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 cancerInfo
- 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
Links
- 239000003814 drug Substances 0.000 title abstract 2
- 229930185605 Bisphenol Natural products 0.000 title 1
- 206010028980 Neoplasm Diseases 0.000 title 1
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 title 1
- 201000011510 cancer Diseases 0.000 title 1
- 229940124597 therapeutic agent Drugs 0.000 title 1
- 125000003118 aryl group Chemical group 0.000 abstract 9
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 4
- 102100030794 Conserved oligomeric Golgi complex subunit 1 Human genes 0.000 abstract 3
- 101100329534 Haloarcula marismortui (strain ATCC 43049 / DSM 3752 / JCM 8966 / VKM B-1809) csg1 gene Proteins 0.000 abstract 3
- 101000920124 Homo sapiens Conserved oligomeric Golgi complex subunit 1 Proteins 0.000 abstract 3
- 101100422777 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) SUR1 gene Proteins 0.000 abstract 3
- 125000002252 acyl group Chemical group 0.000 abstract 3
- 229920006395 saturated elastomer Polymers 0.000 abstract 3
- 229910006069 SO3H Inorganic materials 0.000 abstract 2
- 102000001307 androgen receptors Human genes 0.000 abstract 2
- 108010080146 androgen receptors Proteins 0.000 abstract 2
- AOJDZKCUAATBGE-UHFFFAOYSA-N bromomethane Chemical compound Br[CH2] AOJDZKCUAATBGE-UHFFFAOYSA-N 0.000 abstract 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 2
- HFPGRVHMFSJMOL-UHFFFAOYSA-N dibromomethane Chemical compound Br[CH]Br HFPGRVHMFSJMOL-UHFFFAOYSA-N 0.000 abstract 2
- 125000000896 monocarboxylic acid group Chemical group 0.000 abstract 2
- 125000001424 substituent group Chemical group 0.000 abstract 2
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 abstract 2
- XXJGBENTLXFVFI-UHFFFAOYSA-N 1-amino-methylene Chemical compound N[CH2] XXJGBENTLXFVFI-UHFFFAOYSA-N 0.000 abstract 1
- 101100277337 Arabidopsis thaliana DDM1 gene Chemical group 0.000 abstract 1
- 101100294106 Caenorhabditis elegans nhr-3 gene Proteins 0.000 abstract 1
- 101100294115 Caenorhabditis elegans nhr-4 gene Proteins 0.000 abstract 1
- 101100516554 Caenorhabditis elegans nhr-5 gene Proteins 0.000 abstract 1
- 101100516563 Caenorhabditis elegans nhr-6 gene Proteins 0.000 abstract 1
- 102100035249 Carbonyl reductase [NADPH] 3 Human genes 0.000 abstract 1
- 101000737274 Homo sapiens Carbonyl reductase [NADPH] 3 Proteins 0.000 abstract 1
- 101100533890 Hypocrea jecorina (strain QM6a) sor3 gene Proteins 0.000 abstract 1
- 101100533874 Hypocrea jecorina (strain QM6a) sor5 gene Proteins 0.000 abstract 1
- 206010060862 Prostate cancer Diseases 0.000 abstract 1
- 208000000236 Prostatic Neoplasms Diseases 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 101150113676 chr1 gene Chemical group 0.000 abstract 1
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- CBOIHMRHGLHBPB-UHFFFAOYSA-N hydroxymethyl Chemical compound O[CH2] CBOIHMRHGLHBPB-UHFFFAOYSA-N 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- ROWMQJJMCWDJDT-UHFFFAOYSA-N tribromomethane Chemical compound Br[C](Br)Br ROWMQJJMCWDJDT-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C57/00—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
- C07C57/30—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing six-membered aromatic rings
- C07C57/38—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing six-membered aromatic rings polycyclic
-
- 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
- A61K31/075—Ethers or acetals
- A61K31/085—Ethers or acetals having an ether linkage to aromatic ring nuclear carbon
- A61K31/09—Ethers or acetals having an ether linkage to aromatic ring nuclear carbon having two or more such linkages
-
- 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
- A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
- A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
- A61K31/22—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/08—Drugs for disorders of the urinary system of the prostate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/10—Anti-acne agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/14—Drugs for dermatological disorders for baldness or alopecia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- 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
- A61P5/24—Drugs for disorders of the endocrine system of the sex hormones
- A61P5/28—Antiandrogens
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C15/00—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts
- C07C15/12—Polycyclic non-condensed hydrocarbons
- C07C15/16—Polycyclic non-condensed hydrocarbons containing at least two phenyl groups linked by one single acyclic carbon atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/20—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring
- C07C43/225—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/20—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring
- C07C43/23—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing hydroxy or O-metal groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/62—Halogen-containing esters
- C07C69/63—Halogen-containing esters of saturated acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing 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)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Epidemiology (AREA)
- Dermatology (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Ophthalmology & Optometry (AREA)
- Diabetes (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).
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)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| HUE034458T2 (en) | 2008-07-02 | 2018-02-28 | British Columbia Cancer Agency Branch | Diglycidyl ether derivatives, therapeutics and methods for their use |
| WO2011082487A1 (en) | 2010-01-06 | 2011-07-14 | British Columbia Cancer Agency Branch | Bisphenol derivatives and their use as androgen receptor activity modulators |
| US20140248263A1 (en) * | 2011-04-08 | 2014-09-04 | The University Of British Columbia | 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 |
| AP2015008838A0 (en) * | 2013-05-10 | 2015-11-30 | Univ British Columbia Industry Liaison Office | Ester derivatives of androgen receptor modulators and methods for their use |
| US9375496B2 (en) | 2013-09-09 | 2016-06-28 | British Columbia Cancer Agency Branch | Halogenated compounds for cancer imaging and treatment and methods for their use |
| 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 |
| PT3988541T (pt) | 2015-01-13 | 2024-09-03 | British Columbia Cancer Agency Branch | Compostos heterocíclicos para visualização e tratamento de cancro e métodos para o seu uso |
| US10471023B2 (en) | 2015-03-12 | 2019-11-12 | 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 |
| US11485713B2 (en) | 2018-05-25 | 2022-11-01 | 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 |
| US20210323931A1 (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)
| 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 |
| DE3170223D1 (en) | 1981-01-13 | 1985-06-05 | Teijin Ltd | 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 |
| US4904760A (en) | 1987-04-27 | 1990-02-27 | Mitsubishi Gas Chemical Co., Inc. | Thermosetting resin composition from cyanate ester and non-branched aromatic compound |
| WO1988009782A1 (en) * | 1987-06-01 | 1988-12-15 | The Dow Chemical Company | Process for making propargyl ethers of hydroxyaromatic compounds |
| US5155196A (en) | 1987-06-01 | 1992-10-13 | The Dow Chemical Company | Polymer resulting from the cure of a preformed chromene-containing mixture |
| 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 |
| AR011626A1 (es) | 1997-02-07 | 2000-08-30 | Shell Int Research | Un procedimiento para la elaboracion de compuestos epoxidos, resinas epoxidas obtenidas mediante dicho procedimiento y un procedimiento para laelaboracion de compuestos intermedios para la elaboracion de compuestos epoxidos |
| 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 |
| AU4494399A (en) | 1998-06-30 | 2000-01-24 | University Of British Columbia, The | 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 |
| WO2001027622A1 (en) | 1999-10-14 | 2001-04-19 | Bristol-Myers Squibb Company | Crystallographic structure of the androgen receptor ligand binding domain |
| 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 |
| US7344700B2 (en) | 2002-02-28 | 2008-03-18 | 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 |
| JP2007524677A (ja) | 2004-02-13 | 2007-08-30 | ザ ユニバーシティ オブ ブリティッシュ コロンビア | 放射性標識化合物及び組成物、それらの前駆体及びそれらの製造方法 |
| 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 |
| WO2006018723A2 (en) | 2004-08-18 | 2006-02-23 | 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 |
| HUE034458T2 (en) | 2008-07-02 | 2018-02-28 | British Columbia Cancer Agency Branch | Diglycidyl ether derivatives, therapeutics and methods for their use |
| WO2011082487A1 (en) | 2010-01-06 | 2011-07-14 | British Columbia Cancer Agency Branch | Bisphenol derivatives and their use as androgen receptor activity modulators |
| WO2011082488A1 (en) | 2010-01-06 | 2011-07-14 | British Columbia Cancer Agency Branch | Bisphenol derivative therapeutics and methods for their use |
| US20140248263A1 (en) | 2011-04-08 | 2014-09-04 | The University Of British Columbia | 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 |
| AP2015008838A0 (en) | 2013-05-10 | 2015-11-30 | Univ British Columbia Industry Liaison Office | Ester derivatives of androgen receptor modulators and methods for their use |
| 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 |
| US9375496B2 (en) | 2013-09-09 | 2016-06-28 | British Columbia Cancer Agency Branch | Halogenated compounds for cancer imaging and treatment and methods for their use |
-
2011
- 2011-01-06 WO PCT/CA2011/000019 patent/WO2011082487A1/en not_active Ceased
- 2011-01-06 EP EP11731645.5A patent/EP2521707B1/en not_active Not-in-force
- 2011-01-06 AR ARP110100034A patent/AR079846A1/es unknown
- 2011-01-06 CA CA2786319A patent/CA2786319C/en active Active
- 2011-01-06 US US13/520,729 patent/US9388112B2/en active Active
- 2011-01-06 JP JP2012547415A patent/JP5940982B2/ja active Active
Also Published As
| Publication number | Publication date |
|---|---|
| US20130131167A1 (en) | 2013-05-23 |
| EP2521707A4 (en) | 2013-07-24 |
| EP2521707B1 (en) | 2017-06-14 |
| JP2013516435A (ja) | 2013-05-13 |
| EP2521707A1 (en) | 2012-11-14 |
| JP5940982B2 (ja) | 2016-06-29 |
| WO2011082487A8 (en) | 2013-01-17 |
| US9388112B2 (en) | 2016-07-12 |
| WO2011082487A1 (en) | 2011-07-14 |
| CA2786319A1 (en) | 2011-07-14 |
| CA2786319C (en) | 2019-03-12 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AR079846A1 (es) | Agentes terapeuticos derivados de bisfenol que contienen un grupo aquiral y su uso en el tratamiento del cancer | |
| 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. | |
| CO6470846A2 (es) | Derivados aminobut´ricos sustituidos como inhibidores de neprilisina | |
| AR126076A1 (es) | Compuestos de benzotia(di)azepina y su uso como moduladores del ácido biliar | |
| 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 | |
| NI201200012A (es) | Profármacos que comprenden un conjugado de insulina - conector | |
| PE20250759A1 (es) | Conjugado de anticuerpo bispecifico-farmaco de camptotecina y uso farmaceutico de este | |
| 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. | |
| ES2660001T3 (es) | Comprimido estable que contiene un derivado de 4,5-epoximorfinano | |
| AR043998A1 (es) | Acidos fenoxiaceticos | |
| 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 | |
| HN2011003097A (es) | Derivados amino-propionicos sustituidos como inhibidores de neprilisina | |
| AR070429A1 (es) | Derivados de 1,3 tiazol como inhibidores de estearoil - coa -desaturasa | |
| AR090493A1 (es) | Acidos indaniloxidihidrobenzofuranilaceticos | |
| AR078049A1 (es) | Moduladores de lxr | |
| AR086357A1 (es) | Derivados de indazol sustituidos activos como inhibidores de quinasas | |
| AR078151A1 (es) | Conjugados de acidos grasos y niacina, composiciones farmaceuticas que los contienen y uso de los mismos en el tratamiento de enfermedades metabolicas. | |
| AR072816A1 (es) | Derivados heterociclicos de piridazina, inhibidores de smo, composiciones farmaceuticas que los comprenden y uso de los mismos como agentes anticancer. | |
| UY33731A (es) | ?derivados de ácido amino-fenil-pentanoico sustituidos como inhibidores de nep? |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FB | Suspension of granting procedure |