ES2572387T3 - Compuestos anti-infecciosos - Google Patents
Compuestos anti-infecciososInfo
- Publication number
- ES2572387T3 ES2572387T3 ES11711032T ES11711032T ES2572387T3 ES 2572387 T3 ES2572387 T3 ES 2572387T3 ES 11711032 T ES11711032 T ES 11711032T ES 11711032 T ES11711032 T ES 11711032T ES 2572387 T3 ES2572387 T3 ES 2572387T3
- Authority
- ES
- Spain
- Prior art keywords
- group
- heterocyclyl
- heteroaryl
- cycloalkyl
- benzyl
- Prior art date
- Legal status (The legal status 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 status listed.)
- Active
Links
Classifications
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- 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
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- 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
- A61P31/04—Antibacterial agents
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- 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
- A61P31/04—Antibacterial agents
- A61P31/06—Antibacterial agents for tuberculosis
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D243/00—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms
- C07D243/06—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4
- C07D243/10—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
- C07D243/14—1,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines
- C07D243/16—1,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines substituted in position 5 by aryl radicals
- C07D243/18—1,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines substituted in position 5 by aryl radicals substituted in position 2 by nitrogen, oxygen or sulfur atoms
- C07D243/20—Nitrogen atoms
-
- 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
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Communicable Diseases (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Pulmonology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
Un compuesto que tiene la fórmula general Ib:**Fórmula** en la que X, Y y Z son CH; o es 1; n es 0; m es 0, 1, 2, 3 o 4; A es C>=O; W es NH; R2, cada vez que aparece, se selecciona independientemente entre el grupo que consiste en hidrógeno, halógeno, alquilo C1-C10, cicloalquilo C3-C10, alquenilo C2-C10, cicloalquenilo C3-C10, alquinilo C2-C10, haloalquilo C1-C10, -OH, -OR5, alcoxi C1-C10, cicloalcoxi C3-C10, cicloalquilalcoxi C3-C15, cicloalquilalquilo C3-C15, -CN, -NO2, - NH2, -N(R5)2, -C(O)R5, -C(O)OR5, -C(O)N(R5)2, -SR5,-S(O)R5, -S(O)2R5, -S(O)2N(RS)2, arilo, por ejemplo fenilo, bencilo, heteroarilo y heterociclilo; R3, cada vez que aparece, se selecciona independientemente entre el grupo que consiste en hidrógeno, halógeno, alquilo C1-C10, cicloalquilo C3-C10, hidroxilo, -OR6, -CN, -NO2, -NH2, -N(R6)C(O)R6,-C(O)R6, -C(O)OR6, -C(O)N(R6)2, -S(O)R6, -S(O)2R6, -S(O)2N(R6)2, arilo, por ejemplo fenilo, bencilo, heteroarilo, heterociclilo o dos grupos de R3 están conectados entre sí para hacer anillos cíclicos y heterocíclicos de cinco o seis miembros, R5 y R6, cada vez que aparecen, se seleccionan independientemente entre el grupo que consiste en hidrógeno, alquilo C1-C10, cicloalquilo C3-C10, alquenilo C2-C10, cicloalquenilo C3-C10, alquinilo C2-C10, haloalquilo C1-C10, arilo, por ejemplo fenilo, bencilo, heteroarilo y heterociclilo; R10 es un resto seleccionado entre el grupo que consiste en**Fórmula** en las que m' es 0, 1, 2, 3 o 4 y n' es 0, 1, 2 o 3; R11, cada vez que aparece, se selecciona independientemente entre el grupo que consiste en hidrógeno, alquilo C1-C10, cicloalquilo C3-C10, alquenilo C2-C10, cicloalquenilo C3-C10, alquinilo C2-C10, haloalquilo C1-C10, -OH, - OR13, alcoxi C1-C10, cicloalcoxi C3-C10, cicloalquilalcoxi C3-C15, cicloalquilalquilo C3-C15, -NH2, -N(R13)2, -C(O)R13, -COOR13, -C(O)N(R13)2, -S(O)R13, -S(O)2R13, -S(O)2N(R13)2, arilo, por ejemplo fenilo, bencilo, heteroarilo y heterociclilo; R12, cada vez que aparece, se selecciona independientemente entre el grupo que consiste en hidrógeno, alquilo C1-C10, cicloalquilo C3-C10, alquenilo C2-C10, cicloalquenilo C3-C10, alquinilo C2-C10, haloalquilo C1-C10, hidroxilo, - OR14, -C(O)R14, -C(O)OR14, -CN, -NO2, -NH2, -N(R14)2, -C(O)N(R14)2, S(O)R14, -S(O)2R14, -S(O)2N(R14)2, arilo, por ejemplo fenilo, bencilo, heteroarilo y heterociclilo; R3, cada vez que aparece, se selecciona independientemente entre el grupo que consiste en hidrógeno, alquilo C1-C10, cicloalquilo C3-C10, alquenilo C2-C10, cicloalquenilo C3-C10, alquinilo C2-C10, haloalquilo C1-C10, arilo, por ejemplo fenilo, bencilo, heteroarilo y heterociclilo; y R14, cada vez que aparece, se selecciona independientemente entre el grupo que consiste en hidrógeno, alquilo C1-C8 opcionalmente sustituido con al menos un hidroxilo o halógeno; cicloalquilo C3-C7, alquenilo C2-C10, cicloalquenilo C3-C10, alquinilo C2-C10, haloalquilo C1-C10, arilo, por ejemplo fenilo, bencilo, heteroarilo y heterociclilo, y sales farmacéuticamente aceptables del mismo para uso en el tratamiento de una infección bacteriana.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US31511310P | 2010-03-18 | 2010-03-18 | |
US201161440937P | 2011-02-09 | 2011-02-09 | |
PCT/EP2011/001345 WO2011113606A1 (en) | 2010-03-18 | 2011-03-18 | Anti-infective compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
ES2572387T3 true ES2572387T3 (es) | 2016-05-31 |
Family
ID=44021876
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES11711032T Active ES2572387T3 (es) | 2010-03-18 | 2011-03-18 | Compuestos anti-infecciosos |
Country Status (18)
Country | Link |
---|---|
US (1) | US8865734B2 (es) |
EP (1) | EP2547678B1 (es) |
JP (1) | JP5944837B2 (es) |
KR (1) | KR101732212B1 (es) |
CN (1) | CN102869661B (es) |
AU (1) | AU2011229423B2 (es) |
BR (1) | BR112012023576B1 (es) |
CA (1) | CA2793086C (es) |
ES (1) | ES2572387T3 (es) |
HK (1) | HK1180683A1 (es) |
IL (1) | IL221940A (es) |
MX (1) | MX345762B (es) |
NZ (1) | NZ602311A (es) |
PL (1) | PL2547678T3 (es) |
RU (1) | RU2576662C2 (es) |
SG (2) | SG184073A1 (es) |
WO (1) | WO2011113606A1 (es) |
ZA (1) | ZA201206814B (es) |
Families Citing this family (108)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9309238B2 (en) | 2009-11-05 | 2016-04-12 | University Of Notre Dame Du Lac | Imidazo [1,2-a]pyridine compounds, synthesis thereof, and methods of using same |
US9284301B2 (en) | 2010-03-25 | 2016-03-15 | Merck Sharp & Dohme Corp. | Soluble guanylate cyclase activators |
EP2575473B1 (en) | 2010-05-27 | 2016-01-20 | Merck Sharp & Dohme Corp. | Soluble guanylate cyclase activators |
WO2012045729A1 (en) * | 2010-10-05 | 2012-04-12 | Glaxo Group Limited | Imidazo [1, 2 -a] pyridine and pyrazolo [1, 5 -a] pyridine derivatives as trpv1 antagonists |
KR20140093610A (ko) | 2011-04-21 | 2014-07-28 | 재단법인 한국파스퇴르연구소 | 소염 화합물 |
MX2013014082A (es) | 2011-05-30 | 2014-03-21 | Astellas Pharma Inc | Compuestos de imidazopiridina. |
US9309250B2 (en) | 2011-06-22 | 2016-04-12 | Vertex Pharmaceuticals Incorporated | Substituted pyrrolo[2,3-b]pyrazines as ATR kinase inhibitors |
AU2012324517A1 (en) * | 2011-10-21 | 2014-05-22 | Torrent Pharmaceuticals Limited | Novel substituted imidazopyrimidines as Gpbar1 receptor modulators |
US8765959B2 (en) * | 2011-12-23 | 2014-07-01 | Boehringer Ingelheim International Gmbh | Piperidine derivatives |
RU2696278C2 (ru) * | 2012-07-18 | 2019-08-01 | Юниверсити Оф Нотр Дам Дю Лак | 5,5-гетероароматические противоинфекционные соединения |
WO2014021383A1 (ja) * | 2012-07-31 | 2014-02-06 | 協和発酵キリン株式会社 | 縮環複素環化合物 |
US8778964B2 (en) * | 2012-11-05 | 2014-07-15 | Bayer Pharma Aktiengesellschaft | Hydroxy-substituted imidazo[1,2-a]-pyridinecarboxamides and their use |
US8796305B2 (en) | 2012-11-05 | 2014-08-05 | Bayer Pharma Aktiengesellschaft | Carboxy-substituted imidazo[1,2-a]pyridinecarboxamides and their use |
US9126998B2 (en) | 2012-11-05 | 2015-09-08 | Bayer Pharma AG | Amino-substituted imidazo[1,2-a]pyridinecarboxamides and their use |
US9624214B2 (en) | 2012-11-05 | 2017-04-18 | Bayer Pharma Aktiengesellschaft | Amino-substituted imidazo[1,2-a]pyridinecarboxamides and their use |
AU2013353117A1 (en) | 2012-11-30 | 2015-06-04 | Astellas Pharma Inc. | Imidazopyridine compound |
BR112015012454B1 (pt) | 2012-12-07 | 2022-07-05 | Vertex Pharmaceuticals Incorporated | Compostos inibidores de atr quinase, seu uso e composição farmacêutica compreendendo os mesmos |
WO2014143241A1 (en) | 2013-03-15 | 2014-09-18 | Vertex Pharmaceuticals Incorporated | Compounds useful as inhibitors of atr kinase |
EP2970286A1 (en) | 2013-03-15 | 2016-01-20 | Vertex Pharmaceuticals Inc. | Fused pyrazolopyrimidine derivatives useful as inhibitors of atr kinase |
US8969360B2 (en) | 2013-03-15 | 2015-03-03 | Vertex Pharmaceuticals Incorporated | Compounds useful as inhibitors of ATR kinase |
CA2914100A1 (en) | 2013-06-04 | 2014-12-11 | Bayer Pharma Aktiengesellschaft | 3-aryl-substituted imidazo[1,2-a]pyridines and the use thereof |
WO2015009525A1 (en) * | 2013-07-17 | 2015-01-22 | Global Alliance For Tb Drug Development | Azaindole compounds, synthesis thereof, and methods of using the same |
EP3027615B1 (en) * | 2013-08-02 | 2021-07-21 | Institut Pasteur Korea | Anti-infective compounds |
CN105934435B (zh) | 2013-12-06 | 2019-02-22 | 沃泰克斯药物股份有限公司 | 用作atr激酶抑制剂的化合物,其制备,及其放射性标记的衍生物 |
HUE046273T2 (hu) | 2014-02-13 | 2020-02-28 | Incyte Corp | Ciklopropilaminok mint LSD1 inhibitorok |
US9527835B2 (en) | 2014-02-13 | 2016-12-27 | Incyte Corporation | Cyclopropylamines as LSD1 inhibitors |
US9493442B2 (en) | 2014-02-13 | 2016-11-15 | Incyte Corporation | Cyclopropylamines as LSD1 inhibitors |
CR20200362A (es) | 2014-02-13 | 2020-10-26 | Incyte Corp | CICLOPROPILAMINA COMO INHIBIDORES DE LA LSD1 (Divisional 2016-0395) |
CA2939793A1 (en) | 2014-02-19 | 2015-08-27 | Bayer Pharma Aktiengesellschaft | 3-(pyrimidine-2-yl)imidazo[1,2-a]pyridines |
JP2017508810A (ja) | 2014-03-21 | 2017-03-30 | バイエル・ファルマ・アクティエンゲゼルシャフト | シアノ置換イミダゾ[1,2−a]ピリジンカルボキサミドおよびその使用 |
US20170057958A1 (en) | 2014-05-02 | 2017-03-02 | Bayer Pharma Aktiengesellschaft | Enantiomers of the n-(2-amino-5-fluoro-2-methylpentyl)-8-[(2,6-difluorobenzyl)oxy]-2-methylimidazo[1,2-a]pyridine-3-carboxamide, as well as of the di- and trifluoro derivatives for the treatment of cardiovascular diseases |
CN103965193B (zh) * | 2014-05-30 | 2016-04-06 | 浙江司太立制药股份有限公司 | N-(苯氧烷基)咪唑并[1,2-a]吡啶-3-酰胺类化合物及其制备方法 |
CN107074863B (zh) | 2014-06-05 | 2019-12-03 | 沃泰克斯药物股份有限公司 | Atr激酶抑制剂的制备方法及其不同的固体形式 |
SG11201610500WA (en) | 2014-06-17 | 2017-01-27 | Vertex Pharma | Method for treating cancer using a combination of chk1 and atr inhibitors |
US9758523B2 (en) | 2014-07-10 | 2017-09-12 | Incyte Corporation | Triazolopyridines and triazolopyrazines as LSD1 inhibitors |
US9695167B2 (en) | 2014-07-10 | 2017-07-04 | Incyte Corporation | Substituted triazolo[1,5-a]pyridines and triazolo[1,5-a]pyrazines as LSD1 inhibitors |
US9695168B2 (en) | 2014-07-10 | 2017-07-04 | Incyte Corporation | Substituted imidazo[1,5-α]pyridines and imidazo[1,5-α]pyrazines as LSD1 inhibitors |
TW201613925A (en) | 2014-07-10 | 2016-04-16 | Incyte Corp | Imidazopyrazines as LSD1 inhibitors |
EP3227287B1 (de) | 2014-12-02 | 2019-08-07 | Bayer Pharma Aktiengesellschaft | Heteroaryl-substituierte imidazo[1,2-a]pyridine und ihre verwendung |
US9944647B2 (en) | 2015-04-03 | 2018-04-17 | Incyte Corporation | Heterocyclic compounds as LSD1 inhibitors |
UA125171C2 (uk) * | 2015-07-02 | 2022-01-26 | Янссен Саєнсиз Айрленд Юсі | Антибактеріальні сполуки |
JP7427363B2 (ja) | 2015-08-12 | 2024-02-05 | インサイト・ホールディングス・コーポレイション | Lsd1阻害剤の塩 |
KR20180053386A (ko) | 2015-09-17 | 2018-05-21 | 마빈 제이. 밀러 | 마이코박테리아 감염에 대해 유용한 벤질 아민-함유 헤테로사이클릭 화합물 및 조성물 |
EP3355926A4 (en) | 2015-09-30 | 2019-08-21 | Vertex Pharmaceuticals Inc. | METHOD FOR THE TREATMENT OF CANCER WITH A COMBINATION OF DNA DAMAGING AGENTS AND ATR INHIBITORS |
MA52119A (fr) | 2015-10-19 | 2018-08-29 | Ncyte Corp | Composés hétérocycliques utilisés comme immunomodulateurs |
SG10202004618TA (en) | 2015-11-19 | 2020-06-29 | Incyte Corp | Heterocyclic compounds as immunomodulators |
EP3386979B1 (de) | 2015-12-10 | 2020-07-29 | Bayer Pharma Aktiengesellschaft | 2-phenyl-3-(piperazinomethyl)imidazo[1,2-a]pyridin-derivate als blocker der task-1 und task-2 kanäle zur behandlung von schlafbedingten atemstörungen |
CA3007699A1 (en) | 2015-12-10 | 2017-06-15 | Bayer Pharma Aktiengesellschaft | Substituted perhydropyrrolo[3,4-c]pyrrole derivatives and the use of same |
US20170174679A1 (en) | 2015-12-22 | 2017-06-22 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
EP3421454B9 (en) * | 2016-02-26 | 2023-08-09 | Otsuka Pharmaceutical Co., Ltd. | Piperidine derivative |
ES2963148T3 (es) | 2016-04-22 | 2024-03-25 | Incyte Corp | Formulaciones de un inhibidor de LSD1 |
WO2017192961A1 (en) | 2016-05-06 | 2017-11-09 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
TW201808902A (zh) | 2016-05-26 | 2018-03-16 | 美商英塞特公司 | 作為免疫調節劑之雜環化合物 |
EA201990044A1 (ru) | 2016-06-16 | 2019-05-31 | Янссен Сайенсиз Айрлэнд Анлимитед Компани | Гетероциклические соединения в качестве антибактериальных средств |
WO2017216281A1 (en) | 2016-06-16 | 2017-12-21 | Janssen Sciences Ireland Uc | Heterocyclic compounds as antibacterials |
MD3472167T2 (ro) | 2016-06-20 | 2023-02-28 | Incyte Corp | Compuși heterociclici ca imunomodulatori |
ES2930092T3 (es) | 2016-07-14 | 2022-12-07 | Incyte Corp | Compuestos heterocíclicos como inmunomoduladores |
JOP20190005A1 (ar) | 2016-07-20 | 2019-01-20 | Bayer Ag | مركبات ديازاهيترو ثنائية الحلقة مستبدلة واستخداماتها |
CN106279123B (zh) * | 2016-08-15 | 2018-09-04 | 郑州大学 | 3-(苯磺酰甲基)咪唑并杂环类化合物及其合成方法 |
JOP20190024A1 (ar) | 2016-08-26 | 2019-02-19 | Gilead Sciences Inc | مركبات بيروليزين بها استبدال واستخداماتها |
ES2941716T3 (es) | 2016-08-29 | 2023-05-25 | Incyte Corp | Compuestos heterocíclicos como inmunomoduladores |
CA3047980A1 (en) | 2016-12-22 | 2018-06-28 | Incyte Corporation | Tetrahydro imidazo[4,5-c]pyridine derivatives as pd-l1 internalization inducers |
ES2874756T3 (es) | 2016-12-22 | 2021-11-05 | Incyte Corp | Derivados de triazolo[1,5-A]piridina como inmunomoduladores |
MX2019007416A (es) | 2016-12-22 | 2019-12-11 | Incyte Corp | Derivados de benzooxazol como inmunomoduladores. |
ES2899402T3 (es) | 2016-12-22 | 2022-03-11 | Incyte Corp | Derivados de piridina como inmunomoduladores |
MA47676A (fr) | 2017-03-01 | 2021-06-02 | Janssen Sciences Ireland Unlimited Co | Polythérapie |
WO2018184976A1 (de) | 2017-04-05 | 2018-10-11 | Bayer Pharma Aktiengesellschaft | Substituierte imidazo[1,2-a]pyridincarboxamide und ihre verwendung |
WO2018227427A1 (en) | 2017-06-14 | 2018-12-20 | Bayer Aktiengesellschaft | Substituted bridged diazepane derivatives and use thereof |
JOP20190284A1 (ar) | 2017-06-14 | 2019-12-11 | Bayer Pharma AG | مركبات إيميدازوبيريميدين مستبدلة بديازا ثنائي الحلقة واستخدامها للمعالجة من اضطرابات التنفس |
EP3428815A1 (en) | 2017-07-11 | 2019-01-16 | Institut Pasteur | Docking method based on saturation transfer difference nmr data, and means for its implementation |
CN111246848A (zh) | 2017-10-05 | 2020-06-05 | 快尔生物技术公司 | 与抗结核药物组合的环稠和的噻唑并2-吡啶酮 |
JP7319977B2 (ja) | 2017-12-06 | 2023-08-02 | リン バイオサイエンス,インコーポレイテッド | チューブリン阻害剤 |
JP7184383B2 (ja) * | 2018-02-01 | 2022-12-06 | ザ・ユニバーシティ・オブ・シドニー | 抗癌性化合物 |
CN108159049B (zh) * | 2018-02-01 | 2021-01-05 | 中国科学院广州生物医药与健康研究院 | 一种吡啶类化合物的新用途 |
ES2962605T3 (es) | 2018-02-26 | 2024-03-20 | Gilead Sciences Inc | Compuestos de pirrolizina sustituidos como inhibidores de la replicación del VHB |
CN117903140A (zh) | 2018-02-27 | 2024-04-19 | 因赛特公司 | 作为a2a/a2b抑制剂的咪唑并嘧啶和三唑并嘧啶 |
JP7372255B2 (ja) | 2018-03-30 | 2023-10-31 | インサイト・コーポレイション | 免疫調節剤としての複素環式化合物 |
HRP20230306T1 (hr) | 2018-05-11 | 2023-05-12 | Incyte Corporation | Derivati tetrahidro-imidazo[4,5-c]piridina kao pd-l1 imunomodulatori |
MA52940A (fr) | 2018-05-18 | 2021-04-28 | Incyte Corp | Dérivés de pyrimidine fusionnés utilisés en tant qu'inhibiteurs de a2a/a2b |
JP7490631B2 (ja) | 2018-07-05 | 2024-05-27 | インサイト・コーポレイション | A2a/a2b阻害剤としての縮合ピラジン誘導体 |
WO2020047198A1 (en) | 2018-08-31 | 2020-03-05 | Incyte Corporation | Salts of an lsd1 inhibitor and processes for preparing the same |
CN109651363B (zh) * | 2019-01-03 | 2020-06-26 | 东华理工大学 | 胺甲基化咪唑并[1,2-a]吡啶化合物及制备方法 |
TWI829857B (zh) | 2019-01-29 | 2024-01-21 | 美商英塞特公司 | 作為a2a / a2b抑制劑之吡唑并吡啶及三唑并吡啶 |
WO2021018387A1 (en) | 2019-07-30 | 2021-02-04 | Qurient Co., Ltd. | Different forms of 6-chloro-2-ethyl-n-(4-(4-(4-(trifluoromethoxy)phenyl)piperidine-1-yl)benzyl)imidazo[1,2-a]pyridine-3-carboxamide |
US11753406B2 (en) | 2019-08-09 | 2023-09-12 | Incyte Corporation | Salts of a PD-1/PD-L1 inhibitor |
TW202124379A (zh) * | 2019-09-10 | 2021-07-01 | 日商鹽野義製藥股份有限公司 | 對分枝桿菌感染有用之含苄胺的5,6-雜芳族化合物 |
CA3149868A1 (en) | 2019-09-13 | 2021-03-18 | Jerome Emile Georges Guillemont | Antibacterial compounds |
CA3155852A1 (en) | 2019-09-30 | 2021-04-08 | Incyte Corporation | PYRIDO[3,2-D]PYRIMIDINE COMPOUNDS AS IMMUNOMODULATORS |
KR20220075335A (ko) | 2019-09-30 | 2022-06-08 | 얀센 사이언시즈 아일랜드 언리미티드 컴퍼니 | 항균 화합물 |
WO2021063914A1 (en) | 2019-09-30 | 2021-04-08 | Janssen Sciences Ireland Unlimited Company | 4-quinolinone antibacterial compounds |
WO2021096849A1 (en) | 2019-11-11 | 2021-05-20 | Incyte Corporation | Salts and crystalline forms of a pd-1/pd-l1 inhibitor |
CN114786670A (zh) * | 2019-12-20 | 2022-07-22 | 奎利恩特有限公司 | 一种药物口服剂型 |
JP2023517519A (ja) * | 2020-03-02 | 2023-04-26 | シロナックス・リミテッド | フェロトーシス阻害剤ジアリールアミンパラアセトアミド類 |
CN111393435A (zh) * | 2020-03-16 | 2020-07-10 | 青岛吉澳医药科技有限公司 | 氮杂吲哚酰胺类化合物及其制备方法和用途 |
US11718622B2 (en) | 2020-03-16 | 2023-08-08 | Exelixis Inc. | Heterocyclic adenosine receptor antagonists |
WO2022016021A1 (en) | 2020-07-15 | 2022-01-20 | Third Harmonic Bio, Inc. | Crystalline forms of a selective c-kit kinase inhibitor |
US11760756B2 (en) | 2020-11-06 | 2023-09-19 | Incyte Corporation | Crystalline form of a PD-1/PD-L1 inhibitor |
WO2022099018A1 (en) | 2020-11-06 | 2022-05-12 | Incyte Corporation | Process of preparing a pd-1/pd-l1 inhibitor |
US11866434B2 (en) | 2020-11-06 | 2024-01-09 | Incyte Corporation | Process for making a PD-1/PD-L1 inhibitor and salts and crystalline forms thereof |
US11744823B2 (en) | 2020-11-19 | 2023-09-05 | Third Harmonic Bio, Inc. | Pharmaceutical compositions of a selective c-kit kinase inhibitor and methods for making and using same |
WO2022119899A1 (en) * | 2020-12-02 | 2022-06-09 | Shionogi & Co., Ltd. | A medicament for treating mycobacterial infection characterized by combining a cytochrome bc1 inhibitor with clarithromycin or azithromycin |
JP2024510478A (ja) | 2021-03-16 | 2024-03-07 | ヤンセン・サイエンシズ・アイルランド・アンリミテッド・カンパニー | 抗菌化合物 |
BR112023018654A2 (pt) | 2021-03-17 | 2023-10-03 | Janssen Sciences Ireland Unlimited Co | Compostos antibacterianos |
CA3211592A1 (en) | 2021-03-17 | 2022-09-22 | Jerome Emile Georges Guillemont | Antibacterial compounds |
WO2022214519A1 (en) | 2021-04-07 | 2022-10-13 | Janssen Sciences Ireland Unlimited Company | Antibacterial compounds |
WO2022214520A1 (en) | 2021-04-07 | 2022-10-13 | Janssen Sciences Ireland Unlimited Company | Antibacterial compounds |
TW202325274A (zh) | 2021-10-28 | 2023-07-01 | 愛爾蘭商健生科學愛爾蘭無限公司 | 抗菌化合物 |
WO2024089170A1 (en) | 2022-10-27 | 2024-05-02 | Janssen Sciences Ireland Unlimited Company | Antibacterial compounds |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE598759A (es) * | 1960-01-04 | |||
US3133076A (en) * | 1961-04-06 | 1964-05-12 | Simes | Phenyl-imidazo(1, 2-a)pyridine-6-car-boxylic acids and their esters |
US3105834A (en) * | 1961-10-11 | 1963-10-01 | Norwich Pharma Co | 2-(5-nitro-2-furyl)-imidazo [1, 2-alpha]-pyridine or-pyrimidine |
US6080767A (en) * | 1996-01-02 | 2000-06-27 | Aventis Pharmaceuticals Products Inc. | Substituted n-[(aminoiminomethyl or aminomethyl)phenyl]propyl amides |
HUP0203739A3 (en) * | 1999-10-08 | 2004-07-28 | Gruenenthal Gmbh | Bicyclic imidazo-3-yl-amine derivatives which are substituted on the sixth ring, process for their preparation and pharmaceutical compositions containing them |
AU2001264932A1 (en) * | 2000-05-26 | 2001-12-11 | Neurogen Corporation | Oxo-imidazopyrimidine-carboxamides and their use as gaba brain receptor ligands |
US7563788B2 (en) * | 2004-03-19 | 2009-07-21 | Pfizer Inc. | Substituted Imidazo[1,2-a]pyridines as Antibacterial Agents |
US20080234318A1 (en) | 2005-08-31 | 2008-09-25 | Kristjan Gudmundsson | Chemical Compounds |
WO2007034282A2 (en) * | 2005-09-19 | 2007-03-29 | Pfizer Products Inc. | Diaryl-imidazole compounds condensed with a heterocycle as c3a receptor antagonists |
WO2007034278A2 (en) * | 2005-09-19 | 2007-03-29 | Pfizer Products Inc. | Fused imidazole derivatives as c3a receptor antagonists |
MX2009006863A (es) * | 2006-12-20 | 2009-08-28 | Schering Corp | Inhibidores novedosos de c-jun-n-terminal cinasas. |
TW200901969A (en) * | 2007-06-06 | 2009-01-16 | Smithkline Beecham Corp | Chemical compounds |
JP5412429B2 (ja) * | 2007-07-23 | 2014-02-12 | クレストーン・インコーポレーテッド | 抗細菌性アミド及びスルホンアミド置換複素環式尿素化合物 |
CN103983627A (zh) | 2008-06-17 | 2014-08-13 | 韩国巴斯德研究所 | 作为抗结核病药的吡啶并嘧啶化合物 |
WO2011050245A1 (en) | 2009-10-23 | 2011-04-28 | Yangbo Feng | Bicyclic heteroaryls as kinase inhibitors |
US9309238B2 (en) | 2009-11-05 | 2016-04-12 | University Of Notre Dame Du Lac | Imidazo [1,2-a]pyridine compounds, synthesis thereof, and methods of using same |
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HK1180683A1 (zh) | 2013-10-25 |
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CA2793086C (en) | 2018-08-21 |
MX2012010671A (es) | 2013-04-03 |
SG184073A1 (en) | 2012-10-30 |
AU2011229423A1 (en) | 2012-09-27 |
JP5944837B2 (ja) | 2016-07-05 |
SG10201502109VA (en) | 2015-05-28 |
IL221940A (en) | 2017-03-30 |
AU2011229423B2 (en) | 2015-12-10 |
WO2011113606A1 (en) | 2011-09-22 |
WO2011113606A8 (en) | 2012-10-26 |
CN102869661A (zh) | 2013-01-09 |
KR20130028723A (ko) | 2013-03-19 |
RU2576662C2 (ru) | 2016-03-10 |
CN102869661B (zh) | 2015-08-05 |
RU2012144317A (ru) | 2014-04-27 |
KR101732212B1 (ko) | 2017-05-02 |
ZA201206814B (en) | 2016-03-30 |
US20130065884A1 (en) | 2013-03-14 |
CA2793086A1 (en) | 2011-09-22 |
MX345762B (es) | 2017-02-15 |
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