NO20111199A1 - Indolderivater som antikreftmidler - Google Patents

Indolderivater som antikreftmidler Download PDF

Info

Publication number: NO20111199A1
Authority: NO; Norway
Prior art keywords: formula; compound; compounds; solvent; treatment
Prior art date: 2009-02-04

Application number

NO20111199A

Other languages

English (en)

Norwegian (no)

Inventor

Bruno Schoentjes

Sophie Descamps

Nathalie Claudie Isabelle Amblard

Original Assignee

Janssen Pharmaceutica Nv

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.)

2009-02-04

Filing date

2011-09-02

Publication date

2011-11-04

2011-09-02 Application filed by Janssen Pharmaceutica Nv filed Critical Janssen Pharmaceutica Nv

2011-11-04 Publication of NO20111199A1 publication Critical patent/NO20111199A1/no

Links

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Classifications

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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/14—Drugs for disorders of the endocrine system of the thyroid hormones, e.g. T3, T4
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/06—Antianaemics
- 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
- C07D401/10—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 carbon chain containing aromatic rings

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Chemical & Material Sciences (AREA)
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Medicinal Chemistry (AREA)
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Pharmacology & Pharmacy (AREA)
Life Sciences & Earth Sciences (AREA)
Animal Behavior & Ethology (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
General Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Engineering & Computer Science (AREA)
Bioinformatics & Cheminformatics (AREA)
Diabetes (AREA)
Immunology (AREA)
Neurology (AREA)
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Physical Education & Sports Medicine (AREA)
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Neurosurgery (AREA)
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Ophthalmology & Optometry (AREA)
Rheumatology (AREA)
Endocrinology (AREA)
Psychiatry (AREA)
Hospice & Palliative Care (AREA)
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Transplantation (AREA)
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Oncology (AREA)
Urology & Nephrology (AREA)
Dermatology (AREA)
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Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Plural Heterocyclic Compounds (AREA)
Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

NO20111199A 2009-02-04 2011-09-02 Indolderivater som antikreftmidler NO20111199A1 (no)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
EP09152089		2009-02-04
PCT/EP2010/051316 WO2010089327A2 (fr)	2009-02-04	2010-02-03	Dérivés d'indole en tant qu'agents anti-cancéreux

Publications (1)

Publication Number	Publication Date
NO20111199A1 true NO20111199A1 (no)	2011-11-04

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NO20111199A NO20111199A1 (no)	2009-02-04	2011-09-02	Indolderivater som antikreftmidler

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US (1)	US8541442B2 (fr)
EP (1)	EP2393801B1 (fr)
JP (1)	JP5612611B2 (fr)
KR (1)	KR101730407B1 (fr)
CN (1)	CN102307868B (fr)
AR (1)	AR075235A1 (fr)
AU (1)	AU2010210178B2 (fr)
BR (1)	BRPI1008855B8 (fr)
CA (1)	CA2749209C (fr)
CL (1)	CL2011001860A1 (fr)
CO (1)	CO6341625A2 (fr)
EA (1)	EA021883B1 (fr)
ES (1)	ES2639752T3 (fr)
IL (1)	IL214427A (fr)
MX (1)	MX2011008195A (fr)
MY (1)	MY152018A (fr)
NO (1)	NO20111199A1 (fr)
NZ (1)	NZ594186A (fr)
SG (1)	SG173495A1 (fr)
TW (1)	TWI476189B (fr)
UA (1)	UA107455C2 (fr)
WO (1)	WO2010089327A2 (fr)
ZA (1)	ZA201105695B (fr)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2841517B2 (ja)	1989-08-11	1998-12-24	株式会社ツムラ	入浴剤
JP2872763B2 (ja)	1990-06-28	1999-03-24	紀伊産業株式会社	携帯用肛門洗浄器
CA2853729A1 (fr) *	2011-10-28	2013-05-02	Board Of Regents, The University Of Texas System	Nouvelles compositions et procedes pour traiter le cancer
WO2014085486A2 (fr)	2012-11-30	2014-06-05	Waters Technologies Corporation	Procédés et appareil pour l'analyse de métabolites de la vitamine d
CN108239083B (zh)	2016-12-26	2021-08-17	阿里根公司	芳香烃受体调节剂
CN106632303A (zh) *	2017-01-09	2017-05-10	湖南华腾制药有限公司	一种6‑噻唑基吲哚衍生物的制备方法
WO2019099977A2 (fr)	2017-11-20	2019-05-23	Ariagen, Inc.	Composés d'indole et leur utilisation
CN108659003B (zh) *	2018-04-14	2021-01-26	上海朝晖药业有限公司	一种治疗口腔溃疡的化合物的制备方法
AU2020205139A1 (en) *	2019-01-04	2021-08-19	Jiangsu Hengrui Medicine Co., Ltd.	6-oxo-1,6-dihydropyridazine derivative, preparation method therefor and medical use thereof
US20220162169A1 (en) *	2019-02-20	2022-05-26	Jiangsu Hengrui Medicine Co., Ltd.	6-oxo-1,6-dihydropyridazine prodrug derivative, preparation method therefor, and application thereof in medicine
AU2020258394A1 (en)	2019-04-15	2021-10-28	Ariagen, Inc.	Chiral indole compounds and their use
WO2024102758A2 (fr) *	2022-11-08	2024-05-16	The General Hospital Corporation	Séries n-(n-aminoalkyl)phénanthridiunium de fluorophores sensibles au chlorure et leurs procédés d'utilisation

Family Cites Families (19)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR901228A (fr)	1943-01-16	1945-07-20	Deutsche Edelstahlwerke Ag	Système d'aimant à entrefer annulaire
AUPO863197A0 (en)	1997-08-18	1997-09-11	Fujisawa Pharmaceutical Co., Ltd.	Novel derivatives
US6309492B1 (en)	1998-09-16	2001-10-30	Marc A. Seidner	Polymer fill coating for laminate or composite wood products and method of making same
UA71587C2 (uk)	1998-11-10	2004-12-15	Шерінг Акцієнгезелльшафт	Аміди антранілової кислоти та їхнє застосування як лікарських засобів
BR9915940A (pt)	1998-12-02	2001-09-11	Pfizer Prod Inc	Métodos e composições para restaurar a estabilidade conformacional de uma proteìna da famìlia p53
AU1734401A (en)	1999-12-09	2001-06-18	Mitsubishi Pharma Corporation	Carboxyamido derivatives
JP2004508421A (ja)	2000-09-15	2004-03-18	アノーメッド　インコーポレイティド	ケモカインレセプター結合性ヘテロ環式化合物
ES2566056T3 (es)	2001-03-29	2016-04-08	Eli Lilly And Company	N-(2-ariletil)bencilaminas como antagonistas del receptor 5-HT6
AU2002357728A1 (en)	2001-11-09	2003-05-19	The Regents Of The University Of California	Alpha-helix mimicry by a class of organic molecules
PL370176A1 (en)	2001-11-13	2005-05-16	3-Dimensional Pharmaceuticals, Inc.	Substituted 1,4-benzodiazepines and uses thereof for the treatment of cancer
ES2301717T3 (es)	2001-12-18	2008-07-01	F. Hoffmann-La Roche Ag	Cis-2,4,5-trifenil-imidazolinas y su utilizacion para el tratamiento de tumores.
GB0215650D0 (en)	2002-07-05	2002-08-14	Cyclacel Ltd	Bisarylsufonamide compounds
JP5156378B2 (ja)	2004-09-22	2013-03-06	ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ	ＭＤＭ２とｐ５３の間の相互作用の阻害剤
DE602007007065D1 (de)	2006-03-22	2010-07-22	Janssen Pharmaceutica Nv	Cycloalkylaminderivate als inhibitoren der wechselwirkung zwischen mdm2 und p53
US8232298B2 (en)	2006-03-22	2012-07-31	Janssen Pharmaceutica N.V.	Inhibitors of the interaction between MDM2 and P53
US20100129933A1 (en) *	2007-04-26	2010-05-27	Forschungszentrum Karlsruhe Gmbh	Method for detecting the binding between mdm2 and the proteasome
PA8792401A1 (es)	2007-08-06	2009-03-31	Janssen Pharmaceutica Nv	Fenilendiaminas
JO2704B1 (en)	2007-09-21	2013-03-03	جانسين فارماسوتيكا ان في	Interference inhibition factors between MD2 and B53
US8288377B2 (en)	2007-09-21	2012-10-16	Janssen Pharmaceutica N.V.	Inhibitors of the interaction between MDM2 and p53

2010
- 2010-02-03 MY MYPI2011003583 patent/MY152018A/en unknown
- 2010-02-03 MX MX2011008195A patent/MX2011008195A/es active IP Right Grant
- 2010-02-03 NZ NZ594186A patent/NZ594186A/xx not_active IP Right Cessation
- 2010-02-03 SG SG2011055431A patent/SG173495A1/en unknown
- 2010-02-03 KR KR1020117020348A patent/KR101730407B1/ko not_active Expired - Fee Related
- 2010-02-03 CN CN201080007001.9A patent/CN102307868B/zh not_active Expired - Fee Related
- 2010-02-03 BR BRPI1008855A patent/BRPI1008855B8/pt not_active IP Right Cessation
- 2010-02-03 WO PCT/EP2010/051316 patent/WO2010089327A2/fr not_active Ceased
- 2010-02-03 AR ARP100100298A patent/AR075235A1/es unknown
- 2010-02-03 EP EP10702310.3A patent/EP2393801B1/fr active Active
- 2010-02-03 EA EA201170997A patent/EA021883B1/ru not_active IP Right Cessation
- 2010-02-03 US US13/147,707 patent/US8541442B2/en not_active Expired - Fee Related
- 2010-02-03 ES ES10702310.3T patent/ES2639752T3/es active Active
- 2010-02-03 CA CA2749209A patent/CA2749209C/fr active Active
- 2010-02-03 AU AU2010210178A patent/AU2010210178B2/en not_active Ceased
- 2010-02-03 TW TW099103103A patent/TWI476189B/zh not_active IP Right Cessation
- 2010-02-03 JP JP2011548674A patent/JP5612611B2/ja not_active Expired - Fee Related
- 2010-03-02 UA UAA201109449A patent/UA107455C2/uk unknown
2011
- 2011-07-12 CO CO11087033A patent/CO6341625A2/es not_active Application Discontinuation
- 2011-08-02 CL CL2011001860A patent/CL2011001860A1/es unknown
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- 2011-08-03 IL IL214427A patent/IL214427A/en active IP Right Grant
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Also Published As

Publication number	Publication date
NZ594186A (en)	2012-12-21
BRPI1008855B8 (pt)	2021-05-25
TWI476189B (zh)	2015-03-11
MX2011008195A (es)	2011-09-06
IL214427A (en)	2016-02-29
SG173495A1 (en)	2011-09-29
JP2012516872A (ja)	2012-07-26
CN102307868A (zh)	2012-01-04
US8541442B2 (en)	2013-09-24
JP5612611B2 (ja)	2014-10-22
US20110294846A1 (en)	2011-12-01
BRPI1008855B1 (pt)	2020-05-12
KR101730407B1 (ko)	2017-04-26
MY152018A (en)	2014-08-15
CA2749209A1 (fr)	2010-08-12
AU2010210178A1 (en)	2011-07-28
CN102307868B (zh)	2016-06-22
EA021883B1 (ru)	2015-09-30
EP2393801B1 (fr)	2017-07-12
AU2010210178B2 (en)	2014-06-05
CO6341625A2 (es)	2011-11-21
EA201170997A1 (ru)	2012-01-30
EP2393801A2 (fr)	2011-12-14
WO2010089327A2 (fr)	2010-08-12
WO2010089327A3 (fr)	2010-10-21
UA107455C2 (uk)	2015-01-12
KR20110116195A (ko)	2011-10-25
BRPI1008855A2 (pt)	2016-03-15
CA2749209C (fr)	2017-01-10
ZA201105695B (en)	2014-01-29
IL214427A0 (en)	2011-09-27
AR075235A1 (es)	2011-03-16
CL2011001860A1 (es)	2012-07-20
TW201038552A (en)	2010-11-01
ES2639752T3 (es)	2017-10-30

Publication	Publication Date	Title
NO20111199A1 (no)	2011-11-04	Indolderivater som antikreftmidler
CA2783624C (fr)	2019-08-20	Composes heteroaryle et utilisations associees
EP2953943B1 (fr)	2017-04-12	Dihydropyrimidinones bicycliques substituées et leur utilisation à titre d'inhibiteurs de l'activité élastase neutrophile
RU2477724C2 (ru)	2013-03-20	Ингибиторы взаимодействия между mdm2 и p53
EP2964617B1 (fr)	2017-04-12	Dihydropyrimidinones bicycliques substituées et leur utilisation en tant qu'inhibiteurs de l'activité élastase de neutrophiles
RS51007B (sr)	2010-10-31	Supstituisani piridinil i pirimidinil derivati kao modulatori metabolizma i lečenje poremećaja proisteklih iz toga
JP2017509687A (ja)	2017-04-06	大環状ピリミジン誘導体
EP3019493A1 (fr)	2016-05-18	Dihydroquinoxalinones et dihydropyridopyrazinones inhibitrices de protéine bet modifiées
WO2009019274A1 (fr)	2009-02-12	Phénylènediamines substituées utilisables en tant qu'inhibiteurs de l'interaction entre mdm2 et p53
EP3174876B1 (fr)	2019-12-18	Dihydropyrimidinones bicycliques substituées et leur utilisation en tant qu'inhibiteurs de l'activité de l'élastase neutrophile
JP6457523B2 (ja)	2019-01-23	医薬組成物のためのスルホキシイミン置換キナゾリン
HK1163674B (en)	2017-09-29	Indole derivatives as anticancer agents
HK1163674A (en)	2012-09-14	Indole derivatives as anticancer agents
TW202128653A (zh)	2021-08-01	作為parp7抑制劑的嗒酮

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