[go: up one dir, main page]

PE20130382A1 - Derivados de n-(imidazopirimidin-7-il)-heteroarilamida y su uso como inhibidores de pde10a - Google Patents

Derivados de n-(imidazopirimidin-7-il)-heteroarilamida y su uso como inhibidores de pde10a

Info

Publication number
PE20130382A1
PE20130382A1 PE2012001636A PE2012001636A PE20130382A1 PE 20130382 A1 PE20130382 A1 PE 20130382A1 PE 2012001636 A PE2012001636 A PE 2012001636A PE 2012001636 A PE2012001636 A PE 2012001636A PE 20130382 A1 PE20130382 A1 PE 20130382A1
Authority
PE
Peru
Prior art keywords
amide
lower alkyl
imidazopyrimidin
heteroarylamide
pde10a
Prior art date
Application number
PE2012001636A
Other languages
English (en)
Inventor
Sanchez Ruben Alvarez
Konrad Bleicher
Alexander Flohr
Luca Gobbi
Katrin Groebke Zbinden
Mathias Koerner
Bernd Kuhn
Jens-Uwe Peters
Markus Rudolph
Original Assignee
Hoffmann La Roche
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 Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of PE20130382A1 publication Critical patent/PE20130382A1/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
    • 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
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with 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
    • A61P25/14Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • 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
    • A61P25/22Anxiolytics
    • 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
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/30Drugs for disorders of the nervous system for treating abuse or dependence
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Biomedical Technology (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Psychiatry (AREA)
  • Psychology (AREA)
  • Anesthesiology (AREA)
  • Hospice & Palliative Care (AREA)
  • Pain & Pain Management (AREA)
  • Addiction (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

SE REFIERE A UN COMPUESTO DERIVADO DE N-(IMIDAZOPIRIMIDIN-7-IL)-HETEROARILAMIDA DE FORMULA (I) DONDE R1 ES FENILO O TIENILO OPCIONALMENTE SUSTUIDO CON OH, HALOGENO, ALQUILO INFERIOR, ENTRE OTROS; R2 ES UN HETEROARILO MONOCICLICO DE 5 O 6 ESLABONES QUE TIENE DE 1 A 3 HETEROATOMOS OPCIONALMENTE SUSTITUIDO CON NITRO, ALQUILO INFERIOR, ALCOXI INFERIOR, ENTRE OTROS; R8 ES HIDROGENO, ALQUILO INFERIOR, ALCOXI INFERIOR, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: 4-[(2-FLUOR-ETIL)-METIL-AMIDA]3-{[2-(3-FLUORMETOXIFENIL)-IMIDAZOL[1,2-a]PIRIMIDIN-7-IL]-AMIDA}DEL ACIDO 2-METIL-2H-PIRAZOL-3,4-DICARBOXILICO, 2-[(2-FENIL-IMIDAZO[1,2-a]PIRIMIDIN-7-IL)-AMIDA] 3-[(2,2,2-TRIFLUOR-ETIL)-AMIDA] DEL ACIDO PIRAZINA-2,3- DICARBOXILICO, ENTRE OTROS. REFERIDO ADEMAS A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE LA FOSFODIESTERASA 10A (PDE10A) SIENDO UTILES PARA EL TRATAMIENTO TERAPEUTICO Y/O PROFILACTICO DE LOS TRANSTORNOS PSICOTICOS, LA ESQUIZOFRENIA, TRANSTORNO DE LA ALUCINACION ENTRE OTROS.
PE2012001636A 2010-03-26 2011-03-23 Derivados de n-(imidazopirimidin-7-il)-heteroarilamida y su uso como inhibidores de pde10a PE20130382A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP10158011 2010-03-26

Publications (1)

Publication Number Publication Date
PE20130382A1 true PE20130382A1 (es) 2013-03-30

Family

ID=43989818

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2012001636A PE20130382A1 (es) 2010-03-26 2011-03-23 Derivados de n-(imidazopirimidin-7-il)-heteroarilamida y su uso como inhibidores de pde10a

Country Status (25)

Country Link
US (1) US8410117B2 (es)
EP (1) EP2552918B1 (es)
JP (1) JP5764196B2 (es)
KR (1) KR20130073876A (es)
CN (1) CN102791714B (es)
AR (1) AR080785A1 (es)
AU (1) AU2011231668A1 (es)
BR (1) BR112012024199A2 (es)
CA (1) CA2786213A1 (es)
CL (1) CL2012002497A1 (es)
CR (1) CR20120443A (es)
EC (1) ECSP12012174A (es)
ES (1) ES2478448T3 (es)
IL (1) IL220932A0 (es)
MA (1) MA34069B1 (es)
MX (1) MX2012010880A (es)
NZ (1) NZ600927A (es)
PE (1) PE20130382A1 (es)
PH (1) PH12012501772A1 (es)
RU (1) RU2562066C2 (es)
SG (1) SG183824A1 (es)
TW (1) TWI478924B (es)
UA (1) UA108640C2 (es)
WO (1) WO2011117264A1 (es)
ZA (1) ZA201206257B (es)

Families Citing this family (43)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2827724A1 (en) 2011-02-18 2012-08-23 Allergan, Inc. Substituted 6,7-dialkoxy-3-isoquinolinol derivatives as inhibitors of phosphodiesterase 10 (pde10a)
CA2852936A1 (en) 2011-10-20 2013-04-25 Glaxosmithkline Llc Substituted bicyclic aza-heterocycles and analogues as sirtuin modulators
EP2768834B1 (en) * 2011-10-20 2016-04-27 Glaxosmithkline LLC Substituted bicyclic aza-heterocycles and analogues as sirtuin modulators
KR20140077965A (ko) * 2011-10-20 2014-06-24 글락소스미스클라인 엘엘씨 시르투인 조절제로서의 치환된 비시클릭 아자-헤테로사이클 및 유사체
MX348635B (es) * 2012-08-17 2017-06-22 Hoffmann La Roche Proceso para preparación de derivados de ácido pirazol carboxílico.
WO2014071044A1 (en) 2012-11-01 2014-05-08 Allergan, Inc. Substituted 6,7-dialkoxy-3-isoquinoline derivatives as inhibitors of phosphodiesterase 10 (pde10a)
CA2888324A1 (en) * 2012-11-07 2014-05-15 Alexander Flohr Triazolo compounds
CN102964308B (zh) * 2012-11-30 2015-03-18 中国药科大学 新型嘧啶类化合物、其制备方法、包含此类化合物的药物组合物及其用途
TR201904614T4 (en) 2013-02-27 2019-05-21 Mochida Pharm Co Ltd Novel pyrazole derivative.
JP6130055B2 (ja) * 2013-05-23 2017-05-17 エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft 造影剤としての2−フェニルイミダゾ[1.2−a]ピリミジン
US10039764B2 (en) 2013-07-12 2018-08-07 University Of South Alabama Treatment and diagnosis of cancer and precancerous conditions using PDE10A inhibitors and methods to measure PDE10A expression
EP3049411B1 (en) * 2013-09-26 2017-04-26 F. Hoffmann-La Roche AG Imidazo[1,2-a]pyridin-7-amines as imaging tools
US9200016B2 (en) 2013-12-05 2015-12-01 Allergan, Inc. Substituted 6, 7-dialkoxy-3-isoquinoline derivatives as inhibitors of phosphodiesterase 10 (PDE 10A)
PL408251A1 (pl) * 2014-05-19 2015-11-23 Celon Pharma Spółka Z Ograniczoną Odpowiedzialnością Skondensowane pochodne triazolu jako inhibitory fosfodiesterazy 10A
JP6568855B2 (ja) * 2014-07-30 2019-08-28 持田製薬株式会社 ピラゾール誘導体の製造方法
JP6827621B2 (ja) * 2015-09-29 2021-02-10 オンコセラピー・サイエンス株式会社 Suv39h2を阻害するための二環式化合物およびその使用
TW201718581A (zh) 2015-10-19 2017-06-01 英塞特公司 作為免疫調節劑之雜環化合物
LT3377488T (lt) 2015-11-19 2023-01-10 Incyte Corporation Heterocikliniai junginiai, kaip imunomoduliatoriai
US20170174679A1 (en) 2015-12-22 2017-06-22 Incyte Corporation Heterocyclic compounds as immunomodulators
MA44860A (fr) 2016-05-06 2019-03-13 Incyte Holdings Corp Composés hétérocycliques utilisés comme immunomodulateurs
WO2017205464A1 (en) 2016-05-26 2017-11-30 Incyte Corporation Heterocyclic compounds as immunomodulators
HUE060256T2 (hu) 2016-06-20 2023-02-28 Incyte Corp Heterociklusos vegyületek mint immunmodulátorok
US20180016260A1 (en) 2016-07-14 2018-01-18 Incyte Corporation Heterocyclic compounds as immunomodulators
ES2941716T3 (es) 2016-08-29 2023-05-25 Incyte Corp Compuestos heterocíclicos como inmunomoduladores
WO2018119266A1 (en) 2016-12-22 2018-06-28 Incyte Corporation Benzooxazole derivatives as immunomodulators
JP7303108B2 (ja) 2016-12-22 2023-07-04 インサイト・コーポレイション 免疫調節剤としての二環式複素芳香環化合物
CN116115764A (zh) 2016-12-22 2023-05-16 因赛特公司 四氢咪唑并[4,5-c]吡啶衍生物作为pd-l1内在化诱导剂
EP3558989B1 (en) 2016-12-22 2021-04-14 Incyte Corporation Triazolo[1,5-a]pyridine derivatives as immunomodulators
WO2018119221A1 (en) 2016-12-22 2018-06-28 Incyte Corporation Pyridine derivatives as immunomodulators
TWI674260B (zh) 2017-02-01 2019-10-11 德商菲尼克斯製藥股份有限公司 芳基烴受體(AhR)調節劑化合物
TWI752155B (zh) 2017-02-01 2022-01-11 德商菲尼克斯製藥股份有限公司 芳香烴受體(AhR)調節劑化合物
ES3030010T3 (en) 2018-03-30 2025-06-26 Incyte Corp Heterocyclic compounds as immunomodulators
BR112020022936A2 (pt) 2018-05-11 2021-02-02 Incyte Corporation derivados de tetra-hidro-imidazo[4,5-c]piridina como imunomoduladores de pd-l1
BR112020013697A2 (pt) 2018-11-06 2020-12-01 H. Lundbeck A/S compostos para tratamento de sintomas negativos e comprometimentos cognitivos
WO2020094591A1 (en) 2018-11-06 2020-05-14 H. Lundbeck A/S Pde10a inhibitors for treating negative symptoms and cognitive impairments in a patient suffering from schizophrenia
CA3150434A1 (en) 2019-08-09 2021-02-18 Incyte Corporation Salts of a pd-1/pd-l1 inhibitor
IL291471B2 (en) 2019-09-30 2025-04-01 Incyte Corp Pyrimido[3,2–D]pyrimidine compounds as immunomodulators
MX2022004741A (es) * 2019-10-21 2022-05-16 Sk Biopharmaceuticals Co Ltd Uso de compuestos de imidazopirimidina o imidazotriazina para prevencion, alivio, o tratamiento de trastornos cognitivos, o para mejorar la funcion cognitiva.
JP2023500395A (ja) 2019-11-11 2023-01-05 インサイト・コーポレイション Pd-1/pd-l1阻害剤の塩及び結晶形態
US11760756B2 (en) 2020-11-06 2023-09-19 Incyte Corporation Crystalline form of a PD-1/PD-L1 inhibitor
US11780836B2 (en) 2020-11-06 2023-10-10 Incyte Corporation Process of preparing a PD-1/PD-L1 inhibitor
TW202233616A (zh) 2020-11-06 2022-09-01 美商英塞特公司 用於製備pd-1/pd-l1抑制劑以及其鹽及結晶形式之方法
CN115572282B (zh) * 2021-07-05 2024-07-09 华东理工大学 含芳杂环结构的吡唑酰胺类化合物及其制备方法和应用

Family Cites Families (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES493459A0 (es) 1980-07-17 1981-07-01 Consejo Superior Investigacion Procedimiento para la preparacion de 3(6 5)-formilpira- zol-4-carboxilatos de alquilo
SK9892001A3 (en) * 1999-11-10 2002-04-04 Ortho Mcneil Pharm Inc Substituted 2-aryl-3-(heteroaryl)-imidazo[1,2-a]pyrimidines, and related pharmaceutical compositions and methods
AU783521B2 (en) 2000-05-24 2005-11-03 Merck Sharp & Dohme Limited 3-phenyl-imidazo-pyrimidine derivatives as ligands for GABA receptors
US6596731B2 (en) * 2001-03-27 2003-07-22 Hoffmann-La Roche Inc. Substituted imidazo[1,2-A] pyridine derivatives
FR2825705B1 (fr) 2001-06-08 2005-05-20 Aventis Pharma Sa Nouveaux composes heterocycliques, leur preparation et leur utilisation comme medicaments, notamment comme anti-bacteriens
ZA200601706B (en) * 2003-07-30 2007-09-26 S A L V A T Lab Sa Substituted imidazopyrimidines for the prevention and treatment of cancer
CA2534432A1 (en) 2003-07-31 2005-02-10 Bayer Pharmaceuticals Corporation Methods for treating diabetes and related disorders using pde10a inhibitors
WO2007034282A2 (en) * 2005-09-19 2007-03-29 Pfizer Products Inc. Diaryl-imidazole compounds condensed with a heterocycle as c3a receptor antagonists
WO2007082806A1 (en) * 2006-01-17 2007-07-26 F. Hoffmann-La Roche Ag Aryl-isoxazol-4-yl-imidazo[1,2-a]pyridine useful for the treatment of alzheimer’s disease via gaba receptors
US7951824B2 (en) 2006-02-17 2011-05-31 Hoffman-La Roche Inc. 4-aryl-pyridine-2-carboxyamide derivatives
DK2497470T3 (en) * 2006-11-22 2015-12-07 Incyte Holdings Corp Imidazotriaziner and imidazopyrimidines as kinase inhibitors
EP1964841A1 (en) * 2007-02-28 2008-09-03 sanofi-aventis Imidazo[1,2-a]azine and their use as pharmaceuticals
DE102007048716A1 (de) * 2007-10-11 2009-04-23 Merck Patent Gmbh Imidazo[1,2-a]pyrimidinderivate
FR2926556B1 (fr) * 2008-01-22 2010-02-19 Sanofi Aventis Derives de carboxamides n-azabicycliques, leur preparation et leur application en therapeutique
TWI501965B (zh) * 2008-06-20 2015-10-01 Lundbeck & Co As H 作為pde10a酵素抑制劑之新穎苯基咪唑衍生物

Also Published As

Publication number Publication date
CN102791714B (zh) 2015-03-25
KR20130073876A (ko) 2013-07-03
SG183824A1 (en) 2012-10-30
AR080785A1 (es) 2012-05-09
CA2786213A1 (en) 2011-09-29
US20110237564A1 (en) 2011-09-29
RU2012143794A (ru) 2014-05-10
EP2552918B1 (en) 2014-06-11
PH12012501772A1 (en) 2017-07-26
CL2012002497A1 (es) 2013-03-22
WO2011117264A1 (en) 2011-09-29
JP5764196B2 (ja) 2015-08-12
US8410117B2 (en) 2013-04-02
IL220932A0 (en) 2012-09-24
ES2478448T3 (es) 2014-07-22
AU2011231668A1 (en) 2012-07-19
HK1173440A1 (en) 2013-05-16
ZA201206257B (en) 2013-05-29
TWI478924B (zh) 2015-04-01
UA108640C2 (uk) 2015-05-25
MX2012010880A (es) 2012-10-15
NZ600927A (en) 2013-08-30
TW201136937A (en) 2011-11-01
CR20120443A (es) 2012-10-11
JP2013523673A (ja) 2013-06-17
EP2552918A1 (en) 2013-02-06
BR112012024199A2 (pt) 2016-07-05
ECSP12012174A (es) 2012-10-30
MA34069B1 (fr) 2013-03-05
RU2562066C2 (ru) 2015-09-10
CN102791714A (zh) 2012-11-21

Similar Documents

Publication Publication Date Title
PE20130382A1 (es) Derivados de n-(imidazopirimidin-7-il)-heteroarilamida y su uso como inhibidores de pde10a
PE20190913A1 (es) Derivados aromaticos de sulfonamida
PE20141540A1 (es) Derivados de 2-amino-4-(piridin-2-il)-5,6-dihidro-4h-1,3-oxazina y su uso como inhibidores de bace-1 y/o bace-2
PE20142301A1 (es) Uracilos sustituidos biciclicamente y uso de los mismos
CO6612267A2 (es) Nuevos derivados de 1,1 dióxido- 5 fenil- 2,3,4-5tetrahidro- 1,4-benzotiazepina y composiciones farmaceúticas que los comprenden
PE20140934A1 (es) Derivados de pirazol
PE20140192A1 (es) Derivados de bencimidazol como inhibidores de cinasa pi3
CO6341581A2 (es) Derivados de heteroarilo como inhibidores de dgat1
JO3025B1 (ar) الأندازولات المستبدلة بالأوكسازول كمثبطات كيناز pi3
PE20130279A1 (es) Compuestos heteroarilo nitrogenados
PE20121471A1 (es) Derivados de sulfonamida heterociclicos utiles como inhibidores de mek
MX2012004311A (es) Derivados de ciclohexano spiro condensados como inhibidores de lipasa sensible a hormonas (hsl) utiles en el tratamiento de diabetes.
PE20151538A1 (es) Nuevos compuestos como inhibidores de reorganizado durante la transfeccion (ret)
PE20120834A1 (es) Derivados de furopirimidindiona como moduladores de trpa1
PE20121352A1 (es) Derivados de heteroarilo que contienen n como inhibidores de cinasa jak3
PE20140927A1 (es) Compuestos heterociclicos como inhibidores de cinasas
PE20142019A1 (es) Nuevos derivados de acidos indaniloxidihidrobenzofuranilaceticos y sus usos como agonistas del receptor gpr40
CY1121248T1 (el) Πολυμορφικες μορφες κι αλατα 6-(1h-ινδολ-4-υλ)-4-(5-{[4-(1-μεθυλαιθυλο)-1-πιπεραζινυλ]μεθυλο}-1,3-οξαζολ-2-υλ)-1η-ινδαζολιου ως αναστολεις ρi3κ για χρηση στη θεραπεια π.χ. αναπνευστικων διαταραχων
PE20130155A1 (es) Derivados de ariletinilo
PE20141529A1 (es) Derivados de biciclo [3,2,1] octilamida y sus usos
PE20141682A1 (es) Derivados de (4-fenilimidazol-2-il) etilamina utiles como moduladores de canal de sodio
PE20120062A1 (es) Derivados de 1-bencil-2-amino-tetralina como inhibidores del transportador de glicina glyt1
AR086100A1 (es) Compuestos de cromenona y composiciones farmaceuticas que los contienen
PE20141380A1 (es) Imidazopiridazinas como inhibidores de quinasa akt
PE20141167A1 (es) Piridopirazinas sustituidas como inhibidores novedosos de ptk

Legal Events

Date Code Title Description
FA Abandonment or withdrawal