MA64509B1 - Composés hétérocycliques utilisés comme immunomodulateurs - Google Patents

Composés hétérocycliques utilisés comme immunomodulateurs

Info

Publication number
MA64509B1
MA64509B1 MA64509A MA64509A MA64509B1 MA 64509 B1 MA64509 B1 MA 64509B1 MA 64509 A MA64509 A MA 64509A MA 64509 A MA64509 A MA 64509A MA 64509 B1 MA64509 B1 MA 64509B1
Authority
MA
Morocco
Prior art keywords
immunomodulators
compounds used
heterocyclic compounds
compounds
amelioration
Prior art date
Application number
MA64509A
Other languages
English (en)
Inventor
Liangxing Wu
Wenqing Yao
Kaijiong Xiao
Original Assignee
Incyte Corporation
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=66625434&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MA64509(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Incyte Corporation filed Critical Incyte Corporation
Publication of MA64509B1 publication Critical patent/MA64509B1/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D519/00Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
    • 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
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • 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
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04Antibacterial agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/10Antimycotics
    • 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
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • 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
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • A61P37/04Immunostimulants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/06Antianaemics
    • 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

Landscapes

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

Abstract

L'invention concerne des composés de formule (I), des procédés d'utilisation des composés comme immunomodulateurs et des compositions pharmaceutiques comprenant de tels composés. Les composés sont utiles dans le traitement, la prévention ou lamélioration de maladies ou de troubles tels que le cancer ou les infections.
MA64509A 2018-05-11 2019-05-10 Composés hétérocycliques utilisés comme immunomodulateurs MA64509B1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201862670249P 2018-05-11 2018-05-11
US201862688164P 2018-06-21 2018-06-21
EP23152736.7A EP4219492B1 (fr) 2018-05-11 2019-05-10 Composés hétérocycliques utilisés comme immunomodulateurs

Publications (1)

Publication Number Publication Date
MA64509B1 true MA64509B1 (fr) 2025-02-28

Family

ID=66625434

Family Applications (1)

Application Number Title Priority Date Filing Date
MA64509A MA64509B1 (fr) 2018-05-11 2019-05-10 Composés hétérocycliques utilisés comme immunomodulateurs

Country Status (35)

Country Link
US (5) US10618916B2 (fr)
EP (3) EP4219492B1 (fr)
JP (2) JP7328995B2 (fr)
KR (1) KR102806565B1 (fr)
CN (2) CN112752756B (fr)
AU (2) AU2019267824B2 (fr)
BR (1) BR112020022936A2 (fr)
CA (1) CA3099994A1 (fr)
CL (2) CL2020002922A1 (fr)
CO (1) CO2020015437A2 (fr)
CR (1) CR20200614A (fr)
DK (2) DK4219492T3 (fr)
EC (1) ECSP20079887A (fr)
ES (2) ES2943028T3 (fr)
FI (2) FI3790877T3 (fr)
HR (2) HRP20230306T1 (fr)
HU (2) HUE070093T2 (fr)
IL (1) IL278605B2 (fr)
JO (1) JOP20200288A1 (fr)
LT (2) LT4219492T (fr)
MA (1) MA64509B1 (fr)
MD (2) MD3790877T2 (fr)
MX (2) MX2020012045A (fr)
PE (1) PE20211918A1 (fr)
PH (1) PH12020551927A1 (fr)
PL (2) PL4219492T3 (fr)
PT (2) PT4219492T (fr)
RS (2) RS66459B1 (fr)
SA (1) SA520420524B1 (fr)
SG (1) SG11202011165TA (fr)
SI (2) SI4219492T1 (fr)
SM (2) SMT202500077T1 (fr)
TW (2) TW202425987A (fr)
WO (1) WO2019217821A1 (fr)
ZA (1) ZA202403924B (fr)

Families Citing this family (113)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RS61089B1 (sr) 2012-06-13 2020-12-31 Incyte Holdings Corp Supstituisana triciklična jedinjenja kao inhibitori fgfr
DK2986610T5 (en) 2013-04-19 2018-12-10 Incyte Holdings Corp BICYCLIC HETEROCYCLES AS FGFR INHIBITORS
SG11201706287PA (en) 2015-02-20 2017-09-28 Incyte Corp Bicyclic heterocycles as fgfr inhibitors
MA41551A (fr) 2015-02-20 2017-12-26 Incyte Corp Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4
WO2017070089A1 (fr) 2015-10-19 2017-04-27 Incyte Corporation Composés hétérocycliques utilisés comme immunomodulateurs
ES2928856T3 (es) 2015-11-19 2022-11-23 Incyte Corp Compuestos heterocíclicos como inmunomoduladores
WO2017106634A1 (fr) 2015-12-17 2017-06-22 Incyte Corporation Dérivés de n-phényl-pyridine-2-carboxamide et leur utilisation comme modulateurs d'interactions protéine/protéine pd-1/pd-l1
TWI850624B (zh) 2015-12-22 2024-08-01 美商英塞特公司 作為免疫調節劑之雜環化合物
ES2906460T3 (es) 2016-05-06 2022-04-18 Incyte Corp Compuestos heterocíclicos como inmunomoduladores
TW201808902A (zh) 2016-05-26 2018-03-16 美商英塞特公司 作為免疫調節劑之雜環化合物
PT3472167T (pt) 2016-06-20 2022-11-11 Incyte Corp Compostos heterocíclicos como imunomoduladores
WO2018005374A1 (fr) 2016-06-27 2018-01-04 Chemocentryx, Inc. Composés immunomodulateurs
US20180016260A1 (en) 2016-07-14 2018-01-18 Incyte Corporation Heterocyclic compounds as immunomodulators
MA46045A (fr) 2016-08-29 2021-04-28 Incyte Corp Composés hétérocycliques utilisés comme immunomodulateurs
TW201835049A (zh) 2016-12-22 2018-10-01 美商英塞特公司 作為免疫調節劑之雜環化合物
US20180179201A1 (en) 2016-12-22 2018-06-28 Incyte Corporation Heterocyclic compounds as immunomodulators
JP7101678B2 (ja) 2016-12-22 2022-07-15 インサイト・コーポレイション 免疫調節剤としての複素環式化合物
EP3558973B1 (fr) 2016-12-22 2021-09-15 Incyte Corporation Dérivés pyridine utilisés en tant qu'immunomodulateurs
RS63710B1 (sr) 2016-12-22 2022-11-30 Incyte Corp Derivati tetrahidro imidazo[4,5-c] piridina kao induktori internalizacije pd-l1
US11130740B2 (en) 2017-04-25 2021-09-28 Arbutus Biopharma Corporation Substituted 2,3-dihydro-1H-indene analogs and methods using same
AR111960A1 (es) 2017-05-26 2019-09-04 Incyte Corp Formas cristalinas de un inhibidor de fgfr y procesos para su preparación
AU2018306619B2 (en) 2017-07-28 2022-06-02 Chemocentryx, Inc. Immunomodulator compounds
EP3664793B1 (fr) 2017-08-08 2022-06-29 ChemoCentryx, Inc. Immunomodulateurs macrocycliques
TWI796596B (zh) 2018-02-13 2023-03-21 美商基利科學股份有限公司 Pd‐1/pd‐l1抑制劑
WO2019165043A2 (fr) 2018-02-22 2019-08-29 Chemocentryx, Inc. Indane-amines utiles en tant qu'antagonistes de pd-l1
PE20251291A1 (es) 2018-02-27 2025-05-14 Incyte Corp Imidazopirimidinas y triazolopirimidinas como inhibidores de a2a/a2b
US12083118B2 (en) 2018-03-29 2024-09-10 Arbutus Biopharma Corporation Substituted 1,1′-biphenyl compounds, analogues thereof, and methods using same
RS66699B1 (sr) 2018-03-30 2025-05-30 Incyte Corp Heterociklična jedinjenja kao imunomodulatori
KR102591947B1 (ko) 2018-04-19 2023-10-25 길리애드 사이언시즈, 인코포레이티드 Pd-1/pd-l1 억제제
WO2019213544A2 (fr) 2018-05-04 2019-11-07 Incyte Corporation Formes solides d'un inhibiteur de fgfr et leurs procédés de préparation
KR20210018264A (ko) 2018-05-04 2021-02-17 인사이트 코포레이션 Fgfr 억제제의 염
TW202425987A (zh) 2018-05-11 2024-07-01 美商英塞特公司 作為免疫調節劑之雜環化合物
JP7391046B2 (ja) 2018-05-18 2023-12-04 インサイト・コーポレイション A2a/a2b阻害剤としての縮合ピリミジン誘導体
US11161850B2 (en) 2018-07-05 2021-11-02 Incyte Corporation Fused pyrazine derivatives as A2A / A2B inhibitors
MX2021000100A (es) 2018-07-13 2021-03-25 Gilead Sciences Inc Inhibidores de muerte programada-1 (pd-1)/ ligando de muerte programada 1 (pd-l1).
US11066404B2 (en) 2018-10-11 2021-07-20 Incyte Corporation Dihydropyrido[2,3-d]pyrimidinone compounds as CDK2 inhibitors
JP7158577B2 (ja) 2018-10-24 2022-10-21 ギリアード サイエンシーズ, インコーポレイテッド Pd-1/pd-l1阻害剤
US11596692B1 (en) 2018-11-21 2023-03-07 Incyte Corporation PD-L1/STING conjugates and methods of use
TWI829857B (zh) 2019-01-29 2024-01-21 美商英塞特公司 作為a2a / a2b抑制劑之吡唑并吡啶及三唑并吡啶
WO2020168197A1 (fr) 2019-02-15 2020-08-20 Incyte Corporation Composés de pyrrolo[2,3-d]pyrimidinone en tant qu'inhibiteurs de cdk2
EA202192260A1 (ru) 2019-02-15 2021-12-17 Инсайт Корпорейшн Биомаркеры циклин-зависимой киназы 2 и их применение
US11472791B2 (en) 2019-03-05 2022-10-18 Incyte Corporation Pyrazolyl pyrimidinylamine compounds as CDK2 inhibitors
US11628162B2 (en) 2019-03-08 2023-04-18 Incyte Corporation Methods of treating cancer with an FGFR inhibitor
WO2020205560A1 (fr) 2019-03-29 2020-10-08 Incyte Corporation Composés sulfonylamides utilisés comme inhibiteurs de la cdk2
WO2020223558A1 (fr) 2019-05-01 2020-11-05 Incyte Corporation Composés aminés tricycliques en tant qu'inhibiteurs de cdk2
US11440914B2 (en) 2019-05-01 2022-09-13 Incyte Corporation Tricyclic amine compounds as CDK2 inhibitors
BR112021022659A2 (pt) 2019-05-15 2022-03-29 Chemocentryx Inc Compostos triarílicos para o tratamento de doenças pd-l1
MA55325A (fr) 2019-06-20 2022-04-27 Chemocentryx Inc Composés pour le traitement de maladies pd-l1
WO2021007269A1 (fr) 2019-07-09 2021-01-14 Incyte Corporation Hétérocycles bicycliques en tant qu'inhibiteurs de fgfr
AU2020310897B2 (en) 2019-07-10 2025-07-17 Chemocentryx, Inc. Indanes as PD-L1 inhibitors
TW202115059A (zh) 2019-08-09 2021-04-16 美商英塞特公司 Pd—1/pd—l1抑制劑之鹽
EP4013750A1 (fr) 2019-08-14 2022-06-22 Incyte Corporation Composés imidazolyl-pyrimidinylamines utilisés comme inhibiteurs de la cdk2
JP7559059B2 (ja) 2019-09-30 2024-10-01 インサイト・コーポレイション 免疫調節剤としてのピリド[3,2-d]ピリミジン化合物
WO2021067374A1 (fr) 2019-10-01 2021-04-08 Incyte Corporation Hétérocycles bicycliques en tant qu'inhibiteurs de fgfr
GEAP202516803A (en) 2019-10-11 2025-10-10 Incyte Corp Bicyclic amines as cdk2 inhibitors
EP4045151A1 (fr) 2019-10-14 2022-08-24 Incyte Corporation Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr
US11566028B2 (en) 2019-10-16 2023-01-31 Incyte Corporation Bicyclic heterocycles as FGFR inhibitors
AU2020368392B2 (en) 2019-10-16 2026-01-08 Chemocentryx, Inc. Heteroaryl-biphenyl amines for the treatment of PD-L1 diseases
CR20220215A (es) 2019-10-16 2022-09-14 Chemocentryx Inc Heteroaril bifenil amidas para el tratamiento de enfermedades relacionadas con el ligando pd-l1
PH12022551136A1 (en) * 2019-11-11 2023-10-09 Incyte Corp Salts and crystalline forms of a pd-1/pd-l1 inhibitor
WO2021113479A1 (fr) 2019-12-04 2021-06-10 Incyte Corporation Hétérocycles tricycliques en tant qu'inhibiteurs de fgfr
IL293001A (en) 2019-12-04 2022-07-01 Incyte Corp Derivatives of fgfr repressors
JP2023509155A (ja) * 2020-01-03 2023-03-07 上▲海▼翰森生物医▲薬▼科技有限公司 ビフェニル系誘導体阻害剤、その調製方法及び使用
AU2020417813A1 (en) 2020-01-03 2022-08-25 Incyte Corporation Combination therapy comprising A2A/A2B and PD-1/PD-L1 inhibitors
JP7387208B2 (ja) * 2020-01-07 2023-11-28 アビスコ セラピューティクス カンパニー リミテッド ビフェニル基フッ素置換二重結合誘導体、その製造方法と薬学的な応用
US12012409B2 (en) 2020-01-15 2024-06-18 Incyte Corporation Bicyclic heterocycles as FGFR inhibitors
CN115697343A (zh) 2020-03-06 2023-02-03 因赛特公司 包含axl/mer和pd-1/pd-l1抑制剂的组合疗法
WO2021211864A1 (fr) 2020-04-16 2021-10-21 Incyte Corporation Inhibiteurs de kras tricycliques fusionnés
US11739102B2 (en) 2020-05-13 2023-08-29 Incyte Corporation Fused pyrimidine compounds as KRAS inhibitors
WO2021254005A1 (fr) * 2020-06-17 2021-12-23 上海和誉生物医药科技有限公司 Immunosuppresseur, son procédé de préparation et son utilisation
WO2022047093A1 (fr) 2020-08-28 2022-03-03 Incyte Corporation Composés d'imidazole vinylique en tant qu'inhibiteurs de kras
CN116940567A (zh) * 2020-09-02 2023-10-24 斯克里普斯研究学院 干扰素基因刺激物sting的激动剂
CN114249726A (zh) * 2020-09-21 2022-03-29 深圳微芯生物科技股份有限公司 联苯类化合物、其制备方法及应用
US11767320B2 (en) 2020-10-02 2023-09-26 Incyte Corporation Bicyclic dione compounds as inhibitors of KRAS
WO2022089511A1 (fr) 2020-10-29 2022-05-05 深圳微芯生物科技股份有限公司 Composé biphényle utilisé en tant qu'immunomodulateur, son procédé de préparation et son application
TW202233616A (zh) 2020-11-06 2022-09-01 美商英塞特公司 用於製備pd-1/pd-l1抑制劑以及其鹽及結晶形式之方法
TW202233615A (zh) 2020-11-06 2022-09-01 美商英塞特公司 Pd—1/pd—l1抑制劑之結晶形式
US11780836B2 (en) 2020-11-06 2023-10-10 Incyte Corporation Process of preparing a PD-1/PD-L1 inhibitor
JP2024502005A (ja) 2020-12-29 2024-01-17 インサイト・コーポレイション A2a/a2b阻害剤、pd-1/pd-l1阻害剤、及び抗cd73抗体を含む併用療法
CN116710460B (zh) * 2021-01-18 2025-09-19 上海齐鲁制药研究中心有限公司 联苯衍生物及其应用
AU2022214735A1 (en) 2021-02-01 2023-08-31 Shenzhen Chipscreen Biosciences, Co., Ltd. Biphenyl compound as immunomodulator, preparation method therefor and use thereof
JP2024513575A (ja) 2021-04-12 2024-03-26 インサイト・コーポレイション Fgfr阻害剤及びネクチン-4標的化剤を含む併用療法
TW202313610A (zh) 2021-06-09 2023-04-01 美商英塞特公司 作為fgfr抑制劑之三環雜環
WO2022261160A1 (fr) 2021-06-09 2022-12-15 Incyte Corporation Hétérocycles tricycliques en tant qu'inhibiteurs de fgfr
US11981671B2 (en) 2021-06-21 2024-05-14 Incyte Corporation Bicyclic pyrazolyl amines as CDK2 inhibitors
PE20241127A1 (es) 2021-07-07 2024-05-24 Incyte Corp Compuestos triciclicos como inhibidores de kras
JP2024529347A (ja) 2021-07-14 2024-08-06 インサイト・コーポレイション Krasの阻害剤としての三環式化合物
WO2023034290A1 (fr) 2021-08-31 2023-03-09 Incyte Corporation Composés de naphtyridine en tant qu'inhibiteurs de kras
WO2023049697A1 (fr) 2021-09-21 2023-03-30 Incyte Corporation Composés hétéro-tricycliques utilisés en tant qu'inhibiteurs de kras
US20230149409A1 (en) * 2021-09-24 2023-05-18 Incyte Corporation Treatment of human papillomavirus-associated cancers by pd-l1 inhibitors
JP2024537824A (ja) 2021-10-01 2024-10-16 インサイト・コーポレイション ピラゾロキノリンkras阻害剤
WO2023064857A1 (fr) 2021-10-14 2023-04-20 Incyte Corporation Composés de quinoléine utiles en tant qu'inhibiteurs de kras
CN114209815B (zh) * 2021-11-22 2024-04-26 山东大学 一种药物组合物及其制备方法和应用
EP4436578A1 (fr) 2021-11-22 2024-10-02 Incyte Corporation Polythérapie comprenant un inhibiteur de fgfr et un inhibiteur de kras
US11976073B2 (en) 2021-12-10 2024-05-07 Incyte Corporation Bicyclic amines as CDK2 inhibitors
WO2023107705A1 (fr) 2021-12-10 2023-06-15 Incyte Corporation Amines bicycliques utilisées comme inhibiteurs de cdk12
CN118660889A (zh) 2021-12-22 2024-09-17 因赛特公司 Fgfr抑制剂的盐和固体形式以及其制备方法
CN118382617A (zh) * 2022-03-07 2024-07-23 上海和誉生物医药科技有限公司 一种全对称联苯基衍生物及其制备方法和应用
WO2023207933A1 (fr) * 2022-04-26 2023-11-02 深圳微芯生物科技股份有限公司 Forme cristalline de composé biphényle utilisée en tant qu'immunomodulateur et son procédé de préparation
TW202346308A (zh) * 2022-04-26 2023-12-01 大陸商深圳微芯生物科技股份有限公司 作為免疫調節劑的聯苯類化合物的鹽型、晶型及其製備方法
PE20250927A1 (es) 2022-06-08 2025-04-02 Incyte Corp Compuestos triciclicos de triazolo como inhibidores de dgk
WO2024015731A1 (fr) 2022-07-11 2024-01-18 Incyte Corporation Composés tricycliques fusionnés en tant qu'inhibiteurs de mutants kras g12v
US20240217989A1 (en) 2022-11-18 2024-07-04 Incyte Corporation Heteroaryl Fluoroalkenes As DGK Inhibitors
AR131101A1 (es) 2023-01-12 2025-02-19 Incyte Corp Heteroarilfluoroalquenos como inhibidores de dgk
WO2024196989A1 (fr) * 2023-03-20 2024-09-26 University Of Central Florida Research Foundation, Inc. Thérapie antipaludique
WO2024220645A1 (fr) 2023-04-18 2024-10-24 Incyte Corporation Inhibiteurs de 2-azabicyclo [2.2.1] heptane kras
US20240390340A1 (en) 2023-04-18 2024-11-28 Incyte Corporation Pyrrolidine kras inhibitors
US20250066363A1 (en) 2023-08-24 2025-02-27 Incyte Corporation Bicyclic DGK Inhibitors
WO2025080593A1 (fr) 2023-10-09 2025-04-17 Incyte Corporation Polythérapie utilisant un inhibiteur de kras g12d et un inhibiteur de pd-1 ou un inhibiteur de pd-l1
WO2025096738A1 (fr) 2023-11-01 2025-05-08 Incyte Corporation Inhibiteurs de kras
TW202523667A (zh) 2023-12-05 2025-06-16 美商英塞特公司 作為dgk抑制劑之三環三唑并化合物
WO2025122695A1 (fr) 2023-12-06 2025-06-12 Incyte Corporation Polythérapie comprenant des inhibiteurs de dgk et des inhibiteurs de pd-1/pd-l1
US20250195536A1 (en) 2023-12-13 2025-06-19 Incyte Corporation Bicyclooctane kras inhibitors

Family Cites Families (366)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3272781A (en) 1963-08-07 1966-09-13 American Potash & Chem Corp Boroureas of phosphinoborine polymers
FR1425700A (fr) 1965-02-22 1966-01-24 Basf Ag Composés formant des complexes métalliques et procédé pour les préparer et les utiliser
US4208328A (en) 1978-04-27 1980-06-17 General Electric Company Alkyl 3,5-dihydroxy-4-(2-benzothiazolyl)benzoates
US4789711A (en) 1986-12-02 1988-12-06 Ciba-Geigy Corporation Multifunctional epoxide resins
JPH0611031Y2 (ja) 1988-02-27 1994-03-23 タマパック株式会社 ゴルフ用パッティンググリーン
DE3828535A1 (de) 1988-08-23 1990-03-08 Basf Ag Benzimidazol-2-carbonsaeureanilide, ihre verwendung als lichtschutzmittel fuer organisches material und mit diesen aniliden stabilisiertes organisches material
US5077164A (en) 1989-06-21 1991-12-31 Minolta Camera Kabushiki Kaisha Photosensitive member containing an azo dye
DE69421982T2 (de) 1993-09-20 2000-03-30 Fuji Photo Film Co., Ltd. Positiv arbeitende Photoresistzusammensetzung
JP3461397B2 (ja) 1995-01-11 2003-10-27 富士写真フイルム株式会社 ポジ型フオトレジスト組成物
WO1998027108A2 (fr) 1996-12-16 1998-06-25 Fujisawa Pharmaceutical Co., Ltd. Nouveaux composes amide
JPH10316853A (ja) 1997-05-15 1998-12-02 Sumitomo Bakelite Co Ltd 半導体多層配線用層間絶縁膜樹脂組成物及び該絶縁膜の製造方法
EP1019391A1 (fr) 1997-10-02 2000-07-19 Merck & Co. Inc. Inhibiteurs de la prenyl-proteine transferase
AU2745899A (en) 1998-03-05 1999-09-20 Nissan Chemical Industries Ltd. Anilide compounds and herbicide
JP2000128984A (ja) 1998-10-28 2000-05-09 Sumitomo Bakelite Co Ltd ポリベンゾオキサゾール前駆体及び樹脂
JP2000128986A (ja) 1998-10-28 2000-05-09 Sumitomo Bakelite Co Ltd ポリベンゾオキサゾール前駆体及びポリベンゾオキサゾール
JP2000128987A (ja) 1998-10-28 2000-05-09 Sumitomo Bakelite Co Ltd ポリベンゾオキサゾール前駆体及びポリベンゾオキサゾール
US6297351B1 (en) 1998-12-17 2001-10-02 Sumitomo Bakelite Company Limited Polybenzoxazole resin and precursor thereof
UA70976C2 (uk) 1998-12-18 2004-11-15 Аксіз Фармасьютікелз, Інк. (гетеро)арилбіциклічні гетероарильні похідні, їх одержання та використання як інгібіторів протеаз
JP2000212281A (ja) 1999-01-27 2000-08-02 Sumitomo Bakelite Co Ltd ポリベンゾオキサゾ―ル前駆体及びポリベンゾオキサゾ―ル樹脂
WO2001007409A1 (fr) 1999-07-23 2001-02-01 Astrazeneca Uk Limited Derives de carbazole et leur utilisation en tant que ligands du recepteur de neuropeptide y5
JP2001114893A (ja) 1999-10-15 2001-04-24 Sumitomo Bakelite Co Ltd ポリベンゾオキサゾール樹脂およびその前駆体
US6372907B1 (en) 1999-11-03 2002-04-16 Apptera Corporation Water-soluble rhodamine dye peptide conjugates
JP2001163975A (ja) 1999-12-03 2001-06-19 Sumitomo Bakelite Co Ltd ポリベンゾオキサゾール樹脂及びその前駆体
SK13752001A3 (sk) 1999-12-27 2002-07-02 Japan Tobacco, Inc. Zlúčeniny s fúzovanými kruhmi a ich použitie ako liečiv
AU2001240542A1 (en) 2000-02-01 2001-08-14 Basf Aktiengesellschaft Heterocyclic compounds and their use as parp inhibitors
US6521618B2 (en) 2000-03-28 2003-02-18 Wyeth 3-cyanoquinolines, 3-cyano-1,6-naphthyridines, and 3-cyano-1,7-naphthyridines as protein kinase inhibitors
AU2001249679A1 (en) 2000-03-31 2001-10-15 Ortho-Mcneil Pharmaceutical, Inc. Phenyl-substituted imidazopyridines
WO2001081312A2 (fr) 2000-04-24 2001-11-01 Merck Frosst Canada & Co. Methode de traitement se basant sur l'utilisation de derives de phenyle et de biaryle comme inhibiteurs de prostaglandine e
KR100786927B1 (ko) 2000-06-28 2007-12-17 스미스클라인비이참피이엘시이 습식 분쇄방법
WO2002014321A1 (fr) 2000-08-11 2002-02-21 The Regents Of The University Of California Utilisation d'inhibiteurs de stat-6 comme agents therapeutiques
EP1343785A2 (fr) 2000-12-13 2003-09-17 Basf Aktiengesellschaft Utilisation d'imidazoazines substituees, nouvelles imidazoazines, procede permettant de les produire et agents les contenant
WO2002048147A2 (fr) 2000-12-15 2002-06-20 Glaxo Group Limited Composes therapeutiques
SE0100567D0 (sv) 2001-02-20 2001-02-20 Astrazeneca Ab Compounds
JP2004532194A (ja) 2001-03-14 2004-10-21 エリ リリー アンド カンパニー レチノイドxレセプターモジュレータ
US7034030B2 (en) 2001-03-30 2006-04-25 Smithkline Beecham Corporation Pyralopyridines, process for their preparation and use as therapeutic compounds
EP1377575B1 (fr) 2001-04-10 2006-07-05 SmithKline Beecham Corporation Composes de pyrazolopyridine antiviraux
JP2002316966A (ja) 2001-04-19 2002-10-31 Ueno Seiyaku Oyo Kenkyusho:Kk ビナフトール誘導体およびその製法
WO2002088124A2 (fr) 2001-04-27 2002-11-07 Smithkline Beecham Corporation Composes therapeutiques
AR035543A1 (es) 2001-06-26 2004-06-16 Japan Tobacco Inc Agente terapeutico para la hepatitis c que comprende un compuesto de anillo condensado, compuesto de anillo condensado, composicion farmaceutica que lo comprende, compuestos de benzimidazol, tiazol y bifenilo utiles como intermediarios para producir dichos compuestos, uso del compuesto de anillo con
JP2005507878A (ja) 2001-09-07 2005-03-24 スミスクライン ビーチャム コーポレーション ヘルペス感染症を治療するためのピラゾロ−ピリジン類
TWI320039B (en) 2001-09-21 2010-02-01 Lactam-containing compounds and derivatives thereof as factor xa inhibitors
CA2461369A1 (fr) 2001-10-09 2003-04-17 Pharmacia & Upjohn Company Carbazoles arylsulfonyl tetrahydro et hexahydro substitues utiles comme ligands du recepteur 5-ht-6
WO2003031587A2 (fr) 2001-10-09 2003-04-17 The Regents Of The University Of California Utilisation d'inhibiteurs de stat-6 comme agents therapeutiques
CA2466279A1 (fr) 2001-11-13 2003-05-22 Dana-Farber Cancer Institute, Inc. Agents modulant l'activite de cellules immunes et procedes d'utilisation associes
JP4024579B2 (ja) 2002-01-22 2007-12-19 住友ベークライト株式会社 プラスチック光導波路用材料及び光導波路
NZ575692A (en) 2002-04-11 2009-10-30 Vertex Pharma Inhibitors of Serine Proteases, Particularly Hepatitis C Virus NS3-NS4 Protease
BR0309475A (pt) 2002-04-23 2005-03-01 Shionogi & Co Derivados de pirazolo-[1,5-a]-pirimidina e inibidores de nad(p)h oxidase que contêm os mesmos
US20060004010A1 (en) 2002-07-10 2006-01-05 Hiromu Habashita Ccr4 antagonist and medical use thereof
WO2004006906A2 (fr) 2002-07-15 2004-01-22 Combinatorx, Incorporated Methodes de traitement de neoplasmes
JP2004059761A (ja) 2002-07-30 2004-02-26 Sumitomo Bakelite Co Ltd ポリベンゾオキサゾール樹脂、その前駆体及びこれらを用いた光導波路材料並びに光導波路
JP2004091369A (ja) 2002-08-30 2004-03-25 Sumitomo Pharmaceut Co Ltd 新規ビフェニル化合物
JPWO2004035522A1 (ja) 2002-08-30 2006-02-16 株式会社 ビーエフ研究所 プリオン蛋白蓄積性疾患の診断プローブおよび治療薬ならびにプリオン蛋白の染色剤
US7153863B2 (en) 2002-10-03 2006-12-26 Smithkline Beecham Corporation Therapeutic compounds based on pyrazolopyridline derivatives
US7582630B2 (en) 2002-10-15 2009-09-01 Smithkline Beecham Corporation Pyradazine compounds as GSK-3 inhibitors
ES2367430T3 (es) 2002-12-23 2011-11-03 Wyeth Llc Anticuerpos contra pd-1 y sus usos.
KR100624406B1 (ko) 2002-12-30 2006-09-18 삼성에스디아이 주식회사 비페닐 유도체 및 이를 채용한 유기 전계 발광 소자
US7320989B2 (en) 2003-02-28 2008-01-22 Encysive Pharmaceuticals, Inc. Pyridine, pyrimidine, quinoline, quinazoline, and naphthalene urotensin-II receptor antagonists
US7078419B2 (en) 2003-03-10 2006-07-18 Boehringer Ingelheim Pharmaceuticals, Inc. Cytokine inhibitors
AR043633A1 (es) 2003-03-20 2005-08-03 Schering Corp Ligandos de receptores de canabinoides
JP4595288B2 (ja) 2003-03-25 2010-12-08 住友ベークライト株式会社 ポリベンゾオキサゾール樹脂、その前駆体及びこれらを用いた光導波路材料並びに光導波路
WO2004089940A1 (fr) 2003-04-11 2004-10-21 Glenmark Pharmaceuticals S.A. Nouveaux composes heterocycliques pour le traitement des affections inflammatoires et allergiques, leur procede de preparation et compositions pharmaceutiques les contenant
JP2005002330A (ja) 2003-05-19 2005-01-06 Sumitomo Electric Ind Ltd 光学樹脂材料、光学素子、光モジュール、フッ素化ポリマー前駆体及びフッ素化ポリマー
ES2467160T3 (es) 2003-05-19 2014-06-12 Irm Llc Compuestos y composiciones inmunosupresores
US20060183746A1 (en) 2003-06-04 2006-08-17 Currie Kevin S Certain imidazo[1,2-a]pyrazin-8-ylamines and method of inhibition of Bruton's tyrosine kinase by such compounds
US7405295B2 (en) 2003-06-04 2008-07-29 Cgi Pharmaceuticals, Inc. Certain imidazo[1,2-a]pyrazin-8-ylamines and method of inhibition of Bruton's tyrosine kinase by such compounds
US20070010573A1 (en) 2003-06-23 2007-01-11 Xianqi Kong Methods and compositions for treating amyloid-related diseases
US7393848B2 (en) 2003-06-30 2008-07-01 Cgi Pharmaceuticals, Inc. Certain heterocyclic substituted imidazo[1,2-A]pyrazin-8-ylamines and methods of inhibition of Bruton's tyrosine kinase by such compounds
WO2005007628A1 (fr) 2003-07-11 2005-01-27 Bristol-Myers Squibb Company Derives de tetrahydroquinoleine constituant des modulateurs des recepteurs des cannabinoides
WO2005004863A1 (fr) 2003-07-11 2005-01-20 Merck Patent Gmbh Benzimidazole carboxamides utilises en tant qu'inhibiteurs de la kinase raf
EP1661879A4 (fr) 2003-08-04 2006-11-29 Ono Pharmaceutical Co Compose d'ether de diphenyle, sa methode de preparation et d'utilisation
WO2005014543A1 (fr) 2003-08-06 2005-02-17 Japan Tobacco Inc. Compose a cycle condense utilise comme inhibiteur de la polymerase du vhc
US7504401B2 (en) 2003-08-29 2009-03-17 Locus Pharmaceuticals, Inc. Anti-cancer agents and uses thereof
JP4895811B2 (ja) 2003-09-11 2012-03-14 ケミア,インコーポレイテッド サイトカイン阻害剤
EP1673343A4 (fr) 2003-10-08 2008-09-10 Irm Llc Composes et compositions convenant comme inhibiteurs de proteine-kinases
EP1679309A4 (fr) 2003-10-24 2007-03-28 Ono Pharmaceutical Co Medicament antistress et usage medical correspondant
WO2005047290A2 (fr) 2003-11-11 2005-05-26 Cellular Genomics Inc. Certaines imidazo[1,2-a]pyrazin-8-ylamines, procede de fabrication et methode d'utilisation
WO2005063710A1 (fr) 2003-12-23 2005-07-14 Basf Aktiengesellschaft Anilides d'acide 3-trifluoromethylpicolinique et leur utilisation comme fongicides
EP1715867A4 (fr) 2004-02-12 2009-04-15 Merck & Co Inc Amides bipyridyles en tant que modulateurs du r cepteur-5 metabotropique du glutamate
JPWO2005077948A1 (ja) 2004-02-16 2008-01-10 第一製薬株式会社 抗真菌作用複素環化合物
GB0403864D0 (en) 2004-02-20 2004-03-24 Ucl Ventures Modulator
JP2005248082A (ja) 2004-03-05 2005-09-15 Sumitomo Electric Ind Ltd ポリベンゾオキサゾール樹脂前駆体の製造方法およびポリベンゾオキサゾール樹脂の製造方法
US7432278B2 (en) 2004-03-08 2008-10-07 The University Of North Carolina At Chapel Hill Dicationic imidazo[1,2-a]pyridines and 5,6,7,8-tetrahydro-imidazo[1,2-a]pyridines as antiprotozoal agents
AU2005221140A1 (en) 2004-03-08 2005-09-22 Amgen Inc. Therapeutic modulation of PPAR (gamma) activity
EP1761496A2 (fr) 2004-03-31 2007-03-14 Janssen Pharmaceutica N.V. Heterocycles ne comprenant pas d`imidazole utilisables comme ligands des recepteurs histamine h3
JP2005290301A (ja) 2004-04-02 2005-10-20 Sumitomo Electric Ind Ltd ポリベンゾオキサゾール樹脂前駆体の製造方法およびポリベンゾオキサゾール樹脂の製造方法
WO2005099656A2 (fr) 2004-04-06 2005-10-27 The Procter & Gamble Company Composes de teinture de la keratine, compositions de teinture de la keratine contenant ces composes et leurs utilisations
NZ550114A (en) 2004-04-20 2011-02-25 Transtech Pharma Inc Substituted thiazole and pyrimidine derivatives as melanocortin receptor modulators
DE102004021716A1 (de) 2004-04-30 2005-12-01 Grünenthal GmbH Substituierte Imidazo[1,2-a]pyridin-Verbindungen und Arzneimittel enthaltend substituierte Imidazo[1,2-a]pyridin-Verbindungen
CA2560387C (fr) 2004-05-03 2013-09-24 Boehringer Ingelheim Pharmaceuticals, Inc. Inhibiteurs de cytokines
PE20060748A1 (es) 2004-09-21 2006-10-01 Smithkline Beecham Corp Derivados de indolcarboxamida como inhibidores de quinasa ikk2
JP2008514611A (ja) 2004-09-23 2008-05-08 ワイス C型肝炎ウイルスによる感染を処置するためのカルバゾールおよびシクロペンタインドールの誘導体
US7713973B2 (en) 2004-10-15 2010-05-11 Takeda Pharmaceutical Company Limited Kinase inhibitors
AU2005304473A1 (en) 2004-11-10 2006-05-18 Cgi Pharmaceuticals, Inc. Imidazo[1 , 2-a] pyrazin-8-ylamines useful as modulators of kinase activity
DE102004054665A1 (de) 2004-11-12 2006-05-18 Bayer Cropscience Gmbh Substituierte bi- und tricyclische Pyrazol-Derivate Verfahren zur Herstellung und Verwendung als Herbizide und Pflanzenwachstumsregulatoren
AU2006218403A1 (en) 2005-03-03 2006-09-08 Sirtris Pharmaceuticals, Inc. Fused heterocyclic compounds and their use as sirtuin modulators
JP2008533032A (ja) 2005-03-10 2008-08-21 シージーアイ ファーマシューティカルズ,インコーポレイティド 或る種の置換アミド、その製造方法及び使用方法
JP2006290883A (ja) 2005-03-17 2006-10-26 Nippon Nohyaku Co Ltd 置換ヘテロ環カルボン酸アニリド誘導体、その中間体及び農園芸用薬剤並びにその使用方法
US7906522B2 (en) 2005-04-28 2011-03-15 Kyowa Hakko Kirin Co., Ltd 2-aminoquinazoline derivatives
AU2006244885B2 (en) 2005-05-09 2011-03-31 E. R. Squibb & Sons, L.L.C. Human monoclonal antibodies to programmed death 1(PD-1) and methods for treating cancer using anti-PD-1 antibodies alone or in combination with other immunotherapeutics
BRPI0610863A2 (pt) 2005-05-20 2010-08-03 Array Biopharma Inc compostos inibidores de raf e métodos para sua utilização
AU2006265108C1 (en) 2005-07-01 2013-01-17 E. R. Squibb & Sons, L.L.C. Human monoclonal antibodies to programmed death ligand 1 (PD-L1)
US20080220968A1 (en) 2005-07-05 2008-09-11 Ge Healthcare Bio-Sciences Ab [1, 2, 4] Triazolo [1, 5-A] Pyrimidine Derivatives as Chromatographic Adsorbent for the Selective Adsorption of Igg
WO2007034282A2 (fr) 2005-09-19 2007-03-29 Pfizer Products Inc. Composes de biphenylimidazole utilises comme antagonistes du recepteur du c3a
US7723336B2 (en) 2005-09-22 2010-05-25 Bristol-Myers Squibb Company Fused heterocyclic compounds useful as kinase modulators
US20070078136A1 (en) 2005-09-22 2007-04-05 Bristol-Myers Squibb Company Fused heterocyclic compounds useful as kinase modulators
EP2597087B1 (fr) 2005-10-25 2016-03-30 Shionogi&Co., Ltd. Dérivés dihydrooxazine et tétrahydropyrimidine comme inhibiteurs de BACE 1
US8518964B2 (en) 2005-11-22 2013-08-27 Merck Sharp & Dohme Corp. Tricyclic compounds useful as inhibitors of kinases
WO2007067711A2 (fr) 2005-12-08 2007-06-14 Amphora Discovery Corporation Certains types d'entites chimiques, compositions et methode de modulation de trpv1
JPWO2007069565A1 (ja) 2005-12-12 2009-05-21 小野薬品工業株式会社 二環式複素環化合物
US20090281075A1 (en) 2006-02-17 2009-11-12 Pharmacopeia, Inc. Isomeric purinones and 1h-imidazopyridinones as pkc-theta inhibitors
WO2007096764A2 (fr) 2006-02-27 2007-08-30 Glenmark Pharmaceuticals S.A. Dérivés d'hétéroaryles bicycliques en tant que modulateurs des récepteurs cannabinoïdes
JPWO2007102531A1 (ja) 2006-03-08 2009-07-23 武田薬品工業株式会社 併用薬
AU2007233709A1 (en) 2006-03-31 2007-10-11 Novartis Ag Organic compounds
EP2023919A4 (fr) 2006-05-08 2010-12-22 Molecular Neuroimaging Llc Composés et sondes amyloïdes de ceux-ci pour des utilisations thérapeutiques et en imagerie
WO2007146712A2 (fr) 2006-06-09 2007-12-21 Kemia, Inc. Thérapie à base d'inhibiteurs de cytokine
US20080280891A1 (en) 2006-06-27 2008-11-13 Locus Pharmaceuticals, Inc. Anti-cancer agents and uses thereof
EP2044061A2 (fr) 2006-07-20 2009-04-08 Mehmet Kahraman Inhibiteurs de la rho kinase à base de benzothiophène
DE102006035018B4 (de) 2006-07-28 2009-07-23 Novaled Ag Oxazol-Triplett-Emitter für OLED-Anwendungen
WO2008021745A2 (fr) 2006-08-16 2008-02-21 Itherx Pharmaceuticals, Inc. Inhibiteurs de la pénétration du virus de l'hépatite c
TWI389895B (zh) 2006-08-21 2013-03-21 Infinity Discovery Inc 抑制bcl蛋白質與結合夥伴間之交互作用的化合物及方法
WO2008027812A2 (fr) 2006-08-28 2008-03-06 Forest Laboratories Holdings Limited Dérivés d'imidazopyridine et d'imidazopyrimidine
US20100160292A1 (en) 2006-09-11 2010-06-24 Cgi Pharmaceuticals, Inc Kinase Inhibitors, and Methods of Using and Identifying Kinase Inhibitors
US7838523B2 (en) 2006-09-11 2010-11-23 Cgi Pharmaceuticals, Inc. Certain substituted amides, method of making, and method of use thereof
CN101573348A (zh) 2006-09-11 2009-11-04 矩阵实验室有限公司 作为pde-4和pde-10的抑制剂的二苯并呋喃衍生物
PE20081370A1 (es) 2006-09-11 2008-11-28 Cgi Pharmaceuticals Inc Determinadas amidas sustituidas, metodo de elaboracion y metodo de uso de las mismas
AR063706A1 (es) 2006-09-11 2009-02-11 Cgi Pharmaceuticals Inc Determinadas amidas sustituidas, el uso de las mismas para el tratamiento de enfermedades mediadas por la inhibicion de la actividad de btk y composiciones farmaceuticas que las comprenden.
FR2906250B1 (fr) 2006-09-22 2008-10-31 Sanofi Aventis Sa Derives de 2-aryl-6phenyl-imidazo(1,2-a) pyridines, leur preparation et leur application en therapeutique
EP2074107A2 (fr) 2006-10-27 2009-07-01 Wyeth a Corporation of the State of Delaware Composes tricycliques servant d'inhibiteurs des metalloproteases matricielles
HRP20130626T1 (en) 2006-11-08 2013-08-31 Bristol-Myers Squibb Company Pyridinone compounds
GB0623209D0 (en) 2006-11-21 2007-01-03 F2G Ltd Antifungal agents
WO2008064317A1 (fr) 2006-11-22 2008-05-29 University Of Medicine And Dentistry Of New Jersey Composés actifs de récepteurs opioïdes lipophiles
WO2008064318A2 (fr) 2006-11-22 2008-05-29 University Of Medicine And Dentistry Of New Jersey Composés actifs de récepteurs opioïdes périphériques
JP2010513253A (ja) 2006-12-14 2010-04-30 ベーリンガー インゲルハイム インテルナショナール ゲーエムベーハー 炎症の治療に有用なベンゾオキサゾール類
ES2415863T3 (es) 2006-12-22 2013-07-29 Incyte Corporation Heterociclos sustituidos como inhibidores de Janus Quinasas
EP1964841A1 (fr) 2007-02-28 2008-09-03 sanofi-aventis Imidazo[1,2-a]azine et son utilisation en tant que produit pharmaceutique
EP2137158A4 (fr) 2007-02-28 2012-04-18 Methylgene Inc Inhibiteurs à petite molécule de protéines arginine méthyltransférases (prmt)
EP1964840A1 (fr) 2007-02-28 2008-09-03 sanofi-aventis Imidazo[1,2-a]pyridines et leur utilisation en tant que produits pharmaceutiques
JP2008218327A (ja) 2007-03-07 2008-09-18 Hitachi Ltd 電解質、電解質膜、それを用いた膜電極接合体、燃料電池電源及び燃料電池電源システム
JP2010120852A (ja) 2007-03-09 2010-06-03 Daiichi Sankyo Co Ltd 新規なジアミド誘導体
CN101679350B (zh) 2007-03-22 2014-03-12 阿斯利康(瑞典)有限公司 用于治疗炎性疾病的喹啉衍生物
AU2008245082B8 (en) 2007-04-24 2012-09-13 Shionogi & Co., Ltd. Aminodihydrothiazine derivatives substituted with a cyclic group
JP5383483B2 (ja) 2007-04-24 2014-01-08 塩野義製薬株式会社 アルツハイマー症治療用医薬組成物
WO2008134553A1 (fr) 2007-04-26 2008-11-06 Xenon Pharmaceuticals Inc. Procédés de traitement de maladies associées aux canaux sodiques au moyen de composés bicycliques
WO2008141249A1 (fr) 2007-05-10 2008-11-20 Acadia Pharmaceuticals Inc. Imidazol (1,2-a)pyridines et composés associés à activité au niveau des récepteurs cannabinoïdes cb2
CA2691357C (fr) 2007-06-18 2014-09-23 N.V. Organon Anticorps diriges contre le recepteur humain de mort programmee pd-1
WO2009027733A1 (fr) 2007-08-24 2009-03-05 Astrazeneca Ab Dérivés de (2-pyridin-3-ylimidazo[1,2-b]pyridazin-6-yl)urée en tant qu'agents antibactériens
US8080542B2 (en) 2007-09-20 2011-12-20 Amgen, Inc. S1P receptor modulating compounds and use thereof
CL2008002793A1 (es) 2007-09-20 2009-09-04 Cgi Pharmaceuticals Inc Compuestos derivados de amidas sustituidas, inhibidores de la actividad de btk; composicion farmaceutica que los comprende; utiles en el tratamiento del cancer, trastornos oseos, enfermedades autoinmunes, entre otras
DE102007048716A1 (de) 2007-10-11 2009-04-23 Merck Patent Gmbh Imidazo[1,2-a]pyrimidinderivate
TW200932219A (en) 2007-10-24 2009-08-01 Astellas Pharma Inc Oxadiazolidinedione compound
JP2011500778A (ja) 2007-10-25 2011-01-06 アストラゼネカ・アクチエボラーグ ピリジン及びピラジン誘導体−083
US7868001B2 (en) 2007-11-02 2011-01-11 Hutchison Medipharma Enterprises Limited Cytokine inhibitors
WO2009062059A2 (fr) 2007-11-08 2009-05-14 Pharmacopeia, Inc. Purinones et 1h-imidazopyridinones isomères comme inhibiteurs de pkc-thêta
JP5489296B2 (ja) 2007-12-13 2014-05-14 メルク・シャープ・アンド・ドーム・コーポレーション Janusキナーゼの阻害剤
RU2364597C1 (ru) 2007-12-14 2009-08-20 Андрей Александрович Иващенко ГЕТЕРОЦИКЛИЧЕСКИЕ ИНГИБИТОРЫ Hh-СИГНАЛЬНОГО КАСКАДА, ЛЕКАРСТВЕННЫЕ КОМПОЗИЦИИ НА ИХ ОСНОВЕ И СПОСОБ ЛЕЧЕНИЯ ЗАБОЛЕВАНИЙ, СВЯЗАННЫХ С АББЕРАНТНОЙ АКТИВНОСТЬЮ Hh СИГНАЛЬНОЙ СИСТЕМЫ
EP2230913B1 (fr) 2007-12-19 2017-10-18 Syngenta Participations AG Composés insecticides
AU2008345225A1 (en) 2007-12-21 2009-07-09 University Of Rochester Method for altering the lifespan of eukaryotic organisms
EP2231659A4 (fr) 2007-12-21 2011-10-26 Univ Sydney Ligands de la protéine de translocation
HUE026064T2 (en) 2008-01-18 2016-05-30 Eisai R&D Man Co Ltd Condensed aminodihydrothiazine derivatives
WO2009096202A1 (fr) 2008-01-31 2009-08-06 Konica Minolta Holdings, Inc. Composé aromatique polycyclique halogéné et son procédé de production
MX2010009416A (es) 2008-02-26 2010-09-24 Novartis Ag Compuestos heterociclicos como inhibidores de cxcr2.
EP2095818A1 (fr) 2008-02-29 2009-09-02 AEterna Zentaris GmbH Utilisation d'antagonistes LHRH dans des doses n'impliquant pas de castration
EP2262837A4 (fr) 2008-03-12 2011-04-06 Merck Sharp & Dohme Protéines de liaison avec pd-1
FR2928921B1 (fr) 2008-03-21 2010-04-23 Sanofi Aventis Derives polysubstitues de 2-aryl-6-phenyl-imidazo°1,2-a!pyridines, leur preparation et leur application en therapeutique
FR2928922B1 (fr) 2008-03-21 2010-04-23 Sanofi Aventis Derives de 2-aryl-6-phenyl-imidazo°1,2-a!pyridines polysubstitues, leur preparation et leur application en therapeutique
FR2928924B1 (fr) 2008-03-21 2010-04-23 Sanofi Aventis Derives polysubstitues de 6-heteroaryle-imidazo°1,2-a! pyridines, leur preparation et leur application en therapeutique
EP2271646A1 (fr) 2008-03-31 2011-01-12 Takeda Pharmaceutical Company Limited Inhibiteurs de kinase 1 de régulation de signal d'apoptose
KR101034351B1 (ko) 2008-05-14 2011-05-16 한국화학연구원 신규 벤즈옥사졸로 치환된 피리딘 유도체 또는 이의약학적으로 허용가능한 염, 이의 제조방법 및 이를유효성분으로 함유하는 이상세포 성장 질환의 예방 및치료용 약학적 조성물
JP5774982B2 (ja) 2008-05-19 2015-09-09 サノビオン ファーマシューティカルズ インクSunovion Pharmaceuticals Inc. イミダゾ[1,2−a]ピリジン化合物
MX2010012961A (es) 2008-05-29 2011-03-03 Sirtris Pharmaceuticals Inc Star Imidazopiridina y analogos relacionados como moduladores de sirtuina.
EP2280946B1 (fr) 2008-06-05 2016-02-10 Glaxo Group Limited Dérivés de 4-carboxamide indazole utiles en tant qu'inhibiteurs de p13 kinases
US8476430B2 (en) 2008-07-24 2013-07-02 Bristol-Myers Squibb Company Fused heterocyclic compounds useful as kinase modulators
US9540322B2 (en) 2008-08-18 2017-01-10 Yale University MIF modulators
US9643922B2 (en) 2008-08-18 2017-05-09 Yale University MIF modulators
JP2011231017A (ja) 2008-09-09 2011-11-17 Nissan Chem Ind Ltd 光学活性エポキシ化合物及び光学活性スルホキシド化合物の製造方法、並びに該方法に用いる配位子、錯体及び該錯体の製造方法
PL2342226T3 (pl) 2008-09-26 2017-01-31 Dana-Farber Cancer Institute, Inc. Ludzkie przeciwciała anty-PD-1, PD-L1 i PD-L2 oraz ich zastosowania
US8598174B2 (en) 2008-11-12 2013-12-03 Genetech, Inc. Pyridazinones, method of making, and method of use thereof
WO2010064020A1 (fr) 2008-12-04 2010-06-10 Proximagen Ltd. Composés imidazopyridines
PT2376535T (pt) 2008-12-09 2017-06-23 Hoffmann La Roche Anticorpos anti-pd-l1 e a sua utilização para a melhoria do funcionamento das células t
ES2490867T3 (es) 2008-12-19 2014-09-04 Bristol-Myers Squibb Company Inhibidores de carbazol y carbolina quinasas
AR074830A1 (es) 2008-12-19 2011-02-16 Cephalon Inc Pirrolotriazinas como inhibidores de alk y jak2
SG171815A1 (en) 2008-12-19 2011-07-28 Bristol Myers Squibb Co Carbazole carboxamide compounds useful as kinase inhibitors
JP5624275B2 (ja) 2008-12-22 2014-11-12 ユー・ディー・シー アイルランド リミテッド 有機電界発光素子
RU2505540C2 (ru) 2008-12-23 2014-01-27 Эббви Инк. Антивирусные соединения
WO2010074284A1 (fr) 2008-12-26 2010-07-01 味の素株式会社 Composé de pyrazolopyrimidine
EP3192811A1 (fr) 2009-02-09 2017-07-19 Université d'Aix-Marseille Anticorps pd-1 et pd-l1 et leurs utilisations
JP2010202530A (ja) 2009-02-27 2010-09-16 Tokyo Institute Of Technology 含ヘテロ芳香族化合物および光学材料
KR20100101055A (ko) 2009-03-07 2010-09-16 주식회사 메디젠텍 세포핵에서 세포질로의 gsk3의 이동을 억제하는 화합물을 함유하는 세포핵에서 세포질로의 gsk3 이동 관련 질환의 치료 또는 예방용 약학적 조성물
CN104030987B (zh) 2009-04-02 2017-04-12 默克雪兰诺有限公司 二氢乳清酸脱氢酶抑制剂
KR20120034613A (ko) 2009-04-16 2012-04-12 센트로 내셔널 드 인베스티가시오네스 온콜로지카스 (씨엔아이오) 키나아제 억제제로서 사용을 위한 이미다조피라진
US8338441B2 (en) 2009-05-15 2012-12-25 Gilead Sciences, Inc. Inhibitors of human immunodeficiency virus replication
EP2448410A4 (fr) 2009-06-30 2013-12-18 Siga Technologies Inc Traitement et prévention d'infections par le virus de la dengue
US8993604B2 (en) 2009-06-30 2015-03-31 Siga Technologies, Inc. Treatment and prevention of dengue virus infections
TWI491606B (zh) 2009-07-13 2015-07-11 Gilead Sciences Inc 調節細胞凋亡信號之激酶的抑制劑
JP2011057661A (ja) 2009-08-14 2011-03-24 Bayer Cropscience Ag 殺虫性カルボキサミド類
UA108363C2 (uk) 2009-10-08 2015-04-27 Похідні імінотіадіазиндіоксиду як інгібітори bace, композиція на їх основі і їх застосування
US9095596B2 (en) 2009-10-15 2015-08-04 Southern Research Institute Treatment of neurodegenerative diseases, causation of memory enhancement, and assay for screening compounds for such
DK2488525T3 (en) 2009-10-16 2018-08-06 Melinta Therapeutics Inc ANTIMICROBIAL COMPOUNDS AND PROCEDURES FOR PREPARING AND USING THEREOF
WO2011050245A1 (fr) 2009-10-23 2011-04-28 Yangbo Feng Hétéroaryles bicycliques formant inhibiteurs de la kinase
EP2504028A4 (fr) 2009-11-24 2014-04-09 Amplimmune Inc Inhibition simultanée de pd-l1/pd-l2
JPWO2011078221A1 (ja) 2009-12-24 2013-05-09 味の素株式会社 イミダゾピリダジン化合物
US20130022629A1 (en) 2010-01-04 2013-01-24 Sharpe Arlene H Modulators of Immunoinhibitory Receptor PD-1, and Methods of Use Thereof
WO2011097607A1 (fr) 2010-02-08 2011-08-11 Southern Research Institute Traitement antiviral et dosage pour cribler des antiviraux
TW201136919A (en) 2010-03-02 2011-11-01 Merck Sharp & Amp Dohme Corp Inhibitors of hepatitis C virus NS5B polymerase
WO2011109254A1 (fr) 2010-03-04 2011-09-09 Merck Sharp & Dohme Corp. Inhibiteurs de catéchol o-méthyl transférase et utilisation associée dans le traitement de troubles psychotiques
KR101732212B1 (ko) 2010-03-18 2017-05-02 재단법인 한국파스퇴르연구소 항감염성 화합물
US8410117B2 (en) 2010-03-26 2013-04-02 Hoffmann-La Roche Inc. Imidazopyrimidine derivatives
US8685969B2 (en) 2010-06-16 2014-04-01 Bristol-Myers Squibb Company Carboline carboxamide compounds useful as kinase inhibitors
US9163087B2 (en) 2010-06-18 2015-10-20 The Brigham And Women's Hospital, Inc. Bi-specific antibodies against TIM-3 and PD-1 for immunotherapy in chronic immune conditions
US8907053B2 (en) 2010-06-25 2014-12-09 Aurigene Discovery Technologies Limited Immunosuppression modulating compounds
CN102295642B (zh) 2010-06-25 2016-04-06 中国人民解放军军事医学科学院毒物药物研究所 2-芳基咪唑并[1,2-a]吡啶-3-乙酰胺衍生物、其制备方法及用途
EP2402345A1 (fr) 2010-06-29 2012-01-04 Basf Se Composés pyrazoliques bicycliques condenses
CN101891895B (zh) 2010-07-28 2011-11-30 南京航空航天大学 基于桥联双水杨醛结构的苯并噻唑类金属配位聚合物及其制法及应用
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
US8633200B2 (en) 2010-09-08 2014-01-21 Bristol-Myers Squibb Company Inhibitors of human immunodeficiency virus replication
CN101993415B (zh) 2010-09-15 2013-08-14 北京韩美药品有限公司 作为Hedgehog通路抑制剂的化合物以及包含该化合物的药物组合物及其应用
US8921381B2 (en) 2010-10-04 2014-12-30 Baruch S. Blumberg Institute Inhibitors of secretion of hepatitis B virus antigens
WO2012052745A1 (fr) 2010-10-21 2012-04-26 Centro Nacional De Investigaciones Oncológicas (Cnio) Combinaisons d'inhibiteurs de pi3k avec un second agent antitumoral
EP2444084A1 (fr) 2010-10-21 2012-04-25 Centro Nacional de Investigaciones Oncológicas (CNIO) Utilisation d'inhibiteurs de PI3K pour le traitement de l'obésité
US20140243324A1 (en) 2010-11-18 2014-08-28 Ligand Pharmaceuticals Incorporated Use of hematopoietic growth factor mimetics
UY33808A (es) 2010-12-17 2012-07-31 Syngenta Participations Ag Compuestos insecticidas
TWI617559B (zh) 2010-12-22 2018-03-11 江蘇恆瑞醫藥股份有限公司 2-芳基咪唑并[1,2-b]嗒.2-苯基咪唑并[1,2-a]吡啶,和2-苯基咪唑并[1,2-a]吡衍生物
PE20140471A1 (es) 2011-01-04 2014-04-13 Novartis Ag Moduladores de la via del complemento y usos de los mismos
CA2825098C (fr) 2011-01-27 2020-03-10 Universite De Montreal Pyrazolopyridine et derives de pyrazolopyrimidine en tant que modulateurs du recepteur de la melanocortine-4
US8921368B2 (en) 2011-03-17 2014-12-30 Bristol-Myers Squibb Company Pyrrolopyridazine JAK3 inhibitors and their use for the treatment of inflammatory and autoimmune diseases
US9464065B2 (en) 2011-03-24 2016-10-11 The Scripps Research Institute Compounds and methods for inducing chondrogenesis
US9499502B2 (en) 2011-04-13 2016-11-22 Merck Sharp & Dohme Corp. 5-substituted iminothiazines and their mono- and dioxides as BACE inhibitors, compositions, and their use
CN102796103A (zh) 2011-05-23 2012-11-28 南京英派药业有限公司 6-(芳基甲酰)咪唑并[1,2-a]嘧啶和6-(芳基甲酰)[1,2,4]三唑并[4,3-a]嘧啶作为Hedgehog抑制剂及其应用
DK2713722T3 (en) 2011-05-31 2017-07-03 Celgene Int Ii Sarl Newly known GLP-1 receptor stabilizers and modulators
GB201109763D0 (en) 2011-06-10 2011-07-27 Ucl Business Plc Compounds
WO2012175991A1 (fr) 2011-06-24 2012-12-27 Pharminox Limited Composés pentacycliques fusionnés anti-prolifératifs
CN103732596B (zh) 2011-07-08 2016-06-01 诺华股份有限公司 吡咯并嘧啶衍生物
EP2548877A1 (fr) 2011-07-19 2013-01-23 MSD Oss B.V. Dérivés de 4-(pyridine condensée à 5 chaînons)benzamide comme inhibiteurs de BTK
WO2013033901A1 (fr) 2011-09-08 2013-03-14 Merck Sharp & Dohme Corp. Dérivés benzofuranes substitués par un hétérocycle et leurs procédés d'utilisation pour le traitement de maladies virales
WO2013040528A1 (fr) 2011-09-16 2013-03-21 Microbiotix, Inc. Composés antimicrobiens
WO2013043521A1 (fr) 2011-09-22 2013-03-28 Merck Sharp & Dohme Corp. Composés pyrazolopyridyle à utiliser en tant qu'inhibiteurs de l'aldostérone synthase
JP6040677B2 (ja) 2011-09-29 2016-12-07 東洋インキScホールディングス株式会社 太陽電池封止材用樹脂組成物
KR20140084146A (ko) 2011-10-13 2014-07-04 노파르티스 아게 신규 옥사진 유도체 및 질환의 치료에서의 그의 용도
CA2852939A1 (fr) 2011-10-20 2013-04-25 Glaxosmithkline Llc Aza-heterocycles bicycliques substitues et analogues en tant que modulateurs des sirtuines
JP2014530850A (ja) 2011-10-21 2014-11-20 トレント・ファーマシューティカルズ・リミテッドTorrent Pharmaceuticals Limited Gpbar1受容体調節剤としての新規置換イミダゾピリミジン
WO2013120040A1 (fr) 2012-02-10 2013-08-15 Children's Medical Center Corporation Inhibition d'une voie ciblée pour améliorer la structure, le fonctionnement et l'activité musculaires dans la dystrophie musculaire
US9034882B2 (en) 2012-03-05 2015-05-19 Bristol-Myers Squibb Company Inhibitors of human immunodeficiency virus replication
IN2014MN01897A (fr) 2012-03-09 2015-07-10 Carna Biosciences Inc
RU2711077C9 (ru) 2012-03-15 2020-08-11 Селджен Кар Ллс Соли ингибитора киназы рецептора эпидермального фактора роста
SG11201401189WA (en) 2012-04-20 2014-09-26 Gilead Sciences Inc Benzothiazol- 6 -yl acetic acid derivatives and their use for treating an hiv infection
WO2013157021A1 (fr) 2012-04-20 2013-10-24 Advinus Therapeutics Limited Composés bicycliques, compositions et applications médicinales de ceux-ci
WO2013163404A1 (fr) 2012-04-27 2013-10-31 The Uab Research Foundation Traitement d'infections virales avec arn viraux traduits par un mécanisme non médié par l'ires
WO2013191113A1 (fr) 2012-06-18 2013-12-27 住友化学株式会社 Composé hétérocyclique fusionné
WO2014007228A1 (fr) 2012-07-03 2014-01-09 小野薬品工業株式会社 Composé ayant une activité agoniste sur un récepteur de la somatostatine, et leur utilisation à des fins médicales
JP6259823B2 (ja) 2012-07-13 2018-01-10 ユーシービー バイオファルマ エスピーアールエル Tnf活性の調節物質としてのイミダゾピリジン誘導体
GB201212513D0 (en) 2012-07-13 2012-08-29 Ucb Pharma Sa Therapeutic agents
JP2015178457A (ja) 2012-07-25 2015-10-08 杏林製薬株式会社 ピラゾロピリジン誘導体、またはその薬理学的に許容される塩
EP2892899B1 (fr) 2012-09-06 2018-03-21 Bristol-Myers Squibb Company Inhibiteurs de jak3 de type imidazopyridazine et leur utilisation pour le traitement de maladies inflammatoires et auto-immunes
BR112015006019B1 (pt) 2012-09-26 2021-01-05 F. Hoffmann-La Roche Ag composto e uso de um composto
WO2014061693A1 (fr) 2012-10-17 2014-04-24 塩野義製薬株式会社 Nouveau dérivé carbocyclique non aromatique ou hétérocyclique non aromatique
US9163027B2 (en) 2012-11-21 2015-10-20 Stategics, Inc. Substituted triazolo-pyrimidine compounds for modulating cell proliferation differentiation and survival
JP6037804B2 (ja) 2012-12-03 2016-12-07 富士フイルム株式会社 ガス分離膜
AU2014207691B2 (en) 2013-01-15 2018-08-30 Incyte Holdings Corporation Thiazolecarboxamides and pyridinecarboxamide compounds useful as Pim kinase inhibitors
CN104968660A (zh) 2013-01-22 2015-10-07 霍夫曼-拉罗奇有限公司 作为bace1抑制剂的氟-[1,3]噁嗪类化合物
CN103933036B (zh) 2013-01-23 2017-10-13 中国人民解放军军事医学科学院毒物药物研究所 2‑芳基咪唑并[1,2‑α]吡啶‑3‑乙酰胺衍生物在制备防治PTSD的药物中的用途
WO2014121085A1 (fr) 2013-01-31 2014-08-07 Thomas Jefferson University Protéines de fusion à base de pd-l1 et pd-l2 et leurs utilisations
AU2014221799B2 (en) 2013-02-27 2017-09-28 Mochida Pharmaceutical Co., Ltd. Novel pyrazole derivative
KR20150124985A (ko) 2013-03-08 2015-11-06 암젠 인크 베타-세크레타제 억제제로서 퍼플루오르화된 사이클로프로필 융합된 1,3-옥사진-2-아민 화합물 및 그의 사용 방법
JP2016516399A (ja) 2013-03-13 2016-06-09 オーストラリアン ニュークリア サイエンス アンド テクノロジー オーガニゼーション 非機能性tspo遺伝子を有するトランスジェニック非ヒト生物
CN104045552B (zh) 2013-03-13 2019-06-11 江苏先声药业有限公司 作为神经保护剂的药用化合物
ES2705247T3 (es) 2013-03-14 2019-03-22 Univ Columbia 4-fenilpiperidinas, su preparación y uso
US9527842B2 (en) 2013-03-14 2016-12-27 VIIV Healthcare UK (No.5) Limited Inhibitors of human immunodeficiency virus replication
CA2906086A1 (fr) 2013-03-14 2014-09-25 Celtaxsys, Inc. Inhibiteurs de la leucotriene a4 hydrolase
PE20151719A1 (es) 2013-03-14 2015-11-19 Curadev Pharma Private Ltd Inhibidores de la ruta de quinurenina
US9308236B2 (en) 2013-03-15 2016-04-12 Bristol-Myers Squibb Company Macrocyclic inhibitors of the PD-1/PD-L1 and CD80(B7-1)/PD-L1 protein/protein interactions
BR112015021983B1 (pt) 2013-03-15 2022-03-03 Plexxikon, Inc Compostos heterocíclicos, composições farmacêuticas que os compreendem e usos dos mesmos
WO2014181287A1 (fr) 2013-05-09 2014-11-13 Piramal Enterprises Limited Composés hétérocyclyliques et leurs utilisations
UY35630A (es) 2013-06-26 2015-01-30 Abbvie Inc Carboxamidas primarias como inhibidores de btk
HUE049733T2 (hu) 2013-07-02 2020-10-28 Syngenta Participations Ag Növényvédõszerként aktív biciklusos vagy triciklusos heterociklusok kéntartalmú szubsztituensekkel
SG10201800325PA (en) 2013-07-17 2018-02-27 Otsuka Pharma Co Ltd Cyanotriazole compounds
KR20160034379A (ko) 2013-07-25 2016-03-29 다나-파버 캔서 인스티튜트 인크. 전사 인자의 억제제 및 그의 용도
EP2835375A1 (fr) 2013-08-09 2015-02-11 Fundació Institut Català d'Investigació Química Composés salphen bis et composites de matériau carboné les comprenant
KR101715090B1 (ko) 2013-08-28 2017-03-13 한국화학연구원 신규한 화합물 또는 이의 약학적으로 허용가능한 염, 및 이를 유효성분으로 함유하는 인플루엔자 바이러스 감염으로 인한 질환의 예방 또는 치료용 약학적 조성물
SG11201601225RA (en) 2013-09-04 2016-03-30 Bristol Myers Squibb Co Compounds useful as immunomodulators
HUE039014T2 (hu) 2013-09-06 2018-12-28 Aurigene Discovery Tech Ltd 1,3,4-Oxadiazol és 1,3,4-tiadiazol származékok, mint immunomodulátorok
DK3041827T3 (en) 2013-09-06 2018-07-16 Aurigene Discovery Tech Ltd 1,2,4-OXADIAZOLD DERIVATIVES AS IMMUNE MODULATORS
WO2015036927A1 (fr) 2013-09-10 2015-03-19 Aurigene Discovery Technologies Limited Dérivés peptidomimétiques d'immunomodulation
JP6336870B2 (ja) 2013-09-30 2018-06-06 日本ポリプロ株式会社 ビフェノール化合物及びそれを用いるオレフィン重合用触媒並びにオレフィン重合体の製造方法
FR3012140B1 (fr) 2013-10-18 2016-08-26 Arkema France Unite et procede pour la purification de methacrylate de methyle brut
GB201321733D0 (en) 2013-12-09 2014-01-22 Ucb Pharma Sa Therapeutic agents
GB201321746D0 (en) 2013-12-09 2014-01-22 Ucb Pharma Sa Therapeutic agents
GB201321743D0 (en) 2013-12-09 2014-01-22 Ucb Pharma Sa Therapeutic agents
GB201321736D0 (en) 2013-12-09 2014-01-22 Ucb Pharma Sa Therapeutic agents
WO2015095337A2 (fr) 2013-12-18 2015-06-25 The Rockefeller University Dérivés pyrazolo [1,5-a]pyrimidine carboxamide pour le traitement de troubles cognitifs
TW201540705A (zh) 2014-01-03 2015-11-01 拜耳作物科學股份有限公司 做為殺蟲劑之新穎吡唑基雜芳基醯胺類
US20160356794A1 (en) 2014-02-10 2016-12-08 Merck Sharp & Dohme Corp. Antibodies that bind to human tau and assay for quantifying human tau using the antibodies
US9695205B2 (en) 2014-02-25 2017-07-04 Achillion Pharmaceuticals, Inc. Amide compounds for treatment of complement mediated disorders
US9394365B1 (en) 2014-03-12 2016-07-19 Yeda Research And Development Co., Ltd Reducing systemic regulatory T cell levels or activity for treatment of alzheimer's disease
JP6490464B2 (ja) 2014-03-26 2019-03-27 三井化学株式会社 遷移金属化合物、オレフィン重合用触媒およびオレフィン系重合体の製造方法
DK3125883T3 (da) 2014-04-04 2020-10-19 Iomet Pharma Ltd Indolderivater til anvendelse i medicin
US9850225B2 (en) 2014-04-14 2017-12-26 Bristol-Myers Squibb Company Compounds useful as immunomodulators
WO2015175678A1 (fr) 2014-05-14 2015-11-19 President And Fellows Of Harvard College Matériaux pour diodes électroluminescentes organiques
CN106065009B (zh) 2014-06-28 2019-03-01 广东东阳光药业有限公司 作为丙型肝炎抑制剂的化合物及其在药物中的应用
CN104211726B (zh) 2014-08-11 2017-06-16 中南民族大学 非茂类三齿双核钛配合物、制备方法及用途
EP3193608A4 (fr) 2014-09-17 2018-05-02 Epizyme, Inc. Inhibiteurs de carm1 et leurs utilisations
JP6777638B2 (ja) 2014-09-19 2020-10-28 マッカイ メディカル ファンデーション ザ プレスビュテロス チャーチ イン タイワン マッカイ メモリアル ホスピタル ベンゾ複素環化合物および薬剤
BR112017006305B1 (pt) 2014-10-06 2024-02-20 Merck Patent Gmbh Compostos heteroarila, seus usos, e composição farmacêutica
WO2016094688A1 (fr) 2014-12-10 2016-06-16 Massachusetts Institute Of Technology Dérivés fusionnés de 1,3-azole utiles pour le traitement de maladies prolifératives
JP6853619B2 (ja) 2015-01-16 2021-03-31 大塚製薬株式会社 シアノトリアゾール化合物の医薬用途
DE112016000383A5 (de) 2015-01-20 2017-10-05 Cynora Gmbh Organische Moleküle, insbesondere zur Verwendung in optoelektronischen Bauelementen
WO2016118404A1 (fr) 2015-01-20 2016-07-28 Merck Sharp & Dohme Corp. Dioxydes d'iminothiadiazine portant un substituant lié à une amine, utilisés en tant qu'inhibiteurs de bace, compositions les contenant et leur utilisation
WO2016156282A1 (fr) 2015-04-02 2016-10-06 Bayer Cropscience Aktiengesellschaft Nouveaux composés de triazole pour contrôler des champignons nocifs phytopathogènes
WO2017035405A1 (fr) 2015-08-26 2017-03-02 Achillion Pharmaceuticals, Inc. Composés amino pour le traitement de troubles immunitaires et inflammatoires
US10745382B2 (en) 2015-10-15 2020-08-18 Bristol-Myers Squibb Company Compounds useful as immunomodulators
WO2017070089A1 (fr) 2015-10-19 2017-04-27 Incyte Corporation Composés hétérocycliques utilisés comme immunomodulateurs
US10633370B2 (en) 2015-10-21 2020-04-28 University of Pittsburgh—of the Commonwealth System of Higher Education Phenyl indole allosteric inhibitors of p97 ATPase
US9603950B1 (en) 2015-10-25 2017-03-28 Institute Of Nuclear Energy Research Compounds of imaging agent with HDAC inhibitor for treatment of Alzheimer syndrome and method of synthesis thereof
KR101717601B1 (ko) 2015-11-10 2017-03-20 한국화학연구원 신규한 화합물 또는 이의 약학적으로 허용가능한 염, 및 이를 유효성분으로 함유하는 인플루엔자 바이러스 감염으로 인한 질환의 예방 또는 치료용 약학적 조성물
ES2928856T3 (es) 2015-11-19 2022-11-23 Incyte Corp Compuestos heterocíclicos como inmunomoduladores
WO2017106634A1 (fr) 2015-12-17 2017-06-22 Incyte Corporation Dérivés de n-phényl-pyridine-2-carboxamide et leur utilisation comme modulateurs d'interactions protéine/protéine pd-1/pd-l1
HRP20210698T1 (hr) 2015-12-22 2021-09-17 Immatics Biotechnologies Gmbh Peptidi i kombinacija peptida za uporabu u imunoterapiji protiv karcinoma dojke i drugih karcinoma
WO2017107052A1 (fr) 2015-12-22 2017-06-29 Merck Sharp & Dohme Corp. Activateurs solubles de guanylate cyclase
MX2018007527A (es) 2015-12-22 2018-09-07 Syngenta Participations Ag Derivados de pirazol activos como pesticidas.
TWI850624B (zh) 2015-12-22 2024-08-01 美商英塞特公司 作為免疫調節劑之雜環化合物
AU2016378482A1 (en) 2015-12-22 2018-07-12 Synthon B.V. Pharmaceutical composition comprising amorphous lenalidomide and an antioxidant
KR101653560B1 (ko) 2016-02-02 2016-09-12 한국화학연구원 신규한 화합물 또는 이의 약학적으로 허용가능한 염, 및 이를 유효성분으로 함유하는 인플루엔자 바이러스 감염으로 인한 질환의 예방 또는 치료용 약학적 조성물
EP3445339B1 (fr) 2016-04-22 2023-08-23 Incyte Corporation Formulations d'un inhibiteur de lsd1
ES2906460T3 (es) 2016-05-06 2022-04-18 Incyte Corp Compuestos heterocíclicos como inmunomoduladores
TW201808902A (zh) 2016-05-26 2018-03-16 美商英塞特公司 作為免疫調節劑之雜環化合物
RU2754856C2 (ru) 2016-06-20 2021-09-08 Новартис Аг Кристаллические формы соединения триазолопиримидина
PT3472167T (pt) 2016-06-20 2022-11-11 Incyte Corp Compostos heterocíclicos como imunomoduladores
PL3471755T3 (pl) 2016-06-20 2020-10-19 Elanco Us Inc. Pegylowany interferon świni i sposoby jego stosowania
JP7054529B2 (ja) 2016-06-21 2022-04-14 エックス4 ファーマシューティカルズ, インコーポレイテッド Cxcr4阻害剤およびその使用
US20180016260A1 (en) 2016-07-14 2018-01-18 Incyte Corporation Heterocyclic compounds as immunomodulators
AU2017305399A1 (en) 2016-08-03 2019-01-31 Arising International, Inc. Symmetric or semi-symmetric compounds useful as immunomodulators
MA46045A (fr) 2016-08-29 2021-04-28 Incyte Corp Composés hétérocycliques utilisés comme immunomodulateurs
CN110167560B (zh) 2016-08-30 2023-08-18 四相制药公司 四环素化合物和治疗方法
MY203083A (en) 2016-12-21 2024-06-07 Acerta Pharma Bv Imidazopyrazine inhibitors of bruton's tyrosine kinase
TWI795381B (zh) 2016-12-21 2023-03-11 比利時商健生藥品公司 作為malt1抑制劑之吡唑衍生物
EP3558973B1 (fr) 2016-12-22 2021-09-15 Incyte Corporation Dérivés pyridine utilisés en tant qu'immunomodulateurs
TW201835049A (zh) 2016-12-22 2018-10-01 美商英塞特公司 作為免疫調節劑之雜環化合物
US20180179201A1 (en) 2016-12-22 2018-06-28 Incyte Corporation Heterocyclic compounds as immunomodulators
US20180177784A1 (en) 2016-12-22 2018-06-28 Incyte Corporation Heterocyclic compounds as immunomodulators
SG10201911240PA (en) 2016-12-22 2020-02-27 Calithera Biosciences Inc Compositions and methods for inhibiting arginase activity
RS63710B1 (sr) 2016-12-22 2022-11-30 Incyte Corp Derivati tetrahidro imidazo[4,5-c] piridina kao induktori internalizacije pd-l1
JP7101678B2 (ja) 2016-12-22 2022-07-15 インサイト・コーポレイション 免疫調節剤としての複素環式化合物
JOP20180040A1 (ar) 2017-04-20 2019-01-30 Gilead Sciences Inc مثبطات pd-1/pd-l1
AU2018306619B2 (en) 2017-07-28 2022-06-02 Chemocentryx, Inc. Immunomodulator compounds
EP3664793B1 (fr) 2017-08-08 2022-06-29 ChemoCentryx, Inc. Immunomodulateurs macrocycliques
US11787766B2 (en) 2017-08-18 2023-10-17 Shanghai Ennovabio Pharmaceuticals Co., Ltd. Compound having PD-L1 inhibitory activity, preparation method therefor and use thereof
TWI796596B (zh) 2018-02-13 2023-03-21 美商基利科學股份有限公司 Pd‐1/pd‐l1抑制劑
RS66699B1 (sr) 2018-03-30 2025-05-30 Incyte Corp Heterociklična jedinjenja kao imunomodulatori
CN111936475B (zh) 2018-04-03 2024-05-10 贝达药业股份有限公司 免疫调节剂及其组合物和制备方法
KR102591947B1 (ko) 2018-04-19 2023-10-25 길리애드 사이언시즈, 인코포레이티드 Pd-1/pd-l1 억제제
TW202425987A (zh) 2018-05-11 2024-07-01 美商英塞特公司 作為免疫調節劑之雜環化合物
WO2020036491A1 (fr) 2018-08-15 2020-02-20 Moonshine Solutions As Procédé et dispositif d'alimentation d'un liquide à un revêtement
JP7158577B2 (ja) 2018-10-24 2022-10-21 ギリアード サイエンシーズ, インコーポレイテッド Pd-1/pd-l1阻害剤
KR20210089195A (ko) 2018-11-02 2021-07-15 상하이 맥시노벨 파마수티컬스 씨오., 엘티디. 비페닐계 화합물, 이의 중간체, 제조 방법, 약학 조성물 및 용도
US11596692B1 (en) 2018-11-21 2023-03-07 Incyte Corporation PD-L1/STING conjugates and methods of use
CN120463702A (zh) 2019-01-31 2025-08-12 贝达药业股份有限公司 免疫调节剂,组合物及其方法
GB201911210D0 (en) 2019-08-06 2019-09-18 Amlo Biosciences Ltd Clinical management of oropharyngeal squamous cell carcinoma
TW202115059A (zh) 2019-08-09 2021-04-16 美商英塞特公司 Pd—1/pd—l1抑制劑之鹽
CA3155090A1 (fr) 2019-09-20 2021-03-25 Transgene Combinaison d'un poxvirus codant pour des polypeptides hpv et il-2 avec un anticorps anti-pd-l1
JP7559059B2 (ja) 2019-09-30 2024-10-01 インサイト・コーポレイション 免疫調節剤としてのピリド[3,2-d]ピリミジン化合物
PH12022551136A1 (en) 2019-11-11 2023-10-09 Incyte Corp Salts and crystalline forms of a pd-1/pd-l1 inhibitor
EP4146216A4 (fr) 2020-05-04 2024-05-29 Beyondspring Pharmaceuticals Inc. Trithérapie pour améliorer la destruction de cellules cancéreuses dans des cancers à faible immunogénicité
TW202233615A (zh) 2020-11-06 2022-09-01 美商英塞特公司 Pd—1/pd—l1抑制劑之結晶形式
TW202233616A (zh) 2020-11-06 2022-09-01 美商英塞特公司 用於製備pd-1/pd-l1抑制劑以及其鹽及結晶形式之方法
US11780836B2 (en) 2020-11-06 2023-10-10 Incyte Corporation Process of preparing a PD-1/PD-L1 inhibitor
TW202241420A (zh) 2020-12-18 2022-11-01 美商英塞特公司 Pd-l1抑制劑之口服調配物
US20230149409A1 (en) 2021-09-24 2023-05-18 Incyte Corporation Treatment of human papillomavirus-associated cancers by pd-l1 inhibitors

Also Published As

Publication number Publication date
US10906920B2 (en) 2021-02-02
RS66459B1 (sr) 2025-02-28
PL4219492T3 (pl) 2025-03-24
CL2021002995A1 (es) 2022-06-24
MX2020012045A (es) 2021-03-29
SG11202011165TA (en) 2020-12-30
PT4219492T (pt) 2025-02-25
DK3790877T3 (da) 2023-04-24
ZA202403924B (en) 2025-04-30
EP3790877B1 (fr) 2023-03-01
US10618916B2 (en) 2020-04-14
US20210115068A1 (en) 2021-04-22
CN112752756B (zh) 2024-06-25
KR20210018282A (ko) 2021-02-17
MD4219492T2 (ro) 2025-04-30
JP7328995B2 (ja) 2023-08-17
CL2020002922A1 (es) 2021-04-16
TW202425987A (zh) 2024-07-01
EP4520328A2 (fr) 2025-03-12
AU2019267824B2 (en) 2023-10-05
JOP20200288A1 (ar) 2020-11-11
LT4219492T (lt) 2025-03-10
IL278605A (fr) 2021-01-31
CO2020015437A2 (es) 2021-01-18
CN112752756A (zh) 2021-05-04
SI3790877T1 (sl) 2023-06-30
EP4520328A3 (fr) 2025-04-16
AU2019267824A1 (en) 2021-01-07
ECSP20079887A (es) 2021-03-31
MD3790877T2 (ro) 2023-08-31
ES3014294T3 (en) 2025-04-21
EP3790877A1 (fr) 2021-03-17
JP2023162216A (ja) 2023-11-08
HRP20230306T1 (hr) 2023-05-12
CA3099994A1 (fr) 2019-11-04
US20190345170A1 (en) 2019-11-14
US20250084104A1 (en) 2025-03-13
PL3790877T3 (pl) 2023-06-12
SMT202300127T1 (it) 2023-05-12
AU2023227554A1 (en) 2023-09-28
DK4219492T3 (da) 2025-02-03
IL278605B1 (en) 2024-11-01
PT3790877T (pt) 2023-05-10
JP2021524842A (ja) 2021-09-16
US12187743B2 (en) 2025-01-07
KR102806565B1 (ko) 2025-05-14
HRP20250173T1 (hr) 2025-04-11
SMT202500077T1 (it) 2025-03-12
CR20200614A (es) 2021-04-27
EP4219492A1 (fr) 2023-08-02
PE20211918A1 (es) 2021-09-28
US11414433B2 (en) 2022-08-16
CN118908978A (zh) 2024-11-08
IL278605B2 (en) 2025-03-01
BR112020022936A2 (pt) 2021-02-02
EP4219492B1 (fr) 2024-11-27
US20220348594A1 (en) 2022-11-03
ES2943028T3 (es) 2023-06-08
WO2019217821A1 (fr) 2019-11-14
PH12020551927A1 (en) 2021-06-14
RS64188B1 (sr) 2023-06-30
TW201946626A (zh) 2019-12-16
FI3790877T3 (fi) 2023-05-09
HUE070093T2 (hu) 2025-05-28
MX2023013685A (es) 2024-01-08
SI4219492T1 (sl) 2025-04-30
SA520420524B1 (ar) 2024-02-15
LT3790877T (lt) 2023-05-10
FI4219492T3 (fi) 2025-02-17
US20200277309A1 (en) 2020-09-03
TWI821288B (zh) 2023-11-11
HUE061503T2 (hu) 2023-07-28

Similar Documents

Publication Publication Date Title
MA64509B1 (fr) Composés hétérocycliques utilisés comme immunomodulateurs
MA64121B1 (fr) Composés hétérocycliques utilisés comme immunomodulateurs
MA47043A1 (fr) Composés indole carboxamides utiles comme inhibiteurs de kinase
MA39783A (fr) Dérivés de quinoxaline utiles en tant que modulateurs de la fgfr kinase
MA52288B1 (fr) Modulateurs d'enzymes de modification de méthyle, compositions et utilisations de ceux-ci
MA41179A (fr) Composés inhibiteurs de parg
MA40290A1 (fr) Agents immunorégulateurs
WO2019035864A8 (fr) Activateurs de la pyruvate kinase destinés à être utilisés dans le traitement de troubles sanguins
MA40111B1 (fr) Dérivés du tétrahydronaphtalène inhibant la protéine mcl-1
MA45020B1 (fr) Dérivés sulfonamides aromatiques
MA43979B1 (fr) Dérivés de 1h-indazole-3-carboxamide et composés similaires en tant qu'inhibiteurs du facteur d pour le traitement de maladies characterisés par une activité aberrante du système complémentaire, comme p.E. Troubles immunologiques
MA44674B1 (fr) Inhibiteurs de bromodomaine
MA31683B1 (fr) Composes et procedes pour moduler fxr
MA40955B1 (fr) 2-amino-6-(difluorométhyl)-5,5-difluoro-6-phényl-3,4,5,6-tétrahydropyridines comme inhibiteurs de bace1
MA54133A (fr) Composés d'aminopyrazine diol utilisés comme inhibiteurs de pi3k-y
MA46229B1 (fr) Composés d'hétéroaryle carboxamide en tant qu'inhibiteurs de ripk2
MA38425B1 (fr) Composés bicycliques pour une utilisation comme agonistes selectifs pour le recepteur s1p1
MA39253A1 (fr) Composés hétéroaryle bicycliques substitués utilisés comme agonistes de rxr
MA53372B1 (fr) Pyridopyrimidinones comme inhibiteurs du récepteur h4 de l'histamine
EA202190766A1 (ru) Иммуномодуляторы, их композиции и способы применения
MA53898B1 (fr) Dérivés de 4-pyrazin-2-ylméthyl-morpholine et leur utilisation comme médicament
MA52220B1 (fr) Composés hétérocycliques utilisés comme immunomodulateurs
EP4230226A4 (fr) Composition pour le traitement de maladies rétiniennes ou choroïdiennes, contenant un inhibiteur d'acta2 comme principe actif
EP4205737A4 (fr) Composition pour la prévention, l'amélioration ou le traitement de maladies inflammatoires ou de maladies immunitaires comprenant la gancaonine n en tant que principe actif
MA43263B1 (fr) Composés hétérocycliques utilisés comme immunomodulateurs