CY1112670T1 - Παραγωγα του 5.6-bisaryl-2-πυριδιν-καρβοξαμιδιου, η παρασκευη τους και η εφαρμογη τους σε θεραπευτικη αγωγη ως ανταγωνιστες των υποδοχεων στην ουροτενσινη ii - Google Patents

Παραγωγα του 5.6-bisaryl-2-πυριδιν-καρβοξαμιδιου, η παρασκευη τους και η εφαρμογη τους σε θεραπευτικη αγωγη ως ανταγωνιστες των υποδοχεων στην ουροτενσινη ii

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Publication number
CY1112670T1
CY1112670T1 CY20121100089T CY121100089T CY1112670T1 CY 1112670 T1 CY1112670 T1 CY 1112670T1 CY 20121100089 T CY20121100089 T CY 20121100089T CY 121100089 T CY121100089 T CY 121100089T CY 1112670 T1 CY1112670 T1 CY 1112670T1
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CY
Cyprus
Prior art keywords
application
bisaryl
carboxamide
pyridin
preparation
Prior art date
Application number
CY20121100089T
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English (en)
Inventor
Jean-Michel Altenburger
Valérie FOSSEY
Daniel Galtier
Frédéric PETIT
Original Assignee
Sanofi
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Publication date
Application filed by Sanofi filed Critical Sanofi
Publication of CY1112670T1 publication Critical patent/CY1112670T1/el

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    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/08—Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
    • 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
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    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
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    • A61P25/00—Drugs for disorders of the nervous system
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    • A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
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    • A—HUMAN NECESSITIES
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    • A61P25/28—Drugs 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
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    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
    • C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/81—Amides; Imides
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    • C07D—HETEROCYCLIC COMPOUNDS
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    • C07D241/10—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D241/14—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members 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
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    • 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
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    • C07D405/00—Heterocyclic 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
    • C07D405/02—Heterocyclic 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
    • C07D405/04—Heterocyclic 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 directly linked by a ring-member-to-ring-member bond

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Cardiology (AREA)
  • Diabetes (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pulmonology (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychiatry (AREA)
  • Endocrinology (AREA)
  • Urology & Nephrology (AREA)
  • Pain & Pain Management (AREA)
  • Vascular Medicine (AREA)
  • Otolaryngology (AREA)
  • Anesthesiology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Rheumatology (AREA)
  • Emergency Medicine (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

Η εφεύρεση αφορά ενώσεις οι οποίες αντιστοιχούν στο χημικό τύπο (Ι): στον οποίο τα Χ, Υ, Α, Β, W, Ζ, p, R1, R2 και R3 είναι όπως ορίστηκαν στην περιγραφή. Διαδικασία παρασκευής και εφαρμογή σε θεραπευτική αγωγή.
CY20121100089T 2008-02-07 2012-01-25 Παραγωγα του 5.6-bisaryl-2-πυριδιν-καρβοξαμιδιου, η παρασκευη τους και η εφαρμογη τους σε θεραπευτικη αγωγη ως ανταγωνιστες των υποδοχεων στην ουροτενσινη ii CY1112670T1 (el)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR0800651A FR2927330B1 (fr) 2008-02-07 2008-02-07 Derives de 5,6-bisaryl-2-pyridine-carboxamide, leur preparation et leur application en therapeutique comme antagonistes des recepteurs a l'urotensine ii
EP09721603A EP2238110B1 (fr) 2008-02-07 2009-02-05 Dérivés de 5.6-bisaryl-2-pyr1dine-carboxamide, leur préparatio leur application en thérapeutique comme antagonistes des recepteurs a l'urotensine ii

Publications (1)

Publication Number Publication Date
CY1112670T1 true CY1112670T1 (el) 2016-02-10

Family

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Family Applications (1)

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CY20121100089T CY1112670T1 (el) 2008-02-07 2012-01-25 Παραγωγα του 5.6-bisaryl-2-πυριδιν-καρβοξαμιδιου, η παρασκευη τους και η εφαρμογη τους σε θεραπευτικη αγωγη ως ανταγωνιστες των υποδοχεων στην ουροτενσινη ii

Country Status (22)

Country Link
US (2) US8466292B2 (el)
EP (1) EP2238110B1 (el)
JP (1) JP2011511046A (el)
KR (1) KR20100116183A (el)
CN (1) CN101981008B (el)
AR (1) AR070573A1 (el)
AT (1) ATE530527T1 (el)
AU (1) AU2009227091B2 (el)
BR (1) BRPI0907719A2 (el)
CA (1) CA2715096A1 (el)
CY (1) CY1112670T1 (el)
DK (1) DK2238110T3 (el)
ES (1) ES2375339T3 (el)
FR (1) FR2927330B1 (el)
HR (1) HRP20120069T1 (el)
IL (1) IL207356A0 (el)
MX (1) MX2010008713A (el)
PL (1) PL2238110T3 (el)
PT (1) PT2238110E (el)
RU (1) RU2497808C2 (el)
SI (1) SI2238110T1 (el)
WO (1) WO2009115665A1 (el)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10703722B2 (en) 2010-04-27 2020-07-07 Calcimedica, Inc. Compounds that modulate intracellular calcium
CN104837832B (zh) * 2012-10-05 2019-04-26 里格尔药品股份有限公司 Gdf-8抑制剂
MX369491B (es) 2013-12-24 2019-11-11 Bristol Myers Squibb Co Compuestos tricíclicos como agentes anticancerígenos.
ES2959658T3 (es) 2015-02-27 2024-02-27 Calcimedica Inc Tratamiento de la pancreatitis
WO2016183114A1 (en) 2015-05-11 2016-11-17 Bristol-Myers Squibb Company Tricyclic compounds as anticancer agents
WO2017019757A1 (en) 2015-07-28 2017-02-02 Bristol-Myers Squibb Company Tgf beta receptor antagonists
CA2995094A1 (en) * 2015-08-07 2017-02-16 Calcimedica, Inc. Use of crac channel inhibitors for the treatment of stroke and traumatic brain injury
KR20180042370A (ko) 2015-08-25 2018-04-25 브리스톨-마이어스 스큅 컴퍼니 Tgf 베타 수용체 길항제
BR112018010410A8 (pt) 2015-11-23 2019-02-26 Five Prime Therapeutics Inc método para tratar câncer em um sujeito, composição e métodos de aumento do número de células nk e de aumento do número de uma ou mais células positivas para pd-l1
SG10201913033UA (en) 2016-03-04 2020-03-30 Bristol Myers Squibb Co Combination therapy with anti-cd73 antibodies
TW202106676A (zh) 2019-04-05 2021-02-16 美商凱麥拉醫療公司 Stat降解劑及其用途

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE0100902D0 (sv) * 2001-03-15 2001-03-15 Astrazeneca Ab Compounds
SE0104332D0 (sv) * 2001-12-19 2001-12-19 Astrazeneca Ab Therapeutic agents
EP2415760A3 (en) * 2003-02-20 2012-02-22 Encysive Pharmaceuticals, Inc. CCR-9 antagonists
CA2517166A1 (en) * 2003-02-28 2004-09-16 Encysive Pharmaceuticals Inc. Pyridine, pyrimidine, quinoline, quinazoline, and naphthalene urotensin-ii receptor antagonists
FR2856684B1 (fr) * 2003-06-26 2008-04-11 Sanofi Synthelabo Derives de diphenylpyridine, leur preparation et leur application en therapeutique
FR2904827B1 (fr) * 2006-08-11 2008-09-19 Sanofi Aventis Sa Derives de 5,6-bisaryl-2-pyridine-carboxamide, leur preparation et leur application en therapeutique comme antiganistes des recepteurs a l'urotensine ii

Also Published As

Publication number Publication date
ATE530527T1 (de) 2011-11-15
WO2009115665A1 (fr) 2009-09-24
EP2238110B1 (fr) 2011-10-26
HRP20120069T1 (hr) 2012-02-29
US8653276B2 (en) 2014-02-18
CN101981008A (zh) 2011-02-23
US8466292B2 (en) 2013-06-18
KR20100116183A (ko) 2010-10-29
CN101981008B (zh) 2013-07-31
PT2238110E (pt) 2012-01-02
CA2715096A1 (fr) 2009-09-24
RU2497808C2 (ru) 2013-11-10
PL2238110T3 (pl) 2012-03-30
US20110009426A1 (en) 2011-01-13
BRPI0907719A2 (pt) 2015-07-14
US20130252974A1 (en) 2013-09-26
ES2375339T3 (es) 2012-02-29
AR070573A1 (es) 2010-04-21
AU2009227091A1 (en) 2009-09-24
FR2927330A1 (fr) 2009-08-14
DK2238110T3 (da) 2012-02-20
RU2010137115A (ru) 2012-03-20
AU2009227091B2 (en) 2013-05-23
EP2238110A1 (fr) 2010-10-13
MX2010008713A (es) 2010-09-09
JP2011511046A (ja) 2011-04-07
SI2238110T1 (sl) 2012-02-29
IL207356A0 (en) 2010-12-30
FR2927330B1 (fr) 2010-02-19

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