PE20091556A1 - Derivado heterociclico fusionado y su uso - Google Patents
Derivado heterociclico fusionado y su usoInfo
- Publication number
- PE20091556A1 PE20091556A1 PE2009000279A PE2009000279A PE20091556A1 PE 20091556 A1 PE20091556 A1 PE 20091556A1 PE 2009000279 A PE2009000279 A PE 2009000279A PE 2009000279 A PE2009000279 A PE 2009000279A PE 20091556 A1 PE20091556 A1 PE 20091556A1
- Authority
- PE
- Peru
- Prior art keywords
- oxo
- piperidin
- phenylethyl
- carboxamide
- dihydro
- Prior art date
Links
Classifications
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- 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
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic 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
- A61K31/4353—Heterocyclic 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
- A61K31/4365—Heterocyclic 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 having sulfur as a ring hetero atom, e.g. ticlopidine
-
- 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
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- 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
- 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
- C07D471/12—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 three hetero rings
- C07D471/14—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
- C07D491/048—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered
-
- 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
Abstract
REFERIDA A UN COMPUESTO DE FORMULA (I) DONDE A ES ANILLO DE 5 A 7 MIEMBROS OPCIONALMENTE SUSTITUIDO; X ES O, S O NR1; R1 ES H, HIDROCARBURO DE FORMA OPCIONAL; R2 ES CARBAMOILO OPCIONALMENTE SUSTITUIDO; R3 ES OH OPCIONALMENTE SUSTITUIDO. SON COMPUESTOS SELECCIONADOS: N-[1-(2-HIDROXIETIL)PIPERIDIN-4-IL]-3-METOXI-1-METIL-4-OXO-5-(2-OXO-2-FENILETIL)-4,5-DIHIDRO-1H-PIRROLO[3,2-c]QUINOLIN-2-CARBOXAMIDA; N-[1-(2-HIDROXIACETIL)PIPERIDIN-4-IL]-3-METOXI-1-METIL-4-OXO-5-(2-OXO-2-FENILETIL)-4,5-DIHIDRO-1H-PIRROLO[3,2-c]QUINOLIN-2-CARBOXAMIDA; 3-ETOXI-6-ETIL-N-[1-(HIDROXIACETIL)PIPERIDIN-4-IL]-1-METIL-4-OXO-5-(2-OXO-2-FENILETIL)-4,5-DIHIDRO-1H-PIRROLO[3,2-c]PIRIDIN-2-CARBOXAMIDA; ENTRE OTROS. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE PROTEINA Smo, UTILES PARA EL TRATAMIENTO DEL CANCER
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2008045134 | 2008-02-26 | ||
JP2008256755 | 2008-10-01 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20091556A1 true PE20091556A1 (es) | 2009-11-03 |
Family
ID=40905094
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2009000279A PE20091556A1 (es) | 2008-02-26 | 2009-02-25 | Derivado heterociclico fusionado y su uso |
Country Status (28)
Country | Link |
---|---|
US (2) | US8399449B2 (es) |
EP (1) | EP2247588B1 (es) |
JP (2) | JP4719317B2 (es) |
KR (1) | KR101569949B1 (es) |
CN (1) | CN102015705B (es) |
AR (1) | AR070479A1 (es) |
AU (1) | AU2009217982B2 (es) |
BR (1) | BRPI0908417B1 (es) |
CA (1) | CA2716773C (es) |
CL (1) | CL2009000429A1 (es) |
CO (1) | CO6321277A2 (es) |
CR (1) | CR11661A (es) |
DO (1) | DOP2010000260A (es) |
EA (1) | EA020144B1 (es) |
EC (1) | ECSP10010496A (es) |
ES (1) | ES2586252T3 (es) |
GE (1) | GEP20125664B (es) |
HK (1) | HK1150274A1 (es) |
IL (1) | IL207735A (es) |
JO (1) | JO3259B1 (es) |
MA (1) | MA32164B1 (es) |
MX (1) | MX2010009372A (es) |
MY (1) | MY150379A (es) |
NZ (1) | NZ587719A (es) |
PE (1) | PE20091556A1 (es) |
TW (1) | TWI480282B (es) |
WO (1) | WO2009107850A2 (es) |
ZA (1) | ZA201006063B (es) |
Families Citing this family (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2716773C (en) | 2008-02-26 | 2016-04-26 | Takeda Pharmaceutical Company Limited | Fused heterocyclic derivative and use thereof |
US20160016982A1 (en) | 2009-07-31 | 2016-01-21 | Thar Pharmaceuticals, Inc. | Crystallization method and bioavailability |
US9169279B2 (en) | 2009-07-31 | 2015-10-27 | Thar Pharmaceuticals, Inc. | Crystallization method and bioavailability |
NO2459176T3 (es) | 2009-07-31 | 2018-02-24 | ||
JPWO2011013752A1 (ja) * | 2009-07-31 | 2013-01-10 | 塩野義製薬株式会社 | 縮合へテロ環誘導体を含有する医薬組成物 |
EP2471793B1 (en) * | 2009-08-26 | 2016-10-05 | Takeda Pharmaceutical Company Limited | Fused heterocyclic ring derivative and use thereof |
JP5599802B2 (ja) * | 2009-08-26 | 2014-10-01 | 武田薬品工業株式会社 | 縮合複素環誘導体およびその用途 |
WO2011024869A1 (ja) * | 2009-08-26 | 2011-03-03 | 武田薬品工業株式会社 | 縮合複素環誘導体およびその用途 |
WO2011024873A1 (ja) * | 2009-08-26 | 2011-03-03 | 武田薬品工業株式会社 | 縮合複素環誘導体およびその用途 |
WO2012071517A2 (en) | 2010-11-24 | 2012-05-31 | Thar Pharmaceuticals, Inc. | Novel crystalline forms |
WO2012154731A1 (en) * | 2011-05-08 | 2012-11-15 | Vanderbilt University | Substituted 1h-pyrrolo[3,2-c]quinolin-4(5h)-one analogs as positive allosteric modulators of the muscarinic acetylcholine receptor m4 |
CA2873097A1 (en) | 2012-05-11 | 2013-11-14 | Todd M. Hansen | Pyridazine and pyridine derivatives as nampt inhibitors |
US9782418B2 (en) * | 2013-12-03 | 2017-10-10 | Celestra Life Science Llc | Rationale-based design of a targeted therapy for cancer |
JP6353031B2 (ja) | 2014-03-19 | 2018-07-04 | 株式会社東芝 | 電池用電極材料、非水電解質電池、電池パック及び車 |
EP3127907A4 (en) * | 2014-03-31 | 2018-04-04 | Boston Biomedical, Inc. | New tricyclic quinone derivative |
CA2986083A1 (en) | 2015-06-11 | 2016-12-15 | Basilea Pharmaceutica International AG | Efflux-pump inhibitors and therapeutic uses thereof |
US9962378B2 (en) * | 2015-09-17 | 2018-05-08 | Macau University Of Science And Technology | ROS1 inhibitor and its use |
HUE057240T2 (hu) | 2016-02-01 | 2022-04-28 | Takeda Pharmaceuticals Co | Kokristály |
US10195218B2 (en) | 2016-05-31 | 2019-02-05 | Grunenthal Gmbh | Crystallization method and bioavailability |
CA3045306A1 (en) | 2016-11-29 | 2018-06-07 | Boston Biomedical, Inc. | Naphthofuran derivatives, preparation, and methods of use thereof |
JP7091201B2 (ja) | 2018-09-14 | 2022-06-27 | 株式会社東芝 | 活物質、電極、二次電池、電池パック、及び車両 |
RU2711968C1 (ru) * | 2018-11-22 | 2020-01-24 | федеральное государственное бюджетное образовательное учреждение высшего образования "Пермский национальный исследовательский политехнический университет" | Анальгезирующее средство |
CN110172068A (zh) * | 2019-06-05 | 2019-08-27 | 河南龙湖生物技术有限公司 | 具有抗肿瘤活性的苯并噻唑类化合物及其制备方法和应用 |
KR20230031285A (ko) | 2020-06-26 | 2023-03-07 | 라퀄리아 파마 인코포레이티드 | 레티노이드와 암 치료제의 병용 요법이 효과적인 암 환자를 선별하는 방법 및 레티노이드와 암 치료제의 병용 의약 |
CN113292477B (zh) * | 2021-06-01 | 2023-06-02 | 四川大学 | 一种铱催化的碳氢活化反应合成异吲哚-1-酮类化合物的方法 |
CN113429422B (zh) * | 2021-07-26 | 2022-05-10 | 中国人民解放军军事科学院军事医学研究院 | 一种噻吩并喹诺酮类化合物及其制备方法和应用 |
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JP3012684B2 (ja) | 1989-12-08 | 2000-02-28 | 大日本製薬株式会社 | チエノキノリン誘導体、チエノナフチリジン誘導体およびそれらの塩 |
WO1993013664A2 (en) | 1992-01-11 | 1993-07-22 | Schering Agrochemicals Limited | Biheterocyclic fungicidal compounds |
FR2695126B1 (fr) * | 1992-08-27 | 1994-11-10 | Sanofi Elf | Dérivés d'acide thiényl ou pyrrolyl carboxyliques, leur préparation et médicaments les contenant. |
JP3223289B2 (ja) | 1992-10-22 | 2001-10-29 | 東洋アルミニウム株式会社 | 肉類調理器具および肉類調理方法 |
SK18542000A3 (sk) | 1998-06-04 | 2001-12-03 | Abbott Laboratories | Protizápalové zlúčeniny inhibujúce bunkovú adhéziu |
EP1181296A1 (en) | 1999-06-03 | 2002-02-27 | Abbott Laboratories | Cell adhesion-inhibiting antiinflammatory compounds |
EP1217000A1 (en) | 2000-12-23 | 2002-06-26 | Aventis Pharma Deutschland GmbH | Inhibitors of factor Xa and factor VIIa |
EP1465869B1 (en) | 2001-12-21 | 2013-05-15 | Exelixis Patent Company LLC | Modulators of lxr |
WO2004020599A2 (en) | 2002-08-29 | 2004-03-11 | Curis, Inc. | Hedgehog antagonists, methods and uses related thereto |
JP2006151810A (ja) | 2002-12-26 | 2006-06-15 | Daiichi Asubio Pharma Co Ltd | ジヒドロチエノキノリン誘導体及びそれを含む細胞接着阻害剤 |
US20050043346A1 (en) | 2003-08-08 | 2005-02-24 | Pharmacia Italia S.P.A. | Pyridylpyrrole derivatives active as kinase inhibitors |
US20070060595A1 (en) | 2003-10-10 | 2007-03-15 | Toshio Yoshizawa | Novel fused heterocyclic compound and use thereof |
US20080249154A1 (en) * | 2003-12-26 | 2008-10-09 | Ono Pharmaceutical Co., Ltd. | Preventive and/or Therapeutic Agent For Disease In Which Mitochondrial Benzodiazephine Receptor Participates |
BRPI0509745A (pt) | 2004-04-08 | 2007-09-25 | Topotarget As | compostos de difenil ox-indol-2-ona e seu uso no tratamento de cáncer |
GB0420722D0 (en) | 2004-09-17 | 2004-10-20 | Addex Pharmaceuticals Sa | Novel allosteric modulators |
MX2008002165A (es) | 2005-08-16 | 2008-04-29 | Irm Llc | Compuestos y composiciones como inhibidores de la proteina cinasa. |
AR056560A1 (es) * | 2005-10-06 | 2007-10-10 | Astrazeneca Ab | Pirrolopiridinonas como moduladores cb1 |
WO2007085188A1 (en) * | 2006-01-27 | 2007-08-02 | Shanghai Hengrui Pharmaceutical Co. Ltd. | Pyrrolo [3,2-c] pyridine-4-one 2-indolinone protein kinase inhibitors |
JP2009536156A (ja) * | 2006-04-14 | 2009-10-08 | ノバルティス アクチエンゲゼルシャフト | ヘッジホッグ経路関連障害の処置におけるビアリールカルボキサミドの使用 |
EA018441B1 (ru) * | 2007-03-14 | 2013-08-30 | ЭКСЕЛИКСИС ПАТЕНТ КОМПАНИ ЭлЭлСи | Ингибиторы пути хеджхога |
PE20090188A1 (es) * | 2007-03-15 | 2009-03-20 | Novartis Ag | Compuestos heterociclicos como moduladores de la senda de hedgehog |
CA2716773C (en) | 2008-02-26 | 2016-04-26 | Takeda Pharmaceutical Company Limited | Fused heterocyclic derivative and use thereof |
-
2009
- 2009-02-25 CA CA2716773A patent/CA2716773C/en active Active
- 2009-02-25 NZ NZ587719A patent/NZ587719A/en unknown
- 2009-02-25 EP EP09714922.3A patent/EP2247588B1/en active Active
- 2009-02-25 JO JOP/2009/0079A patent/JO3259B1/ar active
- 2009-02-25 CN CN2009801148111A patent/CN102015705B/zh active Active
- 2009-02-25 ES ES09714922.3T patent/ES2586252T3/es active Active
- 2009-02-25 WO PCT/JP2009/054007 patent/WO2009107850A2/en active Application Filing
- 2009-02-25 PE PE2009000279A patent/PE20091556A1/es active IP Right Grant
- 2009-02-25 AU AU2009217982A patent/AU2009217982B2/en active Active
- 2009-02-25 TW TW098105923A patent/TWI480282B/zh active
- 2009-02-25 CL CL2009000429A patent/CL2009000429A1/es unknown
- 2009-02-25 MX MX2010009372A patent/MX2010009372A/es active IP Right Grant
- 2009-02-25 JP JP2010533355A patent/JP4719317B2/ja active Active
- 2009-02-25 GE GEAP200911952A patent/GEP20125664B/en unknown
- 2009-02-25 AR ARP090100644A patent/AR070479A1/es active IP Right Grant
- 2009-02-25 KR KR1020107021331A patent/KR101569949B1/ko active IP Right Grant
- 2009-02-25 MY MYPI2010004006A patent/MY150379A/en unknown
- 2009-02-25 EA EA201070994A patent/EA020144B1/ru unknown
- 2009-02-25 US US12/919,413 patent/US8399449B2/en active Active
- 2009-02-25 BR BRPI0908417-7A patent/BRPI0908417B1/pt active IP Right Grant
- 2009-02-25 US US12/392,640 patent/US8217176B2/en active Active
-
2010
- 2010-08-22 IL IL207735A patent/IL207735A/en active IP Right Grant
- 2010-08-25 ZA ZA2010/06063A patent/ZA201006063B/en unknown
- 2010-08-26 DO DO2010000260A patent/DOP2010000260A/es unknown
- 2010-08-31 CR CR11661A patent/CR11661A/es unknown
- 2010-09-21 MA MA33195A patent/MA32164B1/fr unknown
- 2010-09-23 EC EC2010010496A patent/ECSP10010496A/es unknown
- 2010-09-23 CO CO10117653A patent/CO6321277A2/es active IP Right Grant
-
2011
- 2011-02-03 JP JP2011022188A patent/JP5490030B2/ja active Active
- 2011-04-29 HK HK11104328.2A patent/HK1150274A1/zh unknown
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