JP5486602B2 - ベンゾオキサゾール化合物および使用方法 - Google Patents
ベンゾオキサゾール化合物および使用方法 Download PDFInfo
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- JP5486602B2 JP5486602B2 JP2011529267A JP2011529267A JP5486602B2 JP 5486602 B2 JP5486602 B2 JP 5486602B2 JP 2011529267 A JP2011529267 A JP 2011529267A JP 2011529267 A JP2011529267 A JP 2011529267A JP 5486602 B2 JP5486602 B2 JP 5486602B2
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- YMYJXFUPMPMETB-UHFFFAOYSA-N C(CN1CCCC1)COc(cc1)ccc1-c([o]c1c2)nc1ccc2OCCCN1CCCC1 Chemical compound C(CN1CCCC1)COc(cc1)ccc1-c([o]c1c2)nc1ccc2OCCCN1CCCC1 YMYJXFUPMPMETB-UHFFFAOYSA-N 0.000 description 2
- 0 COC[C@@](CCC*)*CCCOc(cc1)ccc1-c([o]c1c2)nc1ccc2OCCCN1[C@](COC)CCC1 Chemical compound COC[C@@](CCC*)*CCCOc(cc1)ccc1-c([o]c1c2)nc1ccc2OCCCN1[C@](COC)CCC1 0.000 description 2
- MUUCWDTTXKQBAS-UHFFFAOYSA-N C(CN1CCCCC1)COc(cc1)ccc1-c([o]c1c2)nc1ccc2OCCCN1CCCCC1 Chemical compound C(CN1CCCCC1)COc(cc1)ccc1-c([o]c1c2)nc1ccc2OCCCN1CCCCC1 MUUCWDTTXKQBAS-UHFFFAOYSA-N 0.000 description 1
- JTPXFCYNDOCNSF-ACHIHNKUSA-N C(CN1[C@H](CN2CCCC2)CCC1)COc(cc1)ccc1-c([o]c1c2)nc1ccc2OCCCN1[C@H](CN2CCCC2)CCC1 Chemical compound C(CN1[C@H](CN2CCCC2)CCC1)COc(cc1)ccc1-c([o]c1c2)nc1ccc2OCCCN1[C@H](CN2CCCC2)CCC1 JTPXFCYNDOCNSF-ACHIHNKUSA-N 0.000 description 1
- SFVCPRVZRHWJGV-UHFFFAOYSA-N CCN(CC)CCN(CC)CCCOc(cc1)ccc1-c1nc(ccc(OCCCN(CC)CCN(CC)CC)c2)c2[o]1 Chemical compound CCN(CC)CCN(CC)CCCOc(cc1)ccc1-c1nc(ccc(OCCCN(CC)CCN(CC)CC)c2)c2[o]1 SFVCPRVZRHWJGV-UHFFFAOYSA-N 0.000 description 1
- BIDBFQXZGCIIQQ-UHFFFAOYSA-N CN(C)CCCCCOc(cc1)ccc1-c([o]c1c2)nc1ccc2OCCCCCN(C)C Chemical compound CN(C)CCCCCOc(cc1)ccc1-c([o]c1c2)nc1ccc2OCCCCCN(C)C BIDBFQXZGCIIQQ-UHFFFAOYSA-N 0.000 description 1
- DEFSKWIBKOCUKR-UHFFFAOYSA-N CN(C)CCCN(C)CCCOc(cc1)ccc1-c([o]c1c2)cc1ccc2OCCCN(C)CCCN(C)C Chemical compound CN(C)CCCN(C)CCCOc(cc1)ccc1-c([o]c1c2)cc1ccc2OCCCN(C)CCCN(C)C DEFSKWIBKOCUKR-UHFFFAOYSA-N 0.000 description 1
- ROIKYKIZDHXPGX-UHFFFAOYSA-N CN(C)CCCOc(cc1)cc2c1nc(-c(cccc1)c1OCCCN(C)C)[o]2 Chemical compound CN(C)CCCOc(cc1)cc2c1nc(-c(cccc1)c1OCCCN(C)C)[o]2 ROIKYKIZDHXPGX-UHFFFAOYSA-N 0.000 description 1
- JZXYRPJTHFGAIU-UHFFFAOYSA-N CN(C)CCCOc(cc1)cc2c1nc(-c1cc(OCCCN(C)C)ccc1)[o]2 Chemical compound CN(C)CCCOc(cc1)cc2c1nc(-c1cc(OCCCN(C)C)ccc1)[o]2 JZXYRPJTHFGAIU-UHFFFAOYSA-N 0.000 description 1
- YUNCYHZBORLEBP-UHFFFAOYSA-N CN(C)CCN(C)CCCOc(cc1)ccc1-c([o]c1c2)nc1ccc2OCCCN(C)CCN(C)C Chemical compound CN(C)CCN(C)CCCOc(cc1)ccc1-c([o]c1c2)nc1ccc2OCCCN(C)CCN(C)C YUNCYHZBORLEBP-UHFFFAOYSA-N 0.000 description 1
- KGHFPRIULSDOQM-UHFFFAOYSA-N COCCNCCCOc(cc1)ccc1-c([o]c1c2)nc1ccc2OCCCNCCOC Chemical compound COCCNCCCOc(cc1)ccc1-c([o]c1c2)nc1ccc2OCCCNCCOC KGHFPRIULSDOQM-UHFFFAOYSA-N 0.000 description 1
- LFPGDMCKWMNOOV-CLJLJLNGSA-N COC[C@@H]1N(CCCOc(cc2)ccc2-c([o]c2c3)nc2ccc3OCCCN2[C@@H](COC)CCC2)CCC1 Chemical compound COC[C@@H]1N(CCCOc(cc2)ccc2-c([o]c2c3)nc2ccc3OCCCN2[C@@H](COC)CCC2)CCC1 LFPGDMCKWMNOOV-CLJLJLNGSA-N 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/52—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings condensed with carbocyclic rings or ring systems
- C07D263/54—Benzoxazoles; Hydrogenated benzoxazoles
- C07D263/56—Benzoxazoles; Hydrogenated benzoxazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- 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]
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- 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
- C07D413/12—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 chain containing hetero atoms as chain links
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Rheumatology (AREA)
- Immunology (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Communicable Diseases (AREA)
- Neurosurgery (AREA)
- Pain & Pain Management (AREA)
- Oncology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Dermatology (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)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10067808P | 2008-09-26 | 2008-09-26 | |
| US61/100,678 | 2008-09-26 | ||
| PCT/US2009/058398 WO2010036905A1 (en) | 2008-09-26 | 2009-09-25 | Benzoxazole compounds and methods of use |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2012504133A JP2012504133A (ja) | 2012-02-16 |
| JP2012504133A5 JP2012504133A5 (enExample) | 2012-11-01 |
| JP5486602B2 true JP5486602B2 (ja) | 2014-05-07 |
Family
ID=41203923
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011529267A Active JP5486602B2 (ja) | 2008-09-26 | 2009-09-25 | ベンゾオキサゾール化合物および使用方法 |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US8354400B2 (enExample) |
| EP (1) | EP2350032B1 (enExample) |
| JP (1) | JP5486602B2 (enExample) |
| WO (1) | WO2010036905A1 (enExample) |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3072891A1 (en) | 2015-03-24 | 2016-09-28 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | New Toll-Like Receptor 9 Antagonists |
| US10071079B2 (en) | 2016-06-29 | 2018-09-11 | Bristol-Myers Squibb Company | [1,2,4]triazolo[1,5-a]pyridinyl substituted indole compounds |
| MX391344B (es) | 2016-07-30 | 2025-03-21 | Bristol Myers Squibb Co | Compuestos indol sustituidos con dimetoxifenilo como inhibidores de receptores tipo toll 7, 8 o 9 (tlr7, tlr8 o tlr9). |
| KR102519535B1 (ko) | 2016-09-09 | 2023-04-06 | 브리스톨-마이어스 스큅 컴퍼니 | 피리딜 치환된 인돌 화합물 |
| CN110997656B (zh) | 2017-08-04 | 2023-04-14 | 百时美施贵宝公司 | 用作tlr7/8/9抑制剂的取代的吲哚化合物 |
| ES2921020T3 (es) | 2017-08-04 | 2022-08-16 | Bristol Myers Squibb Co | Compuestos de indol sustituidos con [1,2,4]triazolo[4,3-a]piridinilo |
| CN111448190B (zh) | 2017-11-14 | 2023-09-26 | 百时美施贵宝公司 | 取代的吲哚化合物 |
| CN107759532B (zh) * | 2017-11-23 | 2021-02-12 | 苏州大学 | 一种苯并噁唑-2-乙基肟衍生物、其制备方法及应用 |
| BR112020011668A2 (pt) | 2017-12-15 | 2020-11-17 | Bristol-Myers Squibb Company | compostos de éter de indol substituído |
| FI3728252T3 (fi) | 2017-12-18 | 2023-10-18 | Bristol Myers Squibb Co | 4-atsaindoliyhdisteitä |
| BR112020012084A2 (pt) * | 2017-12-19 | 2020-11-24 | Bristol-Myers Squibb Company | compostos de indol substituído úteis como inibidores de tlr |
| WO2019126082A1 (en) | 2017-12-19 | 2019-06-27 | Bristol-Myers Squibb Company | 6-azaindole compounds |
| JP7313354B2 (ja) * | 2017-12-19 | 2023-07-24 | ブリストル-マイヤーズ スクイブ カンパニー | Tlr阻害剤として有用なアミド置換されたインドール化合物 |
| CA3085942A1 (en) | 2017-12-20 | 2019-06-27 | Bristol-Myers Squibb Company | Aryl and heteroaryl substituted indole compounds |
| BR112020011984A2 (pt) | 2017-12-20 | 2020-11-17 | Bristol-Myers Squibb Company | compostos de amino indol úteis como inibidores de tlr |
| US11299501B2 (en) | 2017-12-20 | 2022-04-12 | Bristol-Myers Squibb Company | Diazaindole compounds |
| ES2963696T3 (es) | 2018-10-24 | 2024-04-01 | Bristol Myers Squibb Co | Compuestos diméricos de indol sustituidos |
| CN112955450A (zh) | 2018-10-24 | 2021-06-11 | 百时美施贵宝公司 | 经取代的吲哚和吲唑化合物 |
| US11807622B2 (en) | 2019-01-30 | 2023-11-07 | Insilico Medicine Ip Limited | TLR 9 inhibitors |
| EP3965888B1 (en) | 2019-05-09 | 2024-08-21 | Bristol-Myers Squibb Company | Substituted benzimidazolone compounds |
| WO2021067326A1 (en) | 2019-10-01 | 2021-04-08 | Bristol-Myers Squibb Company | Substituted bicyclic heteroaryl compounds |
| CN114829350B (zh) | 2019-10-04 | 2024-05-28 | 百时美施贵宝公司 | 经取代的咔唑化合物 |
| KR20230171469A (ko) | 2021-04-16 | 2023-12-20 | 길리애드 사이언시즈, 인코포레이티드 | 티에노피롤 화합물 |
| EP4398989A1 (en) | 2021-09-10 | 2024-07-17 | Gilead Sciences, Inc. | Thienopyrrole compounds |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002051821A1 (en) | 2000-12-22 | 2002-07-04 | Astrazeneca Ab | Therapeutic compounds |
| DE10134775A1 (de) * | 2001-07-06 | 2003-01-30 | Schering Ag | 1-Alkyl-2.aryl-benzimidazolderivate, deren Verwendung zur Herstellung von Arzneimitteln sowie diese Derivate enthaltende pharmazeutische Präparate |
| UA83620C2 (ru) | 2001-12-05 | 2008-08-11 | Уайт | Замещенные бензоксазолы и их аналоги как эстрогенные агенты |
| RU2006110561A (ru) | 2003-09-30 | 2007-10-10 | Янссен Фармацевтика Н.В. (Be) | Соединения бензоимидазола |
| EP1781628A2 (en) | 2004-08-26 | 2007-05-09 | Wyeth a Corporation of the State of Delaware | Prodrug substituted benzoxazoles as estrogenic agents |
| CN101351458A (zh) | 2005-12-01 | 2009-01-21 | 匹兹堡大学 | 作为促淀粉样变蛋白成像剂的同位素标记的苯并噻唑化合物 |
-
2009
- 2009-09-25 US US13/121,012 patent/US8354400B2/en active Active
- 2009-09-25 JP JP2011529267A patent/JP5486602B2/ja active Active
- 2009-09-25 EP EP09793015.0A patent/EP2350032B1/en active Active
- 2009-09-25 WO PCT/US2009/058398 patent/WO2010036905A1/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| US20110183967A1 (en) | 2011-07-28 |
| US8354400B2 (en) | 2013-01-15 |
| JP2012504133A (ja) | 2012-02-16 |
| EP2350032A1 (en) | 2011-08-03 |
| EP2350032B1 (en) | 2016-05-25 |
| WO2010036905A1 (en) | 2010-04-01 |
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