[go: up one dir, main page]

PE20141317A1 - Nuevas formas polimorficas de sal de clorhidrato de 3-(1-{3-[5-(1-metil-piperidin-4-ilmetoxi)-pirimidin-2-il]-bencil}-6-oxo-1,6-dihidro-piridazin-3-il)-benzonitrilo y sus procesos de preparacion - Google Patents

Nuevas formas polimorficas de sal de clorhidrato de 3-(1-{3-[5-(1-metil-piperidin-4-ilmetoxi)-pirimidin-2-il]-bencil}-6-oxo-1,6-dihidro-piridazin-3-il)-benzonitrilo y sus procesos de preparacion

Info

Publication number
PE20141317A1
PE20141317A1 PE2013002901A PE2013002901A PE20141317A1 PE 20141317 A1 PE20141317 A1 PE 20141317A1 PE 2013002901 A PE2013002901 A PE 2013002901A PE 2013002901 A PE2013002901 A PE 2013002901A PE 20141317 A1 PE20141317 A1 PE 20141317A1
Authority
PE
Peru
Prior art keywords
ilmetoxy
pyridazin
benzonitrile
pyrimidin
piperidin
Prior art date
Application number
PE2013002901A
Other languages
English (en)
Inventor
Axel Becker
Clemens Kuehn
Christoph Saal
Oliver Schadt
Dieter Dorsch
Heinz-Hermann Bokel
Frank Stieber
Christina Donini
Original Assignee
Merck Patent Gmbh
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=41572530&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PE20141317(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Merck Patent Gmbh filed Critical Merck Patent Gmbh
Publication of PE20141317A1 publication Critical patent/PE20141317A1/es

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/18—Drugs for disorders of the alimentary tract or the digestive system for pancreatic disorders, e.g. pancreatic enzymes
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/08—Drugs for disorders of the urinary system of the prostate
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/10—Drugs for disorders of the urinary system of the bladder
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/12—Drugs for disorders of the urinary system of the kidneys
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00—Drugs for genital or sexual disorders; Contraceptives
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P21/00—Drugs for disorders of the muscular or neuromuscular system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00—Drugs for disorders of the senses
    • A61P27/02—Ophthalmic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • A—HUMAN NECESSITIES
    • 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
    • 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
    • C07D401/14—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 three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Epidemiology (AREA)
  • Urology & Nephrology (AREA)
  • Neurology (AREA)
  • Endocrinology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Neurosurgery (AREA)
  • Ophthalmology & Optometry (AREA)
  • Oncology (AREA)
  • Pulmonology (AREA)
  • Biomedical Technology (AREA)
  • Hematology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Dermatology (AREA)
  • Reproductive Health (AREA)
  • Diabetes (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

SE REFIERE A FORMAS CRISTALINAS DEL CLORHIDRATO DE 3-(1-{3-[5-(1-METIL-PIPERIDIN-4-ILMETOXI)-PIRIMIDIN-2-IL]-BENCIL}-6-OXO-1,6-DIHIDRO-PIRIDAZIN-3-IL)-BENZONITRILO TALES COMO: A) LA FORMA H1 CUYOS PICOS XRD USANDO RADIACION Cu-Ka1 EXPRESADOS EN GRADOS 2 THETA +/- 0,1� SON 5.9, 8.8, 11.3, 12.2, 14.5, 15.2, 16.0, ENTRE OTROS; B) LA FORMA NF3 CUYOS PICOS XRD USANDO RADIACION Cu-Ka1 EXPRESADOS EN GRADOS 2 THETA +/- 0,1� SON 6.0, 9.9, 12.8, 15.7, 16.3, 16.9, 20.3, ENTRE OTROS; Y C) LA FORMA H2 CUYOS PICOS XRD USANDO RADIACION Cu-Ka1 EXPRESADOS EN GRADOS 2 THETA +/- 0,1� SON 10.1, 10.8, 11.6, 13.0, 13.5, 15.4, 17.8, ENTRE OTROS. TAMBIEN SE REFIERE A UN PROCESO DE PREPARACION Y A UNA COMPOSICION FARMACEUTICA. DICHAS FORMAS CRISTALINAS SON UTILES EN EL TRATAMIENTO DE CANCER
PE2013002901A 2009-01-08 2009-12-04 Nuevas formas polimorficas de sal de clorhidrato de 3-(1-{3-[5-(1-metil-piperidin-4-ilmetoxi)-pirimidin-2-il]-bencil}-6-oxo-1,6-dihidro-piridazin-3-il)-benzonitrilo y sus procesos de preparacion PE20141317A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP09000140 2009-01-08

Publications (1)

Publication Number Publication Date
PE20141317A1 true PE20141317A1 (es) 2014-09-26

Family

ID=41572530

Family Applications (2)

Application Number Title Priority Date Filing Date
PE2013002901A PE20141317A1 (es) 2009-01-08 2009-12-04 Nuevas formas polimorficas de sal de clorhidrato de 3-(1-{3-[5-(1-metil-piperidin-4-ilmetoxi)-pirimidin-2-il]-bencil}-6-oxo-1,6-dihidro-piridazin-3-il)-benzonitrilo y sus procesos de preparacion
PE2011001297A PE20120474A1 (es) 2009-01-08 2009-12-04 Nuevas formas polimorficas de sal de clorhidrato de 3-(1-{3-[5-(1-metil-piperidin-4-ilmetoxi)-pirimidin-2-il]-bencil}-6-oxo-1,6-dihidro-piridazin-3-il)-benzonitrilo y sus procesos de preparacion

Family Applications After (1)

Application Number Title Priority Date Filing Date
PE2011001297A PE20120474A1 (es) 2009-01-08 2009-12-04 Nuevas formas polimorficas de sal de clorhidrato de 3-(1-{3-[5-(1-metil-piperidin-4-ilmetoxi)-pirimidin-2-il]-bencil}-6-oxo-1,6-dihidro-piridazin-3-il)-benzonitrilo y sus procesos de preparacion

Country Status (31)

Country Link
US (3) US8710058B2 (es)
EP (1) EP2373640B1 (es)
JP (2) JP5719781B2 (es)
KR (2) KR101730791B1 (es)
CN (1) CN102272121B (es)
AR (1) AR074996A1 (es)
AU (1) AU2009336839B2 (es)
BR (1) BRPI0922642B8 (es)
CA (4) CA3014648C (es)
CL (1) CL2011001356A1 (es)
CO (1) CO6400191A2 (es)
CY (1) CY1115631T1 (es)
DK (1) DK2373640T3 (es)
EA (1) EA019342B1 (es)
EC (1) ECSP11011248A (es)
ES (1) ES2522629T3 (es)
HR (1) HRP20140908T1 (es)
IL (1) IL213829A0 (es)
MX (3) MX350894B (es)
MY (1) MY160017A (es)
NZ (1) NZ594404A (es)
PE (2) PE20141317A1 (es)
PL (1) PL2373640T3 (es)
PT (1) PT2373640E (es)
SG (2) SG10201504735QA (es)
SI (1) SI2373640T1 (es)
SM (1) SMT201400161B (es)
TW (1) TWI475997B (es)
UA (1) UA106220C2 (es)
WO (1) WO2010078897A1 (es)
ZA (1) ZA201105782B (es)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PE20141317A1 (es) 2009-01-08 2014-09-26 Merck Patent Gmbh Nuevas formas polimorficas de sal de clorhidrato de 3-(1-{3-[5-(1-metil-piperidin-4-ilmetoxi)-pirimidin-2-il]-bencil}-6-oxo-1,6-dihidro-piridazin-3-il)-benzonitrilo y sus procesos de preparacion
CN104203243A (zh) * 2012-03-19 2014-12-10 默克专利股份公司 具有抗肿瘤活性的6-氧代-1,6-二氢-哒嗪衍生物与其他抗肿瘤化合物的组合
RS56485B1 (sr) * 2012-11-02 2018-01-31 Merck Patent Gmbh 6-okso-1,6-dihidro-piridazin derivat za upotrebu u tretmanu hepatocelularnog karcinoma (hcc)
KR20160099724A (ko) * 2014-01-07 2016-08-22 메르크 파텐트 게엠베하 신장 세포 암종 (rcc) 치료를 위해 사용되는 6-옥소-1,6-디히드로-피리다진 유도체
US10532052B2 (en) 2014-12-12 2020-01-14 Merck Patent Gmbh Combination of a 6-oxo-1,6-dihydro-pyridazine derivative having anti-cancer activity with an EGFR inhibitor
ES2922637T3 (es) * 2015-04-03 2022-09-19 Impact Therapeutics Shanghai Inc Forma de dosificación farmacéutica sólida de inhibidor de PARP y aplicación de forma de dosificación farmacéutica sólida de inhibidor de PARP
WO2016192831A1 (en) 2015-05-29 2016-12-08 Merck Patent Gmbh Compositions of anions and cations with pharmacological activity
KR20180092096A (ko) 2017-02-08 2018-08-17 에이비온 주식회사 트리아졸로 피라진 유도체의 신규한 다형체 및 이의 제조 방법
EP3786155B1 (en) * 2018-04-26 2023-08-16 Fujian Akeylink Biotechnology Co., Ltd. Crystal form of c-met inhibitor and salt form thereof and preparation method therefor
PL3996688T3 (pl) * 2019-07-10 2024-02-12 Merck Patent Gmbh Preparat farmaceutyczny
EP4083040A4 (en) 2020-01-21 2024-04-24 Chia Tai Tianqing Pharmaceutical Group Co., Ltd. IRAQ4 INHIBITOR CRYSTAL AND PREPARATION METHOD THEREFOR
WO2022063869A2 (en) 2020-09-24 2022-03-31 Merck Patent Gmbh Compounds for the treatment of viral infections
KR102489160B1 (ko) 2021-05-26 2023-01-18 주식회사 이노큐어테라퓨틱스 피페리딘디온 유도체
WO2022250350A1 (ko) 2021-05-26 2022-12-01 주식회사 이노큐어테라퓨틱스 피페리딘디온 유도체
IL309014A (en) 2021-06-04 2024-01-01 Merck Patent Gmbh Compounds for the treatment of glioblastoma
CN114394957B (zh) * 2021-12-24 2023-05-09 武汉九州钰民医药科技有限公司 Met抑制剂盐酸特泊替尼的制备方法
KR20230155324A (ko) 2022-05-03 2023-11-10 주식회사 이노큐어테라퓨틱스 피페리딘디온 유도체
CN116768868B (zh) * 2023-08-15 2023-12-08 云南省药物研究所 一种哒嗪酮硫代衍生物及其制备方法和应用

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7094909B2 (en) * 2001-06-11 2006-08-22 Agouron Pharmaceuticals, Inc. HIV protease inhibitors, compositions containing the same, their pharmaceutical uses and materials for their synthesis
US7169932B2 (en) * 2001-06-11 2007-01-30 Pfizer Inc. HIV protease inhibitors, compositions containing the same, their pharmaceutical uses, material for their synthesis
ATE554771T1 (de) * 2003-08-19 2012-05-15 Pharmaton Sa Multivitaminsirup für kinder und junge erwachsene
WO2005026114A1 (en) * 2003-09-17 2005-03-24 Pfizer Inc. Hiv protease inhibitors, compositions containing the same and their pharmaceutical uses
TW200616634A (en) * 2004-10-01 2006-06-01 Bristol Myers Squibb Co Crystalline forms and process for preparing spiro-hydantoin compounds
US20070249637A1 (en) * 2004-10-21 2007-10-25 Collins Michael R Inhibitors Of Hepatitis C Virus Protease, And Compositions And Treatments Using The Same
WO2006048744A1 (en) * 2004-11-02 2006-05-11 Pfizer Inc. Methods of preparing indazole compounds
CN101052633A (zh) * 2004-11-02 2007-10-10 辉瑞大药厂 制备吲唑化合物的方法
DE102005057924A1 (de) * 2005-12-05 2007-06-06 Merck Patent Gmbh Pyridazinonderivate
CL2007001166A1 (es) * 2006-04-26 2008-01-25 Piramed Ltd Compuestos derivados de pirimidina condensada, inhibidores de pi3-quinasa; procesos para preparar los compuestos; composicion farmaceutica que los comprende; uso de los compuestos en la preparacion de medicamentos; proceso para preparar la composicion farmaceutica; y kit que incluye a la composicion farmaceutica
US7820812B2 (en) * 2006-07-25 2010-10-26 Abbott Laboratories Methods of manufacturing crystalline forms of rapamycin analogs
US7812032B2 (en) * 2006-07-25 2010-10-12 Abbott Laboratories Crystalline forms of rapamycin analogs
DE102007032507A1 (de) * 2007-07-12 2009-04-02 Merck Patent Gmbh Pyridazinonderivate
PE20141317A1 (es) * 2009-01-08 2014-09-26 Merck Patent Gmbh Nuevas formas polimorficas de sal de clorhidrato de 3-(1-{3-[5-(1-metil-piperidin-4-ilmetoxi)-pirimidin-2-il]-bencil}-6-oxo-1,6-dihidro-piridazin-3-il)-benzonitrilo y sus procesos de preparacion

Also Published As

Publication number Publication date
PT2373640E (pt) 2014-09-30
EA019342B1 (ru) 2014-02-28
EA201101039A1 (ru) 2012-02-28
SMT201400161B (it) 2015-01-15
EP2373640A1 (en) 2011-10-12
CN102272121B (zh) 2014-12-10
US20140200221A1 (en) 2014-07-17
UA106220C2 (ru) 2014-08-11
JP2012514609A (ja) 2012-06-28
BRPI0922642B8 (pt) 2021-05-25
CA3014648A1 (en) 2010-07-15
CA2749012C (en) 2017-01-31
HK1164856A1 (en) 2012-09-28
CA2949515C (en) 2018-10-23
MX2011007322A (es) 2011-07-29
US20110269767A1 (en) 2011-11-03
TWI475997B (zh) 2015-03-11
CO6400191A2 (es) 2012-03-15
HRP20140908T1 (hr) 2014-11-07
DK2373640T3 (da) 2014-10-06
CN102272121A (zh) 2011-12-07
NZ594404A (en) 2013-04-26
TW201029655A (en) 2010-08-16
CA2749012A1 (en) 2010-07-15
PE20120474A1 (es) 2012-05-04
ES2522629T3 (es) 2014-11-17
SG10201504735QA (en) 2015-07-30
EP2373640B1 (en) 2014-07-30
KR101829595B1 (ko) 2018-02-14
ECSP11011248A (es) 2011-10-31
ZA201105782B (en) 2012-04-25
CA3014648C (en) 2021-06-01
JP2015038148A (ja) 2015-02-26
PL2373640T3 (pl) 2014-12-31
AR074996A1 (es) 2011-03-02
CA3097370A1 (en) 2010-07-15
BRPI0922642B1 (pt) 2020-09-29
BRPI0922642A2 (pt) 2016-01-05
AU2009336839A1 (en) 2011-08-25
AU2009336839A8 (en) 2011-09-08
MX363852B (es) 2019-04-05
IL213829A0 (en) 2011-07-31
US9308205B2 (en) 2016-04-12
SG172831A1 (en) 2011-08-29
AU2009336839B2 (en) 2015-12-24
KR20110111472A (ko) 2011-10-11
MX363848B (es) 2019-04-05
MX350894B (es) 2017-09-22
WO2010078897A1 (en) 2010-07-15
US9289427B2 (en) 2016-03-22
MY160017A (en) 2017-02-15
US20150148351A1 (en) 2015-05-28
KR20170047408A (ko) 2017-05-04
CY1115631T1 (el) 2017-01-04
JP5860126B2 (ja) 2016-02-16
US8710058B2 (en) 2014-04-29
SI2373640T1 (sl) 2014-11-28
KR101730791B1 (ko) 2017-04-27
CL2011001356A1 (es) 2011-09-30
JP5719781B2 (ja) 2015-05-20
CA2949515A1 (en) 2010-07-15

Similar Documents

Publication Publication Date Title
PE20141317A1 (es) Nuevas formas polimorficas de sal de clorhidrato de 3-(1-{3-[5-(1-metil-piperidin-4-ilmetoxi)-pirimidin-2-il]-bencil}-6-oxo-1,6-dihidro-piridazin-3-il)-benzonitrilo y sus procesos de preparacion
CL2008000690A1 (es) Compuestos derivados del acido indol-3-propionico; composicion farmaceutica; y uso en el tratamiento de enfermedades tales como hiperlipidemia, hipertension; entre otras.
AR111202A2 (es) Formas cristalinas de cortexolona
CL2013000850A1 (es) Formas cristalinas de 5-(2,6-di-4-morfolinil-4-pirimidinil)-4-trifluoro-metil-piridin-2-amina y de la sal monoclorhidrato composicion farmaceutica; y su uso para el tratamiento de una enfermedad proliferativa como carcionoma de cerebro, de colon, leucemia, mieloma multiple, carcionoma mamario, entre otros.
CL2015002145A1 (es) Preparación, usos y formas sólidas de ácido obeticólico (divisional de solicitud n° 3475-2014)
IL211312A0 (en) Treatment of stroke using isolated placental cells
CL2015001731A1 (es) Compuestos inhibidores de autotaxina; composicion y combinacion farmaceutica; y uso en el tratamiento de enfermedades tales como fibrosis, prurito, cancer, entre otras.
UY32633A (es) Anticuerpos humanizados específicos de la forma protofibrilar del péptido beta-amiloide
CL2008000790A1 (es) Compuestos derivados de purina sustituida; metodo de sintesis; composicion farmaceutica; y uso en el tratamiento de enfermedades tales como aterosclerosis, artritis, psoriasis y cancer.
PE20141792A1 (es) Formas polimorficas de (s)-2-(1-(9h-purin-6-ilamino)propil)-5-fluor-3-fenilquinazolin-4(3h)-ona
EP2459233A4 (en) STROMAL ADIPOSE TISSUE (ASC) CELLS AS ADMINISTRATION DEVICES IN THE TREATMENT OF CANCER
HUE047996T2 (hu) AAV variáns és készítmények, eljárások és alkalmazások sejtekbe, szervekbe és szövetekbe történõ géntranszferhez
TN2012000161A1 (en) Spiro-oxindole mdm2 antagonists
WO2010101964A3 (en) Methods and compositions useful in treating cancer and reducing wnt mediated effects in a cell
CL2009000990A1 (es) Uso de epotilona d para el tratamiento de enfermedades asociadas a tau, tal como enfermedad alzheimer, parkinson, entre otras.
CL2015000916A1 (es) Formas cristalinas del acido (s,e)-4-(2-(3-(3-cloro-2-fluoro-6-(1h-tetrazol-1-il)fenil)acriloil)-5-(4-metil-2-oxopiperazin-1-il)-1,2,3,4-tetrahidroisoquinolin-1-carboxamida)benzoico; proceso de preparacion; composicion farmaceutica; uso en el tratamiento de trastornos tromboembolicos tales como angina , infarto al miocardio, apoplejia, tromboflebitis, entre otros.
FI20100121A0 (fi) Menetelmä nikkelipitoisen raaka-aineen käsittelemiseksi
CL2008001257A1 (es) Compuestos triciclicos, inhibidores de metaloproteinasas matriciales; composicion farmaceutica; y uso en el tratamiento de enfermedades tales como artritis reumatoide, osteoartritis, aterosclerosis, cancer de pulmon, entre otras.
CR20110625A (es) Compuestos biciclicos y triciclicos como inhibidores de kat ii
EP2736437A4 (en) METHOD AND COMPOSITION FOR HYPERTHERMAL TREATMENT OF CELLS
PE20151062A1 (es) PIRIMIDO-[4,5-b]-QUINOLINA-4,5(3H,10H)-DIONAS COMO SUPRESORAS DE MUTACION SIN SENTIDO
WO2012015999A3 (en) Process for the preparation of imatinib mesylate
CL2013000756A1 (es) Forma cristalaina del citrato diacido de (4s)-4-(5-fenil-1,3,4-tiadiazol-2-iloxi)-1-azatriciclo[3.3.1.13,7]decano; proceso de preparacion; composicion farmaceutica; y su uso para tratar o prevenir un trastorno de la memoria, un trastorno cognitivo, neurodegeneracion, entre otros.
IL208951A0 (en) Process for the preparation of 5-(2-amino-pyrimidin-4-yl)-2-aryl-1h-pyrrole-3-carboxamides
CR9613S (es) Contenedor

Legal Events

Date Code Title Description
FC Refusal