学株式会社 組成物、光学フィルム及びその製造方法、光学部材ならびに表示装置
JP2010066630A (ja) 2008-09-12 2010-03-25 Sumitomo Chemical Co Ltd 光学フィルムの製造方法及び光学フィルム
WO2010048149A2 (fr) 2008-10-20 2010-04-29 Kalypsys, Inc. Modulateurs hétérocycliques de gpr119 pour le traitement d'une maladie
AR073920A1 (es) 2008-10-23 2010-12-09 Boehringer Ingelheim Int Derivados urea de nortropanos sustituidos, medicamentos que contienen dichos compuestos , su uso en el tratamiento de enfermedades mediadas por la inhibicion de la enzima 11beta-hidroxiesteroide deshidrogenasa y proceso para su preparacion.
EP2373634B1 (fr) 2008-12-05 2015-11-11 Mochida Pharmaceutical Co., Ltd. Composés de morpholinone en tant qu'inhibiteurs de facteur ixa
US8987242B2 (en) 2008-12-05 2015-03-24 Merck Sharp & Dohme Corp. Morpholinone compounds as factor IXA inhibitors
CA2740195A1 (fr) 2008-12-23 2010-07-01 Abbott Laboratories Composes antiviraux
RU2505540C2 (ru) 2008-12-23 2014-01-27 Эббви Инк. Антивирусные соединения
CN101759683B (zh) 2008-12-25 2011-12-28 哈尔滨誉衡药业股份有限公司 二氢化茚酰胺化合物制备方法、包含其的药物组合物、及其作为蛋白激酶抑制剂的应用
WO2010096371A2 (fr) 2009-02-18 2010-08-26 Boehringer Ingelheim International Gmbh Composés hétérocycliques qui modulent le récepteur cb2
KR101641385B1 (ko) 2009-03-16 2016-07-20 스미또모 가가꾸 가부시끼가이샤 화합물, 광학 필름 및 광학 필름의 제조 방법
JP5899607B2 (ja) 2009-03-16 2016-04-06 住友化学株式会社 化合物、光学フィルム及び光学フィルムの製造方法
JP2011008205A (ja) 2009-05-27 2011-01-13 Fujifilm Corp 二軸性光学異方性膜を作製するための組成物
JP2011006360A (ja) 2009-06-26 2011-01-13 Sumitomo Chemical Co Ltd 化合物、光学フィルム及び光学フィルムの製造方法
GB0912777D0 (en) 2009-07-22 2009-08-26 Eisai London Res Lab Ltd Fused aminodihydropyrimidone derivatives
US20110021531A1 (en) 2009-07-27 2011-01-27 Chobanian Harry Oxazole derivatives useful as inhibitors of faah
US9212177B2 (en) 2009-08-05 2015-12-15 Versitech Limited Antiviral compounds and methods of making and using thereof
KR20120055608A (ko) 2009-08-06 2012-05-31 메르크 파텐트 게엠베하 신규한 이환 우레아 화합물
JP2011042606A (ja) 2009-08-20 2011-03-03 Sumitomo Chemical Co Ltd 化合物、光学フィルム及び光学フィルムの製造方法
EP2470183B1 (fr) 2009-08-26 2015-09-16 Merck Sharp & Dohme Corp. Composés d'amide hétérocyclique comme inhibiteurs de la protéine kinase
AU2010286933A1 (en) 2009-08-31 2012-03-15 Merck Sharp & Dohme Corp. Morpholinone compounds as factor IXa inhibitors
WO2011031896A2 (fr) 2009-09-09 2011-03-17 Avila Therapeutics, Inc. Inhibiteurs de pi3 kinase et leurs utilisations
EA020586B1 (ru) 2009-09-10 2014-12-30 Новартис Аг СУЛЬФОНАМИДЫ В КАЧЕСТВЕ ИНГИБИТОРОВ БЕЛКОВ СЕМЕЙСТВА Bcl-2, ПРЕДНАЗНАЧЕННЫЕ ДЛЯ ЛЕЧЕНИЯ РАКА
WO2011068138A1 (fr) 2009-12-01 2011-06-09 住友化学株式会社 Procédé de préparation de monoesters d'acides cycloalcanedicarboxyliques
KR20120118008A (ko) 2009-12-18 2012-10-25 아이데닉스 파마슈티칼스, 인코포레이티드 5,5-융합 아릴렌 또는 헤테로아릴렌 간염 c 바이러스 억제제
JP2013517281A (ja) 2010-01-13 2013-05-16 テンペロ、ファーマシューティカルズ、インコーポレイテッド 化合物及び方法
EP2533783B8 (fr) 2010-01-13 2015-12-16 Tempero Pharmaceuticals, Inc. COMPOSÉS ET PROCÉDÉS pour l' inhibition d' HDAC
MX2012008801A (es) 2010-01-28 2012-08-17 Merck Sharp & Dohme Composiciones farmaceuticas para el tratamiento de dolor y otras indicaciones.
EA201290774A1 (ru) 2010-02-11 2013-03-29 Вандербилт Юниверсити Пиразолопиридиновые, пиразолопиразиновые, пиразолопиримидиновые, пиразолотиофеновые и пиразолотиазоловые соединения как аллостерические потенциаторы mglur4, композиции и способы лечения неврологических дисфункций
JP5879273B2 (ja) 2010-03-01 2016-03-08 ジーティーエックス・インコーポレイテッド 癌を処置するための化合物
EP2552905B1 (fr) 2010-03-26 2016-10-05 Boehringer Ingelheim International GmbH Inhibiteurs de la kinase B-Raf
WO2011117382A1 (fr) 2010-03-26 2011-09-29 Boehringer Ingelheim International Gmbh Pyridyltriazoles
JP5856606B2 (ja) 2010-04-22 2016-02-10 メルク・シャープ・エンド・ドーム・コーポレイション Faahの調節薬として有用なオキサゾール誘導体
US9725479B2 (en) 2010-04-22 2017-08-08 Ionis Pharmaceuticals, Inc. 5′-end derivatives
WO2011133729A2 (fr) 2010-04-23 2011-10-27 Kineta, Inc. Composés antiviraux
AU2011242688B2 (en) 2010-04-23 2015-01-22 Kineta, Inc. Anti-viral compounds
US20120149715A1 (en) 2010-05-28 2012-06-14 Yi Tsun Richard Kao Compounds and methods for the treatment of viral infections
JP5652011B2 (ja) 2010-06-10 2015-01-14 住友化学株式会社 光学フィルム
EP2593107A1 (fr) 2010-07-12 2013-05-22 Merck Sharp & Dohme Corp. Inhibiteurs de la tyrosine kinase
WO2012016133A2 (fr) 2010-07-29 2012-02-02 President And Fellows Of Harvard College Inhibiteurs de la ros1 kinase pour le traitement de glioblastome et d'autres cancers déficients en p53
WO2012027322A1 (fr) 2010-08-26 2012-03-01 Boehringer Ingelheim International Gmbh Composés oxadiazole, inhibiteurs de la production de leucotriènes
WO2012033390A2 (fr) 2010-09-10 2012-03-15 Green Cross Corporation Nouveau dérivé du thiophène utilisé comme inhibiteur du sglt2 et composition pharmaceutique comprenant ce dérivé
JP2013540145A (ja) 2010-10-21 2013-10-31 ウニベルシテート デス ザールランデス コルチゾール依存性疾患の治療用の選択的cyp11b1阻害剤
WO2012058645A1 (fr) 2010-10-29 2012-05-03 Biogen Idec Ma Inc. Inhibiteurs de tyrosine kinase hétérocycliques
US8710055B2 (en) 2010-12-21 2014-04-29 Boehringer Ingelheim International Gmbh Triazolylphenyl sulfonamides as serine/threonine kinase inhibitors
CN103298822A (zh) 2010-12-23 2013-09-11 索尔维公司 三均配型金属络合物的面式异构体的制备
US20120214803A1 (en) 2011-02-18 2012-08-23 Vifor (International) Ag Novel Sulfonaminoquinoline Hepcidin Antagonists
US8828996B2 (en) 2011-03-14 2014-09-09 Vertex Pharmaceuticals Incorporated Morpholine-spirocyclic piperidine amides as modulators of ion channels
CN102675289B (zh) 2011-03-18 2014-11-05 浙江大德药业集团有限公司 作为蛋白激酶抑制剂的n-苯基苯甲酰胺衍生物
WO2012128582A2 (fr) 2011-03-23 2012-09-27 Hyundai Pharm Co., Ltd. Composé capable d'inhiber la 11-bêta-hydroxystéroïde déshydrogénase de type 1 humaine et composition pharmaceutique en contenant
US20120252721A1 (en) 2011-03-31 2012-10-04 Idenix Pharmaceuticals, Inc. Methods for treating drug-resistant hepatitis c virus infection with a 5,5-fused arylene or heteroarylene hepatitis c virus inhibitor
TW201311149A (zh) * 2011-06-24 2013-03-16 Ishihara Sangyo Kaisha 有害生物防治劑
US9199962B2 (en) 2011-07-07 2015-12-01 Merck Patent Gmbh Substituted azaheterocycles for the treatment of cancer
WO2013009830A1 (fr) 2011-07-13 2013-01-17 Tempero Pharmaceuticals, Inc. Méthodes de traitement
WO2013009810A1 (fr) 2011-07-13 2013-01-17 Tempero Pharmaceuticals, Inc. Méthodes de traitement
WO2013009827A1 (fr) 2011-07-13 2013-01-17 Tempero Pharmaceuticals, Inc. Méthodes de traitement
WO2013042139A1 (fr) 2011-09-23 2013-03-28 Advinus Therapeutics Limited Composés amides, compositions et applications de ceux-ci
EP2776420A1 (fr) 2011-11-09 2014-09-17 Vertex Pharmaceuticals Incorporated Composés de pyrazine utiles comme inhibiteurs de kinase atr
WO2013071090A1 (fr) 2011-11-09 2013-05-16 Vertex Pharmaceuticals Incorporated Composés utiles en tant qu'inhibiteurs de la kinase atr
WO2013071088A1 (fr) 2011-11-09 2013-05-16 Vertex Pharmaceuticals Incorporated Composés utiles comme inhibiteurs de kinase atr
JO3407B1 (ar) 2012-05-31 2019-10-20 Eisai R&D Man Co Ltd مركبات رباعي هيدرو بيرازولو بيريميدين
KR102365952B1 (ko) 2013-10-14 2022-02-22 에자이 알앤드디 매니지먼트 가부시키가이샤 선택적으로 치환된 퀴놀린 화합물
EP3626717A1 (fr) * 2013-10-14 2020-03-25 Eisai R&D Management Co., Ltd. Composés de quinoline sélectivement substitués

Also Published As

Publication number Publication date
EP3057964A1 (fr) 2016-08-24
BR112016008359A2 (fr) 2017-10-03
PL3057964T3 (pl) 2020-05-18
JP6639607B2 (ja) 2020-02-05
PH12016500642B1 (en) 2016-05-30
IL245131B (en) 2018-11-29
HRP20200147T1 (hr) 2020-05-01
PH12016500642A1 (en) 2016-05-30
TWI624467B (zh) 2018-05-21
EP3057964B1 (fr) 2019-12-04
CA2927510A1 (fr) 2015-04-23
MX364657B (es) 2019-05-03
TW201838988A (zh) 2018-11-01
MD20160052A2 (ro) 2016-09-30
ZA201601882B (en) 2019-09-25
KR20180011874A (ko) 2018-02-02
TWI702218B (zh) 2020-08-21
CN106414432B (zh) 2019-06-14
US20180354939A1 (en) 2018-12-13
RU2016118619A (ru) 2017-11-22
JP2016535003A (ja) 2016-11-10
HUE048706T2 (hu) 2020-08-28
EP3995495A1 (fr) 2022-05-11
CY1122776T1 (el) 2021-05-05
SG11201602818TA (en) 2016-05-30
US9428495B2 (en) 2016-08-30
US20180030045A1 (en) 2018-02-01
US20150105370A1 (en) 2015-04-16
ZA201608132B (en) 2019-01-30
IL245131A0 (en) 2016-06-30
US20160326161A1 (en) 2016-11-10
CN106414432A (zh) 2017-02-15
PE20160608A1 (es) 2016-07-08
PT3057964T (pt) 2020-02-25
HK1223092A1 (en) 2017-07-21
RU2016118619A3 (fr) 2018-05-23
USRE47193E1 (en) 2019-01-08
RU2679622C2 (ru) 2019-02-12
AU2014334554B2 (en) 2018-12-06
KR20160068949A (ko) 2016-06-15
BR112016008359B1 (pt) 2022-07-19
IL262970B (en) 2019-10-31
JP2017226700A (ja) 2017-12-28
AR098014A1 (es) 2016-04-27
CL2016000662A1 (es) 2016-12-16
NZ720129A (en) 2021-03-26
ZA201905393B (en) 2020-11-25
CN110105346B (zh) 2023-03-10
CA2927510C (fr) 2022-03-01
AU2018264036B2 (en) 2020-07-16
JP6223563B2 (ja) 2017-11-01
SMT202000076T1 (it) 2020-03-13
MX2016004632A (es) 2016-10-26
JP6420878B2 (ja) 2018-11-07
ES2773303T3 (es) 2020-07-10
RS59911B1 (sr) 2020-03-31
TW201602100A (zh) 2016-01-16
MD4635C1 (ro) 2020-01-31
AU2014334554A1 (en) 2016-06-02
AU2018264036A1 (en) 2018-12-06
WO2015057659A1 (fr) 2015-04-23
JP2019023220A (ja) 2019-02-14
JO3554B1 (ar) 2020-07-05
LT3057964T (lt) 2020-02-25
KR101823488B1 (ko) 2018-01-30
EP3626717A1 (fr) 2020-03-25
MX2019005192A (es) 2019-10-21
ZA201801112B (en) 2020-10-28
US10087174B2 (en) 2018-10-02
UA120039C2 (uk) 2019-09-25
MY192489A (en) 2022-08-23
MA39034A1 (fr) 2018-01-31
KR102103256B1 (ko) 2020-04-23
MX374600B (es) 2025-03-06
IL262970A (en) 2018-12-31
CN110105346A (zh) 2019-08-09
SG10201704327RA (en) 2017-06-29
DK3057964T3 (da) 2020-02-24
SI3057964T1 (sl) 2020-03-31
SG10202103278TA (en) 2021-04-29
MD4635B1 (ro) 2019-06-30

Similar Documents

Publication Publication Date Title
MA39034A1 (fr) Composés de quinoline sélectivement substitués
MX2016004629A (es) Compuestos de quinolina selectivamente sustituidos.
UA113440C2 (xx) Сполуки тетрагідропіразолопіримідину
MA44322A (fr) Compositions comprenant des souches bactériennes
MA42471A (fr) Compositions comprenant des souches bactériennes
MA40682B1 (fr) Anticorps anti-ox40 et procédés d&#39;utilisation correspondants
MA38632B1 (fr) Anticorps anti-récepteur de transferrine et procédés d&#39;utilisation
MA39172A1 (fr) Dérivés bicycliques hétérocycliques comme inhibiteurs de bromodomaines
EP3470424A4 (fr) Séquence de région constante à chaîne lourde d&#39;anticorps pour améliorer l&#39;activité d&#39;anticorps agonistes
CR20160171A (es) NUEVO OCTAHIDRO-CICLOBUTA[1,2-c; 3,4-c] DIPIRROL-2-ILO
MX367879B (es) N-alquil 2-(disustituido)alquiladenosin-5-uronamidas como agonistas a2a.
MA38884A1 (fr) Composé de triazolopyridine, compositions et procédés d&#39;utilisation associés
MA40366A (fr) Dérivés de tétrahydroquinoline à titre d&#39;inhibiteurs des bromodomaines
EP3373935A4 (fr) Dérivés de cyanopyridine utilisés en tant qu&#39;agonistes des récepteurs bêta x du foie, compositions associées et leur utilisation
MA39837B1 (fr) Quinazoline-thf-amines halogénées en tant qu&#39;inhibiteurs de la pde1
MA39076A1 (fr) Dérivé de chromone en tant qu&#39;antagoniste dopaminergique d3 pour son utilisation pour le traitement d&#39;un trouble du spectre autistique
MA38654B1 (fr) Dérivés de type promédicament de triazolopyridines substituées
MA41311B1 (fr) Peptides antagonistes du cgrp
EP3743186A4 (fr) Compositions permettant l&#39;élimination de métaux lourds
MA39355B2 (fr) Anticorps anti-ox40 et procédés d&#39;utilisation correspondants
EP3816158A4 (fr) Dérivés de benzimidazole et leur utilisation en tant qu&#39;inhibiteurs d&#39;idh1
MA38657A1 (fr) Combinaison d&#39;un dérivé d&#39;imidazopyridazine et d&#39;un agent mitotique pour le traitement du cancer
TH158525A (th) สารประกอบเตตระไฮโดรไพราโซโลไพริมิดีน
MA39118A1 (fr) Quinazoline-thf-amines utilisées en tant qu&#39;inhibiteurs de la pde1
MA40553B1 (fr) Derives de pyrimidine eventuellement condensee utiles dans le traitement de maladies inflammatoires, metaboliques, oncologiques et auto-immunes