BR112013003843A2 - "derivados de 2-(arilamino)-3h-imidazo[4,5-b]piridina-6-carboxamida, e composição farmacêutica" - Google Patents
"derivados de 2-(arilamino)-3h-imidazo[4,5-b]piridina-6-carboxamida, e composição farmacêutica"Info
- Publication number
- BR112013003843A2 BR112013003843A2 BR112013003843A BR112013003843A BR112013003843A2 BR 112013003843 A2 BR112013003843 A2 BR 112013003843A2 BR 112013003843 A BR112013003843 A BR 112013003843A BR 112013003843 A BR112013003843 A BR 112013003843A BR 112013003843 A2 BR112013003843 A2 BR 112013003843A2
- Authority
- BR
- Brazil
- Prior art keywords
- arylamino
- imidazo
- pyridine
- carboxamide derivatives
- pharmaceutical composition
- Prior art date
Links
Classifications
-
- 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
-
- 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
- A61K31/437—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 containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Rheumatology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pain & Pain Management (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
derivados de 2-(arilamino-3h-imidazo[4,5-b]piridina-6-carboxamida e seu uso como inibidores de mp-ges-1. esta invenção refere-se aos compostos de fórmula i: seu uso como inibidores de prostaglandina e~ 2~sintase-1 microssômica (mp-ges-1), composições farmacêuticas contendo-a, e seu uso como medicamentos para o tratamento e/ou prevenção de doenças inflamatórias e condições associadas. a, m, w, r^ 1^, r^ 2^, r^ 6^, r^ 7^ têm significados cedidos na descrição.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP10173502 | 2010-08-20 | ||
PCT/EP2011/064257 WO2012022792A1 (en) | 2010-08-20 | 2011-08-19 | 2-(arylamino)-3h-imidazo[4,5-b]pyridine-6-carboxamide derivatives and their use as mpges-1 inhibitors |
Publications (1)
Publication Number | Publication Date |
---|---|
BR112013003843A2 true BR112013003843A2 (pt) | 2016-06-28 |
Family
ID=44474976
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BR112013003843A BR112013003843A2 (pt) | 2010-08-20 | 2011-08-19 | "derivados de 2-(arilamino)-3h-imidazo[4,5-b]piridina-6-carboxamida, e composição farmacêutica" |
Country Status (15)
Country | Link |
---|---|
US (1) | US8586604B2 (pt) |
EP (1) | EP2606046A1 (pt) |
JP (1) | JP5554450B2 (pt) |
KR (1) | KR20130098305A (pt) |
CN (1) | CN103097382A (pt) |
AR (1) | AR082509A1 (pt) |
AU (1) | AU2011290724B2 (pt) |
BR (1) | BR112013003843A2 (pt) |
CA (1) | CA2807089A1 (pt) |
CL (1) | CL2013000351A1 (pt) |
EA (1) | EA201201663A1 (pt) |
MX (1) | MX2013001805A (pt) |
NZ (1) | NZ605432A (pt) |
TW (1) | TW201302741A (pt) |
WO (1) | WO2012022792A1 (pt) |
Families Citing this family (39)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
UY32138A (es) | 2008-09-25 | 2010-04-30 | Boehringer Ingelheim Int | Amidas sustituidas del ácido 2-(2,6-dicloro-fenilamino)-6-fluoro-1-metil-1h-bencimidazol-5-carboxílico y sus sales farmacéuticamente aceptables |
UY32470A (es) | 2009-03-05 | 2010-10-29 | Boehringer Ingelheim Int | Derivados de 2-{2-cloro-5-[(sustituido) metil]fenilamino} -1-metil]fenilamino}-1-metilbencimidazol-5-carboxamidas-n-(sustituidas) y sus sales fisiológicamente aceptables, composiciones conteniéndolos y aplicaciones |
CN101645797B (zh) | 2009-08-25 | 2011-04-13 | 华为技术有限公司 | 自动保护倒换方法、设备和系统 |
US8586604B2 (en) | 2010-08-20 | 2013-11-19 | Boehringer Ingelheim International Gmbh | Inhibitors of the microsomal prostaglandin E2 synthase-1 |
US8937073B2 (en) | 2010-08-20 | 2015-01-20 | Boehringer Ingelheim International Gmbh | Disubstituted tetrahydrofuranyl compounds and their use as B1-receptor antagonists |
US8759537B2 (en) | 2010-08-20 | 2014-06-24 | Boehringer Ingelheim International Gmbh | 3H-imidazo [4, 5-C] pyridine-6-carboxamides as anti-inflammatory agents |
US8486968B2 (en) | 2010-12-10 | 2013-07-16 | Boehringer Ingelheim International Gmbh | Compounds |
UY33779A (es) | 2010-12-10 | 2012-07-31 | Boehringer Ingelheim Int | ?2-(fenilamino)-1H-bencimidazol-5-carboxamidas novedosas? |
US8466186B2 (en) | 2010-12-10 | 2013-06-18 | Boehringer Ingelheim International Gmbh | Compounds |
EP3366683A1 (en) * | 2017-02-28 | 2018-08-29 | Acousia Therapeutics GmbH | Cyclic amides, acteamides and ureas useful as potassium channel openers |
MX2021015452A (es) | 2019-06-25 | 2022-02-11 | Gilead Sciences Inc | Proteinas de fusion flt3l-fc y metodos de uso. |
EP4023638A4 (en) * | 2019-08-26 | 2023-10-04 | Kukje Pharma Co., Ltd. | INDOLE CARBOXAMIDE DERIVATIVE AND PHARMACEUTICAL COMPOSITION CONTAINING SAME |
JP7371243B2 (ja) | 2019-10-18 | 2023-10-30 | フォーティ セブン, インコーポレイテッド | 骨髄異形成症候群及び急性骨髄性白血病を治療するための併用療法 |
CN114599392A (zh) | 2019-10-31 | 2022-06-07 | 四十七公司 | 基于抗cd47和抗cd20的血癌治疗 |
TWI778443B (zh) | 2019-11-12 | 2022-09-21 | 美商基利科學股份有限公司 | Mcl1抑制劑 |
MX2022007930A (es) | 2019-12-24 | 2022-08-08 | Carna Biosciences Inc | Compuestos moduladores de diacilglicerol quinasa. |
WO2021163064A2 (en) | 2020-02-14 | 2021-08-19 | Jounce Therapeutics, Inc. | Antibodies and fusion proteins that bind to ccr8 and uses thereof |
AU2021264550A1 (en) | 2020-05-01 | 2022-11-17 | Gilead Sciences, Inc. | CD73 inhibiting 2,4-dioxopyrimidine compounds |
AU2021267373A1 (en) | 2020-05-06 | 2022-12-08 | Ajax Therapeutics, Inc. | 6-heteroaryloxy benzimidazoles and azabenzimidazoles as JAK2 inhibitors |
TW202302145A (zh) | 2021-04-14 | 2023-01-16 | 美商基利科學股份有限公司 | CD47/SIRPα結合及NEDD8活化酶E1調節次單元之共抑制以用於治療癌症 |
CN113304154A (zh) * | 2021-05-10 | 2021-08-27 | 澳门科技大学 | 嘧啶二酮类化合物作为微粒体前列腺素e2合酶抑制剂的应用 |
US20220389394A1 (en) | 2021-05-18 | 2022-12-08 | Gilead Sciences, Inc. | METHODS OF USING FLT3L-Fc FUSION PROTEINS |
EP4359413A1 (en) | 2021-06-23 | 2024-05-01 | Gilead Sciences, Inc. | Diacylglyercol kinase modulating compounds |
AU2022299051A1 (en) | 2021-06-23 | 2023-12-07 | Gilead Sciences, Inc. | Diacylglyercol kinase modulating compounds |
WO2022271677A1 (en) | 2021-06-23 | 2022-12-29 | Gilead Sciences, Inc. | Diacylglyercol kinase modulating compounds |
CA3222439A1 (en) | 2021-06-23 | 2022-12-29 | Gilead Sciences, Inc. | Diacylglyercol kinase modulating compounds |
AU2022375782A1 (en) | 2021-10-28 | 2024-05-02 | Gilead Sciences, Inc. | Pyridizin-3(2h)-one derivatives |
AU2022376954A1 (en) | 2021-10-29 | 2024-05-02 | Gilead Sciences, Inc. | Cd73 compounds |
AU2022388555A1 (en) | 2021-11-09 | 2024-05-02 | Ajax Therapeutics, Inc. | 6-he tero aryloxy benzimidazoles and azabenzimidazoles as jak2 inhibitors |
WO2023122581A2 (en) | 2021-12-22 | 2023-06-29 | Gilead Sciences, Inc. | Ikaros zinc finger family degraders and uses thereof |
AU2022417491A1 (en) | 2021-12-22 | 2024-05-23 | Gilead Sciences, Inc. | Ikaros zinc finger family degraders and uses thereof |
TW202340168A (zh) | 2022-01-28 | 2023-10-16 | 美商基利科學股份有限公司 | Parp7抑制劑 |
WO2023178181A1 (en) | 2022-03-17 | 2023-09-21 | Gilead Sciences, Inc. | Ikaros zinc finger family degraders and uses thereof |
US20230355796A1 (en) | 2022-03-24 | 2023-11-09 | Gilead Sciences, Inc. | Combination therapy for treating trop-2 expressing cancers |
TW202345806A (zh) | 2022-03-31 | 2023-12-01 | 美商艾伯維有限公司 | 噻唑并〔5,4-b〕吡啶malt-1抑制劑 |
TW202345901A (zh) | 2022-04-05 | 2023-12-01 | 美商基利科學股份有限公司 | 用於治療結腸直腸癌之組合療法 |
TW202400138A (zh) | 2022-04-21 | 2024-01-01 | 美商基利科學股份有限公司 | Kras g12d調節化合物 |
WO2024006929A1 (en) | 2022-07-01 | 2024-01-04 | Gilead Sciences, Inc. | Cd73 compounds |
WO2024064668A1 (en) | 2022-09-21 | 2024-03-28 | Gilead Sciences, Inc. | FOCAL IONIZING RADIATION AND CD47/SIRPα DISRUPTION ANTICANCER COMBINATION THERAPY |
Family Cites Families (41)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3006671A1 (de) | 1980-02-22 | 1981-08-27 | Dr. Karl Thomae Gmbh, 7950 Biberach | Neue benzoxazole, deren herstellung und deren verwendung als arzneumittel |
FI91859C (fi) | 1987-06-17 | 1994-08-25 | Eisai Co Ltd | Analogiamenetelmä antiallergisena aineena aktiivisen bentsotiatsolijohdannaisen valmistamiseksi |
JPH06759B2 (ja) | 1989-09-22 | 1994-01-05 | ファイザー製薬株式会社 | 新規なベンゾイミダゾール化合物 |
DK1114028T3 (da) | 1998-08-26 | 2007-04-30 | Aventis Pharma Ltd | Azabicykliske forbindelser, der modulerer inhibering af celleadhæsion |
ATE325105T1 (de) | 1999-02-16 | 2006-06-15 | Aventis Pharma Ltd | Bicyclische verbindungen und ihre verwendung als integrinrezeptorliganden |
EE200100528A (et) | 1999-04-12 | 2003-02-17 | Aventis Pharma Limited | Asendatud bitsükliline heteroarüülühend, seda sisaldav farmatseutiline kompositsioon ning nende raviotstarbeline kasutamine |
AU4591600A (en) | 1999-05-05 | 2000-11-21 | Aventis Pharma Limited | Substituted bicyclic compounds |
CN1292744C (zh) * | 1999-05-07 | 2007-01-03 | 得克萨斯生物技术公司 | 抑制整联蛋白与其受体结合的羧酸衍生物 |
US6340681B1 (en) | 1999-07-16 | 2002-01-22 | Pfizer Inc | 2-benzimidazolylamine compounds as ORL-1-receptor agonists |
MXPA02003364A (es) | 1999-10-06 | 2002-08-23 | Boehringer Ingelheim Pharma | Compuestos heterociclicos utiles como inhibidores de las cinasas de tirosina. |
FR2833948B1 (fr) | 2001-12-21 | 2004-02-06 | Sod Conseils Rech Applic | Nouveaux derives de benzimidazole et leur utilisation en tant que medicament |
ES2290479T3 (es) | 2002-03-01 | 2008-02-16 | Smithkline Beecham Corporation | Diamino-pirimidinas y su uso como inhibidores de la angiogenesis. |
ES2336094T3 (es) | 2002-03-29 | 2010-04-08 | Novartis Vaccines And Diagnostics, Inc. | Benzazoles sustituidos y uso de los mismos como inhibidores de quinasa raf. |
US7037902B2 (en) | 2002-07-03 | 2006-05-02 | Receptron, Inc. | Affinity small molecules for the EPO receptor |
JP4768265B2 (ja) | 2002-10-15 | 2011-09-07 | シンタ ファーマシューティカルズ コーポレーション | 新規化合物 |
US7265138B2 (en) | 2003-02-10 | 2007-09-04 | Amgen Inc. | Vanilloid receptor ligands and their use in treatments |
FR2851563B1 (fr) | 2003-02-26 | 2005-04-22 | Sod Conseils Rech Applic | Nouveaux derives de benzimidazole et d'imidazo-pyridine et leur utilisation en tant que medicament |
US7531553B2 (en) | 2003-03-21 | 2009-05-12 | Amgen Inc. | Heterocyclic compounds and methods of use |
FR2852957B1 (fr) | 2003-03-31 | 2005-06-10 | Sod Conseils Rech Applic | Nouveaux derives d'imidazo-pyridine et leur utilisation en tant que medicament |
US7329682B2 (en) | 2003-04-03 | 2008-02-12 | Ewha University-Industry Collaboration Foundation | Method for inhibiting 5-lipoxygenase using a benzoxazole derivative |
JP4842829B2 (ja) | 2003-10-31 | 2011-12-21 | 武田薬品工業株式会社 | 含窒素縮合複素環化合物 |
US7470712B2 (en) | 2004-01-21 | 2008-12-30 | Bristol-Myers Squibb Company | Amino-benzazoles as P2Y1 receptor inhibitors |
GB0401334D0 (en) | 2004-01-21 | 2004-02-25 | Novartis Ag | Organic compounds |
CN101006054A (zh) | 2004-06-18 | 2007-07-25 | 比奥里波克斯公司 | 用于炎症治疗的吲哚 |
EP1828143B1 (en) * | 2004-12-17 | 2013-03-20 | Merck Frosst Canada Ltd. | 2-(phenyl or heterocyclic)-1h-phenantrho[9,10-d]imidazoles as mpges-1 inhibitors |
US7723340B2 (en) | 2005-01-13 | 2010-05-25 | Signal Pharmaceuticals, Llc | Haloaryl substituted aminopurines, compositions thereof, and methods of treatment therewith |
US7521446B2 (en) | 2005-01-13 | 2009-04-21 | Signal Pharmaceuticals, Llc | Haloaryl substituted aminopurines, compositions thereof, and methods of treatment therewith |
KR20070114123A (ko) | 2005-01-19 | 2007-11-29 | 바이올리폭스 에이비 | 염증 치료에 유용한 인돌 |
CA2599320A1 (en) | 2005-02-25 | 2006-08-31 | Kudos Pharmaceuticals Limited | Hydrazinomethyl, hydr zonomethyl and 5-membered heterocylic compounds which act as mtor inhibitors and their use as anti cancer agents |
CN102633783A (zh) | 2006-02-10 | 2012-08-15 | 转化技术制药公司 | 作为Aurora激酶抑制剂的苯并唑系衍生物、组合物和使用方法 |
WO2008009924A2 (en) | 2006-07-18 | 2008-01-24 | Biolipox Ab | Indoles useful in the treatment of inflammation |
KR20080027191A (ko) | 2006-09-22 | 2008-03-26 | 이화여자대학교 산학협력단 | 신규한 벤즈옥사졸 유도체, 이의 제조방법 및 이를포함하는 약학 조성물 |
WO2008071944A1 (en) | 2006-12-14 | 2008-06-19 | Boehringer Ingelheim International Gmbh | Benzoxazoles useful in the treatment of inflammation |
WO2008129276A1 (en) | 2007-04-19 | 2008-10-30 | Boehringer Ingelheim International Gmbh | Disulfonamides useful in the treatment of inflammation |
UY32138A (es) | 2008-09-25 | 2010-04-30 | Boehringer Ingelheim Int | Amidas sustituidas del ácido 2-(2,6-dicloro-fenilamino)-6-fluoro-1-metil-1h-bencimidazol-5-carboxílico y sus sales farmacéuticamente aceptables |
UY32470A (es) | 2009-03-05 | 2010-10-29 | Boehringer Ingelheim Int | Derivados de 2-{2-cloro-5-[(sustituido) metil]fenilamino} -1-metil]fenilamino}-1-metilbencimidazol-5-carboxamidas-n-(sustituidas) y sus sales fisiológicamente aceptables, composiciones conteniéndolos y aplicaciones |
US8586604B2 (en) | 2010-08-20 | 2013-11-19 | Boehringer Ingelheim International Gmbh | Inhibitors of the microsomal prostaglandin E2 synthase-1 |
US8759537B2 (en) | 2010-08-20 | 2014-06-24 | Boehringer Ingelheim International Gmbh | 3H-imidazo [4, 5-C] pyridine-6-carboxamides as anti-inflammatory agents |
US8486968B2 (en) | 2010-12-10 | 2013-07-16 | Boehringer Ingelheim International Gmbh | Compounds |
US8466186B2 (en) | 2010-12-10 | 2013-06-18 | Boehringer Ingelheim International Gmbh | Compounds |
UY33779A (es) | 2010-12-10 | 2012-07-31 | Boehringer Ingelheim Int | ?2-(fenilamino)-1H-bencimidazol-5-carboxamidas novedosas? |
-
2011
- 2011-08-17 US US13/211,471 patent/US8586604B2/en not_active Expired - Fee Related
- 2011-08-19 TW TW100129864A patent/TW201302741A/zh unknown
- 2011-08-19 EP EP11751853.0A patent/EP2606046A1/en not_active Withdrawn
- 2011-08-19 CA CA2807089A patent/CA2807089A1/en not_active Abandoned
- 2011-08-19 CN CN2011800390100A patent/CN103097382A/zh active Pending
- 2011-08-19 JP JP2013524454A patent/JP5554450B2/ja not_active Expired - Fee Related
- 2011-08-19 NZ NZ60543211A patent/NZ605432A/en not_active IP Right Cessation
- 2011-08-19 AU AU2011290724A patent/AU2011290724B2/en not_active Expired - Fee Related
- 2011-08-19 KR KR1020137004207A patent/KR20130098305A/ko not_active Application Discontinuation
- 2011-08-19 EA EA201201663A patent/EA201201663A1/ru unknown
- 2011-08-19 BR BR112013003843A patent/BR112013003843A2/pt not_active IP Right Cessation
- 2011-08-19 WO PCT/EP2011/064257 patent/WO2012022792A1/en active Application Filing
- 2011-08-19 MX MX2013001805A patent/MX2013001805A/es unknown
- 2011-08-19 AR ARP110103038A patent/AR082509A1/es unknown
-
2013
- 2013-02-04 CL CL2013000351A patent/CL2013000351A1/es unknown
Also Published As
Publication number | Publication date |
---|---|
JP2013534235A (ja) | 2013-09-02 |
WO2012022792A1 (en) | 2012-02-23 |
AR082509A1 (es) | 2012-12-12 |
JP5554450B2 (ja) | 2014-07-23 |
EA201201663A1 (ru) | 2013-08-30 |
CA2807089A1 (en) | 2012-02-23 |
MX2013001805A (es) | 2013-04-29 |
TW201302741A (zh) | 2013-01-16 |
CL2013000351A1 (es) | 2013-06-21 |
AU2011290724B2 (en) | 2015-11-05 |
AU2011290724A1 (en) | 2013-01-10 |
NZ605432A (en) | 2015-04-24 |
US8586604B2 (en) | 2013-11-19 |
KR20130098305A (ko) | 2013-09-04 |
US20120208839A1 (en) | 2012-08-16 |
CN103097382A (zh) | 2013-05-08 |
EP2606046A1 (en) | 2013-06-26 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
BR112013003843A2 (pt) | "derivados de 2-(arilamino)-3h-imidazo[4,5-b]piridina-6-carboxamida, e composição farmacêutica" | |
GT201300137A (es) | Derivados de imidazo [1,2-b] piridazina e imidazo [4,5-b] piridina como inhibidores de jak | |
BR112013001088A2 (pt) | "derivados substituídos como inibidores a quinase de imidazoquinolina" | |
UA109010C2 (en) | MORPHOLINOPYRIMIDINES AND THEIR APPLICATIONS IN THERAPY | |
BR112013011991A2 (pt) | composto, composição farmacêutica, uso de um composto, método de tratamento, produto, e kit. | |
BR112012012906A2 (pt) | triazolopiridinas | |
MX2011009847A (es) | Agentes antihelminticos y su uso. | |
CO6680683A2 (es) | Inhibiddores de la prostaglandina e2 sintasa-1 microsómica (mpges-1) y composiciones que los contienen, útiles en el tratamiento de enfermedades inflamatorias | |
CO6680667A2 (es) | Derivados ester de ácido borónico cíclico y sus usos terapéuticos | |
UA108926C2 (ru) | LibreOffice? [2,3-D] +" +" !+ | |
GEP20146115B (en) | Thieno [2,3-b] pyridine derivatives as viral replication inhibitors | |
BR112013016595A2 (pt) | inibidores de neprilisina | |
JO3111B1 (ar) | ترايازولوبيريدينات مستبدلة واستخدامها كمثبطات ttk | |
BR112012019765A2 (pt) | composto, e, uso de um composto. | |
IN2014CN04530A (pt) | ||
IN2014CN03130A (pt) | ||
JO3115B1 (ar) | مركبات بيريدازينون واستخدامها كمثبطات daao | |
MX2010001338A (es) | Derivados de pirimidina y piridina y su uso y composiciones farmaceuticas. | |
GEP20135806B (en) | Lactams as beta secretase inhibitors | |
WO2013106761A3 (en) | Antimicrobial agents | |
UA109290C2 (uk) | Спільні кристали і солі інгібіторів ccr3 | |
MX340574B (es) | Imidazo pirazinas. | |
BR112014003063A2 (pt) | "3,4-di-hidro-1h-[1,8]naftiridinonas substituídas com ciclopenta[c]pirrol antibacterianas, composição farmacêutica compreendendo os referidos compostos, processos para preparação destes e uso". | |
MX341577B (es) | Derivados biciclicos de pirimidin-urea o carbamato sustituidos con morfolino como inhibidores del blanco de rapamicina de mamifero. | |
MX2011013869A (es) | Agentes antihelminticos y su uso. |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
B08F | Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette] |
Free format text: REFERENTE A 5A ANUIDADE. |
|
B08K | Patent lapsed as no evidence of payment of the annual fee has been furnished to inpi [chapter 8.11 patent gazette] |
Free format text: EM VIRTUDE DO ARQUIVAMENTO PUBLICADO NA RPI 2386 DE 27-09-2016 E CONSIDERANDO AUSENCIA DE MANIFESTACAO DENTRO DOS PRAZOS LEGAIS, INFORMO QUE CABE SER MANTIDO O ARQUIVAMENTO DO PEDIDO DE PATENTE, CONFORME O DISPOSTO NO ARTIGO 12, DA RESOLUCAO 113/2013. |