IL136145A0 - Heterocyclic compounds for inhibition of gastric acid secretion, processes for their preparation and pharmaceutical compositions thereof - Google Patents

Heterocyclic compounds for inhibition of gastric acid secretion, processes for their preparation and pharmaceutical compositions thereof

Info

Publication number
IL136145A0
IL136145A0 IL13614598A IL13614598A IL136145A0 IL 136145 A0 IL136145 A0 IL 136145A0 IL 13614598 A IL13614598 A IL 13614598A IL 13614598 A IL13614598 A IL 13614598A IL 136145 A0 IL136145 A0 IL 136145A0
Authority
IL
Israel
Prior art keywords
inhibition
processes
preparation
pharmaceutical compositions
heterocyclic compounds
Prior art date
Application number
IL13614598A
Other languages
English (en)
Original Assignee
Astrazeneca Ab
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 Astrazeneca Ab filed Critical Astrazeneca Ab
Publication of IL136145A0 publication Critical patent/IL136145A0/xx

Links

Classifications

    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04Antibacterial agents

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
IL13614598A 1997-11-28 1998-11-18 Heterocyclic compounds for inhibition of gastric acid secretion, processes for their preparation and pharmaceutical compositions thereof IL136145A0 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
SE9704404A SE9704404D0 (sv) 1997-11-28 1997-11-28 New compounds
PCT/SE1998/002091 WO1999028322A1 (en) 1997-11-28 1998-11-18 Heterocyclic compounds for inhibition of gastric acid secretion, processes for their preparation and pharmaceutical compositions thereof

Publications (1)

Publication Number Publication Date
IL136145A0 true IL136145A0 (en) 2001-05-20

Family

ID=20409181

Family Applications (1)

Application Number Title Priority Date Filing Date
IL13614598A IL136145A0 (en) 1997-11-28 1998-11-18 Heterocyclic compounds for inhibition of gastric acid secretion, processes for their preparation and pharmaceutical compositions thereof

Country Status (32)

Country Link
US (1) US6518270B1 (cg-RX-API-DMAC7.html)
EP (1) EP1042324B1 (cg-RX-API-DMAC7.html)
JP (1) JP2001525322A (cg-RX-API-DMAC7.html)
KR (1) KR20010032559A (cg-RX-API-DMAC7.html)
CN (1) CN1142933C (cg-RX-API-DMAC7.html)
AR (1) AR016972A1 (cg-RX-API-DMAC7.html)
AT (1) ATE233263T1 (cg-RX-API-DMAC7.html)
AU (1) AU752187C (cg-RX-API-DMAC7.html)
BR (1) BR9814755A (cg-RX-API-DMAC7.html)
CA (1) CA2311798A1 (cg-RX-API-DMAC7.html)
CZ (1) CZ292349B6 (cg-RX-API-DMAC7.html)
DE (1) DE69811735T2 (cg-RX-API-DMAC7.html)
DK (1) DK1042324T3 (cg-RX-API-DMAC7.html)
EE (1) EE04060B1 (cg-RX-API-DMAC7.html)
ES (1) ES2191356T3 (cg-RX-API-DMAC7.html)
HU (1) HUP0100601A3 (cg-RX-API-DMAC7.html)
ID (1) ID24730A (cg-RX-API-DMAC7.html)
IL (1) IL136145A0 (cg-RX-API-DMAC7.html)
IS (1) IS5486A (cg-RX-API-DMAC7.html)
MY (1) MY121032A (cg-RX-API-DMAC7.html)
NO (1) NO315704B1 (cg-RX-API-DMAC7.html)
NZ (1) NZ504355A (cg-RX-API-DMAC7.html)
PL (1) PL340920A1 (cg-RX-API-DMAC7.html)
PT (1) PT1042324E (cg-RX-API-DMAC7.html)
RU (1) RU2241000C2 (cg-RX-API-DMAC7.html)
SE (1) SE9704404D0 (cg-RX-API-DMAC7.html)
SK (1) SK283904B6 (cg-RX-API-DMAC7.html)
TR (1) TR200001530T2 (cg-RX-API-DMAC7.html)
TW (1) TW515798B (cg-RX-API-DMAC7.html)
UA (1) UA70932C2 (cg-RX-API-DMAC7.html)
WO (1) WO1999028322A1 (cg-RX-API-DMAC7.html)
ZA (1) ZA9810468B (cg-RX-API-DMAC7.html)

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SE9704404D0 (sv) 1997-11-28 1997-11-28 Astra Ab New compounds
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JP2005530739A (ja) * 2002-04-19 2005-10-13 セルラー ジェノミクス,インコーポレーテッド イミダゾ[1,2−a]ピラジン−8−イルアミン、生成方法、および使用方法
AU2003270489A1 (en) 2002-09-09 2004-03-29 Cellular Genomics, Inc. 6-ARYL-IMIDAZO(1,2-a)PYRAZIN-8-YLAMINES, METHOD OF MAKING, AND METHOD OF USE THEREOF
WO2004029057A1 (ja) * 2002-09-25 2004-04-08 Sankyo Company, Limited 内臓痛の治療または予防のための医薬組成物
WO2004029058A1 (ja) * 2002-09-25 2004-04-08 Sankyo Company, Limited 血中ガストリン濃度上昇の抑制のための医薬組成物
EP1575951B1 (en) 2002-12-06 2014-06-25 Debiopharm International SA Heterocyclic compounds, methods of making them and their use in therapy
US7160885B2 (en) 2003-02-10 2007-01-09 Cgi Pharmaceuticals, Inc. Certain 6, 8-(heteroaryl or aryl) disubstituted imidazo[1,2-a]pyrazines as modulators of Hsp90 complex activity
AR043002A1 (es) * 2003-02-18 2005-07-13 Altana Pharma Ag Imidazopirazinas 6-substituidos
JP4880448B2 (ja) * 2003-03-17 2012-02-22 アフィナム ファーマシューティカルズ,インコーポレーテッド 複数の抗生物質を含む組成物、及びそれを用いる方法
WO2005014599A1 (en) 2003-06-04 2005-02-17 Cellular Genomics, Inc. Imidazo[1,2-a]pyrazin-8-ylamines and method of inhibition of bruton’s tyrosine kinase by such compounds
US7393848B2 (en) 2003-06-30 2008-07-01 Cgi Pharmaceuticals, Inc. Certain heterocyclic substituted imidazo[1,2-A]pyrazin-8-ylamines and methods of inhibition of Bruton's tyrosine kinase by such compounds
WO2005019220A2 (en) 2003-08-11 2005-03-03 Cellular Genomics Inc. Substituted imidazo[1,2-a]pyrazines as modulators of kinase activity
EP1974730A1 (en) 2003-11-03 2008-10-01 AstraZeneca AB Imidazo[1,2-a]pyridine derivatives for use in the treatment of sleep disturbance due to silent gastro-esophageal reflux
KR101299399B1 (ko) * 2004-06-04 2013-08-22 아피늄 파마슈티컬스, 인크. 치료제, 및 그의 제조 및 사용 방법
KR101764575B1 (ko) * 2004-07-28 2017-08-03 다케다 야쿠힌 고교 가부시키가이샤 피롤로〔2,3-c〕피리딘 화합물, 그 제조 방법 및 용도
JP2008508347A (ja) * 2004-08-02 2008-03-21 ニコメッド ゲゼルシャフト ミット ベシュレンクテル ハフツング 5置換された1H−ピロロ[3,2−b]ピリジン
US8148529B2 (en) * 2004-09-03 2012-04-03 Yuhan Corporation Pyrrolo[3,2-C] pyridine derivatives and processes for the preparation thereof
PL1784404T3 (pl) 2004-09-03 2012-04-30 Yuhan Corp Pochodne pirolo[2,3-c]pirydyny i sposoby ich wytwarzania
JP4989477B2 (ja) * 2004-09-03 2012-08-01 ユーハン・コーポレイション ピロロ[3,2−c]ピリジン誘導体及びその製造方法
EP1784403B1 (en) * 2004-09-03 2013-07-17 Yuhan Corporation Pyrrolo[3,2-b]pyridine derivatives and processes for the preparation thereof
US7777040B2 (en) 2005-05-03 2010-08-17 Cgi Pharmaceuticals, Inc. Certain substituted ureas, as modulators of kinase activity
JP2009507032A (ja) 2005-09-02 2009-02-19 アボット・ラボラトリーズ 新規なイミダゾ系複素環
WO2007067416A2 (en) * 2005-12-05 2007-06-14 Affinium Pharmaceuticals, Inc. Heterocyclylacrylamide compounds as fabi inhibitors and antibacterial agents
WO2007145921A1 (en) * 2006-06-06 2007-12-21 Schering Corporation Imidazopyrazines as protein kinase inhibitors
JP5468899B2 (ja) * 2006-07-20 2014-04-09 アフィニウム ファーマシューティカルズ, インク. Fabiインヒビターとしてのアクリルアミド誘導体
EP2125802A4 (en) 2007-02-16 2014-08-20 Debiopharm Int Sa SALTS, PRODRUGS AND POLYMORPHES OF FAB I INHIBITORS
JP5496915B2 (ja) 2008-02-13 2014-05-21 シージーアイ ファーマシューティカルズ,インコーポレーテッド 6−アリール−イミダゾ[1,2−a]ピラジン誘導体、その製造方法、及びその使用方法
SG10201707798SA (en) 2008-12-08 2017-10-30 Gilead Connecticut Inc Imidazopyrazine syk inhibitors
US8450321B2 (en) 2008-12-08 2013-05-28 Gilead Connecticut, Inc. 6-(1H-indazol-6-yl)-N-[4-(morpholin-4-yl)phenyl]imidazo-[1,2-A]pyrazin-8-amine, or a pharmaceutically acceptable salt thereof, as a SYK inhibitor
ES2590804T3 (es) 2008-12-08 2016-11-23 Gilead Connecticut, Inc. Inhibidores de Imidazopyrazine Syk
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KR101720885B1 (ko) 2012-06-19 2017-03-28 데비오팜 인터네셔날 에스 에이 (e)-n-메틸-n-((3-메틸벤조푸란-2-일)메틸)-3-(7-옥소-5,6,7,8-테트라히드로-1,8-나프티리딘-3-일)아크릴아미드의전구약물 유도체
KR20170116203A (ko) 2013-07-30 2017-10-18 질레드 코네티컷 인코포레이티드 Syk 억제제의 제제
NZ715776A (en) 2013-07-30 2017-04-28 Gilead Connecticut Inc Polymorph of syk inhibitors
DK3076976T3 (da) 2013-12-04 2020-12-07 Kronos Bio Inc Fremgangsmåder til behandling af cancer
GB201321738D0 (en) * 2013-12-09 2014-01-22 Ucb Pharma Sa Therapeutic Agents
US9290505B2 (en) 2013-12-23 2016-03-22 Gilead Sciences, Inc. Substituted imidazo[1,2-a]pyrazines as Syk inhibitors
TWI735853B (zh) 2013-12-23 2021-08-11 美商克洛諾斯生技有限公司 脾酪胺酸激酶抑制劑
EA201790086A1 (ru) 2014-07-14 2017-07-31 Джилид Сайэнс, Инк. Комбинации для лечения раковых заболеваний
US10751351B2 (en) 2016-02-26 2020-08-25 Debiopharm International S.A. Medicament for treatment of diabetic foot infections
WO2019040298A1 (en) 2017-08-25 2019-02-28 Gilead Sciences, Inc. SYK INHIBITORY POLYMORPHS
LT3923914T (lt) 2019-02-14 2023-07-25 Debiopharm International S.A. Afabicino kompozicija, jos gamybos būdas
US11339168B2 (en) 2019-02-22 2022-05-24 Kronos Bio, Inc. Crystalline forms of 6-(6-aminopyrazin-2-yl)-N-(4-(4-(oxetan-3-yl)piperazin-1-yl)phenyl)imidazo[1,2-a]pyrazin-8-amine as Syk inhibitors
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Also Published As

Publication number Publication date
US6518270B1 (en) 2003-02-11
HUP0100601A2 (hu) 2001-09-28
ID24730A (id) 2000-08-03
RU2241000C2 (ru) 2004-11-27
BR9814755A (pt) 2000-10-03
CZ292349B6 (cs) 2003-09-17
DE69811735T2 (de) 2003-12-18
EE200000315A (et) 2001-10-15
ZA9810468B (en) 1999-05-21
CA2311798A1 (en) 1999-06-10
TW515798B (en) 2003-01-01
HUP0100601A3 (en) 2002-10-28
JP2001525322A (ja) 2001-12-11
DK1042324T3 (da) 2003-05-05
EP1042324B1 (en) 2003-02-26
CN1142933C (zh) 2004-03-24
AU752187C (en) 2003-09-18
IS5486A (is) 2000-05-10
TR200001530T2 (tr) 2000-11-21
UA70932C2 (uk) 2004-11-15
MY121032A (en) 2005-12-30
SK6742000A3 (en) 2001-03-12
EE04060B1 (et) 2003-06-16
CN1284078A (zh) 2001-02-14
AR016972A1 (es) 2001-08-01
PL340920A1 (en) 2001-03-12
KR20010032559A (ko) 2001-04-25
NO20002721D0 (no) 2000-05-26
CZ20001947A3 (cs) 2000-11-15
NO20002721L (no) 2000-07-28
EP1042324A1 (en) 2000-10-11
AU1356599A (en) 1999-06-16
HK1030216A1 (en) 2001-04-27
ATE233263T1 (de) 2003-03-15
SK283904B6 (sk) 2004-04-06
WO1999028322A1 (en) 1999-06-10
DE69811735D1 (de) 2003-04-03
SE9704404D0 (sv) 1997-11-28
ES2191356T3 (es) 2003-09-01
NO315704B1 (no) 2003-10-13
NZ504355A (en) 2001-12-21
PT1042324E (pt) 2003-06-30
AU752187B2 (en) 2002-09-12

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