ME02754B - Ligandi opioidnih receptora i postupci njihove upotrebe i pripreme - Google Patents
Ligandi opioidnih receptora i postupci njihove upotrebe i pripremeInfo
- 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
- Authority
- ME
- Montenegro
- Prior art keywords
- alkyl
- pharmaceutically acceptable
- acceptable salt
- compound
- compound according
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims 3
- 102000003840 Opioid Receptors Human genes 0.000 title 1
- 108090000137 Opioid Receptors Proteins 0.000 title 1
- 239000003446 ligand Substances 0.000 title 1
- 238000004519 manufacturing process Methods 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims 25
- 150000003839 salts Chemical class 0.000 claims 20
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 14
- 125000001475 halogen functional group Chemical group 0.000 claims 10
- 125000000217 alkyl group Chemical group 0.000 claims 9
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 9
- 125000004093 cyano group Chemical group *C#N 0.000 claims 8
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 8
- 238000006467 substitution reaction Methods 0.000 claims 8
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims 7
- 125000003545 alkoxy group Chemical group 0.000 claims 7
- 125000001072 heteroaryl group Chemical group 0.000 claims 4
- 125000002950 monocyclic group Chemical group 0.000 claims 3
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 2
- 230000015572 biosynthetic process Effects 0.000 claims 2
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 claims 1
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 125000004076 pyridyl group Chemical group 0.000 claims 1
- 125000003107 substituted aryl group Chemical group 0.000 claims 1
Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/35—Heterocyclic 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
-
- 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
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/35—Heterocyclic 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
- A61K31/352—Heterocyclic 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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- A—HUMAN NECESSITIES
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- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4433—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with oxygen as a ring hetero atom
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- A—HUMAN NECESSITIES
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- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4436—Non 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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- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/444—Non 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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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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- A61K9/00—Medicinal preparations characterised by special physical form
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- A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
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- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
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- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/96—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings spiro-condensed with carbocyclic rings or ring systems
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- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
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- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
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- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
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- Urology & Nephrology (AREA)
- Psychiatry (AREA)
- Endocrinology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyrane Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- 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
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 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ME02754B true ME02754B (me) | 2018-01-20 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MEP-2017-129A ME02754B (me) | 2011-03-23 | 2012-03-23 | Ligandi opioidnih receptora i postupci njihove upotrebe i pripreme |
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| Country | Link |
|---|---|
| US (8) | US8835488B2 (me) |
| EP (3) | EP3872076A1 (me) |
| JP (6) | JP5912169B2 (me) |
| KR (3) | KR102129247B1 (me) |
| CN (1) | CN103702561B (me) |
| AU (2) | AU2012230761B2 (me) |
| CA (1) | CA2830742C (me) |
| CY (1) | CY1119057T1 (me) |
| DK (2) | DK3290415T3 (me) |
| EA (1) | EA025456B1 (me) |
| ES (2) | ES2857549T3 (me) |
| HR (1) | HRP20171021T1 (me) |
| HU (2) | HUE032948T2 (me) |
| IL (4) | IL228506A (me) |
| LT (1) | LT2688403T (me) |
| ME (1) | ME02754B (me) |
| PL (2) | PL2688403T3 (me) |
| PT (2) | PT3290415T (me) |
| RS (1) | RS56111B1 (me) |
| SI (1) | SI2688403T1 (me) |
| SM (1) | SMT201700325T1 (me) |
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Families Citing this family (60)
| 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)
| 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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