PE20140629A1 - Derivados de fenil-isoxazol y procedimiento para la preparacion de los mismos - Google Patents
Derivados de fenil-isoxazol y procedimiento para la preparacion de los mismosInfo
- Publication number
- PE20140629A1 PE20140629A1 PE2013002002A PE2013002002A PE20140629A1 PE 20140629 A1 PE20140629 A1 PE 20140629A1 PE 2013002002 A PE2013002002 A PE 2013002002A PE 2013002002 A PE2013002002 A PE 2013002002A PE 20140629 A1 PE20140629 A1 PE 20140629A1
- Authority
- PE
- Peru
- Prior art keywords
- phenyl
- methyl
- isoxazole
- preparation
- isoxazol
- Prior art date
Links
- ZBRDJMFLJXFIGJ-UHFFFAOYSA-N 3-phenyl-1,2-oxazole Chemical class O1C=CC(C=2C=CC=CC=2)=N1 ZBRDJMFLJXFIGJ-UHFFFAOYSA-N 0.000 title abstract 2
- 238000002360 preparation method Methods 0.000 title abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 4
- ZUSWDTWYONAOPH-UHFFFAOYSA-N [2-(trifluoromethyl)phenyl]hydrazine;hydrochloride Chemical class [Cl-].[NH3+]NC1=CC=CC=C1C(F)(F)F ZUSWDTWYONAOPH-UHFFFAOYSA-N 0.000 abstract 3
- 229910052736 halogen Inorganic materials 0.000 abstract 3
- 150000002367 halogens Chemical class 0.000 abstract 3
- -1 2-FLUOROPHENYL Chemical class 0.000 abstract 2
- WSFSSNUMVMOOMR-BJUDXGSMSA-N methanone Chemical compound O=[11CH2] WSFSSNUMVMOOMR-BJUDXGSMSA-N 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical class [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 abstract 1
- JIQNWFBLYKVZFY-UHFFFAOYSA-N methoxycyclohexatriene Chemical class COC1=C[C]=CC=C1 JIQNWFBLYKVZFY-UHFFFAOYSA-N 0.000 abstract 1
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical group [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 241000712461 unidentified influenza virus Species 0.000 abstract 1
Classifications
-
- 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
- A61K31/495—Heterocyclic 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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- 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
- A61K31/41—Heterocyclic 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
- A61K31/42—Oxazoles
-
- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/16—Antivirals for RNA viruses for influenza or rhinoviruses
-
- 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
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/08—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members 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
- C07D261/18—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Virology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Pulmonology (AREA)
- Molecular Biology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
SE REFIERE A COMPUESTOS DERIVADOS DE FENIL-ISOXAZOL DE FORMULA (1) DONDE R1, R2 Y R3 SON CADA UNO H, HALOGENO, ALQUILO INFERIOR O ALCOXI INFERIOR OPCIONALMENTE SUSTITUIDOS CON HALOGENO; R4 ES METILO O AMINA; R8 ES UN COMPUESTO DE FORMULA 2 O 3, EN DONDE R5, R6 Y R7 SON CADA UNO H, ALQUILO INFERIOR, HIDROXI, HALOGENO, ENTRE OTROS; R9 ES ALQUILO INFERIOR. SON COMPUESTOS PREFERIDOS: (4-(3-METOXIFENIL)PIPERAZINA-1-IL)(5-METIL-3-(2-(TRIFLUOROMETIL)FENIL)ISOXAZOL-4-IL)METANONA; (4-(2-FLUOROFENIL)PIPERAZINA-1-IL)(5-METIL-3-(2-(TRIFLUOROMETIL)FENIL)ISOXAZOL-4-IL)METANONA; (4-(3,4-DICLOROFENIL)PIPERAZINA-1-IL)(5-METIL-3-(2-(TRIFLUOROMETIL)FENIL)ISOXAZOL-4-IL)METANONA; ENTRE OTROS. TAMBIEN SE REFIERE A UN METODO DE PREPARACION Y A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS INHIBEN LA ACTIVIDAD DEL VIRUS DE LA INFLUENZA
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR1020110036172A KR101369584B1 (ko) | 2011-04-19 | 2011-04-19 | 페닐-이속사졸 유도체 및 그의 제조방법 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20140629A1 true PE20140629A1 (es) | 2014-05-22 |
Family
ID=46514985
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2013002002A PE20140629A1 (es) | 2011-04-19 | 2012-03-30 | Derivados de fenil-isoxazol y procedimiento para la preparacion de los mismos |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US9132126B2 (es) |
| EP (1) | EP2699566B1 (es) |
| JP (1) | JP5833143B2 (es) |
| KR (1) | KR101369584B1 (es) |
| CN (1) | CN103313982B (es) |
| AR (1) | AR086029A1 (es) |
| AU (1) | AU2012246914B2 (es) |
| CA (1) | CA2824757A1 (es) |
| CL (1) | CL2013001910A1 (es) |
| CO (1) | CO6771432A2 (es) |
| EA (1) | EA022336B1 (es) |
| IL (1) | IL227711A0 (es) |
| MX (1) | MX340098B (es) |
| PE (1) | PE20140629A1 (es) |
| PH (1) | PH12013501883A1 (es) |
| SA (1) | SA112330457B1 (es) |
| SG (1) | SG192134A1 (es) |
| TW (1) | TWI434836B (es) |
| UY (1) | UY34023A (es) |
| WO (1) | WO2012144752A1 (es) |
| ZA (1) | ZA201305277B (es) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2018141854A1 (en) | 2017-02-02 | 2018-08-09 | Janssen Vaccines & Prevention B.V. | Piperazine derivatives for influenza virus inhibition |
| CA3052353A1 (en) | 2017-02-02 | 2018-08-09 | Janssen Vaccines & Prevention B.V. | Piperazine derivatives for influenza virus inhibition |
| JP7019727B2 (ja) * | 2017-02-08 | 2022-02-15 | バイオトロン リミティッド | インフルエンザの治療方法 |
| TWI765323B (zh) * | 2019-08-22 | 2022-05-21 | 大陸商四川海思科製藥有限公司 | 抗流感病毒化合物及其製備方法和用途 |
| CN111704587B (zh) * | 2020-06-29 | 2023-04-07 | 遵义医科大学 | 一种三氟甲基化1,3-噁嗪类化合物的合成方法 |
| CN114349746A (zh) * | 2020-11-19 | 2022-04-15 | 中国医学科学院医药生物技术研究所 | 一种含有4-氟苯基片段的吡啶类化合物及其制备方法和应用、药物组合物 |
| JP2024506000A (ja) | 2021-02-04 | 2024-02-08 | 四川海思科制▲薬▼有限公司 | Ha阻害剤化合物の塩及び結晶形 |
Family Cites Families (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8427618D0 (en) * | 1984-11-01 | 1984-12-05 | Shell Int Research | Anticoccidial compositions |
| SK282950B6 (sk) | 1990-04-24 | 2003-01-09 | Biota Scientific Management Pty Ltd | Deriváty alfa-D-neuramínovej kyseliny, spôsob ich prípravy, ich použitie a farmaceutické prípravky na ich báze |
| RU2181357C2 (ru) | 1995-02-27 | 2002-04-20 | Джилид Сайэнс, Инк. | Композиция селективных ингибиторов вирусных или бактериальных нейраминидаз (варианты), соединение и способ лечения или профилактики заболевания гриппом |
| UA74912C2 (en) | 2001-07-06 | 2006-02-15 | Merck & Co Inc | Beta-aminotetrahydroimidazo-(1,2-a)-pyrazines and tetratriazolo-(4,3-a)-pyrazines as inhibitors of dipeptylpeptidase for the treatment or prevention of diabetes |
| ES2180456B1 (es) * | 2001-07-20 | 2004-05-01 | Laboratorios S.A.L.V.A.T., S.A. | Isoxazoles sustituidos y su utilizacion como antibioticos. |
| AU2002337843A1 (en) | 2001-10-12 | 2003-04-22 | Onconova Therapeutics, Inc. | Processes for the preparation of substituted isoxazoles and 2-isoxazolines |
| MXPA04012959A (es) | 2002-06-29 | 2005-05-16 | Zentaris Gmbh | Arilcarbonilpiperacinas y heteroarilcarbonilpiperacinas y su uso para tratamiento de enfermedades de tumor benigno y maligno. |
| AU2003232650A1 (en) | 2003-05-06 | 2004-11-26 | Il Yang Pharm Co., Ltd. | N-phenyl-2-pyrimidine-amine derivatives and process for the preparation thereof |
| KR20050051729A (ko) | 2003-11-28 | 2005-06-02 | 일양약품주식회사 | 사이클로 옥시게나제-2 억제제인 페닐 헤테로사이클의제조방법 |
| CN1687075A (zh) * | 2005-03-24 | 2005-10-26 | 天津药物研究院 | 3-苯基异噁唑-5-甲酰胺基取代β-内酰胺类衍生物及其用途 |
| WO2007008541A2 (en) * | 2005-07-08 | 2007-01-18 | Kalypsys, Inc. | Cellular cholesterol absorption modifiers |
| KR100674813B1 (ko) | 2005-08-05 | 2007-01-29 | 일양약품주식회사 | N-페닐-2-피리미딘-아민 유도체 및 그의 제조방법 |
| AU2007275301A1 (en) * | 2006-07-20 | 2008-01-24 | Amgen Inc. | Substituted azole aromatic heterocycles as inhibitors of 11-beta-HSD-1 |
| WO2009084024A2 (en) | 2007-11-02 | 2009-07-09 | Glenmark Generics Limited | A process for the preparation of r-sit agliptin and its pharmaceutically acceptable salts thereof |
| US20090192326A1 (en) | 2007-11-13 | 2009-07-30 | Nurit Perlman | Preparation of sitagliptin intermediate |
| US8642660B2 (en) | 2007-12-21 | 2014-02-04 | The University Of Rochester | Method for altering the lifespan of eukaryotic organisms |
| KR101044880B1 (ko) | 2008-06-12 | 2011-06-28 | 일양약품주식회사 | 항궤양제 화합물의 합성에 유용한 중간체의 제조방법 |
| KR20100021321A (ko) | 2008-08-14 | 2010-02-24 | 일양약품주식회사 | Ν-페닐-2-피리미딘-아민 유도체의 제조방법 |
| US20100297079A1 (en) * | 2009-05-20 | 2010-11-25 | Chimerix, Inc. | Compounds, compositions and methods for treating viral infection |
| WO2011015037A1 (en) * | 2009-08-05 | 2011-02-10 | The University Of Hongkong | Antiviral compounds and methods of making and using there of cross reference to related applications |
| GB2474748B (en) | 2009-10-01 | 2011-10-12 | Amira Pharmaceuticals Inc | Polycyclic compounds as lysophosphatidic acid receptor antagonists |
| JP5902172B2 (ja) | 2010-09-08 | 2016-04-13 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | 広範囲のインフルエンザ抗ウイルス薬としての新規ピペラジン類似体 |
| ES2564257T3 (es) | 2010-09-28 | 2016-03-21 | Bristol-Myers Squibb Company | Nuevos análogos de piperazina con grupos heteroarilo sustituidos como antivirales de amplio espectro de la gripe |
| KR101956586B1 (ko) | 2012-03-27 | 2019-03-11 | 일양약품주식회사 | 약제학적 조성물 및 이의 제조방법 |
-
2011
- 2011-04-19 KR KR1020110036172A patent/KR101369584B1/ko not_active Expired - Fee Related
-
2012
- 2012-03-30 CN CN201280005377.5A patent/CN103313982B/zh not_active Expired - Fee Related
- 2012-03-30 MX MX2013007661A patent/MX340098B/es active IP Right Grant
- 2012-03-30 WO PCT/KR2012/002362 patent/WO2012144752A1/en not_active Ceased
- 2012-03-30 CA CA2824757A patent/CA2824757A1/en not_active Abandoned
- 2012-03-30 EP EP12774858.0A patent/EP2699566B1/en not_active Not-in-force
- 2012-03-30 PH PH1/2013/501883A patent/PH12013501883A1/en unknown
- 2012-03-30 PE PE2013002002A patent/PE20140629A1/es not_active Application Discontinuation
- 2012-03-30 TW TW101111335A patent/TWI434836B/zh not_active IP Right Cessation
- 2012-03-30 AU AU2012246914A patent/AU2012246914B2/en not_active Ceased
- 2012-03-30 US US13/979,743 patent/US9132126B2/en not_active Expired - Fee Related
- 2012-03-30 JP JP2013551922A patent/JP5833143B2/ja not_active Expired - Fee Related
- 2012-03-30 EA EA201300805A patent/EA022336B1/ru not_active IP Right Cessation
- 2012-03-30 SG SG2013056734A patent/SG192134A1/en unknown
- 2012-04-16 SA SA112330457A patent/SA112330457B1/ar unknown
- 2012-04-16 UY UY0001034023A patent/UY34023A/es not_active Application Discontinuation
- 2012-04-17 AR ARP120101314A patent/AR086029A1/es unknown
-
2013
- 2013-06-27 CL CL2013001910A patent/CL2013001910A1/es unknown
- 2013-07-12 ZA ZA2013/05277A patent/ZA201305277B/en unknown
- 2013-07-29 IL IL227711A patent/IL227711A0/en unknown
- 2013-08-16 CO CO13196001A patent/CO6771432A2/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ZA201305277B (en) | 2014-09-25 |
| TW201309658A (zh) | 2013-03-01 |
| EP2699566A4 (en) | 2014-09-03 |
| IL227711A0 (en) | 2013-09-30 |
| JP5833143B2 (ja) | 2015-12-16 |
| KR101369584B1 (ko) | 2014-03-06 |
| CA2824757A1 (en) | 2012-10-26 |
| EP2699566B1 (en) | 2017-02-22 |
| EA022336B1 (ru) | 2015-12-30 |
| HK1188998A1 (zh) | 2014-05-23 |
| EA201300805A1 (ru) | 2013-11-29 |
| CN103313982A (zh) | 2013-09-18 |
| AU2012246914B2 (en) | 2015-09-24 |
| CO6771432A2 (es) | 2013-10-15 |
| SG192134A1 (en) | 2013-08-30 |
| MX2013007661A (es) | 2013-08-12 |
| US9132126B2 (en) | 2015-09-15 |
| EP2699566A1 (en) | 2014-02-26 |
| CL2013001910A1 (es) | 2014-04-21 |
| NZ613314A (en) | 2015-09-25 |
| CN103313982B (zh) | 2016-02-03 |
| PH12013501883A1 (en) | 2019-06-03 |
| JP2014503601A (ja) | 2014-02-13 |
| WO2012144752A1 (en) | 2012-10-26 |
| UY34023A (es) | 2012-06-29 |
| TWI434836B (zh) | 2014-04-21 |
| US20140031364A1 (en) | 2014-01-30 |
| AU2012246914A1 (en) | 2013-08-15 |
| MX340098B (es) | 2016-06-27 |
| AR086029A1 (es) | 2013-11-13 |
| KR20120118665A (ko) | 2012-10-29 |
| SA112330457B1 (ar) | 2015-08-19 |
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