IL227496B - Pyrazolo[4,3–b]pyridines are converted as drugs - Google Patents

Pyrazolo[4,3–b]pyridines are converted as drugs

Info

Publication number
IL227496B
IL227496B IL227496A IL22749613A IL227496B IL 227496 B IL227496 B IL 227496B IL 227496 A IL227496 A IL 227496A IL 22749613 A IL22749613 A IL 22749613A IL 227496 B IL227496 B IL 227496B
Authority
IL
Israel
Prior art keywords
pyridines
medicaments
substituted pyrazolo
pyrazolo
substituted
Prior art date
Application number
IL227496A
Other languages
English (en)
Hebrew (he)
Other versions
IL227496A0 (en
Inventor
Ei Bachir Kaloun
Karim Bedjeguelal
Remi Rabot
Anna Kruczynski
Philippe Schmitt
Michel Perez
Nicolas Rahier
Original Assignee
Pf Medicament
Ei Bachir Kaloun
Karim Bedjeguelal
Remi Rabot
Anna Kruczynski
Philippe Schmitt
Michel Perez
Nicolas Rahier
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 Pf Medicament, Ei Bachir Kaloun, Karim Bedjeguelal, Remi Rabot, Anna Kruczynski, Philippe Schmitt, Michel Perez, Nicolas Rahier filed Critical Pf Medicament
Publication of IL227496A0 publication Critical patent/IL227496A0/en
Publication of IL227496B publication Critical patent/IL227496B/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non 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
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
    • 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
    • A61K31/4985Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • 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
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Pain & Pain Management (AREA)
  • Psychiatry (AREA)
  • Rheumatology (AREA)
  • Hospice & Palliative Care (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Plural Heterocyclic Compounds (AREA)
IL227496A 2011-01-27 2013-07-16 Pyrazolo[4,3–b]pyridines are converted as drugs IL227496B (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR1150651A FR2970967B1 (fr) 2011-01-27 2011-01-27 Derives de type azaindazole ou diazaindazole comme medicament
PCT/EP2012/051283 WO2012101239A1 (en) 2011-01-27 2012-01-27 Derivatives of azaindazole or diazaindazole type as medicament

Publications (2)

Publication Number Publication Date
IL227496A0 IL227496A0 (en) 2013-09-30
IL227496B true IL227496B (en) 2019-02-28

Family

ID=44318089

Family Applications (2)

Application Number Title Priority Date Filing Date
IL227496A IL227496B (en) 2011-01-27 2013-07-16 Pyrazolo[4,3–b]pyridines are converted as drugs
IL257748A IL257748B (en) 2011-01-27 2018-02-26 Derivatives of pyrazole [4,3-b]pyridine, pyrazolo[4,3-b]pyridine and pyrazolo[4,3-b]pyrazine for use in the treatment of cancer, inflammatory diseases and neurodegenerative diseases,

Family Applications After (1)

Application Number Title Priority Date Filing Date
IL257748A IL257748B (en) 2011-01-27 2018-02-26 Derivatives of pyrazole [4,3-b]pyridine, pyrazolo[4,3-b]pyridine and pyrazolo[4,3-b]pyrazine for use in the treatment of cancer, inflammatory diseases and neurodegenerative diseases,

Country Status (30)

Country Link
US (2) US20130172360A1 (cg-RX-API-DMAC10.html)
EP (1) EP2668184B1 (cg-RX-API-DMAC10.html)
JP (1) JP5931926B2 (cg-RX-API-DMAC10.html)
KR (2) KR101923751B1 (cg-RX-API-DMAC10.html)
CN (1) CN103339129B (cg-RX-API-DMAC10.html)
AR (1) AR084935A1 (cg-RX-API-DMAC10.html)
AU (1) AU2012210467B2 (cg-RX-API-DMAC10.html)
BR (1) BR112013018852B1 (cg-RX-API-DMAC10.html)
CA (1) CA2823824C (cg-RX-API-DMAC10.html)
CY (1) CY1120088T1 (cg-RX-API-DMAC10.html)
DK (1) DK2668184T3 (cg-RX-API-DMAC10.html)
ES (1) ES2661695T3 (cg-RX-API-DMAC10.html)
FR (1) FR2970967B1 (cg-RX-API-DMAC10.html)
HR (1) HRP20180524T1 (cg-RX-API-DMAC10.html)
HU (1) HUE037153T2 (cg-RX-API-DMAC10.html)
IL (2) IL227496B (cg-RX-API-DMAC10.html)
LT (1) LT2668184T (cg-RX-API-DMAC10.html)
MA (1) MA34903B1 (cg-RX-API-DMAC10.html)
MX (1) MX356411B (cg-RX-API-DMAC10.html)
MY (1) MY180666A (cg-RX-API-DMAC10.html)
PL (1) PL2668184T3 (cg-RX-API-DMAC10.html)
PT (1) PT2668184T (cg-RX-API-DMAC10.html)
RS (1) RS57101B1 (cg-RX-API-DMAC10.html)
RU (1) RU2600976C2 (cg-RX-API-DMAC10.html)
SI (1) SI2668184T1 (cg-RX-API-DMAC10.html)
TN (1) TN2013000293A1 (cg-RX-API-DMAC10.html)
TR (1) TR201802944T4 (cg-RX-API-DMAC10.html)
TW (1) TWI546303B (cg-RX-API-DMAC10.html)
UA (1) UA109698C2 (cg-RX-API-DMAC10.html)
WO (1) WO2012101239A1 (cg-RX-API-DMAC10.html)

Families Citing this family (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8754114B2 (en) 2010-12-22 2014-06-17 Incyte Corporation Substituted imidazopyridazines and benzimidazoles as inhibitors of FGFR3
FR2970967B1 (fr) * 2011-01-27 2013-02-15 Pf Medicament Derives de type azaindazole ou diazaindazole comme medicament
US9458147B2 (en) 2012-02-22 2016-10-04 Sanford-Burnham Medical Research Institute Sulfonamide compounds and uses as TNAP inhibitors
CN107652289B (zh) 2012-06-13 2020-07-21 因塞特控股公司 作为fgfr抑制剂的取代的三环化合物
EP2689779A1 (en) 2012-07-27 2014-01-29 Pierre Fabre Medicament Derivatives of azaindazole or diazaindazole type for treating a cancer overexpressing trk
EP2689778A1 (en) * 2012-07-27 2014-01-29 Pierre Fabre Medicament Derivatives of azaindoles or diazaindoles for treating pain
US9388185B2 (en) 2012-08-10 2016-07-12 Incyte Holdings Corporation Substituted pyrrolo[2,3-b]pyrazines as FGFR inhibitors
US9266892B2 (en) 2012-12-19 2016-02-23 Incyte Holdings Corporation Fused pyrazoles as FGFR inhibitors
JP6449244B2 (ja) 2013-04-19 2019-01-09 インサイト・ホールディングス・コーポレイションIncyte Holdings Corporation Fgfr抑制剤としての二環式複素環
US10851105B2 (en) 2014-10-22 2020-12-01 Incyte Corporation Bicyclic heterocycles as FGFR4 inhibitors
EP3233840B1 (en) 2014-12-16 2018-11-21 Eudendron S.r.l. Heterocyclic derivatives modulating activity of certain protein kinases
MA41551A (fr) 2015-02-20 2017-12-26 Incyte Corp Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4
WO2016134294A1 (en) 2015-02-20 2016-08-25 Incyte Corporation Bicyclic heterocycles as fgfr4 inhibitors
ES2751669T3 (es) 2015-02-20 2020-04-01 Incyte Corp Heterociclos bicíclicos como inhibidores FGFR
US10211205B2 (en) * 2016-04-27 2019-02-19 International Business Machines Corporation Field effect transistor structure for reducing contact resistance
CN108570052A (zh) * 2017-03-13 2018-09-25 中国科学院上海药物研究所 五元杂环并吡嗪化合物、制备方法、中间体、组合和应用
AR111960A1 (es) 2017-05-26 2019-09-04 Incyte Corp Formas cristalinas de un inhibidor de fgfr y procesos para su preparación
AU2019264078A1 (en) * 2018-05-02 2020-12-17 Jw Pharmaceutical Corporation Novel heterocycle derivative
PE20210919A1 (es) 2018-05-04 2021-05-19 Incyte Corp Sales de un inhibidor de fgfr
CN119241541A (zh) 2018-05-04 2025-01-03 因赛特公司 Fgfr抑制剂的固体形式和其制备方法
WO2020185532A1 (en) 2019-03-08 2020-09-17 Incyte Corporation Methods of treating cancer with an fgfr inhibitor
EP3725777A1 (en) * 2019-04-17 2020-10-21 Rottapharm Biotech S.r.l. Benzo- and pyrido-pyrazoles as protein kinase inhibitors
US11591329B2 (en) 2019-07-09 2023-02-28 Incyte Corporation Bicyclic heterocycles as FGFR inhibitors
WO2021067374A1 (en) 2019-10-01 2021-04-08 Incyte Corporation Bicyclic heterocycles as fgfr inhibitors
GEP20247679B (en) 2019-10-14 2024-10-10 Incyte Corp Bicyclic heterocycles as fgfr inhibitors
US11566028B2 (en) 2019-10-16 2023-01-31 Incyte Corporation Bicyclic heterocycles as FGFR inhibitors
IL293001A (en) 2019-12-04 2022-07-01 Incyte Corp Derivatives of fgfr repressors
CA3163875A1 (en) 2019-12-04 2021-06-10 Incyte Corporation Tricyclic heterocycles as fgfr inhibitors
JP2023509421A (ja) * 2019-12-31 2023-03-08 アイエフエム デュー インコーポレイテッド Sting活性に関連する状態を治療するための化合物および組成物
US12012409B2 (en) 2020-01-15 2024-06-18 Incyte Corporation Bicyclic heterocycles as FGFR inhibitors
CN115916771B (zh) * 2020-04-02 2025-04-01 浙江华海药业股份有限公司 多靶点的抗肿瘤化合物及其制备方法和应用
WO2022106902A2 (en) 2020-11-20 2022-05-27 2692372 Ontario, Inc. Benzenesulfonamide derivatives and uses thereof
JP2024513575A (ja) 2021-04-12 2024-03-26 インサイト・コーポレイション Fgfr阻害剤及びネクチン-4標的化剤を含む併用療法
WO2022261160A1 (en) 2021-06-09 2022-12-15 Incyte Corporation Tricyclic heterocycles as fgfr inhibitors
AR126101A1 (es) 2021-06-09 2023-09-13 Incyte Corp Heterociclos tricíclicos como inhibidores de fgfr

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ID24653A (id) * 1997-03-19 2000-07-27 Basf Ag Zat-zat terapi
EP1215208B1 (en) 1997-10-27 2006-07-12 Agouron Pharmaceuticals, Inc. 4-Aminothiazole derivatives, their preparation and their use as inhibitors of cyclin-dependent kinases
EP1292586B1 (en) 2000-06-22 2004-08-04 Pfizer Limited Process for the preparation of pyrazolopyrimidinones
AU2003245700A1 (en) * 2002-02-12 2003-09-04 Glaxo Group Limited Pyrazolopyridine derivatives
DE102004061288A1 (de) * 2004-12-14 2006-06-29 Schering Ag 3-Amino-Pyrazolo[3,4b]pyridine als Inhibitoren von Proteintyrosinkinasen, deren Herstellung und Verwendung als Arzneimittel
BRPI0614884A2 (pt) * 2005-08-25 2011-04-19 Hoffmann La Roche inibidores de p38 map cinase e métodos para uso dos mesmos
AU2007275816A1 (en) 2006-07-17 2008-01-24 Merck Sharp & Dohme Corp. 1-hydroxy naphthyridine compounds as anti-HIV agents
CN101594862B (zh) 2006-12-20 2015-11-25 内尔维阿诺医学科学有限公司 作为激酶抑制剂的取代吲唑衍生物
CA2693901C (en) 2007-07-20 2015-12-29 Nerviano Medical Sciences S.R.L. Substituted indazole derivatives active as kinase inhibitors
ES2630026T3 (es) 2008-12-18 2017-08-17 Nerviano Medical Sciences S.R.L. Derivados indazólicos sustituidos activos como inhibidores de cinasa
FR2970967B1 (fr) * 2011-01-27 2013-02-15 Pf Medicament Derives de type azaindazole ou diazaindazole comme medicament

Also Published As

Publication number Publication date
MA34903B1 (fr) 2014-02-01
US20130085144A1 (en) 2013-04-04
FR2970967A1 (fr) 2012-08-03
UA109698C2 (xx) 2015-09-25
TWI546303B (zh) 2016-08-21
KR20180122028A (ko) 2018-11-09
CN103339129A (zh) 2013-10-02
SI2668184T1 (en) 2018-06-29
PL2668184T3 (pl) 2018-06-29
IL257748B (en) 2020-06-30
RS57101B1 (sr) 2018-06-29
IL257748A (en) 2018-04-30
RU2013138624A (ru) 2015-03-10
CA2823824A1 (en) 2012-08-02
EP2668184B1 (en) 2018-01-10
PT2668184T (pt) 2018-03-13
TR201802944T4 (tr) 2018-03-21
JP5931926B2 (ja) 2016-06-08
MX356411B (es) 2018-05-24
BR112013018852B1 (pt) 2021-12-21
MY180666A (en) 2020-12-04
MX2013008673A (es) 2013-12-02
US20130172360A1 (en) 2013-07-04
DK2668184T3 (en) 2018-03-12
RU2600976C2 (ru) 2016-10-27
HK1186737A1 (en) 2014-03-21
JP2014503574A (ja) 2014-02-13
KR101923751B1 (ko) 2018-11-29
CN103339129B (zh) 2015-07-29
WO2012101239A1 (en) 2012-08-02
NZ614432A (en) 2015-03-27
AR084935A1 (es) 2013-07-10
HUE037153T2 (hu) 2018-08-28
TN2013000293A1 (en) 2015-01-20
ES2661695T3 (es) 2018-04-03
BR112013018852A2 (pt) 2017-08-15
CA2823824C (en) 2018-12-11
HRP20180524T1 (hr) 2018-05-04
FR2970967B1 (fr) 2013-02-15
EP2668184A1 (en) 2013-12-04
US8883821B2 (en) 2014-11-11
AU2012210467B2 (en) 2016-07-07
AU2012210467A1 (en) 2013-09-12
IL227496A0 (en) 2013-09-30
TW201247664A (en) 2012-12-01
CY1120088T1 (el) 2018-12-12
LT2668184T (lt) 2018-04-10
KR20140014147A (ko) 2014-02-05

Similar Documents

Publication Publication Date Title
IL227496B (en) Pyrazolo[4,3–b]pyridines are converted as drugs
ZA201906379B (en) 1h-pyrazolo[3,4-b]pyridines and therapeutic uses thereof
ZA201307783B (en) Tri-and tetracylic pyrazolo[3,4-b]pyridine compounds as antineoplastic agent
IL234485A (en) Compounds based on imidazo [2,1 – b] pyridazine
IL235819A0 (en) Preparation of pyrrolo[b–3,2]pyridines
SMT201700539T1 (it) DERIVATI IMIDAZO[1,2-b]PIRIDAZINICI COME INIBITORI DI CHINASI
ZA201206630B (en) Hetaryl-[1,8]naphthyridine derivatives
ZA201307511B (en) Pyrido [2,3-b] pyrazine derivatives and their therapeutical uses
IL232717B (en) 3-cyanoaryl-h1-pyrrolo[b-3,2]pyridine derivatives
IL221479A0 (en) Triazolo [4,5-b] pyridin derivatives
ZA201404074B (en) 6-difluoromethyl-5,6-dihydro-2h-[1,4]oxazin-3-amine derivatives
ZA201301313B (en) Herbicidal isoxazolo[5,4-b]pyridines
IL230740A0 (en) Decorative insulating products for construction
SG11201408816QA (en) 3-(PYRAZOLYL)-1H-PYRROLO[2,3-b]PYRIDINE DERIVATIVES AS KINASE INHIBITORS
IL230834A0 (en) History of pyrido-pyrimidine, their preparation and medicines containing them
ZA201305227B (en) Pharmaceutical composition comprising pyridone derivatives
ZA201304074B (en) Pyrazino[2,3-d]isoxazole derivative
EP2565194A4 (en) IMIDAZO [1,2-a] PYRIDINE DERIVATIVE
PL2729473T3 (pl) Pochodne kwasu karboksylowego z pierścieniem oksazolo[5,4-B]pirydynowym
GB201221462D0 (en) Novel isothiazolo[5,4-b]pyridines
GB201213663D0 (en) Novel isothiazolo[5,4-b]pyridines
GB201211756D0 (en) Novel isothiazolo [4,3-b]pyridines
EP2865747A4 (en) 4,6-HEXADECADIENE-2,4-DICARBOXYLIC ACID DERIVATIVE
AU2011246168A1 (en) Imidazo[1,2-a]pyridine derivative

Legal Events

Date Code Title Description
FF Patent granted
KB Patent renewed