CL2019000778A1 - Derivados de cromano, isocromano y dihidroisobenzofuranos como moduladores alostéricos negativos de mglur2, composiciones y su uso. - Google Patents

Derivados de cromano, isocromano y dihidroisobenzofuranos como moduladores alostéricos negativos de mglur2, composiciones y su uso.

Info

Publication number
CL2019000778A1
CL2019000778A1 CL2019000778A CL2019000778A CL2019000778A1 CL 2019000778 A1 CL2019000778 A1 CL 2019000778A1 CL 2019000778 A CL2019000778 A CL 2019000778A CL 2019000778 A CL2019000778 A CL 2019000778A CL 2019000778 A1 CL2019000778 A1 CL 2019000778A1
Authority
CL
Chile
Prior art keywords
disorders
mglur2
same
vehicle
compositions
Prior art date
Application number
CL2019000778A
Other languages
English (en)
Inventor
Iyassu K Sebhat
Ashok Arasappan
Scott B Hoy
Robert R Wilkening
Duane Demong
Original Assignee
Merck Sharp & Dohme
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 Merck Sharp & Dohme filed Critical Merck Sharp & Dohme
Publication of CL2019000778A1 publication Critical patent/CL2019000778A1/es

Links

Classifications

    • 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
    • A61K31/439Heterocyclic 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 the ring forming part of a bridged ring system, e.g. quinuclidine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/16Amides, e.g. hydroxamic acids
    • A61K31/165Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
    • A61K31/166Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the carbon of a carboxamide group directly attached to the aromatic ring, e.g. procainamide, procarbazine, metoclopramide, labetalol
    • 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
    • A61K31/436Heterocyclic 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 six-membered ring having oxygen as a ring hetero atom, e.g. rapamycin
    • 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
    • A61P25/14Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A61P25/16Anti-Parkinson drugs
    • 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
    • A61P25/20Hypnotics; Sedatives
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D221/00Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00
    • C07D221/02Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00 condensed with carbocyclic rings or ring systems
    • C07D221/22Bridged ring systems
    • C07D221/24Camphidines
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/12Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains three hetero rings
    • C07D491/18Bridged systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/01Hydrocarbons
    • A61K31/015Hydrocarbons carbocyclic
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/02Halogenated hydrocarbons
    • A61K31/025Halogenated hydrocarbons carbocyclic
    • A61K31/03Halogenated hydrocarbons carbocyclic aromatic

Landscapes

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

Abstract

LA PRESENTE INVENCIÓN PROPORCIONA CIERTOS COMPUESTOS DE CROMANO, ISOCROMANO Y DIHIDROISOBENZOFURANO SUSTITUIDOS DE FÓRMULA (I), O UNA SAL FARMACÉUTICAMENTE ACEPTABLE DE LOS MISMOS, EN LA QUE EL ANILLO A ES UN RESTO SELECCIONADO DE, Y EL ANILLO B, N, R1 , R2 , R2A, R3 Y R3A SON COMO SE DEFINEN EN LA PRESENTE MEMORIA. LOS COMPUESTOS DE LA INVENCIÓN SON ÚTILES COMO INHIBIDORES DE MGLUR2, O MODULADORES ALOSTÉRICOS NEGATIVOS DE MGLUR2 (NAM), Y PUEDEN SER ÚTILES EN PROCEDIMIENTOS DE TRATAMIENTO DE UN PACIENTE PARA ENFERMEDADES O TRASTORNOS EN LOS QUE ESTÁ IMPLICADO EL RECEPTOR MGLUR2-NAM, TALES COMO LA ENFERMEDAD DE ALZHEIMER, DETERIORO COGNITIVO, DETERIORO COGNITIVO LEVE, ESQUIZOFRENIA Y OTROS TRASTORNOS DEL ESTADO DE ÁNIMO, TRASTORNOS DEL DOLOR Y TRASTORNOS DEL SUEÑO, MEDIANTE LA ADMINISTRACIÓN AL PACIENTE DE UNA CANTIDAD TERAPÉUTICAMENTE EFICAZ DE UN COMPUESTO DE LA INVENCIÓN, O UNA SAL FARMACÉUTICAMENTE ACEPTABLE DEL MISMO. LA INVENCIÓN TAMBIÉN SE REFIERE A COMPOSICIONES FARMACÉUTICAS QUE COMPRENDEN UN COMPUESTO DE LA INVENCIÓN, O UNA SAL FARMACÉUTICAMENTE ACEPTABLE DEL MISMO, (OPCIONALMENTE EN COMBINACIÓN CON UNO O MÁS INGREDIENTES ACTIVOS ADICIONALES), Y UN VEHÍCULO FARMACÉUTICAMENTE ACEPTABLE, Y AL USO DE LOS COMPUESTOS Y COMPOSICIONES FARMACÉUTICAS DE LA INVENCIÓN EN EL TRATAMIENTO DE TALES ENFERMEDADES.
CL2019000778A 2016-09-27 2019-03-25 Derivados de cromano, isocromano y dihidroisobenzofuranos como moduladores alostéricos negativos de mglur2, composiciones y su uso. CL2019000778A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201662400150P 2016-09-27 2016-09-27

Publications (1)

Publication Number Publication Date
CL2019000778A1 true CL2019000778A1 (es) 2019-05-31

Family

ID=60043302

Family Applications (1)

Application Number Title Priority Date Filing Date
CL2019000778A CL2019000778A1 (es) 2016-09-27 2019-03-25 Derivados de cromano, isocromano y dihidroisobenzofuranos como moduladores alostéricos negativos de mglur2, composiciones y su uso.

Country Status (39)

Country Link
US (4) US10335399B2 (es)
EP (1) EP3519416B1 (es)
JP (3) JP6681517B2 (es)
KR (1) KR102296043B1 (es)
CN (1) CN109983022B (es)
AR (1) AR109714A1 (es)
AU (2) AU2017334870C1 (es)
CA (1) CA3037537C (es)
CL (1) CL2019000778A1 (es)
CO (1) CO2019002673A2 (es)
CR (1) CR20190147A (es)
CY (1) CY1124346T1 (es)
DK (1) DK3519416T3 (es)
DO (1) DOP2019000076A (es)
EA (1) EA038627B1 (es)
EC (1) ECSP19020742A (es)
ES (1) ES2868973T3 (es)
GE (2) GEP20217279B (es)
HR (1) HRP20210793T1 (es)
HU (1) HUE054898T2 (es)
IL (1) IL265366B (es)
JO (1) JOP20190058B1 (es)
LT (1) LT3519416T (es)
MA (1) MA46342B1 (es)
MD (1) MD3519416T2 (es)
MX (1) MX2019003492A (es)
MY (1) MY196807A (es)
NI (1) NI201900025A (es)
PE (1) PE20190609A1 (es)
PH (1) PH12019500597A1 (es)
PL (1) PL3519416T3 (es)
PT (1) PT3519416T (es)
RS (1) RS61890B1 (es)
SI (1) SI3519416T1 (es)
TN (2) TN2020000161A1 (es)
TW (1) TWI764934B (es)
UA (1) UA123687C2 (es)
WO (1) WO2018063955A1 (es)
ZA (1) ZA201901701B (es)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EA038627B1 (ru) * 2016-09-27 2021-09-24 Мерк Шарп И Доум Корп. ПРОИЗВОДНЫЕ ХРОМАНА, ИЗОХРОМАНА И ДИГИДРОИЗОБЕНЗОФУРАНА В КАЧЕСТВЕ НЕГАТИВНЫХ АЛЛОСТЕРИЧЕСКИХ МОДУЛЯТОРОВ РЕЦЕПТОРОВ mGluR2, ИХ КОМПОЗИЦИИ И ПРИМЕНЕНИЕ
CA3087283A1 (en) 2018-01-19 2019-07-25 Cytokinetics, Inc. Dihydrobenzofuran and inden analogs as cardiac sarcomere inhibitors
JP7438148B2 (ja) 2018-06-26 2024-02-26 サイトキネティックス, インコーポレイテッド 心臓サルコメア阻害剤
KR102704291B1 (ko) * 2019-03-01 2024-09-09 노보 노르디스크 에이/에스 융합 3환 화합물의 제조 방법, 및 그의 중간체
MX2023010125A (es) 2021-03-04 2023-09-11 Cytokinetics Inc Inhibidores del sarcomero cardiaco.
WO2023278729A1 (en) * 2021-06-30 2023-01-05 The General Hospital Corporation Chromane imaging ligands

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5552437A (en) 1994-10-27 1996-09-03 Merck Frosst Canada, Inc. Bisarylcarbinol derivatives as inhibitors of leukotriene biosynthesis
US5576338A (en) 1995-02-15 1996-11-19 Merck Frosst Canada, Inc. Bis (biaryl) compounds as inhibitors of leukotriene biosynthesis
WO2005014543A1 (ja) 2003-08-06 2005-02-17 Japan Tobacco Inc. 縮合環化合物及びそのhcvポリメラーゼ阻害剤としての利用
CA2624294A1 (en) 2005-10-05 2007-04-12 Merck Frosst Canada Ltd. Substituted quinolines as inhibitors of leukotriene biosynthesis
AR065093A1 (es) 2007-02-05 2009-05-13 Merck Frosst Canada Ltd Compuestos farmacéuticos inhibidores de la biosintesis de leucotrienos
WO2010021693A2 (en) 2008-08-18 2010-02-25 Yale University Mif modulators
MY161325A (en) * 2009-05-12 2017-04-14 Janssen Pharmaceuticals Inc 1, 2, 4-triazolo[4,3-a]pyridine derivatives and their use for the treatment or prevention of neurological and psychiatric disorders
WO2011075699A2 (en) 2009-12-18 2011-06-23 Sunovion Pharmaceuticals Inc. Compounds for treating disorders mediated by metabotropic glutamate receptor 5, and methods of use thereof
WO2013066736A1 (en) * 2011-11-03 2013-05-10 Merck Sharp & Dohme Corp. QUINOLINE CARBOXAMIDE AND QUINOLINE CARBONITRILE DERIVATIVES AS mGluR2-NEGATIVE ALLOSTERIC MODULATORS, COMPOSITIONS, AND THEIR USE
JO3368B1 (ar) 2013-06-04 2019-03-13 Janssen Pharmaceutica Nv مركبات 6، 7- ثاني هيدرو بيرازولو [5،1-a] بيرازين- 4 (5 يد)- اون واستخدامها بصفة منظمات تفارغية سلبية لمستقبلات ميجلور 2
WO2016029454A1 (en) 2014-08-29 2016-03-03 Merck Sharp & Dohme Corp. TETRAHYDRONAPHTHYRIDINE DERIVATIVES AS mGluR2-NEGATIVE ALLOSTERIC MODULATORS, COMPOSITIONS, AND THEIR USE
US9382208B1 (en) 2015-01-26 2016-07-05 Vanderbilt University Negative allosteric modulators of metabotropic glutamate receptor 2
WO2016149324A1 (en) 2015-03-16 2016-09-22 Vanderbilt University Negative allosteric modulators of metabotropic glutamate receptor 2
JP6471614B2 (ja) 2015-05-29 2019-02-20 株式会社リコー 通信端末、通信システム、通信制御方法、及びプログラム
JP2018154554A (ja) 2015-07-29 2018-10-04 大日本住友製薬株式会社 新規リンカー部位を持つ縮合ピラゾール誘導体およびその医薬用途
EA038627B1 (ru) * 2016-09-27 2021-09-24 Мерк Шарп И Доум Корп. ПРОИЗВОДНЫЕ ХРОМАНА, ИЗОХРОМАНА И ДИГИДРОИЗОБЕНЗОФУРАНА В КАЧЕСТВЕ НЕГАТИВНЫХ АЛЛОСТЕРИЧЕСКИХ МОДУЛЯТОРОВ РЕЦЕПТОРОВ mGluR2, ИХ КОМПОЗИЦИИ И ПРИМЕНЕНИЕ

Also Published As

Publication number Publication date
UA123687C2 (uk) 2021-05-12
JP2020011989A (ja) 2020-01-23
ECSP19020742A (es) 2019-04-30
US20210015800A1 (en) 2021-01-21
EA201990818A1 (ru) 2019-08-30
MY196807A (en) 2023-05-03
TWI764934B (zh) 2022-05-21
TN2020000161A1 (en) 2022-04-04
HRP20210793T1 (hr) 2021-09-03
EP3519416B1 (en) 2021-03-31
AU2017334870B2 (en) 2020-08-20
IL265366A (en) 2019-05-30
US20220218676A1 (en) 2022-07-14
CR20190147A (es) 2019-05-17
NI201900025A (es) 2019-05-27
MA46342A (fr) 2019-08-07
PH12019500597A1 (en) 2019-07-24
AR109714A1 (es) 2019-01-16
AU2020270468A1 (en) 2020-12-10
CO2019002673A2 (es) 2019-03-29
US20180085358A1 (en) 2018-03-29
CA3037537A1 (en) 2018-04-05
KR102296043B1 (ko) 2021-08-30
WO2018063955A1 (en) 2018-04-05
HUE054898T2 (hu) 2021-10-28
PE20190609A1 (es) 2019-04-23
JOP20190058A1 (ar) 2019-03-24
US10335399B2 (en) 2019-07-02
US20190247374A1 (en) 2019-08-15
CA3037537C (en) 2021-06-15
JOP20190058B1 (ar) 2023-09-17
TN2020000160A1 (en) 2022-04-04
ZA201901701B (en) 2023-03-29
DOP2019000076A (es) 2019-07-15
CN109983022B (zh) 2022-06-07
EA038627B1 (ru) 2021-09-24
EP3519416A1 (en) 2019-08-07
MX2019003492A (es) 2019-09-19
MD3519416T2 (ro) 2021-09-30
BR112019005869A8 (pt) 2023-05-02
PL3519416T3 (pl) 2021-09-06
TW201815794A (zh) 2018-05-01
SI3519416T1 (sl) 2021-08-31
JP2019529468A (ja) 2019-10-17
CN109983022A (zh) 2019-07-05
CY1124346T1 (el) 2022-07-22
JP6945605B2 (ja) 2021-10-06
RS61890B1 (sr) 2021-06-30
IL265366B (en) 2021-12-01
AU2017334870A1 (en) 2019-03-28
JP6681517B2 (ja) 2020-04-15
BR112019005869A2 (pt) 2019-06-11
LT3519416T (lt) 2021-06-10
US10806724B2 (en) 2020-10-20
AU2017334870C1 (en) 2020-12-17
JP2020111596A (ja) 2020-07-27
GEP20217266B (en) 2021-06-25
MA46342B1 (fr) 2021-05-31
ES2868973T3 (es) 2021-10-22
DK3519416T3 (da) 2021-05-25
JP6992109B2 (ja) 2022-02-15
GEP20217279B (en) 2021-08-10
AU2020270468B2 (en) 2022-02-17
KR20190056418A (ko) 2019-05-24
PT3519416T (pt) 2021-05-13

Similar Documents

Publication Publication Date Title
CL2019000778A1 (es) Derivados de cromano, isocromano y dihidroisobenzofuranos como moduladores alostéricos negativos de mglur2, composiciones y su uso.
CO2017013708A2 (es) Macrociclos peptídicos contra acinetobacter baumannii.
CR20150628A (es) Derivados de la pirazolopirrolidina y su uso en el tratamiento de enfermedades
ECSP18073366A (es) Derivados de indolina sustituidos como inhibidores de la replicación vírica de dengue
ECSP19083621A (es) Derivados de indolina sustituidos como inhibidores de la replicación vírica de dengue
UY37168A (es) Profármacos de principios activos citotóxicos con grupos enzimáticamente escindibles
NI201900099A (es) Derivados de indolina sustituidos como inhibidores de la replicación vírica de dengue
ECSP18073293A (es) Derivados de indolina sustituidos como inhibidores de la replicación viral del dengue
UY35827A (es) Derivados de triazolopirazina como inhibidores de la proteína brd4
NI201900098A (es) Derivados de indolina sustituidos como inhibidores de la replicación vírica de dengue
ECSP13012967A (es) 1,3-oxazinas como inhibidores de la bace1 y/o de la bace2
ECSP19083640A (es) Derivados de indolina sustituidos como inhibidores de la replicación vírica de dengue
CL2017001073A1 (es) 2,4 diamino-quinolia sustituido como nuevos agentes anticancerigenos
BR112015019412A8 (pt) inibidores de bace1, seus usos, e composição farmacêutica
CO7151509A2 (es) Difluoro-hexahidro-ciclopentaoxacinilos y difluoro-hexahidro-benzooxacinilos como inhibidores de bace1
DOP2019000100A (es) Derivados de naftiridinona y su uso en el tratamiento de la arritmia
UY37622A (es) Derivados de pirazol como inhibidores de bromodominio de la familia bet y su uso en aplicaciones terapéuticas
CR20170426A (es) Inhibidores de bace 1
BR112016007430A2 (pt) 5-aril-1-imino-1-oxo-[1,2,4]tiadiazinas
BR112019017314A2 (pt) composições farmacêuticas para terapia de combinação
CO2022006718A2 (es) Compuestos bicíclicos y métodos para su uso en el tratamiento del síndrome de pitt hopkins
AR110598A1 (es) Profármacos de principios activos citotóxicos con grupos enzimáticamente escindibles
UA109669U (uk) Фармацевтична композиція для лікування застудних захворювань у формі мазі