[go: up one dir, main page]

MA26528A1 - DERIVES HYDROXY SUBSTITUE DE 2-ALKYLIDENE HYDROXYCUMARANONES A ACTIVITE uPA-uPAR ANTAGONISTE COMME AGENT ANTITUMORAL ET/OU ANTIMETASTATIQUE. - Google Patents

DERIVES HYDROXY SUBSTITUE DE 2-ALKYLIDENE HYDROXYCUMARANONES A ACTIVITE uPA-uPAR ANTAGONISTE COMME AGENT ANTITUMORAL ET/OU ANTIMETASTATIQUE.

Info

Publication number
MA26528A1
MA26528A1 MA25200A MA25200A MA26528A1 MA 26528 A1 MA26528 A1 MA 26528A1 MA 25200 A MA25200 A MA 25200A MA 25200 A MA25200 A MA 25200A MA 26528 A1 MA26528 A1 MA 26528A1
Authority
MA
Morocco
Prior art keywords
hydroxycumaranones
upa
alkylidene
antagonist
tumor
Prior art date
Application number
MA25200A
Other languages
English (en)
Inventor
De Cillis Gianpiero
Konig Bernhard
Di Domenico Roberto
Oliva Ambrogio
Original Assignee
Hoffmann La Roche
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 Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of MA26528A1 publication Critical patent/MA26528A1/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic 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
    • C07D405/02Heterocyclic 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
    • C07D405/12Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/34Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
    • A61K31/343Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide condensed with a carbocyclic ring, e.g. coumaran, bufuralol, befunolol, clobenfurol, amiodarone
    • 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
    • A61P35/00Antineoplastic agents
    • A61P35/04Antineoplastic agents specific for metastasis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/08Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
    • C07D211/18Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D211/26Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members 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
    • C07D211/56Nitrogen atoms
    • C07D211/58Nitrogen atoms attached in position 4
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/04Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
    • C07D295/08Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms
    • C07D295/084Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/77Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D307/78Benzo [b] furans; Hydrogenated benzo [b] furans
    • C07D307/82Benzo [b] furans; Hydrogenated benzo [b] furans 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 carbon atoms of the hetero ring
    • C07D307/83Oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic 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
    • C07D405/14Heterocyclic 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 three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Oncology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Furan Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
MA25200A 1997-07-31 1998-07-31 DERIVES HYDROXY SUBSTITUE DE 2-ALKYLIDENE HYDROXYCUMARANONES A ACTIVITE uPA-uPAR ANTAGONISTE COMME AGENT ANTITUMORAL ET/OU ANTIMETASTATIQUE. MA26528A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP97113190 1997-07-31
EP98106946 1998-04-16

Publications (1)

Publication Number Publication Date
MA26528A1 true MA26528A1 (fr) 2004-12-20

Family

ID=26145681

Family Applications (1)

Application Number Title Priority Date Filing Date
MA25200A MA26528A1 (fr) 1997-07-31 1998-07-31 DERIVES HYDROXY SUBSTITUE DE 2-ALKYLIDENE HYDROXYCUMARANONES A ACTIVITE uPA-uPAR ANTAGONISTE COMME AGENT ANTITUMORAL ET/OU ANTIMETASTATIQUE.

Country Status (21)

Country Link
US (1) US6200989B1 (fr)
EP (1) EP1012147B1 (fr)
JP (1) JP3241711B2 (fr)
KR (1) KR100343067B1 (fr)
AR (1) AR013374A1 (fr)
AT (1) ATE308535T1 (fr)
AU (1) AU745839B2 (fr)
BR (1) BR9811589A (fr)
CA (1) CA2296476A1 (fr)
DE (1) DE69832184D1 (fr)
HR (1) HRP20000031A2 (fr)
HU (1) HUP0004221A2 (fr)
ID (1) ID24525A (fr)
IL (1) IL134193A0 (fr)
MA (1) MA26528A1 (fr)
NO (1) NO20000366D0 (fr)
PE (1) PE106099A1 (fr)
PL (1) PL338614A1 (fr)
TR (1) TR200000272T2 (fr)
UY (1) UY25114A1 (fr)
WO (1) WO1999006387A2 (fr)

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU736869B2 (en) * 1999-01-30 2001-08-02 Roche Diagnostics Gmbh O-substituted hydroxycoumaranone derivatives as antitumor and antimetastatic agents
AU2002362030A1 (en) * 2001-11-27 2003-06-10 Fred Hutchinson Cancer Research Center Methods for inhibiting deacetylase activity
AU2002358158A1 (en) * 2001-12-19 2003-06-30 D. Collen Research Foundation Use of urokinase receptor antagonists to modulate ischemiareperfusion injury
WO2004076444A2 (fr) * 2003-02-25 2004-09-10 F. Hoffmann-La Roche Ag Nouveaux derives d'hydroxycoumaranone utilises en tant qu'agents antitumoraux et antimetastatiques a activite biologique amelioree dans des dosages cellulaires et a stabilite amelioree
AU2007310007A1 (en) * 2006-10-27 2008-05-02 Otsuka Chemical Co., Ltd. Amide compound or salt thereof, and biofilm formation inhibitor, biofilm remover and bactericide each using the amide compound or salt thereof
US8258307B2 (en) 2006-11-07 2012-09-04 University Of Tokyo Amide compound or salt thereof, and biofilm inhibitor, biofilm remover and disinfectant containing the same
GB2462022B (en) 2008-06-16 2011-05-25 Biovascular Inc Controlled release compositions of agents that reduce circulating levels of platelets and methods thereof
PT109740B (pt) * 2016-11-14 2020-07-30 Hovione Farmaciencia Sa Processo para a preparação de brometo de umeclidínio
EP4092013A1 (fr) 2017-06-20 2022-11-23 Imbria Pharmaceuticals, Inc. Compositions et procédés pour augmenter l'efficacité du métabolisme cardiaque
US11833156B2 (en) 2017-09-22 2023-12-05 Jubilant Epipad LLC Heterocyclic compounds as pad inhibitors
WO2019077631A1 (fr) 2017-10-18 2019-04-25 Jubilant Biosys Limited Composés imidazo-pyridine à utiliser en tant qu'inhibiteurs de pad
KR20200085836A (ko) 2017-11-06 2020-07-15 주빌런트 프로델 엘엘씨 Pd1/pd-l1 활성화 억제제로서의 피리미딘 유도체
BR112020010322A2 (pt) 2017-11-24 2020-11-17 Jubilant Episcribe Llc composto da fórmula i; composto da fórmula ia; composto da fórmula ib; processo de preparação de compostos da fórmula i; composição farmacêutica; método para o tratamento e/ou prevenção de várias doenças; uso dos compostos; método para o tratamento de câncer; e método para o tratamento e/ou prevenção de uma afecção mediada por prmt5 ou um distúrbio proliferativo ou câncer
SG11202005561XA (en) 2017-12-13 2020-07-29 Praxis Biotech LLC Inhibitors of integrated stress response pathway
CN112105610B (zh) 2018-03-13 2024-01-26 朱比连特普罗德尔有限责任公司 作为pd1/pd-l1相互作用/活化的抑制剂的双环化合物
WO2019236710A1 (fr) * 2018-06-05 2019-12-12 Praxis Biotech LLC Inhibiteurs de la voie de réponse intégrée au stress
EP3866794B1 (fr) 2018-10-17 2024-12-04 Imbria Pharmaceuticals, Inc. Procédés de traitement de maladies rhumatismales à l'aide de composés à base de trimétazidine
JP6611029B1 (ja) * 2018-11-05 2019-11-27 プキョン ナショナル ユニバーシティ インダストリ ユニバーシティ コーポレーション ファウンデーションPukyong National University Industry−University Cooperation Foundation 高周波超音波多焦点変換器、その製造装置、および製造方法
JP2022536663A (ja) 2019-06-12 2022-08-18 プラクシス バイオテック エルエルシー 統合的ストレス応答経路のモジュレーター
US11780811B2 (en) 2020-06-30 2023-10-10 Imbria Pharmaceuticals, Inc. Methods of synthesizing 2-[4-[(2,3,4-trimethoxyphenyl)methyl]piperazin-1-yl]ethyl pyridine-3-carboxylate
US11530184B2 (en) 2020-06-30 2022-12-20 Imbria Pharmaceuticals, Inc. Crystal forms of 2-[4-[(2,3,4-trimethoxyphenyl)methyl]piperazin-1-yl]ethyl pyridine-3-carboxylate
US11883396B2 (en) 2021-05-03 2024-01-30 Imbria Pharmaceuticals, Inc. Methods of treating kidney conditions using modified forms of trimetazidine

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2901336A1 (de) * 1979-01-15 1980-07-24 Boehringer Mannheim Gmbh Neue arylether, verfahren zu deren herstellung sowie diese verbindungen enthaltende arzneimittel
DE3209271A1 (de) 1982-03-13 1983-09-15 Boehringer Mannheim Gmbh, 6800 Mannheim Bicyclische phenolether, verfahren zu deren herstellung sowie diese verbindungen enthaltende arzneimittel
EP0192671B1 (fr) * 1984-08-13 1993-12-29 Biotechnology Australia Pty. Ltd. Minactivin
US5747458A (en) * 1995-06-07 1998-05-05 Chiron Corporation Urokinase receptor ligands

Also Published As

Publication number Publication date
KR20010022362A (ko) 2001-03-15
NO20000366L (no) 2000-01-25
US6200989B1 (en) 2001-03-13
ATE308535T1 (de) 2005-11-15
PL338614A1 (en) 2000-11-06
DE69832184D1 (de) 2005-12-08
ID24525A (id) 2000-07-20
AU745839B2 (en) 2002-04-11
TR200000272T2 (tr) 2000-09-21
BR9811589A (pt) 2000-09-19
JP3241711B2 (ja) 2001-12-25
WO1999006387A3 (fr) 1999-04-22
HRP20000031A2 (en) 2000-10-31
NO20000366D0 (no) 2000-01-25
UY25114A1 (es) 2001-01-31
AU9155998A (en) 1999-02-22
EP1012147A2 (fr) 2000-06-28
HUP0004221A2 (hu) 2001-04-28
WO1999006387A2 (fr) 1999-02-11
JP2001512113A (ja) 2001-08-21
CA2296476A1 (fr) 1999-02-11
AR013374A1 (es) 2000-12-27
IL134193A0 (en) 2001-04-30
PE106099A1 (es) 1999-11-11
KR100343067B1 (ko) 2002-07-03
EP1012147B1 (fr) 2005-11-02

Similar Documents

Publication Publication Date Title
MA26528A1 (fr) DERIVES HYDROXY SUBSTITUE DE 2-ALKYLIDENE HYDROXYCUMARANONES A ACTIVITE uPA-uPAR ANTAGONISTE COMME AGENT ANTITUMORAL ET/OU ANTIMETASTATIQUE.
PT946542E (pt) Derivados de indano ou de di-hidroindol
DE69721347D1 (de) Sprachaktivitätserkennung
NO973756D0 (no) Deteksjon av stemmeaktivitet
DE69716266D1 (de) Sprachaktivitätsdetektor
PT888359E (pt) Derivados de pirimidin-4-ona como pesticida
BR9611820A (pt) Derivados de quinolina
NO990918D0 (no) Ringformet kateter
MA26503A1 (fr) Derives de 5'-desoxy-cytidine.
EP0891347A4 (fr) Derives triterpenes possedant une activite immunosuppressive
FR2746875B1 (fr) Garniture de friction
PT1025114E (pt) Derivados de eritromicina-cetolido 6-o-substituido 3'-n-modificados possuindo actividade antibacteriana
EP0920622A4 (fr) Detection de microbacteries
ATA38796A (de) Möbelbeschlagteil
FI955584A7 (fi) Ääniaktiviteetin tunnistaminen
MA26440A1 (fr) Derives de n-benzylazolium
AUPN748496A0 (en) Bird activity platform
ZA975366B (en) Preparation of substituted 3-aryl-5-haloalkyl-pyrazoles having herbicidal activity.
DE59602693D1 (de) Lenk- oder Bockrolle
EP0804205A4 (fr) Derives de 4-aza-19-norandrostane
PT796843E (pt) Derivados de 1,25-di-hidroxi-16,22,23-trisde-hidro-colecalciferol
KR970053464U (ko) 휴지걸이
AT3511U3 (de) Briefkasten oder briefkastenanlage
ES1033459Y (es) Criolla de adorno.
UA25779A (uk) Спосіб діагhостики раhhіх порушеhь фуhкціоhальhої активhості печіhки