SE8300736D0 - Novel pharmacologically active compounds - Google Patents

Novel pharmacologically active compounds

Info

Publication number
SE8300736D0
SE8300736D0 SE8300736A SE8300736A SE8300736D0 SE 8300736 D0 SE8300736 D0 SE 8300736D0 SE 8300736 A SE8300736 A SE 8300736A SE 8300736 A SE8300736 A SE 8300736A SE 8300736 D0 SE8300736 D0 SE 8300736D0
Authority
SE
Sweden
Prior art keywords
active compounds
pharmacologically active
novel pharmacologically
novel
compounds
Prior art date
Application number
SE8300736A
Other languages
English (en)
Swedish (sv)
Inventor
A E Brendstrom
S A I Carlsson
B I M Kellsson
P L Lindberg
Original Assignee
Haessle 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 Haessle Ab filed Critical Haessle Ab
Priority to SE8300736A priority Critical patent/SE8300736D0/xx
Publication of SE8300736D0 publication Critical patent/SE8300736D0/xx
Priority to SE8400688A priority patent/SE8400688L/xx
Priority to DE3404610A priority patent/DE3404610A1/de
Priority to FI840547A priority patent/FI840547A/fi
Priority to IT47675/84A priority patent/IT1177553B/it
Priority to FR8402093A priority patent/FR2543551B1/fr
Priority to NZ207102A priority patent/NZ207102A/en
Priority to GB08403540A priority patent/GB2134523B/en
Priority to NO840504A priority patent/NO840504L/no
Priority to AU24456/84A priority patent/AU578891B2/en
Priority to AT0043584A priority patent/AT386825B/de
Priority to BE0/212366A priority patent/BE898880A/fr
Priority to DK59184A priority patent/DK59184A/da
Priority to CH660/84A priority patent/CH666892A5/de
Priority to LU85209A priority patent/LU85209A1/fr
Priority to ZA841011A priority patent/ZA841011B/xx
Priority to NL8400446A priority patent/NL8400446A/nl
Priority to JP59022067A priority patent/JPS59181277A/ja
Priority to GB868610503A priority patent/GB8610503D0/en
Priority to GB08610790A priority patent/GB2174988B/en
Priority to SE8700499A priority patent/SE8700499L/xx
Priority to SE8700498A priority patent/SE8700498D0/xx
Priority to NO882001A priority patent/NO882001D0/no
Priority to US07/408,719 priority patent/US5039806A/en
Priority to CY1555A priority patent/CY1555A/xx

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
    • C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
    • C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
    • C07D235/24—Benzimidazoles; 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
    • 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
    • A61P1/04—Drugs 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
    • C—CHEMISTRY; METALLURGY
    • 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
    • C07D213/62—Oxygen or sulfur atoms
    • C07D213/63—One oxygen atom
    • C07D213/68—One oxygen atom attached in position 4
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
    • C07D217/12—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with radicals, substituted by hetero atoms, attached to carbon atoms of the nitrogen-containing ring
    • C07D217/14—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with radicals, substituted by hetero atoms, attached to carbon atoms of the nitrogen-containing ring other than aralkyl radicals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
    • C07D217/12—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with radicals, substituted by hetero atoms, attached to carbon atoms of the nitrogen-containing ring
    • C07D217/14—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with radicals, substituted by hetero atoms, attached to carbon atoms of the nitrogen-containing ring other than aralkyl radicals
    • C07D217/16—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with radicals, substituted by hetero atoms, attached to carbon atoms of the nitrogen-containing ring other than aralkyl radicals substituted by oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
    • C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
    • C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
    • C07D235/24—Benzimidazoles; 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
    • C07D235/28—Sulfur atoms
    • 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
    • C07D401/12—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 linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • 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
    • C07D405/12—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 linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
    • C07D407/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04—Ortho-condensed systems

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Engineering & Computer Science (AREA)
  • Animal Behavior & Ethology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pyridine Compounds (AREA)
  • Other In-Based Heterocyclic Compounds (AREA)
SE8300736A 1983-02-11 1983-02-11 Novel pharmacologically active compounds SE8300736D0 (sv)

Priority Applications (25)

Application Number Priority Date Filing Date Title
SE8300736A SE8300736D0 (sv) 1983-02-11 1983-02-11 Novel pharmacologically active compounds
SE8400688A SE8400688L (sv) 1983-02-11 1984-02-09 Nya farmakologiskt aktiva foreningar
DE3404610A DE3404610A1 (de) 1983-02-11 1984-02-09 Benzimidazolderivate, verfahren zu deren herstellung und sie enthaltende arzneimittel
JP59022067A JPS59181277A (ja) 1983-02-11 1984-02-10 新規な薬理学的に活性な化合物
AT0043584A AT386825B (de) 1983-02-11 1984-02-10 Verfahren zur herstellung von neuen benzimidazolderivaten und von deren salzen
LU85209A LU85209A1 (de) 1983-02-11 1984-02-10 Benzimidazoles substitues,procede pour leur preparation et compositions pharmaceutiques les contenant,inhibant la secretion d'acide gastrique ou exercant un effet cytoprotecteur du tube digestif
FR8402093A FR2543551B1 (fr) 1983-02-11 1984-02-10 Benzimidapoles substitues, procede pour leur preparation et compositions pharmaceutiques les contenant, inhibant la secretion d'acide gastrique ou exercant un effet cytoprotecteur du tube digestif
NZ207102A NZ207102A (en) 1983-02-11 1984-02-10 Benzimidazole derivatives and pharmaceutical compositions
GB08403540A GB2134523B (en) 1983-02-11 1984-02-10 Novel pharmacologically active compounds
NO840504A NO840504L (no) 1983-02-11 1984-02-10 Nye farmakologisk aktive forbindelser
AU24456/84A AU578891B2 (en) 1983-02-11 1984-02-10 Substituted 2-pyridylobenzimidazole derivatives
FI840547A FI840547A (fi) 1983-02-11 1984-02-10 Nya farmakologiskt aktiva foereningar.
BE0/212366A BE898880A (fr) 1983-02-11 1984-02-10 Nouveaux benzimidazoles, preparations pharmaceutiques qui les contiennent et leur preparation
DK59184A DK59184A (da) 1983-02-11 1984-02-10 Farmakologisk virksomme forbindelser og terapeutisk acceptable salte deraf
CH660/84A CH666892A5 (de) 1983-02-11 1984-02-10 Pharmakologisch aktive verbindungen, die zur verhuetung und behandlung von magengeschwueren verwendbar sind.
IT47675/84A IT1177553B (it) 1983-02-11 1984-02-10 Composti farmacologicamente attivi per il trattamento di affezioni gastrointestinali e procedimento di preparazione
ZA841011A ZA841011B (en) 1983-02-11 1984-02-10 Novel pharmacologically active compounds
NL8400446A NL8400446A (nl) 1983-02-11 1984-02-10 Farmaceutisch werkzame verbindingen, werkwijzen ter bereiding ervan alsmede samenstellingen, die deze verbindingen bevatten.
GB868610503A GB8610503D0 (en) 1983-02-11 1986-04-29 Pyridyl alkylthiobenzimidazole derivatives
GB08610790A GB2174988B (en) 1983-02-11 1986-05-02 Intermediates for pyridyl alkylthio-benzimidazole derivatives
SE8700499A SE8700499L (sv) 1983-02-11 1987-02-10 Nya farmakologiskt aktiva foreningar
SE8700498A SE8700498D0 (sv) 1983-02-11 1987-02-10 Novel pharmaceologically active compounds
NO882001A NO882001D0 (no) 1983-02-11 1988-05-06 Analogifremgangsmaate til fremstilling av farmakologisk aktive forbindelser.
US07/408,719 US5039806A (en) 1983-02-11 1989-09-18 Novel pharmacologically active compound pyridyl methylsulfinyl benzimidazole
CY1555A CY1555A (en) 1983-02-11 1991-03-22 Pyridyl alkylthio-benzimidazole derivatives

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SE8300736A SE8300736D0 (sv) 1983-02-11 1983-02-11 Novel pharmacologically active compounds

Publications (1)

Publication Number Publication Date
SE8300736D0 true SE8300736D0 (sv) 1983-02-11

Family

ID=20349994

Family Applications (3)

Application Number Title Priority Date Filing Date
SE8300736A SE8300736D0 (sv) 1983-02-11 1983-02-11 Novel pharmacologically active compounds
SE8700499A SE8700499L (sv) 1983-02-11 1987-02-10 Nya farmakologiskt aktiva foreningar
SE8700498A SE8700498D0 (sv) 1983-02-11 1987-02-10 Novel pharmaceologically active compounds

Family Applications After (2)

Application Number Title Priority Date Filing Date
SE8700499A SE8700499L (sv) 1983-02-11 1987-02-10 Nya farmakologiskt aktiva foreningar
SE8700498A SE8700498D0 (sv) 1983-02-11 1987-02-10 Novel pharmaceologically active compounds

Country Status (19)

Country Link
US (1) US5039806A (xx)
JP (1) JPS59181277A (xx)
AT (1) AT386825B (xx)
AU (1) AU578891B2 (xx)
BE (1) BE898880A (xx)
CH (1) CH666892A5 (xx)
CY (1) CY1555A (xx)
DE (1) DE3404610A1 (xx)
DK (1) DK59184A (xx)
FI (1) FI840547A (xx)
FR (1) FR2543551B1 (xx)
GB (3) GB2134523B (xx)
IT (1) IT1177553B (xx)
LU (1) LU85209A1 (xx)
NL (1) NL8400446A (xx)
NO (1) NO840504L (xx)
NZ (1) NZ207102A (xx)
SE (3) SE8300736D0 (xx)
ZA (1) ZA841011B (xx)

Families Citing this family (110)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE8300736D0 (sv) * 1983-02-11 1983-02-11 Haessle Ab Novel pharmacologically active compounds
US5077407A (en) * 1983-07-01 1991-12-31 The Upjohn Company Substituted 2-[monoannelated (3,4-,4,5-, and 5,6-) pyridylalkylenesulfinyl]benzimidazoles
CA1259070A (en) * 1983-07-01 1989-09-05 Upjohn Company (The) Substituted 2-¬monoannelated(3,4-,4,5-, and 5,6-)- pyridylalkylenesulfinyl|-benzimidazoles
US4575554A (en) * 1983-12-05 1986-03-11 The Upjohn Company Substituted 2-pyridylmethylthio- and sulfinyl-benzimidazoles as gastric antisecretory agents
ZW4585A1 (en) * 1984-04-19 1985-11-20 Hoffmann La Roche Imidazole derivatives
CA1341314C (en) 1984-07-06 2001-11-06 David Cox Derivatives of benzimidazole, benzothiazole and benzoxazole
SE8404065D0 (sv) * 1984-08-10 1984-08-10 Haessle Ab Novel biologically active compounds
JPS6150978A (ja) * 1984-08-16 1986-03-13 Takeda Chem Ind Ltd ピリジン誘導体およびその製造法
JPS6150979A (ja) * 1984-08-16 1986-03-13 Takeda Chem Ind Ltd ピリジン誘導体およびその製造法
US4619997A (en) * 1984-09-06 1986-10-28 The Upjohn Company Substituted 2-pyridylmethylthio and sulfinyl-benzimidazoles as gastric antisecretory agents
KR890000387B1 (ko) * 1984-09-24 1989-03-16 디 엎존 캄파니 2-(피리딜알켄술 피닐)벤즈 이미드아졸류의 n-치환 유도체의 제조방법
AU568441B2 (en) * 1984-09-24 1987-12-24 Upjohn Company, The 2-(pyridylalkenesulfinyl) benzimidazole derivatives
IL76839A (en) * 1984-10-31 1988-08-31 Byk Gulden Lomberg Chem Fab Picoline derivatives,processes for the preparation thereof and pharmaceutical compositions containing the same
DE3509333A1 (de) * 1985-03-15 1986-09-18 Hoechst Ag, 6230 Frankfurt Substituierte benzimidazolderivate, verfahren zu ihrer herstellung, sie enthaltende pharmazeutische zubereitungen und ihre verwendung als magensaeuresekretionshemmer
US5869513A (en) * 1985-05-24 1999-02-09 G. D. Searle & Co. 2- (1H-benzimidazol-2-ylsulfinyl)methyl!benzenamines
AU5768886A (en) 1985-05-24 1986-11-27 G.D. Searle & Co. 2-((1-h-benzimidazol-2-ylsulfinyl)methyl)benzenamines
US4738975A (en) * 1985-07-02 1988-04-19 Takeda Chemical Industries, Ltd. Pyridine derivatives, and use as anti-ulcer agents
DK337086A (da) * 1985-08-12 1987-02-13 Hoffmann La Roche Benzimidazolderivater
SE8505112D0 (sv) * 1985-10-29 1985-10-29 Haessle Ab Novel pharmacological compounds
US6749864B2 (en) 1986-02-13 2004-06-15 Takeda Chemical Industries, Ltd. Stabilized pharmaceutical composition
US5433959A (en) * 1986-02-13 1995-07-18 Takeda Chemical Industries, Ltd. Stabilized pharmaceutical composition
CA1327010C (en) * 1986-02-13 1994-02-15 Tadashi Makino Stabilized solid pharmaceutical composition containing antiulcer benzimidazole compound and its production
ES2032394T3 (es) * 1986-02-20 1993-02-16 Hoechst Aktiengesellschaft Procedimiento para preparar derivados de tienoimidazol sustituidos.
JPS62201884A (ja) * 1986-02-28 1987-09-05 Tokyo Tanabe Co Ltd ベンズイミダゾール誘導体及びその製造法
ATE56717T1 (de) * 1986-07-01 1990-10-15 Shionogi & Co Substituierte isoquinolinderivate und antiulcusmittel.
US4772619A (en) * 1986-07-17 1988-09-20 G. D. Searle & Co. [(1H-benzimidazol-2-ylsulfinyl)methyl]-2-pyridinamines
US4687775A (en) * 1986-07-17 1987-08-18 G. D. Searle & Co. 2-[(Imidazo[1,2-a]pyridinylmethyl)sulfinyl]-1H-benzimidazoles
US4721718A (en) * 1986-08-18 1988-01-26 G. D. Searle & Co. 2-[(imidazo[1,2-a]pyridin-3-ylmethyl)sulfinyl]-1H-benzimidazoles useful in the treatment and prevention of ulcers
SE8604566D0 (sv) * 1986-10-27 1986-10-27 Haessle Ab Novel compunds
EP0786461A1 (en) * 1986-11-13 1997-07-30 Eisai Co., Ltd. Pyridine derivatives, pharmaceutical compositions comprising the same, the use of the same for the manufacture of medicaments having therapeutic or preventative value, and a process for preparing the same
FI90544C (fi) * 1986-11-13 1994-02-25 Eisai Co Ltd Menetelmä lääkeaineina käyttökelpoisten 2-pyridin-2-yyli-metyylitio- ja sulfinyyli-1H-bensimidatsolijohdannaisten valmistamiseksi
NZ234564A (en) * 1986-11-21 1991-04-26 Haessle Ab 1-substituted benzimidazoles and pharmaceutical compositions
US5026560A (en) * 1987-01-29 1991-06-25 Takeda Chemical Industries, Ltd. Spherical granules having core and their production
US4942245A (en) * 1987-04-20 1990-07-17 Kyorin Pharmaceutical Co., Ltd. Benzimidazole Derivatives
US4839365A (en) * 1987-05-19 1989-06-13 Shinogi & Co., Ltd. Thienopyridine derivatives useful in treating gastric ulcers
FI96860C (fi) * 1987-06-17 1996-09-10 Eisai Co Ltd Analogiamenetelmä lääkeaineena käytettävän pyridiinijohdannaisen valmistamiseksi
JP2718945B2 (ja) * 1987-06-17 1998-02-25 エーザイ株式会社 ピリジン誘導体及びそれを含有する潰瘍治療剤
US4920230A (en) * 1987-06-29 1990-04-24 Takeda Chemical Industries, Ltd. Method of producing nitrogen-containing heteroaromatic compounds having an alkoxy group
WO1989000566A1 (en) * 1987-07-21 1989-01-26 Yoshitomi Pharmaceutical Industries, Ltd. Pyridine compounds and medicinal use thereof
KR920003928B1 (ko) * 1988-09-20 1992-05-18 히사미쯔세이야꾸 가부시기가이샤 신규의 디벤즈[b,e]옥세핀유도체
AT391693B (de) * 1988-11-15 1990-11-12 Cl Pharma Verfahren zur herstellung von 3-5-dimethyl-4methoxypyridinderivaten sowie neues zwischenprodukt hierfuer
EG19302A (en) * 1988-12-22 1994-11-30 Haessle Ab Compound with gastric acid inhibitory effect and process for its preparation
US4965269A (en) * 1989-12-20 1990-10-23 Ab Hassle Therapeutically active chloro substituted benzimidazoles
SE9002043D0 (sv) * 1990-06-07 1990-06-07 Astra Ab Improved method for synthesis
SE9002206D0 (sv) 1990-06-20 1990-06-20 Haessle Ab New compounds
WO1992012976A1 (en) * 1991-01-16 1992-08-06 Yoshitomi Pharmaceutical Industries, Ltd. Use of pyridine compound as selective drug and novel pyridine compound
ES2037609B1 (es) * 1991-12-02 1994-04-01 Techquin Etablissment Procedimiento para la obtencion del 2-(((3-metil-4-(2,2,2-trifluroetoxi)-2-piridinil)-metil)sulfinil)-1h-benzimidazol.
ES2037608B1 (es) * 1991-12-02 1994-04-01 Techquin Etablissment Procedimiento para la obtencion del 2 (((3-metil-4-(2,2,2,-trifluoroetoxi)-2-piridinil)-metil)sulfinil)-1h-benzimidazol".
US5504082A (en) * 1992-06-01 1996-04-02 Yoshitomi Pharmaceutical Industries, Ltd. Pyridine compound and pharmaceutical compostions
WO1993024480A1 (en) * 1992-06-01 1993-12-09 Yoshitomi Pharmaceutical Industries, Ltd. Pyridine compound and medicinal use thereof
KR0144793B1 (ko) * 1992-07-08 1998-07-15 제임스 클리프튼 보올딩 돼지에서 위궤양을 완화시키기 위한 벤즈이미다졸
SG52479A1 (en) * 1992-07-28 1998-09-28 Astra Ab Injection and injection kit containing omeprazole and its analogs
TW280770B (xx) 1993-10-15 1996-07-11 Takeda Pharm Industry Co Ltd
PT731801E (pt) 1993-12-01 2002-04-29 Byk Gulden Lomberg Chem Fab Aminoalquilaminopiridinas substituidas
KR0142815B1 (ko) * 1994-12-02 1998-07-15 정도언 신규한 5-피롤릴-6-할로게노-2피리딜메틸설피닐벤즈이미다졸 유도체
KR0179401B1 (ko) * 1994-02-28 1999-03-20 송택선 신규한 5-피롤릴-2-피리딜메틸설피닐벤즈이미다졸 유도체
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DK59184D0 (da) 1984-02-10
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US5039806A (en) 1991-08-13
FI840547A0 (fi) 1984-02-10
FR2543551B1 (fr) 1987-08-21
NZ207102A (en) 1987-09-30
IT8447675A0 (it) 1984-02-10
GB8610503D0 (en) 1986-06-04
GB2134523A (en) 1984-08-15
ZA841011B (en) 1984-09-26
LU85209A1 (de) 1985-09-12
GB2174988A (en) 1986-11-19
BE898880A (fr) 1984-08-10
SE8700499D0 (sv) 1987-02-10
GB8403540D0 (en) 1984-03-14
GB8610790D0 (en) 1986-06-11
ATA43584A (de) 1988-03-15
GB2174988B (en) 1987-08-26
SE8700498L (sv) 1987-02-10
SE8700498D0 (sv) 1987-02-10
CY1555A (en) 1991-03-22
CH666892A5 (de) 1988-08-31
DK59184A (da) 1984-08-12
JPS59181277A (ja) 1984-10-15
AU578891B2 (en) 1988-11-10
IT1177553B (it) 1987-08-26
NL8400446A (nl) 1984-09-03
DE3404610A1 (de) 1984-08-16
NO840504L (no) 1984-08-13
SE8700499L (sv) 1987-02-10
AU2445684A (en) 1984-08-16

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