GT200900032A - Derivados de oxazolidona como moduladors pr - Google Patents
Derivados de oxazolidona como moduladors prInfo
- Publication number
- GT200900032A GT200900032A GT200900032A GT200900032A GT200900032A GT 200900032 A GT200900032 A GT 200900032A GT 200900032 A GT200900032 A GT 200900032A GT 200900032 A GT200900032 A GT 200900032A GT 200900032 A GT200900032 A GT 200900032A
- Authority
- GT
- Guatemala
- Prior art keywords
- endomyromatimatomy
- distribution
- modulators
- oxazolidone derivatives
- tautommers
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/42—Oxazoles
- A61K31/422—Oxazoles not condensed and containing further heterocyclic rings
-
- 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
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/18—Feminine contraceptives
-
- 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
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/24—Drugs for disorders of the endocrine system of the sex hormones
- A61P5/30—Oestrogens
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D263/34—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D263/48—Nitrogen atoms not forming part of a nitro radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic 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
- C07D413/04—Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D453/00—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids
- C07D453/06—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing isoquinuclidine ring systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Endocrinology (AREA)
- Diabetes (AREA)
- Reproductive Health (AREA)
- Gynecology & Obstetrics (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Steroid Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
ESTA SOLICITUD PRESENTA COMPUESTOS DERIVADOS DE OXAZOLIDONA, SALES FARMACÉUTICAMENTE ACEPTABLES, TAUTÓMEROS, METABOLITOS O PROFÁRMACOS DE LOS MISMOS, LOS CUALES SON ÚTILES PARA TRATAR UNA VARIEDAD DE AFECCIONES RELACIONADAS CON HORMONAS QUE INCLUYEN CONTRACEPCIÓN TRATAR O PREVENIR MIOMAS UTERINOS, ENDOMETRIOSIS, METRORRAGIA DISFUNCIONAL, LIOMIOMATA UTERINO, SÍNDROME DE OVARIO POLIQUÍSTICO O CARCINOMAS DEPENDIENTES DE HORMONA, QUE PROPORCIONA HORMONOTERAPIA RESTITUTIVA, QUE ESTIMULA LA INGESTIÓN DE ALIMENTO O SINCRONIZACIÓN DEL ESTRO.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US83789806P | 2006-08-15 | 2006-08-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
GT200900032A true GT200900032A (es) | 2011-03-29 |
Family
ID=39082681
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GT200900032A GT200900032A (es) | 2006-08-15 | 2009-02-12 | Derivados de oxazolidona como moduladors pr |
Country Status (22)
Country | Link |
---|---|
US (1) | US7618990B2 (es) |
EP (1) | EP2054410A2 (es) |
JP (1) | JP2010500409A (es) |
KR (1) | KR20090039774A (es) |
CN (1) | CN101501031B (es) |
AR (1) | AR062327A1 (es) |
AU (1) | AU2007284599B2 (es) |
BR (1) | BRPI0716622A2 (es) |
CA (1) | CA2659208A1 (es) |
CR (1) | CR10617A (es) |
GT (1) | GT200900032A (es) |
IL (1) | IL196886A0 (es) |
MX (1) | MX2009001698A (es) |
NO (1) | NO20090457L (es) |
NZ (1) | NZ574753A (es) |
PE (1) | PE20070753A1 (es) |
RU (1) | RU2009105113A (es) |
SA (1) | SA07280440B1 (es) |
SV (1) | SV2009003168A (es) |
TW (1) | TW200815428A (es) |
WO (1) | WO2008021331A2 (es) |
ZA (1) | ZA200901055B (es) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2008112495A1 (en) * | 2007-03-09 | 2008-09-18 | Wyeth | Synthesis and characterization of polymorph form iii of 4-(2,(4,4-dimethyl-2-oxooxazolidin-3-yl)thiazol-4-yl)benzonitrile |
PE20081803A1 (es) * | 2007-03-09 | 2008-12-11 | Wyeth Corp | Sintesis y caracterizacion de la forma ii polimorfica de 4-(2-(4,4-dimetil-2-oxooxazolidin-3-il)tiazol-4-il)benzonitrilo |
CN101525310B (zh) * | 2009-04-21 | 2019-04-16 | 大连九信精细化工有限公司 | 1-苯甲酰基-3-(2-羟基-1,1-二甲基乙基)硫脲的合成方法 |
ES2550319T3 (es) * | 2010-09-28 | 2015-11-06 | Radius Health, Inc | Moduladores selectivos del receptor de andrógenos |
US9120818B2 (en) * | 2010-12-14 | 2015-09-01 | Merck Sharp & Dohme Corp. | Process and intermediates for preparing macrolactams |
US9902719B2 (en) | 2014-07-03 | 2018-02-27 | Celgene Quanticel Research, Inc. | Inhibitors of lysine specific demethylase-1 |
Family Cites Families (51)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3493565A (en) | 1966-03-14 | 1970-02-03 | Squibb & Sons Inc | 3-amino-5-(nitrofuryl)-1,2,4-oxadiazole derivatives |
DE1670338A1 (de) | 1966-03-14 | 1972-08-10 | Heyden Chem Fab | Verfahren zur Herstellung von antimikrobiell wirksamen Nitrofuranderivaten |
NL6809997A (es) * | 1967-08-04 | 1969-02-06 | ||
GB1224995A (en) | 1968-09-20 | 1971-03-10 | Delalande Sa | New 5-propargyloxymethyl-2-substituted oxazolidinones and their process of preparation |
CA1076582A (en) * | 1975-10-28 | 1980-04-29 | Charles J. Paget | Antiviral thiazolinyl or thiazinyl ketobenzimidazoles |
US4293558A (en) * | 1975-10-28 | 1981-10-06 | Eli Lilly And Company | Antiviral thiazolinyl benzimidazoles and derivatives |
US4008243A (en) * | 1975-11-19 | 1977-02-15 | Eli Lilly And Company | Antiviral thiazolinyl or thiazinyl benzimidazole esters |
US4268679A (en) * | 1980-02-19 | 1981-05-19 | Ppg Industries, Inc. | 3-[5- or 3-Substituted-5- or 3-isoxazolyl]-1-allyl or alkyl-4-substituted-5-substituted or unsubstituted-2-imidazolidinones |
US4426527A (en) * | 1982-02-12 | 1984-01-17 | Ppg Industries, Inc. | 3-[5- Or 3-substituted-1,2,4-oxadiazol-3- or -5-yl]-1-substituted-4-substituted-5-substituted or unsubstituted-2-imidazolidinones |
DE3227329A1 (de) | 1982-07-22 | 1984-01-26 | Basf Ag, 6700 Ludwigshafen | Verfahren zur herstellung von 2-n,n-disubstituierten aminothiazolen |
US4756744A (en) * | 1985-06-24 | 1988-07-12 | Ppg Industries, Inc. | Herbicidally active 4-aminoalkylamino-3-isoxazolyl-2-imidazolidinone derivatives |
DE3723797A1 (de) | 1987-07-18 | 1989-01-26 | Merck Patent Gmbh | Oxazolidinone |
CA2095429A1 (en) | 1990-11-06 | 1992-05-07 | Paul E. Bender | Imidazolidinone compounds |
ES2245660T3 (es) | 1990-11-30 | 2006-01-16 | Otsuka Pharmaceutical Co., Ltd. | Derivados de azol y su utilizacion como inhibidores de los radicales superoxidos. |
DE4335876A1 (de) * | 1993-10-17 | 1995-04-20 | Schering Ag | Kombination von Progesteronantagonisten und Antiöstrogenen mit partialer agonistischer Wirkung für die Hormonsubstitutions-Therapie für peri- und postmenopausale Frauen |
JPH07149745A (ja) | 1993-11-30 | 1995-06-13 | Hisamitsu Pharmaceut Co Inc | 新規な2−アミノチアゾール誘導体 |
WO1995015955A1 (de) | 1993-12-06 | 1995-06-15 | Basf Aktiengesellschaft | 2,4-diaminothiazole und ihre herstellung |
DE4425613A1 (de) * | 1994-07-20 | 1996-01-25 | Bayer Ag | 5-gliedrige Heteroaryl-oxazolidinone |
DE19540027A1 (de) | 1995-10-27 | 1997-04-30 | Gruenenthal Gmbh | Substituierte Imidazolidin-2,4-dion-Verbindungen als pharmazeutische Wirkstoffe |
US5714607A (en) * | 1995-12-01 | 1998-02-03 | American Cyanamid Company | Process improvement in the synthesis of N- 3-(3-cyano-pyrazolo 1,5-a!pyrimidin-7-yl)phenyl!-N-ethylacetamide |
DE19601264A1 (de) * | 1996-01-16 | 1997-07-17 | Bayer Ag | Pyrido-annellierte Thienyl- und Furanyl-Oxazolidinone |
HRP970049A2 (en) | 1996-02-06 | 1998-04-30 | Bayer Ag | New heteroaryl oxazolidinones |
DE19649095A1 (de) | 1996-02-06 | 1997-08-07 | Bayer Ag | Neue Heteroaryl-Oxazolidinone |
DE19604223A1 (de) | 1996-02-06 | 1997-08-07 | Bayer Ag | Neue substituierte Oxazolidinone |
US5972372A (en) * | 1996-07-31 | 1999-10-26 | The Population Council, Inc. | Intravaginal rings with insertable drug-containing core |
JP3192662B2 (ja) | 1996-07-31 | 2001-07-30 | 日研化学株式会社 | 6―フェニルテトラヒドロ―1,3―オキサジン―2―オン誘導体及びそれを含む医薬組成物 |
US5819742A (en) * | 1996-11-06 | 1998-10-13 | Family Health International | Vaginal device for preventing conception or the transmission of sexually transmitted diseases, or both |
DE19732928C2 (de) | 1997-07-31 | 2000-05-18 | Gruenenthal Gmbh | Verwendung substituierter Imidazolidin-2,4-dion-Verbindungen als Schmerzmittel |
CA2302417A1 (en) * | 1997-10-27 | 1999-05-06 | Takeda Chemical Industries, Ltd. | Adenosine a3 receptor antagonists |
EP1049682A1 (en) * | 1998-01-23 | 2000-11-08 | Versicor, Inc. | Oxazolidinone combinatorial libraries, compositions and methods of preparation |
US6562844B2 (en) * | 1998-01-23 | 2003-05-13 | Pharmacia & Upjohn Company | Oxazolidinone combinatorial libraries, compositions and methods of preparation |
WO1999042455A1 (en) | 1998-02-19 | 1999-08-26 | Tularik Inc. | Antiviral agents |
JP2001261652A (ja) | 2000-03-21 | 2001-09-26 | Suntory Ltd | 二置換イミノヘテロサイクリック化合物 |
AU2001244618A1 (en) | 2000-03-30 | 2001-10-15 | Takeda Chemical Industries Ltd. | Substituted 1,3-thiazole compounds, their production and use |
GB0009803D0 (en) * | 2000-04-25 | 2000-06-07 | Astrazeneca Ab | Chemical compounds |
DE10034623A1 (de) | 2000-07-17 | 2002-01-31 | Bayer Ag | Heterocyclisch substituierte Pyridine als Cytokin-Inhibitoren |
DE10034622A1 (de) | 2000-07-17 | 2002-01-31 | Bayer Ag | Substituierte Imidazol-Derivate und deren Verwendung zur Herstellung von Arzneimitteln |
DE10034628A1 (de) | 2000-07-17 | 2002-01-31 | Bayer Ag | Pyridinhaltige Oxazolidinone als Cytokin-Inhibitoren |
US20020115669A1 (en) * | 2000-08-31 | 2002-08-22 | Wiedeman Paul E. | Oxazolidinone chemotherapeutic agents |
FR2823209B1 (fr) | 2001-04-04 | 2003-12-12 | Fournier Lab Sa | Nouvelles thiohydantoines et leur utilisation en therapeutique |
GB0118407D0 (en) | 2001-07-27 | 2001-09-19 | Cipla Ltd | Oxazolidinone derivatives as antibacterial agents |
KR100437972B1 (ko) * | 2001-10-27 | 2004-07-02 | 한국과학기술연구원 | 피롤리디논 유도체, 이의 제조 방법 및 이를 포함하는제약 조성물 |
US7119111B2 (en) | 2002-05-29 | 2006-10-10 | Amgen, Inc. | 2-oxo-1,3,4-trihydroquinazolinyl derivatives and methods of use |
PL375532A1 (en) | 2002-08-08 | 2005-11-28 | Smithkline Beecham Corporation | Benzimidazol-1-yl-thiophene compounds for the treatment of cancer |
TWI324596B (en) * | 2002-08-26 | 2010-05-11 | Nat Health Research Institutes | Imidazolamino compounds |
AU2003258433A1 (en) | 2002-08-28 | 2004-03-19 | Merck Frosst Canada Ltd | Oxazolidin-2-one and thiazolidin-2-one derivatives for use as ep4 receptor agonists in the treatment of glaucoma |
US20040167192A1 (en) * | 2003-01-16 | 2004-08-26 | David Solow-Cordero | Methods of treating conditions associated with an Edg-7 receptor |
US7169797B2 (en) * | 2003-02-14 | 2007-01-30 | Abbott Laboratories | Protein-tyrosine phosphatase inhibitors and uses thereof |
WO2004087698A2 (en) | 2003-03-25 | 2004-10-14 | Vertex Pharmaceuticals Incorporated | Thiazoles useful as inhibitors of protein kinases |
CN100387594C (zh) | 2003-04-03 | 2008-05-14 | 麦克公司 | 二芳基取代的吡唑类代谢型谷氨酸受体-5调节剂 |
US7514567B2 (en) | 2003-07-08 | 2009-04-07 | Astrazeneca Ab | Oxazolidinone nicotinic acetylcholine receptor agonists |
-
2007
- 2007-07-31 TW TW096127981A patent/TW200815428A/zh unknown
- 2007-08-10 AR ARP070103552A patent/AR062327A1/es not_active Application Discontinuation
- 2007-08-13 US US11/891,748 patent/US7618990B2/en not_active Expired - Fee Related
- 2007-08-13 KR KR1020097002974A patent/KR20090039774A/ko not_active Application Discontinuation
- 2007-08-13 MX MX2009001698A patent/MX2009001698A/es active IP Right Grant
- 2007-08-13 RU RU2009105113/04A patent/RU2009105113A/ru not_active Application Discontinuation
- 2007-08-13 BR BRPI0716622-2A patent/BRPI0716622A2/pt not_active IP Right Cessation
- 2007-08-13 WO PCT/US2007/017931 patent/WO2008021331A2/en active Application Filing
- 2007-08-13 CA CA002659208A patent/CA2659208A1/en not_active Abandoned
- 2007-08-13 NZ NZ574753A patent/NZ574753A/en not_active IP Right Cessation
- 2007-08-13 JP JP2009524654A patent/JP2010500409A/ja active Pending
- 2007-08-13 AU AU2007284599A patent/AU2007284599B2/en not_active Ceased
- 2007-08-13 EP EP07836789A patent/EP2054410A2/en not_active Withdrawn
- 2007-08-13 CN CN2007800302230A patent/CN101501031B/zh not_active Expired - Fee Related
- 2007-08-14 SA SA07280440A patent/SA07280440B1/ar unknown
- 2007-08-15 PE PE2007001100A patent/PE20070753A1/es not_active Application Discontinuation
-
2009
- 2009-01-29 NO NO20090457A patent/NO20090457L/no not_active Application Discontinuation
- 2009-02-03 IL IL196886A patent/IL196886A0/en unknown
- 2009-02-12 GT GT200900032A patent/GT200900032A/es unknown
- 2009-02-12 SV SV2009003168A patent/SV2009003168A/es unknown
- 2009-02-13 CR CR10617A patent/CR10617A/es unknown
- 2009-02-13 ZA ZA200901055A patent/ZA200901055B/xx unknown
Also Published As
Publication number | Publication date |
---|---|
NO20090457L (no) | 2009-04-27 |
BRPI0716622A2 (pt) | 2013-10-08 |
NZ574753A (en) | 2011-04-29 |
US20080045556A1 (en) | 2008-02-21 |
SV2009003168A (es) | 2010-01-14 |
CA2659208A1 (en) | 2008-02-21 |
KR20090039774A (ko) | 2009-04-22 |
SA07280440B1 (ar) | 2010-10-20 |
TW200815428A (en) | 2008-04-01 |
JP2010500409A (ja) | 2010-01-07 |
MX2009001698A (es) | 2009-02-25 |
AU2007284599B2 (en) | 2011-07-21 |
CR10617A (es) | 2009-03-12 |
PE20070753A1 (es) | 2008-08-14 |
ZA200901055B (en) | 2009-12-30 |
CN101501031A (zh) | 2009-08-05 |
RU2009105113A (ru) | 2010-09-27 |
CN101501031B (zh) | 2012-02-01 |
IL196886A0 (en) | 2009-11-18 |
US7618990B2 (en) | 2009-11-17 |
WO2008021331A3 (en) | 2008-05-22 |
EP2054410A2 (en) | 2009-05-06 |
AU2007284599A1 (en) | 2008-02-21 |
AR062327A1 (es) | 2008-10-29 |
WO2008021331A2 (en) | 2008-02-21 |
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