MA35342B1 - Composés de-pipéridinyle utiles comme inhibiteurs de la tankyrase - Google Patents
Composés de-pipéridinyle utiles comme inhibiteurs de la tankyraseInfo
- Publication number
- MA35342B1 MA35342B1 MA36745A MA36745A MA35342B1 MA 35342 B1 MA35342 B1 MA 35342B1 MA 36745 A MA36745 A MA 36745A MA 36745 A MA36745 A MA 36745A MA 35342 B1 MA35342 B1 MA 35342B1
- Authority
- MA
- Morocco
- Prior art keywords
- tankyrase
- inhibitors
- compounds useful
- piperidinyl compounds
- formula
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic 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
- C07D401/02—Heterocyclic 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
- C07D401/04—Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic 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
- C07D401/14—Heterocyclic 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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic 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
- C07D471/02—Heterocyclic 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
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic 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
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic 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
- C07D491/02—Heterocyclic 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
- C07D491/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic 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
- C07D491/02—Heterocyclic 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
- C07D491/04—Ortho-condensed systems
- C07D491/044—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
- C07D491/052—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being six-membered
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic 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
- C07D498/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
L'invention concerne des composés représentés par la formule (i). L'invention concerne aussi des compositions pharmaceutiques et des combinaisons comprenant un composé représenté par la formule (i), ainsi que l'utilisation de tels composés comme inhibiteurs de la tankyrase et dans le traitement de troubles liés à la signalisation de wnt et à la signalisation des tankyrases 1 et 2, lesdits troubles comprenant notamment, mais pas exclusivement, le cancer.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201161507321P | 2011-07-13 | 2011-07-13 | |
PCT/IB2012/053613 WO2013008217A1 (fr) | 2011-07-13 | 2012-07-13 | Composés de 4-pipéridinyle utiles comme inhibiteurs de la tankyrase |
Publications (1)
Publication Number | Publication Date |
---|---|
MA35342B1 true MA35342B1 (fr) | 2014-08-01 |
Family
ID=46604017
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MA36745A MA35342B1 (fr) | 2011-07-13 | 2014-02-10 | Composés de-pipéridinyle utiles comme inhibiteurs de la tankyrase |
Country Status (20)
Country | Link |
---|---|
US (2) | US9163003B2 (fr) |
EP (1) | EP2731940B1 (fr) |
JP (1) | JP5957077B2 (fr) |
KR (1) | KR20140051944A (fr) |
CN (1) | CN103797006B (fr) |
AP (1) | AP2014007400A0 (fr) |
AU (1) | AU2012282076A1 (fr) |
BR (1) | BR112014000792A2 (fr) |
CA (1) | CA2841932A1 (fr) |
CO (1) | CO6880065A2 (fr) |
CR (1) | CR20140071A (fr) |
DO (1) | DOP2014000012A (fr) |
EA (1) | EA201490272A1 (fr) |
ES (1) | ES2548513T3 (fr) |
IL (1) | IL230430A0 (fr) |
MA (1) | MA35342B1 (fr) |
MX (1) | MX2014000536A (fr) |
TN (1) | TN2014000016A1 (fr) |
WO (1) | WO2013008217A1 (fr) |
ZA (1) | ZA201400374B (fr) |
Families Citing this family (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103781776A (zh) * | 2011-07-13 | 2014-05-07 | 诺华股份有限公司 | 用作端锚聚合酶抑制剂的新的2-哌啶-1-基-乙酰胺化合物 |
DK2822656T3 (en) | 2012-03-07 | 2017-01-30 | Inst Of Cancer Research: Royal Cancer Hospital (The) | 3-aryl-5-substituted-isoquinolin-1-one compounds and their therapeutic use |
EP2970121B1 (fr) * | 2013-03-15 | 2017-12-13 | Araxes Pharma LLC | Inhibiteurs covalents de k-ras g12c |
DK3030554T3 (en) * | 2013-08-07 | 2018-06-06 | Merck Patent Gmbh | PIPERIDINUREADERIVATIVES |
JP6456392B2 (ja) | 2013-09-11 | 2019-01-23 | インスティチュート オブ キャンサー リサーチ:ロイヤル キャンサー ホスピタル | 3−アリール−5−置換イソキノリン−1−オン化合物及びその治療的使用 |
WO2015135461A1 (fr) * | 2014-03-10 | 2015-09-17 | 四川海思科制药有限公司 | Dérivé de dihydrobenzofurane-pipéridine-cétone substitué, sa préparation et son utilisation |
WO2015169421A1 (fr) | 2014-05-07 | 2015-11-12 | Merck Patent Gmbh | Dérivés hétérocyclyl-butanamides |
WO2016006975A2 (fr) * | 2014-07-11 | 2016-01-14 | St Pharm Co., Ltd. | Nouveaux dérivés imidazotriazinone ou imidazopyrazinone et leur utilisation |
KR101739003B1 (ko) | 2014-07-11 | 2017-05-23 | 에스티팜 주식회사 | 신규한 트리아졸로피리미디논 또는 트리아졸로피리디논 유도체, 및 이들의 용도 |
KR20160007347A (ko) | 2014-07-11 | 2016-01-20 | 에스티팜 주식회사 | 신규한 이미다조트리아지논 또는 이미다조피라지논 유도체, 및 이들의 용도 |
WO2016006974A2 (fr) * | 2014-07-11 | 2016-01-14 | St Pharm Co., Ltd. | Nouveaux dérivés triazolopyrimidinone ou triazolopyridinone et leur utilisation |
SG11201803584RA (en) | 2015-11-02 | 2018-05-30 | Merck Patent Gmbh | 1,4-dicarbonyl-piperidyl derivatives |
KR101777475B1 (ko) * | 2015-12-08 | 2017-09-11 | 에스티팜 주식회사 | 신규한 디히드로피라노피리미디논 유도체 및 이들의 용도 |
AU2016378723B2 (en) | 2015-12-22 | 2021-09-30 | SHY Therapeutics LLC | Compounds for the treatment of cancer and inflammatory disease |
WO2017156350A1 (fr) | 2016-03-09 | 2017-09-14 | K-Gen, Inc. | Méthodes de traitement du cancer |
EP3642209B1 (fr) | 2017-06-21 | 2023-11-29 | Shy Therapeutics LLC | Composés interagissant avec la superfamille ras destinés à être utilisés dans le traitement de cancers, de maladies inflammatoires, de rasopathies et de maladies fibrotiques |
WO2020114892A1 (fr) | 2018-12-03 | 2020-06-11 | Merck Patent Gmbh | 4-hétéroarylcarbonyl-n-(phényle ou hétéroaryl) pipéridine-1-carboxamides servant d'inhibiteurs de tankyrases |
MX2022001952A (es) * | 2019-08-15 | 2022-06-02 | Black Diamond Therapeutics Inc | Compuestos de alquinil quinazolina. |
WO2022146614A1 (fr) * | 2020-12-03 | 2022-07-07 | Washington University | Méthodes de traitement et de prévention d'une maladie rénale |
Family Cites Families (31)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20020022636A1 (en) | 1997-09-03 | 2002-02-21 | Jia-He Li | Oxo-substituted compounds, process of making, and compositions and methods for inhibiting parp activity |
WO2000042025A1 (fr) | 1999-01-14 | 2000-07-20 | Meiji Seika Kaisha, Ltd. | Inhibiteurs de poly(adp-ribose) polymerase consistant en des derives de pyrimidine |
US6710058B2 (en) * | 2000-11-06 | 2004-03-23 | Bristol-Myers Squibb Pharma Company | Monocyclic or bicyclic carbocycles and heterocycles as factor Xa inhibitors |
DE10056312A1 (de) | 2000-11-14 | 2002-05-16 | Bayer Ag | Substituierte Amidoalkyluracile und ihre Verwendung |
AUPR201600A0 (en) | 2000-12-11 | 2001-01-11 | Fujisawa Pharmaceutical Co., Ltd. | Quinazolinone derivative |
JPWO2002094790A1 (ja) | 2001-05-23 | 2004-09-09 | 三菱ウェルファーマ株式会社 | 縮合ヘテロ環化合物およびその医薬用途 |
ATE424388T1 (de) | 2001-12-06 | 2009-03-15 | Merck & Co Inc | Mitotische kinesinhemmer |
DE10201240A1 (de) | 2002-01-15 | 2003-07-24 | Bayer Ag | Substituierte Alkyluracile und ihre Verwendung |
AUPS019702A0 (en) | 2002-01-29 | 2002-02-21 | Fujisawa Pharmaceutical Co., Ltd. | Condensed heterocyclic compounds |
RU2292337C2 (ru) | 2002-02-19 | 2007-01-27 | Оно Фармасьютикал Ко., Лтд. | Конденсированные производные пиридазина и лекарственные препараты, содержащие данные соединения в качестве активного ингредиента |
AUPS137402A0 (en) | 2002-03-26 | 2002-05-09 | Fujisawa Pharmaceutical Co., Ltd. | Novel tricyclic compounds |
TWI275390B (en) | 2002-04-30 | 2007-03-11 | Wyeth Corp | Process for the preparation of 7-substituted-3- quinolinecarbonitriles |
US7183287B2 (en) | 2003-04-03 | 2007-02-27 | Pharmacia Corporation | Substituted pyrimidinones |
WO2004111014A1 (fr) | 2003-06-06 | 2004-12-23 | Vertex Pharmaceuticals Incorporated | Derives de pyrimidne utilises en tant que modulateurs de transporteurs de cassette de liaison a l'atp |
NL1026826C2 (nl) | 2003-08-13 | 2007-01-04 | Pharmacia Corp | Gesubstitueerde pyridinonen. |
US7439254B2 (en) | 2003-12-08 | 2008-10-21 | Cytokinetics, Inc. | Compounds, compositions, and methods |
GB0405101D0 (en) * | 2004-03-06 | 2004-04-07 | Astrazeneca Ab | Compounds |
US7375102B2 (en) | 2004-06-28 | 2008-05-20 | Amgen Sf, Llc | Tetrahydroquinazolin-4(3H)-one-related and tetrahydropyrido[2,3-D]pyrimidin-4(3H)-one-related compounds, compositions and methods for their use |
EA012416B1 (ru) * | 2004-06-30 | 2009-10-30 | Янссен Фармацевтика Н.В. | Производные замещенного 2-алкилхиназолинона как ингибиторы parp |
PL1789390T3 (pl) | 2004-09-02 | 2012-04-30 | Genentech Inc | Pirydylowe inhibitory szlaku sygnałowego hedgehog |
GB0510390D0 (en) | 2005-05-20 | 2005-06-29 | Novartis Ag | Organic compounds |
WO2007002701A2 (fr) | 2005-06-27 | 2007-01-04 | Amgen Inc. | Composes et compositions d'aryl nitrile et leurs utilisations dans le traitement de maladies inflammatoires et de troubles associes |
PL2021337T3 (pl) * | 2006-04-25 | 2010-06-30 | Lilly Co Eli | Inhibitory dehydrogenazy 11-beta-hydroksysteroidowej typu 1 |
US8466150B2 (en) | 2006-12-28 | 2013-06-18 | Abbott Laboratories | Inhibitors of poly(ADP-ribose)polymerase |
PE20140100A1 (es) | 2007-09-12 | 2014-02-12 | Genentech Inc | Combinaciones de compuestos inhibidores de fosfoinositida 3-quinasa y agentes quimioterapeuticos |
US8354528B2 (en) | 2007-10-25 | 2013-01-15 | Genentech, Inc. | Process for making thienopyrimidine compounds |
WO2009059994A2 (fr) | 2007-11-05 | 2009-05-14 | Novartis Ag | Procédés et compositions pour mesurer l'activation de wnt et pour traiter des cancers liés à wnt |
KR101179753B1 (ko) | 2007-11-06 | 2012-09-04 | 제일약품주식회사 | 신규한 트리시클릭 유도체 또는 이의 약학적으로허용가능한 염, 이의 제조방법 및 이를 포함하는 약학조성물 |
EP2219646A4 (fr) | 2007-12-21 | 2010-12-22 | Univ Rochester | Procédé permettant de modifier la durée de vie d'organismes eucaryotes |
EP2271626B1 (fr) | 2008-03-27 | 2014-11-26 | Janssen Pharmaceutica, N.V. | Tétrahydrophénanthridinones et tétrahydrocyclopentaquinolinones comme inhibiteurs de la polymérisation de la tubuline et de parp |
CN103781776A (zh) * | 2011-07-13 | 2014-05-07 | 诺华股份有限公司 | 用作端锚聚合酶抑制剂的新的2-哌啶-1-基-乙酰胺化合物 |
-
2012
- 2012-07-13 CN CN201280043558.7A patent/CN103797006B/zh not_active Expired - Fee Related
- 2012-07-13 AP AP2014007400A patent/AP2014007400A0/xx unknown
- 2012-07-13 CA CA 2841932 patent/CA2841932A1/fr not_active Abandoned
- 2012-07-13 US US14/154,173 patent/US9163003B2/en not_active Ceased
- 2012-07-13 ES ES12742957.9T patent/ES2548513T3/es active Active
- 2012-07-13 BR BR112014000792A patent/BR112014000792A2/pt not_active IP Right Cessation
- 2012-07-13 MX MX2014000536A patent/MX2014000536A/es not_active Application Discontinuation
- 2012-07-13 WO PCT/IB2012/053613 patent/WO2013008217A1/fr active Application Filing
- 2012-07-13 KR KR20147003628A patent/KR20140051944A/ko not_active Application Discontinuation
- 2012-07-13 JP JP2014519688A patent/JP5957077B2/ja not_active Expired - Fee Related
- 2012-07-13 EP EP12742957.9A patent/EP2731940B1/fr not_active Not-in-force
- 2012-07-13 AU AU2012282076A patent/AU2012282076A1/en not_active Abandoned
- 2012-07-13 EA EA201490272A patent/EA201490272A1/ru unknown
- 2012-07-13 US US15/786,125 patent/USRE46942E1/en active Active
-
2014
- 2014-01-13 IL IL230430A patent/IL230430A0/en unknown
- 2014-01-15 TN TNP2014000016A patent/TN2014000016A1/en unknown
- 2014-01-17 ZA ZA2014/00374A patent/ZA201400374B/en unknown
- 2014-01-22 DO DO2014000012A patent/DOP2014000012A/es unknown
- 2014-02-10 MA MA36745A patent/MA35342B1/fr unknown
- 2014-02-12 CR CR20140071A patent/CR20140071A/es unknown
- 2014-02-13 CO CO14031176A patent/CO6880065A2/es not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
BR112014000792A2 (pt) | 2017-10-31 |
ZA201400374B (en) | 2014-10-29 |
TN2014000016A1 (en) | 2015-07-01 |
CR20140071A (es) | 2014-10-16 |
JP5957077B2 (ja) | 2016-07-27 |
CA2841932A1 (fr) | 2013-01-17 |
AP2014007400A0 (en) | 2014-01-31 |
IL230430A0 (en) | 2014-03-31 |
MX2014000536A (es) | 2014-12-05 |
NZ620426A (en) | 2015-08-28 |
EP2731940B1 (fr) | 2015-08-19 |
JP2014522855A (ja) | 2014-09-08 |
USRE46942E1 (en) | 2018-07-10 |
WO2013008217A1 (fr) | 2013-01-17 |
EP2731940A1 (fr) | 2014-05-21 |
AU2012282076A1 (en) | 2014-02-27 |
DOP2014000012A (es) | 2014-07-31 |
KR20140051944A (ko) | 2014-05-02 |
ES2548513T3 (es) | 2015-10-19 |
CO6880065A2 (es) | 2014-02-28 |
EA201490272A1 (ru) | 2014-05-30 |
US20150126513A1 (en) | 2015-05-07 |
CN103797006A (zh) | 2014-05-14 |
US9163003B2 (en) | 2015-10-20 |
CN103797006B (zh) | 2016-01-27 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
MA35342B1 (fr) | Composés de-pipéridinyle utiles comme inhibiteurs de la tankyrase | |
MA37762B1 (fr) | Composés n-aryltriazole utilisés comme antagonistes de lpar | |
MA37764A1 (fr) | Composés n-alkyltriazole utilisés comme antagonistes de lpar | |
MA38398B1 (fr) | Composés biaryle amides en tant qu'inhibiteurs de kinase | |
EA201201665A1 (ru) | Новые соединения | |
MA35184B1 (fr) | Antagonistes de trpv4 | |
MA41562B1 (fr) | Agonistes d'apj 4-hydroxy-3-(heteroaryl)pyridine-2-one a utiliser dans le traitement de troubles cardio-vasculaires | |
MA53399B1 (fr) | Pyrazoles substitués en tant qu`inhibiteurs de la kallicréine plasmatique humaine | |
MA39211B1 (fr) | Composés tricycliques comme agents anti-cancers | |
MA39995B1 (fr) | Composés destinés à traiter l'amyotrophie spinale | |
ME01284B (fr) | Composés organiques | |
MD20150043A2 (ro) | Inhibitori ai histon-demetilazelor | |
MA37959A2 (fr) | Dérivés de 5-phénoxy-3h-pyrimidin-4-one et leur utilisation en tant qu'inhibiteurs de la transcriptase inverse du vih | |
MA34837B1 (fr) | Composés indoliques ou analogues de ceux-ci utiles dans le traitement de la dégénérescence maculaire liée à l'âge (dmla) | |
MA38661A1 (fr) | Composés hétéro-aromatiques et leur utilisation en tant que ligands d1 de la dopamine | |
MA40225A (fr) | Composés dihydroisoquinolinone substitués | |
MA34896B1 (fr) | Inhibiteurs du virus de l'hepatite c | |
MA37886A1 (fr) | Nouvelles pyridinones bicycliques | |
MA39165A1 (fr) | Dérivés de benzimidazole-proline pour leurs utilisations dans le traitement du syndrome des etats crepusculaires | |
MA37439A1 (fr) | Inhibiteurs de dgat1 à ponts éthers cycliques pour le traitement de troubles medies par l'acyle coa-diacylglycerol transferase 1 (dgat1). | |
MA43409B1 (fr) | Composés polycycliques à utiliser en tant qu'inhibiteurs de la tyrosine kinase de bruton | |
MA37765A1 (fr) | Composés de pyrazole substitués utilisés comme antagonistes de lpar | |
MA38810A1 (fr) | Inhibiteurs de rorc2 méthodes d'utilisation associées | |
MA39152B1 (fr) | Cyclopentanes substitués en 1,2 utilisés comme antagonistes du récepteur d'orexine | |
MA38410B1 (fr) | Composés d'azétidinyloxyphénylpyrrolidine |