DK2864328T3 - PHARMACEUTICAL ACTIVE RELATIONS - Google Patents

PHARMACEUTICAL ACTIVE RELATIONS Download PDF

Info

Publication number
DK2864328T3
DK2864328T3 DK13731470.4T DK13731470T DK2864328T3 DK 2864328 T3 DK2864328 T3 DK 2864328T3 DK 13731470 T DK13731470 T DK 13731470T DK 2864328 T3 DK2864328 T3 DK 2864328T3
Authority
DK
Denmark
Prior art keywords
compound
compounds
pharmaceutically acceptable
solvate
acceptable salt
Prior art date
Application number
DK13731470.4T
Other languages
Danish (da)
English (en)
Inventor
Julian Blagg
Vassilios Bavetsias
Spyridon Linardopoulos
Andrew S Moore
Original Assignee
The Institute Of Cancer Res Royal Cancer Hospital
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 The Institute Of Cancer Res Royal Cancer Hospital filed Critical The Institute Of Cancer Res Royal Cancer Hospital
Application granted granted Critical
Publication of DK2864328T3 publication Critical patent/DK2864328T3/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/06Peri-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
DK13731470.4T 2012-06-21 2013-06-21 PHARMACEUTICAL ACTIVE RELATIONS DK2864328T3 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB1211021.9A GB201211021D0 (en) 2012-06-21 2012-06-21 Pharmaceutically active compounds
PCT/GB2013/051633 WO2013190319A1 (en) 2012-06-21 2013-06-21 Pharmaceutically active compounds

Publications (1)

Publication Number Publication Date
DK2864328T3 true DK2864328T3 (en) 2018-03-12

Family

ID=46641296

Family Applications (1)

Application Number Title Priority Date Filing Date
DK13731470.4T DK2864328T3 (en) 2012-06-21 2013-06-21 PHARMACEUTICAL ACTIVE RELATIONS

Country Status (23)

Country Link
US (1) US9447092B2 (en:Method)
EP (1) EP2864328B8 (en:Method)
JP (1) JP6159397B2 (en:Method)
CN (1) CN104470922B (en:Method)
AU (1) AU2013279040B2 (en:Method)
BR (1) BR112014032142B1 (en:Method)
CA (1) CA2876357C (en:Method)
CY (1) CY1120608T1 (en:Method)
DK (1) DK2864328T3 (en:Method)
ES (1) ES2660159T3 (en:Method)
GB (1) GB201211021D0 (en:Method)
HR (1) HRP20180386T1 (en:Method)
HU (1) HUE036048T2 (en:Method)
IN (1) IN2015MN00045A (en:Method)
LT (1) LT2864328T (en:Method)
NO (1) NO2864328T3 (en:Method)
PL (1) PL2864328T3 (en:Method)
PT (1) PT2864328T (en:Method)
RS (1) RS56996B1 (en:Method)
RU (1) RU2654942C2 (en:Method)
SI (1) SI2864328T1 (en:Method)
SM (1) SMT201800128T1 (en:Method)
WO (1) WO2013190319A1 (en:Method)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB201522532D0 (en) * 2015-12-21 2016-02-03 Cancer Rec Tech Ltd Novel pyrrolo[3,2-c]pyridine-6-amino derivatives
US11340215B2 (en) 2016-02-26 2022-05-24 Japanese Foundation For Cancer Research Screening method of anticancer agent focused on function of HP1 and evaluation system
GB2592622B (en) * 2020-03-04 2022-08-03 Ellipses Pharma Ltd Formulations of a dual aurora kinase/FLT3 inhibitor
GB2596038B (en) * 2020-03-04 2022-12-14 Ellipses Pharma Ltd Salts and polymorphic forms of (6-chloro-7-(4-(4-chlorobenzyl)piperazin-1-yl)-2-(1,3-dimethyl-1H-pyrazol-4-yl)-3H-imidazo[4,5-B]pyridine)

Family Cites Families (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9624482D0 (en) 1995-12-18 1997-01-15 Zeneca Phaema S A Chemical compounds
US6184225B1 (en) 1996-02-13 2001-02-06 Zeneca Limited Quinazoline derivatives as VEGF inhibitors
DE69709319T2 (de) 1996-03-05 2002-08-14 Astrazeneca Ab, Soedertaelje 4-anilinochinazolin derivate
GB9718972D0 (en) 1996-09-25 1997-11-12 Zeneca Ltd Chemical compounds
GB9714249D0 (en) 1997-07-08 1997-09-10 Angiogene Pharm Ltd Vascular damaging agents
GB9900334D0 (en) 1999-01-07 1999-02-24 Angiogene Pharm Ltd Tricylic vascular damaging agents
GB9900752D0 (en) 1999-01-15 1999-03-03 Angiogene Pharm Ltd Benzimidazole vascular damaging agents
CA2406979A1 (en) 2000-05-31 2001-12-06 Astrazeneca Ab Indole derivatives with vascular damaging activity
UA73993C2 (uk) 2000-06-06 2005-10-17 Астразенека Аб Хіназолінові похідні для лікування пухлин та фармацевтична композиція
BR0112224A (pt) 2000-07-07 2003-06-10 Angiogene Pharm Ltd Composto, composição farmacêutica, uso de um composto ou de um sal, solvato ou pró-droga farmaceuticamente aceitável do mesmo, e, processo para preparar um composto
HUP0301742A3 (en) 2000-07-07 2005-08-29 Angiogene Pharm Ltd Colchinol derivatives as angiogenesis inhibitors, process for producing them, pharmaceutical compositions containing them and their use
WO2003004488A1 (en) * 2001-07-03 2003-01-16 Chiron Corporation Indazole benzimidazole compounds as tyrosine and serine/threonine kinase inhibitors
TWI372050B (en) * 2003-07-03 2012-09-11 Astex Therapeutics Ltd (morpholin-4-ylmethyl-1h-benzimidazol-2-yl)-1h-pyrazoles
CN102127078A (zh) * 2005-07-14 2011-07-20 安斯泰来制药株式会社 Janus激酶3的杂环类抑制剂
US8088761B2 (en) * 2005-12-22 2012-01-03 Cancer Research Technology Limited Enzyme inhibitors
CN101616920A (zh) * 2007-01-30 2009-12-30 比奥根艾迪克Ma公司 1-H-吡唑并(3,4b)嘧啶衍生物及其作为有丝分裂激酶调节剂的用途
WO2009001021A1 (en) 2007-06-26 2008-12-31 Chroma Therapeutics Ltd. Imidazopyridine derivatives useful as enzyme inhibitors for the treatment of cell proliferative and autoimmune diseases
CN102143746A (zh) * 2008-07-03 2011-08-03 埃克塞利希斯股份有限公司 Cdk 调节剂
AR082986A1 (es) * 2010-09-14 2013-01-23 Exelixis Inc DERIVADOS DE PURINA COMO INHIBIDORES DE PI3K-d, METODOS PARA SU PREPARACION, FORMULACIONES FARMACEUTICAS QUE LOS COMPRENDEN Y SU USO EN EL TRATAMIENTO DE ENFERMEDADES HIPERPROLIFERATIVAS

Also Published As

Publication number Publication date
JP2015520222A (ja) 2015-07-16
US9447092B2 (en) 2016-09-20
CY1120608T1 (el) 2019-12-11
RS56996B1 (sr) 2018-05-31
BR112014032142A2 (pt) 2017-06-27
HRP20180386T1 (hr) 2018-04-20
EP2864328B1 (en) 2017-12-06
PT2864328T (pt) 2018-03-12
SMT201800128T1 (it) 2018-05-02
RU2015101702A (ru) 2016-08-10
US20150266868A1 (en) 2015-09-24
RU2654942C2 (ru) 2018-05-25
ES2660159T3 (es) 2018-03-21
LT2864328T (lt) 2018-04-10
WO2013190319A1 (en) 2013-12-27
GB201211021D0 (en) 2012-08-01
HUE036048T2 (hu) 2018-06-28
IN2015MN00045A (en:Method) 2015-10-16
BR112014032142B1 (pt) 2022-03-03
AU2013279040A1 (en) 2015-01-29
EP2864328A1 (en) 2015-04-29
PL2864328T3 (pl) 2018-06-29
SI2864328T1 (en) 2018-04-30
CA2876357A1 (en) 2013-12-27
NO2864328T3 (en:Method) 2018-05-05
EP2864328B8 (en) 2018-01-24
CN104470922B (zh) 2016-08-24
JP6159397B2 (ja) 2017-07-05
AU2013279040B2 (en) 2017-11-16
CN104470922A (zh) 2015-03-25
CA2876357C (en) 2020-07-14

Similar Documents

Publication Publication Date Title
EP2958898B1 (en) 2-(hetero)aryl-benzimidazole and imidazopyridine derivatives as inhibitors of asparagime emethyl transferase
US11787786B2 (en) Fused 1,4-dihydrodioxin derivatives as inhibitors of heat shock transcription factor 1
US20220402912A1 (en) Inhibitor compounds
EP3575299B1 (en) N2-phenyl-pyrido[3,4-d]pyrimidine-2,8-diamine derivatives and their use as mps1 inhibitors
DK2864328T3 (en) PHARMACEUTICAL ACTIVE RELATIONS
AU2016375851B2 (en) Novel pyrrolo[3,2-c]pyridine-6-amino derivatives
WO2013190320A1 (en) Imidazopyridines as inhibitors of aurora kinase and/or flt3
AU2020311297A1 (en) DERIVATIVES OF 4-(IMIDAZO[l,2-a]PYRIDIN-3-YL)-N-(PYRIDINYL)PYRIMIDIN- 2-AMINE AS THERAPEUTIC AGENTS
EP4584267A1 (en) Novel compounds as ck2 inhibitors
HK40010173A (en) N2-phenyl-pyrido[3,4-d]pyrimidine-2,8-diamine derivatives and their use as mps1 inhibitors
HK40010173B (en) N2-phenyl-pyrido[3,4-d]pyrimidine-2,8-diamine derivatives and their use as mps1 inhibitors
HK1262217B (en) Pyrrolo[3,2-c]pyridine-6-amino derivatives
HK1262217A1 (en) Pyrrolo[3,2-c]pyridine-6-amino derivatives
HK1113352A1 (en) Chemical compounds