CN105209467B - 咪唑并吡咯烷酮衍生物及其在治疗疾病中的用途 - Google Patents
咪唑并吡咯烷酮衍生物及其在治疗疾病中的用途 Download PDFInfo
- Publication number
- CN105209467B CN105209467B CN201480028176.6A CN201480028176A CN105209467B CN 105209467 B CN105209467 B CN 105209467B CN 201480028176 A CN201480028176 A CN 201480028176A CN 105209467 B CN105209467 B CN 105209467B
- Authority
- CN
- China
- Prior art keywords
- dimethyl
- bases
- methyl
- chlorophenyl
- oxo
- 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.)
- Expired - Fee Related
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- 0 *C(C(CCCCC1)C1C1C2C1)(C(C=CC=C/C=C/C1)=CC1=C)N2C1=CC=CC=CC=CC=C1 Chemical compound *C(C(CCCCC1)C1C1C2C1)(C(C=CC=C/C=C/C1)=CC1=C)N2C1=CC=CC=CC=CC=C1 0.000 description 27
- ZLBKAFXGTXIMBN-HSZRJFAPSA-N CC(C)C[n]1c(C2CCOCC2)nc(C2=O)c1[C@@H](c(cc1)ccc1Cl)N2c(cc1C)n[n]2c1nnc2C Chemical compound CC(C)C[n]1c(C2CCOCC2)nc(C2=O)c1[C@@H](c(cc1)ccc1Cl)N2c(cc1C)n[n]2c1nnc2C ZLBKAFXGTXIMBN-HSZRJFAPSA-N 0.000 description 1
- IQIUDSWFPYGIST-UHFFFAOYSA-N CC(C)[n]1c(-c2c(C)[o]nc2C)nc(C2=O)c1C(c(cc1)ccc1Cl)N2C(C=C1C)=CN(C)C1=O Chemical compound CC(C)[n]1c(-c2c(C)[o]nc2C)nc(C2=O)c1C(c(cc1)ccc1Cl)N2C(C=C1C)=CN(C)C1=O IQIUDSWFPYGIST-UHFFFAOYSA-N 0.000 description 1
- MIQUVIUEZWYUSK-UHFFFAOYSA-N CC(C)[n]1c(C2CCN(C)CC2)nc2c1C(c1ccc(C)cc1)NC2=O Chemical compound CC(C)[n]1c(C2CCN(C)CC2)nc2c1C(c1ccc(C)cc1)NC2=O MIQUVIUEZWYUSK-UHFFFAOYSA-N 0.000 description 1
- LRWMKIGMKUKHBW-UHFFFAOYSA-N CC(C)[n]1c([Br]=C)nc(C2=O)c1C(c(cc1)ccc1Cl)N2C(C=C1C)=CN(C)C1=O Chemical compound CC(C)[n]1c([Br]=C)nc(C2=O)c1C(c(cc1)ccc1Cl)N2C(C=C1C)=CN(C)C1=O LRWMKIGMKUKHBW-UHFFFAOYSA-N 0.000 description 1
- OMWRONONTICAKU-UHFFFAOYSA-N CC(C)[n]1c([Br]=C)nc(C2=O)c1C(c(cc1)ccc1Cl)N2c(cc1C)c[n]2c1nnc2C Chemical compound CC(C)[n]1c([Br]=C)nc(C2=O)c1C(c(cc1)ccc1Cl)N2c(cc1C)c[n]2c1nnc2C OMWRONONTICAKU-UHFFFAOYSA-N 0.000 description 1
- MSXMEGOUYCSMJA-UHFFFAOYSA-N CC1=CC(N(C(c2c3nc(-c4ncc[s]4)[nH]2)c(cc2)ccc2Cl)C3=O)=CN(C)C1=O Chemical compound CC1=CC(N(C(c2c3nc(-c4ncc[s]4)[nH]2)c(cc2)ccc2Cl)C3=O)=CN(C)C1=O MSXMEGOUYCSMJA-UHFFFAOYSA-N 0.000 description 1
- HHNLWTVZGFCDMU-UHFFFAOYSA-N CC1=CC(N(Cc2c3[nH]c(Br)n2)C3c(cc2)ccc2Cl)=CN(C)C1=O Chemical compound CC1=CC(N(Cc2c3[nH]c(Br)n2)C3c(cc2)ccc2Cl)=CN(C)C1=O HHNLWTVZGFCDMU-UHFFFAOYSA-N 0.000 description 1
- WKQWDISUQXTCNU-UHFFFAOYSA-N CCCCOC(c([n]1Cc(cc2)ccc2OC)c(C=O)nc1Br)=O Chemical compound CCCCOC(c([n]1Cc(cc2)ccc2OC)c(C=O)nc1Br)=O WKQWDISUQXTCNU-UHFFFAOYSA-N 0.000 description 1
- VGGTVIRRIHHUEK-UHFFFAOYSA-N CCCCOC(c1c(C(OCCCC)=O)nc[nH]1)=O Chemical compound CCCCOC(c1c(C(OCCCC)=O)nc[nH]1)=O VGGTVIRRIHHUEK-UHFFFAOYSA-N 0.000 description 1
- ZMMRTYNERZVMQC-UHFFFAOYSA-N CCOC(c1c(C(c(cc2)ccc2Cl)Nc(cc2C)nc3c2nn[n]3C)[n](CC=C)c(Br)n1)=O Chemical compound CCOC(c1c(C(c(cc2)ccc2Cl)Nc(cc2C)nc3c2nn[n]3C)[n](CC=C)c(Br)n1)=O ZMMRTYNERZVMQC-UHFFFAOYSA-N 0.000 description 1
- ZNWDKSZGTKLHML-UHFFFAOYSA-N CCOC(c1c(C(c(cc2)ccc2Cl)O)[n](C2COC2)c(Br)n1)=O Chemical compound CCOC(c1c(C(c(cc2)ccc2Cl)O)[n](C2COC2)c(Br)n1)=O ZNWDKSZGTKLHML-UHFFFAOYSA-N 0.000 description 1
- CYPCWFKNFJRMQN-UHFFFAOYSA-N CCOC(c1c[n](C)cn1)=O Chemical compound CCOC(c1c[n](C)cn1)=O CYPCWFKNFJRMQN-UHFFFAOYSA-N 0.000 description 1
- SKXLTOZZAXFBRR-UHFFFAOYSA-N CCOCC(c1c(C(c(cc2)ccc2Cl)NC(C=C2C)=CN(C)C2=O)[n](C2CC2)c([Br]=C)n1)=O Chemical compound CCOCC(c1c(C(c(cc2)ccc2Cl)NC(C=C2C)=CN(C)C2=O)[n](C2CC2)c([Br]=C)n1)=O SKXLTOZZAXFBRR-UHFFFAOYSA-N 0.000 description 1
- OSOMHZBGIZCTKM-OAQYLSRUSA-N CC[n]1c(-c(cccn2)c2OC)nc([C@@H](c(cc2)ccc2Cl)N2C(C=C3C)=CN(C)C3=O)c1C2=O Chemical compound CC[n]1c(-c(cccn2)c2OC)nc([C@@H](c(cc2)ccc2Cl)N2C(C=C3C)=CN(C)C3=O)c1C2=O OSOMHZBGIZCTKM-OAQYLSRUSA-N 0.000 description 1
- UCTNVNGRNJPSOM-UHFFFAOYSA-N CC[n]1c(C(N(C2c(cc3)ccc3Cl)c(cc3C)cc4c3nn[n]4C)=O)c2nc1C Chemical compound CC[n]1c(C(N(C2c(cc3)ccc3Cl)c(cc3C)cc4c3nn[n]4C)=O)c2nc1C UCTNVNGRNJPSOM-UHFFFAOYSA-N 0.000 description 1
- HDNRAPAFJLXKBV-UHFFFAOYSA-N CCc(cc1)ccc1OC Chemical compound CCc(cc1)ccc1OC HDNRAPAFJLXKBV-UHFFFAOYSA-N 0.000 description 1
- AIJFPNKGGAPZFJ-UHFFFAOYSA-N CNCc(cc1)ccc1OC Chemical compound CNCc(cc1)ccc1OC AIJFPNKGGAPZFJ-UHFFFAOYSA-N 0.000 description 1
- XDKPXRURANQQLJ-UHFFFAOYSA-N COc(nc1)cc(N)c1F Chemical compound COc(nc1)cc(N)c1F XDKPXRURANQQLJ-UHFFFAOYSA-N 0.000 description 1
- IDPURXSQCKYKIJ-UHFFFAOYSA-N COc1ccc(CN)cc1 Chemical compound COc1ccc(CN)cc1 IDPURXSQCKYKIJ-UHFFFAOYSA-N 0.000 description 1
- VFDAORCFAAAXRV-UHFFFAOYSA-N Cc1cc(N(C(c2c3nc(-c(cccn4)c4OC)[nH]2)c(cc2)ccc2Cl)C3=O)c[n]2c1nnc2C(F)F Chemical compound Cc1cc(N(C(c2c3nc(-c(cccn4)c4OC)[nH]2)c(cc2)ccc2Cl)C3=O)c[n]2c1nnc2C(F)F VFDAORCFAAAXRV-UHFFFAOYSA-N 0.000 description 1
- MAFPDYCUAPCXQA-UHFFFAOYSA-N Cc1cc(N(C(c2c3nc(C4=CCOCC4)[n]2C2COC2)c(cc2)ccc2Cl)C3=N)cc2c1nn[n]2C Chemical compound Cc1cc(N(C(c2c3nc(C4=CCOCC4)[n]2C2COC2)c(cc2)ccc2Cl)C3=N)cc2c1nn[n]2C MAFPDYCUAPCXQA-UHFFFAOYSA-N 0.000 description 1
- RXXHXYQFQDTPDM-UHFFFAOYSA-N Cc1cc(N)c[n]2c1nnc2CF Chemical compound Cc1cc(N)c[n]2c1nnc2CF RXXHXYQFQDTPDM-UHFFFAOYSA-N 0.000 description 1
- XRQOPEVIGOZEJD-UHFFFAOYSA-N Cc1nnc(c(C)c2)[n]1cc2N(C(c1c2nc(-c(cc3)cnc3OC)[n]1C)c(cc1)ccc1Cl)C2=O Chemical compound Cc1nnc(c(C)c2)[n]1cc2N(C(c1c2nc(-c(cc3)cnc3OC)[n]1C)c(cc1)ccc1Cl)C2=O XRQOPEVIGOZEJD-UHFFFAOYSA-N 0.000 description 1
- PCLIMKBDDGJMGD-UHFFFAOYSA-N O=C(CCC1=O)N1Br Chemical compound O=C(CCC1=O)N1Br PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
-
- 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
- A61K31/41—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
- A61K31/4192—1,2,3-Triazoles
-
- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/5025—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/513—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim having oxo groups directly attached to the heterocyclic ring, e.g. cytosine
-
- 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
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP13169390 | 2013-05-27 | ||
| EP13169390.5 | 2013-05-27 | ||
| EP13177676 | 2013-07-23 | ||
| EP13177676.7 | 2013-07-23 | ||
| PCT/IB2014/061715 WO2014191894A1 (en) | 2013-05-27 | 2014-05-26 | Imidazopyrrolidinone derivatives and their use in the treatment of disease |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN105209467A CN105209467A (zh) | 2015-12-30 |
| CN105209467B true CN105209467B (zh) | 2018-06-08 |
Family
ID=50979826
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201480028176.6A Expired - Fee Related CN105209467B (zh) | 2013-05-27 | 2014-05-26 | 咪唑并吡咯烷酮衍生物及其在治疗疾病中的用途 |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US9890166B2 (enExample) |
| EP (2) | EP3004109A1 (enExample) |
| JP (1) | JP6373978B2 (enExample) |
| KR (1) | KR20160012194A (enExample) |
| CN (1) | CN105209467B (enExample) |
| AU (1) | AU2014272774B2 (enExample) |
| BR (1) | BR112015029491A2 (enExample) |
| CA (1) | CA2913697A1 (enExample) |
| EA (1) | EA029312B1 (enExample) |
| MX (1) | MX2015016344A (enExample) |
| WO (1) | WO2014191894A1 (enExample) |
Families Citing this family (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2909778T3 (es) | 2013-03-15 | 2022-05-10 | Incyte Holdings Corp | Heterociclos tricíclicos como inhibidores de proteína BET para su uso en el tratamiento de una enfermedad proliferativa en combinación con un inhibidor de Janus quinasas |
| EP3004109A1 (en) | 2013-05-27 | 2016-04-13 | Novartis AG | Imidazopyrrolidinone derivatives and their use in the treatment of disease |
| WO2015004533A2 (en) | 2013-06-21 | 2015-01-15 | Zenith Epigenetics Corp. | Novel substituted bicyclic compounds as bromodomain inhibitors |
| WO2015002754A2 (en) | 2013-06-21 | 2015-01-08 | Zenith Epigenetics Corp. | Novel bicyclic bromodomain inhibitors |
| ES2635560T3 (es) | 2013-07-08 | 2017-10-04 | Incyte Holdings Corporation | Heterociclos tricíclicos como inhibidores de la proteína NET |
| WO2015015318A2 (en) | 2013-07-31 | 2015-02-05 | Zenith Epigenetics Corp. | Novel quinazolinones as bromodomain inhibitors |
| RS63733B1 (sr) | 2013-10-18 | 2022-12-30 | Celgene Quanticel Research Inc | Inhibitori bromodomena |
| CA2931249A1 (en) * | 2013-11-21 | 2015-05-28 | Novartis Ag | Pyrrolopyrrolone derivatives and their use as bet inhibitors |
| US9315501B2 (en) | 2013-11-26 | 2016-04-19 | Incyte Corporation | Bicyclic heterocycles as BET protein inhibitors |
| WO2015081203A1 (en) | 2013-11-26 | 2015-06-04 | Incyte Corporation | Bicyclic heterocycles as bet protein inhibitors |
| WO2015095492A1 (en) | 2013-12-19 | 2015-06-25 | Incyte Corporation | Tricyclic heterocycles as bet protein inhibitors |
| SG10201809353TA (en) | 2014-04-23 | 2018-11-29 | Incyte Corp | 1H-PYRROLO[2,3-c]PYRIDIN-7(6H)-ONES AND PYRAZOLO[3,4-c]PYRIDIN-7(6H)-ONES AS INHIBITORS OF BET PROTEINS |
| WO2016044130A1 (en) | 2014-09-15 | 2016-03-24 | Incyte Corporation | Tricyclic heterocycles for use as bet protein inhibitors |
| WO2016087936A1 (en) | 2014-12-01 | 2016-06-09 | Zenith Epigenetics Corp. | Substituted pyridinones as bromodomain inhibitors |
| WO2016087942A1 (en) | 2014-12-01 | 2016-06-09 | Zenith Epigenetics Corp. | Substituted pyridines as bromodomain inhibitors |
| US10292968B2 (en) | 2014-12-11 | 2019-05-21 | Zenith Epigenetics Ltd. | Substituted heterocycles as bromodomain inhibitors |
| US10231953B2 (en) | 2014-12-17 | 2019-03-19 | Zenith Epigenetics Ltd. | Inhibitors of bromodomains |
| GB201504694D0 (en) | 2015-03-19 | 2015-05-06 | Glaxosmithkline Ip Dev Ltd | Covalent conjugates |
| AR104259A1 (es) * | 2015-04-15 | 2017-07-05 | Celgene Quanticel Res Inc | Inhibidores de bromodominio |
| AR106520A1 (es) | 2015-10-29 | 2018-01-24 | Incyte Corp | Forma sólida amorfa de un inhibidor de proteína bet |
| MX2018009870A (es) | 2016-02-15 | 2018-11-29 | Cemm Forschungszentrum Fuer Molekulare Medizin Gmbh | Inhibidores de taf1 para la terapia del cancer. |
| TWI830533B (zh) | 2016-06-20 | 2024-01-21 | 美商英塞特公司 | Bet抑制劑之結晶固體形式 |
| TW201822637A (zh) | 2016-11-07 | 2018-07-01 | 德商拜耳廠股份有限公司 | 用於控制動物害蟲的經取代磺醯胺類 |
| AU2017359288A1 (en) | 2016-11-14 | 2019-05-30 | Cemm - Forschungszentrum Für Molekulare Medizin Gmbh | Combination of a BRD4 inhibitor and an antifolate for the therapy of cancer |
| TW201837026A (zh) | 2017-01-10 | 2018-10-16 | 德商拜耳廠股份有限公司 | 作為除害劑之雜環衍生物(二) |
| UY37556A (es) | 2017-01-10 | 2018-07-31 | Bayer Ag | Derivados heterocíclicos como pesticidas |
| WO2018161871A1 (zh) * | 2017-03-06 | 2018-09-13 | 罗欣生物科技(上海)有限公司 | 作为p53-MDM2抑制剂的咪唑并吡咯酮化合物 |
| AU2018242612B2 (en) * | 2017-03-31 | 2020-05-21 | Novartis Ag | Dose and regimen for an HDM2-p53 interaction inhibitor in hematological tumors |
| WO2019067021A1 (en) * | 2017-09-28 | 2019-04-04 | The General Hospital Corporation | COMPOUNDS FOR THE TREATMENT OF CONDITIONS ASSOCIATED WITH ABNORMAL STEROIDOGENESIS |
| EP3750885A4 (en) * | 2018-02-06 | 2021-10-27 | Shanghai Haihe Pharmaceutical Co., Ltd. | COMPOUND PRESENTING AN INHIBITORING ACTIVITY OF BET, ITS PREPARATION PROCESS AND ITS USE |
| WO2019174576A1 (zh) * | 2018-03-12 | 2019-09-19 | 罗欣药业(上海)有限公司 | 咪唑并吡咯酮化合物及其应用 |
| TW202102492A (zh) * | 2019-03-15 | 2021-01-16 | 日商日本曹達股份有限公司 | 雜環化合物及農園藝用殺菌劑 |
| WO2021047466A1 (zh) * | 2019-09-12 | 2021-03-18 | 罗欣药业(上海)有限公司 | 一种p53-MDM2抑制剂的晶型及其制备方法 |
| US11833155B2 (en) | 2020-06-03 | 2023-12-05 | Incyte Corporation | Combination therapy for treatment of myeloproliferative neoplasms |
| US20230247994A1 (en) | 2020-07-02 | 2023-08-10 | Bayer Aktiengesellschaft | Heterocyclene derivatives as pest control agents |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
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- 2014-05-26 BR BR112015029491A patent/BR112015029491A2/pt active Search and Examination
- 2014-05-26 KR KR1020157036223A patent/KR20160012194A/ko not_active Withdrawn
- 2014-05-26 CN CN201480028176.6A patent/CN105209467B/zh not_active Expired - Fee Related
- 2014-05-26 EA EA201592256A patent/EA029312B1/ru not_active IP Right Cessation
- 2014-05-26 WO PCT/IB2014/061715 patent/WO2014191894A1/en not_active Ceased
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- 2014-05-26 AU AU2014272774A patent/AU2014272774B2/en not_active Ceased
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| AU2014272774A1 (en) | 2015-11-26 |
| EA029312B1 (ru) | 2018-03-30 |
| JP2016520116A (ja) | 2016-07-11 |
| CN105209467A (zh) | 2015-12-30 |
| JP6373978B2 (ja) | 2018-08-15 |
| WO2014191894A1 (en) | 2014-12-04 |
| EP3004109A1 (en) | 2016-04-13 |
| KR20160012194A (ko) | 2016-02-02 |
| EA201592256A1 (ru) | 2016-04-29 |
| CA2913697A1 (en) | 2014-12-04 |
| EP3412675A1 (en) | 2018-12-12 |
| BR112015029491A2 (pt) | 2017-07-25 |
| US20160108047A1 (en) | 2016-04-21 |
| MX2015016344A (es) | 2016-03-01 |
| US9890166B2 (en) | 2018-02-13 |
| AU2014272774B2 (en) | 2016-12-08 |
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