MA32734B1 - Antagonisme smoothened pour traitement de troubles lies a la voie de signalisation hedgehog - Google Patents

Antagonisme smoothened pour traitement de troubles lies a la voie de signalisation hedgehog

Info

Publication number
MA32734B1
MA32734B1 MA33801A MA33801A MA32734B1 MA 32734 B1 MA32734 B1 MA 32734B1 MA 33801 A MA33801 A MA 33801A MA 33801 A MA33801 A MA 33801A MA 32734 B1 MA32734 B1 MA 32734B1
Authority
MA
Morocco
Prior art keywords
smoothened
hedgehog signaling
disorders related
inhibitors
formula
Prior art date
Application number
MA33801A
Other languages
Arabic (ar)
English (en)
Inventor
Marion Dorsch
John E Monahan
Michael Patrick Morrissey
Shifeng Pan
Juliet Williams
Original Assignee
Novartis Ag
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=41314595&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MA32734(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Novartis Ag filed Critical Novartis Ag
Publication of MA32734B1 publication Critical patent/MA32734B1/fr

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
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • 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
    • A61K31/167Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the nitrogen of a carboxamide group directly attached to the aromatic ring, e.g. lidocaine, paracetamol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/365Lactones
    • A61K31/366Lactones having six-membered rings, e.g. delta-lactones
    • 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
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/41641,3-Diazoles
    • A61K31/41841,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
    • 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
    • A61K31/4402Non condensed pyridines; Hydrogenated derivatives thereof only substituted in position 2, e.g. pheniramine, bisacodyl
    • 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
    • A61K31/4433Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with oxygen as a ring hetero atom
    • 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
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/4545Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
    • 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
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/4738Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/4745Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
    • 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
    • A61K31/50Pyridazines; Hydrogenated pyridazines
    • A61K31/502Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with carbocyclic ring systems, e.g. cinnoline, phthalazine
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

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)
  • Pain & Pain Management (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

La présente invention concerne des procédés qui permettent de moduler, par exemple, d'exercer un effet antagoniste sur l'activité de la voie de signalisation Hedgehog, et de traiter des troubles liées à la voie de signalisation Hedgehog tels que des cancers (par exemple, le médulloblastome). En particulier, l'invention concerne des procédés permettant d'inhiber des états de croissance aberrante résultant de phénotypes tels que la perte de fonction Ptch, le gain de fonction Hedgehog, le gain de fonction Smoothened ou le gain de fonction GIi par administration à un mammifère de combinaisons d'inhibiteurs Smoothened (par exemple, un composé de formule I, de formule II, ou de formule III, ou un quelconque des composés se trouvant dans la liste de référence incluse dans la description) et des inhibiteurs de la voie de signalisation de la biosynthèse du cholestérol (par exemple, des statines), des inhibiteurs GIi, et/ou des inhibiteurs de la Phosphatidylinositol 3-kinase (P13K).
MA33801A 2008-10-01 2011-04-29 Antagonisme smoothened pour traitement de troubles lies a la voie de signalisation hedgehog MA32734B1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US10185808P 2008-10-01 2008-10-01
US10185108P 2008-10-01 2008-10-01
PCT/EP2009/062537 WO2010037715A1 (fr) 2008-10-01 2009-09-28 Antagonisme smoothened pour le traitement de troubles liés à la voie de signalisation hedgehog

Publications (1)

Publication Number Publication Date
MA32734B1 true MA32734B1 (fr) 2011-10-02

Family

ID=41314595

Family Applications (1)

Application Number Title Priority Date Filing Date
MA33801A MA32734B1 (fr) 2008-10-01 2011-04-29 Antagonisme smoothened pour traitement de troubles lies a la voie de signalisation hedgehog

Country Status (16)

Country Link
US (2) US8778927B2 (fr)
EP (3) EP2617414A3 (fr)
JP (2) JP5773873B2 (fr)
KR (1) KR101624000B1 (fr)
CN (2) CN102170873B (fr)
AU (1) AU2009299927B2 (fr)
BR (1) BRPI0920533A2 (fr)
CA (1) CA2738868C (fr)
CL (1) CL2011000710A1 (fr)
IL (1) IL211678A (fr)
MA (1) MA32734B1 (fr)
MX (1) MX340304B (fr)
RU (1) RU2519200C2 (fr)
TW (1) TWI478916B (fr)
WO (1) WO2010037715A1 (fr)
ZA (1) ZA201101725B (fr)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20100041663A1 (en) 2008-07-18 2010-02-18 Novartis Ag Organic Compounds as Smo Inhibitors
RU2519200C2 (ru) * 2008-10-01 2014-06-10 Новартис Аг Применение антагонистов smoothened для лечения связанных с путем hedgehog нарушений
ES2588981T3 (es) * 2010-10-05 2016-11-08 Genentech, Inc. Smoothened mutante y métodos de uso de la misma
TWI574687B (zh) * 2011-01-03 2017-03-21 古利斯股份有限公司 具有鋅結合部份之刺蝟拮抗劑
US9708299B2 (en) 2011-01-03 2017-07-18 Genentech, Inc. Hedgehog antagonists having zinc binding moieties
US20120184529A1 (en) * 2011-01-14 2012-07-19 Demario Mark D Combination therapy
US20120207840A1 (en) * 2011-02-10 2012-08-16 Aura Biosciences, Inc. Virion Derived Protein Nanoparticles For Delivering Diagnostic Or Therapeutic Agents For The Treatment Of Non-Melanoma Skin Cancer
US9248128B2 (en) 2012-01-27 2016-02-02 New York University Method for enhancing remyelination using GLI1 inhibitors
CN104177363B (zh) * 2013-05-24 2018-06-05 江苏先声药业有限公司 双环杂环胺类Hedgehog信号通路抑制剂
CN105518027A (zh) * 2013-09-17 2016-04-20 豪夫迈·罗氏有限公司 使用抗lgr5抗体的方法
US9970935B2 (en) * 2014-02-06 2018-05-15 The Brigham And Women's Hospital, Inc. Uses of GLI1 in detecting tissue fibrosis
US20170290849A1 (en) * 2014-09-05 2017-10-12 The Trustees Of Columbia University In The City Of New York AKT and SHH Pathway Inhibitor Combination Therapy for Treating Basal Cell Carcinomas
EP3560924B1 (fr) 2015-04-02 2021-03-31 Merck Patent GmbH Imidazolonyl-quinoléines et leur utilisation comme inhibiteurs du atm kinase
WO2017007634A1 (fr) * 2015-07-06 2017-01-12 The Board Of Regents Of The University Of Texas System Composés benzamide ou benzamine à utiliser en tant qu'anticancéreux pour le traitement de cancers humains
WO2017156350A1 (fr) 2016-03-09 2017-09-14 K-Gen, Inc. Méthodes de traitement du cancer
US10548908B2 (en) 2016-09-15 2020-02-04 Nostopharma, LLC Compositions and methods for preventing and treating heterotopic ossification and pathologic calcification
EP3624798A1 (fr) * 2017-05-18 2020-03-25 Institut National de la Sante et de la Recherche Medicale (INSERM) Méthodes et compositions pharmaceutiques pour le traitement de maladies mastocytaires
WO2018218114A1 (fr) * 2017-05-26 2018-11-29 Institute For Cancer Research D/B/A The Research Institute Of Fox Chase Cancer Center Utilisation du cholestérol pour favoriser la survie et la prolifération de cellules de médulloblastomes primaires
CN110856722A (zh) * 2018-08-26 2020-03-03 中国农业科学院上海兽医研究所(中国动物卫生与流行病学中心上海分中心) 环靶明或其衍生物的用途

Family Cites Families (34)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4681893A (en) * 1986-05-30 1987-07-21 Warner-Lambert Company Trans-6-[2-(3- or 4-carboxamido-substituted pyrrol-1-yl)alkyl]-4-hydroxypyran-2-one inhibitors of cholesterol synthesis
US7709454B2 (en) * 1997-06-20 2010-05-04 New York University Methods and compositions for inhibiting tumorigenesis
CO5090829A1 (es) 1998-07-21 2001-10-30 Novartis Ag Compuestos organicos de la formula i, utiles como inhibido res de la proteina de transferencia de triglicerido microso mal y de la secrecion de la apolipoproteina b.
WO2001005767A1 (fr) 1999-07-20 2001-01-25 Novartis Ag Composes organiques
US8354397B2 (en) * 2001-07-27 2013-01-15 Curis, Inc. Mediators of hedgehog signaling pathways, compositions and uses related thereto
BR0312597A (pt) * 2002-07-11 2005-05-10 Combinatorx Inc Combinações de drogas para o tratamento de neoplasmas
US7135575B2 (en) * 2003-03-03 2006-11-14 Array Biopharma, Inc. P38 inhibitors and methods of use thereof
WO2005094864A2 (fr) 2004-03-30 2005-10-13 Max-Planck Gesellschaft zur Förderung der Wissenschaften e.V. Traitement de tumeurs qui secretent du wnt et du hedgehog avec des inhibiteurs de biogenese de particule de lipoproteine
KR20140048343A (ko) * 2004-09-02 2014-04-23 제넨테크, 인크. 헤지호그 신호전달에 대한 피리딜 억제제
CA2583812A1 (fr) 2004-10-28 2006-05-11 Irm Llc Composes et compositions servant de modulateurs de la voie de signalisation hedgehog
GB0510390D0 (en) * 2005-05-20 2005-06-29 Novartis Ag Organic compounds
FR2889087B1 (fr) 2005-07-28 2008-09-12 Saint Gobain Ct Recherches Support de cuisson pour ceramiques et procede d'obtention
JP3996173B2 (ja) 2005-07-29 2007-10-24 ヤマト株式会社 塗装用マスキング材
AU2007204208A1 (en) 2006-01-11 2007-07-19 Astrazeneca Ab Morpholino pyrimidine derivatives and their use in therapy
JO2660B1 (en) * 2006-01-20 2012-06-17 نوفارتيس ايه جي Pi-3 inhibitors and methods of use
US20090029997A1 (en) 2006-01-23 2009-01-29 Laboratoires Serono Sa Thiazole Derivatives and Use Thereof
WO2007087395A2 (fr) 2006-01-25 2007-08-02 Osi Pharmaceuticals, Inc. INHIBITEURS DE mTOR INSATURES
US7517995B2 (en) 2006-04-06 2009-04-14 Boehringer Ingelheim International Gmbh Thiazolyl-dihydro-cyclopentapyrazole
US20070238746A1 (en) 2006-04-06 2007-10-11 Trixi Brandl Thiazolyl-dihydro-chinazoline
KR20090006089A (ko) * 2006-04-14 2009-01-14 노파르티스 아게 헤지호그 경로 관련 질환의 치료에서의 바이아릴카르복스아미드의 용도
US8252792B2 (en) 2006-04-26 2012-08-28 F. Hoffman-La Roche Ag Pyrimidine derivatives as PI3K inhibitors
DK2024372T3 (da) 2006-04-26 2010-09-20 Hoffmann La Roche Thieno[3,2-d]pyrimidin-derivat, der er egnet som P13K inhibitor
JP2009535388A (ja) 2006-05-03 2009-10-01 アストラゼネカ アクチボラグ ピラゾール誘導体、及びそのpi3k阻害薬としての使用
GB0608854D0 (en) 2006-05-04 2006-06-14 Chroma Therapeutics Ltd P13 kinase inhibitors
GB0608823D0 (en) 2006-05-04 2006-06-14 Chroma Therapeutics Ltd Inhibitors of P13 kinase
UA93548C2 (uk) 2006-05-05 2011-02-25 Айерем Елелсі Сполуки та композиції як модулятори хеджхогівського сигнального шляху
WO2007139492A1 (fr) 2006-05-30 2007-12-06 Actar Ab Dérivés hexahydropyrimidine, tétrahydroimidazole ou octahydroazépane
PE20080948A1 (es) 2006-07-25 2008-09-10 Irm Llc Derivados de imidazol como moduladores de la senda de hedgehog
EP1972631A1 (fr) * 2007-03-23 2008-09-24 Novartis AG Imidazopyridazines comme inhibiteurs de kinase lipide PI3K
MY159181A (en) * 2006-11-21 2016-12-30 Univ Putra Malaysia Use of an anti-cancer compound
PE20090188A1 (es) * 2007-03-15 2009-03-20 Novartis Ag Compuestos heterociclicos como moduladores de la senda de hedgehog
CN101820950B (zh) * 2007-06-07 2015-01-21 Irm责任有限公司 作为刺猬蛋白信号通路调节剂的联苯基甲酰胺类化合物
US20100041663A1 (en) * 2008-07-18 2010-02-18 Novartis Ag Organic Compounds as Smo Inhibitors
RU2519200C2 (ru) * 2008-10-01 2014-06-10 Новартис Аг Применение антагонистов smoothened для лечения связанных с путем hedgehog нарушений

Also Published As

Publication number Publication date
ZA201101725B (en) 2011-12-28
US8778927B2 (en) 2014-07-15
MX340304B (es) 2016-07-05
AU2009299927A1 (en) 2010-04-08
IL211678A0 (en) 2011-06-30
RU2519200C2 (ru) 2014-06-10
JP2015180654A (ja) 2015-10-15
CL2011000710A1 (es) 2011-08-05
JP2012504573A (ja) 2012-02-23
CA2738868C (fr) 2017-01-17
BRPI0920533A2 (pt) 2020-12-15
US20140200217A1 (en) 2014-07-17
CN102170873B (zh) 2014-07-30
RU2011117059A (ru) 2012-11-10
WO2010037715A1 (fr) 2010-04-08
TW201018672A (en) 2010-05-16
EP2346499A1 (fr) 2011-07-27
CN103784457A (zh) 2014-05-14
EP3023097A1 (fr) 2016-05-25
CN102170873A (zh) 2011-08-31
EP2617414A3 (fr) 2013-11-06
JP5773873B2 (ja) 2015-09-02
KR20110066200A (ko) 2011-06-16
AU2009299927B2 (en) 2013-05-30
TWI478916B (zh) 2015-04-01
MX2011003468A (es) 2011-04-21
KR101624000B1 (ko) 2016-05-24
US20110183962A1 (en) 2011-07-28
CA2738868A1 (fr) 2010-04-08
EP2617414A2 (fr) 2013-07-24
IL211678A (en) 2016-12-29

Similar Documents

Publication Publication Date Title
MA32734B1 (fr) Antagonisme smoothened pour traitement de troubles lies a la voie de signalisation hedgehog
MA30781B1 (fr) Inhibiteur de kinase
MA34300B1 (fr) Composés azotés hétérocycliques convenant comme inhibiteurs de la pde10
TNSN07305A1 (fr) Agonistes de pyy et leurs utilisations
MA32558B1 (fr) Composes organiques
TN2011000454A1 (fr) Derives de benzofurannyle utilises comme inhibiteurs de glucokinase
MA34797B1 (fr) Hétéroaryles et leurs utilisations
TNSN08196A1 (fr) Derives de pyrazine
MA30988B1 (fr) Composes destines a inhiber la progression mitotique
MA30784B1 (fr) Derives phenyliques et utilisation de ceux-ci en tant qu'immunomodulateurs.
MX2009005604A (es) Inhibidores espiro cetona de acetil-coa carboxilasa.
MA35639B1 (fr) Compose heterocyclique aromatique dihydroxy
MA41562B1 (fr) Agonistes d'apj 4-hydroxy-3-(heteroaryl)pyridine-2-one a utiliser dans le traitement de troubles cardio-vasculaires
MA32171B1 (fr) Compose heterocyclique
MA29772B1 (fr) Benzimidazoles substitues et procedes de preparation
MA40225B1 (fr) Composés dihydroisoquinolinone substitués
TW200736229A (en) Substituted 1H-benzimidazole-4-carboxamides are potent PARP inhibitors
MA43409B1 (fr) Composés polycycliques à utiliser en tant qu'inhibiteurs de la tyrosine kinase de bruton
MA33662B1 (fr) Composés de spiropipéridine et leur utilisation pharmaceutique pour le traitement du diabète
BRPI0922135A2 (pt) composto de cromeno e derivado do mesmo.
MA31574B1 (fr) Dérivés de pyrazole et leur utilisation comme inhibiteurs de raf
MA32104B1 (fr) Dérivés d'oxime en tant qu'inhibiteurs de hsp90
MA30663B1 (fr) Derives d'ester de l'acide aminophosphorique et modulateur du recepteur s1p contenant ledit derive en tant que principe actif
WO2008066755A3 (fr) Inhibiteurs de tyrosine kinase en tant qu'agents anti-kinétolastides et anti-apicomplexes
MA34385B1 (fr) Composés hétérocycliques condensés comme inhibiteurs de phosphodiestérases (pdes)