BR9605267A - Inibidor de angiogenese - Google Patents

Inibidor de angiogenese

Info

Publication number
BR9605267A
BR9605267A BR9605267A BR9605267A BR9605267A BR 9605267 A BR9605267 A BR 9605267A BR 9605267 A BR9605267 A BR 9605267A BR 9605267 A BR9605267 A BR 9605267A BR 9605267 A BR9605267 A BR 9605267A
Authority
BR
Brazil
Prior art keywords
angiogenesis inhibitor
angiogenesis
inhibitor
Prior art date
Application number
BR9605267A
Other languages
English (en)
Inventor
Jun Inoue
Masayuki Nakamura
Chiho Fukiage
Mitsuyoshi Azuma
Yuka Yoshida
Original Assignee
Senju Pharma Co
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 Senju Pharma Co filed Critical Senju Pharma Co
Publication of BR9605267A publication Critical patent/BR9605267A/pt

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/55—Protease inhibitors
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/15—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
    • C07C311/16—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom
    • C07C311/19—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom to an acyclic carbon atom of a hydrocarbon radical substituted by carboxyl groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
    • C07D303/02—Compounds containing oxirane rings
    • C07D303/48—Compounds containing oxirane rings with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms, e.g. ester or nitrile radicals

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • General Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Immunology (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Epidemiology (AREA)
  • Animal Behavior & Ethology (AREA)
  • Engineering & Computer Science (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Peptides Or Proteins (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)
BR9605267A 1995-10-25 1996-10-25 Inibidor de angiogenese BR9605267A (pt)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP27748595 1995-10-25
JP24804696 1996-09-19

Publications (1)

Publication Number Publication Date
BR9605267A true BR9605267A (pt) 1998-07-21

Family

ID=26538555

Family Applications (1)

Application Number Title Priority Date Filing Date
BR9605267A BR9605267A (pt) 1995-10-25 1996-10-25 Inibidor de angiogenese

Country Status (13)

Country Link
US (2) US6057290A (pt)
EP (2) EP0927716B1 (pt)
AR (1) AR004694A1 (pt)
AT (3) ATE230275T1 (pt)
AU (1) AU716495B2 (pt)
BR (1) BR9605267A (pt)
CA (1) CA2188817C (pt)
DE (3) DE69625575T2 (pt)
ES (2) ES2190139T3 (pt)
HU (1) HUP9602943A3 (pt)
MX (1) MX9605156A (pt)
NO (1) NO964514L (pt)
PL (1) PL316669A1 (pt)

Families Citing this family (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1997003060A1 (fr) * 1995-07-13 1997-01-30 Senju Pharmaceutical Co., Ltd. Derives de la piperazine et leurs utilisations
US6214800B1 (en) * 1995-10-25 2001-04-10 Senju Pharmaceutical Co., Ltd. Angiogenesis inhibitor
DE19718826A1 (de) * 1997-05-05 1998-11-12 Marion S Dr Eckmiller Verwendung biologisch aktiver Wirkstoffe zum Beeinflussen des Extrazellulär-Raumes von Sinneszellen und Verfahren zur Wirkstoff-Administrationssteuerung
WO1999011640A1 (fr) * 1997-09-04 1999-03-11 Nippon Chemiphar Co., Ltd. Derives d'epoxysuccinamide
US6015787A (en) * 1997-11-04 2000-01-18 New England Medical Center Hospitals, Inc. Cell-permeable protein inhibitors of calpain
DE69925578T2 (de) 1998-03-05 2006-04-27 Senju Pharmaceutical Co., Ltd. Pharmazeutische zusammenstellung zur vorbeugung und behandlung von mit zellkrankheiten des augenhintergrundes zusammenhängenden krankheiten
KR20010041967A (ko) 1998-03-20 2001-05-25 요시다 쇼지 뇌조직 장애를 예방 및 치료하기 위한 시스테인프로테아제 억제제 함유 약제학적 조성물
GB9819860D0 (en) * 1998-09-12 1998-11-04 Zeneca Ltd Chemical compounds
CN1398189A (zh) 1998-12-23 2003-02-19 G.D.西尔公司 用于***形成的放疗与cox－2抑制剂的联合治疗
WO2000058280A1 (fr) * 1999-03-26 2000-10-05 Shionogi & Co., Ltd. Derives de sulfonamide carbocyclique
KR20010001270A (ko) * 1999-06-03 2001-01-05 복성해 혈관신생을 억제하는 새로운 이소쿠마린 유도체
WO2001026648A1 (fr) 1999-10-13 2001-04-19 Senju Pharmaceutical Co., Ltd. Preparation d'adhesif a usage ophtalmique pour l'absorption par voie percutanee
AU1735001A (en) * 1999-12-10 2001-06-18 Senju Pharmaceutical Co., Ltd. Cyclodextrin-containing pharmaceutical composition
JPWO2002034252A1 (ja) * 2000-10-26 2004-03-04 千寿製薬株式会社 ジペプチジルアルデヒド誘導体含有医薬組成物
WO2002048096A1 (fr) * 2000-12-12 2002-06-20 Senju Pharmaceutical Co., Ltd. Derives d'hydrazone et utilisation de ceux-ci dans des medicaments
NZ529098A (en) 2001-06-06 2005-08-26 Lilly Co Eli Benzoylsulfonamides and sulfonylbenzamidines for use as antitumour agents
US7115607B2 (en) * 2001-07-25 2006-10-03 Amgen Inc. Substituted piperazinyl amides and methods of use
WO2003078415A1 (fr) * 2002-03-15 2003-09-25 Senju Pharmaceutical Co., Ltd. Derive de l'hemiacetal cyclique et son utilisation
ATE473216T1 (de) 2002-03-29 2010-07-15 Senju Pharma Co Hydroxymorpholinonderivat und dessen medizinische verwendung
EP1354586A1 (en) * 2002-04-20 2003-10-22 Aventis Pharma Deutschland GmbH The use of hydroxpyridone-derivatives in wound healing
ATE448198T1 (de) * 2002-07-22 2009-11-15 Senju Pharma Co Neue alpha-ketoamidderivate und deren verwendung
GB0314262D0 (en) 2003-06-19 2003-07-23 Univ Nottingham Trent Novel compounds and methods of using the same
US7615556B2 (en) * 2006-01-27 2009-11-10 Bristol-Myers Squibb Company Piperazinyl derivatives as modulators of chemokine receptor activity
US8236798B2 (en) 2009-05-07 2012-08-07 Abbott Gmbh & Co. Kg Carboxamide compounds and their use as calpain inhibitors
EP2541716A1 (en) 2010-02-25 2013-01-02 Panasonic Corporation Demand and supply control apparatus, demand and supply control method, and program
CN103052382B (zh) 2010-07-14 2014-10-22 千寿制药株式会社 α-酮酰胺衍生物的固体分散体
GB201218084D0 (en) 2012-10-09 2012-11-21 Univ Aston Novel compounds and methods for use in medicine
GB201220474D0 (en) * 2012-11-14 2012-12-26 Sagetis Biotech Sl Polypeptides
US20210145930A1 (en) * 2018-05-07 2021-05-20 NeuroTheranostics, Inc. Multiple layer article with interactive reinforcements linear ribbon fiber reinforcement for composite forms
WO2022187491A1 (en) * 2021-03-03 2022-09-09 The Texas A& M University System Inhibitors of cysteine proteases

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS50137951A (pt) 1974-04-27 1975-11-01
JPS5754157A (en) 1980-09-19 1982-03-31 Nippon Kayaku Co Ltd L-argininal derivative and its preparation
PT84170B (pt) * 1986-01-24 1989-03-30 Sanofi Sa Processo para a preparacao de derivados n alfa-substituidos das n alfa-aril-sulfonilaminoacil d-amidinofenil-alaninamidas
JP2536754B2 (ja) * 1987-05-08 1996-09-18 日本ケミファ株式会社 ピペラジン誘導体
JPH0832698B2 (ja) * 1987-05-08 1996-03-29 日本ケミファ株式会社 ピペラジン誘導体
JP2701932B2 (ja) * 1989-04-10 1998-01-21 サントリー株式会社 タンパク質分解酵素阻害剤
US5510531A (en) 1989-04-10 1996-04-23 Suntory Limited Proteinase inhibitor
EP0395309B1 (en) * 1989-04-28 1995-12-27 Takara Shuzo Co. Ltd. Human calpastatin-like polypeptide
JPH06506921A (ja) 1991-02-22 1994-08-04 ザ・デュポン・メルク・ファーマシュウティカル・カンパニー 置換α−アミノアルデヒドおよび誘導体
EP0504938A3 (en) * 1991-03-22 1993-04-14 Suntory Limited Prophylactic and therapeutic agent for bone diseases comprising di- or tripeptide derivative as active ingredient
CA2071621C (en) * 1991-06-19 1996-08-06 Ahihiko Hosoda Aldehyde derivatives
JP2848232B2 (ja) 1993-02-19 1999-01-20 武田薬品工業株式会社 アルデヒド誘導体
US5607831A (en) 1993-03-25 1997-03-04 The United States Of America As Represented By The Department Of Health And Human Services In vitro methods for assessing the susceptibility of HIV-1-infected individuals to cysteine protease-mediated activation-induced programmed cell death
US5658885A (en) 1993-04-27 1997-08-19 The Dupont Merck Pharmaceutical Company Amidino and guanidino substituted boronic acid inhibitors of trypsin-like enzymes
JP3599287B2 (ja) * 1993-04-28 2004-12-08 三菱化学株式会社 スルホンアミド誘導体
EP0783489A1 (en) * 1994-09-27 1997-07-16 Takeda Chemical Industries, Ltd. Aldehyde derivatives as upsteine protease inhibitors
US5614649A (en) 1994-11-14 1997-03-25 Cephalon, Inc. Multicatalytic protease inhibitors
EP0731107A1 (en) * 1995-02-13 1996-09-11 Takeda Chemical Industries, Ltd. Production of aldehyde derivatives
WO1996035711A1 (en) 1995-05-10 1996-11-14 Chiroscience Limited Peptide compounds which inhibit metalloproteinase and tnf liberation, and their therapeutic use
WO1997003060A1 (fr) * 1995-07-13 1997-01-30 Senju Pharmaceutical Co., Ltd. Derives de la piperazine et leurs utilisations
WO1997021690A1 (en) 1995-11-28 1997-06-19 Cephalon, Inc. D-amino acid derived inhibitors of cysteine and serine proteases

Also Published As

Publication number Publication date
DE69625575D1 (de) 2003-02-06
ES2190139T3 (es) 2003-07-16
ATE230275T1 (de) 2003-01-15
AR004694A1 (es) 1999-03-10
NO964514L (no) 1997-04-28
DE69628050T2 (de) 2004-04-01
CA2188817A1 (en) 1997-04-26
DE69625575T2 (de) 2003-09-25
EP0927716B1 (en) 2003-05-07
DE69628050D1 (de) 2003-06-12
DE69625622D1 (de) 2003-02-06
HUP9602943A3 (en) 1998-03-02
DE69625622T2 (de) 2003-08-14
PL316669A1 (en) 1997-04-28
US6551999B1 (en) 2003-04-22
AU716495B2 (en) 2000-02-24
US6057290A (en) 2000-05-02
EP0771565A2 (en) 1997-05-07
NO964514D0 (no) 1996-10-24
MX9605156A (es) 1998-05-31
ATE239698T1 (de) 2003-05-15
ATE230389T1 (de) 2003-01-15
CA2188817C (en) 2010-01-26
EP0771565A3 (en) 1998-11-04
AU7038496A (en) 1997-05-01
EP0927716A1 (en) 1999-07-07
ES2193615T3 (es) 2003-11-01
EP0771565B1 (en) 2003-01-02
HUP9602943A2 (en) 1997-08-28

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Legal Events

Date Code Title Description
FA10 Dismissal: dismissal - article 33 of industrial property law