WO2000027819A2 - Anthranilsäureamide und deren verwendung als arzneimittel - Google Patents

Anthranilsäureamide und deren verwendung als arzneimittel Download PDF

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Publication number
WO2000027819A2
WO2000027819A2 PCT/EP1999/008478 EP9908478W WO0027819A2 WO 2000027819 A2 WO2000027819 A2 WO 2000027819A2 EP 9908478 W EP9908478 W EP 9908478W WO 0027819 A2 WO0027819 A2 WO 0027819A2
Authority
WO
WIPO (PCT)
Prior art keywords
group
stands
hydrogen
halogen
methyl
Prior art date
Application number
PCT/EP1999/008478
Other languages
German (de)
English (en)
French (fr)
Other versions
WO2000027819A3 (de
Inventor
Andreas Huth
Dieter Seidelmann
Karl-Heinz Thierauch
Guido Bold
Paul William Manley
Pascal Furet
Jeanette Marjorie Wood
Jürgen Mestan
Jose Brüggen
Stefano Ferrari
Martin Krüger
Eckhard Ottow
Andreas Menrad
Michael Schirner
Original Assignee
Schering Aktiengesellschaft
Novartis Aktiengesellschaft
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
Priority claimed from GBGB9824579.8A external-priority patent/GB9824579D0/en
Priority claimed from DE1999110396 external-priority patent/DE19910396C2/de
Priority to UA2001063917A priority Critical patent/UA71587C2/uk
Priority to CA002350208A priority patent/CA2350208A1/en
Priority to SK607-2001A priority patent/SK6072001A3/sk
Priority to NZ511413A priority patent/NZ511413A/en
Priority to HU0104425A priority patent/HUP0104425A3/hu
Priority to EA200100524A priority patent/EA004701B1/ru
Priority to AU10454/00A priority patent/AU771180B2/en
Priority to EP99953967A priority patent/EP1129074A2/de
Application filed by Schering Aktiengesellschaft, Novartis Aktiengesellschaft filed Critical Schering Aktiengesellschaft
Priority to EEP200100258A priority patent/EE200100258A/xx
Priority to JP2000580999A priority patent/JP2002529452A/ja
Priority to US09/831,506 priority patent/US7122547B1/en
Priority to PL99348349A priority patent/PL348349A1/xx
Priority to BR9915553-2A priority patent/BR9915553A/pt
Publication of WO2000027819A2 publication Critical patent/WO2000027819A2/de
Publication of WO2000027819A3 publication Critical patent/WO2000027819A3/de
Priority to NO20012245A priority patent/NO320647B1/no
Priority to HK02103628A priority patent/HK1041882A1/xx

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C237/00Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
    • C07C237/28Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton
    • C07C237/32Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton having the nitrogen atom of the carboxamide group bound to an acyclic carbon atom of a hydrocarbon radical substituted by oxygen atoms
    • 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
    • C07D401/14Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/12Drugs for disorders of the urinary system of the kidneys
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/06Antipsoriatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • A61P27/06Antiglaucoma agents or miotics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • 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
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/14Vasoprotectives; Antihaemorrhoidals; Drugs for varicose therapy; Capillary stabilisers
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/36Radicals substituted by singly-bound nitrogen atoms
    • C07D213/38Radicals substituted by singly-bound nitrogen atoms having only hydrogen or hydrocarbon radicals attached to the substituent nitrogen atom
    • 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
    • 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
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/12Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Ophthalmology & Optometry (AREA)
  • Diabetes (AREA)
  • Urology & Nephrology (AREA)
  • Dermatology (AREA)
  • Cardiology (AREA)
  • Vascular Medicine (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Rheumatology (AREA)
  • Epidemiology (AREA)
  • Obesity (AREA)
  • Endocrinology (AREA)
  • Immunology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Emergency Medicine (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Hematology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Indole Compounds (AREA)
  • Pyridine Compounds (AREA)
PCT/EP1999/008478 1998-11-10 1999-11-09 Anthranilsäureamide und deren verwendung als arzneimittel WO2000027819A2 (de)

Priority Applications (15)

Application Number Priority Date Filing Date Title
UA2001063917A UA71587C2 (uk) 1998-11-10 1999-09-11 Аміди антранілової кислоти та їхнє застосування як лікарських засобів
PL99348349A PL348349A1 (en) 1998-11-10 1999-11-09 Antrhranilic acid amides and the use thereof as medicaments
BR9915553-2A BR9915553A (pt) 1998-11-10 1999-11-09 Amidas de ácido antranìlico e seu emprego como medicamento
JP2000580999A JP2002529452A (ja) 1998-11-10 1999-11-09 アントラニル酸アミド及び医薬剤としてのその使用
NZ511413A NZ511413A (en) 1998-11-10 1999-11-09 Antrhranilic acid amides and the use thereof as medicaments
HU0104425A HUP0104425A3 (en) 1998-11-10 1999-11-09 Anthranilic acid amides and the use thereof for the treatment of angiogenesis
EA200100524A EA004701B1 (ru) 1998-11-10 1999-11-09 Амиды антраниловой кислоты и их применение в качестве лекарственных средств
AU10454/00A AU771180B2 (en) 1998-11-10 1999-11-09 Antrhranilic acid amides and the use thereof as medicaments
EP99953967A EP1129074A2 (de) 1998-11-10 1999-11-09 Anthranilsäureamide und deren verwendung als arzneimittel
CA002350208A CA2350208A1 (en) 1998-11-10 1999-11-09 Antrhranilic acid amides and the use thereof as medicaments
EEP200100258A EE200100258A (et) 1998-11-10 1999-11-09 Antraniilhappe amiidid ja nende kasutamine ravimitena
SK607-2001A SK6072001A3 (en) 1998-11-10 1999-11-09 Anthranilic acid amides and the use thereof as medicaments
US09/831,506 US7122547B1 (en) 1998-11-10 1999-11-09 Anthranilic acid amides and the use thereof as medicaments
NO20012245A NO320647B1 (no) 1998-11-10 2001-05-07 Anthranilsyreamider og anvendelse derav for fremstilling av medikamenter
HK02103628A HK1041882A1 (en) 1998-11-10 2002-05-14 Anthranilic acid amides and their use in manufacturing pharmaceutical agents.

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
GBGB9824579.8A GB9824579D0 (en) 1998-11-10 1998-11-10 Organic compounds
GB9824579.8 1998-11-10
DE19910396.8 1999-03-03
DE1999110396 DE19910396C2 (de) 1999-03-03 1999-03-03 Anthranilsäureamide und deren Verwendung als Arzneimittel

Publications (2)

Publication Number Publication Date
WO2000027819A2 true WO2000027819A2 (de) 2000-05-18
WO2000027819A3 WO2000027819A3 (de) 2000-08-17

Family

ID=26052266

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP1999/008478 WO2000027819A2 (de) 1998-11-10 1999-11-09 Anthranilsäureamide und deren verwendung als arzneimittel

Country Status (23)

Country Link
US (1) US7122547B1 (US07122547-20061017-C00064.png)
EP (1) EP1129074A2 (US07122547-20061017-C00064.png)
JP (1) JP2002529452A (US07122547-20061017-C00064.png)
KR (2) KR100777476B1 (US07122547-20061017-C00064.png)
CN (1) CN1151133C (US07122547-20061017-C00064.png)
AU (1) AU771180B2 (US07122547-20061017-C00064.png)
BG (1) BG65371B1 (US07122547-20061017-C00064.png)
BR (1) BR9915553A (US07122547-20061017-C00064.png)
CA (1) CA2350208A1 (US07122547-20061017-C00064.png)
CZ (1) CZ20011631A3 (US07122547-20061017-C00064.png)
EA (1) EA004701B1 (US07122547-20061017-C00064.png)
EE (1) EE200100258A (US07122547-20061017-C00064.png)
HK (1) HK1041882A1 (US07122547-20061017-C00064.png)
HR (1) HRP20010402A2 (US07122547-20061017-C00064.png)
HU (1) HUP0104425A3 (US07122547-20061017-C00064.png)
NO (1) NO320647B1 (US07122547-20061017-C00064.png)
NZ (1) NZ511413A (US07122547-20061017-C00064.png)
PL (1) PL348349A1 (US07122547-20061017-C00064.png)
SK (1) SK6072001A3 (US07122547-20061017-C00064.png)
TR (1) TR200101307T2 (US07122547-20061017-C00064.png)
UA (1) UA71587C2 (US07122547-20061017-C00064.png)
WO (1) WO2000027819A2 (US07122547-20061017-C00064.png)
YU (1) YU31801A (US07122547-20061017-C00064.png)

Cited By (131)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001085719A1 (de) * 2000-05-09 2001-11-15 Schering Aktiengesellschaft Ortho substituierte anthranilsäureamide und deren verwendung als arzneimittel
WO2001085671A2 (de) * 2000-05-09 2001-11-15 Schering Aktiengesellschaft Anthranylamide und deren verwendung als arzneimittel
WO2001097786A2 (en) * 2000-06-21 2001-12-27 F. Hoffmann-La Roche Ag Benzothiazole derivatives
WO2002046181A2 (en) * 2000-12-07 2002-06-13 Cv Therapeutics, Inc. Abca-1 elevating compounds against coronary artery disease or atherosclerosis
WO2002066470A1 (en) * 2001-01-12 2002-08-29 Amgen Inc. Substituted alkylamine derivatives and methods of use
WO2002090352A2 (de) * 2001-05-08 2002-11-14 Schering Aktiengesellschaft Selektive anthranylamidpyridinamide als vegfr-2 und vegfr-3 inhibitoren
WO2002090349A1 (de) * 2001-05-08 2002-11-14 Schering Aktiengesellschaft N-oxidanthranylamid-derivate und deren verwendung als arzneimittel
DE10123587A1 (de) * 2001-05-08 2002-11-21 Schering Ag Cyanoanthranylamid-Derivate und deren Verwendung als Arzneimittel
DE10123573A1 (de) * 2001-05-08 2002-11-28 Schering Ag N-Oxidanthranylamid-Derivate und deren Verwendung als Arzneimittel
WO2002100833A1 (fr) * 2001-06-12 2002-12-19 Sumitomo Pharmaceuticals Company, Limited Inhibiteurs de rho kinase
WO2002055501A3 (en) * 2001-01-12 2002-12-19 Amgen Inc. N-pyridyl carboxamide derivatives and pharmaceutical compositions containing them
WO2003000678A1 (de) * 2001-05-08 2003-01-03 Schering Aktiengesellschaft Cyanoanthranylamid-derivate und deren verwendung als arzneimittel
WO2002068406A3 (en) * 2001-01-12 2003-04-24 Amgen Inc Substituted amine derivatives and their use for the treatment of angiogenesis
WO2004005279A2 (en) * 2002-07-09 2004-01-15 Amgen Inc. Substituted anthranilic amide derivatives and methods of use
WO2004007481A2 (en) * 2002-07-17 2004-01-22 Amgen Inc. Substituted amine derivatives and methods of use in the treatment of angiogenesis relates disorders
WO2004007458A1 (en) 2002-07-17 2004-01-22 Amgen Inc. Substituted 2-alkylamine nicotinic amide derivatives and use there of
EP1388341A1 (en) * 2002-08-07 2004-02-11 Aventis Pharma Deutschland GmbH Acylamino-substituted heteroaromatic compounds and their use as pharmaceuticals
DE10235690A1 (de) * 2002-07-31 2004-02-19 Schering Ag VEGFR-2 und VEGFR-3 inhibitorische Anthranylamidpyridinamide
WO2004050610A2 (en) * 2002-12-04 2004-06-17 Gene Logic Inc. Modulators of melanocortin receptor
WO2004063330A2 (en) 2003-01-06 2004-07-29 Osi Pharmaceuticals, Inc. (2-carboxamido) (3-amino) thiophene compounds
WO2004072069A1 (en) * 2003-02-14 2004-08-26 Glaxo Group Limited Carboxamide derivatives
WO2004078723A1 (ja) 2003-03-07 2004-09-16 Santen Pharmaceutical Co. Ltd. 4-ピリジルアルキルチオ基を置換基として有する新規化合物
US6818661B2 (en) * 2000-05-09 2004-11-16 Novartis Ag Anthranylalkyl and cycloalkyl amides and use thereof as VEGF receptor inhibitors
WO2004103306A2 (en) 2003-05-19 2004-12-02 Irm Llc Immunosuppressant compounds and compositions
WO2004108133A2 (en) * 2003-06-05 2004-12-16 Vertex Pharmaceuticals Incorporated Modulators of vr1 receptor
WO2004111005A1 (de) * 2003-06-13 2004-12-23 Schering Aktiengesellschaft Vegfr-2 und vegfr-3 inhibitorische anthranylamidpyridone
WO2005000833A1 (en) 2003-05-19 2005-01-06 Irm, Llc Immunosuppressant compounds and compositions
WO2005004864A1 (en) * 2003-07-11 2005-01-20 Merck Patent Gmbh Benzimidazole derivatives as raf kinase inhibitors
WO2004069792A3 (en) * 2003-02-03 2005-01-20 Janssen Pharmaceutica Nv Quinoline-derived amide modulators of vanilloid vr1 receptor
US6864255B2 (en) 2001-04-11 2005-03-08 Amgen Inc. Substituted triazinyl amide derivatives and methods of use
WO2005047273A1 (en) * 2003-11-14 2005-05-26 Novartis Ag Thiazole and pyrazole derivatives as flt-3 kinase inhibitors
WO2005054179A2 (en) 2003-12-03 2005-06-16 Leo Pharma A/S Hydroxamic acid esters and pharmaceutical use thereof
EP1568368A1 (en) * 2004-02-26 2005-08-31 Schering Aktiengesellschaft Pharmaceutical combination comprising a CDK inhibitor and a VEGF receptor inhibitor
WO2005085202A1 (de) * 2004-02-26 2005-09-15 Merck Patent Gmbh Pyridinamid-derivate als kinase-inhibitoren
WO2005085188A2 (en) * 2004-03-02 2005-09-15 Compass Pharmaceuticals Llc Compounds and methods for anti-tumor therapy
WO2006047574A1 (en) 2004-10-26 2006-05-04 Osi Pharmaceuticals, Inc. (2-carboxamido)(3-amino) thiophene compounds
US7087761B2 (en) 2003-01-07 2006-08-08 Hoffmann-La Roche Inc. Cyclization process for substituted benzothiazole derivatives
US7094789B2 (en) 2002-07-22 2006-08-22 Asahi Kasei Pharma Corporation 5-substituted isoquinoline derivatives
US7101868B2 (en) 2001-01-12 2006-09-05 Amgen Inc. Substituted arylamine derivatives and methods of use
US7129245B2 (en) * 1998-12-23 2006-10-31 Eli Lilly And Company Aromatic amides
US7132438B2 (en) 2001-10-09 2006-11-07 Amgen Inc. Benzimidazole derivatives
CN1300113C (zh) * 2001-11-08 2007-02-14 诺瓦提斯公司 邻氨基苯甲酰胺和其作为vegf受体酪氨酸激酶抑制剂的用途
WO2007038459A2 (en) 2005-09-27 2007-04-05 Novartis Ag Carboxyamine compounds and their use in the treatment of hdac dependent diseases
US7202260B2 (en) 2003-06-13 2007-04-10 Schering Ag VEGFR-2 and VEGFR-3 inhibitory anthranilamide pyridones
US7238808B2 (en) 2005-03-23 2007-07-03 Hoffmann-La Roche Inc. Acetylenyl-pyrazolo-pyrimidine derivatives
WO2007107543A1 (en) 2006-03-22 2007-09-27 Janssen Pharmaceutica N.V. Inhibitors of the interaction between mdm2 and p53
US7338956B2 (en) 2002-08-07 2008-03-04 Sanofi-Aventis Deutschland Gmbh Acylamino-substituted heteroaromatic compounds and their use as pharmaceuticals
WO2008037477A1 (en) 2006-09-29 2008-04-03 Novartis Ag Pyrazolopyrimidines as p13k lipid kinase inhibitors
US7368446B2 (en) 2004-05-24 2008-05-06 Hoffmann-La Roche Inc. 4-hydroxy-4-methyl-piperidine-1-carboxylic acid (4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-amide
JP2008518894A (ja) * 2004-11-03 2008-06-05 バイエル・シエーリング・ファーマ アクチエンゲゼルシャフト Vegf受容体キナーゼインヒビターとしてのアントラニルアミドピリジンウレア
JP2008518893A (ja) * 2004-11-03 2008-06-05 バイエル・シエーリング・ファーマ アクチエンゲゼルシャフト 血管内皮成長因子(vegf)受容体キナーゼインヒビターとしてのニコチンアミドピリジンウレア
EP1944026A2 (en) 2002-05-16 2008-07-16 Novartis AG Use of EDG receptor binding agents in cancer
WO2008093677A1 (ja) 2007-01-29 2008-08-07 Santen Pharmaceutical Co., Ltd. 血管新生阻害活性を有する新規オキサジアゾール誘導体およびチアジアゾール誘導体
EP1975166A1 (en) * 2007-03-30 2008-10-01 Bayer Schering Pharma AG Synthesis of anthranilamides
US7459563B2 (en) 2004-11-05 2008-12-02 Hoffmann-La Roche Inc. Process for the preparation of isonicotinic acid derivatives
EP2022498A2 (en) 2005-11-21 2009-02-11 Novartis AG Neuroendocrine tumour treatment
US7504404B2 (en) 2005-09-27 2009-03-17 Hoffmann-La Roche Inc. Compounds as metabotropic glutamate receptor antagonists
US7544703B2 (en) 2004-02-17 2009-06-09 Santen Pharmaceutical Co., Ltd. Cyclic compound having 4-pyridylalkylthio group having substituted or unsubstituted amino group introduced therein
US7572794B2 (en) 2004-11-03 2009-08-11 Bayer Schering Pharma Ag Anthranilamide pyridinureas as vascular endothelial growth factor (VEGF) receptor kinase inhibitors
US7615565B2 (en) 2002-07-31 2009-11-10 Bayer Schering Pharma Aktiengesellschaft VEGFR-2 and VEGFR-3 inhibitory anthranilamide pyridines
WO2010022725A1 (en) 2008-08-27 2010-03-04 Leo Pharma A/S Pyridine derivatives as vegfr-2 receptor and protein tyrosine kinase inhibitors
WO2010043050A1 (en) 2008-10-16 2010-04-22 Celator Pharmaceuticals Corporation Combinations of a liposomal water-soluble camptothecin with cetuximab or bevacizumab
WO2010071794A1 (en) 2008-12-18 2010-06-24 Novartis Ag New polymorphic form of 1- (4- { l- [ (e) -4-cyclohexyl--3-trifluoromethyl-benzyloxyimino] -ethyl) -2-ethyl-benzy l) -azetidine-3-carboxylic
WO2010080455A1 (en) 2008-12-18 2010-07-15 Novartis Ag New salts
WO2010080409A1 (en) 2008-12-18 2010-07-15 Novartis Ag Hemifumarate salt of 1- [4- [1- ( 4 -cyclohexyl-3 -trifluoromethyl-benzyloxyimino ) -ethyl] -2 -ethyl-benzyl] -a zetidine-3-carboxylic acid
EP2210643A2 (en) 2001-07-19 2010-07-28 Novartis AG Combinations comprising epothilones and pharmaceutical uses thereof
WO2010088335A1 (en) 2009-01-29 2010-08-05 Novartis Ag Substituted benzimidazoles for the treatment of astrocytomas
EP2253319A1 (en) 2001-05-16 2010-11-24 Novartis AG Combination comprising N-{5-[4-(4-methyl-piperazino-methyl)-benzoylamido]-2-methylphenyl}-4-(3-pyridyl)-2pyrimidine-amine and a chemotherapeutic agent.
WO2010149755A1 (en) 2009-06-26 2010-12-29 Novartis Ag 1, 3-disubstituted imidazolidin-2-one derivatives as inhibitors of cyp 17
EP2269603A1 (en) 2001-02-19 2011-01-05 Novartis AG Treatment of solid tumours with rapamycin derivatives
EP2270008A1 (en) 2005-05-20 2011-01-05 Novartis AG 1,3-dihydro-imidazo[4,5-c]quinolin-2-ones as lipid kinase and/or pi3 kinases inhibitors
EP2272511A1 (en) 2006-05-09 2011-01-12 Novartis AG Combination comprising an iron chelator and an anti-neoplastic agent and use thereof
WO2011015652A1 (en) 2009-08-07 2011-02-10 Novartis Ag 3-heteroarylmethyl-imidazo[1,2-b]pyridazin-6-yl derivatives as c-met tyrosine kinase modulators
WO2011018454A1 (en) 2009-08-12 2011-02-17 Novartis Ag Heterocyclic hydrazone compounds and their uses to treat cancer and inflammation
WO2011020861A1 (en) 2009-08-20 2011-02-24 Novartis Ag Heterocyclic oxime compounds
WO2011022439A1 (en) 2009-08-17 2011-02-24 Intellikine, Inc. Heterocyclic compounds and uses thereof
US7897774B2 (en) 2005-03-03 2011-03-01 Santen Pharmaceutical Co., Ltd. Cyclic compound having quinolylalkylthio group
WO2011023677A1 (en) 2009-08-26 2011-03-03 Novartis Ag Tetra-substituted heteroaryl compounds and their use as mdm2 and/or mdm4 modulators
US7906511B2 (en) 2005-03-31 2011-03-15 Santen Pharmaceutical Co., Ltd. Cyclic compound having pyrimidinylalkylthio group
US7906533B2 (en) 2004-11-03 2011-03-15 Bayer Schering Pharma Ag Nicotinamide pyridinureas as vascular endothelial growth factor (VEGF) receptor kinase inhibitors
WO2011029915A1 (en) 2009-09-10 2011-03-17 Novartis Ag Ether derivatives of bicyclic heteroaryls
EP2308855A1 (en) 2002-03-15 2011-04-13 Novartis AG 2,4-Diaminopyrimidine derivatives
WO2011054828A1 (en) 2009-11-04 2011-05-12 Novartis Ag Heterocyclic sulfonamide derivatives useful as mek inhibitors
WO2011064211A1 (en) 2009-11-25 2011-06-03 Novartis Ag Benzene-fused 6-membered oxygen-containing heterocyclic derivatives of bicyclic heteroaryls
WO2011070030A1 (en) 2009-12-08 2011-06-16 Novartis Ag Heterocyclic sulfonamide derivatives
WO2011076786A1 (en) 2009-12-22 2011-06-30 Novartis Ag Substituted isoquinolinones and quinazolinones
US7989462B2 (en) 2003-07-03 2011-08-02 Myrexis, Inc. 4-arylamin-or-4-heteroarylamino-quinazolines and analogs as activators of caspases and inducers of apoptosis and the use thereof
EP2359818A1 (en) 2007-02-15 2011-08-24 Novartis AG Combination of LBH589 with HSP 90 inhibitors for treating cancer
WO2011157793A1 (en) 2010-06-17 2011-12-22 Novartis Ag Piperidinyl substituted 1,3-dihydro-benzoimidazol-2-ylideneamine derivatives
WO2011157787A1 (en) 2010-06-17 2011-12-22 Novartis Ag Biphenyl substituted 1,3-dihydro-benzoimidazol-2-ylideneamine derivatives
EP2409969A1 (en) 2004-06-24 2012-01-25 Novartis AG Pyrimidine urea derivatives as kinase inhibitors
US8106190B2 (en) * 2005-11-30 2012-01-31 Astellas Pharma Inc. 2-aminobenzamide derivatives
WO2012035078A1 (en) 2010-09-16 2012-03-22 Novartis Ag 17α-HYDROXYLASE/C17,20-LYASE INHIBITORS
WO2012066095A1 (en) 2010-11-19 2012-05-24 Novartis Ag Crystalline form of an inhibitor of mdm2/4 and p53 interaction
WO2012107500A1 (en) 2011-02-10 2012-08-16 Novartis Ag [1, 2, 4] triazolo [4, 3 -b] pyridazine compounds as inhibitors of the c-met tyrosine kinase
WO2012116237A2 (en) 2011-02-23 2012-08-30 Intellikine, Llc Heterocyclic compounds and uses thereof
US8258145B2 (en) 2005-01-03 2012-09-04 Myrexis, Inc. Method of treating brain cancer
WO2012120469A1 (en) 2011-03-08 2012-09-13 Novartis Ag Fluorophenyl bicyclic heteroaryl compounds
WO2012149413A1 (en) 2011-04-28 2012-11-01 Novartis Ag 17α-HYDROXYLASE/C17,20-LYASE INHIBITORS
US8309562B2 (en) 2003-07-03 2012-11-13 Myrexis, Inc. Compounds and therapeutical use thereof
WO2012168884A1 (en) 2011-06-09 2012-12-13 Novartis Ag Heterocyclic sulfonamide derivatives
WO2012175487A1 (en) 2011-06-20 2012-12-27 Novartis Ag Cyclohexyl isoquinolinone compounds
WO2012175520A1 (en) 2011-06-20 2012-12-27 Novartis Ag Hydroxy substituted isoquinolinone derivatives
WO2013038362A1 (en) 2011-09-15 2013-03-21 Novartis Ag 6 - substituted 3 - (quinolin- 6 - ylthio) - [1,2,4] triazolo [4, 3 -a] pyradines as tyrosine kinase
EP2591775A1 (en) 2006-04-05 2013-05-15 Novartis AG Combinations comprising mtor inhibitors for treating cancer
WO2013080141A1 (en) 2011-11-29 2013-06-06 Novartis Ag Pyrazolopyrrolidine compounds
WO2013096049A1 (en) 2011-12-23 2013-06-27 Novartis Ag Compounds for inhibiting the interaction of bcl2 with binding partners
WO2013096059A1 (en) 2011-12-23 2013-06-27 Novartis Ag Compounds for inhibiting the interaction of bcl2 with binding partners
WO2013096055A1 (en) 2011-12-23 2013-06-27 Novartis Ag Compounds for inhibiting the interaction of bcl2 with binding partners
WO2013096051A1 (en) 2011-12-23 2013-06-27 Novartis Ag Compounds for inhibiting the interaction of bcl2 with binding partners
WO2013096060A1 (en) 2011-12-23 2013-06-27 Novartis Ag Compounds for inhibiting the interaction of bcl2 with binding partners
EP2628726A1 (en) 2008-03-26 2013-08-21 Novartis AG Hydroxamate-based inhibitors of deacetylases b
US8541442B2 (en) 2009-02-04 2013-09-24 Janssen Pharmaceutica N.V. Indole derivatives as anticancer agents
WO2013149581A1 (en) 2012-04-03 2013-10-10 Novartis Ag Combination products with tyrosine kinase inhibitors and their use
WO2013175417A1 (en) 2012-05-24 2013-11-28 Novartis Ag Pyrrolopyrrolidinone compounds
WO2014115077A1 (en) 2013-01-22 2014-07-31 Novartis Ag Substituted purinone compounds
WO2014115080A1 (en) 2013-01-22 2014-07-31 Novartis Ag Pyrazolo[3,4-d]pyrimidinone compounds as inhibitors of the p53/mdm2 interaction
WO2014151147A1 (en) 2013-03-15 2014-09-25 Intellikine, Llc Combination of kinase inhibitors and uses thereof
WO2014155268A2 (en) 2013-03-25 2014-10-02 Novartis Ag Fgf-r tyrosine kinase activity inhibitors - use in diseases associated with lack of or reduced snf5 activity
US8853406B2 (en) 2007-08-06 2014-10-07 Janssen Pharmaceutica Nv Substituted phenylenediamines as inhibitors of the interaction between MDM2 and P53
WO2015022662A1 (en) 2013-08-14 2015-02-19 Novartis Ag Compounds and compositions as inhibitors of mek
WO2015022663A1 (en) 2013-08-14 2015-02-19 Novartis Ag Compounds and compositions as inhibitors of mek
WO2015022664A1 (en) 2013-08-14 2015-02-19 Novartis Ag Compounds and compositions as inhibitors of mek
WO2015084804A1 (en) 2013-12-03 2015-06-11 Novartis Ag Combination of mdm2 inhibitor and braf inhibitor and their use
WO2016016822A1 (en) 2014-07-31 2016-02-04 Novartis Ag Combination therapy
EP3064502A1 (en) 2012-01-26 2016-09-07 Novartis AG Imidazopyrrolidinone compounds
US9725427B2 (en) 2012-03-16 2017-08-08 Biohaven Pharmaceutical Holding Company Limited Prodrugs of riluzole and their method of use
WO2019077037A1 (en) 2017-10-18 2019-04-25 Chemotherapeutisches Forschungsinstitut Georg-Speyer-Haus METHODS AND COMPOUNDS FOR ENHANCED IMMUNE CELL THERAPY
WO2019119486A1 (zh) 2017-12-21 2019-06-27 中国科学院合肥物质科学研究院 一类嘧啶类衍生物激酶抑制剂
EP3797765A1 (en) 2006-06-27 2021-03-31 Novartis AG S1p receptor modulators for treating multiple sclerosis
WO2021097256A1 (en) 2019-11-14 2021-05-20 Cohbar, Inc. Cxcr4 antagonist peptides

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7427390B2 (en) * 2004-03-10 2008-09-23 Schering Ag Radiohalogenated benzamide derivatives and their use in tumor diagnosis and tumor therapy
DE102004011720B4 (de) * 2004-03-10 2008-04-03 Bayer Schering Pharma Aktiengesellschaft Radiohalogenierte Benzamidderivate und deren Verwendung in der Tumordiagnostik und Tumortherapie
DE102004039876A1 (de) * 2004-06-23 2006-01-26 Lanxess Deutschland Gmbh Herstellung von fluorierten 1,3-Benzodioxanen
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
US8247556B2 (en) * 2005-10-21 2012-08-21 Amgen Inc. Method for preparing 6-substituted-7-aza-indoles
JP5162574B2 (ja) * 2006-03-22 2013-03-13 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及びp53間の相互作用のインヒビターとしての環式アルキルアミン誘導体
WO2008077809A1 (en) * 2006-12-22 2008-07-03 F. Hoffmann-La Roche Ag Process for the manufacture of 7-oxa-bicyclo derivatives
CA2841142C (en) 2010-06-23 2020-12-15 Ryan D. Morin Biomarkers for non-hodgkin lymphomas and uses thereof
US9175331B2 (en) 2010-09-10 2015-11-03 Epizyme, Inc. Inhibitors of human EZH2, and methods of use thereof
KR102061353B1 (ko) 2010-09-10 2020-01-02 에피자임, 인코포레이티드 인간 ezh2의 억제제 및 이의 사용 방법
EP2681216B1 (en) 2011-02-28 2017-09-27 Epizyme, Inc. Substituted 6,5-fused bicyclic heteroaryl compounds
JO3438B1 (ar) 2011-04-13 2019-10-20 Epizyme Inc مركبات بنزين مستبدلة بأريل أو أريل غير متجانس
TW201733984A (zh) 2011-04-13 2017-10-01 雅酶股份有限公司 經取代之苯化合物
CN102603729A (zh) * 2012-01-12 2012-07-25 贵州大学 N-(2-(取代苯并噻唑-2-氨基甲酰基)-取代苯基)吡啶甲酰胺类衍生物
LT3184523T (lt) 2012-04-13 2020-02-10 Epizyme Inc N-((4,6-dimetil-2-okso-1,2-dihidropiridin-3-il)metil)-5-(etil (tetrahidro-2h-piran-4-il)amino)-4-metil-4'-(morfolinometil)-[1,1'-bifenil]-3-karboksamido hidrobromidas, skirtas naudoti hematologinės sistemos proliferacinio sutrikimo gydymui
TWI588131B (zh) 2012-10-15 2017-06-21 雅酶股份有限公司 經取代苯化合物
CN103130696B (zh) * 2013-03-21 2014-06-11 山东大学 邻氨基苯甲酰胺类化合物及其制备方法与应用
CN103405434A (zh) * 2013-08-22 2013-11-27 中国药科大学 Vegfr-2抑制剂及其用途
PL3057962T3 (pl) 2013-10-16 2024-01-29 Epizyme, Inc. Postać soli chlorowodorku do inhibicji ezh2
CN104163794A (zh) * 2013-10-17 2014-11-26 中国药科大学 2-氨基芳环类血管内皮生长因子受体(vegfr)抑制剂及其制备方法和用途
CA3166630A1 (en) 2020-01-03 2021-07-08 Berg Llc Polycyclic amides as ube2k modulators for treating cancer
WO2022222890A1 (en) * 2021-04-19 2022-10-27 Shanghai Yao Yuan Biotechnology Co., Ltd. Benzothiazole and quinoline derivatives for use in treating kawasaki disease

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3409668A (en) * 1964-11-07 1968-11-05 Palazzo Giuseppe Substituted anthranilamides and process for the preparation thereof
DE2652144A1 (de) * 1976-11-16 1978-05-18 Merck Patent Gmbh Neue chinazolindione
DE3406416A1 (de) * 1983-02-28 1984-08-30 American Cyanamid Co., Wayne, N.J. N-((omega)-(1h-imidazol-l-yl)-alkyl)-arylamide
EP0564356A1 (fr) * 1992-04-01 1993-10-06 Fournier Industrie Et Sante Dérivés de 4-phénylaminométhylimidazole, procédé de préparation, antagonistes des récepteurs angiotensin II et leur application en thérapeutique

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3226394A (en) * 1964-06-16 1965-12-28 Shulton Inc Pyridylethylated anthranilamides and derivatives thereof
JPS5744672B2 (US07122547-20061017-C00064.png) 1974-05-24 1982-09-22
US4568687A (en) * 1983-02-28 1986-02-04 American Cyanamid Company N-[2-4-(1H-Imidazol-1-yl)alkyl]-arylamides and pharmaceutical compositions
CA2155662A1 (en) * 1993-12-27 1995-07-06 Fumihiro Ozaki Anthranilic acid derivative
WO1997034895A1 (de) * 1996-03-15 1997-09-25 Novartis Ag NEUE N-7 HETEROCYCLYL-PYRROLO[2,3-d]PYRIMIDINE UND IHRE VERWENDUNG

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3409668A (en) * 1964-11-07 1968-11-05 Palazzo Giuseppe Substituted anthranilamides and process for the preparation thereof
DE2652144A1 (de) * 1976-11-16 1978-05-18 Merck Patent Gmbh Neue chinazolindione
DE3406416A1 (de) * 1983-02-28 1984-08-30 American Cyanamid Co., Wayne, N.J. N-((omega)-(1h-imidazol-l-yl)-alkyl)-arylamide
EP0564356A1 (fr) * 1992-04-01 1993-10-06 Fournier Industrie Et Sante Dérivés de 4-phénylaminométhylimidazole, procédé de préparation, antagonistes des récepteurs angiotensin II et leur application en thérapeutique

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
CHEMICAL ABSTRACTS, vol. 85, no. 3, 19. Juli 1976 (1976-07-19) Columbus, Ohio, US; abstract no. 21433p, NODA, KANJI ET AL: "Quinazoline compounds" Seite 701; XP002135867 & JP 50 157383 A (HISAMITSU PHARMACEUTICAL CO., LTD., JAPAN) 19. Dezember 1975 (1975-12-19) *
DATABASE CHEMABS [Online] CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US MONTGINOUL, C. ET AL: "Analgesic, anticonvulsant and anti-inflammatory activities of 1H,3H-quinazoline-2,4-diones" retrieved from STN Database accession no. 110:165551h XP002135868 & ANN. PHARM. FR. (1989), 46(4), 223-32, *
HARDTMANN, GOETZ E. ET AL: "Chemistry of 2H-3,1-benzoxazine-2,4(1H)-dione (isatoic anhydrides). 1. Synthesis of N-substituted 2H-3,1-benzoxazine-2,4(1H)-diones" JOURNAL OF HETEROCYCLIC CHEMISTRY., Bd. 12, Nr. 3, 1975, Seiten 565-572, XP002135866 HETEROCORPORATION. PROVO., US ISSN: 0022-152X *
PASTOR, G. ET AL: "Synthesis of new 1H,3H-quinazoline-2,4-diones" BULLETIN DE LA SOCIETE CHIMIQUE DE FRANCE., Bd. 5-6, Nr. 2, 1975, Seiten 1331-1338, XP002135865 SOCIETE FRANCAISE DE CHIMIE. PARIS., FR ISSN: 0037-8968 *

Cited By (224)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7129245B2 (en) * 1998-12-23 2006-10-31 Eli Lilly And Company Aromatic amides
WO2001085719A1 (de) * 2000-05-09 2001-11-15 Schering Aktiengesellschaft Ortho substituierte anthranilsäureamide und deren verwendung als arzneimittel
WO2001085671A2 (de) * 2000-05-09 2001-11-15 Schering Aktiengesellschaft Anthranylamide und deren verwendung als arzneimittel
US6818661B2 (en) * 2000-05-09 2004-11-16 Novartis Ag Anthranylalkyl and cycloalkyl amides and use thereof as VEGF receptor inhibitors
WO2001085671A3 (de) * 2000-05-09 2002-04-11 Schering Ag Anthranylamide und deren verwendung als arzneimittel
US7012081B2 (en) 2000-05-09 2006-03-14 Schering Ag Anthranyl amides and their use as medicaments
US7081468B2 (en) 2000-05-09 2006-07-25 Schering Ag Ortho-substituted anthranilic acid amides and their use as medicaments
US7479491B2 (en) * 2000-05-09 2009-01-20 Novartis Ag Azanthranylalkyl and -cycloalkyl amides and their use as VEGF receptor inhibitors
US6963000B2 (en) 2000-06-21 2005-11-08 Hoffman-La Roche Inc. Benzothiazole derivatives with activity as adenosine receptor ligands
US7317007B2 (en) 2000-06-21 2008-01-08 Hoffmann-La Roche Inc. Benzothiazole derivatives with activity as adenosine receptor ligands
WO2001097786A3 (en) * 2000-06-21 2002-12-12 Hoffmann La Roche Benzothiazole derivatives
US6835732B2 (en) 2000-06-21 2004-12-28 Hoffman-La Roche Inc. Benzothiazole derivatives with activity as adenosine receptor ligands
WO2001097786A2 (en) * 2000-06-21 2001-12-27 F. Hoffmann-La Roche Ag Benzothiazole derivatives
US6521754B2 (en) 2000-06-21 2003-02-18 Hoffman-La Roche Inc. Benzothiazole derivatives with activity as adenosine receptor ligands
AU2001281817B2 (en) * 2000-06-21 2005-11-24 F. Hoffmann-La Roche Ag Benzothiazole derivatives
WO2002046181A3 (en) * 2000-12-07 2002-12-27 Cv Therapeutics Inc Abca-1 elevating compounds against coronary artery disease or atherosclerosis
AU2002225978B2 (en) * 2000-12-07 2005-08-11 Gilead Palo Alto, Inc. ABCA-1 elevating compounds against coronary artery disease or atherosclerosis
US6548548B2 (en) 2000-12-07 2003-04-15 Cv Therapeutics, Inc. ABCA-1 elevating compounds
WO2002046181A2 (en) * 2000-12-07 2002-06-13 Cv Therapeutics, Inc. Abca-1 elevating compounds against coronary artery disease or atherosclerosis
WO2002066470A1 (en) * 2001-01-12 2002-08-29 Amgen Inc. Substituted alkylamine derivatives and methods of use
EP1798230A1 (en) * 2001-01-12 2007-06-20 Amgen Inc. Substituted alkylamine derivatives and methods of use
US7101868B2 (en) 2001-01-12 2006-09-05 Amgen Inc. Substituted arylamine derivatives and methods of use
US7102009B2 (en) 2001-01-12 2006-09-05 Amgen Inc. Substituted amine derivatives and methods of use
US7514564B2 (en) 2001-01-12 2009-04-07 Amgen Inc. Substituted amine derivatives and methods of use
CN1313464C (zh) * 2001-01-12 2007-05-02 安姆根有限公司 取代的烷基胺衍生物、其制备方法、含其的组合物及其用途
US6995162B2 (en) 2001-01-12 2006-02-07 Amgen Inc. Substituted alkylamine derivatives and methods of use
WO2002068406A3 (en) * 2001-01-12 2003-04-24 Amgen Inc Substituted amine derivatives and their use for the treatment of angiogenesis
EP2311808A1 (en) 2001-01-12 2011-04-20 Amgen Inc. Substituted alkylamine derivatives and methods of use
US7105682B2 (en) 2001-01-12 2006-09-12 Amgen Inc. Substituted amine derivatives and methods of use
US6878714B2 (en) 2001-01-12 2005-04-12 Amgen Inc. Substituted alkylamine derivatives and methods of use
CZ303356B6 (cs) * 2001-01-12 2012-08-08 Amgen Inc. Substituovaný alkylaminový derivát a farmaceutická kompozice s jeho obsahem
US8058445B2 (en) 2001-01-12 2011-11-15 Amgen Inc. Substituted pyridinecarboxamides for the treatment of cancer
US8642624B2 (en) 2001-01-12 2014-02-04 Amgen Inc. Substituted alkylamine derivatives and methods of use
EP2311829A1 (en) 2001-01-12 2011-04-20 Amgen Inc. Substituted alkylamine derivatives and methods of use
WO2002055501A3 (en) * 2001-01-12 2002-12-19 Amgen Inc. N-pyridyl carboxamide derivatives and pharmaceutical compositions containing them
BG66160B1 (bg) * 2001-01-12 2011-09-30 Amgen Inc. Заместени алкиламинови производни и използването им
US7687643B2 (en) 2001-01-12 2010-03-30 Amgen Inc. Process for preparing 3,3-dimethylindolines
EP3345602A1 (en) 2001-02-19 2018-07-11 Novartis AG Rapamycin derivative for treating advanced solid tumours
EP2783686A1 (en) 2001-02-19 2014-10-01 Novartis AG Combination of a rapamycin derivative and letrozole for treating breast cancer
EP3406249A1 (en) 2001-02-19 2018-11-28 Novartis AG Treatment of breast tumors with a rapamycin derivative in combination with an aromatase inhibitor
EP3351246A1 (en) 2001-02-19 2018-07-25 Novartis AG Rapamycin derivative for the treatment of a solid tumor associated with deregulated angiogenesis
EP3342411A1 (en) 2001-02-19 2018-07-04 Novartis AG Rapamycin derivative for treating pancreas cancer
EP2762140A1 (en) 2001-02-19 2014-08-06 Novartis AG Treatment of solid brain tumours with a rapamycin derivative
EP2269603A1 (en) 2001-02-19 2011-01-05 Novartis AG Treatment of solid tumours with rapamycin derivatives
EP2269604A1 (en) 2001-02-19 2011-01-05 Novartis AG Treatment of solid tumours with rapamycin derivatives
EP2764865A2 (en) 2001-02-19 2014-08-13 Novartis AG Cancer treatment
US6864255B2 (en) 2001-04-11 2005-03-08 Amgen Inc. Substituted triazinyl amide derivatives and methods of use
WO2003000678A1 (de) * 2001-05-08 2003-01-03 Schering Aktiengesellschaft Cyanoanthranylamid-derivate und deren verwendung als arzneimittel
DE10123573A1 (de) * 2001-05-08 2002-11-28 Schering Ag N-Oxidanthranylamid-Derivate und deren Verwendung als Arzneimittel
WO2002090352A2 (de) * 2001-05-08 2002-11-14 Schering Aktiengesellschaft Selektive anthranylamidpyridinamide als vegfr-2 und vegfr-3 inhibitoren
US7429592B2 (en) 2001-05-08 2008-09-30 Schering Aktienegesellschaft Cyanoanthranilamide derivatives and the use thereof as medicaments
DE10123587B4 (de) * 2001-05-08 2005-04-07 Schering Ag Cyanoanthranylamid-Derivate und deren Verwendung als Arzneimittel
JP2004528379A (ja) * 2001-05-08 2004-09-16 シエーリング アクチエンゲゼルシャフト Vegfr−2およびvegfr−3インヒビターとしての選択的アントラニルアミドピリジンアミド
WO2002090349A1 (de) * 2001-05-08 2002-11-14 Schering Aktiengesellschaft N-oxidanthranylamid-derivate und deren verwendung als arzneimittel
DE10123587A1 (de) * 2001-05-08 2002-11-21 Schering Ag Cyanoanthranylamid-Derivate und deren Verwendung als Arzneimittel
DE10123573B4 (de) * 2001-05-08 2005-06-02 Schering Ag N-Oxidanthranylamid-Derivate und deren Verwendung als Arzneimittel
WO2002090352A3 (de) * 2001-05-08 2003-05-01 Schering Ag Selektive anthranylamidpyridinamide als vegfr-2 und vegfr-3 inhibitoren
US7459470B2 (en) 2001-05-08 2008-12-02 Schering Ag N-oxide anthranylamide derivatives and their use as medicaments
EP2253319A1 (en) 2001-05-16 2010-11-24 Novartis AG Combination comprising N-{5-[4-(4-methyl-piperazino-methyl)-benzoylamido]-2-methylphenyl}-4-(3-pyridyl)-2pyrimidine-amine and a chemotherapeutic agent.
US7199147B2 (en) 2001-06-12 2007-04-03 Dainippon Sumitomo Pharma Co., Ltd. Rho kinase inhibitors
WO2002100833A1 (fr) * 2001-06-12 2002-12-19 Sumitomo Pharmaceuticals Company, Limited Inhibiteurs de rho kinase
JPWO2002100833A1 (ja) * 2001-06-12 2004-09-24 住友製薬株式会社 Rhoキナーゼ阻害剤
EP2210643A2 (en) 2001-07-19 2010-07-28 Novartis AG Combinations comprising epothilones and pharmaceutical uses thereof
US7132438B2 (en) 2001-10-09 2006-11-07 Amgen Inc. Benzimidazole derivatives
US7635774B2 (en) 2001-10-09 2009-12-22 Amgen Inc. Benzimidazole derivatives
CN1300113C (zh) * 2001-11-08 2007-02-14 诺瓦提斯公司 邻氨基苯甲酰胺和其作为vegf受体酪氨酸激酶抑制剂的用途
EP2308855A1 (en) 2002-03-15 2011-04-13 Novartis AG 2,4-Diaminopyrimidine derivatives
EP1955696A2 (en) 2002-05-16 2008-08-13 Novartis AG Use of EDG receptor binding agents in cancer
EP1944026A2 (en) 2002-05-16 2008-07-16 Novartis AG Use of EDG receptor binding agents in cancer
AU2003256481B2 (en) * 2002-07-09 2007-08-09 Amgen Inc. Substituted anthranilic amide derivatives and methods of use
JP2006502112A (ja) * 2002-07-09 2006-01-19 アムジエン・インコーポレーテツド 置換アントラニルアミド誘導体および使用方法
WO2004005279A2 (en) * 2002-07-09 2004-01-15 Amgen Inc. Substituted anthranilic amide derivatives and methods of use
US7307088B2 (en) 2002-07-09 2007-12-11 Amgen Inc. Substituted anthranilic amide derivatives and methods of use
WO2004005279A3 (en) * 2002-07-09 2004-03-11 Amgen Inc Substituted anthranilic amide derivatives and methods of use
WO2004007458A1 (en) 2002-07-17 2004-01-22 Amgen Inc. Substituted 2-alkylamine nicotinic amide derivatives and use there of
WO2004007481A2 (en) * 2002-07-17 2004-01-22 Amgen Inc. Substituted amine derivatives and methods of use in the treatment of angiogenesis relates disorders
WO2004007481A3 (en) * 2002-07-17 2004-02-19 Amgen Inc Substituted amine derivatives and methods of use in the treatment of angiogenesis relates disorders
US7094789B2 (en) 2002-07-22 2006-08-22 Asahi Kasei Pharma Corporation 5-substituted isoquinoline derivatives
US7615565B2 (en) 2002-07-31 2009-11-10 Bayer Schering Pharma Aktiengesellschaft VEGFR-2 and VEGFR-3 inhibitory anthranilamide pyridines
DE10235690A1 (de) * 2002-07-31 2004-02-19 Schering Ag VEGFR-2 und VEGFR-3 inhibitorische Anthranylamidpyridinamide
EP1388341A1 (en) * 2002-08-07 2004-02-11 Aventis Pharma Deutschland GmbH Acylamino-substituted heteroaromatic compounds and their use as pharmaceuticals
US7338956B2 (en) 2002-08-07 2008-03-04 Sanofi-Aventis Deutschland Gmbh Acylamino-substituted heteroaromatic compounds and their use as pharmaceuticals
JP2005538123A (ja) * 2002-08-07 2005-12-15 アベンティス・ファーマ・ドイチユラント・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング アシルアミノ−置換複素芳香族化合物および医薬としてのそれらの使用
JP4778230B2 (ja) * 2002-08-07 2011-09-21 サノフィ−アベンティス・ドイチュラント・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング アシルアミノ−置換複素芳香族化合物および医薬としてのそれらの使用
WO2004014369A1 (en) * 2002-08-07 2004-02-19 Aventis Pharma Deutschland Gmbh Acylamino-substituted heteroaromatic compounds and their use as pharmaceuticals
US7365070B2 (en) 2002-12-04 2008-04-29 Ore Pharmaceuticals Inc. Modulators of melanocortin receptor
WO2004050610A2 (en) * 2002-12-04 2004-06-17 Gene Logic Inc. Modulators of melanocortin receptor
US7790719B2 (en) 2002-12-04 2010-09-07 Ore Pharmaceuticals, Inc. Modulators of melanocortin receptor
WO2004050610A3 (en) * 2002-12-04 2004-08-26 Millennium Pharm Inc Modulators of melanocortin receptor
US7696225B2 (en) 2003-01-06 2010-04-13 Osi Pharmaceuticals, Inc. (2-carboxamido)(3-Amino) thiophene compounds
US6949563B2 (en) 2003-01-06 2005-09-27 Graham Michael Wynne (2-carboxamido)(3-amino)thiophene compounds
WO2004063330A2 (en) 2003-01-06 2004-07-29 Osi Pharmaceuticals, Inc. (2-carboxamido) (3-amino) thiophene compounds
US7087761B2 (en) 2003-01-07 2006-08-08 Hoffmann-La Roche Inc. Cyclization process for substituted benzothiazole derivatives
WO2004069792A3 (en) * 2003-02-03 2005-01-20 Janssen Pharmaceutica Nv Quinoline-derived amide modulators of vanilloid vr1 receptor
EP2308848A1 (en) * 2003-02-03 2011-04-13 Janssen Pharmaceutica NV Quinoline-derived amide modulators of vanilloid VR1 receptor
US8394828B2 (en) 2003-02-03 2013-03-12 Janssen Pharmaceutica, Nv Quinoline-derived amide modulators of vanilloid VR1 receptor
WO2004072069A1 (en) * 2003-02-14 2004-08-26 Glaxo Group Limited Carboxamide derivatives
US7531558B2 (en) 2003-02-14 2009-05-12 Glaxo Group Limited Carboxamide derivatives
WO2004078723A1 (ja) 2003-03-07 2004-09-16 Santen Pharmaceutical Co. Ltd. 4-ピリジルアルキルチオ基を置換基として有する新規化合物
US8518973B2 (en) 2003-03-07 2013-08-27 Santen Pharmaceutical Co., Ltd. Compounds having 4-pyridylalkylthio group as a substituent
US8207194B2 (en) 2003-03-07 2012-06-26 Santen Pharmaceutical Co., Ltd. Compounds having a 4-pyridylalkylthio group as a substituent
EP2527326A1 (en) 2003-03-07 2012-11-28 Santen Pharmaceutical Co., Ltd Novel compounds having 4-pyridylalkylthio group as substituent
US7534802B2 (en) 2003-03-07 2009-05-19 Santen Pharmaceutical Co., Ltd. Compounds having 4-pyridylalkylthio group as substituent
WO2004103306A2 (en) 2003-05-19 2004-12-02 Irm Llc Immunosuppressant compounds and compositions
WO2005000833A1 (en) 2003-05-19 2005-01-06 Irm, Llc Immunosuppressant compounds and compositions
EP3272736A1 (en) 2003-05-19 2018-01-24 Novartis Ag Immunosuppressant compounds and compositions
EP2644195A1 (en) 2003-05-19 2013-10-02 Irm Llc Immunosuppressant Compounds and Compositions
EP2514743A1 (en) 2003-05-19 2012-10-24 Irm Llc Immunosuppressant Compounds and Compositions
WO2004108133A2 (en) * 2003-06-05 2004-12-16 Vertex Pharmaceuticals Incorporated Modulators of vr1 receptor
WO2004108133A3 (en) * 2003-06-05 2005-03-31 Vertex Pharma Modulators of vr1 receptor
JP2006526660A (ja) * 2003-06-05 2006-11-24 バーテックス ファーマシューティカルズ インコーポレイテッド Vr1レセプターのモジュレーター
WO2004111005A1 (de) * 2003-06-13 2004-12-23 Schering Aktiengesellschaft Vegfr-2 und vegfr-3 inhibitorische anthranylamidpyridone
US7202260B2 (en) 2003-06-13 2007-04-10 Schering Ag VEGFR-2 and VEGFR-3 inhibitory anthranilamide pyridones
US8309562B2 (en) 2003-07-03 2012-11-13 Myrexis, Inc. Compounds and therapeutical use thereof
US7989462B2 (en) 2003-07-03 2011-08-02 Myrexis, Inc. 4-arylamin-or-4-heteroarylamino-quinazolines and analogs as activators of caspases and inducers of apoptosis and the use thereof
WO2005004864A1 (en) * 2003-07-11 2005-01-20 Merck Patent Gmbh Benzimidazole derivatives as raf kinase inhibitors
US7691886B2 (en) 2003-07-11 2010-04-06 Merck Patent Gmbh Benzimidazole derivatives as raf kinase inhibitors
WO2005047273A1 (en) * 2003-11-14 2005-05-26 Novartis Ag Thiazole and pyrazole derivatives as flt-3 kinase inhibitors
WO2005054179A2 (en) 2003-12-03 2005-06-16 Leo Pharma A/S Hydroxamic acid esters and pharmaceutical use thereof
US7544703B2 (en) 2004-02-17 2009-06-09 Santen Pharmaceutical Co., Ltd. Cyclic compound having 4-pyridylalkylthio group having substituted or unsubstituted amino group introduced therein
WO2005085202A1 (de) * 2004-02-26 2005-09-15 Merck Patent Gmbh Pyridinamid-derivate als kinase-inhibitoren
EP1568368A1 (en) * 2004-02-26 2005-08-31 Schering Aktiengesellschaft Pharmaceutical combination comprising a CDK inhibitor and a VEGF receptor inhibitor
WO2005085188A3 (en) * 2004-03-02 2006-06-15 Compass Pharmaceuticals Llc Compounds and methods for anti-tumor therapy
WO2005085188A2 (en) * 2004-03-02 2005-09-15 Compass Pharmaceuticals Llc Compounds and methods for anti-tumor therapy
US7368446B2 (en) 2004-05-24 2008-05-06 Hoffmann-La Roche Inc. 4-hydroxy-4-methyl-piperidine-1-carboxylic acid (4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-amide
EP2409969A1 (en) 2004-06-24 2012-01-25 Novartis AG Pyrimidine urea derivatives as kinase inhibitors
EP2418205A1 (en) 2004-06-24 2012-02-15 Novartis AG Pyrimidine urea derivatives as kinase inhibitors
WO2006047574A1 (en) 2004-10-26 2006-05-04 Osi Pharmaceuticals, Inc. (2-carboxamido)(3-amino) thiophene compounds
US7906533B2 (en) 2004-11-03 2011-03-15 Bayer Schering Pharma Ag Nicotinamide pyridinureas as vascular endothelial growth factor (VEGF) receptor kinase inhibitors
JP2008518893A (ja) * 2004-11-03 2008-06-05 バイエル・シエーリング・ファーマ アクチエンゲゼルシャフト 血管内皮成長因子(vegf)受容体キナーゼインヒビターとしてのニコチンアミドピリジンウレア
JP2008518894A (ja) * 2004-11-03 2008-06-05 バイエル・シエーリング・ファーマ アクチエンゲゼルシャフト Vegf受容体キナーゼインヒビターとしてのアントラニルアミドピリジンウレア
US7572794B2 (en) 2004-11-03 2009-08-11 Bayer Schering Pharma Ag Anthranilamide pyridinureas as vascular endothelial growth factor (VEGF) receptor kinase inhibitors
US7902229B2 (en) 2004-11-03 2011-03-08 Bayer Schering Pharma Ag Anthranilamide pyridinureas as vascular endothelial growth factor (VEGF) receptor kinase inhibitors
US7459563B2 (en) 2004-11-05 2008-12-02 Hoffmann-La Roche Inc. Process for the preparation of isonicotinic acid derivatives
US8258145B2 (en) 2005-01-03 2012-09-04 Myrexis, Inc. Method of treating brain cancer
US7897774B2 (en) 2005-03-03 2011-03-01 Santen Pharmaceutical Co., Ltd. Cyclic compound having quinolylalkylthio group
US8063048B2 (en) 2005-03-23 2011-11-22 Hoffmann-La Roche Inc. Acetylenyl-pyrazolo-pyrimidine derivatives
US7718661B2 (en) 2005-03-23 2010-05-18 Hoffmann-La Roche Inc. Acetylenyl-pyrazolo-pyrimidine derivatives
US7238808B2 (en) 2005-03-23 2007-07-03 Hoffmann-La Roche Inc. Acetylenyl-pyrazolo-pyrimidine derivatives
US7446113B2 (en) 2005-03-23 2008-11-04 Hoffman-La Roche Inc. Acetylenyl-pyrazolo-pyrimidine derivatives
US7906511B2 (en) 2005-03-31 2011-03-15 Santen Pharmaceutical Co., Ltd. Cyclic compound having pyrimidinylalkylthio group
US8507485B2 (en) 2005-03-31 2013-08-13 Santen Pharmaceutical Co., Ltd. Cyclic compound having pyrimidinylalkylthio group
EP2292617A1 (en) 2005-05-20 2011-03-09 Novartis AG 1,3-dihydro-imidazo[4,5-c]quinolin-2-ones as lipid kinase and/or pi3 kinase inhibitors
EP2270008A1 (en) 2005-05-20 2011-01-05 Novartis AG 1,3-dihydro-imidazo[4,5-c]quinolin-2-ones as lipid kinase and/or pi3 kinases inhibitors
US8093263B2 (en) 2005-09-27 2012-01-10 Hoffmann-La Roche Inc. Substituted pyrazolo [1,5-a] pyrimidines as metabotropic glutamate antagonists
WO2007038459A2 (en) 2005-09-27 2007-04-05 Novartis Ag Carboxyamine compounds and their use in the treatment of hdac dependent diseases
US7504404B2 (en) 2005-09-27 2009-03-17 Hoffmann-La Roche Inc. Compounds as metabotropic glutamate receptor antagonists
US8349844B2 (en) 2005-09-27 2013-01-08 Hoffmann-La Roche Inc. Substituted pyrazolo [1,5-A] pyrimidines as metabotropic glutamate antagonists
EP2022498A2 (en) 2005-11-21 2009-02-11 Novartis AG Neuroendocrine tumour treatment
EP2275103A2 (en) 2005-11-21 2011-01-19 Novartis AG mTOR inhibitors in the treatment of endocrine tumors
US8106190B2 (en) * 2005-11-30 2012-01-31 Astellas Pharma Inc. 2-aminobenzamide derivatives
US8232298B2 (en) 2006-03-22 2012-07-31 Janssen Pharmaceutica N.V. Inhibitors of the interaction between MDM2 and P53
WO2007107543A1 (en) 2006-03-22 2007-09-27 Janssen Pharmaceutica N.V. Inhibitors of the interaction between mdm2 and p53
EP2591775A1 (en) 2006-04-05 2013-05-15 Novartis AG Combinations comprising mtor inhibitors for treating cancer
EP2272511A1 (en) 2006-05-09 2011-01-12 Novartis AG Combination comprising an iron chelator and an anti-neoplastic agent and use thereof
EP3797765A1 (en) 2006-06-27 2021-03-31 Novartis AG S1p receptor modulators for treating multiple sclerosis
WO2008037477A1 (en) 2006-09-29 2008-04-03 Novartis Ag Pyrazolopyrimidines as p13k lipid kinase inhibitors
US8063034B2 (en) 2007-01-29 2011-11-22 Santen Pharmaceutical Co., Ltd. Oxadiazole derivatives and thiadiazole derivatives having neovascularization inhibitory activity
WO2008093677A1 (ja) 2007-01-29 2008-08-07 Santen Pharmaceutical Co., Ltd. 血管新生阻害活性を有する新規オキサジアゾール誘導体およびチアジアゾール誘導体
EP2359818A1 (en) 2007-02-15 2011-08-24 Novartis AG Combination of LBH589 with HSP 90 inhibitors for treating cancer
EP2491923A2 (en) 2007-02-15 2012-08-29 Novartis AG Combinations of therapeutic agents for treating cancer
EP1975166A1 (en) * 2007-03-30 2008-10-01 Bayer Schering Pharma AG Synthesis of anthranilamides
WO2008119569A1 (en) * 2007-03-30 2008-10-09 Bayer Schering Pharma Aktiengesellschaft Synthesis of anthranilamides
US8853406B2 (en) 2007-08-06 2014-10-07 Janssen Pharmaceutica Nv Substituted phenylenediamines as inhibitors of the interaction between MDM2 and P53
EP2628726A1 (en) 2008-03-26 2013-08-21 Novartis AG Hydroxamate-based inhibitors of deacetylases b
WO2010022725A1 (en) 2008-08-27 2010-03-04 Leo Pharma A/S Pyridine derivatives as vegfr-2 receptor and protein tyrosine kinase inhibitors
WO2010043050A1 (en) 2008-10-16 2010-04-22 Celator Pharmaceuticals Corporation Combinations of a liposomal water-soluble camptothecin with cetuximab or bevacizumab
WO2010080409A1 (en) 2008-12-18 2010-07-15 Novartis Ag Hemifumarate salt of 1- [4- [1- ( 4 -cyclohexyl-3 -trifluoromethyl-benzyloxyimino ) -ethyl] -2 -ethyl-benzyl] -a zetidine-3-carboxylic acid
WO2010080455A1 (en) 2008-12-18 2010-07-15 Novartis Ag New salts
WO2010071794A1 (en) 2008-12-18 2010-06-24 Novartis Ag New polymorphic form of 1- (4- { l- [ (e) -4-cyclohexyl--3-trifluoromethyl-benzyloxyimino] -ethyl) -2-ethyl-benzy l) -azetidine-3-carboxylic
WO2010088335A1 (en) 2009-01-29 2010-08-05 Novartis Ag Substituted benzimidazoles for the treatment of astrocytomas
US8541442B2 (en) 2009-02-04 2013-09-24 Janssen Pharmaceutica N.V. Indole derivatives as anticancer agents
WO2010149755A1 (en) 2009-06-26 2010-12-29 Novartis Ag 1, 3-disubstituted imidazolidin-2-one derivatives as inhibitors of cyp 17
WO2011015652A1 (en) 2009-08-07 2011-02-10 Novartis Ag 3-heteroarylmethyl-imidazo[1,2-b]pyridazin-6-yl derivatives as c-met tyrosine kinase modulators
WO2011018454A1 (en) 2009-08-12 2011-02-17 Novartis Ag Heterocyclic hydrazone compounds and their uses to treat cancer and inflammation
WO2011022439A1 (en) 2009-08-17 2011-02-24 Intellikine, Inc. Heterocyclic compounds and uses thereof
WO2011020861A1 (en) 2009-08-20 2011-02-24 Novartis Ag Heterocyclic oxime compounds
WO2011023677A1 (en) 2009-08-26 2011-03-03 Novartis Ag Tetra-substituted heteroaryl compounds and their use as mdm2 and/or mdm4 modulators
WO2011029915A1 (en) 2009-09-10 2011-03-17 Novartis Ag Ether derivatives of bicyclic heteroaryls
WO2011054828A1 (en) 2009-11-04 2011-05-12 Novartis Ag Heterocyclic sulfonamide derivatives useful as mek inhibitors
WO2011064211A1 (en) 2009-11-25 2011-06-03 Novartis Ag Benzene-fused 6-membered oxygen-containing heterocyclic derivatives of bicyclic heteroaryls
WO2011070030A1 (en) 2009-12-08 2011-06-16 Novartis Ag Heterocyclic sulfonamide derivatives
WO2011076786A1 (en) 2009-12-22 2011-06-30 Novartis Ag Substituted isoquinolinones and quinazolinones
WO2011157793A1 (en) 2010-06-17 2011-12-22 Novartis Ag Piperidinyl substituted 1,3-dihydro-benzoimidazol-2-ylideneamine derivatives
WO2011157787A1 (en) 2010-06-17 2011-12-22 Novartis Ag Biphenyl substituted 1,3-dihydro-benzoimidazol-2-ylideneamine derivatives
WO2012035078A1 (en) 2010-09-16 2012-03-22 Novartis Ag 17α-HYDROXYLASE/C17,20-LYASE INHIBITORS
WO2012066095A1 (en) 2010-11-19 2012-05-24 Novartis Ag Crystalline form of an inhibitor of mdm2/4 and p53 interaction
WO2012107500A1 (en) 2011-02-10 2012-08-16 Novartis Ag [1, 2, 4] triazolo [4, 3 -b] pyridazine compounds as inhibitors of the c-met tyrosine kinase
US9127000B2 (en) 2011-02-23 2015-09-08 Intellikine, LLC. Heterocyclic compounds and uses thereof
WO2012116237A2 (en) 2011-02-23 2012-08-30 Intellikine, Llc Heterocyclic compounds and uses thereof
WO2012120469A1 (en) 2011-03-08 2012-09-13 Novartis Ag Fluorophenyl bicyclic heteroaryl compounds
WO2012149413A1 (en) 2011-04-28 2012-11-01 Novartis Ag 17α-HYDROXYLASE/C17,20-LYASE INHIBITORS
WO2012168884A1 (en) 2011-06-09 2012-12-13 Novartis Ag Heterocyclic sulfonamide derivatives
WO2012175520A1 (en) 2011-06-20 2012-12-27 Novartis Ag Hydroxy substituted isoquinolinone derivatives
WO2012175487A1 (en) 2011-06-20 2012-12-27 Novartis Ag Cyclohexyl isoquinolinone compounds
WO2013038362A1 (en) 2011-09-15 2013-03-21 Novartis Ag 6 - substituted 3 - (quinolin- 6 - ylthio) - [1,2,4] triazolo [4, 3 -a] pyradines as tyrosine kinase
WO2013080141A1 (en) 2011-11-29 2013-06-06 Novartis Ag Pyrazolopyrrolidine compounds
WO2013096059A1 (en) 2011-12-23 2013-06-27 Novartis Ag Compounds for inhibiting the interaction of bcl2 with binding partners
WO2013096049A1 (en) 2011-12-23 2013-06-27 Novartis Ag Compounds for inhibiting the interaction of bcl2 with binding partners
WO2013096055A1 (en) 2011-12-23 2013-06-27 Novartis Ag Compounds for inhibiting the interaction of bcl2 with binding partners
WO2013096051A1 (en) 2011-12-23 2013-06-27 Novartis Ag Compounds for inhibiting the interaction of bcl2 with binding partners
WO2013096060A1 (en) 2011-12-23 2013-06-27 Novartis Ag Compounds for inhibiting the interaction of bcl2 with binding partners
EP3064502A1 (en) 2012-01-26 2016-09-07 Novartis AG Imidazopyrrolidinone compounds
EP3272754A1 (en) 2012-01-26 2018-01-24 Novartis AG Imidazopyrrolidinone compounds
US9725427B2 (en) 2012-03-16 2017-08-08 Biohaven Pharmaceutical Holding Company Limited Prodrugs of riluzole and their method of use
US10844026B2 (en) 2012-03-16 2020-11-24 Biohaven Pharmaceutical Holding Company Ltd. Prodrugs of riluzole and their method of use
US11440893B2 (en) 2012-03-16 2022-09-13 Biohaven Pharmaceutical Holding Company Ltd. Prodrugs of riluzole and their method of use
US10562870B2 (en) 2012-03-16 2020-02-18 Biohaven Pharmaceutical Holding Company Ltd. Prodrugs of riluzole and their method of use
WO2013149581A1 (en) 2012-04-03 2013-10-10 Novartis Ag Combination products with tyrosine kinase inhibitors and their use
EP3964513A1 (en) 2012-04-03 2022-03-09 Novartis AG Combination products with tyrosine kinase inhibitors and their use
WO2013175417A1 (en) 2012-05-24 2013-11-28 Novartis Ag Pyrrolopyrrolidinone compounds
WO2014115077A1 (en) 2013-01-22 2014-07-31 Novartis Ag Substituted purinone compounds
WO2014115080A1 (en) 2013-01-22 2014-07-31 Novartis Ag Pyrazolo[3,4-d]pyrimidinone compounds as inhibitors of the p53/mdm2 interaction
WO2014151147A1 (en) 2013-03-15 2014-09-25 Intellikine, Llc Combination of kinase inhibitors and uses thereof
WO2014155268A2 (en) 2013-03-25 2014-10-02 Novartis Ag Fgf-r tyrosine kinase activity inhibitors - use in diseases associated with lack of or reduced snf5 activity
WO2015022664A1 (en) 2013-08-14 2015-02-19 Novartis Ag Compounds and compositions as inhibitors of mek
WO2015022663A1 (en) 2013-08-14 2015-02-19 Novartis Ag Compounds and compositions as inhibitors of mek
WO2015022662A1 (en) 2013-08-14 2015-02-19 Novartis Ag Compounds and compositions as inhibitors of mek
WO2015084804A1 (en) 2013-12-03 2015-06-11 Novartis Ag Combination of mdm2 inhibitor and braf inhibitor and their use
WO2016016822A1 (en) 2014-07-31 2016-02-04 Novartis Ag Combination therapy
WO2019077037A1 (en) 2017-10-18 2019-04-25 Chemotherapeutisches Forschungsinstitut Georg-Speyer-Haus METHODS AND COMPOUNDS FOR ENHANCED IMMUNE CELL THERAPY
WO2019119486A1 (zh) 2017-12-21 2019-06-27 中国科学院合肥物质科学研究院 一类嘧啶类衍生物激酶抑制剂
US11602534B2 (en) 2017-12-21 2023-03-14 Hefei Institutes Of Physical Science, Chinese Academy Of Sciences Pyrimidine derivative kinase inhibitors
WO2021097256A1 (en) 2019-11-14 2021-05-20 Cohbar, Inc. Cxcr4 antagonist peptides

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KR20070087027A (ko) 2007-08-27
EP1129074A2 (de) 2001-09-05
AU771180B2 (en) 2004-03-18
EA004701B1 (ru) 2004-06-24
BG105588A (en) 2002-04-30
HUP0104425A3 (en) 2003-05-28
KR20010075689A (ko) 2001-08-09
WO2000027819A3 (de) 2000-08-17
HK1041882A1 (en) 2002-07-26
CZ20011631A3 (cs) 2001-10-17
NO20012245D0 (no) 2001-05-07
SK6072001A3 (en) 2002-01-07
JP2002529452A (ja) 2002-09-10

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