AR113931A1 - Tratamientos de combinación que comprenden la administración de 1h-pirazolo[4,3-b]piridinas - Google Patents

Tratamientos de combinación que comprenden la administración de 1h-pirazolo[4,3-b]piridinas

Info

Publication number
AR113931A1
AR113931A1 ARP180103639A ARP180103639A AR113931A1 AR 113931 A1 AR113931 A1 AR 113931A1 AR P180103639 A ARP180103639 A AR P180103639A AR P180103639 A ARP180103639 A AR P180103639A AR 113931 A1 AR113931 A1 AR 113931A1
Authority
AR
Argentina
Prior art keywords
alkyl
fluoroalkyl
optionally substituted
cyano
substituents selected
Prior art date
Application number
ARP180103639A
Other languages
English (en)
Original Assignee
H Lundbeck As
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 H Lundbeck As filed Critical H Lundbeck As
Publication of AR113931A1 publication Critical patent/AR113931A1/es

Links

Classifications

    • 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
    • A61K31/435Heterocyclic 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
    • A61K31/4353Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • 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
    • A61K31/435Heterocyclic 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
    • A61K31/44Non 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
    • 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
    • A61K31/4965Non-condensed pyrazines
    • A61K31/497Non-condensed pyrazines containing further heterocyclic rings
    • 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/18Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/22Anxiolytics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/24Antidepressants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2300/00Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca

Landscapes

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

Abstract

Reivindicación 1: 1) Un primer compuesto de acuerdo con la fórmula (1) donde L se selecciona entre el grupo que consiste en NH, CH₂, S y O; R¹ se selecciona entre el grupo que consiste en hidrógeno, alquilo C₁₋₅ lineal o ramificado, fluoroalquilo C₁₋₅ y cicloalquilo C₃₋₅ monocíclico saturado; R² se selecciona entre el grupo que consiste en alquilo C₁₋₈ lineal o ramificado, cicloalquilo C₃₋₈ monocíclico saturado, oxetanilo, tetrahidrofuranilo y tetrahidropiranilo; todos los cuales pueden estar opcionalmente sustituidos una o más veces con uno o más sustituyentes seleccionados entre el grupo que consiste en metilo, flúor, hidroxi, ciano y metoxi; R³ es metilo sustituido con fenilo, piridonilo, piridinilo, pirimidinilo o pirazinilo, todos los cuales pueden estar opcionalmente sustituidos una o más veces con uno o más sustituyentes seleccionados entre el grupo que consiste en halógeno, ciano, alquilo C₁₋₃, fluoroalquilo C₁₋₃, fluoroalcoxi C₁₋₃ y alcoxi C₁₋₃; o R³ es metilo sustituido con un heteroarilo de 5 miembros que está opcionalmente sustituido con uno o más sustituyentes seleccionados entre halógeno, ciano, alquilo C₁₋₃, fluoroalquilo C₁₋₃, fluoroalcoxi C₁₋₃ y alcoxi C₁₋₃; o R³ es etilo sustituido con fenilo, piridonilo, piridinilo, pirimidinilo o pirazinilo todos los cuales pueden estar opcionalmente sustituidos una o más veces con uno o más sustituyentes seleccionados entre el grupo que consiste en halógeno, ciano, alquilo C₁₋₃, fluoroalquilo C₁₋₃, fluoroalcoxi C₁₋₃ y alcoxi C₁₋₃; o R³ es etilo sustituido con un heteroarilo de 5 miembros, que está opcionalmente sustituido con uno o más sustituyentes seleccionados entre halógeno, ciano, alquilo C₁₋₃, fluoroalquilo C₁₋₃, fluoroalcoxi C₁₋₃ y alcoxi C₁₋₃; o L es CH₂ y R³ es NH que está sustituido con fenilo, piridonilo, piridinilo, pirimidinilo o pirazinilo todos los cuales pueden estar opcionalmente sustituidos una o más veces con uno o más sustituyentes seleccionados entre el grupo que consiste en halógeno, ciano, alquilo C₁₋₃, fluoroalquilo C₁₋₃, fluoroalcoxi C₁₋₃ y alcoxi C₁₋₃; o L es CH₂ y R³ es NH que está sustituido con un heteroarilo de 5 miembros, que está opcionalmente sustituido con uno o más sustituyentes seleccionados entre halógeno, ciano, alquilo C₁₋₃, fluoroalquilo C₁₋₃, fluoroalcoxi C₁₋₃ y alcoxi C₁₋₃; R⁴ es fenilo, piridinilo o piridonilo todos los cuales pueden estar opcionalmente sustituidos una o más veces con uno o más sustituyentes seleccionados entre el grupo que consiste en halógeno, ciano, alquilo C₁₋₄, fluoroalquilo C₁₋₄, deutereoalquilo C₁₋₄, fluoroalcoxi C₁₋₃, ciclopropiloxi, alcoxi C₁₋₃, deutereoalcoxi C₁₋₃ y -N-R⁵R⁶, en el que R⁵ y R⁶ se seleccionan cada uno independientemente entre H, alquilo C₁₋₃ y deutereoalquilo C₁₋₃; o R⁴ es un heteroarilo de 5 miembros, que está opcionalmente sustituido con uno o más sustituyentes seleccionados entre halógeno, ciano, alquilo C₁₋₄, fluoroalquilo C₁₋₄, deutereoalquilo C₁₋₄, fluoroalcoxi C₁₋₃, ciclopropiloxi, alcoxi C₁₋₃, deutereoalcoxi C₁₋₃ y -N-R⁵R⁶, en el que R⁵ y R⁶ se seleccionan cada uno independientemente entre H, alquilo C₁₋₃ y deutereoalquilo C₁₋₃; o R⁴ es un heterociclo saturado de 4, 5 ó 6 miembros, todos los cuales pueden estar opcionalmente sustituidos con uno o más sustituyentes seleccionados entre oxo, alquilo C₁₋₄ y fluoroalquilo C₁₋₄; o una de sus sales farmacéuticamente aceptables, y 2) un segundo compuesto, compuesto que es útil en el tratamiento de un trastorno psiquiátrico, en donde 1) y 2) son para su uso combinado en el tratamiento de un trastorno psiquiátrico y/o cognitivo.
ARP180103639A 2017-12-14 2018-12-13 Tratamientos de combinación que comprenden la administración de 1h-pirazolo[4,3-b]piridinas AR113931A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DKPA201700708 2017-12-14

Publications (1)

Publication Number Publication Date
AR113931A1 true AR113931A1 (es) 2020-07-01

Family

ID=64959282

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP180103639A AR113931A1 (es) 2017-12-14 2018-12-13 Tratamientos de combinación que comprenden la administración de 1h-pirazolo[4,3-b]piridinas

Country Status (26)

Country Link
US (1) US11634416B2 (es)
EP (1) EP3723807B1 (es)
JP (1) JP7261801B2 (es)
KR (1) KR20200099154A (es)
CN (1) CN111465410B (es)
AR (1) AR113931A1 (es)
AU (1) AU2018385453B2 (es)
BR (1) BR112019016815A2 (es)
CA (1) CA3085201A1 (es)
CL (1) CL2020001548A1 (es)
CO (1) CO2020007129A2 (es)
CY (1) CY1124751T1 (es)
ES (1) ES2899868T3 (es)
HR (1) HRP20211784T1 (es)
HU (1) HUE057202T2 (es)
IL (1) IL275290B2 (es)
LT (1) LT3723807T (es)
MX (1) MX2020006174A (es)
PL (1) PL3723807T3 (es)
PT (1) PT3723807T (es)
RS (1) RS62551B1 (es)
RU (1) RU2020118913A (es)
SG (1) SG11202005361RA (es)
SI (1) SI3723807T1 (es)
WO (1) WO2019115566A1 (es)
ZA (1) ZA202003514B (es)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10034861B2 (en) 2016-07-04 2018-07-31 H. Lundbeck A/S 1H-pyrazolo[4,3-b]pyridines as PDE1 inhibitors
CN111465410B (zh) 2017-12-14 2022-10-25 H.隆德贝克有限公司 包括施用1h-吡唑并[4,3-b]吡啶的组合治疗
AR113926A1 (es) 2017-12-14 2020-07-01 H Lundbeck As Derivados de 1h-pirazolo[4,3-b]piridinas
WO2019121840A1 (en) 2017-12-20 2019-06-27 H. Lundbeck A/S Pyrazolo[3,4-b]pyridines and imidazo[1,5-b]pyridazines as pde1 inhibitors

Family Cites Families (45)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6326379B1 (en) 1998-09-16 2001-12-04 Bristol-Myers Squibb Co. Fused pyridine inhibitors of cGMP phosphodiesterase
DE19942474A1 (de) 1999-09-06 2001-03-15 Merck Patent Gmbh Pyrazolo[4,3-d]pyrimidine
MY144532A (en) 2001-08-20 2011-09-30 Lundbeck & Co As H Novel method for down-regulation of amyloid
GB0230045D0 (en) 2002-12-23 2003-01-29 Glaxo Group Ltd Compounds
ES2319797T3 (es) 2004-07-05 2009-05-12 Astellas Pharma Inc. Derivados de pirazolopiridina.
ATE430746T1 (de) 2004-10-19 2009-05-15 Smithkline Beecham Cork Ltd Crf-rezeptor-antagonisten und zugehörige verfahren
US9248127B2 (en) 2005-02-04 2016-02-02 3M Innovative Properties Company Aqueous gel formulations containing immune response modifiers
TWI320783B (en) 2005-04-14 2010-02-21 Otsuka Pharma Co Ltd Heterocyclic compound
RU2402549C3 (ru) 2005-04-14 2022-03-10 Оцука Фармасьютикал Ко., Лтд. Пиперазин-замещенные бензотиофены для лечения психических расстройств
BRPI0620239B8 (pt) 2005-12-22 2021-05-25 Newron Pharm Spa derivados de 2-feniletilamino.
US8012936B2 (en) 2006-03-29 2011-09-06 New York University Tau fragments for immunotherapy
JP5837278B2 (ja) 2006-12-05 2015-12-24 イントラ−セルラー・セラピーズ・インコーポレイテッドIntra−Cellular Therapies, Inc. 新規使用
CA2680625C (en) 2007-03-14 2016-02-23 Ranbaxy Laboratories Limited Pyrazolo (3, 4-b) pyridine derivatives as phosphodiesterase inhibitors
MA32940B1 (fr) 2008-12-06 2012-01-02 Intra Cellular Therapies Inc Composes organiques
EP2440234A4 (en) 2009-06-10 2013-11-06 Univ New York IMMUNOLOGICAL TARGETING OF PATHOLOGICAL TAU PROTEINS
PL3042917T3 (pl) 2010-08-12 2018-07-31 Eli Lilly And Company Przeciwciała przeciwko peptydowi beta amyloidu N3pGlu i ich zastosowanie
US9499610B2 (en) 2011-04-08 2016-11-22 H. Lundbeck A/S Antibodies specific to pyroglutamated Aβ
EP2699572B1 (en) 2011-04-21 2016-08-10 Origenis GmbH Heterocyclic compounds as kinase inhibitors
EP2828253A1 (en) 2012-03-19 2015-01-28 Abide Therapeutics, Inc. Carbamate compounds and of making and using same
TW201533043A (zh) 2013-04-18 2015-09-01 Lundbeck & Co As H 作爲lrrk2抑制劑的芳基吡咯并吡啶衍生化合物
UA116023C2 (uk) 2013-07-08 2018-01-25 Ф. Хоффманн-Ля Рош Аг Етинільні похідні як антагоністи метаботропного глутаматного рецептора
US20170066741A1 (en) 2014-02-19 2017-03-09 H. Lundbeck A/S 2-Amino-3,5,5-Trifluoro-3,4,5,6-Tetrahydropyridines as BACE1 Inhibitors for Treatment of Alzheimer's Disease
TWI599358B (zh) 2014-09-16 2017-09-21 美國禮來大藥廠 組合療法
US20160083391A1 (en) 2014-09-18 2016-03-24 Sunovion Pharmaceuticals Inc. Tricyclic piperazine derivative
US20160083400A1 (en) 2014-09-18 2016-03-24 Sunovion Pharmaceuticals Inc. Tricyclic guanidine derivative
WO2016042775A1 (en) 2014-09-18 2016-03-24 Sunovion Pharmaceuticals Inc. Tricyclic derivative
TW201629064A (zh) 2014-10-10 2016-08-16 H 朗德貝克公司 作爲pde1抑制劑之三唑並吡酮
CR20170187A (es) 2014-11-10 2018-02-01 H Lundbeck As 2-Amino-3,5-difluoro-6-metil-6-fenil-3,4,5,6-tetrahidropiridinas en calidad de inhibidores de BACE1 para el tratamiento de la enfermedad de Alzheimer
MA40941A (fr) 2014-11-10 2017-09-19 H Lundbeck As 2-amino-5,5-difluoro-6-(fluorométhyl)-6-phényl-3,4,5,6-tétrahydropyridines comme inhibiteurs de bace1
JO3458B1 (ar) 2014-11-10 2020-07-05 H Lundbeck As 2- أمينو-6- (دايفلوروميثيل) – 5، 5- ديفلورو-6-فينيل-3،4، 5، 6-تيتراهيدروبيريدين كمثبطات bace1
US20180044343A1 (en) 2015-03-16 2018-02-15 Sumitomo Dainippon Pharma Co., Ltd. Bicyclic imidazolo derivative
US20160311831A1 (en) 2015-04-22 2016-10-27 H. Lundbeck A/S Imidazotriazinones as PDE1 Inhibitors
JO3711B1 (ar) 2015-07-13 2021-01-31 H Lundbeck As أجسام مضادة محددة لبروتين تاو وطرق استعمالها
US10206909B2 (en) 2015-08-03 2019-02-19 Samumed, Llc 3-(1H-pyrrolo[2,3-B]pyridin-2-yl)-1H-pyrazolo[4,3-B]pyridines and therapeutic uses thereof
PE20181015A1 (es) 2015-08-12 2018-06-26 H Lundbeck As 2-amino-3-fluoro-3-(fluorometil)-6-meti-6-fenil-3,4,5,6-tetrahidropiridinas como inhibidores de bace1
WO2017100276A1 (en) 2015-12-08 2017-06-15 The Arizona Board Of Regents On Behalf Of The University Of Arizona Compositions and methods for treatment, amelioration, and prevention of diabetes-related skin ulcers
GB2563730B (en) 2015-12-09 2021-09-15 Ford Global Tech Llc Alert for left-behind mobile device
US10682354B2 (en) 2016-03-28 2020-06-16 Intra-Cellular Therapies, Inc. Compositions and methods
US10034861B2 (en) * 2016-07-04 2018-07-31 H. Lundbeck A/S 1H-pyrazolo[4,3-b]pyridines as PDE1 inhibitors
JOP20190126A1 (ar) 2016-12-22 2019-05-28 H Lundbeck As بيرازولو [3، 4-b] بيريدينات وإيميدازو [1، 5-b] بيريدازينات على هيئة مثبطات PDE1
AR113926A1 (es) * 2017-12-14 2020-07-01 H Lundbeck As Derivados de 1h-pirazolo[4,3-b]piridinas
CN111465410B (zh) 2017-12-14 2022-10-25 H.隆德贝克有限公司 包括施用1h-吡唑并[4,3-b]吡啶的组合治疗
WO2019121840A1 (en) * 2017-12-20 2019-06-27 H. Lundbeck A/S Pyrazolo[3,4-b]pyridines and imidazo[1,5-b]pyridazines as pde1 inhibitors
US10766893B2 (en) 2017-12-20 2020-09-08 H. Lundbeck A/S 1H-pyrazolo[4,3-b]pyridines as PDE1 inhibitors
TW201927784A (zh) * 2017-12-20 2019-07-16 丹麥商H 朗德貝克公司 作為pde1抑制劑之大環

Also Published As

Publication number Publication date
JP7261801B2 (ja) 2023-04-20
ES2899868T3 (es) 2022-03-15
ZA202003514B (en) 2022-12-21
AU2018385453B2 (en) 2024-02-08
IL275290A (en) 2020-07-30
CY1124751T1 (el) 2022-07-22
SG11202005361RA (en) 2020-07-29
KR20200099154A (ko) 2020-08-21
CA3085201A1 (en) 2019-06-20
AU2018385453A1 (en) 2020-07-02
SI3723807T1 (sl) 2022-01-31
IL275290B2 (en) 2023-06-01
BR112019016815A2 (pt) 2020-04-07
CN111465410A (zh) 2020-07-28
HUE057202T2 (hu) 2022-04-28
JP2021506775A (ja) 2021-02-22
CL2020001548A1 (es) 2020-09-25
MX2020006174A (es) 2022-09-27
PT3723807T (pt) 2021-11-26
CN111465410B (zh) 2022-10-25
EP3723807B1 (en) 2021-10-20
RS62551B1 (sr) 2021-12-31
US20200385381A1 (en) 2020-12-10
HRP20211784T1 (hr) 2022-02-18
RU2020118913A (ru) 2022-01-14
PL3723807T3 (pl) 2022-01-24
CO2020007129A2 (es) 2020-06-19
WO2019115566A1 (en) 2019-06-20
LT3723807T (lt) 2021-12-10
US11634416B2 (en) 2023-04-25
EP3723807A1 (en) 2020-10-21

Similar Documents

Publication Publication Date Title
AR113931A1 (es) Tratamientos de combinación que comprenden la administración de 1h-pirazolo[4,3-b]piridinas
AR110405A1 (es) Compuestos
AR094342A1 (es) Derivados de ácido borónico útiles como agentes antimicrobianos
AR112290A1 (es) Dinucleótidos cíclicos como agentes anticáncer
AR100645A1 (es) Derivados de pirazolo-pirimidina
AR095311A1 (es) 3-pirimidin-4-il-oxazolidin-2-onas como inhibidores de idh mutante
AR094911A1 (es) SALES DE DERIVADOS DE 2-AMINO-1-HIDROXIETIL-8-HIDROXIQUINOLIN-2(1H)-ONA QUE TIENEN ACTIVIDAD AGONISTA DEL RECEPTOR b2 ADRENÉRGICO ASÍ COMO ACTIVIDAD ANTAGONISTA DEL RECEPTOR MUSCARÍNICO M₃
AR109709A1 (es) Inhibidores de la fosfatidilinositol 3-quinasa
AR086817A1 (es) Compuestos inhibidores de la fosfodiesterasa tipo 10a
AR088828A1 (es) DERIVADOS DE CICLOHEXILAMINA QUE TIENEN ACTIVIDAD COMO AGONISTAS ADRENERGICOS b2 Y COMO ANTAGONISTAS MUSCARINICOS M3
AR106053A1 (es) Compuestos imidazo[4,5-c]quinolin-2-ona y su uso para el tratamiento del cáncer
AR112348A1 (es) Compuestos bicíclicos de pirazolo y triazolo como inhibidores de quinasas jak
AR094299A1 (es) Derivados de ftalazin-1(2h)-ona sustituidos
AR094857A1 (es) Derivados de pirrolo[2,3-d]pirimidina
AR113926A1 (es) Derivados de 1h-pirazolo[4,3-b]piridinas
AR091271A1 (es) Pirrolopirimidona y pirrolopiridona, inhibidores de tanquirasa
AR109296A1 (es) Derivados de oxadiazolopiridina para el uso como inhibidores de ghrelin o-aciltransferasa (goat)
AR103742A1 (es) Derivados de trifluorometilpropanamida
AR089623A1 (es) Inhibidores de iap
AR103566A1 (es) Compuestos derivados de heteroarilo y heterociclo condensados
AR114465A1 (es) Compuestos de pirazol sustituidos con heteroarilo y su utilización farmacéutica
AR094797A1 (es) Derivados de pirrolotriazina como inhibidores de pi3k
AR109776A1 (es) Compuestos de p2x₃ y/o p2x₂/₃ y métodos
AR095267A1 (es) Compuestos inhibidores de la fosfodiesterasa del tipo 10a
AR111252A1 (es) Compuestos de isoxazol carboxamida y usos de los mismos