FR23C1031I2 - Derives de lactames en tant qu'inhibiteurs d'idh1 mutants - Google Patents

Derives de lactames en tant qu'inhibiteurs d'idh1 mutants

Info

Publication number
FR23C1031I2
FR23C1031I2 FR23C1031C FR23C1031C FR23C1031I2 FR 23C1031 I2 FR23C1031 I2 FR 23C1031I2 FR 23C1031 C FR23C1031 C FR 23C1031C FR 23C1031 C FR23C1031 C FR 23C1031C FR 23C1031 I2 FR23C1031 I2 FR 23C1031I2
Authority
FR
France
Prior art keywords
lactam derivatives
mutant idh1
idh1 inhibitors
inhibitors
mutant
Prior art date
Legal status (The legal status 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 status listed.)
Active
Application number
FR23C1031C
Other languages
English (en)
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Laboratoires Servier SAS
Original Assignee
Laboratoires Servier SAS
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=48797706&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=FR23C1031(I2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Laboratoires Servier SAS filed Critical Laboratoires Servier SAS
Publication of FR23C1031I1 publication Critical patent/FR23C1031I1/fr
Application granted granted Critical
Publication of FR23C1031I2 publication Critical patent/FR23C1031I2/fr
Active legal-status Critical Current

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic 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
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/06—Dipeptides
    • C07K5/06139—Dipeptides with the first amino acid being heterocyclic
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/005—Enzyme inhibitors
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
    • A61K38/05—Dipeptides
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D205/00—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom
    • C07D205/02—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
    • C07D205/06—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D205/08—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with one oxygen atom directly attached in position 2, e.g. beta-lactams
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
    • C07D207/22—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D207/24—Oxygen or sulfur atoms
    • C07D207/26—2-Pyrrolidones
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
    • C07D207/22—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D207/24—Oxygen or sulfur atoms
    • C07D207/26—2-Pyrrolidones
    • C07D207/273—2-Pyrrolidones with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to other ring carbon atoms
    • C07D207/277—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D207/28—2-Pyrrolidone-5- carboxylic acids; Functional derivatives thereof, e.g. esters, nitriles
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/02—Heterocyclic 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
    • C07D401/04—Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/14—Heterocyclic 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/06—Dipeptides
    • C07K5/06008—Dipeptides with the first amino acid being neutral
    • C07K5/06078—Dipeptides with the first amino acid being neutral and aromatic or cycloaliphatic
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/02—Heterocyclic 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
    • C07D401/12—Heterocyclic 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/06—Dipeptides
    • C07K5/06191—Dipeptides containing heteroatoms different from O, S, or N

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Epidemiology (AREA)
  • Immunology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Biochemistry (AREA)
  • Molecular Biology (AREA)
  • Genetics & Genomics (AREA)
  • Biophysics (AREA)
  • Hematology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Oncology (AREA)
  • Biomedical Technology (AREA)
  • Diabetes (AREA)
  • Neurology (AREA)
  • Dermatology (AREA)
  • Pulmonology (AREA)
  • Rheumatology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Neurosurgery (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Peptides Or Proteins (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
FR23C1031C 2012-01-19 2023-09-07 Derives de lactames en tant qu'inhibiteurs d'idh1 mutants Active FR23C1031I2 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CN2012070601 2012-01-19
PCT/CN2013/000068 WO2013107291A1 (fr) 2012-01-19 2013-01-21 Composés thérapeutiquement actifs et leurs procédés d'utilisation

Publications (2)

Publication Number Publication Date
FR23C1031I1 FR23C1031I1 (fr) 2023-10-13
FR23C1031I2 true FR23C1031I2 (fr) 2024-08-16

Family

ID=48797706

Family Applications (1)

Application Number Title Priority Date Filing Date
FR23C1031C Active FR23C1031I2 (fr) 2012-01-19 2023-09-07 Derives de lactames en tant qu'inhibiteurs d'idh1 mutants

Country Status (42)

Country Link
US (7) US9474779B2 (fr)
EP (3) EP3985001A1 (fr)
JP (4) JP6313714B2 (fr)
KR (3) KR102108507B1 (fr)
CN (2) CN106496090B (fr)
AR (2) AR089768A1 (fr)
AU (3) AU2013211436B2 (fr)
BR (1) BR112014017840B1 (fr)
CA (2) CA3077245A1 (fr)
CL (1) CL2014001891A1 (fr)
CO (1) CO7010834A2 (fr)
CR (2) CR20170097A (fr)
CY (3) CY1120651T1 (fr)
DK (2) DK2804851T3 (fr)
EA (2) EA035662B1 (fr)
EC (1) ECSP14014544A (fr)
ES (2) ES2685746T3 (fr)
FI (1) FIC20230031I1 (fr)
FR (1) FR23C1031I2 (fr)
HK (1) HK1198439A1 (fr)
HR (2) HRP20220017T1 (fr)
HU (3) HUE057264T2 (fr)
IL (3) IL233683B (fr)
IN (1) IN2014DN05986A (fr)
LT (2) LT2804851T (fr)
MX (1) MX351166B (fr)
MY (1) MY178486A (fr)
NI (1) NI201400078A (fr)
NL (1) NL301243I2 (fr)
NO (1) NO2023038I1 (fr)
NZ (2) NZ722400A (fr)
PE (2) PE20190801A1 (fr)
PH (3) PH12014501626B1 (fr)
PL (2) PL2804851T3 (fr)
PT (2) PT2804851T (fr)
RS (2) RS57730B1 (fr)
SG (3) SG10202103521PA (fr)
SI (2) SI3447052T1 (fr)
TW (2) TWI636040B (fr)
UA (2) UA122324C2 (fr)
WO (1) WO2013107291A1 (fr)
ZA (1) ZA202100373B (fr)

Families Citing this family (61)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2740424T3 (es) 2009-03-13 2020-02-05 Agios Pharmaceuticals Inc Métodos y composiciones para trastornos relacionados con la proliferación celular
CN102481300B (zh) 2009-06-29 2015-04-15 安吉奥斯医药品有限公司 治疗性化合物和组合物
EP2491145B1 (fr) 2009-10-21 2016-03-09 Agios Pharmaceuticals, Inc. Procédés et compositions pour des troubles relatifs à la prolifération cellulaire
DK2704721T3 (en) 2011-05-03 2018-07-09 Agios Pharmaceuticals Inc Pyruvate kinase activators for therapeutic use
CN102827170A (zh) 2011-06-17 2012-12-19 安吉奥斯医药品有限公司 治疗活性组合物和它们的使用方法
CN102827073A (zh) 2011-06-17 2012-12-19 安吉奥斯医药品有限公司 治疗活性组合物和它们的使用方法
EP3984997A1 (fr) 2012-01-06 2022-04-20 Les Laboratoires Servier SAS Composés thérapeutiquement actifs et leurs procédés d'utilisation
CA2860858A1 (fr) * 2012-01-19 2013-07-25 Agios Pharmaceuticals, Inc. Composes therapeutiquement actifs et leurs methodes d'utilisation
US9474779B2 (en) 2012-01-19 2016-10-25 Agios Pharmaceuticals, Inc. Therapeutically active compositions and their methods of use
US10202339B2 (en) 2012-10-15 2019-02-12 Agios Pharmaceuticals, Inc. Therapeutic compounds and compositions
WO2015003360A2 (fr) 2013-07-11 2015-01-15 Agios Pharmaceuticals, Inc. Composés thérapeutiquement actifs et leurs méthodes d'utilisation
EP3019490B1 (fr) 2013-07-11 2020-06-03 Agios Pharmaceuticals, Inc. Composés n,6-bis(aryl ou hétéroaryl)-1,3,5-triazine-2,4-diamine comme inhibiteurs d'idh2 mutantes pour le traitement du cancer
US9579324B2 (en) 2013-07-11 2017-02-28 Agios Pharmaceuticals, Inc Therapeutically active compounds and their methods of use
WO2015003355A2 (fr) 2013-07-11 2015-01-15 Agios Pharmaceuticals, Inc. Composés thérapeutiquement actifs et leurs méthodes d'utilisation
CN105593215B (zh) 2013-07-11 2019-01-15 安吉奥斯医药品有限公司 用于治疗癌症的作为idh2突变体抑制剂的2,4-或4,6-二氨基嘧啶化合物
US20150031627A1 (en) * 2013-07-25 2015-01-29 Agios Pharmaceuticals, Inc Therapeutically active compounds and their methods of use
WO2015010297A1 (fr) * 2013-07-25 2015-01-29 Agios Pharmaceuticals, Inc. Composés thérapeutiquement actifs et leurs méthodes d'utilisation
CN103694142A (zh) * 2013-11-28 2014-04-02 浙江科技学院 4-N-Boc-氨基环己酮的制备方法
WO2015127173A1 (fr) * 2014-02-20 2015-08-27 Agios Pharmaceuticals, Inc Composés thérapeutiquement actifs et leurs procédés d'utilisation
WO2015127172A1 (fr) * 2014-02-20 2015-08-27 Agios Pharmaceuticals, Inc. Composés thérapeutiquement actifs et leurs procédés d'utilisation
KR102400737B1 (ko) 2014-03-14 2022-05-20 아지오스 파마슈티컬스 아이엔씨. 치료적으로 활성인 화합물의 약제학적 조성물
RS62178B1 (sr) * 2014-03-14 2021-08-31 Les Laboratoires Servier Sas Farmaceutske kompozicije terapeutski aktivnih jedinjenja
MY195016A (en) 2014-08-04 2023-01-03 Nuevolution As Optionally Fused Heterocyclyl-Substituted Derivatives of Pyrimidine Useful for The Treatment of Inflammatory, Metabolic, Oncologic and Autoimmune Diseases
BR112017006425B8 (pt) 2014-10-01 2023-05-16 Daiichi Sankyo Co Ltd Compostos derivados de isoxazol, seus usos, inibidores de isocitrato desidrogenase 1 mutante e da produção de d-2 hidroxiglutamato, agente antitumoral e composição farmacêutica compreendendo os mesmos
US11234976B2 (en) 2015-06-11 2022-02-01 Agios Pharmaceuticals, Inc. Methods of using pyruvate kinase activators
EP4403173A3 (fr) * 2015-10-15 2024-10-09 Les Laboratoires Servier Polythérapie pour le traitement de tumeurs malignes
CN108697698B (zh) * 2015-10-15 2021-12-03 阿吉奥斯制药公司 用于治疗恶性肿瘤的组合疗法
EA039805B1 (ru) * 2015-11-13 2022-03-15 Аджиос Фармасьютикалз, Инк. Комбинированная терапия для лечения злокачественных опухолей
CA3007363A1 (fr) * 2015-12-04 2017-06-08 Agios Pharmaceuticals, Inc. Methodes de traitement de tumeurs malignes
WO2017140758A1 (fr) 2016-02-19 2017-08-24 Debiopharm International S.A. Dérivés de 2-amino-4-(2-oxazolidinone-3-yl)-pyrimidine fusionnés avec un noyau hétéroaromatique à cinq chaînons en position 5,6 qui sont utiles dans le traitement de divers cancers
JP6856657B2 (ja) * 2016-02-26 2021-04-07 アジオス ファーマシューティカルズ， インコーポレイテッド 血液学的悪性疾患および固形腫瘍の処置のためのｉｄｈ１阻害剤
ES2842448T3 (es) * 2016-03-22 2021-07-14 Lianyungang Runzhong Pharmaceutical Co Ltd Compuesto de sultama y método de aplicación del mismo
WO2018010142A1 (fr) * 2016-07-14 2018-01-18 Shanghai Meton Pharmaceutical Co., Ltd Inhibiteur de l'iso-citrate déshydrogénase (idh)
IL265115B (en) 2016-08-31 2022-07-01 Agios Pharmaceuticals Inc Inhibitors of metabolic processes in the cell
CA3067028A1 (fr) 2017-06-12 2018-12-20 Agios Pharmaceuticals, Inc. Methodes de traitement de tumeurs cerebrales a l'aide d'une polytherapie
KR20200027502A (ko) 2017-06-12 2020-03-12 아지오스 파마슈티컬스 아이엔씨. 병용 요법을 사용한 뇌 종양 치료 방법
FI3686191T3 (fi) * 2017-09-22 2023-01-31 Kiteinen sulfamidiyhdiste
US11066390B2 (en) 2017-11-27 2021-07-20 Assia Chemical Industries Ltd. Solid state forms of Ivosidenib
WO2019161383A1 (fr) * 2018-02-19 2019-08-22 The Regents Of The University Of Colorado, A Body Corporate Quantification d'oxopipéridine par spectrométrie de masse
US11311527B2 (en) 2018-05-16 2022-04-26 Forma Therapeutics, Inc. Inhibiting mutant isocitrate dehydrogenase 1 (mIDH-1)
US11013733B2 (en) 2018-05-16 2021-05-25 Forma Therapeutics, Inc. Inhibiting mutant isocitrate dehydrogenase 1 (mlDH-1)
US10532047B2 (en) 2018-05-16 2020-01-14 Forma Therapeutics, Inc. Solid forms of ((S)-5-((1-(6-chloro-2-oxo-1,2-dihydroquinolin-3-yl)ethyl)amino)-1-methyl-6-oxo-1,6-dihydropyridine-2-carbonitrile
HUE061331T2 (hu) 2018-05-16 2023-06-28 Forma Therapeutics Inc Mutáns IDH-1 gátlása
US11013734B2 (en) 2018-05-16 2021-05-25 Forma Therapeutics, Inc. Treating patients harboring an isocitrate dehydrogenase-1 (IDH-1) mutation
US10980788B2 (en) * 2018-06-08 2021-04-20 Agios Pharmaceuticals, Inc. Therapy for treating malignancies
BR112021000156A2 (pt) 2018-07-06 2021-04-06 Agios Pharmaceuticals, Inc. Formas de ivosidenib e composições farmacêuticas
CA3121202A1 (fr) 2018-11-30 2020-06-04 Nuvation Bio Inc. Composes pyrrole et pyrazole et leurs procedes d'utilisation
CN109535025B (zh) * 2018-12-18 2022-09-09 尚科生物医药（上海）有限公司 一种艾伏尼布中间体3,3-二氟环丁胺盐酸盐的制备方法
WO2020127887A1 (fr) 2018-12-21 2020-06-25 Sandoz Ag Procédé de préparation d'un produit intermédiaire d'ivosidénib
MA56783B1 (fr) 2019-08-08 2023-10-31 Servier Lab Procédé de préparation d'ivosidenib et d'un intermédiaire de celui-ci
TW202120486A (zh) * 2019-08-09 2021-06-01 英商阿帝歐斯製藥有限公司 新穎化合物
US20220324838A1 (en) * 2019-08-09 2022-10-13 Alembic Pharmaceuticals Limited An Improved Process Of Preparation Of Ivosidenib
US20230242503A9 (en) * 2019-08-09 2023-08-03 Artios Pharma Limited Heterocyclic compounds for use in the treatment of cancer
WO2021079380A1 (fr) * 2019-10-23 2021-04-29 Msn Laboratories Private Limited, R&D Center Procédé amélioré de préparation de (2s)-n-{(1s)-1-(2-chlorophényl)-2-[(3,3-difluorocyclobutyl)-amino]-2-oxoéthyl}-1-(4-cyanopyridin-2-yl)-n-(5-fluoropyridin-3-yl)-5-oxopyrrolidine-2-carboxamide
JP2021098692A (ja) 2019-12-20 2021-07-01 ヌエヴォリューション・アクティーゼルスカブＮｕｅｖｏｌｕｔｉｏｎ Ａ／Ｓ 核内受容体に対して活性の化合物
AU2021249530A1 (en) 2020-03-31 2022-12-01 Nuevolution A/S Compounds active towards nuclear receptors
AU2021245397A1 (en) 2020-03-31 2022-10-20 Nuevolution A/S Compounds active towards nuclear receptors
CN111349081B (zh) * 2020-04-28 2021-01-15 宁波大学科学技术学院 一种Ivosidenib及其中间体的手性合成方法
EP4186525A4 (fr) 2020-07-21 2024-04-03 Daiichi Sankyo Company, Limited Médicament combiné de témozolomide et d'inhibiteur de l'enzyme idh1 mutée
CN116332905A (zh) * 2021-12-23 2023-06-27 上海翊石医药科技有限公司 (s)-n-苯基-1-(吡啶-2-基)吡咯烷-2-甲酰胺衍生物
CN118451067A (zh) * 2021-12-30 2024-08-06 上海湃隆生物科技有限公司 一种DNA聚合酶theta抑制剂及其应用

Family Cites Families (163)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2390529A (en) 1942-02-03 1945-12-11 Ernst A H Friedheim Hydrazino-1,3,5-triazino derivatives of substituted phenylarsenic compounds
NL125847C (fr) 1963-02-15
BE754242A (fr) 1970-07-15 1971-02-01 Geigy Ag J R Diamino-s-triazines et dinitro-s-triazines
US3867383A (en) 1971-03-29 1975-02-18 Ciba Geigy Corp Monoanthranilatoanilino-s-triazines
BE793501A (fr) 1971-12-31 1973-06-29 Ciba Geigy Composes heterocycliques et produits phytopharmaceutiques qui en contiennent
CH606334A5 (fr) 1974-06-21 1978-10-31 Ciba Geigy Ag
DE2928485A1 (de) 1979-07-14 1981-01-29 Bayer Ag Verwendung von harnstoffderivaten als arzneimittel bei der behandlung von fettstoffwechselstoerungen
JPS58186682A (ja) 1982-04-27 1983-10-31 日本化薬株式会社 セルロ−ス又はセルロ−ス含有繊維材料の染色法
DE3512630A1 (de) 1985-04-06 1986-10-23 Hoechst Ag, 6230 Frankfurt Verfahren zum faerben oder bedrucken von cellulosefasern oder cellulosemischfasern
US5041443A (en) 1989-02-21 1991-08-20 Dainippon Pharmaceutical Co., Ltd. Medicament for treating cerebral insufficiency diseases, novel 2-(1-piperazinyl)-4-phenylcycloalkanopyrimidine derivatives, and process for the production thereof
DE69010232T2 (de) 1989-03-03 1994-12-01 Dainippon Pharmaceutical Co 2-(1-Piperazinyl)-4-phenylcycloalkanpyridin-Derivate, Verfahren zu deren Herstellung und pharmazeutische Zusammensetzungen, die sie enthalten.
JPH0491034A (ja) 1990-08-02 1992-03-24 Fujimoto Daiagunosuteitsukusu:Kk 中枢神経保護剤
JPH0499768A (ja) 1990-08-17 1992-03-31 Dainippon Pharmaceut Co Ltd ４―（４―フェニルピリジン―２―イル）ピペラジン―１―オキシド誘導体
JPH05140126A (ja) 1991-11-26 1993-06-08 Hokko Chem Ind Co Ltd トリアゾール誘導体および除草剤
CA2131004A1 (fr) 1992-02-28 1993-09-02 Hideshi Kobayashi Derive s-triazine et remede contre les maladies oestrogeno-dependantes renfermant ce derive
IL115420A0 (en) 1994-09-26 1995-12-31 Zeneca Ltd Aminoheterocyclic derivatives
IL117580A0 (en) 1995-03-29 1996-07-23 Merck & Co Inc Inhibitors of farnesyl-protein transferase and pharmaceutical compositions containing them
FR2735127B1 (fr) 1995-06-09 1997-08-22 Pf Medicament Nouvelles piperazines heteroaromatiques utiles comme medicaments.
ES2100129B1 (es) 1995-10-11 1998-02-16 Medichem Sa Nuevos compuestos aminopiridinicos policiclicos inhibidores de acetilcolinesterasa, procedimiento para su preparacion y su utilizacion.
EP0880501A1 (fr) 1996-02-02 1998-12-02 Zeneca Limited Composes heterocycliques utiles en tant qu'agents pharmaceutiques
GB9602166D0 (en) 1996-02-02 1996-04-03 Zeneca Ltd Aminoheterocyclic derivatives
US5807876A (en) 1996-04-23 1998-09-15 Vertex Pharmaceuticals Incorporated Inhibitors of IMPDH enzyme
JPH09291034A (ja) 1996-02-27 1997-11-11 Yoshitomi Pharmaceut Ind Ltd 縮合ピリジン化合物およびその医薬としての用途
US6262113B1 (en) 1996-03-20 2001-07-17 Smithkline Beecham Corporation IL-8 receptor antagonists
JP2000510866A (ja) 1996-05-20 2000-08-22 ダーウィン・ディスカバリー・リミテッド Ｔｎｆとｐｄｅ―ｉｖのインヒビターとしてのキノリンスルホンアミド
US5984882A (en) 1996-08-19 1999-11-16 Angiosonics Inc. Methods for prevention and treatment of cancer and other proliferative diseases with ultrasonic energy
EP0945446A4 (fr) 1996-11-14 1999-12-08 Nissan Chemical Ind Ltd Derives de cyanoethylmelamine et procede de production
US6399358B1 (en) 1997-03-31 2002-06-04 Thomas Jefferson University Human gene encoding human chondroitin 6-sulfotransferase
JPH11158073A (ja) 1997-09-26 1999-06-15 Takeda Chem Ind Ltd アデノシンａ３拮抗剤
US7517880B2 (en) 1997-12-22 2009-04-14 Bayer Pharmaceuticals Corporation Inhibition of p38 kinase using symmetrical and unsymmetrical diphenyl ureas
IL136737A0 (en) 1997-12-22 2001-06-14 Bayer Ag Inhibition of p38 kinase using symmetrical and unsymmetrical diphenyl ureas
AU9064598A (en) 1998-07-10 2000-02-01 Harald Groger Precusors for pna-monomers
US6783965B1 (en) 2000-02-10 2004-08-31 Mountain View Pharmaceuticals, Inc. Aggregate-free urate oxidase for preparation of non-immunogenic polymer conjugates
DK1588716T3 (da) 1998-08-06 2011-05-23 Mountain View Pharmaceuticals Peg-uratoxidase-konjugater og anvendelse deraf
UY25842A1 (es) 1998-12-16 2001-04-30 Smithkline Beecham Corp Antagonistas de receptores de il-8
AU5379900A (en) 1999-06-07 2000-12-28 Shire Biochem Inc. Thiophene integrin inhibitors
JP2003508382A (ja) 1999-08-27 2003-03-04 スージェン・インコーポレーテッド リン酸模倣体およびホスファターゼ阻害剤を用いる治療方法
IL155155A0 (en) 1999-09-17 2003-10-31 Cor Therapeutics Inc BENZAMIDES AND RELATED INHIBITORS OF FACTOR Xa
EP1216231A2 (fr) 1999-09-17 2002-06-26 Millennium Pharmaceuticals, Inc. INHIBITEURS DU FACTEUR Xa
JP4794793B2 (ja) 1999-12-28 2011-10-19 ファーマコペイア， インコーポレイテッド Ｎ−ヘテロ環ＴＮＦ−α発現阻害剤
DE60115394T2 (de) 2000-02-29 2006-10-19 Millennium Pharmaceuticals, Inc., Cambridge Benzamide und ähnliche inhibitoren vom faktor xa
AU8066701A (en) 2000-07-20 2002-02-05 Neurogen Corp Capsaicin receptor ligands
JP4113323B2 (ja) 2000-08-07 2008-07-09 富士フイルム株式会社 アゾ色素及びそれを含むインクジェット記録用インク、並びにインクジェット記録方法
US6525091B2 (en) 2001-03-07 2003-02-25 Telik, Inc. Substituted diarylureas as stimulators for Fas-mediated apoptosis
EP1389194A2 (fr) 2001-04-27 2004-02-18 Vertex Pharmaceuticals Incorporated Inhibiteurs de bace
BR0210291A (pt) 2001-06-11 2004-07-13 Biovitrum Ab Compostos de sulfonamida substituìdos, processo para sua preparação e seu uso como medicamento para o tratamento de distúrbios do sistema nervoso central, obesidade e diabetes do tipo ii
EP1397142A4 (fr) 2001-06-19 2004-11-03 Bristol Myers Squibb Co Inhibiteurs pyrimidine de la phosphodiesterase (pde) 7
DE60238066D1 (de) 2001-08-17 2010-12-02 Basf Se Triazinderivate und deren verwendung als sonnenschutzmittel
JP4753336B2 (ja) 2001-09-04 2011-08-24 日本化薬株式会社 新規アリル化合物及びその製法
US6878196B2 (en) 2002-01-15 2005-04-12 Fuji Photo Film Co., Ltd. Ink, ink jet recording method and azo compound
US20040067234A1 (en) 2002-07-11 2004-04-08 Paz Einat Isocitrate dehydrogenase and uses thereof
SI2256108T1 (sl) 2002-07-18 2016-05-31 Janssen Pharmaceutica N.V. Substituirani triazinski kinazni inhibitorji
JP2004083610A (ja) 2002-08-22 2004-03-18 Fuji Photo Film Co Ltd インクセット、インクカートリッジ、記録方法、プリンター及び記録物
JP2004107220A (ja) 2002-09-13 2004-04-08 Mitsubishi Pharma Corp ＴＮＦ−α産生抑制剤
CL2003002353A1 (es) 2002-11-15 2005-02-04 Vertex Pharma Compuestos derivados de diaminotriazoles, inhibidores d ela proteina quinasa; composicion farmaceutica; procedimiento de preparacion; y su uso del compuesto en el tratamiento de enfermedades de desordenes alergicos, proliferacion, autoinmunes, condic
AU2003293333A1 (en) 2002-12-02 2004-06-23 Arqule, Inc. Method of treating cancers
NZ541050A (en) 2002-12-16 2010-06-25 Genmab As Human monoclonal antibodies against interleukin 8 (IL-8)
WO2004062604A2 (fr) 2003-01-10 2004-07-29 Threshold Pharmaceuticals, Inc. Traitement du cancer par le 2-desoxyglucose
US7358262B2 (en) 2003-01-29 2008-04-15 Whitehead Institute For Biomedical Research Identification of genotype-selective anti-tumor agents
WO2004074438A2 (fr) 2003-02-14 2004-09-02 Smithkline Beecham Corporation Antagonistes de ccr8
WO2004073619A2 (fr) 2003-02-14 2004-09-02 Smithkline Beecham Corporation Antagonistes du recepteur ccr8
EP2239012A3 (fr) 2003-04-11 2011-06-15 High Point Pharmaceuticals, LLC Dérivés amidés substitués et leurs utilisations pharmaceutiques
WO2005013982A1 (fr) 2003-08-06 2005-02-17 Vertex Pharmaceuticals Incorporated Composes d'aminotriazole utiles en tant qu'inhibiteurs des proteines kinases
EP1689722A2 (fr) 2003-10-10 2006-08-16 Bayer Pharmaceuticals Corporation Derives de pyrimidine dans le traitement de troubles hyperproliferatifs
JP4099768B2 (ja) 2003-11-10 2008-06-11 富士電機デバイステクノロジー株式会社 電子写真感光体および該電子写真感光体に起因する干渉縞有無の判定方法
US20070196395A1 (en) 2003-12-12 2007-08-23 Mackerell Alexander Immunomodulatory compounds that target and inhibit the py'binding site of tyrosene kinase p56 lck sh2 domain
BRPI0417213A (pt) 2003-12-24 2007-02-06 Scios Inc tratamento de gliomas malìgnos com inibidores de tgf-beta
JP2005264016A (ja) 2004-03-19 2005-09-29 Fuji Photo Film Co Ltd インクジェット記録用インク、インクセット及びインクジェット記録方法
US7335770B2 (en) 2004-03-24 2008-02-26 Reddy U5 Therapeutics, Inc. Triazine compounds and their analogs, compositions, and methods
GB0412526D0 (en) 2004-06-05 2004-07-14 Leuven K U Res & Dev Type 2 diabetes
CN101083992A (zh) 2004-09-20 2007-12-05 泽农医药公司 抑制人硬脂酰CoA去饱和酶的哒嗪衍生物
JP2008538544A (ja) 2004-09-23 2008-10-30 レディ ユーエス セラピューティックス， インコーポレイテッド 新規ピリミジン化合物、それらの調製のためのプロセスおよびそれらを含む組成物
WO2006038594A1 (fr) 2004-10-04 2006-04-13 Ono Pharmaceutical Co., Ltd. Inhibiteur de canal de calcium de type n
JP2008526723A (ja) 2004-12-30 2008-07-24 アステックス、セラピューティックス、リミテッド Ｃｄｋ、ｇｓｋ及びオーロラキナーゼの活性を調節するピラゾール誘導体
US20080146570A1 (en) 2005-01-25 2008-06-19 Astrazeneca Ab Chemical Compounds
CZ2007700A3 (cs) 2005-04-11 2008-02-27 Savient Pharmaceuticals, Inc. Variantní forma urátoxidázy a její použití
ES2624863T3 (es) 2005-06-08 2017-07-17 Millennium Pharmaceuticals, Inc. Métodos para identificación, evaluación, y tratamiento de pacientes con terapia de cáncer
GB0513702D0 (en) 2005-07-04 2005-08-10 Sterix Ltd Compound
CN101296909B (zh) 2005-08-26 2011-10-12 默克雪兰诺有限公司 吡嗪衍生物及其作为pi3k抑制剂的应用
US8133900B2 (en) 2005-11-01 2012-03-13 Targegen, Inc. Use of bi-aryl meta-pyrimidine inhibitors of kinases
TW200815426A (en) 2006-06-28 2008-04-01 Astrazeneca Ab New pyridine analogues II 333
US8343548B2 (en) 2006-08-08 2013-01-01 Shin-Etsu Chemical Co., Ltd. Solid dosage form comprising solid dispersion
US20100297673A1 (en) 2006-09-20 2010-11-25 Reddy Us Therapeutics Methods and compositions for upregulation of peroxiredoxin activity
US20080109846A1 (en) 2006-10-23 2008-05-08 Ewertz C Christian System and method for audiovisual content playback
CA2669117A1 (fr) 2006-10-26 2008-05-02 Gary A. Flynn Modulateurs d'aquaporine et procedes pour leur utilisation pour le traitement d'un oedeme et d'un desequilibre de fluides
HUP0600810A3 (en) 2006-10-27 2008-09-29 Richter Gedeon Nyrt New sulfonamide derivatives as bradykinin antagonists, process and intermediates for their preparation and pharmaceutical compositions containing them
PE20081229A1 (es) 2006-12-01 2008-08-28 Merck & Co Inc Antagonistas de receptor de orexina de diazepam sustituido
US20100234341A1 (en) 2006-12-04 2010-09-16 Marion Lanier Substituted pyrimidines as adenosine receptor antagonists
RU2452484C2 (ru) 2006-12-08 2012-06-10 Милленниум Фармасьютикалз, Инк. Стандартные лекарственные препараты и способы лечения тромбоза пероральным введением ингибитора фактора ха
AU2007333925B2 (en) 2006-12-15 2013-10-31 Nantbio, Inc. Triazine derivatives and their therapeutical applications
BRPI0810921A2 (pt) 2007-04-30 2014-10-29 Prometic Biosciences Inc Derivados de triazina, composições contendo tais derivados e métodos de tratamento de câncer e doenças autoimunes usando tais compostos
JP2010529193A (ja) 2007-06-11 2010-08-26 ミイカナ セラピューティクス インコーポレイテッド 置換ピラゾール化合物
ES2605230T3 (es) 2007-07-20 2017-03-13 Nerviano Medical Sciences S.R.L. Derivados de indazol sustituidos activos como inhibidores de cinasas
JP5282091B2 (ja) 2007-07-25 2013-09-04 ブリストル−マイヤーズ スクイブ カンパニー トリアジンキナーゼ阻害剤
TW200906818A (en) 2007-07-31 2009-02-16 Astrazeneca Ab Chemical compounds
TW200924778A (en) 2007-10-10 2009-06-16 Takeda Pharmaceutical Amide compound
WO2009051910A1 (fr) * 2007-10-16 2009-04-23 The Regents Of The University Of California Composés ayant une activité augmentant le transport ionique grâce à la cftr mutante et leurs utilisations
US8642660B2 (en) 2007-12-21 2014-02-04 The University Of Rochester Method for altering the lifespan of eukaryotic organisms
JP5277685B2 (ja) 2008-03-26 2013-08-28 富士ゼロックス株式会社 電子写真感光体、画像形成装置、プロセスカートリッジ及び画像形成方法
GB0805477D0 (en) 2008-03-26 2008-04-30 Univ Nottingham Pyrimidines triazines and their use as pharmaceutical agents
US20090281089A1 (en) 2008-04-11 2009-11-12 Genentech, Inc. Pyridyl inhibitors of hedgehog signalling
CN101575408B (zh) 2008-05-09 2013-10-30 Mca技术有限公司 用作阻燃剂和光稳定剂的聚三嗪基化合物
EP3782611B1 (fr) 2008-05-15 2022-07-06 Celgene Corporation Formulations orales d'analogues de cytidine et leurs procédés d'utilisation
FR2932483A1 (fr) 2008-06-13 2009-12-18 Cytomics Systems Composes utiles pour le traitement des cancers.
WO2010007756A1 (fr) 2008-07-14 2010-01-21 塩野義製薬株式会社 Dérivé de pyridine ayant une activité d'inhibition de la ttk
WO2010028179A1 (fr) 2008-09-03 2010-03-11 Dr. Reddy's Laboratories Ltd. Composés hétérocycliques comme modulateurs de gata
EP3266879B1 (fr) 2008-09-03 2019-07-03 The Johns Hopkins University Altérations génétiques de l'isocitrate déshydrogénase et d'autres gènes dans le gliome malin
JP2010079130A (ja) 2008-09-29 2010-04-08 Fuji Xerox Co Ltd 電子写真感光体、プロセスカートリッジ、及び画像形成装置
JP2012509321A (ja) 2008-11-21 2012-04-19 ミレニアム ファーマシューティカルズ， インコーポレイテッド 癌および他の疾患または障害の処置のための、４−［６−メトキシ−７−（３−ピペリジン−１−イル−プロポキシ）キナゾリン−４−イル］ピペラジン−１−カルボン酸（４−イソプロポキシフェニル）−アミドの乳酸塩およびその薬学的組成物
JP2010181540A (ja) 2009-02-04 2010-08-19 Fuji Xerox Co Ltd 電子写真感光体、プロセスカートリッジ、及び画像形成装置
BRPI1008661B8 (pt) 2009-02-06 2021-05-25 Nippon Shinyaku Co Ltd compostos derivados de aminopirazina, seu uso e composição farmacêutica
ES2740424T3 (es) 2009-03-13 2020-02-05 Agios Pharmaceuticals Inc Métodos y composiciones para trastornos relacionados con la proliferación celular
PL2427441T3 (pl) 2009-05-04 2017-06-30 Agios Pharmaceuticals, Inc. Aktywatory PKM2 do stosowania w leczeniu raka
WO2010130638A1 (fr) 2009-05-14 2010-11-18 Evotec Ag Composés sulfamides, compositions pharmaceutiques et leurs utilisations
BRPI1010881A2 (pt) 2009-06-08 2016-05-31 California Capital Equity Llc derivados de triazina e suas aplicações terapêuticas.
WO2010144522A1 (fr) 2009-06-09 2010-12-16 Abraxis Bioscience, Llc Dérivés de la triazine substituée à l'uréidophényle et leurs applications thérapeutiques
US20120277233A1 (en) 2009-06-09 2012-11-01 California Capital Equity, Llc Pyridyl-Triazine Inhibitors of Hedgehog Signaling
CN102481300B (zh) 2009-06-29 2015-04-15 安吉奥斯医药品有限公司 治疗性化合物和组合物
ES2582535T3 (es) 2009-07-10 2016-09-13 Kirk Promotion Ltd. Dispositivo de articulación de la rodilla
JP2013503846A (ja) 2009-09-01 2013-02-04 ファイザー・インク ベンズイミダゾール誘導体
CA2773561A1 (fr) 2009-09-14 2011-03-17 Phusis Therapeutics Inc. Compositions et formulations pharmaceutiques comprenant des inhibiteurs du domaine d'homologie a la pleckstrine et leurs methodes d'utilisation
JP5473851B2 (ja) 2009-09-30 2014-04-16 富士フイルム株式会社 高分子フィルム、位相差フィルム、偏光板及び液晶表示装置
US8652534B2 (en) 2009-10-14 2014-02-18 Berry Pharmaceuticals, LLC Compositions and methods for treatment of mammalian skin
EP2491145B1 (fr) 2009-10-21 2016-03-09 Agios Pharmaceuticals, Inc. Procédés et compositions pour des troubles relatifs à la prolifération cellulaire
US9062076B2 (en) 2009-10-22 2015-06-23 Fibrotech Therapeutics Pty Ltd Fused ring analogues of anti-fibrotic agents
EP2509600B1 (fr) 2009-12-09 2017-08-02 Agios Pharmaceuticals, Inc. Composés thérapeutiquement actifs destinés au traitement d'un cancer caractérisé par une mutation idh
NZ578968A (en) 2010-02-10 2011-03-31 Allans Sheetmetal And Engineering Services Fuel feed system for a pellet fire
WO2011123618A1 (fr) 2010-04-01 2011-10-06 Agios Pharmaceuticals, Inc. Procédés d'identification d'un composé candidat
US20130109643A1 (en) 2010-05-10 2013-05-02 The Johns Hopkins University Metabolic inhibitor against tumors having an idh mutation
WO2012006506A1 (fr) 2010-07-09 2012-01-12 Massachusetts Institute Of Technology Genès, enzymes et flux constituant des cibles métaboliques pour la thérapie contre le cancer
BR112013001122B1 (pt) 2010-07-16 2021-06-08 Agios Pharmaceuticals, Inc composto de fórmula ii, uso do composto e composição farmacêutica compreendendo dito composto
CA2814581C (fr) 2010-10-21 2019-02-12 Biomarin Pharmaceutical Inc. Sel tosylate de la (8s,9r)-5-fluoro-8-(4-fluorophenyl)-9-(1-methyl-1h- 1,2,4-triazol-5-yl)-8,9-dihydro-2h-pyrido[4,3,2-de]phtalazin-3(7h)-one cristallin
WO2012078288A2 (fr) 2010-11-08 2012-06-14 Washington University Méthodes de détermination du risque d'évolutions défavorables dans la leucémie myéloïde aiguë
CN103347866B (zh) 2010-11-29 2016-05-18 加林制药公司 作为治疗呼吸控制不适或疾病的呼吸兴奋剂的新化合物
TWI549947B (zh) 2010-12-29 2016-09-21 阿吉歐斯製藥公司 治療化合物及組成物
WO2012173682A2 (fr) 2011-03-29 2012-12-20 The Broad Institute, Inc. Composés et méthodes de traitement de maladies liées à l'isocitrate déshydrogénase
CA2834692A1 (fr) 2011-05-03 2012-11-08 Agios Pharmaceuticals, Inc. Activateurs de la pyruvate kinase destines a une utilisation therapeutique
TWI555737B (zh) 2011-05-24 2016-11-01 拜耳知識產權公司 含有硫醯亞胺基團之４－芳基－ｎ－苯基－１，３，５－三氮雜苯－２－胺
WO2012170284A1 (fr) 2011-06-06 2012-12-13 Merck Sharp & Dohme Corp. Inhibition médiée par interférence par arn de l'expression du gène de l'isocitrate déshydrogénase (idh1)
CN102827170A (zh) 2011-06-17 2012-12-19 安吉奥斯医药品有限公司 治疗活性组合物和它们的使用方法
CN102827073A (zh) 2011-06-17 2012-12-19 安吉奥斯医药品有限公司 治疗活性组合物和它们的使用方法
US9199962B2 (en) 2011-07-07 2015-12-01 Merck Patent Gmbh Substituted azaheterocycles for the treatment of cancer
WO2013007708A1 (fr) 2011-07-08 2013-01-17 Helmholtz-Zentrum für Infektionsforschung GmbH Médicament pour le traitement du cancer du foie
WO2013016206A1 (fr) 2011-07-22 2013-01-31 University Of Louisville Research Foundation, Inc. Composés anti-biofilm
GEP20166432B (en) 2011-09-27 2016-02-10 Novartis Ag 3-pyrimidin-4-yl-oxazolidin-2-ones as inhibitors of mutant idh
CN102659765B (zh) 2011-12-31 2014-09-10 沈阳药科大学 嘧啶及三嗪类化合物的制备方法和应用
EP3984997A1 (fr) 2012-01-06 2022-04-20 Les Laboratoires Servier SAS Composés thérapeutiquement actifs et leurs procédés d'utilisation
US9474779B2 (en) 2012-01-19 2016-10-25 Agios Pharmaceuticals, Inc. Therapeutically active compositions and their methods of use
CA2860858A1 (fr) 2012-01-19 2013-07-25 Agios Pharmaceuticals, Inc. Composes therapeutiquement actifs et leurs methodes d'utilisation
EP2634259A1 (fr) 2012-03-01 2013-09-04 Deutsches Krebsforschungszentrum Supports et procédés pour la détermination du (D)-2-hydroxyglutarate (D2HG)
KR20140131955A (ko) 2012-03-09 2014-11-14 카나 바이오사이언스 인코포레이션 신규 트리아진 유도체
WO2014015422A1 (fr) 2012-07-27 2014-01-30 Ontario Institute For Cancer Research Nanoparticules à base de cellulose pour administration de médicament
US10202339B2 (en) 2012-10-15 2019-02-12 Agios Pharmaceuticals, Inc. Therapeutic compounds and compositions
US9579324B2 (en) 2013-07-11 2017-02-28 Agios Pharmaceuticals, Inc Therapeutically active compounds and their methods of use
WO2015003360A2 (fr) 2013-07-11 2015-01-15 Agios Pharmaceuticals, Inc. Composés thérapeutiquement actifs et leurs méthodes d'utilisation
US20150031627A1 (en) 2013-07-25 2015-01-29 Agios Pharmaceuticals, Inc Therapeutically active compounds and their methods of use
WO2015127173A1 (fr) 2014-02-20 2015-08-27 Agios Pharmaceuticals, Inc Composés thérapeutiquement actifs et leurs procédés d'utilisation
RS62178B1 (sr) 2014-03-14 2021-08-31 Les Laboratoires Servier Sas Farmaceutske kompozicije terapeutski aktivnih jedinjenja
KR102400737B1 (ko) 2014-03-14 2022-05-20 아지오스 파마슈티컬스 아이엔씨. 치료적으로 활성인 화합물의 약제학적 조성물
CN108697698B (zh) 2015-10-15 2021-12-03 阿吉奥斯制药公司 用于治疗恶性肿瘤的组合疗法
EP4403173A3 (fr) 2015-10-15 2024-10-09 Les Laboratoires Servier Polythérapie pour le traitement de tumeurs malignes
CA3007363A1 (fr) 2015-12-04 2017-06-08 Agios Pharmaceuticals, Inc. Methodes de traitement de tumeurs malignes
JP6856657B2 (ja) 2016-02-26 2021-04-07 アジオス ファーマシューティカルズ， インコーポレイテッド 血液学的悪性疾患および固形腫瘍の処置のためのｉｄｈ１阻害剤

Also Published As

Publication number Publication date
US9850277B2 (en) 2017-12-26
AR122902A2 (es) 2022-10-12
HUE039110T2 (hu) 2018-12-28
HK1198439A1 (en) 2015-04-24
FIC20230031I1 (fi) 2023-10-10
PE20190801A1 (es) 2019-06-10
SG10201608374XA (en) 2016-12-29
EP3447052A1 (fr) 2019-02-27
MY178486A (en) 2020-10-14
HUE057264T2 (hu) 2022-05-28
NL301243I2 (nl) 2023-10-04
AR089768A1 (es) 2014-09-17
CA2861556A1 (fr) 2013-07-25
CO7010834A2 (es) 2014-07-31
PH12014501626A1 (en) 2014-10-13
FR23C1031I1 (fr) 2023-10-13
LT2804851T (lt) 2018-09-10
CY1120651T1 (el) 2019-12-11
HRP20220017T1 (hr) 2022-04-01
CN104136411A (zh) 2014-11-05
PH12017501419A1 (en) 2018-10-08
NI201400078A (es) 2014-10-10
AU2017265100A1 (en) 2017-12-14
IL281942A (en) 2021-05-31
CY2023023I1 (el) 2024-02-16
JP2019031562A (ja) 2019-02-28
CN106496090B (zh) 2020-04-21
HRP20181199T1 (hr) 2018-11-16
US20130190249A1 (en) 2013-07-25
KR102108507B1 (ko) 2020-05-08
US10717764B2 (en) 2020-07-21
US10640534B2 (en) 2020-05-05
KR20190128747A (ko) 2019-11-18
BR112014017840B1 (pt) 2023-01-17
ZA202100373B (en) 2023-04-26
JP6313714B2 (ja) 2018-04-18
IL233683A0 (en) 2014-09-30
EP2804851B1 (fr) 2018-07-18
EP2804851A4 (fr) 2015-06-24
CR20140388A (es) 2014-11-13
PE20141824A1 (es) 2014-12-11
SI2804851T1 (sl) 2018-11-30
US20190315802A1 (en) 2019-10-17
CN106496090A (zh) 2017-03-15
SI3447052T1 (sl) 2022-04-29
JP2015509098A (ja) 2015-03-26
IL264516B (en) 2021-04-29
PH12018501410A1 (en) 2019-08-14
RS57730B1 (sr) 2018-12-31
DK3447052T3 (da) 2022-01-17
EA201491391A1 (ru) 2014-10-30
JP6805220B2 (ja) 2020-12-23
SG11201404190PA (en) 2014-08-28
US20180194802A1 (en) 2018-07-12
SG10202103521PA (en) 2021-05-28
US20240059733A1 (en) 2024-02-22
HUS2300035I1 (hu) 2024-07-28
AU2019283951A1 (en) 2020-01-23
MX351166B (es) 2017-10-04
PL3447052T3 (pl) 2022-05-09
RS62919B1 (sr) 2022-03-31
US9474779B2 (en) 2016-10-25
NZ722400A (en) 2018-02-23
EP3447052B1 (fr) 2021-10-20
CR20170097A (es) 2017-06-30
PT3447052T (pt) 2022-01-18
KR20200049913A (ko) 2020-05-08
EA201692271A1 (ru) 2018-01-31
CA2861556C (fr) 2021-07-13
EP2804851A1 (fr) 2014-11-26
MX2014008744A (es) 2014-08-29
JP2021038263A (ja) 2021-03-11
TW201331177A (zh) 2013-08-01
US11667673B2 (en) 2023-06-06
IL233683B (en) 2019-02-28
BR112014017840A8 (pt) 2017-07-11
PH12017501419B1 (en) 2018-10-08
DK2804851T3 (en) 2018-09-03
EA026723B1 (ru) 2017-05-31
US20160130298A1 (en) 2016-05-12
TW201843136A (zh) 2018-12-16
CN104136411B (zh) 2016-10-12
NZ627053A (en) 2017-01-27
US20170015703A1 (en) 2017-01-19
ES2903390T3 (es) 2022-04-01
UA115047C2 (uk) 2017-09-11
NO2023038I1 (no) 2023-10-13
PH12014501626B1 (en) 2014-10-13
ECSP14014544A (es) 2015-12-31
UA122324C2 (uk) 2020-10-26
PL2804851T3 (pl) 2018-11-30
WO2013107291A1 (fr) 2013-07-25
CA3077245A1 (fr) 2013-07-25
EA035662B1 (ru) 2020-07-23
AU2013211436B2 (en) 2017-08-24
PT2804851T (pt) 2018-10-15
AU2013211436A1 (en) 2014-07-24
KR20140127255A (ko) 2014-11-03
KR102144739B1 (ko) 2020-08-18
BR112014017840A2 (fr) 2017-06-20
IL281942B (en) 2022-03-01
CL2014001891A1 (es) 2014-11-14
IL264516A (en) 2019-02-28
TWI713847B (zh) 2020-12-21
ES2685746T3 (es) 2018-10-11
US20210024575A1 (en) 2021-01-28
IN2014DN05986A (fr) 2015-06-26
AU2019283951B2 (en) 2021-05-13
LT3447052T (lt) 2022-02-10
JP2017101067A (ja) 2017-06-08
EP3985001A1 (fr) 2022-04-20
CY1124988T1 (el) 2023-01-05
AU2017265100B2 (en) 2019-10-03
KR102044730B1 (ko) 2019-11-15
TWI636040B (zh) 2018-09-21

Similar Documents

Publication Publication Date Title
FR23C1031I2 (fr) Derives de lactames en tant qu'inhibiteurs d'idh1 mutants
FR22C1010I2 (fr) Composes heterocycliques fusionnes en tant qu'inhibiteurs de proteine kinase
FR22C1047I1 (fr) Derives de benzimidazole-proline
FR3000492B1 (fr) Nouveaux derives azaindole en tant qu'inhibiteurs multikinases
CR20150120A (es) Nuevos derivados bicíclicos
BR112015003190A2 (pt) haxacianetos de ferro de solubilidade alta
UY34602A (es) ?Derivados de bencimidazolil- e imidazopiridinil-metilamina?
MA41140A (fr) Dérivés de 2,4-dioxo-quinazoline-6-sulfonamide en tant qu'inhibiteurs de la parg
BR112014028334A2 (pt) derivados dipeptídicos de lisina ácido glutâmico.
HK1259439A1 (zh) 確定體細胞誘變原因的方法
BR112013023056A2 (pt) derivados de oxaespiro [2,5] octano e análogos
BR302012004133S1 (pt) "configuração aplicada em barra de chocolate"
FR2979931B1 (fr) Potelet de garde-corps ou d'echafaudage equipe d'un bloqueur perfectionne
CL2014003125A1 (es) Anticuerpos de anti-transglutaminasa 2
ZA201405959B (en) Novel neurokinin 1 receptor antagonist compounds
FR2967353B1 (fr) Derives de quinolinone
DK2854789T3 (da) Genotype- eller fænotype-baserede lægemiddelformuleringer
UY34834A (es) Dispensación de artículos
CO7020921A2 (es) Agonistas de mglu 2/3
FR2987866B1 (fr) Profil de bout d'aube
TH149331B (th) "วิธีการสำหรับฆ่าเชื้อพื้นผิว"
UA23860S (uk) Профіль з'єднувальний
FR2988834B1 (fr) Methode d'interpolation de signal evenementiel
EP2865747A4 (fr) Dérivé d'acide 4,6-hexadécadiène-2,4-dicarboxylique
HN2012002443S1 (es) Set plastico multiusos 4 niveles variedad de colores