MX2018015422A - Compuestos de indol sustituidos con [1,2,4]triazolo[1,5-a]piridini lo. - Google Patents

Compuestos de indol sustituidos con [1,2,4]triazolo[1,5-a]piridini lo.

Info

Publication number
MX2018015422A
MX2018015422A MX2018015422A MX2018015422A MX2018015422A MX 2018015422 A MX2018015422 A MX 2018015422A MX 2018015422 A MX2018015422 A MX 2018015422A MX 2018015422 A MX2018015422 A MX 2018015422A MX 2018015422 A MX2018015422 A MX 2018015422A
Authority
MX
Mexico
Prior art keywords
triazolo
compounds
substituted indole
indole compounds
pyridinyl substituted
Prior art date
Application number
MX2018015422A
Other languages
English (en)
Inventor
J Dyckman Alaric
L Posy Shoshana
S Dodd Dharmpal
P Mussari Christopher
J Lombardo Louis
Kumar Sistla Ramesh
E Macor John
C Sherwood Trevor
Pasunoori Laxman
HEGDE Subramaya
RAMACHANDRA Anupama
Shamsul HAQUE Tasir
Ratna Kumar Sreekantha
Original Assignee
Squibb Bristol Myers Co
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 Squibb Bristol Myers Co filed Critical Squibb Bristol Myers Co
Publication of MX2018015422A publication Critical patent/MX2018015422A/es

Links

Classifications

    • 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
    • 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
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/41961,2,4-Triazoles
    • 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
    • A61K31/4353Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D249/00Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Immunology (AREA)
  • Rheumatology (AREA)
  • Pain & Pain Management (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

La presente invención se refiere a compuestos de la Fórmula (I) (ver Fórmula) o una sal del mismo, en donde R1, R2, R3, R4, R5, m, n y p se definen en la presente. También se describen métodos para usar tals compuestos como inhibidores de la señalización a través del receptor tipo Toll 7, 8 o 9, y composiciones farmacéuticas que comprenden tals compuestos. Estos compuestos son útiles para tratar enfermedades inflamatorias y autoinmunitarias.
MX2018015422A 2016-06-29 2017-06-28 Compuestos de indol sustituidos con [1,2,4]triazolo[1,5-a]piridini lo. MX2018015422A (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
IN201611022328 2016-06-29
US15/635,055 US10071079B2 (en) 2016-06-29 2017-06-27 [1,2,4]triazolo[1,5-a]pyridinyl substituted indole compounds
PCT/US2017/039633 WO2018005586A1 (en) 2016-06-29 2017-06-28 [1,2,4]triazolo[1,5-a]pyridinyl substituted indole compounds

Publications (1)

Publication Number Publication Date
MX2018015422A true MX2018015422A (es) 2019-04-22

Family

ID=60805851

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2018015422A MX2018015422A (es) 2016-06-29 2017-06-28 Compuestos de indol sustituidos con [1,2,4]triazolo[1,5-a]piridini lo.

Country Status (31)

Country Link
US (8) US10071079B2 (es)
EP (1) EP3478682B1 (es)
JP (1) JP6995067B6 (es)
KR (1) KR102473482B1 (es)
CN (1) CN109641895B (es)
AR (1) AR108905A1 (es)
AU (1) AU2017287902B2 (es)
BR (1) BR112018077119A2 (es)
CA (1) CA3029620A1 (es)
CL (1) CL2018003821A1 (es)
CO (1) CO2019000686A2 (es)
CY (1) CY1124514T1 (es)
DK (1) DK3478682T3 (es)
EA (1) EA037530B1 (es)
ES (1) ES2886964T3 (es)
HR (1) HRP20211261T8 (es)
HU (1) HUE056091T2 (es)
IL (1) IL263961B (es)
LT (1) LT3478682T (es)
MX (1) MX2018015422A (es)
MY (1) MY196474A (es)
PE (1) PE20190324A1 (es)
PL (1) PL3478682T3 (es)
PT (1) PT3478682T (es)
RS (1) RS62292B1 (es)
SG (1) SG11201811590RA (es)
SI (1) SI3478682T1 (es)
TW (1) TWI636053B (es)
UY (1) UY37310A (es)
WO (1) WO2018005586A1 (es)
ZA (1) ZA201900571B (es)

Families Citing this family (59)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10071079B2 (en) 2016-06-29 2018-09-11 Bristol-Myers Squibb Company [1,2,4]triazolo[1,5-a]pyridinyl substituted indole compounds
CN109715617B (zh) 2016-07-30 2022-04-19 百时美施贵宝公司 作为tlr7、tlr8或tlr9抑制剂的二甲氧基苯基取代的吲哚化合物
CN109923108B (zh) 2016-09-09 2022-04-29 百时美施贵宝公司 吡啶基取代的吲哚化合物
CN117402852A (zh) 2016-10-14 2024-01-16 精密生物科学公司 对乙肝病毒基因组中的识别序列特异性的工程化大范围核酸酶
JP7266576B2 (ja) * 2017-08-04 2023-04-28 ブリストル-マイヤーズ スクイブ カンパニー [1,2,4]トリアゾロ[4,3-a]ピリジニル置換のインドール化合物
WO2019028302A1 (en) 2017-08-04 2019-02-07 Bristol-Myers Squibb Company SUBSTITUTED INDOLE COMPOUNDS USEFUL AS TLR7 / 8/9 INHIBITORS
CN111448190B (zh) * 2017-11-14 2023-09-26 百时美施贵宝公司 取代的吲哚化合物
CN111527080B (zh) * 2017-12-15 2023-09-22 百时美施贵宝公司 取代的吲哚醚化合物
US11878975B2 (en) * 2017-12-19 2024-01-23 Bristol-Myers Squibb Company Substituted indole compounds useful as TLR inhibitors
WO2019126081A1 (en) 2017-12-19 2019-06-27 Bristol-Myers Squibb Company Amide substituted indole compounds useful as tlr inhibitors
WO2019126082A1 (en) 2017-12-19 2019-06-27 Bristol-Myers Squibb Company 6-azaindole compounds
CA3086431A1 (en) 2017-12-20 2019-06-27 Bristol-Myers Squibb Company Amino indole compounds useful as tlr inhibitors
ES2904773T3 (es) * 2017-12-20 2022-04-06 Bristol Myers Squibb Co Compuestos de diazaindol
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
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
US11420958B2 (en) 2017-12-20 2022-08-23 Bristol-Myers Squibb Company Aryl and heteroaryl substituted indole compounds
WO2019155042A1 (en) 2018-02-12 2019-08-15 F. Hoffmann-La Roche Ag Novel sulfone compounds and derivatives for the treatment and prophylaxis of virus infection
CA3091142C (en) 2018-02-26 2023-04-11 Gilead Sciences, Inc. Substituted pyrrolizine compounds and uses thereof
WO2019195181A1 (en) 2018-04-05 2019-10-10 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
KR20200140867A (ko) 2018-04-06 2020-12-16 인스티튜트 오브 오가닉 케미스트리 앤드 바이오케미스트리 에이에스 씨알 브이.브이.아이. 3'3'-사이클릭 다이뉴클레오티드
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
US11142750B2 (en) 2018-04-12 2021-10-12 Precision Biosciences, Inc. Optimized engineered meganucleases having specificity for a recognition sequence in the Hepatitis B virus genome
WO2019211799A1 (en) 2018-05-03 2019-11-07 Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. 2'3'-cyclic dinucleotide analogue comprising a cyclopentanyl modified nucleotide
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 (en) * 2018-06-13 2019-12-19 F. Hoffmann-La Roche Ag Pyridinyl heterocyclyl compounds for the treatment of autoimmune disease
EP3826724B1 (en) 2018-07-23 2022-10-05 F. Hoffmann-La Roche AG Novel piperazine compounds for the treatment of autoimmune disease
WO2020028097A1 (en) 2018-08-01 2020-02-06 Gilead Sciences, Inc. Solid forms of (r)-11-(methoxymethyl)-12-(3-methoxypropoxy)-3,3-dimethyl-8-0x0-2,3,8,13b-tetrahydro-1h-pyrido[2,1-a]pyrrolo[1,2-c] phthalazine-7-c arboxylic acid
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
EP3847170B1 (en) 2018-09-06 2022-06-22 F. Hoffmann-La Roche AG Novel cyclic amidine compounds for the treatment of autoimmune disease
CN112955450A (zh) * 2018-10-24 2021-06-11 百时美施贵宝公司 经取代的吲哚和吲唑化合物
JP2022505827A (ja) * 2018-10-24 2022-01-14 ブリストル-マイヤーズ スクイブ カンパニー 置換インドール二量体の化合物
TWI721624B (zh) 2018-10-31 2021-03-11 美商基利科學股份有限公司 經取代之6-氮雜苯并咪唑化合物
PE20211655A1 (es) 2018-10-31 2021-08-24 Gilead Sciences Inc Compuestos de 6-azabencimidazol sustituidos como inhibidores de hpk1
US20220152078A1 (en) 2019-03-07 2022-05-19 Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. 2'3'-cyclic dinucleotides and prodrugs thereof
JP7350872B2 (ja) 2019-03-07 2023-09-26 インスティチュート オブ オーガニック ケミストリー アンド バイオケミストリー エーエスシーアール,ヴイ.ヴイ.アイ. 3’3’-環状ジヌクレオチドおよびそのプロドラッグ
US11766447B2 (en) 2019-03-07 2023-09-26 Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. 3′3′-cyclic dinucleotide analogue comprising a cyclopentanyl modified nucleotide as sting modulator
TWI751516B (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
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
JP2022532568A (ja) 2019-05-07 2022-07-15 ブリストル-マイヤーズ スクイブ カンパニー プロドラッグ化合物
TWI826690B (zh) 2019-05-23 2023-12-21 美商基利科學股份有限公司 經取代之烯吲哚酮化物及其用途
CN110146631B (zh) * 2019-06-25 2021-11-12 山西康宝生物制品股份有限公司 一种药用材料中聚乙二醇单甲醚残留量的检测方法
WO2021034804A1 (en) 2019-08-19 2021-02-25 Gilead Sciences, Inc. Pharmaceutical formulations of tenofovir alafenamide
JP7398556B2 (ja) 2019-09-30 2023-12-14 ギリアード サイエンシーズ, インコーポレイテッド Hbvワクチン及びhbvを治療する方法
JP2022552159A (ja) * 2019-10-04 2022-12-15 ブリストル-マイヤーズ スクイブ カンパニー 置換カルバゾール化合物
CN116057068A (zh) 2019-12-06 2023-05-02 精密生物科学公司 对乙型肝炎病毒基因组中的识别序列具有特异性的优化的工程化大范围核酸酶
CN115605493A (zh) 2020-03-20 2023-01-13 吉利德科学公司(Us) 4′-c-取代的-2-卤代-2′-脱氧腺苷核苷的前药及其制备和使用方法
CN115701995A (zh) 2020-06-11 2023-02-14 百时美施贵宝公司 用于治疗皮肤红斑狼疮的tlr7抑制剂与泼尼松龙或羟氯喹的组合
US20230310409A1 (en) 2020-06-22 2023-10-05 Bristol-Myers Squibb Company Treating rheumatoid arthritis
TW202214632A (zh) * 2020-07-27 2022-04-16 大陸商江蘇恆瑞醫藥股份有限公司 吲哚稠環類衍生物、其製備方法及其在醫藥上的應用
TW202227442A (zh) 2020-11-26 2022-07-16 大陸商江蘇恆瑞醫藥股份有限公司 稠合三環化合物、其製備方法及其在醫藥上的應用
AU2022257039A1 (en) 2021-04-16 2023-10-05 Gilead Sciences, Inc. Thienopyrrole compounds
KR20240006683A (ko) 2021-05-13 2024-01-15 길리애드 사이언시즈, 인코포레이티드 TLR8 조절 화합물과 항-HBV siRNA 치료제의 조합물
CN113416188B (zh) * 2021-05-31 2022-12-13 河南偶联生物科技有限公司 一种[1,2,4]三唑并[1,5-a]吡啶化合物的合成方法
KR20240005901A (ko) 2021-06-23 2024-01-12 길리애드 사이언시즈, 인코포레이티드 디아실글리세롤 키나제 조절 화합물
CN117355531A (zh) 2021-06-23 2024-01-05 吉利德科学公司 二酰基甘油激酶调节化合物
EP4359389A1 (en) 2021-06-23 2024-05-01 Gilead Sciences, Inc. Diacylglyercol kinase modulating compounds
CN117377671A (zh) 2021-06-23 2024-01-09 吉利德科学公司 二酰基甘油激酶调节化合物
WO2024015825A1 (en) 2022-07-13 2024-01-18 Bristol-Myers Squibb Company Processes for preparing 5-bromo-3,4-dimethylpyridin-2-amine and 6-bromo-7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridine

Family Cites Families (48)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PL349192A1 (en) 1998-12-18 2002-07-01 Axys Pharmaceuticals Protease inhibitors
EA200600069A1 (ru) 2003-06-20 2006-08-25 Коли Фармасьютикал Гмбх Низкомолекулярные антагонисты toll-подобных рецепторов (tlr)
WO2007115306A2 (en) 2006-04-04 2007-10-11 Myriad Genetics, Inc. Compounds for diseases and disorders
WO2006113458A1 (en) * 2005-04-15 2006-10-26 Bristol-Myers Squibb Company Heterocyclic inhibitors of protein arginine methyl transferases
DE102006033109A1 (de) 2006-07-18 2008-01-31 Grünenthal GmbH Substituierte Heteroaryl-Derivate
US8027888B2 (en) 2006-08-31 2011-09-27 Experian Interactive Innovation Center, Llc Online credit card prescreen systems and methods
US7977352B2 (en) 2006-12-01 2011-07-12 Galapagos Nv Triazolopyridine compounds useful for the treatment of degenerative and inflammatory diseases
WO2008152471A1 (en) 2007-06-12 2008-12-18 Coley Pharmaceutical Group, Inc. Quinazoline derivative useful as toll-like receptor antagonist
WO2009030996A1 (en) 2007-09-05 2009-03-12 Coley Pharmaceutical Group, Inc. Triazole compounds as toll-like receptor (tlr) agonists
FR2926556B1 (fr) * 2008-01-22 2010-02-19 Sanofi Aventis Derives de carboxamides n-azabicycliques, leur preparation et leur application en therapeutique
US8354400B2 (en) 2008-09-26 2013-01-15 Eisai R&D Co., Ltd. Benzoxazole compounds and methods of use
US8785489B2 (en) 2008-10-17 2014-07-22 Boehringer Ingelheim International Gmbh Heteroaryl substituted indole compounds useful as MMP-13 inhibitors
CN102388043A (zh) 2009-02-11 2012-03-21 桑诺维恩药品公司 组胺h3反相激动剂和拮抗剂及其使用方法
AU2010258785A1 (en) 2009-06-10 2012-01-19 Sunovion Pharmaceuticals Inc. Histamine H3 inverse agonists and antagonists and methods of use thereof
TWI462920B (zh) 2009-06-26 2014-12-01 葛萊伯格有限公司 用於治療退化性及發炎疾病之新穎化合物
JP5864417B2 (ja) 2009-07-16 2016-02-17 マリンクロッド エルエルシー トール様受容体9のアンタゴニストとしての(+)−モルフィナンおよびその治療的使用
US9241991B2 (en) 2010-10-21 2016-01-26 The Brigham And Women's Hospital, Inc. Agents, compositions, and methods for treating pruritus and related skin conditions
EP2663550B1 (en) 2011-01-12 2016-12-14 VentiRx Pharmaceuticals, Inc. Substituted benzoazepines as toll-like receptor modulators
BR112013017947A2 (pt) 2011-01-12 2018-12-18 Array Biopharma Inc benzoazepinas substituídas como moduladores de receptor toll-like
CA2837207A1 (en) 2011-06-01 2012-12-06 Janus Biotherapeutics, Inc. Novel immune system modulators
JP6093759B2 (ja) 2011-06-01 2017-03-08 ジャナス バイオセラピューティクス,インク. 新規の免疫系調節剤
EA031618B1 (ru) 2011-06-09 2019-01-31 Ризен Фармасьютикалз Са Соединения-модуляторы gpr-119
BR112014000774B1 (pt) 2011-07-13 2022-03-29 Tiumbio Co., Ltd Compostos imidazóis substituídos por 2-piridila como inibidores de alk5 e/ou alk4, composição farmacêutica compreendendo-os e uso terapêutico dos mesmos
EP2763677B1 (en) 2011-10-04 2020-02-26 Janus Biotherapeutics, Inc. Novel imidazole quinoline-based immune system modulators
MX2014014031A (es) 2012-05-18 2015-02-12 Sumitomo Dainippon Pharma Co Ltd Compuestos de acido carboxilico.
JO3407B1 (ar) 2012-05-31 2019-10-20 Eisai R&D Man Co Ltd مركبات رباعي هيدرو بيرازولو بيريميدين
RS59911B1 (sr) 2013-10-14 2020-03-31 Eisai R&D Man Co Ltd Selektivno supstituisana jedinjenja hinolina
CA2933466A1 (en) 2013-12-13 2015-06-18 Takeda Pharmaceutical Company Limited Pyrrolo[3,2-c]pyridine derivatives as tlr inhibitors
US20170275287A1 (en) 2014-08-22 2017-09-28 Janus Biotherapeutics, Inc. Novel n2, n4, n7, 6-tetrasubstituted pteridine-2,4,7-triamine and 2, 4, 6, 7-tetrasubstituted pteridine compounds and methods of synthesis and use thereof
US9550778B2 (en) 2014-10-03 2017-01-24 Vanderbilt University Substituted 6-aryl-imidazopyridine and 6-aryl-triazolopyridine carboxamide analogs as negative allosteric modulators of mGluR5
CA2995365C (en) 2015-08-13 2021-10-12 Merck Sharp & Dohme Corp. Cyclic di-nucleotide compounds as sting agonists
AU2017289014B2 (en) 2016-06-29 2019-12-05 Hanmi Pharm. Co., Ltd. Glucagon derivative, conjugate thereof, composition comprising same and therapeutic use thereof
CA3029032A1 (en) 2016-06-29 2018-01-04 Henry Johnson Crystalline salts of peptide epoxyketone immunoproteasome inhibitor
US10071079B2 (en) 2016-06-29 2018-09-11 Bristol-Myers Squibb Company [1,2,4]triazolo[1,5-a]pyridinyl substituted indole compounds
CN109715617B (zh) 2016-07-30 2022-04-19 百时美施贵宝公司 作为tlr7、tlr8或tlr9抑制剂的二甲氧基苯基取代的吲哚化合物
CN109923108B (zh) 2016-09-09 2022-04-29 百时美施贵宝公司 吡啶基取代的吲哚化合物
JP7266576B2 (ja) 2017-08-04 2023-04-28 ブリストル-マイヤーズ スクイブ カンパニー [1,2,4]トリアゾロ[4,3-a]ピリジニル置換のインドール化合物
WO2019028302A1 (en) 2017-08-04 2019-02-07 Bristol-Myers Squibb Company SUBSTITUTED INDOLE COMPOUNDS USEFUL AS TLR7 / 8/9 INHIBITORS
CN111448190B (zh) 2017-11-14 2023-09-26 百时美施贵宝公司 取代的吲哚化合物
CN111527080B (zh) 2017-12-15 2023-09-22 百时美施贵宝公司 取代的吲哚醚化合物
RS64728B1 (sr) 2017-12-18 2023-11-30 Bristol Myers Squibb Co Jedinjenja 4-azaindola
US11878975B2 (en) 2017-12-19 2024-01-23 Bristol-Myers Squibb Company Substituted indole compounds useful as TLR inhibitors
WO2019126082A1 (en) 2017-12-19 2019-06-27 Bristol-Myers Squibb Company 6-azaindole compounds
WO2019126081A1 (en) 2017-12-19 2019-06-27 Bristol-Myers Squibb Company Amide substituted indole compounds useful as tlr inhibitors
US11420958B2 (en) 2017-12-20 2022-08-23 Bristol-Myers Squibb Company Aryl and heteroaryl substituted indole compounds
ES2904773T3 (es) 2017-12-20 2022-04-06 Bristol Myers Squibb Co Compuestos de diazaindol
CA3086431A1 (en) 2017-12-20 2019-06-27 Bristol-Myers Squibb Company Amino indole compounds useful as tlr inhibitors
CN112955450A (zh) 2018-10-24 2021-06-11 百时美施贵宝公司 经取代的吲哚和吲唑化合物

Also Published As

Publication number Publication date
AU2017287902A1 (en) 2019-02-14
US20180325874A1 (en) 2018-11-15
US20230255941A1 (en) 2023-08-17
US20180000790A1 (en) 2018-01-04
HRP20211261T8 (hr) 2022-01-21
IL263961A (en) 2019-01-31
HUE056091T2 (hu) 2022-01-28
EP3478682A1 (en) 2019-05-08
IL263961B (en) 2021-01-31
TWI636053B (zh) 2018-09-21
BR112018077119A2 (pt) 2019-04-02
JP6995067B2 (ja) 2022-01-14
ZA201900571B (en) 2020-10-28
RS62292B1 (sr) 2021-09-30
SI3478682T1 (sl) 2021-10-29
SG11201811590RA (en) 2019-01-30
US10478424B2 (en) 2019-11-19
JP6995067B6 (ja) 2023-12-14
US10912766B2 (en) 2021-02-09
KR102473482B1 (ko) 2022-12-01
EP3478682B1 (en) 2021-07-21
CN109641895B (zh) 2021-09-03
HRP20211261T1 (hr) 2021-11-26
PL3478682T3 (pl) 2021-12-13
LT3478682T (lt) 2021-09-27
US10071079B2 (en) 2018-09-11
US11672780B2 (en) 2023-06-13
USRE49880E1 (en) 2024-03-26
USRE49893E1 (en) 2024-04-02
ES2886964T3 (es) 2021-12-21
MY196474A (en) 2023-04-13
DK3478682T3 (da) 2021-09-13
CA3029620A1 (en) 2018-01-04
UY37310A (es) 2018-01-02
USRE49931E1 (en) 2024-04-23
AU2017287902B2 (en) 2021-09-16
CL2018003821A1 (es) 2019-04-22
KR20190022735A (ko) 2019-03-06
WO2018005586A1 (en) 2018-01-04
EA037530B1 (ru) 2021-04-08
CY1124514T1 (el) 2022-07-22
CN109641895A (zh) 2019-04-16
TW201805285A (zh) 2018-02-16
AR108905A1 (es) 2018-10-10
PT3478682T (pt) 2021-09-15
US20200038374A1 (en) 2020-02-06
JP2019523241A (ja) 2019-08-22
PE20190324A1 (es) 2019-03-05
CO2019000686A2 (es) 2019-02-19
EA201990048A1 (ru) 2019-05-31
US20210085651A1 (en) 2021-03-25

Similar Documents

Publication Publication Date Title
MX2018015422A (es) Compuestos de indol sustituidos con [1,2,4]triazolo[1,5-a]piridini lo.
MX2020005873A (es) Compuestos de 6-azaindol.
MX2019000694A (es) Compuestos indol sustituidos con dimetoxifenilo como inhibidores de receptores tipo toll 7, 8 o 9 (tlr7, tlr8 o tlr9).
MX2020005622A (es) Compuestos de indol sustituidos con arilo y heteroarilo.
MX2020006168A (es) Compuestos de 4-azaindol.
MX2020005515A (es) Compuestos de indol sustituidos con amida, utiles como inhibidores de receptores de tipo toll (tlr).
MX2020005462A (es) Compuestos de indol sustituidos utiles como inhibidores de receptores tipo toll (tlr).
EA201990657A1 (ru) Соединения и композиции в качестве ингибиторов эндосомальных toll-подобных рецепторов
MX2020006014A (es) Compuestos de diazaindol.
PH12017502050B1 (en) Naphthyridine compounds as jak kinase inhibitors
GEP20217242B (en) Pyrazolo[1,5-a]pyrazin-4-yl derivatives as jak-inhibitors
MX2020005513A (es) Compuestos de amino indol utiles como inhibidores de receptores tipo toll (tlr).
PH12015502004A1 (en) Tetracyclic bromodomain inhibitors
MX2015011984A (es) Inhibidores de bromodominio de dihidro-pirrolopiridinona.
MX2015012431A (es) Pirrol amida como inhibidores.
MX2020006093A (es) Compuestos de indol eter sustituidos.
NZ736055A (en) Imidazopyrazines and pyrazolopyrimidines and their use as ampa receptor modulators
EA201792374A1 (ru) Азабензимидазолы и их применение в качестве модуляторов рецептора ampa
MX2017011433A (es) Compuestos heterociclicos triciclicos utiles como inhibidores del factor de necrosis tumoral (tnf).
MX2016009581A (es) Derivados de 6-fenil- o 6-(piridin-3-il) indazol y metodos de uso.
PH12017501876A1 (en) Pyridopyrimidones and their use as nmda receptor modulators
UA117318C2 (uk) ПОХІДНІ 7-(МОРФОЛІНІЛ)-2-(N-ПІПЕРАЗИНІЛ)МЕТИЛТІЄНО[2,3-с]ПІРИДИНУ ЯК ПРОТИРАКОВІ ЛІКУВАЛЬНІ ЗАСОБИ
MY195169A (en) Cyclic Ether Derivatives of Pyrazolo[1,5-A]Pyrimidine-3-Carboxyamide
EA201692227A1 (ru) Производные сложных аминоэфиров

Legal Events

Date Code Title Description
FG Grant or registration