HRP20050070B1 - 3-2-[1-(4-(n-((4-metil-piperazin-1-il)-metilkarbonil)-n-metil-amino)-anilino)-1-fenil-metilen]-6-metoksikarbonil-2-indolinon-monoetansulfonat i njegova primjena kao farmaceutskog pripravka - Google Patents

3-2-[1-(4-(n-((4-metil-piperazin-1-il)-metilkarbonil)-n-metil-amino)-anilino)-1-fenil-metilen]-6-metoksikarbonil-2-indolinon-monoetansulfonat i njegova primjena kao farmaceutskog pripravka

Info

Publication number
HRP20050070B1
HRP20050070B1 HRP20050070AA HRP20050070A HRP20050070B1 HR P20050070 B1 HRP20050070 B1 HR P20050070B1 HR P20050070A A HRP20050070A A HR P20050070AA HR P20050070 A HRP20050070 A HR P20050070A HR P20050070 B1 HRP20050070 B1 HR P20050070B1
Authority
HR
Croatia
Prior art keywords
methyl
methylcarbonyl
anilino
piperazin
methylene
Prior art date
Application number
HRP20050070AA
Other languages
English (en)
Inventor
Gerald Jürgen ROTH
Günter Linz
Peter Sieger
Werner Rall
Frank Hilberg
Thomas Bock
Original Assignee
Boehringer Ingelheim Pharma Gmbh & Co.Kg
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=30469050&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=HRP20050070(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Boehringer Ingelheim Pharma Gmbh & Co.Kg filed Critical Boehringer Ingelheim Pharma Gmbh & Co.Kg
Publication of HRP20050070A2 publication Critical patent/HRP20050070A2/xx
Publication of HRP20050070B1 publication Critical patent/HRP20050070B1/hr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/12Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/30Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
    • C07D209/32Oxygen atoms
    • C07D209/34Oxygen atoms in position 2
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Abstract

Prikazani izum se odnosi na spoj 3-Z-[1-(4-(N-((4-metil-piperazin-1-il)-metilkarbonil)-N-metil-amino)-anilino)-1-fenil-metilen]-6-metoksikarbonil-2-indolinon monoetansulfonat formule I i njegovu primjenu u farmaceutskom pripravku. Formula I:
HRP20050070AA 2002-07-24 2005-01-21 3-2-[1-(4-(n-((4-metil-piperazin-1-il)-metilkarbonil)-n-metil-amino)-anilino)-1-fenil-metilen]-6-metoksikarbonil-2-indolinon-monoetansulfonat i njegova primjena kao farmaceutskog pripravka HRP20050070B1 (hr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE10233500A DE10233500A1 (de) 2002-07-24 2002-07-24 3-Z-[1-(4-(N-((4-Methyl-piperazin-1-yl)-methylcarbonyl)-N-methyl-amino)-anilino)-1-phenyl-methylen]-6-methoxycarbonyl-2-indolinon-Monoethansulfonat und dessen Verwendung als Arzneimittel
PCT/EP2003/007822 WO2004013099A1 (en) 2002-07-24 2003-07-18 3-z-[1-(4-(n-((4-methyl-piperazin-1-yl)-methylcarbonyl)-n-methyl-amino)-anilino)-1-phenyl-methylene]-6-methoxycarbonyl-2-indolinone-monoethanesulphonate and the use thereof as a pharmaceutical composition

Publications (2)

Publication Number Publication Date
HRP20050070A2 HRP20050070A2 (en) 2005-12-31
HRP20050070B1 true HRP20050070B1 (hr) 2013-09-30

Family

ID=30469050

Family Applications (1)

Application Number Title Priority Date Filing Date
HRP20050070AA HRP20050070B1 (hr) 2002-07-24 2005-01-21 3-2-[1-(4-(n-((4-metil-piperazin-1-il)-metilkarbonil)-n-metil-amino)-anilino)-1-fenil-metilen]-6-metoksikarbonil-2-indolinon-monoetansulfonat i njegova primjena kao farmaceutskog pripravka

Country Status (36)

Country Link
US (2) US7119093B2 (hr)
EP (2) EP2386543A1 (hr)
JP (1) JP5039279B2 (hr)
KR (1) KR101145691B1 (hr)
CN (1) CN100351235C (hr)
AR (2) AR040662A1 (hr)
AT (1) ATE551322T1 (hr)
AU (1) AU2003254376B2 (hr)
BR (1) BRPI0312811B8 (hr)
CA (1) CA2493310C (hr)
CY (1) CY1112916T1 (hr)
DE (1) DE10233500A1 (hr)
DK (1) DK1527047T3 (hr)
EA (1) EA008684B1 (hr)
EC (1) ECSP055571A (hr)
EG (1) EG24562A (hr)
ES (1) ES2384968T3 (hr)
HK (1) HK1078851A1 (hr)
HR (1) HRP20050070B1 (hr)
IL (2) IL166405A0 (hr)
ME (1) ME00353B (hr)
MX (1) MXPA04012785A (hr)
MY (1) MY136883A (hr)
NO (1) NO330486B1 (hr)
NZ (1) NZ538367A (hr)
PE (1) PE20040704A1 (hr)
PL (1) PL223758B1 (hr)
PT (1) PT1527047E (hr)
RS (1) RS52283B (hr)
SA (1) SA03240446B1 (hr)
SI (1) SI1527047T1 (hr)
TW (1) TWI285635B (hr)
UA (1) UA78352C2 (hr)
UY (1) UY27904A1 (hr)
WO (1) WO2004013099A1 (hr)
ZA (1) ZA200409814B (hr)

Families Citing this family (64)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10233500A1 (de) * 2002-07-24 2004-02-19 Boehringer Ingelheim Pharma Gmbh & Co. Kg 3-Z-[1-(4-(N-((4-Methyl-piperazin-1-yl)-methylcarbonyl)-N-methyl-amino)-anilino)-1-phenyl-methylen]-6-methoxycarbonyl-2-indolinon-Monoethansulfonat und dessen Verwendung als Arzneimittel
US20040204458A1 (en) * 2002-08-16 2004-10-14 Boehringer Ingelheim Pharma Gmbh & Co. Kg Use of Lck inhibitors for treatment of immunologic diseases
US20050043233A1 (en) * 2003-04-29 2005-02-24 Boehringer Ingelheim International Gmbh Combinations for the treatment of diseases involving cell proliferation, migration or apoptosis of myeloma cells or angiogenesis
PE20060777A1 (es) * 2004-12-24 2006-10-06 Boehringer Ingelheim Int Derivados de indolinona para el tratamiento o la prevencion de enfermedades fibroticas
WO2007057397A1 (en) * 2005-11-15 2007-05-24 Boehringer Ingelheim International Gmbh Treatment of cancer
EP1870400A1 (en) * 2006-06-08 2007-12-26 Boehringer Ingelheim Pharma GmbH & Co. KG Salts and crystalline salt forms of an 2-indolinone derivative
ES2435454T3 (es) 2007-06-21 2013-12-19 Janssen Pharmaceutica, N.V. Indolin-2-onas y aza-indolin-2-onas
PE20091445A1 (es) * 2007-12-03 2009-10-19 Boehringer Ingelheim Int Derivados de indolinona y procedimiento para su fabricacion
WO2009071523A1 (en) 2007-12-03 2009-06-11 Boehringer Ingelheim International Gmbh Process for the manufacture of an indolinone derivative
US20170065529A1 (en) 2015-09-09 2017-03-09 Boehringer Ingelheim International Gmbh Pharmaceutical dosage form for immediate release of an indolinone derivative
US20110301177A1 (en) 2008-06-06 2011-12-08 Boehringer Ingelheim International Gmbh Capsule pharmaceutical dosage form comprising a suspension formulation of an indolinone derivative
HUE025821T2 (en) * 2008-06-06 2016-04-28 Boehringer Ingelheim Int drug combination
UA107560C2 (uk) * 2008-06-06 2015-01-26 Фармацевтична лікарська форма для негайного вивільнення похідної індолінону
WO2010081817A1 (en) 2009-01-14 2010-07-22 Boehringer Ingelheim International Gmbh Method for treating colorectal cancer
US8802384B2 (en) * 2009-03-12 2014-08-12 Boehringer Ingelheim International Gmbh Method or system using biomarkers for the monitoring of a treatment
WO2010130758A1 (en) * 2009-05-14 2010-11-18 Boehringer Ingelheim International Gmbh New combination therapy in treatment of cancer and fibrotic diseases
EP2429520A1 (en) 2009-05-14 2012-03-21 Boehringer Ingelheim International GmbH New combination therapy in treatment of oncological and fibrotic diseases
US20120107304A1 (en) 2010-04-27 2012-05-03 Boehringer Ingelheim International Gmbh Combination therapy in treatment of oncological and fibrotic diseases
WO2012068441A2 (en) 2010-11-19 2012-05-24 Ratiopharm Gmbh Intedanib salts and solid state forms thereof
WO2013059740A1 (en) 2011-10-21 2013-04-25 Foundation Medicine, Inc. Novel alk and ntrk1 fusion molecules and uses thereof
EP2875020B1 (en) 2012-07-19 2017-09-06 Boehringer Ingelheim International GmbH Process for the preparation of a fumaric acid salt of 9-[4-(3-chloro-2-fluoro-phenylamino)-7-methoxy- chinazolin-6-yloxy]-1,4-diaza-spiro[5.5]undecan-5-one
AU2013337277B2 (en) 2012-11-05 2018-03-08 Foundation Medicine, Inc. Novel NTRK1 fusion molecules and uses thereof
EP4223770A3 (en) 2012-11-05 2023-10-18 Foundation Medicine, Inc. Novel fusion molecules and uses thereof
WO2014113729A2 (en) 2013-01-18 2014-07-24 Foundation Mecicine, Inc. Methods of treating cholangiocarcinoma
US20140350022A1 (en) * 2013-05-10 2014-11-27 Boehringer Ingelheim International Gmbh Efficacious treatment of NSCLC and predictive clinical marker of the responsiveness of a tumour to a treatment
CN104003925B (zh) * 2013-06-05 2016-03-30 四川大学 吲哚酮化合物或其衍生物及其用途
WO2015009889A1 (en) * 2013-07-18 2015-01-22 Concert Pharmaceuticals, Inc. Deuterated intedanib derivatives and their use for the treatment of proliferative disorders
US20170114323A1 (en) * 2014-06-19 2017-04-27 Whitehead Institute For Biomedical Research Uses of kinase inhibitors for inducing and maintaining pluripotency
CN106008308A (zh) * 2015-03-13 2016-10-12 正大天晴药业集团股份有限公司 尼达尼布乙磺酸盐结晶
WO2016178064A1 (en) 2015-05-06 2016-11-10 Suven Life Sciences Limited Polymorph of nintedanib ethanesulphonate, processes and intermediates thereof
CN105126909B (zh) * 2015-07-13 2018-01-23 淮海工学院 固载钯催化剂在4‑苯乙炔基‑3‑硝基苯甲酸甲酯合成中的应用
CN105001143A (zh) * 2015-07-24 2015-10-28 南京正大天晴制药有限公司 一种制备高纯度乙磺酸尼达尼布的方法
CN106432042A (zh) * 2015-08-13 2017-02-22 南京华威医药科技开发有限公司 尼达尼布乙磺酸水合物的药物新晶型
WO2017077551A2 (en) * 2015-11-03 2017-05-11 Mylan Laboratories Limited An amorphous nintedanib esylate and solid dispersion thereof
CZ2016104A3 (cs) 2016-02-24 2017-09-06 Zentiva, K.S. Krystalické modifikace solí methyl (3Z)-3-{[(4-{methyl[(4-methylpiperazin-1-yl)acetyl]amino}fenyl)amino](fenyl)methyliden}-2-oxo-2,3-dihydro-1H-indol-6-karboxylátu a způsoby jejich přípravy
JP2019511547A (ja) * 2016-04-13 2019-04-25 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング 結腸直腸癌を治療するためのニンテダニブ、トリフルリジンおよびチピラシルの医薬組合せ
EP3246029A1 (en) 2016-05-19 2017-11-22 Boehringer Ingelheim International Gmbh Pharmaceutical combination of nintedanib and capecitabine for the treatment of colorectal cancer
WO2017198202A1 (zh) * 2016-05-19 2017-11-23 上海诚妙医药科技有限公司 尼达尼布的新晶型及其制备方法及其用途
EP3464240A1 (en) 2016-05-27 2019-04-10 Boehringer Ingelheim International GmbH Use of ecm biomarkers for the determining the treatment onset with nintedanib and pirfenidone
EP3463353A1 (en) 2016-06-01 2019-04-10 Boehringer Ingelheim International GmbH Use of ecm biomarkers for the determining the treatment onset with nintedanib and pirfenidone
ITUA20164213A1 (it) 2016-06-08 2017-12-08 Olon Spa Polimorfo di nintedanib
US10772885B2 (en) 2016-09-26 2020-09-15 Reyoung (Suzhou) Biology Science & Technology Co., Ltd. Composition for treating ocular diseases and methods of usage and making
WO2018108669A1 (en) 2016-12-12 2018-06-21 Boehringer Ingelheim International Gmbh Nintedanib for use in methods for the treatment of interstitial lung diseases by coadministration with olodaterol
US10981896B2 (en) * 2017-03-02 2021-04-20 Board Of Regents, The University Of Texas System Indolinone derivatives as inhibitors of maternal embryonic leucine zipper kinase
CN110072849A (zh) * 2017-03-14 2019-07-30 新源生物科技股份有限公司 3-z-[1-(4-(n-((4-甲基-哌嗪-1-基)-甲羰基)-n-甲基-氨基)-苯氨基)-1-苯基-亚甲基]-6-甲氧羰基-2-吲哚满酮的晶型
TWI632133B (zh) * 2017-03-15 2018-08-11 新源生物科技股份有限公司 3-z-[1-(4-(n-((4-甲基-哌嗪-1-基)-甲羰基)-n-甲基-胺基)-苯胺基)-1-苯基-亞甲基]-6-甲氧羰基-2-吲哚啉酮的晶型
TWI676617B (zh) * 2017-03-15 2019-11-11 新源生物科技股份有限公司 3-z-[1-(4-(n-((4-甲基-呱嗪-1-基)-甲羰基)-n-甲基-胺基)-苯胺基)-1-苯基-亞甲基]-6-甲氧羰基-2-吲哚啉酮的晶型
JP2020512364A (ja) 2017-03-28 2020-04-23 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング 筋ジストロフィーの処置方法において使用するためのニンテダニブ
WO2019048974A1 (en) * 2017-09-06 2019-03-14 Glenmark Pharmaceuticals Limited PROCESS FOR PREPARING NINTEDANIB
EA202090977A1 (ru) 2017-10-23 2020-09-04 Бёрингер Ингельхайм Интернациональ Гмбх Новая комбинация активных агентов для лечения прогрессирующих фиброзирующих интерстициальных заболеваний легких (pf-ild)
WO2019097112A1 (en) 2017-11-17 2019-05-23 Fermion Oy Synthesis of a 2-indolinone derivative known as intermediate for preparing nintedanib
FI3761980T3 (fi) 2018-03-07 2024-02-21 Pliant Therapeutics Inc Aminohappoyhdisteitä ja käyttömenetelmiä
EP3806858A4 (en) 2018-06-15 2022-03-09 Handa Pharmaceuticals, Inc. SALTS OF KINASE INHIBITORS AND ASSOCIATED COMPOSITIONS
CN109988094B (zh) * 2019-04-29 2020-04-14 石药集团中奇制药技术(石家庄)有限公司 一种乙磺酸尼达尼布的制备方法
KR20220109439A (ko) 2019-12-04 2022-08-04 이도르시아 파마슈티컬스 리미티드 섬유증 질환의 치료에서 사용하기 위한 아제티딘 lpa1 수용체 길항제와 피르페니돈 및/또는 닌테다닙의 조합
WO2021198253A1 (en) 2020-04-01 2021-10-07 Boehringer Ingelheim International Gmbh Use of biomarkers in the treatment of fibrotic conditions
US11304947B2 (en) 2020-05-22 2022-04-19 Qx Therapeutics Inc. Compositions and methods for treating lung injuries associated with SARS-COV-2 infections
US20240051920A1 (en) * 2020-08-07 2024-02-15 Bdr Lifesciences Private Limited An improved highly efficient process for the preparation of nintedanib and pharmaceutically acceptable salt thereof
CN111848490B (zh) * 2020-08-24 2021-09-24 江西国药有限责任公司 一种高纯度乙磺酸尼达尼布的制备方法
CN113024439A (zh) * 2021-03-28 2021-06-25 郑州大学 尼达尼布乙磺酸盐新晶型ⅰ的制备
EP4098246A1 (en) 2021-05-31 2022-12-07 Lotus Pharmaceutical Co., Ltd. Formulation of nintedanib
WO2023161668A1 (en) 2022-02-28 2023-08-31 Nuformix Technologies Limited Compositions and methods for treatment of idiopathic pulmonary fibrosis
WO2024037982A1 (en) 2022-08-16 2024-02-22 Boehringer Ingelheim International Gmbh Pharmaceutical formulations of nintedanib for intraocular use
KR20240042322A (ko) 2022-09-23 2024-04-02 삼아제약 주식회사 티로신 키나제 저해제를 유효성분으로 하는 약제학적 조성물

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001027080A2 (de) * 1999-10-13 2001-04-19 Boehringer Ingelheim Pharma Kg In 5-stellung substituierte indolinone und ihre verwendung als kinase und cyclin-cdk-komplexe inhibitoren
WO2001027081A1 (de) * 1999-10-13 2001-04-19 Boehringer Ingelheim Pharma Kg In 6-stellung substituierte indolinone, ihre herstellung und ihre verwendung als arzneimittel
WO2002081445A1 (de) * 2001-04-06 2002-10-17 Boehringer Ingelheim Pharma Gmbh & Co. Kg In 6-stellung substituierte indoline und ihre verwendung als kinase-inhibitoren

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB395546A (en) 1931-10-12 1933-07-20 Robert Pauli Scherer Method of and apparatus for making capsules
US2720463A (en) 1950-11-17 1955-10-11 American Cyanamid Co Gelatin capsule casting composition preparation
US2870062A (en) 1956-04-27 1959-01-20 Scherer Corp R P Gelatin composition for capsules
DE3579384D1 (de) 1984-07-24 1990-10-04 Scherer Gmbh R P Oxytetracyclin-hc1-weichgelatinekapseln und verfahren zu ihrer herstellung.
GB9718913D0 (en) * 1997-09-05 1997-11-12 Glaxo Group Ltd Substituted oxindole derivatives
DE19816624A1 (de) * 1998-04-15 1999-10-21 Boehringer Ingelheim Pharma Neue substituierte Indolinone, ihre Herstellung und ihre Verwendung als Arzneimittel
CN1155596C (zh) * 1999-08-23 2004-06-30 索尔瓦药物有限公司 新的苯基哌嗪
US6762180B1 (en) * 1999-10-13 2004-07-13 Boehringer Ingelheim Pharma Kg Substituted indolines which inhibit receptor tyrosine kinases
DE10233500A1 (de) * 2002-07-24 2004-02-19 Boehringer Ingelheim Pharma Gmbh & Co. Kg 3-Z-[1-(4-(N-((4-Methyl-piperazin-1-yl)-methylcarbonyl)-N-methyl-amino)-anilino)-1-phenyl-methylen]-6-methoxycarbonyl-2-indolinon-Monoethansulfonat und dessen Verwendung als Arzneimittel

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001027080A2 (de) * 1999-10-13 2001-04-19 Boehringer Ingelheim Pharma Kg In 5-stellung substituierte indolinone und ihre verwendung als kinase und cyclin-cdk-komplexe inhibitoren
WO2001027081A1 (de) * 1999-10-13 2001-04-19 Boehringer Ingelheim Pharma Kg In 6-stellung substituierte indolinone, ihre herstellung und ihre verwendung als arzneimittel
WO2002081445A1 (de) * 2001-04-06 2002-10-17 Boehringer Ingelheim Pharma Gmbh & Co. Kg In 6-stellung substituierte indoline und ihre verwendung als kinase-inhibitoren

Also Published As

Publication number Publication date
ATE551322T1 (de) 2012-04-15
EG24562A (en) 2009-10-25
JP2005535684A (ja) 2005-11-24
TWI285635B (en) 2007-08-21
UY27904A1 (es) 2004-02-27
NZ538367A (en) 2008-01-31
MY136883A (en) 2008-11-28
AU2003254376B2 (en) 2010-06-17
AU2003254376A1 (en) 2004-02-23
US7119093B2 (en) 2006-10-10
EP1527047A1 (en) 2005-05-04
CA2493310C (en) 2011-01-18
BRPI0312811B8 (pt) 2021-05-25
ECSP055571A (es) 2005-04-18
CN1671660A (zh) 2005-09-21
AR094217A2 (es) 2015-07-15
WO2004013099A1 (en) 2004-02-12
CA2493310A1 (en) 2004-02-12
BR0312811A (pt) 2005-04-19
DE10233500A1 (de) 2004-02-19
KR20050042139A (ko) 2005-05-04
US20060258681A1 (en) 2006-11-16
PE20040704A1 (es) 2004-11-29
PL223758B1 (pl) 2016-10-31
EA008684B1 (ru) 2007-06-29
BRPI0312811B1 (pt) 2019-03-12
JP5039279B2 (ja) 2012-10-03
HRP20050070A2 (en) 2005-12-31
SI1527047T1 (sl) 2012-07-31
PL372996A1 (en) 2005-08-08
MEP53708A (hr) 2011-05-10
DK1527047T3 (da) 2012-07-16
TW200409754A (en) 2004-06-16
EP2386543A1 (en) 2011-11-16
RS52283B (sr) 2012-10-31
NO330486B1 (no) 2011-04-26
RS20050046A (en) 2007-09-21
US20040176392A1 (en) 2004-09-09
CY1112916T1 (el) 2016-04-13
BRPI0312811A8 (pt) 2019-01-02
HK1078851A1 (en) 2006-03-24
IL166405A (en) 2009-11-18
EP1527047B1 (en) 2012-03-28
KR101145691B1 (ko) 2012-05-25
IL166405A0 (en) 2006-01-15
SA03240446B1 (ar) 2007-07-31
EA200500146A1 (ru) 2005-08-25
MXPA04012785A (es) 2005-06-08
AR040662A1 (es) 2005-04-13
PT1527047E (pt) 2012-06-28
UA78352C2 (uk) 2007-03-15
ES2384968T3 (es) 2012-07-16
CN100351235C (zh) 2007-11-28
ME00353B (me) 2011-10-10
ZA200409814B (en) 2006-02-22
NO20050985L (no) 2005-02-23

Similar Documents

Publication Publication Date Title
HRP20050070B1 (hr) 3-2-[1-(4-(n-((4-metil-piperazin-1-il)-metilkarbonil)-n-metil-amino)-anilino)-1-fenil-metilen]-6-metoksikarbonil-2-indolinon-monoetansulfonat i njegova primjena kao farmaceutskog pripravka
NO20070224L (no) 2-karbamid-4-fenyltiazolderivater, fremstilling og terapeutisk anvendelse derav
EE200300459A (et) Uued spirotritsüklilised derivaadid ja nende kasutamine fosfodiesteraas-7 inhibiitoritena
SE0101387D0 (sv) Novel compounds
ATE327977T1 (de) Tetrahydrochinolin-derivate als crth2 antagonisten
PE20130239A1 (es) Compuestos heteroaril-aril-ureas como inhibidores de la quinasa
MXPA05005223A (es) Diaminotriazoles utiles como inhibidores de proteinas cinasas.
MY139522A (en) New alkyl-pyridines as 11-beta inhibitors for diabetes
ATE469136T1 (de) Inhibitoren von 11-beta- hydroxysteroiddehydrogenase typ 1
AU2002344951A1 (en) Substituted piperazine and diazepanes as histamine h3 receptor agonists
SE0202463D0 (sv) Novel compounds
CY1106969T1 (el) Αναστολεις dpp-iv
NO20054848L (no) Substituerte p-diaminobenzenderivater
EA200501268A1 (ru) Ингибирующие вич 1,2,4-триазины
WO2006047415A3 (en) FACTOR Xa COMPOUNDS
BR0316609A (pt) Sinomenina e compostos de sinomenina, sìntese e uso
ATE442846T1 (de) Piperidin- und pyrrolidin-derivate alsantagonisten des histamin-h3-rezeptors
BRPI0417858A (pt) composto, composição farmacêutica, e, uso de uma composição farmacêutica
SE0403171D0 (sv) New compounds
UY27852A1 (es) Difenilazatidinonas cationicamente sustituidas, procedimiento para su preparacion, medicamentos que comprenden estos compuestos y su uso.
DE60219911D1 (de) Pyrrolidin-2-on derivate als faktor xa inhibitoren
UA92195C2 (ru) Оптически активные карбаматы, способ их получения и их применение в качестве фармацевтических промежуточных соединений
RS51858B (en) 4 - [(3-FLUOROPHENOXY) PHENYLMETHYL] PIPERIDINE METANSULPHONATE: ITS USES, PROCESSING METHODS AND PHARMACEUTICAL COMPOSITIONS
MY136859A (en) Pyrrolidine derivatives as factor xa inhibitors
MY144101A (en) Pyrrolidine-3,4-dicarboxamide derivatives

Legal Events

Date Code Title Description
A1OB Publication of a patent application
ARAI Request for the grant of a patent on the basis of the submitted results of a substantive examination of a patent application
B1PR Patent granted
ODRP Renewal fee for the maintenance of a patent

Payment date: 20190715

Year of fee payment: 17

ODRP Renewal fee for the maintenance of a patent

Payment date: 20200713

Year of fee payment: 18

ODRP Renewal fee for the maintenance of a patent

Payment date: 20210713

Year of fee payment: 19

ODRP Renewal fee for the maintenance of a patent

Payment date: 20220713

Year of fee payment: 20

PB20 Patent expired after termination of 20 years

Effective date: 20230718