AR079846A1 - Agentes terapeuticos derivados de bisfenol que contienen un grupo aquiral y su uso en el tratamiento del cancer - Google Patents

Agentes terapeuticos derivados de bisfenol que contienen un grupo aquiral y su uso en el tratamiento del cancer

Info

Publication number
AR079846A1
AR079846A1 ARP110100034A ARP110100034A AR079846A1 AR 079846 A1 AR079846 A1 AR 079846A1 AR P110100034 A ARP110100034 A AR P110100034A AR P110100034 A ARP110100034 A AR P110100034A AR 079846 A1 AR079846 A1 AR 079846A1
Authority
AR
Argentina
Prior art keywords
independently
formula
remainder
chg1
aromatic ring
Prior art date
Application number
ARP110100034A
Other languages
English (en)
Original Assignee
British Columbia Cancer Agency
Univ British Columbia
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
Application filed by British Columbia Cancer Agency, Univ British Columbia filed Critical British Columbia Cancer Agency
Publication of AR079846A1 publication Critical patent/AR079846A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C57/00Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
    • C07C57/30Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing six-membered aromatic rings
    • C07C57/38Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing six-membered aromatic rings polycyclic
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/075Ethers or acetals
    • A61K31/085Ethers or acetals having an ether linkage to aromatic ring nuclear carbon
    • A61K31/09Ethers or acetals having an ether linkage to aromatic ring nuclear carbon having two or more such linkages
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/21Esters, e.g. nitroglycerine, selenocyanates
    • A61K31/215Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
    • A61K31/22Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/08Drugs for disorders of the urinary system of the prostate
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • 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
    • A61P17/10Anti-acne agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/14Drugs for dermatological disorders for baldness or alopecia
    • 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
    • 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
    • A61P5/00Drugs for disorders of the endocrine system
    • A61P5/24Drugs for disorders of the endocrine system of the sex hormones
    • A61P5/28Antiandrogens
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C15/00Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts
    • C07C15/12Polycyclic non-condensed hydrocarbons
    • C07C15/16Polycyclic non-condensed hydrocarbons containing at least two phenyl groups linked by one single acyclic carbon atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C43/00Ethers; Compounds having groups, groups or groups
    • C07C43/02Ethers
    • C07C43/20Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring
    • C07C43/225Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing halogen
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C43/00Ethers; Compounds having groups, groups or groups
    • C07C43/02Ethers
    • C07C43/20Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring
    • C07C43/23Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing hydroxy or O-metal groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/62Halogen-containing esters
    • C07C69/63Halogen-containing esters of saturated acids
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/06Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Epidemiology (AREA)
  • Dermatology (AREA)
  • Emergency Medicine (AREA)
  • Endocrinology (AREA)
  • Diabetes (AREA)
  • Ophthalmology & Optometry (AREA)
  • Urology & Nephrology (AREA)
  • Reproductive Health (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

También se proporcionan usos de dichos compuestos para el tratamiento de diversas indicaciones, que incluyen cáncer de prostata, así como métodos de tratamiento que involucran dichos compuestos. Reivindicacion 1: El uso de un compuesto que tiene la estructura de formula (1) o una sal farmacéuticamente aceptable de dicho compuesto, en donde: X es CH2, CHR1, o CR1R2; cada uno de R1 y R2 es independientemente alquilo C1-10 lineal o ramificado, sustituido o no sustituido, saturado o insaturado, o R1 y R2 juntos forman un alquilo C3-10 cíclico sustituido o no sustituido, saturado o insaturado, en donde el sustituyente opcional se selecciona del grupo que consiste en oxo, OJö', COOH, R3, OH, OR3, F, CI, Br, I, NH2, NHR3, NR32, CN, SH, SR3, SOR3, SO3H, SO3R3, SO2R3, OSO3R3, OR6, CO2R3, CONH2, CONHR3, CONHR6, CONR32, NHR6, OPO3H3, CONR3R6, NR3R6, y NO2; cada R3 es independientemente alquilo C1-10 no sustituido; cada R6 es independientemente acilo C1-10; al menos un Z de un anillo aromático es independientemente C-Q, al menos un Z del otro anillo aromático es independientemente C-T, CF, CCI, CBr, CI, COH, CG1, COG1, CNH2, CNHG1, CNG12, COSO3H, COPO3H2, CSG1, CSOG1, o CSO2G1, y cada Z restante es independientemente C-T, N, CH, CF, CCI, CBr, CI, COH, CG1, COG1, CNH2, CNHG1, CNG12, COSO3H, COPO3H2, CSG1, CSOG1, o CSO2G1; Q es como en resto de formula (2); J es G1, O, CH2, CHG1, CG12, S, NH, NG1, SO, SO2, o NR; M es H, CI, Br, CH2CI, CHCI2, CCI3, CH2Br, CHBr2, CBr3, o C:::CH; L es H o A-D; A es O, S, NH, NG1, N+H2, o N+HG1; D es H, G1, R, o como los restos de formulas (3), o un resto seleccionado de la TABLA 1; cada uno de q, r y t es independientemente 0, 1, 2, 3, 4, 5, 6 o 7; n es 0,1, 2, 3, 4, 5, 6, 7 u 8; T es un resto de formula (4); J2 es G1, O, CH2, CHG1, CG12, S, NH, NG1, SO, SO2, o NR; M2 es H, CH3, CI, Br, CH2CI, CHCI2, CCI3, CH2Br, CHBr2, CBr3, CH2OH, CH2OJö, G1, CH2OG1, CH2OR, CH2OG1OG1', G1OG1', G1OG1'OG1ö, CH2SG1, CH2NH2, CH2NHG1, CH2NG12, o C:::CH; L2 es H o A2-D2; A2 es O, S, SO, SO2, NH, NG1, N+H2, o N+HG1; D2 es H G1, R, restos de formulas (3), o un resto seleccionado de la TABLA 1; cada uno de u, y, j es independientemente 0, 1, 2, 3, 4, 5, 6 o 7; m es 0, 1, 2, 3, 4, 5, 6, 7 u 8; cada uno de Jö y Jö' es independientemente un resto seleccionado de la TABLA 1; cada G1, G1' y G1ö es independientemente alquilo C1-10 lineal o ramificado, o cíclico aromático o cíclico no aromático, sustituido o no sustituido, saturado o insaturado, en donde el sustituyente opcional se selecciona del grupo que consiste en oxo, OJö', COOH, R4, OH, OR4, F, CI, Br, I, NH2, NHR4, NR42, CN, SH, SR4, SO3H, SO3R4, SO2R4, OSO3R4, OR5, CO2R4, CONH2, CONHR4, CONHR5, CONR42, NHR5, OPO3H3, CONR4R5, NR4R5, y NO2; cada R4 es independientemente alquilo C1-10 no sustituido; cada R5 es independientemente acilo C1-10; R es acilo C1-10; y en donde uno o varios de los grupos OH está opcionalmente sustituido para reemplazar el H con un resto seleccionado de la TABLA 1, para preparar un medicamento para modular la actividad del receptor de androgenos (AR), con la condicion de que: i) cuando un Z en la posicion para respecto de X en el anillo aromático es C-Q; n es 1; J es G1, O, CH2, CHG1, CG12, S, NH, o NG1; Les A-D; A esO, S, NH, NG1, N+H2, o N+HG1; y D es H o un resto seleccionado de la TABLA 1, entonces el Z en la posicion para respecto de X en el otro anillo aromático es N, CH, CF, CCI, CBr, CI, COH, CNH2, COSO3H, COPO3H2, C-T, en donde cuando m es 1 y J2 es G1, O, CH2, CHG1, CG12, S, NH, o NG1, entonces L2 es H o A2-D2, en donde A2 es O, S, NH, NG1, N+H2, o N+HG1, y D2 es G1, R, un resto de formula (3), o C-Q, en donde cuando n es 1 y J es G1, O, CH2, CHG1, CG12, S, NH, o NG1, entonces L es H o A-D, en donde A es O, S, NH, NG1, N+H2, o N+HG1, y D es G1, R, un resto de formula (3); ii) cuando un Z en la posicion para respecto de X en el anillo aromático es CG1, COG1, CNHG1, CNG12, CSG1, CSOG1, o CSO2G1, entonces el Z en la posicion para respecto de X en el otro anillo aromático es N, CH, CF, CCI, CBr, CI, COH, CNH2, COSO3H, COPO3H2, C-T, en donde cuando m es 1 y J2 es G1, O, CH2, CHG1, CG12, S, NH, o NG1, entonces L2 es H o A2-D2, en donde A2 es O, S, NH, NG1, N+H2, o N+HG1; y D2 es G1, R, un resto de formula (3), o C-Q, en donde cuando n es 1 y J es G1, O, CH2, CHG1, CG12, S, NH, o NG1, entonces L es H o A-D, en donde A es O, S, NH, NG1, N+H2, o N+HG1, y D es G1, R, un resto de formula; y iii) cuando un Z en la posicion para respecto de X en el anillo aromático es C-T; m es 1; J2 es G1, O, CH2, CHG1, CG12, S, NH, o NG1; L2 es A2-D2; A2 es O, S, NH, NG1, N+H2, o N+HG1; y D2 es H o un resto seleccionado de la TABLA 1, entonces el Z en la posicion para respecto de X en el otro anillo aromático es N, CH, CF, CCI, CBr, CI, COH, CNH2, COSO3H, COPO3H2, C-Q, en donde cuando n es 1 y J es G1, O, CH2, CHG1, CG12, S, NH, o NG1, entonces L es H o A-D, en donde A es O, S, NH, NG1, N+H2, o N+HG1 y D es G1, R, un resto de formula o C-T, en donde cuando m es 1 y J2 es G1, O, CH2, CHG1, CG12, S, NH, o NG1, entonces L2 es H o A2-D2, en donde A2 es O, S, NH, NG1, N+H2, o N+HG1, y D2 es G1, R, o un resto de formula (3).
ARP110100034A 2010-01-06 2011-01-06 Agentes terapeuticos derivados de bisfenol que contienen un grupo aquiral y su uso en el tratamiento del cancer AR079846A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US28223810P 2010-01-06 2010-01-06

Publications (1)

Publication Number Publication Date
AR079846A1 true AR079846A1 (es) 2012-02-22

Family

ID=44305151

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP110100034A AR079846A1 (es) 2010-01-06 2011-01-06 Agentes terapeuticos derivados de bisfenol que contienen un grupo aquiral y su uso en el tratamiento del cancer

Country Status (6)

Country Link
US (1) US9388112B2 (es)
EP (1) EP2521707B1 (es)
JP (1) JP5940982B2 (es)
AR (1) AR079846A1 (es)
CA (1) CA2786319C (es)
WO (1) WO2011082487A1 (es)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105012282A (zh) 2008-07-02 2015-11-04 不列颠哥伦比亚癌症局分支机构 二缩水甘油醚衍生物治疗剂和它们的使用方法
AR079846A1 (es) 2010-01-06 2012-02-22 British Columbia Cancer Agency Agentes terapeuticos derivados de bisfenol que contienen un grupo aquiral y su uso en el tratamiento del cancer
WO2012139039A2 (en) 2011-04-08 2012-10-11 British Columbia Cancer Agency Branch Bisphenol compounds and methods for their use
US9365510B2 (en) 2012-04-16 2016-06-14 British Columbia Cancer Agency Branch Aziridine bisphenol ethers and related compounds and methods for their use
JP6100439B2 (ja) 2013-05-10 2017-03-22 ブリティッシュ コロンビア キャンサー エージェンシー ブランチ アンドロゲン受容体調節薬のエステル誘導体およびそれらの使用のための方法
KR20160054523A (ko) 2013-09-09 2016-05-16 브리티쉬 콜롬비아 캔써 에이전시 브랜치 암 영상화 및 치료용 할로겐화 화합물, 및 이들의 사용 방법
WO2016058082A1 (en) * 2014-10-14 2016-04-21 British Columbia Cancer Agency Branch 18f compounds for cancer imaging and methods for their use
WO2016058080A1 (en) * 2014-10-14 2016-04-21 British Columbia Cancer Agency Branch Fluoro-chloro bisphenol ether compounds and methods for their use
ES2907708T3 (es) 2015-01-13 2022-04-26 British Columbia Cancer Agency Branch Compuestos heterocíclicos para obtención de imágenes y tratamiento del cáncer y métodos para su uso
WO2016141458A1 (en) 2015-03-12 2016-09-15 British Columbia Cancer Agency Branch Bisphenol ether derivatives and methods for using the same
US20170298033A1 (en) 2016-04-15 2017-10-19 The University Of British Columbia Bisphenol derivatives and their use as androgen receptor activity modulators
WO2019226991A1 (en) 2018-05-25 2019-11-28 Essa Pharma, Inc. Androgen receptor modulators and methods for their use
CN108997093A (zh) * 2018-09-11 2018-12-14 中国科学院生态环境研究中心 一种双酚类化合物单取代脂肪醇及其合成方法
CN118684633A (zh) 2018-10-18 2024-09-24 埃萨制药股份有限公司 雄激素受体调节剂及其使用方法
US12109179B2 (en) 2019-03-28 2024-10-08 Essa Pharma Inc. Pharmaceutical compositions and combinations comprising inhibitors of the androgen receptor and uses thereof
WO2021212032A1 (en) 2020-04-17 2021-10-21 Essa Pharma, Inc. Solid forms of an n-terminal domain androgen receptor inhibitor and uses thereof
WO2023046283A1 (en) 2021-09-22 2023-03-30 Fundació Institut De Recerca Biomèdica (Irb Barcelona) Compounds and their use in a method for modulating ar (androgen receptor) transcriptional activity

Family Cites Families (57)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2571217A (en) 1951-10-16 Horace s
US2890189A (en) * 1954-06-14 1959-06-09 Johnson & Son Inc S C Alkali soluble resins and compositions containing the same
FR1389005A (fr) * 1963-01-09 1965-02-12 Bayer Ag Procédé perfectionné pour durcir des polyépoxydes
US4284574A (en) 1979-06-15 1981-08-18 Ciba-Geigy Corporation Diglycidyl ethers of di-secondary alcohols, their preparation, and curable compositions containing them
US4369298A (en) 1980-05-27 1983-01-18 Tokuyama Soda Kabushiki Kaisha Novel cured resin, process for production thereof, and lens composed of said resin from bis(alkyleneoxyphenyl)-diacrylate, bis(alkyleneoxyphenyl)diallyl ether, bis(alkyleneoxyphenyl)diallyl carbonate monomers
EP0056175B1 (en) 1981-01-13 1985-05-02 Teijin Limited Ion-permeable composite membrane and its use in selective separation
PL135932B2 (en) 1983-11-04 1986-01-31 Politechnika Warszawska Process for manufacturing polyfunctional polyols
US5753730A (en) 1986-12-15 1998-05-19 Mitsui Toatsu Chemicals, Inc. Plastic lenses having a high-refractive index, process for the preparation thereof and casting polymerization process for preparing sulfur-containing urethane resin lens and lens prepared thereby
JPH0832844B2 (ja) * 1987-02-09 1996-03-29 パイロツトインキ株式会社 筆記板用不透明性インキ
EP0290860B1 (en) 1987-04-27 1995-01-25 Mitsubishi Gas Chemical Company, Inc. Thermosetting resin composition
US5155196A (en) 1987-06-01 1992-10-13 The Dow Chemical Company Polymer resulting from the cure of a preformed chromene-containing mixture
KR910003821B1 (ko) * 1987-06-01 1991-06-12 더 다우 케미칼 캄파니 하이드록시방향족 화합물의 프로파르길 에테르를 제조하는 방법
DE3821585A1 (de) 1987-09-13 1989-03-23 Hoechst Ag Positiv arbeitendes strahlungsempfindliches gemisch und daraus hergestelltes strahlungsempfindliches aufzeichnungsmaterial fuer hochenergetische strahlung
US4855184A (en) 1988-02-02 1989-08-08 Minnesota Mining And Manufacturing Company Radiation-curable protective coating composition
DE3939760A1 (de) 1989-12-01 1991-06-06 Bayer Ag Verfahren zur lackierung von kunststoffen, lackierte kunststoffe und die verwendung von hierzu geeigneten haftvermittlern
EP0515128A1 (en) 1991-05-23 1992-11-25 Konica Corporation Silver halide color photographic light-sensitive material
JPH0649473A (ja) 1992-08-04 1994-02-22 Asahi Chem Ind Co Ltd 冷媒組成物
DE4323512A1 (de) 1992-09-01 1994-04-28 Agfa Gevaert Ag Fotografisches Aufzeichnungsmaterial
JPH09176240A (ja) 1995-12-27 1997-07-08 Mitsubishi Chem Corp 光重合性組成物
TW482756B (en) 1997-02-07 2002-04-11 Shell Int Research Process for the manufacture of intermediates for epoxy compounds, process for the manufacture of epoxy compounds and epoxy compounds obtained therewith
JPH10316803A (ja) 1997-05-16 1998-12-02 Teijin Chem Ltd 難燃性樹脂組成物
IL125840A (en) 1997-08-22 2002-12-01 Teijin Chemicals Ltd Bromine compound production method
JPH11166087A (ja) 1997-12-04 1999-06-22 Teijin Chem Ltd 難燃性樹脂組成物
CA2302169A1 (en) 1998-06-30 2000-01-13 The University Of British Columbia Inhibitors of androgen-independent activation of androgen receptor
US6245117B1 (en) 1998-08-07 2001-06-12 Ipposha Oil Industries Co., Ltd. Modifier of cellulose fibers and modification method of cellulose fibers
US6218430B1 (en) 1998-08-24 2001-04-17 Ligand Pharmaceuticals Incorporated Vitamin D3 mimics
JP3795679B2 (ja) 1998-09-01 2006-07-12 帝人化成株式会社 臭素化合物の製造方法
JP2003511467A (ja) 1999-10-14 2003-03-25 ブリストル−マイヤーズ スクイブ カンパニー アンドロゲンレセプターリガンド結合ドメインの結晶構造
US6534621B2 (en) 2000-05-18 2003-03-18 Dow Global Technologies Inc. Process for manufacturing a hydroxyester derivative intermediate and epoxy resins prepared therefrom
US6472436B1 (en) 2000-07-17 2002-10-29 The Salk Institute For Biological Studies Methods for protecting cells from amyloid toxicity and for inhibiting amyloid protein production
US6756400B2 (en) 2000-08-31 2004-06-29 Theravance, Inc. Sodium channel modulators
US6646102B2 (en) 2001-07-05 2003-11-11 Dow Global Technologies Inc. Process for manufacturing an alpha-dihydroxy derivative and epoxy resins prepared therefrom
US20030092724A1 (en) * 2001-09-18 2003-05-15 Huaihung Kao Combination sustained release-immediate release oral dosage forms with an opioid analgesic and a non-opioid analgesic
AU2003217304A1 (en) 2002-02-28 2003-09-16 The University Of Tennessee Research Corporation Radiolabeled selective androgen receptor modulators and their use in prostate cancer imaging and therapy
GB0324551D0 (en) 2003-10-21 2003-11-26 Karobio Ab Novel compounds
CA2555597C (en) 2004-02-13 2016-06-14 The University Of British Columbia Radiolabeled compounds and compositions, their precursors and methods for their production
JP2005325301A (ja) * 2004-05-17 2005-11-24 Fuji Photo Film Co Ltd セルロースアシレートドープ組成物、およびセルロースアシレートフィルム
US20090105349A1 (en) 2004-08-18 2009-04-23 Warner-Lambert Company Llc Androgen modulators
JP2006208607A (ja) 2005-01-26 2006-08-10 Fuji Photo Film Co Ltd パターン形成材料、並びにパターン形成装置及び永久パターン形成方法
JP4753601B2 (ja) 2005-03-23 2011-08-24 旭化成イーマテリアルズ株式会社 感光性組成物
EP1717235A3 (en) 2005-04-29 2007-02-28 Bioprojet Phenoxypropylpiperidines and -pyrrolidines and their use as histamine H3-receptor ligands
FR2885904B1 (fr) 2005-05-19 2007-07-06 Aventis Pharma Sa Nouveaux derives du fluorene, compositions les contenant et utilisation
JP2007290980A (ja) 2006-04-21 2007-11-08 Shin Etsu Chem Co Ltd 含フッ素(メタ)アクリル酸エステル
TW200819421A (en) * 2006-10-31 2008-05-01 Univ Nat Chunghsing The method of synthesizing biphenol A, BPA having di-alkoxyl group by using polycarbonate or its waste
JP2010519369A (ja) 2007-02-20 2010-06-03 ビーエーエスエフ ソシエタス・ヨーロピア 高屈折率モノマー、それらの組成物及び使用
CN105012282A (zh) 2008-07-02 2015-11-04 不列颠哥伦比亚癌症局分支机构 二缩水甘油醚衍生物治疗剂和它们的使用方法
US20130109758A1 (en) 2010-01-06 2013-05-02 The University Of British Columbia Bisphenol derivative therapeutics and methods for their use
AR079846A1 (es) 2010-01-06 2012-02-22 British Columbia Cancer Agency Agentes terapeuticos derivados de bisfenol que contienen un grupo aquiral y su uso en el tratamiento del cancer
WO2012139039A2 (en) 2011-04-08 2012-10-11 British Columbia Cancer Agency Branch Bisphenol compounds and methods for their use
WO2012145330A1 (en) 2011-04-18 2012-10-26 The University Of British Columbia Fluorene-9-bisphenol compounds and methods for their use
WO2012145328A1 (en) 2011-04-18 2012-10-26 The University Of British Columbia Dibenzylphenyl compounds and methods for their use
EP2744773B1 (en) 2011-08-19 2016-11-02 British Columbia Cancer Agency Branch Fluorinated bisphenol ether compounds and methods for their use
WO2013028791A1 (en) 2011-08-22 2013-02-28 British Columbia Cancer Agency Branch 18f compounds for cancer imaging and methods for their use
US9365510B2 (en) 2012-04-16 2016-06-14 British Columbia Cancer Agency Branch Aziridine bisphenol ethers and related compounds and methods for their use
JP6100439B2 (ja) 2013-05-10 2017-03-22 ブリティッシュ コロンビア キャンサー エージェンシー ブランチ アンドロゲン受容体調節薬のエステル誘導体およびそれらの使用のための方法
US20150010469A1 (en) 2013-07-03 2015-01-08 British Columbia Cancer Agency Branch Bisphenol ether compounds with novel bridging groups and methods for their use
KR20160054523A (ko) 2013-09-09 2016-05-16 브리티쉬 콜롬비아 캔써 에이전시 브랜치 암 영상화 및 치료용 할로겐화 화합물, 및 이들의 사용 방법

Also Published As

Publication number Publication date
US9388112B2 (en) 2016-07-12
EP2521707A1 (en) 2012-11-14
JP2013516435A (ja) 2013-05-13
WO2011082487A8 (en) 2013-01-17
US20130131167A1 (en) 2013-05-23
JP5940982B2 (ja) 2016-06-29
CA2786319C (en) 2019-03-12
EP2521707B1 (en) 2017-06-14
EP2521707A4 (en) 2013-07-24
WO2011082487A1 (en) 2011-07-14
CA2786319A1 (en) 2011-07-14

Similar Documents

Publication Publication Date Title
AR079975A1 (es) Agentes terapeuticos derivados de bisfenol u metodos para su uso, composiciones farmaceuticas y uso de los mismos
AR075396A1 (es) Derivados de quinazolinas y composiciones farmaceuticas
AR056986A1 (es) Aza heterociclos como inhibidores de quinasas. procedimiento de obtencion y composiciones farmaceuticas
CL2011002859A1 (es) Compuestos espironucleosidos, inhibidores del virus vhc; composicion farmaceutica de dichos compuestos; uso del compuesto para tratar la hepatitis c.
CU20110216A7 (es) Derivados aminobutíricos sustituidos como inhibidores de neprilisina
ECSP11011560A (es) Derivados amino-propiónicos sustituidos como inhibidores de neprilisina
AR049399A1 (es) Difenilimidazopirimidina e -imidazol aminas como inhibidores de b-secretasa y metodo de obtencion de los mismos
AR085039A1 (es) DERIVADOS DE PURINA, COMPOSICIONES FARMACEUTICAS QUE LOS COMPRENDEN Y SU USO EN LA PREPARACION DE MEDICAMENTOS PARA TRATAR ENFERMEDADES MODULADAS POR LA INHIBICION DE LA PI3K DE CLASE I Y/O mTOR
AR062792A1 (es) Derivados azetidinona y metodos de uso de estos
AR051326A1 (es) Pirazolobenzodiazepinas disustituidas
AR067757A1 (es) Derivados de imidazo[4,5-c]piridin-2-ona, composiciones farmaceuticas que los contienen, procedimiento para su preparacion y uso de los mismos como agentes antivirales.
AR063119A1 (es) Derivados de piridinonas sustituidas, composiciones farmaceuticas que los contienen y usos como antagonistas en trastornos asociados a receptores del tipo i de la hormona de melanina(mch-1 o mchr-1)
RU2011133900A (ru) Аналоги циклоспорина для предупреждения или лечения инфекции гепатита с
ES2660001T3 (es) Comprimido estable que contiene un derivado de 4,5-epoximorfinano
AR043998A1 (es) Acidos fenoxiaceticos
UY31730A (es) Derivados polisustituidos de 6-heteroaril-imidazo[1,2-a]piridinas, su preparación y su aplicación en terapéutica.
AR092269A1 (es) Sulfamoilarilamidas y su uso como medicamentos para el tratamiento de la hepatitis b
CR20120237A (es) Derivados del ácido carbamoil-metil-amino-acético sustituido como inhibidores de nep novedosos
AR070429A1 (es) Derivados de 1,3 tiazol como inhibidores de estearoil - coa -desaturasa
AR078049A1 (es) Moduladores de lxr
AR086357A1 (es) Derivados de indazol sustituidos activos como inhibidores de quinasas
UY33731A (es) ?derivados de ácido amino-fenil-pentanoico sustituidos como inhibidores de nep?
AR052256A1 (es) Derivados de tetrahidropirano y su uso como agentes antidiabeticos
CO6230986A2 (es) Compuesto de 4-piridinona y su uso para cancer
RU2014115796A (ru) Модуляторы ror-гамма

Legal Events

Date Code Title Description
FB Suspension of granting procedure