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ME02754B - Ligandi opioidnih receptora i postupci njihove upotrebe i pripreme - Google Patents

Ligandi opioidnih receptora i postupci njihove upotrebe i pripreme

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Publication number
ME02754B
ME02754B MEP-2017-129A MEP2017129A ME02754B ME 02754 B ME02754 B ME 02754B ME P2017129 A MEP2017129 A ME P2017129A ME 02754 B ME02754 B ME 02754B
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ME
Montenegro
Prior art keywords
alkyl
pharmaceutically acceptable
acceptable salt
compound
compound according
Prior art date
Application number
MEP-2017-129A
Other languages
German (de)
English (en)
French (fr)
Inventor
Dennis Yamashita
Dimitar Gotchev
Philip Pitis
Xiao-Tao Chen
Guodong Liu
Catherine C K Yuan
Original Assignee
Trevena Inc
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First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=46877853&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=ME02754(B) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Trevena Inc filed Critical Trevena Inc
Publication of ME02754B publication Critical patent/ME02754B/me

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    • A61K31/35Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
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    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/35Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
    • A61K31/352Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. methantheline 
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    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
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    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4436Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a heterocyclic ring having sulfur as a ring hetero atom
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    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/444Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
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  • Chemical & Material Sciences (AREA)
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  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
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  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Claims (20)

1. Jedinjenje formule IV-1, ili neka njegova farmaceutski prihvatljiva so,: u kojoj: R21 i R22 su nezavisno H ili CH3; A4 je neki opciono supstituisan cikl formule C(CH2)n, u kojoj n = 2-5, pri čemu je opciona supstitucija halo, cijano, C1-C6 alkil, C1-C6 razgranat alkil, halogenovan C1-C6 alkil, hidroksil, C1-C6 alkiloksi, amino, ili C1-C6 alkilamino; B3 je H ili neki opciono supstituisan C1-C6 alkil, pri čemu je opciona supstitucija halo, hidroksi ili C1-C6 alkoksi; B4 je C1-C6 alkilen; D1 je neki opciono supstituisan monociklični ili biciklični aril ili heteroaril, u kom je svaki prsten neki 5, 6 ili 7-člani prsten, a opciona supstitucija je halo, cijano, C1-C6 alkil, C1-C6 razgranat alkil, halogenovan C1-C6 alkil, hidroksil, C1-C6 alkiloksi, amino, ili C1-C6 alkilamino; i B5 je neki opciono supstituisan monociklični ili biciklični aril ili heteroaril, u kom je svaki prsten neki 5, 6, ili 7-člani prsten, a opciona supstitucija je halo, cijano, C1-C6 alkil, C1-C6 razgranat alkil, halogenovan C1-C6 alkil, hidroksil, C1-C6 alkiloksi, amino, ili C1-C6 alkilamino.
2.Jedinjenje prema zahtevu 1, ili neka njegova farmaceutski prihvatljiva so, koje ima strukturu formule VIII: u kojoj su R26 i R27 nezavisno H ili neki njegov izotop.
3.Jedinjenje prema zahtevu 2, ili neka njegova farmaceutski prihvatljiva so, pri čemu jedinjenje ima formulu IX
4.Jedinjenje prema zahtevima 2 ili 3, ili neka njegova farmaceutski prihvatljiva so, pri čemu jedinjenje ima formulu VII-l
5.Jedinjenje prema nekom od zahteva 2-4, ili neka njegova farmaceutski prihvatljiva so, pri čemu jedinjenje ima formulu X
6. Jedinjenje prema nekom od zahteva 1-5, ili neka njegova farmaceutski prihvatljiva so, kod kog je D1 neki opciono supstituisan fenil, pri čemu je opciona supstitucija halo, cijano, C1-C6 alkil, C1-C6 razgranat alkil, halogenovan C1-C6 alkil, hidroksil, C1-C6 alkiloksi, amino, ili C1-C6 alkilamino ili neki opciono supstituisan piridil, pri čemu je opciona supstitucija halo, cijano, C1-C6 alkil, C1-C6 razgranat alkil, halogenovan C1-C6 alkil, hidroksil, C1-C6 alkiloksi, amino, ili C1-C6 alkilamino.
7.Jedinjenje prema nekom od zahteva 1-5, ili neka njegova farmaceutski prihvatljiva so, kod kog je B5 neki opciono supstituisan monociklični ili biciklični heteroaril, u kom je svaki prsten neki 5, 6, ili 7- člani prsten, a opciona supstitucija je halo, cijano, C1-C6 alkil, C1-C6 razgranat alkil, halogenovan C1-C6alkil, hidroksil, C1-C6 alkiloksi, amino, ili C1-C6 alkilamino.
8.Jedinjenje prema nekom od zahteva 1-5, ili neka njegova farmaceutski prihvatljiva so, kod kog je B5 neki opciono supstituisan aril ili heteroaril odabran iz grupe koju čine pri čemu je opciona supstitucija halo, cijano, C1-C6 alkil, C1-C6 razgranat alkil, halogenovan C1-C6 alkil, hidroksil, C1-C6 alkiloksi, amino, ili C1-C6 alkilamino.
9.Jedinjenje prema zahtevima 1-5, ili neka njegova farmaceutski prihvatljiva so, kod kog je B5 odabran iz grupe koju čine u kojima R23, R24, i R30 su svaki nezavisno nula, H, OH, halo, razgranat ili nerazgranat C1-C6 alkil, cijano, C1-C6alkoksi, amino, C1-C6 haloalkil, ili, R23 i R24 zajedno obrazuju neki aril, heteroaril ili ciki koji je vezan za jedan ili više atoma B5; a R25 je H ili neki opciono supstituisan razgranat ili nerazgranat alkil, pri čemu je opciona supstitucija halo, hidroksi ili C1-C3 alkoksi.
10.Jedinjenje prema zahtevu 9, ili neka njegova farmaceutski prihvatljiva so, kod kog su R23, R24, i R30 svaki nezavisno H, NH2, OH, CI, Br, F, I, OMe, CN, ili CH3.
11.Jedinjenje prema zahtevu 9, ili neka njegova farmaceutski prihvatljiva so, kod kog B5 predstavlja
12.Jedinjenje prema zahtevu 9 ili 11, ili neka njegova farmaceutski prihvatljiva so, kod kog R23 predstavlja C1-C6 alkoksi.
13.Jedinjenje prema nekom od zahteva 1-12, ili neka njegova farmaceutski prihvatljiva so, kod kog B3 predstavlja H ili C1-C6 alkil.
14.Jedinjenje prema zahtevu 1, ili neka njegova farmaceutski prihvatljiva so, koje ima formulu:
15.Jedinjenje prema zahtevu 1, ili neka njegova farmaceutski prihvatljiva so, koje ima formulu:
16.Jedinjenje prema zahtevu 1, ili neka njegova farmaceutski prihvatljiva so, koje ima formulu:
17.Jedinjenje prema zahtevu 1, ili neka njegova farmaceutski prihvatljiva so, koje ima formulu:
18.Farmaceutska kompozicija koja obuhvata jedinjenje, ili neku njegovu farmaceutski prihvatljivu so, prema bilo kom od zahteva 1-17 i neki farmaceutski prihvatljiv nosač.
19.Jedinjenje ili neka njegova farmaceutski prihvatljiva so, ili kompozicija prema bilo kom od zahteva 1-18 za upotrebu u tretiranju bola.
20. Postupak pripreme jedinjenja, ili neke njegove farmaceutski prihvatljive soli, prema zahtevu 2, gde R26 i R27 predstavljaju H, pri čemu taj postupak obuhvata: dovođenje u kontakt pod pogodnim uslovima za obrazovanje jedinjenja koje ima strukturu pod pogodnim uslovima za obrazovanje jedinjenja koje ima strukturu
MEP-2017-129A 2011-03-23 2012-03-23 Ligandi opioidnih receptora i postupci njihove upotrebe i pripreme ME02754B (me)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US201161466809P 2011-03-23 2011-03-23
US201261596808P 2012-02-09 2012-02-09
PCT/US2012/030327 WO2012129495A1 (en) 2011-03-23 2012-03-23 Opioid receptor ligands and methods of using and making same
EP12760456.9A EP2688403B1 (en) 2011-03-23 2012-03-23 Opioid receptor ligands and methods of using and making same

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Families Citing this family (60)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PT3290415T (pt) * 2011-03-23 2021-03-29 Trevena Inc Ligandos de recetores opioides e métodos de utilização e fabrico dos mesmos
ES2553449T3 (es) 2011-07-06 2015-12-09 Gilead Sciences, Inc. Compuestos para el tratamiento de VIH
TWI694071B (zh) 2013-03-01 2020-05-21 美商基利科學股份有限公司 治療反轉錄病毒科(Retroviridae)病毒感染之治療性化合物
US10202353B2 (en) 2014-02-28 2019-02-12 Gilead Sciences, Inc. Therapeutic compounds
EP3350166A4 (en) 2015-09-16 2019-05-01 Metacrine, Inc. FARNESOID-X RECEPTOR AGONISTS AND USES THEREOF
JP6905530B2 (ja) 2015-09-16 2021-07-21 メタクリン,インク. ファルネソイドx受容体アゴニストとその使用
EP3350158A4 (en) 2015-09-16 2019-05-08 Metacrine, Inc. Farnesoid x receptor agonists and uses thereof
CN106588899B (zh) * 2015-10-15 2019-11-15 江苏恒瑞医药股份有限公司 吡啶基取代的6-氧杂螺[4.5]癸烷类衍生物、其制备方法及其在医药上的应用
ES2772689T3 (es) * 2015-10-15 2020-07-08 Jiangsu Hengrui Medicine Co Derivado de oxa espiro, método de preparación del mismo y aplicaciones del mismo en medicamentos
CN108366997A (zh) * 2015-12-14 2018-08-03 特维娜有限公司 治疗痛觉过敏的方法
WO2017105881A1 (en) * 2015-12-15 2017-06-22 NeuForm Pharmaceuticals, Inc. Deuterated compounds for treating pain
CN108601775A (zh) * 2015-12-17 2018-09-28 特维娜有限公司 阿片受体配体和细胞色素p450抑制剂的组合
CN107098876B (zh) * 2016-02-23 2021-04-06 江苏恒瑞医药股份有限公司 苯基丙酰胺类衍生物、其制备方法及其在医药上的应用
CN109689646B (zh) * 2016-07-01 2022-09-02 纽弗姆制药有限公司 用于治疗疼痛的氘代化合物
PE20211427A1 (es) 2016-08-19 2021-08-03 Gilead Sciences Inc Compuestos terapeuticos utiles para el tratamiento profilatico o terapeutico de una infeccion por el virus del vih
EP3555072A1 (en) * 2016-12-16 2019-10-23 Esteve Pharmaceuticals, S.A. Tetrahydropyran and tetrahydrothiopyran amide derivatives having multimodal activity against pain
EP3582783B1 (en) * 2017-02-17 2023-06-07 Trevena, Inc. 7-membered aza-heterocyclic containing delta-opioid receptor modulating compounds, methods of using and making the same
KR20190129867A (ko) 2017-02-17 2019-11-20 트레베나, 인코포레이티드. 5-원 아자-헤테로고리 함유 델타-오피오이드 수용체 조절 화합물, 및 그의 사용 및 제조 방법
IL269068B (en) 2017-03-15 2022-09-01 Metacrine Inc Paranoid x receptor agonists and uses thereof
SG11201908330PA (en) 2017-03-15 2019-10-30 Metacrine Inc Farnesoid x receptor agonists and uses thereof
BR112019020691A2 (pt) * 2017-04-14 2020-05-12 Jiangsu Hengrui Medicine Co., Ltd. Composição farmacêutica contendo agonista do mor e agonista do kor, e usos da mesma
CN108727347B (zh) * 2017-04-14 2020-06-16 江苏恒瑞医药股份有限公司 一种阿片样物质受体(mor)激动剂的晶型及其制备方法
WO2018188643A1 (zh) * 2017-04-14 2018-10-18 江苏恒瑞医药股份有限公司 一种阿片样物质受体(mor)激动剂的盐、其富马酸盐i晶型及制备方法
CN115124520A (zh) * 2017-07-04 2022-09-30 四川海思科制药有限公司 阿片受体激动剂及其应用
AR112412A1 (es) 2017-08-17 2019-10-23 Gilead Sciences Inc Formas de sal de colina de un inhibidor de la cápside del vih
AR112413A1 (es) 2017-08-17 2019-10-23 Gilead Sciences Inc Formas sólidas de un inhibidor de la cápside del vih
WO2019052557A1 (zh) 2017-09-18 2019-03-21 上海华汇拓医药科技有限公司 μ-阿片受体激动剂及其制备方法和在医药领域的应用
MX395589B (es) * 2017-09-28 2025-03-25 Jiangsu Hengrui Medicine Co Método para preparar derivado de oxaespirociclo e intermediario del mismo.
CN111148515B (zh) * 2017-10-13 2022-07-19 山东绿叶制药有限公司 2,6-二氧杂螺[4,5]癸烷类衍生物、其制备方法及其在医药上的应用
BR112020010429A2 (pt) 2017-12-06 2020-11-24 Jiangsu Hengrui Medicine Co., Ltd. uso de agonista de kor em combinação com agonista de mor na preparação de fármaco para tratamento da dor
BR112020015712A2 (pt) 2018-02-05 2020-12-08 Alkermes, Inc. Compostos para tratamento de dor
EP3752495B1 (en) 2018-02-15 2023-07-19 Gilead Sciences, Inc. Pyridine derivatives and their use for treating hiv infection
TWI823164B (zh) 2018-02-16 2023-11-21 美商基利科學股份有限公司 用於製備有療效化合物之方法及中間物
CN111836807A (zh) * 2018-04-28 2020-10-27 四川科伦博泰生物医药股份有限公司 氧杂螺环类化合物及其制备方法和用途
CN111163778B (zh) * 2018-05-14 2023-01-24 江苏恒瑞医药股份有限公司 一种mor受体激动剂药物组合物
CA3103522C (en) 2018-07-16 2023-11-21 Gilead Sciences, Inc. Capsid inhibitors for the treatment of hiv
HRP20251321T1 (hr) 2018-09-18 2025-12-05 Eli Lilly And Company Agonisti farnezoid x receptora i njihova primjena
WO2020073985A1 (zh) * 2018-10-12 2020-04-16 江苏恒瑞医药股份有限公司 一种阿片样物质受体(mor)激动剂的结晶形式及制备方法
CN112638906B (zh) * 2018-10-12 2022-05-27 江苏恒瑞医药股份有限公司 一种阿片样物质受体(mor)激动剂的结晶形式及制备方法
WO2020147848A1 (zh) * 2019-01-17 2020-07-23 上海海雁医药科技有限公司 三环取代的氧杂螺环衍生物、其制法与医药上的用途
CN111662284B (zh) * 2019-03-06 2021-08-10 上海海雁医药科技有限公司 双杂环取代的氧杂螺环衍生物、其制法与医药上的用途
KR20220106165A (ko) 2019-11-26 2022-07-28 길리애드 사이언시즈, 인코포레이티드 Hiv의 예방을 위한 캡시드 억제제
KR102847070B1 (ko) 2020-01-17 2025-08-14 상하이 하이옌 파마슈티컬 테크놀로지 컴퍼니, 리미티드 아자비시클릭 치환된 옥사스피로 유도체, 이의 제조 방법 및 의학적 용도
CN114269751B (zh) 2020-01-17 2024-04-16 上海海雁医药科技有限公司 光学纯的氧杂螺环取代的吡咯并吡唑衍生物、其制法与医药上的用途
CN113214264B (zh) * 2020-01-21 2022-08-09 上海海雁医药科技有限公司 二氢吡咯并五元杂芳基取代的氧杂螺环衍生物、其制法与医药上的用途
AU2021239956A1 (en) 2020-03-18 2022-10-13 Eli Lilly And Company Formulations of a farnesoid X receptor agonist
KR20230027275A (ko) 2020-06-25 2023-02-27 길리애드 사이언시즈, 인코포레이티드 Hiv 치료용 캡시드 저해제
CN114269738B (zh) * 2020-08-10 2023-09-29 成都苑东生物制药股份有限公司 一种mor受体激动剂化合物、制备方法及其用途
CN112694485B (zh) * 2020-09-10 2023-04-07 四川海品信医药科技有限公司 一种阿片受体激动剂噻吩类化合物及其制备方法
JP7751645B2 (ja) 2020-12-29 2025-10-08 上海海雁医薬科技有限公司 オキシスピロ環置換ピロロピラゾール誘導体及びその中間体並びにその調製方法
EP4361154A4 (en) * 2021-07-13 2025-06-18 Shanghai Haiyan Pharmaceutical Technology Co., Ltd. Pharmaceutically acceptable salt of a Mor receptor agonist, polymorph thereof, and use thereof
CN115677675B (zh) * 2021-07-21 2025-09-12 成都苑东生物制药股份有限公司 一种6-氧杂螺[4,5]癸烷类化合物的盐、制备方法及用途
AU2022322838B2 (en) * 2021-08-02 2024-12-12 Jiangsu Nhwa Pharmaceutical Co., Ltd Oxaspiro derivative, and preparation method therefor and use thereof
CN116075505A (zh) * 2021-08-31 2023-05-05 天地恒一制药股份有限公司 阿片受体激动剂及其制备方法和用途
JP7736929B2 (ja) 2021-12-03 2025-09-09 ギリアード サイエンシーズ, インコーポレイテッド Hivウイルス感染症のための治療化合物
FI4445900T3 (fi) 2021-12-03 2025-08-05 Gilead Sciences Inc Terapeuttisia yhdisteitä hiv-virusinfektiota varten
TW202342448A (zh) 2021-12-03 2023-11-01 美商基利科學股份有限公司 用於hiv病毒感染之治療性化合物
CN116041336B (zh) * 2022-01-21 2024-07-09 成都硕德药业有限公司 一种6-氧杂螺[4,5]癸烷类化合物的新晶型、用途及其制备方法
CN116589451B (zh) * 2022-02-11 2024-07-09 成都硕德药业有限公司 一种6-氧杂螺[4,5]癸烷类化合物的新晶型、用途及其制备方法
CN118638109B (zh) * 2024-04-30 2025-10-28 中山大学 一种阿片类药物-奥赛利定的制备方法

Family Cites Families (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5825980B2 (ja) 1976-02-12 1983-05-31 ヤマサ醤油株式会社 サイクリックヌクレオチドの定量法
US4602035A (en) * 1983-12-07 1986-07-22 Hoechst-Roussel Pharmaceuticals Inc. Antidepressant (3-aryl-2,3-dihydrobenzofuran-3-yl)alkylamines
US5223530A (en) 1990-07-31 1993-06-29 Sri, International Arylcycloalkanepolyalkylamine ligands
US5401629A (en) 1990-08-07 1995-03-28 The Salk Institute Biotechnology/Industrial Associates, Inc. Assay methods and compositions useful for measuring the transduction of an intracellular signal
WO1996005166A1 (en) * 1994-08-11 1996-02-22 Yamanouchi Pharmaceutical Co., Ltd. Substituted amine derivative and medicinal composition containing the same
ES2247604T3 (es) 1995-06-12 2006-03-01 G.D. SEARLE & CO. Composiciones que comprenden un inhibidor de ciclooxigenasa-2 y un inhibidor de 5-lipoxigenasa.
US6071918A (en) 1999-07-21 2000-06-06 Dupont Pharmaceuticals Company Combination of an opioid antagonist and a selective serotonin reuptake inhibitor for treatment of alcoholism and alcohol dependence
GB0130261D0 (en) * 2001-12-18 2002-02-06 Pfizer Ltd Lactams as tachykinin antagonists
TW200307539A (en) * 2002-02-01 2003-12-16 Bristol Myers Squibb Co Cycloalkyl inhibitors of potassium channel function
CN1305852C (zh) * 2002-09-19 2007-03-21 伊莱利利公司 作为阿片受体拮抗剂的二芳基醚
KR101255074B1 (ko) * 2003-10-01 2013-04-16 아돌로 코포레이션 스피로시클릭 헤테로시클릭 유도체 및 이의 사용 방법
WO2007041341A2 (en) * 2005-09-29 2007-04-12 The Trustees Of Columbia University In The City Of New York Identification of anti-cancer compounds and compounds for treating huntington's disease and methods of treatment thereof
WO2007081966A2 (en) * 2006-01-09 2007-07-19 University Of Southern California Small molecules for treating cancer and abnormal cell proliferation disorders
US7645767B2 (en) 2006-08-31 2010-01-12 Trinity Laboratories, Inc. Pharmaceutical compositions for treating chronic pain and pain associated with neuropathy
WO2008057857A1 (en) * 2006-11-01 2008-05-15 Bristol-Myers Squibb Company MODULATORS OF GLUCOCORTICOID RECEPTOR, AP-1, AND/OR NF-ϰB ACTIVITY AND USE THEREOF
US8067447B2 (en) * 2006-11-01 2011-11-29 Bristol-Myers Squibb Company Modulators of glucocorticoid receptor, AP-1, and/or NF-κB activity and use thereof
US20090028873A1 (en) 2007-07-27 2009-01-29 Auspex Pharmaceuticals, Inc. Substituted cyclohexanols
CA2719742C (en) 2008-03-27 2016-11-08 Gruenenthal Gmbh Substituted spirocyclic cyclohexane derivatives
FR2939136B1 (fr) * 2008-12-02 2010-12-03 Galderma Res & Dev Nouveaux composes 4-(heterocycloalkyl)-benzene-1,3-diol comme inhibiteurs de la tyrosinase, leur procede de preparation et leur utilisation en medecine humaine ainsi qu'en cosmetique
EP2415471A1 (en) 2010-08-03 2012-02-08 Laboratorios Del. Dr. Esteve, S.A. Use of sigma ligands in opioid-induced hyperalgesia
FR2967672B1 (fr) * 2010-11-22 2012-12-28 Sanofi Aventis Derives de nitrobenzothiazoles, leur preparation et leurs applications therapeutiques
PT3290415T (pt) * 2011-03-23 2021-03-29 Trevena Inc Ligandos de recetores opioides e métodos de utilização e fabrico dos mesmos
CN108366997A (zh) 2015-12-14 2018-08-03 特维娜有限公司 治疗痛觉过敏的方法

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