KR102329062B1 - Nlrp3 조정제로서의 치환된 이미다조-퀴놀린 - Google Patents
Nlrp3 조정제로서의 치환된 이미다조-퀴놀린 Download PDFInfo
- Publication number
- KR102329062B1 KR102329062B1 KR1020197026922A KR20197026922A KR102329062B1 KR 102329062 B1 KR102329062 B1 KR 102329062B1 KR 1020197026922 A KR1020197026922 A KR 1020197026922A KR 20197026922 A KR20197026922 A KR 20197026922A KR 102329062 B1 KR102329062 B1 KR 102329062B1
- Authority
- KR
- South Korea
- Prior art keywords
- cancer
- optionally substituted
- independently selected
- alkyl
- ring atoms
- 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
- 0 CCN(Cc1nc(cnc2c3ccc(Br)c2)c3[n]1*)C(OC(C)(C)C)=O Chemical compound CCN(Cc1nc(cnc2c3ccc(Br)c2)c3[n]1*)C(OC(C)(C)C)=O 0.000 description 3
- LBNGSUIDEKJIHE-UHFFFAOYSA-N COc1ccc(CNc(c(ccc(Br)c2)c2nc2)c2N)cc1 Chemical compound COc1ccc(CNc(c(ccc(Br)c2)c2nc2)c2N)cc1 LBNGSUIDEKJIHE-UHFFFAOYSA-N 0.000 description 3
- CMIZRIHEZIDQQR-UHFFFAOYSA-N CC(c1nc(c(N)nc2c3ccc(-[n](cc4)nc4-c4cccc(C(C5)CN(Cc6nc(c(N)nc7c8ccc(-[n]9nccc9)c7)c8[nH]6)C5=O)c4)c2)c3[nH]1)N(CCC1)C1=O Chemical compound CC(c1nc(c(N)nc2c3ccc(-[n](cc4)nc4-c4cccc(C(C5)CN(Cc6nc(c(N)nc7c8ccc(-[n]9nccc9)c7)c8[nH]6)C5=O)c4)c2)c3[nH]1)N(CCC1)C1=O CMIZRIHEZIDQQR-UHFFFAOYSA-N 0.000 description 1
- NHVBBCSWTMFGKS-UHFFFAOYSA-N CCN(CC(Nc(cnc1c2ccc(Br)c1)c2NCc(cc1)ccc1OC)=O)C(OC(C)(C)C)=O Chemical compound CCN(CC(Nc(cnc1c2ccc(Br)c1)c2NCc(cc1)ccc1OC)=O)C(OC(C)(C)C)=O NHVBBCSWTMFGKS-UHFFFAOYSA-N 0.000 description 1
- RQBGAKPSPNRXME-UHFFFAOYSA-N CCN(Cc1nc(c(N)nc2c3ccc(-c4n[nH]cc4)c2)c3[nH]1)C(CC(C)(C)O)=O Chemical compound CCN(Cc1nc(c(N)nc2c3ccc(-c4n[nH]cc4)c2)c3[nH]1)C(CC(C)(C)O)=O RQBGAKPSPNRXME-UHFFFAOYSA-N 0.000 description 1
- HFOYWBJEBIHIKY-UHFFFAOYSA-N CCNC(N(CC)Cc1nc(c(N)nc2c3ccc(-c4n[nH]cc4)c2)c3[nH]1)=O Chemical compound CCNC(N(CC)Cc1nc(c(N)nc2c3ccc(-c4n[nH]cc4)c2)c3[nH]1)=O HFOYWBJEBIHIKY-UHFFFAOYSA-N 0.000 description 1
- BCHBBTXLYOTBSO-UHFFFAOYSA-N CCNCc1nc(c(N)nc2c3ccc(-c4n[nH]cc4)c2)c3[nH]1 Chemical compound CCNCc1nc(c(N)nc2c3ccc(-c4n[nH]cc4)c2)c3[nH]1 BCHBBTXLYOTBSO-UHFFFAOYSA-N 0.000 description 1
- GMEIICVBNRVSCK-UHFFFAOYSA-N CCNc(c(ccc(Br)c1)c1nc1)c1[N+]([O-])=O Chemical compound CCNc(c(ccc(Br)c1)c1nc1)c1[N+]([O-])=O GMEIICVBNRVSCK-UHFFFAOYSA-N 0.000 description 1
- UJALIOOXECLGCE-UHFFFAOYSA-N CC[n]1c(c(ccc(-c2ccn[nH]2)c2)c2nc2N)c2nc1CN(CCC1)C1=O Chemical compound CC[n]1c(c(ccc(-c2ccn[nH]2)c2)c2nc2N)c2nc1CN(CCC1)C1=O UJALIOOXECLGCE-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N CN(CCC1)C1=O Chemical compound CN(CCC1)C1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- QWGYOJNUAVBJQG-UHFFFAOYSA-N CN(CCN1Cc2nc(c(N)nc3c4ccc(-c5n[nH]cc5)c3)c4[nH]2)C1=O Chemical compound CN(CCN1Cc2nc(c(N)nc3c4ccc(-c5n[nH]cc5)c3)c4[nH]2)C1=O QWGYOJNUAVBJQG-UHFFFAOYSA-N 0.000 description 1
- TZTSHNQAPSVLFP-UHFFFAOYSA-N CN1c2cnc(cc(cc3)Br)c3c2N(Cc(cc2)ccc2OC)C1CN(CCC1)C1=O Chemical compound CN1c2cnc(cc(cc3)Br)c3c2N(Cc(cc2)ccc2OC)C1CN(CCC1)C1=O TZTSHNQAPSVLFP-UHFFFAOYSA-N 0.000 description 1
- KLCKUDQXMFLINZ-UHFFFAOYSA-N COC(CCC[n]1c(c(ccc(-c2cccnc2)c2)c2nc2N)c2nc1CN(CCC1)C1=O)=O Chemical compound COC(CCC[n]1c(c(ccc(-c2cccnc2)c2)c2nc2N)c2nc1CN(CCC1)C1=O)=O KLCKUDQXMFLINZ-UHFFFAOYSA-N 0.000 description 1
- ZZBGCQGOYPTFOD-UHFFFAOYSA-N COc1ccc(CNc(c(ccc(Br)c2)c2nc2)c2NC(CN(CCC2)C2=O)=O)cc1 Chemical compound COc1ccc(CNc(c(ccc(Br)c2)c2nc2)c2NC(CN(CCC2)C2=O)=O)cc1 ZZBGCQGOYPTFOD-UHFFFAOYSA-N 0.000 description 1
- WFCFWWVGJPUYSB-UHFFFAOYSA-N COc1ccc(C[n]2c(c(ccc(-c3ccc[s]3)c3)c3nc3N)c3nc2CN(CCC2)C2=O)cc1 Chemical compound COc1ccc(C[n]2c(c(ccc(-c3ccc[s]3)c3)c3nc3N)c3nc2CN(CCC2)C2=O)cc1 WFCFWWVGJPUYSB-UHFFFAOYSA-N 0.000 description 1
- CMPZZWILVOFBAI-UHFFFAOYSA-N COc1ccc(C[n]2c(c(ccc(Br)c3)c3nc3)c3nc2CN(CCC2)C2=O)cc1 Chemical compound COc1ccc(C[n]2c(c(ccc(Br)c3)c3nc3)c3nc2CN(CCC2)C2=O)cc1 CMPZZWILVOFBAI-UHFFFAOYSA-N 0.000 description 1
- CIMKJBCYDRWELN-UHFFFAOYSA-N COc1ccc(C[n]2c3c(ccc(Br)c4)c4nc(N)c3nc2CN(CCC2)C2=O)cc1 Chemical compound COc1ccc(C[n]2c3c(ccc(Br)c4)c4nc(N)c3nc2CN(CCC2)C2=O)cc1 CIMKJBCYDRWELN-UHFFFAOYSA-N 0.000 description 1
- PRKFXZLNYSLGFM-UHFFFAOYSA-N Cc(cc1)n[n]1-c(cc1)cc(nc2N)c1c1c2nc(CN(CCC2)C2=O)[nH]1 Chemical compound Cc(cc1)n[n]1-c(cc1)cc(nc2N)c1c1c2nc(CN(CCC2)C2=O)[nH]1 PRKFXZLNYSLGFM-UHFFFAOYSA-N 0.000 description 1
- NKXLFIRVAWTULK-UHFFFAOYSA-N Cc1ccccc1-c(cc1)cc(nc2N)c1c1c2nc(CN(CCC2)C2=O)[nH]1 Chemical compound Cc1ccccc1-c(cc1)cc(nc2N)c1c1c2nc(CN(CCC2)C2=O)[nH]1 NKXLFIRVAWTULK-UHFFFAOYSA-N 0.000 description 1
- GXLILILGCUMCCT-UHFFFAOYSA-N Nc1nc(cc(C2CCCCC2)cc2)c2c2c1nc(CN(CCC1)C1=O)[nH]2 Chemical compound Nc1nc(cc(C2CCCCC2)cc2)c2c2c1nc(CN(CCC1)C1=O)[nH]2 GXLILILGCUMCCT-UHFFFAOYSA-N 0.000 description 1
- MAYUQEFJDWXDJY-UHFFFAOYSA-N Nc1nc(cc(C2CCCCCC2)cc2)c2c2c1nc(CN(CCC1)C1=O)[nH]2 Chemical compound Nc1nc(cc(C2CCCCCC2)cc2)c2c2c1nc(CN(CCC1)C1=O)[nH]2 MAYUQEFJDWXDJY-UHFFFAOYSA-N 0.000 description 1
- CUGJDYZZSOKNFX-UHFFFAOYSA-N Nc1nc(cc(cc2)-c(cccc3)c3Cl)c2c2c1nc(CN(CCC1)C1=O)[nH]2 Chemical compound Nc1nc(cc(cc2)-c(cccc3)c3Cl)c2c2c1nc(CN(CCC1)C1=O)[nH]2 CUGJDYZZSOKNFX-UHFFFAOYSA-N 0.000 description 1
- DVWLCXVKZJGIDP-UHFFFAOYSA-N Nc1nc(cc(cc2)-c(cncc3)c3Cl)c2c2c1nc(CN(CCC1)C1=O)[nH]2 Chemical compound Nc1nc(cc(cc2)-c(cncc3)c3Cl)c2c2c1nc(CN(CCC1)C1=O)[nH]2 DVWLCXVKZJGIDP-UHFFFAOYSA-N 0.000 description 1
- OKGMAMRERZMWGK-UHFFFAOYSA-N Nc1nc(cc(cc2)-c3cc(Cl)cnc3)c2c2c1nc(CN(CCC1)C1=O)[nH]2 Chemical compound Nc1nc(cc(cc2)-c3cc(Cl)cnc3)c2c2c1nc(CN(CCC1)C1=O)[nH]2 OKGMAMRERZMWGK-UHFFFAOYSA-N 0.000 description 1
- KRIXKRZTVXIJMD-UHFFFAOYSA-N Nc1nc(cc(cc2)-c3ccc[s]3)c2c2c1nc(CN(CCC1)C1=O)[nH]2 Chemical compound Nc1nc(cc(cc2)-c3ccc[s]3)c2c2c1nc(CN(CCC1)C1=O)[nH]2 KRIXKRZTVXIJMD-UHFFFAOYSA-N 0.000 description 1
- SUBWHJLGYZCPRD-UHFFFAOYSA-N Nc1nc(cc(cc2)-c3ccccc3)c2c2c1nc(CN(CCC1)C1=O)[nH]2 Chemical compound Nc1nc(cc(cc2)-c3ccccc3)c2c2c1nc(CN(CCC1)C1=O)[nH]2 SUBWHJLGYZCPRD-UHFFFAOYSA-N 0.000 description 1
- CPEIEELXLVHTMK-UHFFFAOYSA-N Nc1nc(cc(cc2)-c3ccccc3C#N)c2c2c1nc(CN(CCC1)C1=O)[nH]2 Chemical compound Nc1nc(cc(cc2)-c3ccccc3C#N)c2c2c1nc(CN(CCC1)C1=O)[nH]2 CPEIEELXLVHTMK-UHFFFAOYSA-N 0.000 description 1
- NMYPBTVWAQKBTP-UHFFFAOYSA-N Nc1nc(cc(cc2)-c3ccccc3F)c2c2c1nc(CN(CCC1)C1=O)[nH]2 Chemical compound Nc1nc(cc(cc2)-c3ccccc3F)c2c2c1nc(CN(CCC1)C1=O)[nH]2 NMYPBTVWAQKBTP-UHFFFAOYSA-N 0.000 description 1
- MXDOKFILKVEESM-UHFFFAOYSA-N Nc1nc(cc(cc2)-c3cccnc3)c2c2c1nc(CN(CC(C1)c3ccccc3)C1=O)[nH]2 Chemical compound Nc1nc(cc(cc2)-c3cccnc3)c2c2c1nc(CN(CC(C1)c3ccccc3)C1=O)[nH]2 MXDOKFILKVEESM-UHFFFAOYSA-N 0.000 description 1
- LFBOXCRWRBYQGB-UHFFFAOYSA-N Nc1nc(cc(cc2)-c3n[nH]cc3)c2c2c1nc(CN(CCCC1)C1=O)[nH]2 Chemical compound Nc1nc(cc(cc2)-c3n[nH]cc3)c2c2c1nc(CN(CCCC1)C1=O)[nH]2 LFBOXCRWRBYQGB-UHFFFAOYSA-N 0.000 description 1
- PNKXYAGYOPOZJD-UHFFFAOYSA-N Nc1nc(cc(cc2)-c3n[nH]cc3)c2c2c1nc(CN(CCO1)C1=O)[nH]2 Chemical compound Nc1nc(cc(cc2)-c3n[nH]cc3)c2c2c1nc(CN(CCO1)C1=O)[nH]2 PNKXYAGYOPOZJD-UHFFFAOYSA-N 0.000 description 1
- ARYHTUPFQTUBBG-UHFFFAOYSA-N OB(c1ccc[s]1)O Chemical compound OB(c1ccc[s]1)O ARYHTUPFQTUBBG-UHFFFAOYSA-N 0.000 description 1
- JGPIWNNFLKDTSR-UHFFFAOYSA-N OC(CN(CCC1)C1=O)=O Chemical compound OC(CN(CCC1)C1=O)=O JGPIWNNFLKDTSR-UHFFFAOYSA-N 0.000 description 1
- KGTVATADCQABRD-UHFFFAOYSA-N [O-][N+](c(cnc1c2ccc(Br)c1)c2Cl)=O Chemical compound [O-][N+](c(cnc1c2ccc(Br)c1)c2Cl)=O KGTVATADCQABRD-UHFFFAOYSA-N 0.000 description 1
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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4738—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4745—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
-
- 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- 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
- A61P35/00—Antineoplastic 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (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)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Immunology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Optical Communication System (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Transducers For Ultrasonic Waves (AREA)
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201762460677P | 2017-02-17 | 2017-02-17 | |
| US62/460,677 | 2017-02-17 | ||
| US201762490881P | 2017-04-27 | 2017-04-27 | |
| US62/490,881 | 2017-04-27 | ||
| US201762573991P | 2017-10-18 | 2017-10-18 | |
| US62/573,991 | 2017-10-18 | ||
| PCT/US2018/018484 WO2018152396A1 (en) | 2017-02-17 | 2018-02-16 | Substituted imidazo-quinolines as nlrp3 modulators |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20190117657A KR20190117657A (ko) | 2019-10-16 |
| KR102329062B1 true KR102329062B1 (ko) | 2021-11-18 |
Family
ID=61283434
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020197026922A Active KR102329062B1 (ko) | 2017-02-17 | 2018-02-16 | Nlrp3 조정제로서의 치환된 이미다조-퀴놀린 |
Country Status (29)
| Country | Link |
|---|---|
| US (4) | US10533005B2 (enExample) |
| EP (2) | EP3510034B1 (enExample) |
| JP (1) | JP7003143B6 (enExample) |
| KR (1) | KR102329062B1 (enExample) |
| CN (1) | CN110325534B (enExample) |
| AU (1) | AU2018221076B2 (enExample) |
| CA (1) | CA3053949A1 (enExample) |
| CL (1) | CL2019002324A1 (enExample) |
| CO (1) | CO2019008932A2 (enExample) |
| CY (1) | CY1123305T1 (enExample) |
| DK (1) | DK3510034T3 (enExample) |
| ES (2) | ES2799900T3 (enExample) |
| HR (1) | HRP20201087T1 (enExample) |
| HU (1) | HUE050965T2 (enExample) |
| IL (1) | IL268640B (enExample) |
| LT (1) | LT3510034T (enExample) |
| ME (1) | ME03801B (enExample) |
| MX (1) | MX390065B (enExample) |
| MY (1) | MY194054A (enExample) |
| PE (1) | PE20191552A1 (enExample) |
| PL (1) | PL3510034T3 (enExample) |
| PT (1) | PT3510034T (enExample) |
| RS (1) | RS60548B1 (enExample) |
| SG (1) | SG11201907451XA (enExample) |
| SI (1) | SI3510034T1 (enExample) |
| SM (1) | SMT202000375T1 (enExample) |
| TW (1) | TWI674261B (enExample) |
| WO (1) | WO2018152396A1 (enExample) |
| ZA (1) | ZA201906104B (enExample) |
Families Citing this family (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106397592A (zh) * | 2015-07-31 | 2017-02-15 | 苏州康宁杰瑞生物科技有限公司 | 针对程序性死亡配体(pd-l1)的单域抗体及其衍生蛋白 |
| IL263616B2 (en) | 2016-07-07 | 2025-01-01 | Univ Leland Stanford Junior | Antibody-adjuvant conjugates |
| TWI674261B (zh) | 2017-02-17 | 2019-10-11 | 美商英能腫瘤免疫股份有限公司 | Nlrp3 調節劑 |
| SG11202000248UA (en) | 2017-07-14 | 2020-02-27 | Innate Tumor Immunity Inc | Nlrp3 modulators |
| EP3658539B1 (en) | 2017-07-24 | 2024-02-21 | Novartis AG | Compounds and compositions for treating conditions associated with nlrp activity |
| JP2020531453A (ja) | 2017-08-15 | 2020-11-05 | インフレイゾーム リミテッド | Nlrp3阻害剤としてのスルホニルウレアおよびスルホニルチオウレア |
| WO2019034692A1 (en) | 2017-08-15 | 2019-02-21 | Inflazome Limited | SULFONYLURATES AND SULFONYLTHIOURES AS INHIBITORS OF NLRP3 |
| WO2019034693A1 (en) | 2017-08-15 | 2019-02-21 | Inflazome Limited | SULFONYLURATES AND SULFONYLTHIOURES AS INHIBITORS OF NLRP3 |
| BR112020007593A2 (pt) | 2017-10-18 | 2020-09-24 | Incyte Corporation | derivados de imidazol condensados substituídos por grupos hidróxi terciários como inibidores de pi3k-gama |
| JP2021502364A (ja) | 2017-11-09 | 2021-01-28 | インフレイゾーム リミテッド | 新規なスルホンアミドカルボキサミド化合物 |
| US12221434B2 (en) | 2017-11-09 | 2025-02-11 | Inflazome Limited | Sulfonamide carboxamide compounds |
| WO2019166619A1 (en) | 2018-03-02 | 2019-09-06 | Inflazome Limited | Novel compounds |
| WO2019209896A1 (en) | 2018-04-25 | 2019-10-31 | Innate Tumor Immunity, Inc. | Nlrp3 modulators |
| SG11202101486RA (en) | 2018-08-16 | 2021-03-30 | Innate Tumor Immunity Inc | Substitued 4-amino-1h-imidazo[4,5-c]quinoline compounds and improved methods for their preparation |
| EP3837014B1 (en) | 2018-08-16 | 2022-10-19 | Innate Tumor Immunity, Inc. | Imidazo[4,5-c]quinoline derived nlrp3-modulators |
| JP7433291B2 (ja) * | 2018-08-16 | 2024-02-19 | イネイト・テューマー・イミュニティ・インコーポレイテッド | イミダゾ[4,5-c]キノリン誘導体のNLRP3モジュレーター |
| CR20250050A (es) | 2018-09-05 | 2025-03-19 | Incyte Corp | Formas cristalinas de un inhibidor de fosfoinositida 3–quinasa (pi3k) (divisional 2021-0165) |
| CN111253390B (zh) * | 2018-11-30 | 2023-10-03 | 四川科伦博泰生物医药股份有限公司 | 并环化合物、其制备方法及用途 |
| EP3911641A1 (en) * | 2019-01-14 | 2021-11-24 | Innate Tumor Immunity, Inc. | Nlrp3 modulators |
| WO2020150114A1 (en) * | 2019-01-14 | 2020-07-23 | Innate Tumor Immunity, Inc. | Heterocyclic nlrp3 modulators, for use in the treatment of cancer |
| WO2020150116A1 (en) * | 2019-01-14 | 2020-07-23 | Innate Tumor Immunity, Inc. | Nlrp3 modulators |
| US20220056043A1 (en) | 2019-02-19 | 2022-02-24 | Sichuan Kelun-Biotech Biopharmaceutical Co., Ltd. | Nitrogen-containing fused cyclic compound, preparation method therefor and use thereof |
| AU2020241686A1 (en) | 2019-03-15 | 2021-11-04 | Bolt Biotherapeutics, Inc. | Immunoconjugates targeting HER2 |
| CN116854706B (zh) * | 2019-04-18 | 2025-11-04 | 四川科伦博泰生物医药股份有限公司 | 稠环化合物、其制备方法及用途 |
| UY38687A (es) | 2019-05-17 | 2023-05-15 | Novartis Ag | Inhibidores del inflamasoma nlrp3, composiciones, combinaciones de los mismos y métodos para su uso |
| AU2020407871A1 (en) | 2019-12-20 | 2022-06-30 | Nammi Therapeutics, Inc. | Formulated and/or co-formulated liposome compositions containing toll-like receptor ("TLR") agonist prodrugs useful in the treatment of cancer and methods thereof |
| KR20220127848A (ko) * | 2020-01-10 | 2022-09-20 | 인네이트 튜머 이뮤니티, 인코포레이티드 | Nlrp3 조정제 |
| KR102409345B1 (ko) * | 2020-09-22 | 2022-06-16 | 가톨릭대학교 산학협력단 | Nlrp3 인플라마좀 억제제 및 이의 용도 |
| UY40374A (es) | 2022-08-03 | 2024-02-15 | Novartis Ag | Inhibidores de inflamasoma nlrp3 |
| CN116874340B (zh) * | 2023-07-10 | 2024-04-05 | 湖北航天化学技术研究所 | 一种苯基炸药类含能共晶化合物及其制备方法 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005123079A2 (en) | 2004-06-14 | 2005-12-29 | 3M Innovative Properties Company | Urea substituted imidazopyridines, imidazoquinolines, and imidazonaphthyridines |
| WO2010088924A1 (en) | 2009-02-06 | 2010-08-12 | Telormedix Sa | Pharmaceutical compositions comprising imidazoquinolin(amines) and derivatives thereof suitable for local administration |
| WO2013033345A1 (en) | 2011-08-30 | 2013-03-07 | Regents Of The University Of Minnesota | Immunomodulators and immunomodulator conjugates |
Family Cites Families (66)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US948029A (en) * | 1909-04-23 | 1910-02-01 | James Harvey Leffler | Reclining-chair. |
| CA1271477A (en) | 1983-11-18 | 1990-07-10 | John F. Gerster | 1h-imidazo[4,5-c]quinolin-4-amines |
| US5389640A (en) | 1991-03-01 | 1995-02-14 | Minnesota Mining And Manufacturing Company | 1-substituted, 2-substituted 1H-imidazo[4,5-c]quinolin-4-amines |
| HU222251B1 (hu) * | 1991-03-01 | 2003-05-28 | Minnesota Mining And Manufacturing Company | 1-és 2-helyzetben szubsztituált 1H-imidazo[4,5-c]kinolin-4-amin-származékok előállításában alkalmazható 1- és 2-helyzetben szubsztituált 1H-imidazo[4,5-c]kinolin-4-(szubsztituált)-származékok |
| US5268376A (en) | 1991-09-04 | 1993-12-07 | Minnesota Mining And Manufacturing Company | 1-substituted 1H-imidazo[4,5-c]quinolin-4-amines |
| JPH1180156A (ja) | 1997-09-04 | 1999-03-26 | Hokuriku Seiyaku Co Ltd | 1−(置換アリール)アルキル−1h−イミダゾピリジン−4−アミン誘導体 |
| WO2000037504A2 (en) | 1998-12-23 | 2000-06-29 | Pfizer Inc. | Human monoclonal antibodies to ctla-4 |
| EP1212422B1 (en) | 1999-08-24 | 2007-02-21 | Medarex, Inc. | Human ctla-4 antibodies and their uses |
| GB0023008D0 (en) | 2000-09-20 | 2000-11-01 | Glaxo Group Ltd | Improvements in vaccination |
| US7927613B2 (en) | 2002-02-15 | 2011-04-19 | University Of South Florida | Pharmaceutical co-crystal compositions |
| NZ540826A (en) | 2002-12-20 | 2008-07-31 | 3M Innovative Properties Co | Aryl / hetaryl substituted imidazoquinolines |
| JP2006517974A (ja) | 2003-02-13 | 2006-08-03 | スリーエム イノベイティブ プロパティズ カンパニー | Irm化合物およびトル様受容体8に関する方法および組成物 |
| WO2005018555A2 (en) | 2003-08-14 | 2005-03-03 | 3M Innovative Properties Company | Lipid-modified immune response modifiers |
| EP1658076B1 (en) | 2003-08-27 | 2013-03-06 | 3M Innovative Properties Company | Aryloxy and arylalkyleneoxy substituted imidazoquinolines |
| CA2537450C (en) | 2003-09-05 | 2012-04-17 | Anadys Pharmaceuticals, Inc. | Administration of tlr7 ligands and prodrugs thereof for treatment of infection by hepatitis c virus |
| RU2409576C2 (ru) * | 2003-11-25 | 2011-01-20 | 3М Инновейтив Пропертиз Компани | Системы, содержащие имидазольное кольцо с заместителями, и способы их получения |
| CA2549216A1 (en) | 2003-12-04 | 2005-08-25 | 3M Innovative Properties Company | Sulfone substituted imidazo ring ethers |
| EP1730143A2 (en) | 2004-03-24 | 2006-12-13 | 3M Innovative Properties Company | Amide substituted imidazopyridines, imidazoquinolines, and imidazonaphthyridines |
| JP2007530579A (ja) * | 2004-06-10 | 2007-11-01 | スリーエム イノベイティブ プロパティズ カンパニー | アミド置換イミダゾピリジン、イミダゾキノリン、およびイミダゾナフチリジン |
| WO2005123080A2 (en) | 2004-06-15 | 2005-12-29 | 3M Innovative Properties Company | Nitrogen-containing heterocyclyl substituted imidazoquinolines and imidazonaphthyridines |
| WO2006065280A2 (en) | 2004-06-18 | 2006-06-22 | 3M Innovative Properties Company | Isoxazole, dihydroisoxazole, and oxadiazole substituted imidazo ring compounds and methods |
| US20070259881A1 (en) | 2004-06-18 | 2007-11-08 | Dellaria Joseph F Jr | Substituted Imidazo Ring Systems and Methods |
| BRPI0515316A (pt) | 2004-09-14 | 2008-07-15 | Chiron Corp | compostos de imidazoquinolina |
| JP2008526752A (ja) | 2004-12-30 | 2008-07-24 | スリーエム イノベイティブ プロパティズ カンパニー | 免疫応答調節剤化合物の多経路投与 |
| WO2006091394A2 (en) | 2005-02-11 | 2006-08-31 | Coley Pharmaceutical Group, Inc. | Substituted imidazoquinolines and imidazonaphthyridines |
| EP1851218A2 (en) | 2005-02-23 | 2007-11-07 | 3M Innovative Properties Company | Hydroxyalkyl substituted imidazoquinoline compounds and methods |
| WO2006098852A2 (en) | 2005-02-23 | 2006-09-21 | Coley Pharmaceutical Group, Inc. | Hydroxyalkyl substituted imidazoquinolines |
| KR101411165B1 (ko) | 2005-07-01 | 2014-06-25 | 메다렉스, 엘.엘.시. | 예정 사멸 리간드 1 (피디-엘1)에 대한 인간 모노클로날항체 |
| WO2007079086A1 (en) * | 2005-12-28 | 2007-07-12 | Coley Pharmaceutical Group, Inc. | Pyrazoloalkyl substituted imidazo ring compounds and methods |
| JP5400763B2 (ja) | 2007-05-08 | 2014-01-29 | アストラゼネカ・アクチエボラーグ | 免疫調節特性を有するイミダゾキノリン類 |
| NZ600758A (en) | 2007-06-18 | 2013-09-27 | Merck Sharp & Dohme | Antibodies to human programmed death receptor pd-1 |
| EP2009002A1 (en) | 2007-06-21 | 2008-12-31 | Institut National De La Sante Et De La Recherche Medicale (Inserm) | New process for the manufacture of 1H-imidazo [4,5-c]-quinoline ring systems |
| WO2010077634A1 (en) | 2008-12-09 | 2010-07-08 | Genentech, Inc. | Anti-pd-l1 antibodies and their use to enhance t-cell function |
| NZ599405A (en) | 2009-11-24 | 2014-09-26 | Medimmune Ltd | Targeted binding agents against b7-h1 |
| PL2699264T3 (pl) | 2011-04-20 | 2018-08-31 | Medimmune, Llc | Przeciwciała i inne cząsteczki wiążące B7-H1 i PD-1 |
| US8728486B2 (en) | 2011-05-18 | 2014-05-20 | University Of Kansas | Toll-like receptor-7 and -8 modulatory 1H imidazoquinoline derived compounds |
| EP2785375B1 (en) | 2011-11-28 | 2020-07-22 | Merck Patent GmbH | Anti-pd-l1 antibodies and uses thereof |
| US9856320B2 (en) | 2012-05-15 | 2018-01-02 | Bristol-Myers Squibb Company | Cancer immunotherapy by disrupting PD-1/PD-L1 signaling |
| CN104736168B (zh) | 2012-05-31 | 2018-09-21 | 索伦托治疗有限公司 | 与pd-l1结合的抗原结合蛋白 |
| EP2674170B1 (en) * | 2012-06-15 | 2014-11-19 | Invivogen | Novel compositions of TLR7 and/or TLR8 agonists conjugated to lipids |
| US9295732B2 (en) | 2013-02-22 | 2016-03-29 | Invivogen | Conjugated TLR7 and/or TLR8 and TLR2 polycationic agonists |
| HRP20210122T1 (hr) | 2013-05-02 | 2021-04-16 | Anaptysbio, Inc. | Protutijela usmjerena protiv programirane smrti-1 (pd-1) |
| PE20160080A1 (es) | 2013-05-18 | 2016-02-21 | Aduro Biotech Inc | Composiciones y metodos para activar la senalizacion que depende del estimulador del gen de interferon |
| CN111423511B (zh) | 2013-05-31 | 2024-02-23 | 索伦托药业有限公司 | 与pd-1结合的抗原结合蛋白 |
| US9227969B2 (en) | 2013-08-14 | 2016-01-05 | Novartis Ag | Compounds and compositions as inhibitors of MEK |
| ES2792183T3 (es) | 2013-09-13 | 2020-11-10 | Beigene Switzerland Gmbh | Anticuerpos anti-PD1 y su uso como productos terapéuticos y de diagnóstico |
| PE20160953A1 (es) | 2013-12-12 | 2016-09-26 | Shanghai hengrui pharmaceutical co ltd | Anticuerpo pd-1, fragmento de union al antigeno de este y uso medico de este |
| US10654807B2 (en) | 2013-12-20 | 2020-05-19 | The University Of Kansas | Toll-like receptor 8 agonists |
| TWI681969B (zh) | 2014-01-23 | 2020-01-11 | 美商再生元醫藥公司 | 針對pd-1的人類抗體 |
| JOP20200094A1 (ar) | 2014-01-24 | 2017-06-16 | Dana Farber Cancer Inst Inc | جزيئات جسم مضاد لـ pd-1 واستخداماتها |
| CN112546231A (zh) * | 2014-07-09 | 2021-03-26 | 博笛生物科技有限公司 | 用于治疗癌症的联合治疗组合物和联合治疗方法 |
| CN112546238A (zh) | 2014-09-01 | 2021-03-26 | 博笛生物科技有限公司 | 用于治疗肿瘤的抗-pd-l1结合物 |
| GB201418004D0 (en) | 2014-10-10 | 2014-11-26 | Isis Innovation | Polymer adjuvant |
| MX2017011644A (es) | 2015-03-13 | 2017-12-04 | Cytomx Therapeutics Inc | Anticuerpos anti-pdl1, anticuerpos anti-pdl1 activables y metodos de uso de los mismos. |
| CN107849144B (zh) | 2015-05-29 | 2021-09-17 | 艾吉纳斯公司 | 抗-ctla-4抗体及其使用方法 |
| WO2017024465A1 (en) | 2015-08-10 | 2017-02-16 | Innovent Biologics (Suzhou) Co., Ltd. | Pd-1 antibodies |
| AR105654A1 (es) | 2015-08-24 | 2017-10-25 | Lilly Co Eli | Anticuerpos pd-l1 (ligando 1 de muerte celular programada) |
| EP3344262A4 (en) | 2015-09-01 | 2019-03-20 | Innate Tumor Immunity, Inc. | IMMUNOCELLS WITH INCREASED IMMUNITY OR RESISTANCE TO AN IMMUNOSUPPRESSIVE CYTOKINE AND USE THEREOF |
| HK1257840A1 (zh) | 2015-09-01 | 2019-11-01 | Agenus Inc. | 抗-pd-1抗体及其使用方法 |
| CN115252792A (zh) | 2016-01-07 | 2022-11-01 | 博笛生物科技有限公司 | 用于治疗肿瘤的抗-egfr组合 |
| US10730871B2 (en) | 2016-01-28 | 2020-08-04 | Regents Of The University Of Minnesota | Immunomodulators and immunomodulator conjugates |
| WO2017132827A1 (en) | 2016-02-02 | 2017-08-10 | Innovent Biologics (Suzhou) Co., Ltd. | Pd-1 antibodies |
| CN111491362B (zh) | 2016-02-02 | 2023-10-24 | 华为技术有限公司 | 确定发射功率的方法、用户设备和基站 |
| US10533007B2 (en) | 2016-04-19 | 2020-01-14 | Innate Tumor Immunity, Inc. | NLRP3 modulators |
| MX2018012249A (es) * | 2016-04-19 | 2019-02-07 | Innate Tumor Immunity Inc | Moduladores de nlpr3. |
| TWI674261B (zh) | 2017-02-17 | 2019-10-11 | 美商英能腫瘤免疫股份有限公司 | Nlrp3 調節劑 |
-
2018
- 2018-02-14 TW TW107105417A patent/TWI674261B/zh active
- 2018-02-16 HR HRP20201087TT patent/HRP20201087T1/hr unknown
- 2018-02-16 LT LTEP18707612.0T patent/LT3510034T/lt unknown
- 2018-02-16 ME MEP-2020-149A patent/ME03801B/me unknown
- 2018-02-16 RS RS20200830A patent/RS60548B1/sr unknown
- 2018-02-16 HU HUE18707612A patent/HUE050965T2/hu unknown
- 2018-02-16 SM SM20200375T patent/SMT202000375T1/it unknown
- 2018-02-16 AU AU2018221076A patent/AU2018221076B2/en active Active
- 2018-02-16 WO PCT/US2018/018484 patent/WO2018152396A1/en not_active Ceased
- 2018-02-16 EP EP18707612.0A patent/EP3510034B1/en active Active
- 2018-02-16 MY MYPI2019004704A patent/MY194054A/en unknown
- 2018-02-16 CA CA3053949A patent/CA3053949A1/en active Pending
- 2018-02-16 KR KR1020197026922A patent/KR102329062B1/ko active Active
- 2018-02-16 SI SI201830085T patent/SI3510034T1/sl unknown
- 2018-02-16 ES ES18707612T patent/ES2799900T3/es active Active
- 2018-02-16 PL PL18707612T patent/PL3510034T3/pl unknown
- 2018-02-16 PT PT187076120T patent/PT3510034T/pt unknown
- 2018-02-16 DK DK18707612.0T patent/DK3510034T3/da active
- 2018-02-16 SG SG11201907451XA patent/SG11201907451XA/en unknown
- 2018-02-16 JP JP2019544636A patent/JP7003143B6/ja active Active
- 2018-02-16 CN CN201880012493.7A patent/CN110325534B/zh active Active
- 2018-02-16 EP EP20169634.1A patent/EP3753938B1/en active Active
- 2018-02-16 ES ES20169634T patent/ES2978510T3/es active Active
- 2018-02-16 US US15/898,258 patent/US10533005B2/en active Active
- 2018-02-16 MX MX2019009788A patent/MX390065B/es unknown
- 2018-02-16 PE PE2019001718A patent/PE20191552A1/es unknown
-
2019
- 2019-08-12 IL IL268640A patent/IL268640B/en unknown
- 2019-08-16 CL CL2019002324A patent/CL2019002324A1/es unknown
- 2019-08-16 CO CONC2019/0008932A patent/CO2019008932A2/es unknown
- 2019-09-16 ZA ZA2019/06104A patent/ZA201906104B/en unknown
- 2019-11-25 US US16/693,420 patent/US20200157096A1/en not_active Abandoned
-
2020
- 2020-07-16 CY CY20201100649T patent/CY1123305T1/el unknown
-
2021
- 2021-05-06 US US17/313,319 patent/US11827632B2/en active Active
-
2023
- 2023-10-17 US US18/488,092 patent/US12351580B2/en active Active
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005123079A2 (en) | 2004-06-14 | 2005-12-29 | 3M Innovative Properties Company | Urea substituted imidazopyridines, imidazoquinolines, and imidazonaphthyridines |
| WO2010088924A1 (en) | 2009-02-06 | 2010-08-12 | Telormedix Sa | Pharmaceutical compositions comprising imidazoquinolin(amines) and derivatives thereof suitable for local administration |
| WO2013033345A1 (en) | 2011-08-30 | 2013-03-07 | Regents Of The University Of Minnesota | Immunomodulators and immunomodulator conjugates |
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR102329062B1 (ko) | Nlrp3 조정제로서의 치환된 이미다조-퀴놀린 | |
| CN109071535B (zh) | Nlrp3调节剂 | |
| KR102711180B1 (ko) | Nlrp3 조정제 | |
| KR102768379B1 (ko) | 이미다조[4,5-c]퀴놀린 유래 NLRP3-조정제 | |
| KR102817037B1 (ko) | 이미다조[4,5-c]퀴놀린 유래 NLRP3-조정제 | |
| KR102815870B1 (ko) | 암의 치료에 사용하기 위한 헤테로시클릭 nlrp3 조정제 | |
| KR20210116529A (ko) | Nlrp3 조정제 | |
| US12338228B2 (en) | NLRP3 modulators | |
| KR102903509B1 (ko) | 암의 치료에 사용하기 위한 nlrp3-조정제로서의 치환된 퀴나졸린 | |
| KR20220127848A (ko) | Nlrp3 조정제 | |
| EA037780B1 (ru) | Модуляторы nlrp3 | |
| HK40003517A (en) | Substituted imidazo-quinolines as nlrp3 modulators | |
| HK40003517B (en) | Substituted imidazo-quinolines as nlrp3 modulators | |
| BR112019016625B1 (pt) | Imidazo-quinolinas substituídas como moduladores de nlrp3, composições farmacêuticas e seus usos para tratar câncer | |
| KR20210114456A (ko) | 암의 치료에 사용하기 위한 nlrp3-조정제로서의 치환된 퀴나졸린 | |
| NZ757257B2 (en) | Substituted imidazo-quinolines as nlrp3 modulators |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PA0105 | International application |
St.27 status event code: A-0-1-A10-A15-nap-PA0105 |
|
| PG1501 | Laying open of application |
St.27 status event code: A-1-1-Q10-Q12-nap-PG1501 |
|
| A201 | Request for examination | ||
| A302 | Request for accelerated examination | ||
| E13-X000 | Pre-grant limitation requested |
St.27 status event code: A-2-3-E10-E13-lim-X000 |
|
| P11-X000 | Amendment of application requested |
St.27 status event code: A-2-2-P10-P11-nap-X000 |
|
| P13-X000 | Application amended |
St.27 status event code: A-2-2-P10-P13-nap-X000 |
|
| PA0201 | Request for examination |
St.27 status event code: A-1-2-D10-D11-exm-PA0201 |
|
| PA0302 | Request for accelerated examination |
St.27 status event code: A-1-2-D10-D17-exm-PA0302 St.27 status event code: A-1-2-D10-D16-exm-PA0302 |
|
| P11-X000 | Amendment of application requested |
St.27 status event code: A-2-2-P10-P11-nap-X000 |
|
| P13-X000 | Application amended |
St.27 status event code: A-2-2-P10-P13-nap-X000 |
|
| R17-X000 | Change to representative recorded |
St.27 status event code: A-3-3-R10-R17-oth-X000 |
|
| E902 | Notification of reason for refusal | ||
| PE0902 | Notice of grounds for rejection |
St.27 status event code: A-1-2-D10-D21-exm-PE0902 |
|
| E13-X000 | Pre-grant limitation requested |
St.27 status event code: A-2-3-E10-E13-lim-X000 |
|
| P11-X000 | Amendment of application requested |
St.27 status event code: A-2-2-P10-P11-nap-X000 |
|
| P13-X000 | Application amended |
St.27 status event code: A-2-2-P10-P13-nap-X000 |
|
| R17-X000 | Change to representative recorded |
St.27 status event code: A-3-3-R10-R17-oth-X000 |
|
| E701 | Decision to grant or registration of patent right | ||
| PE0701 | Decision of registration |
St.27 status event code: A-1-2-D10-D22-exm-PE0701 |
|
| GRNT | Written decision to grant | ||
| PR0701 | Registration of establishment |
St.27 status event code: A-2-4-F10-F11-exm-PR0701 |
|
| PR1002 | Payment of registration fee |
St.27 status event code: A-2-2-U10-U12-oth-PR1002 Fee payment year number: 1 |
|
| PG1601 | Publication of registration |
St.27 status event code: A-4-4-Q10-Q13-nap-PG1601 |
|
| PR1001 | Payment of annual fee |
St.27 status event code: A-4-4-U10-U11-oth-PR1001 Fee payment year number: 4 |
|
| PR1001 | Payment of annual fee |
St.27 status event code: A-4-4-U10-U11-oth-PR1001 Fee payment year number: 5 |