WO2014155268A3 - Fgf-r tyrosine kinase activity inhibitors - use in diseases associated with lack of or reduced snf5 activity - Google Patents
Fgf-r tyrosine kinase activity inhibitors - use in diseases associated with lack of or reduced snf5 activity Download PDFInfo
- Publication number
- WO2014155268A3 WO2014155268A3 PCT/IB2014/060087 IB2014060087W WO2014155268A3 WO 2014155268 A3 WO2014155268 A3 WO 2014155268A3 IB 2014060087 W IB2014060087 W IB 2014060087W WO 2014155268 A3 WO2014155268 A3 WO 2014155268A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- activity
- snf5
- lack
- inhibitors
- fgf
- Prior art date
Links
- 230000000694 effects Effects 0.000 title abstract 8
- 201000010099 disease Diseases 0.000 title abstract 5
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title abstract 5
- 239000003112 inhibitor Substances 0.000 title abstract 5
- 102000004022 Protein-Tyrosine Kinases Human genes 0.000 title abstract 2
- 108090000412 Protein-Tyrosine Kinases Proteins 0.000 title abstract 2
- 101100533768 Tetraodon fluviatilis smarcb1 gene Proteins 0.000 title 1
- 101000835860 Homo sapiens SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily B member 1 Proteins 0.000 abstract 5
- 102100025746 SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily B member 1 Human genes 0.000 abstract 5
- 230000002062 proliferating effect Effects 0.000 abstract 4
- 230000000069 prophylactic effect Effects 0.000 abstract 4
- 230000001225 therapeutic effect Effects 0.000 abstract 4
- 239000003814 drug Substances 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 abstract 2
Classifications
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- 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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- 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
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with 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
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7088—Compounds having three or more nucleosides or nucleotides
- A61K31/713—Double-stranded nucleic acids or oligonucleotides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
FGF-R tyrosine Kinase Activity Inhibitors useful in Case of Lack of SNF5 Activity. The invention relates to the use of FGF-R inhibitors in the (prophylactic and/or therapeutic) treatment of proliferative diseases that depend on at least partial lack of SNF5 activity, the use of said inhibitors for the preparation of a pharmaceutical composition (medicament) for said use, said inhibitors for use in a method of (therapeutic and/or prophylactic) treatment of a proliferative disease depends on at least partial lack of SNF5 activity, a method of (prophylactic and/or therapeutic) treatment of a proliferative disease that depends on at least partial lack of SNF5 activity and a pharmaceutical composition (medicament) for use in the (prophylactic and/or therapeutic) treatment of a proliferative disease that depends on at least partial lack of SNF5 activity, as well as related invention embodiments.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201361804797P | 2013-03-25 | 2013-03-25 | |
US61/804,797 | 2013-03-25 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2014155268A2 WO2014155268A2 (en) | 2014-10-02 |
WO2014155268A3 true WO2014155268A3 (en) | 2014-12-04 |
Family
ID=50483186
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/IB2014/060087 WO2014155268A2 (en) | 2013-03-25 | 2014-03-24 | Fgf-r tyrosine kinase activity inhibitors - use in diseases associated with lack of or reduced snf5 activity |
Country Status (1)
Country | Link |
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WO (1) | WO2014155268A2 (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
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CN112877425A (en) * | 2021-04-22 | 2021-06-01 | 宁夏医科大学 | Application of reagent for detecting SNF5 gene expression in preparation of atherosclerosis diagnosis product |
Family Cites Families (34)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR901228A (en) | 1943-01-16 | 1945-07-20 | Deutsche Edelstahlwerke Ag | Ring gap magnet system |
EP0100172B1 (en) | 1982-07-23 | 1987-08-12 | Imperial Chemical Industries Plc | Amide derivatives |
US5093330A (en) | 1987-06-15 | 1992-03-03 | Ciba-Geigy Corporation | Staurosporine derivatives substituted at methylamino nitrogen |
US5395855A (en) | 1990-05-07 | 1995-03-07 | Ciba-Geigy Corporation | Hydrazones |
NZ243082A (en) | 1991-06-28 | 1995-02-24 | Ici Plc | 4-anilino-quinazoline derivatives; pharmaceutical compositions, preparatory processes, and use thereof |
AU661533B2 (en) | 1992-01-20 | 1995-07-27 | Astrazeneca Ab | Quinazoline derivatives |
TW225528B (en) | 1992-04-03 | 1994-06-21 | Ciba Geigy Ag | |
RO119721B1 (en) | 1992-10-28 | 2005-02-28 | Genentech Inc. | Antagonists of vascular endotelial cell growth factor |
GB9314893D0 (en) | 1993-07-19 | 1993-09-01 | Zeneca Ltd | Quinazoline derivatives |
DE122005000053I2 (en) | 1995-03-30 | 2008-01-17 | Pfizer Prod Inc | quinazoline derivatives |
GB9508538D0 (en) | 1995-04-27 | 1995-06-14 | Zeneca Ltd | Quinazoline derivatives |
US5747498A (en) | 1996-05-28 | 1998-05-05 | Pfizer Inc. | Alkynyl and azido-substituted 4-anilinoquinazolines |
US5880141A (en) | 1995-06-07 | 1999-03-09 | Sugen, Inc. | Benzylidene-Z-indoline compounds for the treatment of disease |
EA001428B1 (en) | 1995-07-06 | 2001-02-26 | Новартис Аг | Pyrrolopyrimidines and pharmaceutical compositions |
US5760041A (en) | 1996-02-05 | 1998-06-02 | American Cyanamid Company | 4-aminoquinazoline EGFR Inhibitors |
GB9603095D0 (en) | 1996-02-14 | 1996-04-10 | Zeneca Ltd | Quinazoline derivatives |
CN1145614C (en) | 1996-04-12 | 2004-04-14 | 沃尼尔·朗伯公司 | Irreversible inhibitors of tyrosine kinases |
WO1997049688A1 (en) | 1996-06-24 | 1997-12-31 | Pfizer Inc. | Phenylamino-substituted tricyclic derivatives for treatment of hyperproliferative diseases |
DE19638745C2 (en) | 1996-09-11 | 2001-05-10 | Schering Ag | Monoclonal antibodies against the extracellular domain of the human VEGF receptor protein (KDR) |
AU4342997A (en) | 1996-09-13 | 1998-04-02 | Sugen, Inc. | Use of quinazoline derivatives for the manufacture of a medicament in the reatment of hyperproliferative skin disorders |
EP0837063A1 (en) | 1996-10-17 | 1998-04-22 | Pfizer Inc. | 4-Aminoquinazoline derivatives |
CO4950519A1 (en) | 1997-02-13 | 2000-09-01 | Novartis Ag | PHTHALAZINES, PHARMACEUTICAL PREPARATIONS THAT UNDERSTAND THEM AND THE PROCESS FOR THEIR PREPARATION |
CO4940418A1 (en) | 1997-07-18 | 2000-07-24 | Novartis Ag | MODIFICATION OF A CRYSTAL OF A DERIVATIVE OF N-PHENYL-2-PIRIMIDINAMINE, PROCESSES FOR ITS MANUFACTURE AND USE |
GB9721069D0 (en) | 1997-10-03 | 1997-12-03 | Pharmacia & Upjohn Spa | Polymeric derivatives of camptothecin |
DE69942097D1 (en) | 1998-08-11 | 2010-04-15 | Novartis Ag | ISOCHINOLINE DERIVATIVES WITH ANGIOGENESIS-HEMMENDER EFFECT |
UA71587C2 (en) | 1998-11-10 | 2004-12-15 | Шерінг Акцієнгезелльшафт | Anthranilic acid amides and use thereof as medicaments |
GB9824579D0 (en) | 1998-11-10 | 1999-01-06 | Novartis Ag | Organic compounds |
EP1140173B2 (en) | 1998-12-22 | 2013-04-03 | Genentech, Inc. | Vascular endothelial cell growth factor antagonists and uses thereof |
ATE329596T1 (en) | 1999-03-30 | 2006-07-15 | Novartis Pharma Gmbh | PHTHALAZINE DERIVATIVES FOR THE TREATMENT OF INFLAMMATORY DISEASES |
PE20020354A1 (en) | 2000-09-01 | 2002-06-12 | Novartis Ag | HYDROXAMATE COMPOUNDS AS HISTONE-DESACETILASE (HDA) INHIBITORS |
TWI238824B (en) | 2001-05-14 | 2005-09-01 | Novartis Ag | 4-amino-5-phenyl-7-cyclobutyl-pyrrolo[2,3-d]pyrimidine derivatives |
GB0119249D0 (en) | 2001-08-07 | 2001-10-03 | Novartis Ag | Organic compounds |
GB0512324D0 (en) | 2005-06-16 | 2005-07-27 | Novartis Ag | Organic compounds |
AR079257A1 (en) | 2009-12-07 | 2012-01-04 | Novartis Ag | CRYSTAL FORMS OF 3- (2,6-DICLORO-3-5-DIMETOXI-PHENYL) -1- {6- [4- (4-ETIL-PIPERAZIN-1-IL) -PENYL-AMINO] -PIRIMIDIN-4- IL} -1-METHYL-UREA AND SALTS OF THE SAME |
-
2014
- 2014-03-24 WO PCT/IB2014/060087 patent/WO2014155268A2/en active Application Filing
Non-Patent Citations (5)
Title |
---|
ANONYMOUS: "Final report: Therapeutically targeting aberrant chromatin remodeling in sarcomas (Project Number: SFA09-20)", 1 February 2011 (2011-02-01), XP002726892, Retrieved from the Internet <URL:https://www.curesarcoma.org/documents/uploads/Roberts_Final_Report.pdf> [retrieved on 20140709] * |
KLENKE F M ET AL: "Tyrosine kinase inhibitor SU6668 represses chondrosarcoma growth via antiangiogenesis in vivo", BMC CANCER, vol. 7, 17 March 2007 (2007-03-17), XP002123128, ISSN: 1471-2407 * |
KONECNY GOTTFRIED E ET AL: "Activity of the Fibroblast Growth Factor Receptor Inhibitors Dovitinib (TKI258) and NVP-BGJ398 in Human Endometrial Cancer Cells", MOLECULAR CANCER THERAPEUTICS, vol. 12, no. 5, 26 February 2013 (2013-02-26), pages 632 - 642, XP002726890 * |
LOCH DAVID C ET AL: "Lineage-Specific Biomarkers Predict Response to FGFR Inhibition", CANCER DISCOVERY, vol. 2, no. 12, December 2012 (2012-12-01), pages 1081 - 1083, XP002726889 * |
WÖHRLE SIMON ET AL: "Fibroblast growth factor receptors as novel therapeutic targets in SNF5-deleted malignant rhabdoid tumors.", PLOS ONE, vol. 8, no. 10, E77652, 30 October 2013 (2013-10-30), pages 1 - 11, XP002726891, ISSN: 1932-6203, DOI: 10.1371/journal.pone.0077652 * |
Also Published As
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WO2014155268A2 (en) | 2014-10-02 |
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