IL111148A0 - Imidazol-4- ylpiperidine derivatives, their preparation and their application in therapeutics - Google Patents

Imidazol-4- ylpiperidine derivatives, their preparation and their application in therapeutics

Info

Publication number
IL111148A0
IL111148A0 IL11114894A IL11114894A IL111148A0 IL 111148 A0 IL111148 A0 IL 111148A0 IL 11114894 A IL11114894 A IL 11114894A IL 11114894 A IL11114894 A IL 11114894A IL 111148 A0 IL111148 A0 IL 111148A0
Authority
IL
Israel
Prior art keywords
imidazol
therapeutics
preparation
application
ylpiperidine
Prior art date
Application number
IL11114894A
Other languages
English (en)
Original Assignee
Synthelabo
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 Synthelabo filed Critical Synthelabo
Publication of IL111148A0 publication Critical patent/IL111148A0/xx

Links

Classifications

    • 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
    • C07D471/00—Heterocyclic 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
    • C07D471/02—Heterocyclic 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
    • C07D471/06—Peri-condensed systems
    • 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic 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
    • C07D487/06—Peri-condensed systems

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
IL11114894A 1993-10-04 1994-10-03 Imidazol-4- ylpiperidine derivatives, their preparation and their application in therapeutics IL111148A0 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR9311771A FR2710915B1 (fr) 1993-10-04 1993-10-04 Dérivés de pipéridine, leur préparation et leur utilisation en thérapeutique.

Publications (1)

Publication Number Publication Date
IL111148A0 true IL111148A0 (en) 1994-12-29

Family

ID=9451496

Family Applications (1)

Application Number Title Priority Date Filing Date
IL11114894A IL111148A0 (en) 1993-10-04 1994-10-03 Imidazol-4- ylpiperidine derivatives, their preparation and their application in therapeutics

Country Status (18)

Country Link
US (1) US5589476A (xx)
EP (1) EP0646583A1 (xx)
JP (1) JPH07179466A (xx)
KR (1) KR950011435A (xx)
CN (1) CN1109471A (xx)
AU (1) AU7432994A (xx)
CA (1) CA2133491A1 (xx)
CZ (1) CZ241994A3 (xx)
FI (1) FI944600A (xx)
FR (1) FR2710915B1 (xx)
HU (1) HUT71120A (xx)
IL (1) IL111148A0 (xx)
NO (1) NO943682L (xx)
NZ (1) NZ264596A (xx)
PL (1) PL305288A1 (xx)
RU (1) RU94036003A (xx)
SK (1) SK119494A3 (xx)
ZA (1) ZA947710B (xx)

Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5500423A (en) * 1994-09-09 1996-03-19 Hoechst-Roussel Pharmaceuticals Inc. 5,6-dihydro-4H-imidazo[4,5,1-ij]quinolines
FR2731708B1 (fr) * 1995-03-13 1997-04-30 Synthelabo Derives de piperidine, leur procede de preparation et leur application en therapeutique
ATE230988T1 (de) * 1995-09-18 2003-02-15 Glaxo Group Ltd Die verwendung von ondansetron zur herstellung eines medikamentes zur behandlung von tremor
FR2747678B1 (fr) * 1996-04-22 1998-05-22 Synthelabo Composes derives d'imidazobenzoxazine, leurs procedes de preparation et leurs utilisations en therapeutique
FR2753196B1 (fr) * 1996-09-12 1998-10-23 Synthelabo Derives d'indazole tricyclique, leur preparation et leur application en therapeutique
DK1104289T3 (da) * 1998-08-21 2006-05-15 Novartis Ag Hidtil ukendte orale formuleringer for 5-HT4-agonister eller -antagonister
IT1303123B1 (it) 1998-10-13 2000-10-30 Rotta Research Lab Derivati basici di benz(e)isoindol-1-oni e pirrolo(3,4-c)chinolin-1-oni ad attivita' 5ht3 antagonista, loro preparazione ed
GB9918425D0 (en) * 1999-08-04 1999-10-06 Novartis Ag Organic compounds
FR2812878B1 (fr) * 2000-08-08 2002-10-11 Sanofi Synthelabo Derives de benzimidazole, leur preparation et leur application en therapeutique
FR2816619B1 (fr) * 2000-11-15 2003-01-31 Sanofi Synthelabo Derives de benzimidazole, leur preparation et leur application en therapeutique
CN1446218A (zh) * 2000-08-08 2003-10-01 圣诺菲-合成实验室公司 苯并咪唑衍生物,它们的制备方法以及它们的治疗应用
FR2816942B1 (fr) * 2000-11-23 2003-05-09 Sanofi Synthelabo Derives de benzimidazole, leur preparation et leur application en therapeutique
FR2816941B1 (fr) * 2000-11-23 2003-01-31 Sanofi Synthelabo Derives de benzimidazole, leur preparation et leur application en therapeutique
US20040242635A1 (en) * 2001-03-30 2004-12-02 Painter Rachel J. Encapsulated dyes in cosmetic compositions
WO2003104233A1 (en) * 2002-06-07 2003-12-18 Altana Pharma Ag 4,5-dihydro-imidazo (4,5,1-ij) quinolin-6-ones derivatives and their use as poly (adp-ribosyl) transferase (parp) inhibitors
UA119848C2 (uk) 2013-03-15 2019-08-27 Інсайт Холдинґс Корпорейшн Трициклічні гетероцикли як інгібітори білків бет
US9290514B2 (en) 2013-07-08 2016-03-22 Incyte Holdings Corporation Tricyclic heterocycles as BET protein inhibitors
US9399640B2 (en) 2013-11-26 2016-07-26 Incyte Corporation Substituted pyrrolo[2,3-c]pyridines and pyrazolo[3,4-c]pyridines as BET protein inhibitors
WO2015081189A1 (en) 2013-11-26 2015-06-04 Incyte Corporation Bicyclic heterocycles as bet protein inhibitors
US9309246B2 (en) 2013-12-19 2016-04-12 Incyte Corporation Tricyclic heterocycles as BET protein inhibitors
EA039678B1 (ru) 2014-04-23 2022-02-24 Инсайт Корпорейшн 1H-ПИРРОЛО[2,3-c]ПИРИДИН-7(6H)-ОНЫ И ПИРАЗОЛО[3,4-c]ПИРИДИН-7(6H)-ОНЫ В КАЧЕСТВЕ ИНГИБИТОРОВ БЕЛКОВ BET
TWI712603B (zh) 2014-09-15 2020-12-11 美商英塞特公司 作為ｂｅｔ蛋白抑制劑之三環雜環
US20170121347A1 (en) 2015-10-29 2017-05-04 Incyte Corporation Amorphous solid form of a bet protein inhibitor
PT3472157T (pt) 2016-06-20 2023-05-30 Incyte Corp Formas sólidas cristalinas de um inibidor bet
US11833155B2 (en) 2020-06-03 2023-12-05 Incyte Corporation Combination therapy for treatment of myeloproliferative neoplasms

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4939138A (en) * 1988-12-29 1990-07-03 Sterling Drug Inc. 2- and 3-aminomethyl-6-arylcarbonyl-2,3-dihydropyrrolo(1,2,3-DE)-1,4-benzoxazines
FR2674855B1 (fr) * 1991-04-03 1994-01-14 Synthelabo Derives de piperidine, leur preparation et leur application en therapeutique.

Also Published As

Publication number Publication date
US5589476A (en) 1996-12-31
HU9402832D0 (en) 1995-01-30
FR2710915B1 (fr) 1995-11-24
RU94036003A (ru) 1996-08-10
ZA947710B (en) 1995-08-10
CA2133491A1 (en) 1995-04-05
AU7432994A (en) 1995-04-13
CN1109471A (zh) 1995-10-04
NO943682L (no) 1995-04-05
NO943682D0 (no) 1994-10-03
CZ241994A3 (en) 1995-04-12
HUT71120A (en) 1995-11-28
FR2710915A1 (fr) 1995-04-14
PL305288A1 (en) 1995-04-18
JPH07179466A (ja) 1995-07-18
KR950011435A (ko) 1995-05-15
FI944600A0 (fi) 1994-10-03
EP0646583A1 (fr) 1995-04-05
FI944600A (fi) 1995-04-05
SK119494A3 (en) 1995-05-10
NZ264596A (en) 1995-11-27

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