FI892498A0 - Aromatiska och heterocykliska karboxiamidderivat saosom antitumoera aemnen. - Google Patents

Aromatiska och heterocykliska karboxiamidderivat saosom antitumoera aemnen.

Info

Publication number
FI892498A0
FI892498A0 FI892498A FI892498A FI892498A0 FI 892498 A0 FI892498 A0 FI 892498A0 FI 892498 A FI892498 A FI 892498A FI 892498 A FI892498 A FI 892498A FI 892498 A0 FI892498 A0 FI 892498A0
Authority
FI
Finland
Prior art keywords
antitumoera
aemnen
saosom
heterocyclic
carboxyamide derivatives
Prior art date
Application number
FI892498A
Other languages
English (en)
Other versions
FI892498A (fi
Inventor
Anton Franz Josef Fliri
Rodney Caughren Schnur
Original Assignee
Pfizer
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 Pfizer filed Critical Pfizer
Publication of FI892498A0 publication Critical patent/FI892498A0/fi
Publication of FI892498A publication Critical patent/FI892498A/fi

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D277/00Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/60Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
    • C07D277/62Benzothiazoles
    • C07D277/68Benzothiazoles 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
    • C07D277/82Nitrogen atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Engineering & Computer Science (AREA)
  • Hematology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Diabetes (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Steroid Compounds (AREA)
  • Graft Or Block Polymers (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
FI892498A 1988-05-24 1989-05-23 Aromatiska och heterocykliska karboxiamidderivat saosom antitumoera aemnen. FI892498A (fi)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US19803488A 1988-05-24 1988-05-24

Publications (2)

Publication Number Publication Date
FI892498A0 true FI892498A0 (fi) 1989-05-23
FI892498A FI892498A (fi) 1989-11-25

Family

ID=22731735

Family Applications (1)

Application Number Title Priority Date Filing Date
FI892498A FI892498A (fi) 1988-05-24 1989-05-23 Aromatiska och heterocykliska karboxiamidderivat saosom antitumoera aemnen.

Country Status (25)

Country Link
EP (1) EP0343893B1 (fi)
JP (1) JPH0678331B2 (fi)
KR (1) KR910006864B1 (fi)
CN (1) CN1023700C (fi)
AT (1) ATE79114T1 (fi)
AU (1) AU601905B2 (fi)
CA (1) CA1328871C (fi)
DD (1) DD283815A5 (fi)
DE (1) DE68902358T2 (fi)
DK (1) DK249389A (fi)
ES (1) ES2043012T3 (fi)
FI (1) FI892498A (fi)
GR (1) GR3005844T3 (fi)
HU (1) HU202507B (fi)
IE (1) IE891667L (fi)
IL (1) IL90337A0 (fi)
MX (1) MX173140B (fi)
MY (1) MY106035A (fi)
NO (1) NO172389C (fi)
NZ (1) NZ229234A (fi)
PL (1) PL154875B1 (fi)
PT (1) PT90622B (fi)
SU (1) SU1681728A3 (fi)
YU (1) YU47019B (fi)
ZA (1) ZA893862B (fi)

Families Citing this family (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2790299B2 (ja) * 1989-02-01 1998-08-27 保土谷化学工業株式会社 ペンゾチアゾール誘導体
US5262400A (en) * 1991-06-20 1993-11-16 Merck & Co., Inc. 4α-substituted avermectin derivatives
CZ293323B6 (cs) * 1995-08-30 2004-04-14 G. D. Searle & Co. Meta-guanidinové, močovinové, thiomočovinové nebo azacyklické deriváty aminobenzoové kyseliny jako antagonisty integrinů
US6100423A (en) * 1995-08-30 2000-08-08 G. D. Searle & Co. Amino benzenepropanoic acid compounds and derivatives thereof
US5716281A (en) * 1995-11-27 1998-02-10 Sega Enterprises, Ltd. Game apparatus using a vehicle with an optical image synthesizing system
TW513418B (en) * 1996-07-31 2002-12-11 Otsuka Pharma Co Ltd Thiazole derivatives, their production and use
IL135176A0 (en) 1997-11-10 2001-05-20 Bristol Myers Squibb Co Benzothiazole derivatives and pharmaceutical compositions containing the same
SI0928793T1 (en) * 1998-01-02 2002-10-31 F. Hoffmann-La Roche Ag Thiazole derivatives
AU3406599A (en) * 1998-04-09 1999-11-01 Institut Fur Diagnostikforschung Gmbh An Der Freien Universitat Berlin Novel benzyl guanidine derivatives for therapy and (in-vivo) and (in-vitro) diagnosis
MXPA02012596A (es) 2000-06-21 2003-04-10 Hoffmann La Roche Derivados de benzotiazol.
US6624163B2 (en) * 2001-11-29 2003-09-23 Hoffman-La Roche Inc. Benzothiazole derivatives
GB0130868D0 (en) * 2001-12-24 2002-02-06 Univ Strathclyde New compounds
CN100357283C (zh) * 2002-04-02 2007-12-26 中国科学院上海药物研究所 一类甲硫氨酰氨肽酶抑制剂
US7087761B2 (en) 2003-01-07 2006-08-08 Hoffmann-La Roche Inc. Cyclization process for substituted benzothiazole derivatives
PT1753760E (pt) 2004-05-24 2008-02-12 Hoffmann La Roche '' - metoxi - 7 - morfolin - 4 - il - benzotiazol - 2 - il) - amida do ácido 4 - hidroxi - 4 - metil - piperidina - 1 - carboxílico''
DE602005008095D1 (de) 2004-11-05 2008-08-21 Hoffmann La Roche Verfahren zur herstellung von isonikotinsäurederivaten
RU2412943C2 (ru) 2005-03-23 2011-02-27 Ф. Хоффманн-Ля Рош Аг ПРОИЗВОДНЫЕ АЦЕТИЛЕНИЛ-ПИРАЗОЛО-ПИРИМИДИНА В КАЧЕСТВЕ АНТАГОНИСТОВ mGluR2
ATE463495T1 (de) 2005-09-27 2010-04-15 Hoffmann La Roche Oxadiazolylpyrazolopyrimidine als mglur2- antagonisten
EP1994017A2 (en) * 2006-03-15 2008-11-26 4Sc Ag Novel heterocyclic nf-kb inhibitors
GB0619325D0 (en) 2006-09-30 2006-11-08 Univ Strathclyde New compounds
US20110178070A1 (en) * 2008-06-24 2011-07-21 Takeda Pharmaceutical Company Limited PI3K/mTOR INHIBITORS
US9499790B2 (en) 2010-08-26 2016-11-22 Kyoto University Method for promoting differentiation of pluripotent stem cells into cardiac muscle cells
EP2748172B1 (en) * 2011-09-30 2017-12-06 Kineta, Inc. Anti-viral compounds
KR101996343B1 (ko) 2012-01-27 2019-07-05 고쿠리츠 다이가쿠 호진 교토 다이가쿠 전능성 줄기세포의 심근분화 유도방법
WO2014136519A1 (ja) 2013-03-08 2014-09-12 国立大学法人京都大学 Egf受容体阻害剤を含む多能性幹細胞の心筋分化促進剤
WO2015037706A1 (ja) * 2013-09-13 2015-03-19 国立大学法人京都大学 多能性幹細胞の心筋分化を促進する化合物
JP6651218B2 (ja) 2014-05-30 2020-02-19 国立大学法人京都大学 低分子化合物を用いた多能性幹細胞の心筋分化誘導法
CN109776486A (zh) * 2019-02-26 2019-05-21 武汉松石科技股份有限公司 一种硫酸亚丙酯的制备方法
CN110590735B (zh) * 2019-09-30 2021-07-23 江苏国泰超威新材料有限公司 一种环状硫酸酯的制备方法

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61225168A (ja) * 1985-03-30 1986-10-06 Nippon Tokushu Noyaku Seizo Kk 新規ベンズアミド、その製法及び殺虫剤
KR930005004B1 (ko) * 1985-04-15 1993-06-11 쟈안센 파아마슈우티카 엔. 부이. 치환된 n-[(4-피페리디닐)알킬]이환 축합 옥사졸아민 및 티아졸아민의 제조방법
GB8611606D0 (en) * 1986-05-13 1986-06-18 Fbc Ltd Fungicides

Also Published As

Publication number Publication date
PT90622A (pt) 1989-11-30
CN1037898A (zh) 1989-12-13
ATE79114T1 (de) 1992-08-15
NO892059L (no) 1989-11-27
YU105989A (en) 1990-08-31
DE68902358D1 (de) 1992-09-10
SU1681728A3 (ru) 1991-09-30
DK249389D0 (da) 1989-05-23
NO172389C (no) 1993-07-14
MX173140B (es) 1994-02-02
MX16158A (es) 1993-06-01
AU601905B2 (en) 1990-09-20
EP0343893B1 (en) 1992-08-05
ES2043012T3 (es) 1993-12-16
GR3005844T3 (fi) 1993-06-07
DK249389A (da) 1989-11-27
IL90337A0 (en) 1989-12-15
NZ229234A (en) 1990-09-26
HU202507B (en) 1991-03-28
EP0343893A1 (en) 1989-11-29
DD283815A5 (de) 1990-10-24
JPH0678331B2 (ja) 1994-10-05
MY106035A (en) 1995-03-31
PL279613A1 (en) 1989-11-27
CN1023700C (zh) 1994-02-09
NO892059D0 (no) 1989-05-23
YU47019B (sh) 1994-11-15
PL154875B1 (en) 1991-09-30
AU3509889A (en) 1989-11-30
DE68902358T2 (de) 1992-12-10
CA1328871C (en) 1994-04-26
HUT51606A (en) 1990-05-28
KR890017248A (ko) 1989-12-15
FI892498A (fi) 1989-11-25
JPH0217181A (ja) 1990-01-22
ZA893862B (en) 1991-01-30
PT90622B (pt) 1994-10-31
IE891667L (en) 1989-11-24
KR910006864B1 (ko) 1991-09-09
NO172389B (no) 1993-04-05

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Legal Events

Date Code Title Description
FD Application lapsed
FD Application lapsed

Owner name: PFIZER INC.