HUE033615T2 - Imidazol-karboxamidok, és FAAH inhibitorként történõ alkalmazásuk - Google Patents

Imidazol-karboxamidok, és FAAH inhibitorként történõ alkalmazásuk Download PDF

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Publication number
HUE033615T2
HUE033615T2 HUE14752676A HUE14752676A HUE033615T2 HU E033615 T2 HUE033615 T2 HU E033615T2 HU E14752676 A HUE14752676 A HU E14752676A HU E14752676 A HUE14752676 A HU E14752676A HU E033615 T2 HUE033615 T2 HU E033615T2
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HU
Hungary
Prior art keywords
salt
compound
disease
active
faah
Prior art date
Application number
HUE14752676A
Other languages
English (en)
Hungarian (hu)
Inventor
Carla Patricia Da Costa Pereira Rosa
De Noronha Rita Gusmâo
Laszlo Erno Kiss
Original Assignee
Bial - Portela & Ca S A
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
Priority claimed from GB201313203A external-priority patent/GB201313203D0/en
Priority claimed from GB201313202A external-priority patent/GB201313202D0/en
Priority claimed from GB201313204A external-priority patent/GB201313204D0/en
Application filed by Bial - Portela & Ca S A filed Critical Bial - Portela & Ca S A
Publication of HUE033615T2 publication Critical patent/HUE033615T2/hu

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    • 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
    • C07D405/02Heterocyclic 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 two hetero rings
    • C07D405/12Heterocyclic 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 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
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/41641,3-Diazoles
    • A61K31/41781,3-Diazoles not condensed 1,3-diazoles and containing further heterocyclic rings, e.g. pilocarpine, nitrofurantoin
    • 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
    • A61K31/454Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
    • 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
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D235/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
    • C07D235/02Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
    • C07D235/04Benzimidazoles; Hydrogenated benzimidazoles
    • C07D235/24Benzimidazoles; Hydrogenated benzimidazoles 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 in position 2
    • 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

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Addiction (AREA)
  • Psychiatry (AREA)
  • Pain & Pain Management (AREA)
  • Epidemiology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Rheumatology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Immunology (AREA)
  • Diabetes (AREA)
  • Pulmonology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Psychology (AREA)
  • Child & Adolescent Psychology (AREA)
  • Ophthalmology & Optometry (AREA)
  • Hospice & Palliative Care (AREA)
  • Otolaryngology (AREA)
  • Anesthesiology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Dermatology (AREA)
HUE14752676A 2013-07-24 2014-07-24 Imidazol-karboxamidok, és FAAH inhibitorként történõ alkalmazásuk HUE033615T2 (hu)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB201313203A GB201313203D0 (en) 2013-07-24 2013-07-24 Urea compound and its use as an enzyme inhibitor
GB201313202A GB201313202D0 (en) 2013-07-24 2013-07-24 Urea Compound And Its Use As An Enzyme Inhibitor
GB201313204A GB201313204D0 (en) 2013-07-24 2013-07-24 Urea compound and its use as an enzyme inhibitor

Publications (1)

Publication Number Publication Date
HUE033615T2 true HUE033615T2 (hu) 2017-12-28

Family

ID=51358056

Family Applications (1)

Application Number Title Priority Date Filing Date
HUE14752676A HUE033615T2 (hu) 2013-07-24 2014-07-24 Imidazol-karboxamidok, és FAAH inhibitorként történõ alkalmazásuk

Country Status (20)

Country Link
US (2) US10501447B2 (cg-RX-API-DMAC7.html)
EP (1) EP3024825B1 (cg-RX-API-DMAC7.html)
JP (1) JP6449277B2 (cg-RX-API-DMAC7.html)
KR (1) KR20160034359A (cg-RX-API-DMAC7.html)
CN (1) CN105793247B (cg-RX-API-DMAC7.html)
AU (1) AU2014293731B2 (cg-RX-API-DMAC7.html)
CA (1) CA2918993C (cg-RX-API-DMAC7.html)
CY (1) CY1119482T1 (cg-RX-API-DMAC7.html)
DK (1) DK3024825T3 (cg-RX-API-DMAC7.html)
ES (1) ES2640800T3 (cg-RX-API-DMAC7.html)
HR (1) HRP20171378T1 (cg-RX-API-DMAC7.html)
HU (1) HUE033615T2 (cg-RX-API-DMAC7.html)
LT (1) LT3024825T (cg-RX-API-DMAC7.html)
MX (1) MX362315B (cg-RX-API-DMAC7.html)
PL (1) PL3024825T3 (cg-RX-API-DMAC7.html)
PT (1) PT3024825T (cg-RX-API-DMAC7.html)
RS (1) RS56297B1 (cg-RX-API-DMAC7.html)
RU (1) RU2671404C2 (cg-RX-API-DMAC7.html)
SI (1) SI3024825T1 (cg-RX-API-DMAC7.html)
WO (1) WO2015012708A1 (cg-RX-API-DMAC7.html)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MY172113A (en) 2017-07-05 2019-11-14 Frimline Private Ltd A pharmaceutical composition for neuropathic pain
US10702487B2 (en) 2017-08-19 2020-07-07 Frimline Private Limited Pharmaceutical composition for prevention of diet induced obesity
PH12018000227B1 (en) 2017-09-05 2019-03-11 Frimline Private Ltd A pharmaceutical composition for improving or preventing progression of chronic kidney disease

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2458965C3 (de) 1974-12-13 1979-10-11 Bayer Ag, 5090 Leverkusen 3-Amino-indazol-N-carbonsäure-Derivate, Verfahren zu ihrer Herstellung sowie sie enthaltende Arzneimittel
EP0014810A3 (en) 1979-01-18 1980-11-26 Fbc Limited Pesticidal pyrazoles, their production, compositions and uses, as well as intermediates and their preparation
JPH01203366A (ja) 1988-02-10 1989-08-16 Mitsui Petrochem Ind Ltd N−置換イミダゾール誘導体
JP3457669B2 (ja) 1992-10-28 2003-10-20 富山化学工業株式会社 新規な1,2−ベンゾイソオキサゾール誘導体またはその塩,それらからなる脳保護剤
DE102004005172A1 (de) 2004-02-02 2005-08-18 Aventis Pharma Deutschland Gmbh Indazolderivate als Inhibitoren der Hormon Sensitiven Lipase
ES2639621T3 (es) * 2004-12-30 2017-10-27 Janssen Pharmaceutica N.V. Derivados de fenilamida del ácido 4-(bencil)-piperazina-1-carboxílico y compuestos relacionados como moduladores de la amida hidrolasa de ácidos grasos (FAAH) para el tratamiento de la ansiedad, el dolor y otras afecciones
FI20075264A0 (fi) 2007-04-18 2007-04-18 Kuopion Yliopisto Heterosykliset fenyylikarbamaatit uusina FAAH-inhibiittoreina
US8324241B2 (en) 2008-04-11 2012-12-04 Bristol-Myers Squibb Company Triazolo compounds useful as DGAT1 inhibitors
BRPI0923819B1 (pt) * 2008-12-24 2021-11-09 Bial-Portela & Ca, S.A. Compostos inibidores de hidrolase amida de ácidos graxos, composições e usos dos mesmos
CA2806701A1 (en) 2010-07-29 2012-02-02 Bial - Portela & Ca, S.A. Process for the synthesis of substituted urea compounds
FR2965262A1 (fr) 2010-09-24 2012-03-30 Sanofi Aventis Derives de nicotinamide, leur preparation et leur application en therapeutique
MX365772B (es) 2012-07-24 2019-06-13 Bial Portela & Ca Sa Compuestos de urea y su uso como inhibidores de enzimas.

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Publication number Publication date
EP3024825A1 (en) 2016-06-01
CN105793247B (zh) 2018-03-16
AU2014293731B2 (en) 2018-03-08
MX2016000797A (es) 2016-09-08
JP6449277B2 (ja) 2019-01-09
SI3024825T1 (sl) 2017-11-30
CY1119482T1 (el) 2018-03-07
ES2640800T3 (es) 2017-11-06
DK3024825T3 (en) 2017-10-02
PL3024825T3 (pl) 2017-12-29
RS56297B1 (sr) 2017-12-29
JP2016525543A (ja) 2016-08-25
RU2671404C2 (ru) 2018-10-31
WO2015012708A1 (en) 2015-01-29
KR20160034359A (ko) 2016-03-29
PT3024825T (pt) 2017-09-28
LT3024825T (lt) 2017-12-11
EP3024825B1 (en) 2017-06-21
US10501447B2 (en) 2019-12-10
CA2918993C (en) 2021-08-24
HRP20171378T1 (hr) 2017-12-15
US20160176854A1 (en) 2016-06-23
CN105793247A (zh) 2016-07-20
AU2014293731A1 (en) 2016-02-11
US20200255412A1 (en) 2020-08-13
CA2918993A1 (en) 2015-01-29
MX362315B (es) 2019-01-11
RU2016104221A (ru) 2017-08-29

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