CN102164902B - 作为吲哚胺2,3-双加氧酶的抑制剂的1,2,5-噁二唑 - Google Patents
作为吲哚胺2,3-双加氧酶的抑制剂的1,2,5-噁二唑 Download PDFInfo
- Publication number
- CN102164902B CN102164902B CN200980134351.9A CN200980134351A CN102164902B CN 102164902 B CN102164902 B CN 102164902B CN 200980134351 A CN200980134351 A CN 200980134351A CN 102164902 B CN102164902 B CN 102164902B
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- Prior art keywords
- amino
- compound
- formula
- oxadiazol
- hydroxyl
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- 0 C*(C*(C)Nc1n[o]nc1C(Nc1ccc(*)c(*)c1)=N)CNS(*)(=O)=O Chemical compound C*(C*(C)Nc1n[o]nc1C(Nc1ccc(*)c(*)c1)=N)CNS(*)(=O)=O 0.000 description 5
- GEIBPCGRQDDQIL-UHFFFAOYSA-N Bc1cc(NC(c2[nH+][O-]nc2NCCCNS(N)(=O)=O)=N)ccc1F Chemical compound Bc1cc(NC(c2[nH+][O-]nc2NCCCNS(N)(=O)=O)=N)ccc1F GEIBPCGRQDDQIL-UHFFFAOYSA-N 0.000 description 1
- GTBRSAGWQONNHB-UHFFFAOYSA-N CCC(CO1)=C(c2n[o]nc2N)N(c(cc2[Br]=C)ccc2F)C1=O Chemical compound CCC(CO1)=C(c2n[o]nc2N)N(c(cc2[Br]=C)ccc2F)C1=O GTBRSAGWQONNHB-UHFFFAOYSA-N 0.000 description 1
- CCAWBVLOBBODJJ-UHFFFAOYSA-N COCCNc1n[o]nc1/C(/Nc(cc1[Br]=C)ccc1F)=N/O Chemical compound COCCNc1n[o]nc1/C(/Nc(cc1[Br]=C)ccc1F)=N/O CCAWBVLOBBODJJ-UHFFFAOYSA-N 0.000 description 1
- YSHMAIJLHYKYRI-UHFFFAOYSA-N COCCNc1n[o]nc1C(Cl)=N Chemical compound COCCNc1n[o]nc1C(Cl)=N YSHMAIJLHYKYRI-UHFFFAOYSA-N 0.000 description 1
- XBMQLVNSZCCEBK-UHFFFAOYSA-N COCCNc1n[o]nc1C(NCc1cc(Br)c[o]1)=N Chemical compound COCCNc1n[o]nc1C(NCc1cc(Br)c[o]1)=N XBMQLVNSZCCEBK-UHFFFAOYSA-N 0.000 description 1
- BRMQXHBGKGGEIA-UHFFFAOYSA-N NCc1cc(Cl)c[o]1 Chemical compound NCc1cc(Cl)c[o]1 BRMQXHBGKGGEIA-UHFFFAOYSA-N 0.000 description 1
- KSPQRCXTMVWZFF-UHFFFAOYSA-N Nc1n[o]nc1C(N1c2cc(C(F)(F)F)ccc2)=NOC1=O Chemical compound Nc1n[o]nc1C(N1c2cc(C(F)(F)F)ccc2)=NOC1=O KSPQRCXTMVWZFF-UHFFFAOYSA-N 0.000 description 1
- INPRBMPXWJHPJB-UHFFFAOYSA-N O=C(C(F)(F)F)Nc1n[o]nc1C1=NOC2OC2N1c1cc(C(F)(F)F)ccc1 Chemical compound O=C(C(F)(F)F)Nc1n[o]nc1C1=NOC2OC2N1c1cc(C(F)(F)F)ccc1 INPRBMPXWJHPJB-UHFFFAOYSA-N 0.000 description 1
- YOJWJBSELPLSAP-UHFFFAOYSA-N OCCCNc1n[o]nc1C(N1c(cc2C(F)(F)F)ccc2F)=NOC1=O Chemical compound OCCCNc1n[o]nc1C(N1c(cc2C(F)(F)F)ccc2F)=NOC1=O YOJWJBSELPLSAP-UHFFFAOYSA-N 0.000 description 1
Classifications
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- 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
- A61K31/4245—Oxadiazoles
-
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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- A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
- A61K39/39533—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals
- A61K39/3955—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals against proteinaceous materials, e.g. enzymes, hormones, lymphokines
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- C07D271/02—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
- C07D271/08—1,2,5-Oxadiazoles; Hydrogenated 1,2,5-oxadiazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/04—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
-
- 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
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- 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
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
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- Engineering & Computer Science (AREA)
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- Immunology (AREA)
- Epidemiology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Oncology (AREA)
- Virology (AREA)
- Psychiatry (AREA)
- Communicable Diseases (AREA)
- Pain & Pain Management (AREA)
- Ophthalmology & Optometry (AREA)
- Dermatology (AREA)
- Mycology (AREA)
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- Molecular Biology (AREA)
- Physical Education & Sports Medicine (AREA)
- AIDS & HIV (AREA)
- Pulmonology (AREA)
- Transplantation (AREA)
- Hospice & Palliative Care (AREA)
- Hematology (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201410287499.9A CN104042611B (zh) | 2008-07-08 | 2009-07-07 | 作为吲哚胺2,3-双加氧酶的抑制剂的1,2,5-噁二唑 |
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US7887608P | 2008-07-08 | 2008-07-08 | |
| US61/078876 | 2008-07-08 | ||
| US61/078,876 | 2008-07-08 | ||
| US15087309P | 2009-02-09 | 2009-02-09 | |
| US61/150,873 | 2009-02-09 | ||
| US61/150873 | 2009-02-09 | ||
| PCT/US2009/049794 WO2010005958A2 (en) | 2008-07-08 | 2009-07-07 | 1,2,5-oxadiazoles as inhibitors of indoleamine 2,3-dioxygenase |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201410287499.9A Division CN104042611B (zh) | 2008-07-08 | 2009-07-07 | 作为吲哚胺2,3-双加氧酶的抑制剂的1,2,5-噁二唑 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN102164902A CN102164902A (zh) | 2011-08-24 |
| CN102164902B true CN102164902B (zh) | 2014-07-23 |
Family
ID=41128289
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN200980134351.9A Expired - Fee Related CN102164902B (zh) | 2008-07-08 | 2009-07-07 | 作为吲哚胺2,3-双加氧酶的抑制剂的1,2,5-噁二唑 |
| CN201410287499.9A Expired - Fee Related CN104042611B (zh) | 2008-07-08 | 2009-07-07 | 作为吲哚胺2,3-双加氧酶的抑制剂的1,2,5-噁二唑 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201410287499.9A Expired - Fee Related CN104042611B (zh) | 2008-07-08 | 2009-07-07 | 作为吲哚胺2,3-双加氧酶的抑制剂的1,2,5-噁二唑 |
Country Status (36)
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI651311B (zh) | 2013-11-08 | 2019-02-21 | 英塞特控股公司 | 用於合成吲哚胺2,3-雙加氧酶抑制劑之方法 |
| CN104042611B (zh) * | 2008-07-08 | 2019-05-14 | 因塞特控股公司 | 作为吲哚胺2,3-双加氧酶的抑制剂的1,2,5-噁二唑 |
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| DK1879573T3 (da) | 2005-05-10 | 2013-02-25 | Incyte Corp | Modulatorer af indolamin 2,3-dioxygenase og fremgangsmåder til anvendelse deraf |
| ES2540561T3 (es) | 2005-12-20 | 2015-07-10 | Incyte Corporation | N-hidroxiamidinoheterociclos como moduladores de indolamina 2,3-dioxigenasa |
| CL2007002650A1 (es) | 2006-09-19 | 2008-02-08 | Incyte Corp | Compuestos derivados de heterociclo n-hidroxiamino; composicion farmaceutica, util para tratar cancer, infecciones virales y desordenes neurodegenerativos entre otras. |
| CA2663057C (en) * | 2006-09-19 | 2015-12-08 | Incyte Corporation | N-hydroxyamidinoheterocycles as modulators of indoleamine 2,3-dioxygenase |
| US8299295B2 (en) | 2009-10-15 | 2012-10-30 | Johnson Matthey Public Limited Company | Polymorphs of bromfenac sodium and methods for preparing bromfenac sodium polymorphs |
| GB0919757D0 (en) * | 2009-11-12 | 2009-12-30 | Johnson Matthey Plc | Polymorphs of bromfenac sodium and methods for preparing bromfenac sodium polymorphs |
| NO2694640T3 (enExample) | 2011-04-15 | 2018-03-17 | ||
| ES2903205T3 (es) * | 2011-11-09 | 2022-03-31 | Kyowa Kirin Co Ltd | Compuestos heterocíclicos que contienen nitrógeno |
| GB201120860D0 (en) | 2011-12-05 | 2012-01-18 | Cambridge Entpr Ltd | Cancer immunotherapy |
| US20150182490A1 (en) | 2012-06-26 | 2015-07-02 | Del Mar Pharmaceuticals | Methods for treating tyrosine-kinase-inhibitor-resistant malignancies in patients with genetic polymorphisms or ahi1 dysregulations or mutations employing dianhydrogalactitol, diacetyldianhydrogalactitol, dibromodulcitol, or analogs or derivatives thereof |
| CA2889182A1 (en) | 2012-10-26 | 2014-05-01 | The University Of Chicago | Synergistic combination of immunologic inhibitors for the treatment of cancer |
| CN105492011A (zh) | 2013-04-08 | 2016-04-13 | 丹尼斯·M·布朗 | 不理想给药化学化合物的治疗增效 |
| PH12020550847A1 (en) * | 2014-02-04 | 2022-05-11 | Incyte Corp | Combination of a pd-1 antagonist and an ido1 inhibitor for treating cancer |
| KR20160146747A (ko) | 2014-03-31 | 2016-12-21 | 제넨테크, 인크. | 항혈관신생제 및 ox40 결합 효능제를 포함하는 조합 요법 |
| SG11201607969XA (en) | 2014-03-31 | 2016-10-28 | Genentech Inc | Anti-ox40 antibodies and methods of use |
| LT3148579T (lt) | 2014-05-28 | 2021-05-25 | Agenus Inc. | Anti-gitr antikūnai ir jų panaudojimo būdai |
| JP2017525753A (ja) | 2014-06-06 | 2017-09-07 | フレクサス・バイオサイエンシーズ・インコーポレイテッドFlexus Biosciences, Inc. | 免疫調節剤 |
| MX372995B (es) * | 2014-07-17 | 2020-04-13 | Chdi Foundation Inc | Metodos y composiciones para el tratamiento de trastornos relacionados con vih. |
| CN105481789B (zh) * | 2014-09-15 | 2020-05-19 | 中国科学院上海有机化学研究所 | 一种吲哚胺-2,3-双加氧酶抑制剂及其制备方法 |
| UY36390A (es) | 2014-11-05 | 2016-06-01 | Flexus Biosciences Inc | Compuestos moduladores de la enzima indolamina 2,3-dioxigenasa (ido), sus métodos de síntesis y composiciones farmacéuticas que los contienen |
| AR102537A1 (es) | 2014-11-05 | 2017-03-08 | Flexus Biosciences Inc | Agentes inmunomoduladores |
| EA201790806A1 (ru) | 2014-11-05 | 2017-11-30 | Флексус Байосайенсиз, Инк. | Иммунорегулирующие средства |
| WO2016100851A1 (en) | 2014-12-18 | 2016-06-23 | Lankenau Institute For Medical Research | Methods and compositions for the treatment of retinopathy and other ocular diseases |
| WO2016123573A1 (en) | 2015-01-30 | 2016-08-04 | President And Fellows Of Harvard College | Peritumoral and intratumoral materials for cancer therapy |
| SG11201606876RA (en) | 2015-03-04 | 2016-10-28 | Gilead Sciences Inc | Toll like receptor modulator compounds |
| BR112017019699A2 (pt) * | 2015-03-17 | 2018-09-04 | Pfizer Inc. | derivados substituídos por 3-indol, composições farmacêuticas e métodos para uso |
| WO2016155545A1 (zh) * | 2015-03-31 | 2016-10-06 | 江苏恒瑞医药股份有限公司 | 含氨磺酰基的1,2,5-噁二唑类衍生物、其制备方法及其在医药上的应用 |
| MX2017012805A (es) | 2015-04-07 | 2018-04-11 | Genentech Inc | Complejo de unión a antígenos con actividad agonista y métodos de uso. |
| CN106715440B (zh) | 2015-04-21 | 2019-02-22 | 江苏恒瑞医药股份有限公司 | 咪唑并异吲哚类衍生物、其制备方法及其在医药上的应用 |
| DK3303394T3 (da) | 2015-05-29 | 2020-07-06 | Agenus Inc | Anti-ctla-4-antistoffer og fremgangsmåder til anvendelse deraf |
| US9891882B2 (en) * | 2015-06-01 | 2018-02-13 | Nagravision S.A. | Methods and systems for conveying encrypted data to a communication device |
| EP3303397A1 (en) | 2015-06-08 | 2018-04-11 | H. Hoffnabb-La Roche Ag | Methods of treating cancer using anti-ox40 antibodies and pd-1 axis binding antagonists |
| AU2016274585A1 (en) | 2015-06-08 | 2017-12-14 | Genentech, Inc. | Methods of treating cancer using anti-OX40 antibodies |
| WO2017002078A1 (en) | 2015-07-02 | 2017-01-05 | Glaxosmithkline Intellectual Property Development Limited | Inhibitors of indoleamine 2,3-dioxygenase |
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Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104042611B (zh) * | 2008-07-08 | 2019-05-14 | 因塞特控股公司 | 作为吲哚胺2,3-双加氧酶的抑制剂的1,2,5-噁二唑 |
| TWI651311B (zh) | 2013-11-08 | 2019-02-21 | 英塞特控股公司 | 用於合成吲哚胺2,3-雙加氧酶抑制劑之方法 |
| TWI696618B (zh) | 2013-11-08 | 2020-06-21 | 美商英塞特控股公司 | 用於合成吲哚胺2,3-雙加氧酶抑制劑之方法 |
| TWI775079B (zh) | 2013-11-08 | 2022-08-21 | 美商英塞特控股公司 | 用於合成吲哚胺2,3-雙加氧酶抑制劑之方法 |
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