[go: up one dir, main page]

MX2019012336A - Compuestos inhibidores del transportador vesicular de monoaminas 2 (vmat2) y composiciones de los mismos. - Google Patents

Compuestos inhibidores del transportador vesicular de monoaminas 2 (vmat2) y composiciones de los mismos.

Info

Publication number
MX2019012336A
MX2019012336A MX2019012336A MX2019012336A MX2019012336A MX 2019012336 A MX2019012336 A MX 2019012336A MX 2019012336 A MX2019012336 A MX 2019012336A MX 2019012336 A MX2019012336 A MX 2019012336A MX 2019012336 A MX2019012336 A MX 2019012336A
Authority
MX
Mexico
Prior art keywords
sup
compounds
compositions
inhibitor compounds
vmat2 inhibitor
Prior art date
Application number
MX2019012336A
Other languages
English (en)
Inventor
Nicole Harriott
Donald Hettinger
Shawn Branum
Jeffrey C Culhane
Original Assignee
Neurocrine Biosciences Inc
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=62111264&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MX2019012336(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Neurocrine Biosciences Inc filed Critical Neurocrine Biosciences Inc
Publication of MX2019012336A publication Critical patent/MX2019012336A/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/4985Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

Se proporciona un compuesto seleccionado de compuestos de fórmula (I) y sales, solvatos e hidratos farmacéuticamente aceptables de los mismos: (Ver formula) en la que R1, R2, R3 y R4 son tal como se definen en el presente documento. Tales compuestos son inhibidores del transportador vesicular de monoaminas 2 (VMAT2) y tienen utilidad para tratar, por ejemplo, enfermedades y trastornos neurológicos y psiquiátricos. También se dan a conocer composiciones que contienen tales compuestos en combinación con un portador farmacéuticamente aceptable, así como métodos relativos a su uso en sujetos que lo necesitan.
MX2019012336A 2017-04-19 2018-04-17 Compuestos inhibidores del transportador vesicular de monoaminas 2 (vmat2) y composiciones de los mismos. MX2019012336A (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201762487413P 2017-04-19 2017-04-19
US201862652837P 2018-04-04 2018-04-04
PCT/US2018/028031 WO2018195121A1 (en) 2017-04-19 2018-04-17 Vmat2 inhibitor compounds and compositions thereof

Publications (1)

Publication Number Publication Date
MX2019012336A true MX2019012336A (es) 2020-07-14

Family

ID=62111264

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2019012336A MX2019012336A (es) 2017-04-19 2018-04-17 Compuestos inhibidores del transportador vesicular de monoaminas 2 (vmat2) y composiciones de los mismos.

Country Status (17)

Country Link
US (1) US11040970B2 (es)
EP (1) EP3612532B1 (es)
JP (1) JP7170662B2 (es)
KR (1) KR20190140968A (es)
CN (1) CN110770236B (es)
AU (1) AU2018254429A1 (es)
BR (1) BR112019021853A2 (es)
CA (1) CA3060251A1 (es)
CL (1) CL2019002919A1 (es)
CO (1) CO2019011604A2 (es)
ES (1) ES2971230T3 (es)
JO (1) JOP20190239A1 (es)
MA (1) MA50145A (es)
MX (1) MX2019012336A (es)
PE (1) PE20191784A1 (es)
TW (1) TW201841913A (es)
WO (1) WO2018195121A1 (es)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EA201991786A1 (ru) 2017-01-27 2020-01-16 Нейрокрин Байосайенсиз, Инк. Способы введения некоторых vmat2-ингибиторов
IL301770B2 (en) 2017-09-21 2024-06-01 Neurocrine Biosciences Inc High dose valbenazine formulation and related preparations, methods and kits
MY198713A (en) 2017-10-10 2023-09-19 Neurocrine Biosciences Inc Methods for the administration of certain vmat2 inhibitors
WO2019241555A1 (en) * 2018-06-14 2019-12-19 Neurocrine Biosciences, Inc. Vmat2 inhibitor compounds, compositions, and methods relating thereto
SG11202100303QA (en) 2018-08-15 2021-02-25 Neurocrine Biosciences Inc Methods for the administration of certain vmat2 inhibitors
WO2020086765A1 (en) * 2018-10-24 2020-04-30 Neurocrine Biosciences, Inc. Processes for preparing a vmat2 inhibitor
CN115175734B (zh) 2019-09-30 2024-04-19 因赛特公司 作为免疫调节剂的吡啶并[3,2-d]嘧啶化合物
CA3160131A1 (en) 2019-11-11 2021-05-20 Incyte Corporation Salts and crystalline forms of a pd-1/pd-l1 inhibitor
IL305054A (en) 2021-03-22 2023-10-01 Neurocrine Biosciences Inc VMAT2 inhibitors and methods of use
WO2022232380A1 (en) 2021-04-29 2022-11-03 Neurocrine Biosciences, Inc. Processes for preparing a vmat2 inhibitor
TW202322816A (zh) 2021-08-20 2023-06-16 美商紐羅克里生物科學有限公司 篩選 vmat2 抑制劑之方法

Family Cites Families (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5798119A (en) 1995-06-13 1998-08-25 S. C. Johnson & Son, Inc. Osmotic-delivery devices having vapor-permeable coatings
GB0106177D0 (en) 2001-03-13 2001-05-02 Hoffmann La Roche Piperazine derivatives
BRPI0411509A (pt) 2003-06-20 2006-07-25 Hoffmann La Roche compostos, processo para a sua manufatura, composições farmacêuticas que compreendem os mesmos, método para tratamento e/ou profilaxia de enfermidades que estão associadas com dpp-iv e sua utilização
CA2575979A1 (en) 2004-08-13 2006-02-23 Omeros Corporation Novel serotonin receptor ligands and their uses thereof
CA2668689C (en) 2006-11-08 2015-12-29 Neurocrine Biosciences Inc. Substituted 3-isobutyl-9,10-dimethoxy-1,3,4,6,7,11b-hexahydro-2h-pyrido[2,1-a]isoquinolin-2-ol compounds and methods relating thereto
FR2912145B1 (fr) 2007-02-02 2009-03-06 Servier Lab Nouveaux derives tricycliques,leur procede de preparation et les compositions pharmaceutiques qui les contiennent
WO2009126305A1 (en) 2008-04-11 2009-10-15 The Trustees Of Columbia University Glucose metabolism modulating compounds
EP2610254B1 (en) 2008-09-18 2015-11-25 Auspex Pharmaceuticals, Inc. Deuterated benzoquinoline derivatives as inhibitors of vesicular monoamine transporter 2
CA2784830C (en) 2009-12-18 2018-03-27 Sunovion Pharmaceuticals Inc. Compounds for treating disorders mediated by metabotropic glutamate receptor 5, and methods of use thereof
CN102285984B (zh) 2010-11-25 2012-10-10 江苏威凯尔医药科技有限公司 (2R,3R,11bR)-二氢丁苯那嗪及相关化合物的制备方法
EP2835372B1 (en) 2012-09-19 2016-05-04 Fujian Institute Of Research On The Structure Of Matter, Chinese Academy Of Sciences Thiophene [2, 3-d]pyrimidine derivative, and preparation method and use thereof
RU2021128797A (ru) 2014-02-07 2021-11-26 Ньюрокрайн Байосайенсиз, Инк. Фармацевтические композиции, содержащие антипсихотическое лекарственное средство и ингибитор vmat2, и их применение
CA2974540C (en) * 2015-02-06 2023-09-26 Neurocrine Biosciences, Inc. [9,10-dimethoxy-3-(2-methylpropyl)-1h,2h,3h,4h,6h,7h,11bh-pyrido-[2,1-a]isoquinolin-2-yl]methanol and compounds, compositions and methods relating thereto
PL3558990T3 (pl) 2016-12-22 2022-12-19 Incyte Corporation Pochodne tetrahydroimidazo[4,5-c]pirydyny jako induktory internalizacji pd-l1
MX391981B (es) 2016-12-22 2025-03-21 Incyte Corp Derivados de benzooxazol como inmunomoduladores.

Also Published As

Publication number Publication date
WO2018195121A1 (en) 2018-10-25
ES2971230T3 (es) 2024-06-04
JOP20190239A1 (ar) 2019-10-09
AU2018254429A1 (en) 2019-11-07
KR20190140968A (ko) 2019-12-20
CN110770236A (zh) 2020-02-07
US11040970B2 (en) 2021-06-22
CO2019011604A2 (es) 2019-10-31
BR112019021853A2 (pt) 2020-05-26
JP7170662B2 (ja) 2022-11-14
JP2020517607A (ja) 2020-06-18
CN110770236B (zh) 2023-03-24
EP3612532B1 (en) 2023-12-13
CA3060251A1 (en) 2018-10-25
CL2019002919A1 (es) 2020-01-17
TW201841913A (zh) 2018-12-01
EP3612532A1 (en) 2020-02-26
US20200131173A1 (en) 2020-04-30
PE20191784A1 (es) 2019-12-24
EP3612532C0 (en) 2023-12-13
MA50145A (fr) 2020-07-29

Similar Documents

Publication Publication Date Title
MX2019012336A (es) Compuestos inhibidores del transportador vesicular de monoaminas 2 (vmat2) y composiciones de los mismos.
MX375718B (es) [9,10-dimetoxi-3-(2-metilpropil)-1h,2h,3h,4h,6h,7h,11bh-pirido-[2,1-a]isoquinolin-2-il]metanol y compuestos, composiciones y metodos relacionados con los mismos.
MX2022008066A (es) Compuestos triciclicos sustituidos.
MX2020001776A (es) Sulfonilureas y sulfoniltioureas como inhibidores de nlrp3.
MX2017010230A (es) Derivados de mono- y poliazanaftaleno sustituidos y su uso.
HUP0402454A2 (hu) Szubsztituált kinazolinszármazékok mint az aurora kinázok inhibitorai, eljárás az előállításukra és ezeket tartalmazó gyógyszerkészítmények
MX2009004910A (es) Compuestos sustituidos de 3-isobutil-9,10-dimetoxi-1,3,4,6,7,11-b- hexahidro-2h-pirido[2,1-a] isoquinolin-2-ol y métodos que se relacionan al mismo.
MX371167B (es) Inhibidores de inhibidores del factor beta de crecimiento de transformacion (tgf-beta).
NZ532494A (en) Dibenzylamine compound and medicinal use thereof
MX2015008971A (es) Derivados de pirimidina pirido- o pirrolo-fusionados como inhibidores de autotaxina para tratar dolor.
MX2020010181A (es) Compuestos de piperidina como inhibidores covalentes de menina.
MX2016006685A (es) Compuestos heterociclicos de n-acilimino.
MX2022016515A (es) Nuevo inhibidor de la secrecion de acido y uso del mismo.
EA200601178A1 (ru) Морфолинилсодержащие бензимидазолы в качестве ингибиторов репликации респираторно-синцитиального вируса
PH12022550436A1 (en) Alpha-d-galactopyranoside derivatives
CR20200643A (es) Nuev0s compuestos de piridina y pirazina com0 inhibidores del receptor connabinoide 2
SG10201806809QA (en) 1-heterocyclyl isochromanyl compounds and analogs for treating cns disorders
TN2021000025A1 (en) Novel heterocyclic amine derivative and pharmaceutical composition comprising same
MY195576A (en) Novel Amino-Imidazopyridine Derivatives as Janus Kinase Inhibitors and Pharmaceutical use Thereof
MX2025000174A (es) Compuestos y metodos terapeuticos.
SA522441473B1 (ar) Cdk7 مركبات مفيدة لتثبيط
CR20230479A (es) Formas de sales y sólidas de un inhibidor de cinasas
MX2024002674A (es) Derivados de tiadiazolona utiles como activadores de ampk.
CR20230218A (es) Nuevos derivados de indazol acetileno
MX2023003631A (es) Indazoles a manera de inhibidores de cinasa 1 progenitora hematopoyetica (hpk1) y metodos de uso de los mismos.