MA54543A - Inhibiteurs de kif18a - Google Patents

Inhibiteurs de kif18a

Info

Publication number
MA54543A
MA54543A MA054543A MA54543A MA54543A MA 54543 A MA54543 A MA 54543A MA 054543 A MA054543 A MA 054543A MA 54543 A MA54543 A MA 54543A MA 54543 A MA54543 A MA 54543A
Authority
MA
Morocco
Prior art keywords
kif18a
inhibitors
kif18a inhibitors
Prior art date
Application number
MA054543A
Other languages
English (en)
Inventor
Abhisek Banerjee
Matthew Paul Bourbeau
James Alexander Brown
Jian Jeffrey Chen
Michael J Frohn
Lei Jia
Kexue Li
Qingyian Liu
Jonathan Dante Low
Vu Ma
Ana Elena Minatti
Liping H Pettus
Nuria A Tamayo
Mary Catherine Walton
Original Assignee
Amgen Inc
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 Amgen Inc filed Critical Amgen Inc
Publication of MA54543A publication Critical patent/MA54543A/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • 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
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/4545Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
    • 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
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D419/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms
    • C07D419/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04Ortho-condensed systems
    • C07D491/044Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/10Spiro-condensed systems
    • C07D491/107Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
MA054543A 2018-12-20 2019-12-20 Inhibiteurs de kif18a MA54543A (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201862783061P 2018-12-20 2018-12-20

Publications (1)

Publication Number Publication Date
MA54543A true MA54543A (fr) 2022-03-30

Family

ID=69187977

Family Applications (1)

Application Number Title Priority Date Filing Date
MA054543A MA54543A (fr) 2018-12-20 2019-12-20 Inhibiteurs de kif18a

Country Status (25)

Country Link
US (4) US11236069B2 (fr)
EP (1) EP3897852A1 (fr)
JP (1) JP7407196B2 (fr)
KR (1) KR102875569B1 (fr)
CN (2) CN120398830A (fr)
AR (1) AR117490A1 (fr)
AU (1) AU2019403486B2 (fr)
BR (1) BR112021011989A2 (fr)
CA (1) CA3123871A1 (fr)
CL (1) CL2021001634A1 (fr)
CO (1) CO2021008224A2 (fr)
CR (1) CR20210387A (fr)
EA (1) EA202191730A1 (fr)
IL (1) IL283639B2 (fr)
JO (1) JOP20210154B1 (fr)
MA (1) MA54543A (fr)
MX (1) MX2021007156A (fr)
PE (1) PE20211475A1 (fr)
PH (1) PH12021551409A1 (fr)
SA (1) SA521422303B1 (fr)
SG (1) SG11202106520VA (fr)
TW (1) TWI844602B (fr)
UA (1) UA129950C2 (fr)
UY (1) UY38526A (fr)
WO (1) WO2020132648A1 (fr)

Families Citing this family (68)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MX2021007157A (es) 2018-12-20 2021-08-16 Amgen Inc Heteroarilamidas utiles como inhibidores de kif18a.
CA3123227A1 (fr) * 2018-12-20 2020-06-25 Amgen Inc. Amides d'heteroaryle utiles en tant qu'inhibiteurs de kif18a
PE20211475A1 (es) 2018-12-20 2021-08-05 Amgen Inc Inhibidores de kif18a
WO2020132651A1 (fr) 2018-12-20 2020-06-25 Amgen Inc. Inhibiteurs de kif18a
CA3147272A1 (fr) 2019-08-02 2021-02-11 Amgen Inc. Inhibiteurs de kif18a
US12540129B2 (en) 2019-08-02 2026-02-03 Amgen Inc. KIF18A inhibitors
TW202203919A (zh) * 2020-04-14 2022-02-01 美商安進公司 用於治療贅生性疾病之kif18a抑制劑
MX2023004518A (es) 2020-10-20 2023-06-19 Amgen Inc Compuestos espiro heterocíclicos y métodos de uso.
US20230406860A1 (en) 2020-10-27 2023-12-21 Amgen Inc. Heterocyclic spiro compounds and methods of use
JP2024517693A (ja) 2021-04-29 2024-04-23 アムジエン・インコーポレーテツド 2-アミノベンゾチアゾール化合物及びその使用方法
CA3224249A1 (fr) 2021-06-25 2022-12-29 Hangzhou Innogate Pharma Co., Ltd. Compose destine a etre utilise en tant qu'inhibiteur de kif18a
TW202321213A (zh) 2021-07-21 2023-06-01 美商安進公司 Kif18a抑制劑化合物之鹽和固態形式
WO2023028564A1 (fr) 2021-08-26 2023-03-02 Volastra Therapeutics, Inc. Inhibiteurs spiro-indoliniques de la kif18a
WO2023088441A1 (fr) 2021-11-19 2023-05-25 微境生物医药科技(上海)有限公司 Inhibiteur de kif18a
CA3248925A1 (fr) * 2022-01-26 2023-08-03 Amgen Inc. Synthèse d'un inhibiteur de kif18a
MX2024010045A (es) 2022-02-16 2024-08-26 Amgen Inc Compuestos de quinazolina y uso de los mismos como inhibidores de proteinas mutantes kras.
MX2024010043A (es) 2022-02-16 2024-08-26 Amgen Inc Compuestos de quinazolina y uso de los mismos como inhibidores de proteinas kras mutantes.
EP4495113A4 (fr) * 2022-03-17 2026-02-18 Wigen Biomedicine Tech Shanghai Co Ltd Inhibiteur de kif18a
AU2023254325A1 (en) * 2022-04-15 2024-10-17 Wuhan Humanwell Innovative Drug Research and Development Center Limited Company Kif18a inhibitor and use thereof
WO2023217232A1 (fr) * 2022-05-13 2023-11-16 上海湃隆生物科技有限公司 Inhibiteur de kinésine kif18a et son utilisation
CN116554151B (zh) * 2022-05-13 2024-09-20 上海湃隆生物科技有限公司 驱动蛋白kif18a抑制剂及其应用
US20250382298A1 (en) 2022-06-30 2025-12-18 Suzhou Genhouse Bio Co., Ltd. Nitrogen-containing compound and use thereof
CN117510463A (zh) * 2022-08-05 2024-02-06 长春金赛药业有限责任公司 Kif18a抑制剂化合物、药物组合物及其制备方法和应用
WO2024032661A1 (fr) * 2022-08-11 2024-02-15 山东轩竹医药科技有限公司 Inhibiteur de kif18a et son utilisation
US20260062416A1 (en) * 2022-08-12 2026-03-05 Accent Therapeutics, Inc. Inhibitors of kif18a and uses thereof
WO2024039829A1 (fr) 2022-08-18 2024-02-22 Accent Therapeutics, Inc. Inhibiteurs de kif18a et leurs utilisations
JP2025533411A (ja) * 2022-09-08 2025-10-07 長春金賽薬業有限責任公司 Kif18a阻害剤化合物、医薬組成物並びにその製造方法及び応用
CN119907796A (zh) * 2022-09-09 2025-04-29 海南先声再明医药股份有限公司 酰胺类化合物、其组合物及用途
CN119562952A (zh) * 2022-09-30 2025-03-04 山东轩竹医药科技有限公司 Kif18a抑制剂
WO2024067675A1 (fr) * 2022-09-30 2024-04-04 长春金赛药业有限责任公司 Composé inhibiteur de kif18a à cycle condensé, composition pharmaceutique, procédé de préparation correspondant et utilisation associée
CN117917405A (zh) * 2022-10-21 2024-04-23 杭州邦顺制药有限公司 Kif18a蛋白抑制剂
PE20252237A1 (es) 2022-11-14 2025-09-15 Amgen Inc Inhibidores macrociclicos de kras y metodos de uso
WO2024109923A1 (fr) * 2022-11-24 2024-05-30 InventisBio Co., Ltd. Composés hétérocycliques, leurs procédés de préparation et leurs utilisations
CN115594664B (zh) * 2022-11-25 2023-02-24 英矽智能科技(上海)有限公司 一类螺环衍生物作为kif18a抑制剂
WO2024114730A1 (fr) * 2022-11-30 2024-06-06 微境生物医药科技(上海)有限公司 Composition pharmaceutique pour le traitement du cancer
WO2024114787A1 (fr) * 2022-12-02 2024-06-06 深圳众格生物科技有限公司 Composé amide ou urée
CN120265626A (zh) * 2022-12-14 2025-07-04 浙江海正药业股份有限公司 芳香酰胺类衍生物、其制备方法和其在医药上的应用
CN120641408A (zh) * 2022-12-16 2025-09-12 抟相医药(上海)有限公司 含氮化合物、药物组合物及其用途
WO2024137984A1 (fr) * 2022-12-22 2024-06-27 Accent Therapeutics, Inc. Inhibiteurs de kif18a et utilisations associées
CN120752230A (zh) * 2022-12-28 2025-10-03 英矽智能科技知识产权有限公司 Kif18a的抑制剂及其用途
CN120569373A (zh) * 2023-01-05 2025-08-29 浙江海正药业股份有限公司 芳香酰胺类衍生物及其制备方法和医药上的用途
AU2024208850A1 (en) * 2023-01-20 2025-06-12 Insilico Medicine Ip Limited Inhibitors of kif18a and uses thereof
WO2024183710A1 (fr) * 2023-03-06 2024-09-12 武汉人福创新药物研发中心有限公司 Composé inhibiteur de kif18a et son utilisation
CN115947717B (zh) * 2023-03-09 2023-05-30 英矽智能科技(上海)有限公司 一类kif18a抑制剂
KR20250154490A (ko) 2023-03-10 2025-10-28 쯔지앙 하이썬 파머슈티컬 컴퍼니, 리미티드 방향족 아미드 유도체, 이의 제조 방법, 및 그의 용도
CN121002013A (zh) * 2023-04-18 2025-11-21 南京同诺康医药科技有限公司 Kif18a抑制剂及其制备方法和用途
CN116535400B (zh) * 2023-04-26 2024-08-16 上海湃隆生物科技有限公司 氮杂螺环化合物及其应用
WO2025021003A1 (fr) 2023-07-21 2025-01-30 浙江海正药业股份有限公司 Dérivé d'amide aromatique, son procédé de préparation et son utilisation
WO2025026392A1 (fr) * 2023-08-02 2025-02-06 上海湃隆生物科技有限公司 Inhibiteur de kinésine kif18a et son utilisation
WO2025035759A1 (fr) * 2023-08-17 2025-02-20 深圳市祥根生物有限公司 Inhibiteur de kif18a et son utilisation
CN121712776A (zh) * 2023-09-26 2026-03-20 上海湃隆生物科技有限公司 驱动蛋白kif18a抑制剂及其应用
WO2025077882A1 (fr) * 2023-10-13 2025-04-17 武汉人福创新药物研发中心有限公司 Forme saline et forme cristalline d'un composé inhibiteur de kif18a, leur procédé de préparation et leur utilisation
WO2025081019A1 (fr) * 2023-10-13 2025-04-17 Iambic Therapeutics, Inc. Composés modulateurs de kif et méthodes d'utilisation
WO2025163351A1 (fr) * 2024-02-02 2025-08-07 Satyarx Pharma Innovations Pvt Ltd Nouveaux composés hétérocycliques utilisés en tant qu'inhibiteurs de kif18a
TW202600556A (zh) * 2024-03-07 2026-01-01 大陸商長春金賽藥業有限責任公司 Kif18a抑制劑的可藥用鹽、晶型及其製備方法和用途
WO2025185704A1 (fr) * 2024-03-07 2025-09-12 长春金赛药业有限责任公司 Forme cristalline d'un inhibiteur de kif18a, son procédé de préparation et son utilisation
WO2025190325A1 (fr) * 2024-03-13 2025-09-18 海南先声再明医药股份有限公司 Combinaison pharmaceutique d'inhibiteur de kif18a et d'inhibiteur de tubuline et son utilisation
WO2025194054A1 (fr) 2024-03-14 2025-09-18 Amgen Inc. Composés spirocycliques utilisés en tant que modulateurs de kras et leurs utilisations
TW202602882A (zh) 2024-03-14 2026-01-16 美商安進公司 作為kras調節劑的大環化合物及其用途
WO2025195205A1 (fr) * 2024-03-21 2025-09-25 甫康(上海)健康科技有限责任公司 Composé sulfanilamide et son utilisation
WO2025217247A1 (fr) 2024-04-10 2025-10-16 Amgen Inc. Inhibiteurs spiro-hétérocycliques ancrés de protéines mutantes kras g12c et leurs utilisations
WO2025230862A1 (fr) 2024-04-29 2025-11-06 Amgen Inc. Composés aminés macrocycliques utilisés en tant que modulateurs de kras et leurs utilisations
WO2025230878A1 (fr) 2024-04-29 2025-11-06 Amgen Inc. Composés macrocycliques utilisés en tant que modulateurs de kras et leurs utilisations
WO2025240582A1 (fr) 2024-05-14 2025-11-20 Amgen Inc. Composés macrocycliques utilisés en tant que modulateurs de kras et leurs utilisations
WO2025242166A1 (fr) * 2024-05-22 2025-11-27 InventisBio Co., Ltd. Composés hétérocycliques, leurs procédés de préparation et leurs utilisations
WO2026007956A1 (fr) * 2024-07-02 2026-01-08 长春金赛药业有限责任公司 Utilisation d'un inhibiteur de kif18a pour le traitement du cancer de l'ovaire
WO2026021411A1 (fr) * 2024-07-23 2026-01-29 Insilico Medicine Ip Limited Inhibiteurs de kif18a et leurs utilisations
WO2026055477A1 (fr) 2024-09-06 2026-03-12 Amgen Inc. Composés macrocycliques constituant des modulateurs de kras et leurs utilisations

Family Cites Families (224)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PT72878B (en) 1980-04-24 1983-03-29 Merck & Co Inc Process for preparing mannich-base hydroxamic acid pro-drugs for the improved delivery of non-steroidal anti-inflammatory agents
DE3381783D1 (de) 1982-03-03 1990-09-13 Genentech Inc Menschliches antithrombin iii, dns sequenzen dafuer, expressions- und klonierungsvektoren die solche sequenzen enthalten und damit transformierte zellkulturen, verfahren zur expression von menschlichem antithrombin iii und diese enthaltende pharmazeutische zusammensetzungen.
GB8827305D0 (en) 1988-11-23 1988-12-29 British Bio Technology Compounds
JP2762522B2 (ja) 1989-03-06 1998-06-04 藤沢薬品工業株式会社 血管新生阻害剤
US5112946A (en) 1989-07-06 1992-05-12 Repligen Corporation Modified pf4 compositions and methods of use
PT98990A (pt) 1990-09-19 1992-08-31 American Home Prod Processo para a preparacao de esteres de acidos carboxilicos de rapamicina
US5892112A (en) 1990-11-21 1999-04-06 Glycomed Incorporated Process for preparing synthetic matrix metalloprotease inhibitors
US5120842A (en) 1991-04-01 1992-06-09 American Home Products Corporation Silyl ethers of rapamycin
US5100883A (en) 1991-04-08 1992-03-31 American Home Products Corporation Fluorinated esters of rapamycin
US5118678A (en) 1991-04-17 1992-06-02 American Home Products Corporation Carbamates of rapamycin
CA2102780C (fr) 1991-05-10 2007-01-09 Alfred P. Spada Composes de type bis-monoaryle, aryle bicyclique et (ou) heteroaryle inhibant l'activite de tyrosine kinase des recepteurs de l'egf et (ou) du pdgf
US5118677A (en) 1991-05-20 1992-06-02 American Home Products Corporation Amide esters of rapamycin
NZ243082A (en) 1991-06-28 1995-02-24 Ici Plc 4-anilino-quinazoline derivatives; pharmaceutical compositions, preparatory processes, and use thereof
US5151413A (en) 1991-11-06 1992-09-29 American Home Products Corporation Rapamycin acetals as immunosuppressant and antifungal agents
GB9125660D0 (en) 1991-12-03 1992-01-29 Smithkline Beecham Plc Novel compound
GB9300059D0 (en) 1992-01-20 1993-03-03 Zeneca Ltd Quinazoline derivatives
US5521184A (en) 1992-04-03 1996-05-28 Ciba-Geigy Corporation Pyrimidine derivatives and processes for the preparation thereof
ZA935112B (en) 1992-07-17 1994-02-08 Smithkline Beecham Corp Rapamycin derivatives
ZA935111B (en) 1992-07-17 1994-02-04 Smithkline Beecham Corp Rapamycin derivatives
US5256790A (en) 1992-08-13 1993-10-26 American Home Products Corporation 27-hydroxyrapamycin and derivatives thereof
GB9221220D0 (en) 1992-10-09 1992-11-25 Sandoz Ag Organic componds
US5258389A (en) 1992-11-09 1993-11-02 Merck & Co., Inc. O-aryl, O-alkyl, O-alkenyl and O-alkynylrapamycin derivatives
PT669929E (pt) 1992-11-13 2007-04-30 Immunex Corp Ligando de elk, uma citoquina
US5455258A (en) 1993-01-06 1995-10-03 Ciba-Geigy Corporation Arylsulfonamido-substituted hydroxamic acids
US5629327A (en) 1993-03-01 1997-05-13 Childrens Hospital Medical Center Corp. Methods and compositions for inhibition of angiogenesis
US5516658A (en) 1993-08-20 1996-05-14 Immunex Corporation DNA encoding cytokines that bind the cell surface receptor hek
JPH08503971A (ja) 1993-10-01 1996-04-30 チバ−ガイギー アクチェンゲゼルシャフト ピリミジンアミン誘導体及びその調製のための方法
US5656643A (en) 1993-11-08 1997-08-12 Rhone-Poulenc Rorer Pharmaceuticals Inc. Bis mono-and bicyclic aryl and heteroaryl compounds which inhibit EGF and/or PDGF receptor tyrosine kinase
WO1995014023A1 (fr) 1993-11-19 1995-05-26 Abbott Laboratories Analogues semi-synthetiques de rapamycine (macrolides) utilises comme immunomodulateurs
PT734389E (pt) 1993-12-17 2000-09-29 Novartis Ag Derivados de rapamicina uteis como imunossupressores
US5700823A (en) 1994-01-07 1997-12-23 Sugen, Inc. Treatment of platelet derived growth factor related disorders such as cancers
IL112249A (en) 1994-01-25 2001-11-25 Warner Lambert Co Pharmaceutical compositions containing di and tricyclic pyrimidine derivatives for inhibiting tyrosine kinases of the epidermal growth factor receptor family and some new such compounds
IL112248A0 (en) 1994-01-25 1995-03-30 Warner Lambert Co Tricyclic heteroaromatic compounds and pharmaceutical compositions containing them
WO1995024190A2 (fr) 1994-03-07 1995-09-14 Sugen, Inc. Inhibiteurs de tyrosine-kinase receptrice destines a inhiber les troubles lies a la proliferation cellulaire et compositions les contenant
AU702522B2 (en) 1994-04-15 1999-02-25 Amgen, Inc. HEK5, HEK7, HEK8, HEK11, new EPH-like receptor protein tyrosine kinases
DE59500788D1 (de) 1994-05-03 1997-11-20 Ciba Geigy Ag Pyrrolopyrimidinderivate mit antiproliferativer Wirkung
US6303769B1 (en) 1994-07-08 2001-10-16 Immunex Corporation Lerk-5 dna
US5919905A (en) 1994-10-05 1999-07-06 Immunex Corporation Cytokine designated LERK-6
US6057124A (en) 1995-01-27 2000-05-02 Amgen Inc. Nucleic acids encoding ligands for HEK4 receptors
US5863949A (en) 1995-03-08 1999-01-26 Pfizer Inc Arylsulfonylamino hydroxamic acid derivatives
DE69536015D1 (de) 1995-03-30 2009-12-10 Pfizer Prod Inc Chinazolinone Derivate
JP4249804B2 (ja) 1995-04-03 2009-04-08 ノバルティス・アクチエンゲゼルシャフト ピラゾール誘導体およびその製造法
JP3053222B2 (ja) 1995-04-20 2000-06-19 ファイザー・インコーポレーテッド Mmpおよびtnf抑制剤としてのアリールスルホニルヒドロキサム酸誘導体
GB9508538D0 (en) 1995-04-27 1995-06-14 Zeneca Ltd Quinazoline derivatives
US5747498A (en) 1996-05-28 1998-05-05 Pfizer Inc. Alkynyl and azido-substituted 4-anilinoquinazolines
US5650415A (en) 1995-06-07 1997-07-22 Sugen, Inc. Quinoline compounds
US5880141A (en) 1995-06-07 1999-03-09 Sugen, Inc. Benzylidene-Z-indoline compounds for the treatment of disease
CZ292233B6 (cs) 1995-06-09 2003-08-13 Novartis Ag Deriváty rapamycinu a jejich použití jako léčiv
EP0836605B1 (fr) 1995-07-06 2002-02-06 Novartis AG Pyrrolopyrimidines et leurs procedes de preparation
DE19534177A1 (de) 1995-09-15 1997-03-20 Merck Patent Gmbh Cyclische Adhäsionsinhibitoren
AR004010A1 (es) 1995-10-11 1998-09-30 Glaxo Group Ltd Compuestos heterociclicos
GB9523675D0 (en) 1995-11-20 1996-01-24 Celltech Therapeutics Ltd Chemical compounds
ATE225343T1 (de) 1995-12-20 2002-10-15 Hoffmann La Roche Matrix-metalloprotease inhibitoren
AU1441497A (en) 1996-01-23 1997-08-20 Novartis Ag Pyrrolopyrimidines and processes for their preparation
JP3406763B2 (ja) 1996-01-30 2003-05-12 東レ・ダウコーニング・シリコーン株式会社 シリコーンゴム組成物
GB9603095D0 (en) 1996-02-14 1996-04-10 Zeneca Ltd Quinazoline derivatives
GB9603097D0 (en) 1996-02-14 1996-04-10 Zeneca Ltd Quinazoline compounds
DE19608588A1 (de) 1996-03-06 1997-09-11 Thomae Gmbh Dr K Pyrimido [5,4-d]pyrimidine, diese Verbindungen enthaltende Arzneimittel, deren Verwendung und Verfahren zu ihrer Herstellung
DE19629652A1 (de) 1996-03-06 1998-01-29 Thomae Gmbh Dr K 4-Amino-pyrimidin-Derivate, diese Verbindungen enthaltende Arzneimittel, deren Verwendung und Verfahren zu ihrer Herstellung
US6051577A (en) 1996-03-15 2000-04-18 Novartis Ag N-7-heterocyclyl pyrrolo[2,3-D]pyrimidines and the use thereof
JP3370340B2 (ja) 1996-04-12 2003-01-27 ワーナー―ランバート・コンパニー チロシンキナーゼの不可逆的阻害剤
GB9607729D0 (en) 1996-04-13 1996-06-19 Zeneca Ltd Quinazoline derivatives
EP0907642B1 (fr) 1996-06-24 2005-11-02 Pfizer Inc. Derives tricycliques substitues par phenylamino, destines au traitement des maladies hyperproliferatives
EP0818442A3 (fr) 1996-07-12 1998-12-30 Pfizer Inc. Dérivés cycliques de sulfones comme inhibiteurs de métalloprotéinase et de la production du facteur de nécrose des tumeurs
US6258823B1 (en) 1996-07-12 2001-07-10 Ariad Pharmaceuticals, Inc. Materials and method for treating or preventing pathogenic fungal infection
HRP970371A2 (en) 1996-07-13 1998-08-31 Kathryn Jane Smith Heterocyclic compounds
DE69716916T2 (de) 1996-07-13 2003-07-03 Glaxo Group Ltd., Greenford Kondensierte heterozyklische verbindungen als protein kinase inhibitoren
EA199900021A1 (ru) 1996-07-13 1999-08-26 Глаксо, Груп Лимитед Бициклические гетероароматические соединения в качестве ингибиторов протеинтирозинкиназы
CA2260898C (fr) 1996-07-18 2002-05-14 Pfizer Limited Composes a base de phosphinate inhibiteurs des metalloproteases matricielles
DE69738749D1 (de) 1996-08-16 2008-07-17 Schering Corp Zelloberflächen-antigen aus säugetieren und verwandte reagenzien
US6111090A (en) 1996-08-16 2000-08-29 Schering Corporation Mammalian cell surface antigens; related reagents
PL331895A1 (en) 1996-08-23 1999-08-16 Pfizer Arylosulphonylamino derivatives of hydroxamic acid
AU720429B2 (en) 1996-08-23 2000-06-01 Novartis Ag Substituted pyrrolopyrimidines and processes for their preparation
AU4779897A (en) 1996-10-02 1998-04-24 Novartis Ag Fused pyrazole derivatives and processes for their preparation
ID18494A (id) 1996-10-02 1998-04-16 Novartis Ag Turunan pirazola leburan dan proses pembuatannya
ES2239779T3 (es) 1996-10-02 2005-10-01 Novartis Ag Derivados de pirimidina y procedimientos para la preparacion de los mismos.
EP0837063A1 (fr) 1996-10-17 1998-04-22 Pfizer Inc. Dérivés de 4-aminoquinazoline
GB9621757D0 (en) 1996-10-18 1996-12-11 Ciba Geigy Ag Phenyl-substituted bicyclic heterocyclyl derivatives and their use
DE69730151T2 (de) 1997-01-06 2005-08-04 Pfizer Inc. Cyclische sulfonderivate
AU721748B2 (en) 1997-02-03 2000-07-13 Pfizer Products Inc. Arylsulfonylamino hydroxamic acid derivatives
KR20000070751A (ko) 1997-02-05 2000-11-25 로즈 암스트롱, 크리스틴 에이. 트러트웨인 세포 증식 억제제로서의 피리도[2,3-d]피리미딘 및 4-아미노피리미딘
CA2279863A1 (fr) 1997-02-07 1998-08-13 Pfizer Inc. Derives du n-hxdroxy-beta-sulfonyl-propionamide et leur utilisation comme inhibiteurs des metalloproteases matrices
WO1998034918A1 (fr) 1997-02-11 1998-08-13 Pfizer Inc. Derives de l'acide arylsulfonylhydroxamique
CO4950519A1 (es) 1997-02-13 2000-09-01 Novartis Ag Ftalazinas, preparaciones farmaceuticas que las comprenden y proceso para su preparacion
US6150395A (en) 1997-05-30 2000-11-21 The Regents Of The University Of California Indole-3-carbinol (I3C) derivatives and methods
WO1999007701A1 (fr) 1997-08-05 1999-02-18 Sugen, Inc. Derives de quinoxaline tricyclique utiles en tant qu'inhibiteurs de proteine tyrosine kinase
ID23668A (id) 1997-08-08 2000-05-11 Pfizer Prod Inc Turunan asam ariloksiarilsulfonilamino hidroksamat
WO1999020758A1 (fr) 1997-10-21 1999-04-29 Human Genome Sciences, Inc. Proteines tr11, tr11sv1 et tr11sv2 de type recepteur du facteur de necrose tumorale humain
GB9725782D0 (en) 1997-12-05 1998-02-04 Pfizer Ltd Therapeutic agents
RS49779B (sr) 1998-01-12 2008-06-05 Glaxo Group Limited, Biciklična heteroaromatična jedinjenja kao inhibitori protein tirozin kinaze
GB9800575D0 (en) 1998-01-12 1998-03-11 Glaxo Group Ltd Heterocyclic compounds
GB9801690D0 (en) 1998-01-27 1998-03-25 Pfizer Ltd Therapeutic agents
JP2002502607A (ja) 1998-02-09 2002-01-29 ジェネンテク・インコーポレイテッド 新規な腫瘍壊死因子レセプター相同体及びそれをコードする核酸
ES2324846T3 (es) 1998-03-04 2009-08-17 Bristol-Myers Squibb Company Inhibidores de la proteina tirosina quinasa de imidazopirazina heterociclo-sustituida.
PA8469501A1 (es) 1998-04-10 2000-09-29 Pfizer Prod Inc Hidroxamidas del acido (4-arilsulfonilamino)-tetrahidropiran-4-carboxilico
PA8469401A1 (es) 1998-04-10 2000-05-24 Pfizer Prod Inc Derivados biciclicos del acido hidroxamico
IL139934A0 (en) 1998-05-29 2002-02-10 Sugen Inc Pyrrole substituted 2-indolinone derivatives and pharmaceutical compositions containing the same
UA60365C2 (uk) 1998-06-04 2003-10-15 Пфайзер Продактс Інк. Похідні ізотіазолу, спосіб їх одержання, фармацевтична композиція та спосіб лікування гіперпроліферативного захворювання у ссавця
CA2336848A1 (fr) 1998-07-10 2000-01-20 Merck & Co., Inc. Nouveaux inhibiteurs de l'angiogenese
EP1109555A4 (fr) 1998-08-31 2001-11-21 Merck & Co Inc Nouveaux inhibiteurs d'angiogenese
DK1004578T3 (da) 1998-11-05 2004-06-28 Pfizer Prod Inc 5-oxo-pyrrolidin-2-carboxylsyrehydroxamidderivater
CA2359244C (fr) 1999-01-13 2013-10-08 Bayer Healthcare Llc Diphenyle urees a substitution .omega.-carboxy aryle en tant qu'inhibiteurs de la kinase p38
JP4673977B2 (ja) 1999-03-30 2011-04-20 ノバルティス アーゲー 炎症性疾患治療用フタラジン誘導体
GB9912961D0 (en) 1999-06-03 1999-08-04 Pfizer Ltd Metalloprotease inhibitors
US6521424B2 (en) 1999-06-07 2003-02-18 Immunex Corporation Recombinant expression of Tek antagonists
ATE324444T1 (de) 1999-06-07 2006-05-15 Immunex Corp Tek-antagonisten
PT1196186E (pt) 1999-07-12 2008-02-14 Genentech Inc Promoção ou inibição da angiogénese e da cardiovascularização com homólogos de ligandos/receptores do factor de necrose tumoral.
AU783158B2 (en) 1999-08-24 2005-09-29 Ariad Pharmaceuticals, Inc. 28-epirapalogs
MXPA02005101A (es) 1999-10-18 2003-09-25 Alexipharma Inc Derivados de indol canabimimeticos.
CN100376567C (zh) 1999-11-05 2008-03-26 阿斯特拉曾尼卡有限公司 作为vegf抑制剂的喹唑啉衍生物
DK1233943T3 (da) 1999-11-24 2011-08-15 Sugen Inc Ioniserbare indolinon derivater og anvendelse deraf som PTK ligander
US6515004B1 (en) 1999-12-15 2003-02-04 Bristol-Myers Squibb Company N-[5-[[[5-alkyl-2-oxazolyl]methyl]thio]-2-thiazolyl]-carboxamide inhibitors of cyclin dependent kinases
US6727225B2 (en) 1999-12-20 2004-04-27 Immunex Corporation TWEAK receptor
EP1259595B1 (fr) 2000-02-25 2007-04-04 Immunex Corporation Antagonistes des integrines
US6651123B1 (en) 2000-03-30 2003-11-18 International Business Machines Corporation File system locking
US6534309B1 (en) 2000-08-03 2003-03-18 Cytokinetics, Inc. Motor proteins and methods for their use
US6630500B2 (en) 2000-08-25 2003-10-07 Cephalon, Inc. Selected fused pyrrolocarbazoles
ES2556946T3 (es) 2000-12-21 2016-01-21 Novartis Ag Pirimidinaminas como moduladores de la angiogénesis
US7102009B2 (en) 2001-01-12 2006-09-05 Amgen Inc. Substituted amine derivatives and methods of use
US6995162B2 (en) 2001-01-12 2006-02-07 Amgen Inc. Substituted alkylamine derivatives and methods of use
US7105682B2 (en) 2001-01-12 2006-09-12 Amgen Inc. Substituted amine derivatives and methods of use
US20020147198A1 (en) 2001-01-12 2002-10-10 Guoqing Chen Substituted arylamine derivatives and methods of use
US6878714B2 (en) 2001-01-12 2005-04-12 Amgen Inc. Substituted alkylamine derivatives and methods of use
CA2485343A1 (fr) 2002-05-23 2004-05-13 Merck & Co., Inc. Inhibiteurs de kinesine mitotique
US7307088B2 (en) 2002-07-09 2007-12-11 Amgen Inc. Substituted anthranilic amide derivatives and methods of use
TWI329112B (en) 2002-07-19 2010-08-21 Bristol Myers Squibb Co Novel inhibitors of kinases
JP2006507841A (ja) 2002-11-14 2006-03-09 ダーマコン, インコーポレイテッド 機能的siRNAおよび超機能的siRNA
US7423018B2 (en) 2002-12-13 2008-09-09 University Of Massachusetts Kinesin-like proteins and methods of use
AU2004244626A1 (en) 2003-05-23 2004-12-09 The Government Of The United States Of America As Represented By The Secretary, Department Of Health And Human Services GITR ligand and GITR ligand-related molecules and antibodies and uses thereof
WO2005005434A1 (fr) 2003-07-08 2005-01-20 Novartis Ag Utilisation de rapamycine et de derives de rapamycine pour traiter les pertes de masse osseuse
EP1648900A4 (fr) 2003-07-11 2010-02-10 Ariad Pharma Inc Macrocycles contenant du phosphore
US20050048054A1 (en) 2003-07-11 2005-03-03 Shino Hanabuchi Lymphocytes; methods
AR045134A1 (es) 2003-07-29 2005-10-19 Smithkline Beecham Plc Compuesto de 1h - imidazo [4,5-c] piridin-ilo, composicion farmaceutica que lo comprende, proceso para prepararla, su uso para preparar dicha composicion farmaceutica, combinacion farmaceutica, uso de la combinacion farmaceutica para la preparacion de un medicamento, procedimientos para preparar dic
CN1835746A (zh) 2003-08-15 2006-09-20 默克公司 有丝分裂驱动蛋白抑制剂
WO2005055808A2 (fr) 2003-12-02 2005-06-23 Genzyme Corporation Compositions et methodes pour le diagnostic et le traitement du cancer du poumon
TR200808208T1 (tr) 2003-12-09 2008-12-22 The Government Of The United States Of America, As Represented By The Secretary, Department Of Health And Human Services Bir immün tepkinin bastırılması veya proliferatif bir hastalığın tedavisi
GB0409799D0 (en) 2004-04-30 2004-06-09 Isis Innovation Method of generating improved immune response
US7504413B2 (en) 2004-05-06 2009-03-17 Cytokinetics, Inc. N-(4-(imidazo[1,2A]pyridin-YL)phenethyl)benzamide inhibitors of the mitotic kinesin CENP-E for treating certain cellular proliferation diseases
US20060002932A1 (en) 2004-06-04 2006-01-05 Duke University Methods and compositions for enhancement of immunity by in vivo depletion of immunosuppressive cell activity
JP4836280B2 (ja) * 2004-06-18 2011-12-14 ノバルティス バクシンズ アンド ダイアグノスティックス,インコーポレーテッド 癌を治療するためのキネシンスピンドルタンパク質(ksp)阻害剤としてのn−(1−(1−ベンジル−4−フェニル−1h−イミダゾール−2−イル)−2,2−ジメチルプロピル)ベンズアミド誘導体および関連化合物
JP2008509971A (ja) 2004-08-18 2008-04-03 ニコメッド ゲゼルシャフト ミット ベシュレンクテル ハフツング Eg5キネシンのインヒビターとして使用するためのベンゾチエノピリジン
GEP20104906B (en) 2004-08-26 2010-02-25 Pfizer Enantiomerically pure aminoheteroaryl compounds as protein kinase inhibitors
CN101039952A (zh) 2004-10-13 2007-09-19 惠氏公司 作为pi3k抑制剂的17-羟基渥曼青霉素类似物
AU2006230099B2 (en) 2005-03-25 2012-04-19 Gitr, Inc. GITR binding molecules and uses therefor
WO2006114788A1 (fr) 2005-04-25 2006-11-02 Ramot At Tel Aviv University Ltd. Polypeptides de kinesine, polynucleotides codant pour ceux-ci et compositions et leurs methodes d'utilisation
PL2161336T5 (pl) 2005-05-09 2017-10-31 Ono Pharmaceutical Co Ludzkie przeciwciała monoklonalne przeciwko białku Programmed Death 1 (PD-1) oraz sposoby leczenia raka z zastosowaniem samych przeciwciał anty-PD-1 lub w połączeniu z innymi środkami immunoterapeutycznymi
GB0510390D0 (en) 2005-05-20 2005-06-29 Novartis Ag Organic compounds
CA2622870A1 (fr) 2005-09-20 2007-03-29 Pfizer Products Inc. Formes de dosage et procedes de traitement utilisant un inhibiteur de la tyrosine kinase
EP1942888A2 (fr) 2005-11-02 2008-07-16 Cytokinetics, Inc. Entites et compositions chimiques et methodes associees
WO2007133822A1 (fr) 2006-01-19 2007-11-22 Genzyme Corporation Anticorps anti-gitr destinés au traitement du cancer
US20100021420A1 (en) 2006-07-14 2010-01-28 Astex Therapeutics Limited Combinations of pyrazole derivatives for the inhibition of cdks and gsk's
WO2008015265A1 (fr) 2006-08-04 2008-02-07 Æterna Zentaris Gmbh Dérivés de l'anthracène et leur utilisation pour le traitement d'affections tumorales bénignes et malignes
WO2008070740A1 (fr) 2006-12-07 2008-06-12 F.Hoffmann-La Roche Ag Composés inhibant la phosphoinositide 3 kinase et procédés d'utilisation
CN101801413A (zh) 2007-07-12 2010-08-11 托勒克斯股份有限公司 采用gitr结合分子的联合疗法
AU2008298948B2 (en) 2007-09-12 2014-09-04 F. Hoffmann-La Roche Ag Combinations of phosphoinositide 3-kinase inhibitor compounds and chemotherapeutic agents, and methods of use
EP2214675B1 (fr) 2007-10-25 2013-11-20 Genentech, Inc. Procédé de préparation de composés de thiénopyrimidine
KR20110044992A (ko) 2008-07-02 2011-05-03 이머전트 프로덕트 디벨롭먼트 시애틀, 엘엘씨 TGF-β 길항제 다중-표적 결합 단백질
CN102149820B (zh) 2008-09-12 2014-07-23 国立大学法人三重大学 能够表达外源gitr配体的细胞
TW201103904A (en) 2009-06-11 2011-02-01 Hoffmann La Roche Janus kinase inhibitor compounds and methods
PT3023438T (pt) 2009-09-03 2020-05-08 Merck Sharp & Dohme Anticorpos anti-gitr
EP2295543A1 (fr) 2009-09-11 2011-03-16 Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. Procédé de préparation de virus de la grippe
GB0919054D0 (en) 2009-10-30 2009-12-16 Isis Innovation Treatment of obesity
SI2519543T1 (sl) 2009-12-29 2016-08-31 Emergent Product Development Seattle, Llc Beljakovine, ki se vežejo s heterodimeri in njihova uporaba
WO2011085261A1 (fr) * 2010-01-08 2011-07-14 Selexagen Therapeutics, Inc. Inhibiteurs de hedgehog
CN103534257A (zh) 2011-04-05 2014-01-22 辉瑞有限公司 作为原肌球蛋白相关激酶抑制剂的吡咯并[2,3-d]嘧啶衍生物
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
EA201490265A1 (ru) 2011-07-13 2014-12-30 Фармасайкликс, Инк. Ингибиторы тирозинкиназы брутона
WO2013039954A1 (fr) 2011-09-14 2013-03-21 Sanofi Anticorps anti-gitr
WO2013188600A1 (fr) 2012-06-12 2013-12-19 Washington University Signature génique à réponse endocrinienne entraînée par une aberration du nombre de copies
CN103242332B (zh) 2013-05-13 2015-11-04 江西科技师范大学 1-n酰基取代吲哚酮衍生物
JP6397410B2 (ja) 2013-08-09 2018-09-26 武田薬品工業株式会社 芳香環化合物
US20170095479A1 (en) 2014-05-29 2017-04-06 Merck Sharp & Dohme Corp. Methods for Treating Cancer with a WEE1 Inhibitor
EP3233918A1 (fr) 2014-12-19 2017-10-25 Novartis AG Polythérapies
TW201643138A (zh) 2015-04-17 2016-12-16 佛瑪治療公司 作為組蛋白脫乙醯基酶(hdac)抑制劑之3-螺-7-異羥肟酸四氫萘
CA2986235A1 (fr) 2015-05-20 2016-11-24 The Broad Institute, Inc. Neo-antigenes partages
JP7251981B2 (ja) 2016-03-24 2023-04-04 バイエル ファーマ アクチエンゲゼルシャフト 酵素開裂基を有する細胞毒性活性剤のプロドラッグ
EP3737666A4 (fr) 2018-01-12 2022-01-05 Kymera Therapeutics, Inc. Agents de dégradation de protéines et utilisations associées
CN108768023B (zh) 2018-08-13 2020-01-07 珠海格力电器股份有限公司 转子组件及交替极电机
DE102018213662A1 (de) 2018-08-14 2020-02-20 Robert Bosch Gmbh Lautsprecher mit einem darin enthaltenen Leuchtelement
CN109039072B (zh) 2018-08-21 2020-09-08 南京南瑞继保电气有限公司 一种双极双向直流变换器及其控制方法和控制装置
CA3123227A1 (fr) 2018-12-20 2020-06-25 Amgen Inc. Amides d'heteroaryle utiles en tant qu'inhibiteurs de kif18a
PE20211475A1 (es) 2018-12-20 2021-08-05 Amgen Inc Inhibidores de kif18a
MX2021007157A (es) 2018-12-20 2021-08-16 Amgen Inc Heteroarilamidas utiles como inhibidores de kif18a.
WO2020132651A1 (fr) 2018-12-20 2020-06-25 Amgen Inc. Inhibiteurs de kif18a
CA3132338A1 (fr) 2019-04-05 2020-10-08 David Suhy Methodes et compositions ameliorees pour biomarqueurs synthetiques
CN113785076B (zh) 2019-05-03 2024-06-11 株式会社递希真 预测癌症预后的方法及其组合物
US20230093080A1 (en) 2019-07-15 2023-03-23 Kymera Therapeutics, Inc. Protein degraders and uses thereof
WO2021026101A1 (fr) 2019-08-02 2021-02-11 Amgen Inc. Inhibiteurs de kif18a
CA3147272A1 (fr) 2019-08-02 2021-02-11 Amgen Inc. Inhibiteurs de kif18a
US12540129B2 (en) 2019-08-02 2026-02-03 Amgen Inc. KIF18A inhibitors
CN114302880B (zh) 2019-08-02 2025-07-15 美国安进公司 Kif18a抑制剂
EP4103045A4 (fr) 2020-02-16 2024-08-14 Genetikaplus Ltd. Procédés de pronostic thérapeutique
US12187992B2 (en) 2020-02-19 2025-01-07 The Regents Of The University Of California Method and device for early cancer screening
TW202203919A (zh) 2020-04-14 2022-02-01 美商安進公司 用於治療贅生性疾病之kif18a抑制劑
WO2021231413A1 (fr) 2020-05-11 2021-11-18 University Of Vermont Approche de traitement impliquant l'inhibition de kif18a pour des tumeurs instables du point de vue chromosomique
EP4192957A4 (fr) 2020-08-07 2024-09-04 Casma Therapeutics, Inc. Modulateurs de trpml
US20230406860A1 (en) 2020-10-27 2023-12-21 Amgen Inc. Heterocyclic spiro compounds and methods of use
WO2022214054A1 (fr) 2021-04-09 2022-10-13 Nanjing University Conjugué et son procédé de préparation et son utilisation
CA3224249A1 (fr) 2021-06-25 2022-12-29 Hangzhou Innogate Pharma Co., Ltd. Compose destine a etre utilise en tant qu'inhibiteur de kif18a
TW202321213A (zh) 2021-07-21 2023-06-01 美商安進公司 Kif18a抑制劑化合物之鹽和固態形式
WO2023028564A1 (fr) 2021-08-26 2023-03-02 Volastra Therapeutics, Inc. Inhibiteurs spiro-indoliniques de la kif18a
WO2023041055A1 (fr) 2021-09-16 2023-03-23 微境生物医药科技(上海)有限公司 Inhibiteur de kif18a
CN118201923A (zh) 2021-10-15 2024-06-14 海南先声再明医药股份有限公司 三环类化合物
WO2023088441A1 (fr) 2021-11-19 2023-05-25 微境生物医药科技(上海)有限公司 Inhibiteur de kif18a
CA3248925A1 (fr) 2022-01-26 2023-08-03 Amgen Inc. Synthèse d'un inhibiteur de kif18a
WO2023146979A1 (fr) 2022-01-27 2023-08-03 The Board Of Trustees Of The Leland Stanford Junior University Plateforme de cytométrie de masse à cellule unique pour cartographier les effets d'agents candidats sur le cartilage
AU2023254325A1 (en) 2022-04-15 2024-10-17 Wuhan Humanwell Innovative Drug Research and Development Center Limited Company Kif18a inhibitor and use thereof
JP2025515484A (ja) 2022-04-28 2025-05-15 ヴォラストラ セラピューティクス,インコーポレーテッド Kif18aを阻害するための化合物
EP4515234A1 (fr) 2022-04-29 2025-03-05 Amgen Inc. Inhibition de kif18a pour le traitement du cancer
US20250382298A1 (en) 2022-06-30 2025-12-18 Suzhou Genhouse Bio Co., Ltd. Nitrogen-containing compound and use thereof
WO2024032661A1 (fr) 2022-08-11 2024-02-15 山东轩竹医药科技有限公司 Inhibiteur de kif18a et son utilisation
US20260062416A1 (en) 2022-08-12 2026-03-05 Accent Therapeutics, Inc. Inhibitors of kif18a and uses thereof
WO2024039829A1 (fr) 2022-08-18 2024-02-22 Accent Therapeutics, Inc. Inhibiteurs de kif18a et leurs utilisations
JP2025533411A (ja) 2022-09-08 2025-10-07 長春金賽薬業有限責任公司 Kif18a阻害剤化合物、医薬組成物並びにその製造方法及び応用
CN119907796A (zh) 2022-09-09 2025-04-29 海南先声再明医药股份有限公司 酰胺类化合物、其组合物及用途
US20260098043A1 (en) 2022-09-14 2026-04-09 Hainan Simcere Zaiming Pharmeceutical Co., Ltd. Polycyclic compound and use thereof
CN119998300A (zh) 2022-09-29 2025-05-13 海南先声再明医药股份有限公司 一类稠环化合物及其用途
WO2024067675A1 (fr) 2022-09-30 2024-04-04 长春金赛药业有限责任公司 Composé inhibiteur de kif18a à cycle condensé, composition pharmaceutique, procédé de préparation correspondant et utilisation associée
CN119894878A (zh) 2022-10-13 2025-04-25 浙江海正药业股份有限公司 芳香酰胺类衍生物及其制备方法和用途
CN117917405A (zh) 2022-10-21 2024-04-23 杭州邦顺制药有限公司 Kif18a蛋白抑制剂
WO2024099398A1 (fr) 2022-11-10 2024-05-16 南京明德新药研发有限公司 Classe de composés sulfonamide contenant un hétérocycle ortho-condensé et leur utilisation
EP4669309A1 (fr) 2023-02-23 2025-12-31 Volastra Therapeutics, Inc. Formulations solides et formes polymorphes d'inhibiteurs d'indoline de kif18a
WO2025007055A1 (fr) 2023-06-29 2025-01-02 Volastra Therapeutics, Inc. Inhibiteurs d'aryl indol-3-yl cétone et d'aryl indazol-3-yl cétone de kif18a
WO2025090640A1 (fr) 2023-10-23 2025-05-01 Volastra Therapeutics, Inc. Formulations solides et formes polymorphes d'inhibiteurs d'indoline de kif18a

Also Published As

Publication number Publication date
CL2021001634A1 (es) 2021-12-10
CO2021008224A2 (es) 2021-07-30
CN113226473B (zh) 2025-05-13
US20220106293A1 (en) 2022-04-07
US20240317715A1 (en) 2024-09-26
IL283639B2 (en) 2024-06-01
JP7407196B2 (ja) 2023-12-28
AR117490A1 (es) 2021-08-11
CA3123871A1 (fr) 2020-06-25
IL283639B1 (en) 2024-02-01
US20260098029A1 (en) 2026-04-09
JOP20210154B1 (ar) 2023-09-17
AU2019403486A1 (en) 2021-06-24
UY38526A (es) 2020-06-30
SA521422303B1 (ar) 2023-12-11
PE20211475A1 (es) 2021-08-05
TWI844602B (zh) 2024-06-11
TW202034924A (zh) 2020-10-01
BR112021011989A2 (pt) 2021-09-08
PH12021551409A1 (en) 2022-05-16
CR20210387A (es) 2021-08-19
CN113226473A (zh) 2021-08-06
KR102875569B1 (ko) 2025-10-23
UA129950C2 (uk) 2025-09-24
KR20210106474A (ko) 2021-08-30
EA202191730A1 (ru) 2021-08-24
WO2020132648A1 (fr) 2020-06-25
US20200239441A1 (en) 2020-07-30
US12054476B2 (en) 2024-08-06
US12509442B2 (en) 2025-12-30
IL283639A (en) 2021-07-29
EP3897852A1 (fr) 2021-10-27
JOP20210154A1 (ar) 2023-01-30
US11236069B2 (en) 2022-02-01
SG11202106520VA (en) 2021-07-29
CN120398830A (zh) 2025-08-01
MX2021007156A (es) 2021-08-16
JP2022513972A (ja) 2022-02-09
AU2019403486B2 (en) 2025-04-24

Similar Documents

Publication Publication Date Title
IL283639A (en) Kif18a inhibitors
MA54550A (fr) Inhibiteurs de kif18a
EP4007752C0 (fr) Inhibiteurs de kif18a
EP4007753C0 (fr) Inhibiteurs de kif18a
MA52812A (fr) Inhibiteurs de sarm1
EP4007756C0 (fr) Inhibiteurs de kif18a
IL269196A (en) Novel inhibitors
EP3843714A4 (fr) Inhibiteurs de cd73
EP3833355A4 (fr) Inhibiteurs de prmt5
MA52813A (fr) Inhibiteurs de sarm1
DK3740479T3 (da) Dna-pk-hæmmere
EP3788042A4 (fr) Inhibiteurs de bcl-2
MA52413A (fr) Inhibiteurs de cd73
MA52809A (fr) Inhibiteurs de sarm1
EP3541932A4 (fr) Inhibiteurs de crispr-cas9
MA52635A (fr) Inhibiteurs de magl
EP3980011C0 (fr) Inhibiteurs de sarm1
DK3571192T3 (da) Jak1-selektive inhibitorer
EP3856176A4 (fr) Inhibiteurs de vap-1
EP3787635A4 (fr) Inhibiteurs de cd73
EP3817736A4 (fr) Inhibiteurs de pikfyve
EP3773537A4 (fr) Inhibiteurs de stat3
DK3630744T3 (da) Pyrazol-magl-inhibitorer
IL281514A (en) O-glycoprotein-2-acetamido-2-deoxy-3-d-glucopyranosidase inhibitors
EP3856194A4 (fr) Inhibiteurs de vap-1