AR083475A1 - Moduladores de receptores de glutamato metabotropicos - Google Patents

Moduladores de receptores de glutamato metabotropicos

Info

Publication number
AR083475A1
AR083475A1 ARP110103856A ARP110103856A AR083475A1 AR 083475 A1 AR083475 A1 AR 083475A1 AR P110103856 A ARP110103856 A AR P110103856A AR P110103856 A ARP110103856 A AR P110103856A AR 083475 A1 AR083475 A1 AR 083475A1
Authority
AR
Argentina
Prior art keywords
alkyl
ring
amino
represents hydrogen
fluorine
Prior art date
Application number
ARP110103856A
Other languages
English (en)
Inventor
Ronalds Zemribo
Markus Henrich
Ulrich Abel
Sibylle Muller
Holger Kubas
Udo Meyer
Mirko Hechenberger
Valerjans Kauss
Original Assignee
Merz Pharma Gmbh & Co Kgaa
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 Merz Pharma Gmbh & Co Kgaa filed Critical Merz Pharma Gmbh & Co Kgaa
Publication of AR083475A1 publication Critical patent/AR083475A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/04Ortho-condensed 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D215/20Oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/06Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • 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
    • 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
    • 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
    • C07D491/044Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
    • C07D491/052Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being six-membered
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D519/00Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0012Galenical forms characterised by the site of application
    • A61K9/0019Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0087Galenical forms not covered by A61K9/02 - A61K9/7023
    • A61K9/0095Drinks; Beverages; Syrups; Compositions for reconstitution thereof, e.g. powders or tablets to be dispersed in a glass of water; Veterinary drenches
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/10Dispersions; Emulsions
    • A61K9/12Aerosols; Foams
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • A61K9/2004Excipients; Inactive ingredients
    • A61K9/2022Organic macromolecular compounds
    • A61K9/205Polysaccharides, e.g. alginate, gums; Cyclodextrin
    • A61K9/2054Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/48Preparations in capsules, e.g. of gelatin, of chocolate
    • A61K9/4841Filling excipients; Inactive ingredients
    • A61K9/4866Organic macromolecular compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/48Preparations in capsules, e.g. of gelatin, of chocolate
    • A61K9/50Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
    • A61K9/51Nanocapsules; Nanoparticles
    • A61K9/5107Excipients; Inactive ingredients
    • A61K9/513Organic macromolecular compounds; Dendrimers
    • A61K9/5138Organic macromolecular compounds; Dendrimers obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyvinyl pyrrolidone, poly(meth)acrylates
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/70Web, sheet or filament bases ; Films; Fibres of the matrix type containing drug
    • A61K9/7023Transdermal patches and similar drug-containing composite devices, e.g. cataplasms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00Systems containing only non-condensed rings
    • C07C2601/02Systems containing only non-condensed rings with a three-membered ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00Systems containing only non-condensed rings
    • C07C2601/06Systems containing only non-condensed rings with a five-membered ring
    • C07C2601/08Systems containing only non-condensed rings with a five-membered ring the ring being saturated

Abstract

Proceso para la preparación de dichos compuestos. Los compuestos son moduladores de mGluR5 y por ello son de utilidad para el control y la prevención de trastornos neurológicos agudos y/o crónicos.Reivindicación 1: Un compuesto caracterizado porque se selecciona entre aquellos de la fórmula (1) donde R1 representa arilo, heteroarilo, cicloalquilo C3-12, cicloalquenilo C5-12, o heterociclilo; R2 representa hidrógeno, flúor, o alquilo C1-6; R3 representa hidrógeno, flúor, o alquilo C1-6; o R2 y R3 junto con el átomo de carbono al cual se encuentran unidos forman un anillo de entre 3 y 7 miembros que puede ser saturado o insaturado, donde el anillo opcionalmente puede contener uno o dos heteroátomos seleccionados entre azufre, oxígeno, y nitrógeno y donde el anillo puede estar opcionalmente sustituido con uno o más sustituyentes seleccionados entre halógeno, fluorometilo, difluorometilo, trifluorometilo, trifluorometoxi, alquilo C1-6, alcoxi C1-6, amino, hidroxi, ciano, acilo, alquilamino C1-6, di-(alquil C1-6)amino, alquilcarbonilamino C1-6, y oxo; W representa CH2, -CR4R5CH2-, O, S, -CR6R7O-, NR8, o -CR9R10NR11-; Y representa CR12R13, o NR14; R4 representa hidrógeno, flúor, o alquilo C1-6; R5 representa hidrógeno, flúor, o alquilo C1-6; o R4 y R5 junto con el átomo de carbono al cual se encuentran unidos forman un anillo de entre 3 y 7 miembros que puede ser saturado o insaturado, donde el anillo opcionalmente puede contener uno o dos heteroátomos seleccionados entre azufre, oxígeno, y nitrógeno y donde el anillo puede estar opcionalmente sustituido con uno o más sustituyentes seleccionados entre halógeno, fluorometilo, difluorometilo, trifluorometilo, trifluorometoxi, alquilo C1-6, alcoxi C1-6, amino, hidroxi, ciano, acilo, alquilamino C1-6, di-(alquil C1-6)amino, alquilcarbonilamino C1-6, y oxo; R6 representa hidrógeno, flúor, o alquilo C1-6; R7 representa hidrógeno, flúor, o alquilo C1-6; o R6 y R7 junto con el átomo de carbono al cual se encuentran unidos forman un anillo de entre 3 y 7 miembros que puede ser saturado o insaturado, donde el anillo opcionalmente puede contener uno o dos heteroátomos seleccionados entre azufre, oxígeno, y nitrógeno y donde el anillo puede estar opcionalmente sustituido con uno o más sustituyentes seleccionados entre halógeno, fluorometilo, difluorometilo, trifluorometilo, trifluorometoxi, alquilo C1-6, alcoxi C1-6, amino, hidroxi, ciano, acilo, alquilamino C1-6, di-(alquil C1-6)amino, alquilcarbonilamino C1-6, y oxo; R8 representa hidrógeno, alquilo C1-6, o acilo; R9 representa hidrógeno, flúor, o alquilo C1-6; R10 representa hidrógeno, flúor, o alquilo C1-6; o R9 y R10 junto con el átomo de carbono al cual se encuentran unidos forman un anillo de entre 3 y 7 miembros que puede ser saturado o insaturado, donde el anillo opcionalmente puede contener uno o dos heteroátomos seleccionados entre azufre, oxígeno, y nitrógeno y donde el anillo puede estar opcionalmente sustituido con uno o más sustituyentes seleccionados entre halógeno, fluorometilo, difluorometilo, trifluorometilo, trifluorometoxi, alquilo C1-6, alcoxi C1-6, amino, hidroxi, ciano, acilo, alquilamino C1-6, di-(alquil C1-6)amino, alquilcarbonilamino C1-6, y oxo; R11 representa hidrógeno, alquilo C1-6, o acilo; R12 representa hidrógeno, flúor, alquilo C1-6, amino, alquilamino C1-6, di-(alquil C1-6)amino, acilamino, o heterociclilo; R13 representa hidrógeno, flúor, o alquilo C1-6; o R12 y R13 junto con el átomo de carbono al cual se encuentran unidos forman un anillo de entre 3 y 7 miembros que puede ser saturado o insaturado, donde el anillo opcionalmente puede contener uno o dos heteroátomos seleccionados entre azufre, oxígeno, y nitrógeno y donde el anillo puede estar opcionalmente sustituido con uno o más sustituyentes seleccionados entre halógeno, fluorometilo, difluorometilo, trifluorometilo, trifluorometoxi, alquilo C1-6, alcoxi C1-6, amino, hidroxi, ciano, acilo, alquilamino C1-6, di-(alquil C1-6)amino, alquilcarbonilamino C1-6, y oxo; y R14 representa hidrógeno, alquilo C1-6, arilo, o heteroarilo; donde el término “arilo” significa fenilo o naftilo, donde el grupo fenilo o naftilo está opcionalmente sustituido con uno o más sustituyentes, que pueden ser iguales o diferentes, seleccionados en forma independiente entre halógeno, fluorometilo, difluorometilo, trifluorometilo, trifluorometoxi, alquilo C1-6, hidroxialquilo C1-6, alquenilo C2-6, alcoxi C1-6, alcoxi C1-6-alquilo C1-6, amino, hidroxi, nitro, ciano, formilo, alquilcarbonilo C1-6, alcoxicarbonilo C1-6, alquilcarboniloxi C1-6, alquilcarboniloxi C1-6-alquilo C1-6, alquilamino C1-6, di-(alquil C1-6)amino, cicloalquilamino C3-12, alquilcarbonilamino C1-6, fenilcarbonilamino, aminocarbonilo, N-alquilaminocarbonilo C1-6, di-N,N-alquilaminocarbonilo C1-6, pirrolidinilo, piperidinilo, morfolinilo, piperazinilo, cicloalquilo C3-12, piridinilo, y alquilendioxi C1-6; el término “heteroarilo” significa un anillo aromático de 5 ó 6 miembros que contiene entre uno y cuatro heteroátomos seleccionados entre oxígeno, azufre y nitrógeno, o un grupo bicíclico que comprende un anillo de 5 ó 6 miembros que contiene entre uno y cuatro heteroátomos seleccionados entre oxígeno, azufre y nitrógeno fusionado con un anillo benceno o un anillo de 5 ó 6 miembros que contiene entre uno y cuatro heteroátomos seleccionados entre oxígeno, azufre y nitrógeno, donde el grupo heteroarilo puede estar opcionalmente sustituido con uno o más sustituyentes, que pueden ser iguales o diferentes, seleccionados en forma independiente entre halógeno, fluorometilo, difluorometilo, trifluorometilo, trifluorometoxi, alquilo C1-6, hidroxialquilo C1-6, alquenilo C2-6, alcoxi C1-6, amino, hidroxi, nitro, ciano, alquilcarbonilo C1-6, alcoxicarbonilo C1-6, alcoxicarboniloxi C1-6, alquilamino C1-6, y di-(alquil C1-6)amino, cicloalquilamino C3-12, alquilcarbonilamino C1-6, aminocarbonilo, N-alquilaminocarbonilo C1-6, di-N,N-alquilaminocarbonilo C1-6, pirrolidinilo, piperidinilo, morfolinilo, cicloalquilo C3-12, alquilendioxi C1-6, arilo, y piridinilo; e isómeros ópticos, prodrogas, sales farmacéuticamente aceptables, hidratos, solvatos y polimorfos del mismo.
ARP110103856A 2010-10-18 2011-10-18 Moduladores de receptores de glutamato metabotropicos AR083475A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US45529010P 2010-10-18 2010-10-18
EP10187954 2010-10-18

Publications (1)

Publication Number Publication Date
AR083475A1 true AR083475A1 (es) 2013-02-27

Family

ID=43618690

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP110103856A AR083475A1 (es) 2010-10-18 2011-10-18 Moduladores de receptores de glutamato metabotropicos

Country Status (2)

Country Link
AR (1) AR083475A1 (es)
WO (1) WO2012052451A1 (es)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2012084873A1 (en) * 2010-12-20 2012-06-28 Novartis Ag 4- (hetero) aryl - ethynyl - octahydro - indole - 1 - carboxylic acid esters
WO2012151139A1 (en) * 2011-05-03 2012-11-08 Merck Sharp & Dohme Corp. Alkyne benzotriazole derivatives
EP2650284A1 (en) * 2012-04-10 2013-10-16 Merz Pharma GmbH & Co. KGaA Heterocyclic derivatives as metabotropic glutamate receptor modulators
MX358311B (es) 2012-04-17 2018-08-14 Fujifilm Corp Compuesto heterociclico que contiene nitrogeno o sal del mismo.
EP3191441B1 (en) 2014-09-09 2020-02-19 Boehringer Ingelheim International Trading (Shanghai) Co. Ltd. Novel process for preparation of spiro[2.5]octane-5,7-dione and spiro[3.5]nonane-6,8-dione
KR20210009357A (ko) * 2018-05-17 2021-01-26 브리스톨-마이어스 스큅 컴퍼니 Ror 감마 조정제로서의 트리시클릭 술폰 화합물

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL7305644A (es) 1972-04-20 1973-10-23
DE2856393C2 (de) 1978-12-27 1983-04-28 Merz + Co GmbH & Co, 6000 Frankfurt Arzneimittel zur Behandlung von Morbus Parkinson
DE58905637D1 (de) 1989-04-14 1993-10-21 Merz & Co Gmbh & Co Verwendung von Adamantan-Derivaten zur Prävention und Behandlung der cerebralen Ischämie.
WO2003076416A1 (en) 2002-03-08 2003-09-18 Warner-Lambert Company Llc Oxo azabicyclic compounds
BR0313724A (pt) 2002-08-13 2005-06-28 Warner Lambert Co Derivados de azaisoquinolina como inibidores de metaloproteinase de matriz
MXPA05001785A (es) 2002-08-13 2005-04-25 Warner Lambert Co Derivados de cromona como inhibidores de las metaloproteinasas de matriz.
TWI301760B (en) 2004-02-27 2008-10-11 Merz Pharma Gmbh & Co Kgaa Tetrahydroquinolinones and their use as antagonists of metabotropic glutamate receptors
WO2007023242A1 (en) 2005-08-24 2007-03-01 Merz Pharma Gmbh & Co. Kgaa Tetrahydroquinolinones and their use as modulators of metabotropic glutamate receptors
US20080045521A1 (en) 2006-06-09 2008-02-21 Astrazeneca Ab Phenylalanine derivatives
WO2010063487A1 (en) 2008-12-05 2010-06-10 Merz Pharma Gmbh & Co. Kgaa Pyrazolopyrimidines, a process for their preparation and their use as medicine

Also Published As

Publication number Publication date
WO2012052451A1 (en) 2012-04-26

Similar Documents

Publication Publication Date Title
AR083475A1 (es) Moduladores de receptores de glutamato metabotropicos
AR077796A1 (es) Moduladores de receptores de glutamato metabotropicos
AR076435A1 (es) Compuestos de indazoles sustituidos, composiciones farmaceuticas que los contienen y procesos de obtencion de los mismos
PE20181024A1 (es) Derivados de ciclohexano sustituido con amido
AR061567A1 (es) Compuestos puros enantiomericamente para el tratamiento de desordenes proliferativos
CR20160548A (es) Nuevos Derivados de Pirazolo Pirimidina y su Uso como Inhibidores de MALT1
AR052902A1 (es) Derivados de piridazina, composicion farmaceutica que los contiene y su uso como agentes terapeuticos para enfermedades mediadas por la estearoil-coa desaturasa
AR068846A1 (es) Compuestos derivados de pirrolo (2,3d)-pirimidina inhibidores de la actividad de pkb, composiciones farmaceuticas que los contienen, proceso de preparacion y uso de los mismos como agentes anticancer
ES2590504T3 (es) N-ciclilamidas como nematicidas
AR055592A1 (es) Derivados de 2-amino-5-cicloalquil-hidantoina como moduladores y/o inhibidores de la beta-secretasa(bace)
ES2659397T3 (es) 2-azabicíclicos sustituidos y su uso como moduladores receptores de orexinas
AR082799A1 (es) Derivados de quinolina y quinoxalina como inhibidores de quinasa
AR053186A1 (es) Derivados del 1- bencil indol carboxamida
AR078172A1 (es) Fenoximetil dihidro oxazolopirimidinonas sustituidas y uso de las mismas como moduladores de receptores metabotropicos de mglur
AR100810A1 (es) Inhibidores de fosfatidilinositol 3-quinasa
AR056103A1 (es) Compuestos de(piran-piperidinil)benzimidazol, composiciones farmaceuticas que los comprenden, proceso de preparacion y usos en el tratamiento de afecciones mediadas por agonistas del receptor muscarinico m1
AR100806A1 (es) Inhibidores de fosfatidilinositol 3-quinasa
AR067646A1 (es) Ariloxazoles sustituidos y su uso
PE20161368A1 (es) Inhibidores de diacilglicerol aciltranferasa 2
AR110282A1 (es) Compuestos de amida bicíclica y uso de éstos en el tratamiento de enfermedades mediadas por rip1
AR086036A1 (es) DERIVADOS DE ETINILO COMO MODULADORES ALOSTERICOS POSITIVOS DE (mGluR5)
AR076401A1 (es) Bisaril alquinilamidas como moduladores alostericos negativos del receptor metabotropico de glutamato 5 (mglur5)
AR085088A1 (es) Inhibidores de histona desacetilasa y composiciones farmaceuticas que los contienen
PE20161369A1 (es) Inhibidores de monoacilglicerol aciltransferasa 2 (mgat2) de dihidropiridinona sustituidos con tetrazolona
PE20181853A1 (es) 1,5-dihidro-4h-pirazolo[3,4-d]pirimidin-4-onas y 1,5-dihidro-4h-pirazolo[4,3-c]piridin-4-onas como inhibidores de pde1

Legal Events

Date Code Title Description
FB Suspension of granting procedure