AU2016279052A1 - Benzodiazepine derivatives, compositions, and methods for treating cognitive impairment - Google Patents
Benzodiazepine derivatives, compositions, and methods for treating cognitive impairment Download PDFInfo
- Publication number
- AU2016279052A1 AU2016279052A1 AU2016279052A AU2016279052A AU2016279052A1 AU 2016279052 A1 AU2016279052 A1 AU 2016279052A1 AU 2016279052 A AU2016279052 A AU 2016279052A AU 2016279052 A AU2016279052 A AU 2016279052A AU 2016279052 A1 AU2016279052 A1 AU 2016279052A1
- Authority
- AU
- Australia
- Prior art keywords
- alkyl
- aliphatic
- pct
- aryl
- compound
- 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.)
- Abandoned
Links
- 0 Cc1c(*)c(*)c(*)[n]1C Chemical compound Cc1c(*)c(*)c(*)[n]1C 0.000 description 18
- OEZAAXHZEMTBOV-DUXPYHPUSA-N C/C(/C=O)=C\N Chemical compound C/C(/C=O)=C\N OEZAAXHZEMTBOV-DUXPYHPUSA-N 0.000 description 1
- WJLCGJBPFXMFBX-UHFFFAOYSA-N CC(C)(C)OC(Nc1c(CC(Nc(cc2)c-3cc2OC)=O)[n]-3nn1)=O Chemical compound CC(C)(C)OC(Nc1c(CC(Nc(cc2)c-3cc2OC)=O)[n]-3nn1)=O WJLCGJBPFXMFBX-UHFFFAOYSA-N 0.000 description 1
- MPIHEDXFMFURFJ-UHFFFAOYSA-N CC(C)OCc1nnc(-c2c3)[n]1Cc1c(C#C)nc(C)[n]1-c2ccc3Cl Chemical compound CC(C)OCc1nnc(-c2c3)[n]1Cc1c(C#C)nc(C)[n]1-c2ccc3Cl MPIHEDXFMFURFJ-UHFFFAOYSA-N 0.000 description 1
- FFAYLHLKYBYKBJ-UHFFFAOYSA-N CC(C)c1nc(-c(nc2)c(C[n]3c(-c4c5)nnc3COC)[n]2-c4ccc5OC)n[o]1 Chemical compound CC(C)c1nc(-c(nc2)c(C[n]3c(-c4c5)nnc3COC)[n]2-c4ccc5OC)n[o]1 FFAYLHLKYBYKBJ-UHFFFAOYSA-N 0.000 description 1
- FOTIBFXYPVRLQJ-UHFFFAOYSA-N CC(C)c1ncn[o]1 Chemical compound CC(C)c1ncn[o]1 FOTIBFXYPVRLQJ-UHFFFAOYSA-N 0.000 description 1
- WAPNOHKVXSQRPX-UHFFFAOYSA-N CC(c1ccccc1)O Chemical compound CC(c1ccccc1)O WAPNOHKVXSQRPX-UHFFFAOYSA-N 0.000 description 1
- IVNOKTXCSGASKK-UHFFFAOYSA-N CCN(CC)Cc1c(Cc2c(C(OCC)=O)nc[n]2-c(cc2)c-3cc2OC)[n]-3nn1 Chemical compound CCN(CC)Cc1c(Cc2c(C(OCC)=O)nc[n]2-c(cc2)c-3cc2OC)[n]-3nn1 IVNOKTXCSGASKK-UHFFFAOYSA-N 0.000 description 1
- WFGXLYYYFZGMLS-UHFFFAOYSA-N CCOC(c(nc1)c(C[n]2c(Br)nnc2-c2c3)[n]1-c2ccc3OC)=O Chemical compound CCOC(c(nc1)c(C[n]2c(Br)nnc2-c2c3)[n]1-c2ccc3OC)=O WFGXLYYYFZGMLS-UHFFFAOYSA-N 0.000 description 1
- HWEPWRLPVGAZSU-UHFFFAOYSA-N CCOC(c(nc1)c2[n]1-c(ccc(C)c1)c1-[n]1nnc(C)c1C2)=O Chemical compound CCOC(c(nc1)c2[n]1-c(ccc(C)c1)c1-[n]1nnc(C)c1C2)=O HWEPWRLPVGAZSU-UHFFFAOYSA-N 0.000 description 1
- GCXVREYOHINKNN-UHFFFAOYSA-N CCOC(c(nc1)c2[n]1-c(ccc(C)c1)c1-[n]1nnc(Cc3cccnc3)c1C2)=O Chemical compound CCOC(c(nc1)c2[n]1-c(ccc(C)c1)c1-[n]1nnc(Cc3cccnc3)c1C2)=O GCXVREYOHINKNN-UHFFFAOYSA-N 0.000 description 1
- LIXVTBXWPUHDGS-UHFFFAOYSA-N CCOC(c(nc1)c2[n]1-c(ccc(F)c1)c1-[n]1nnc(C)c1C2)=C Chemical compound CCOC(c(nc1)c2[n]1-c(ccc(F)c1)c1-[n]1nnc(C)c1C2)=C LIXVTBXWPUHDGS-UHFFFAOYSA-N 0.000 description 1
- ZYZQIAZMXMKALR-UHFFFAOYSA-N CCOC(c(nc1)c2[n]1-c(ccc(F)c1)c1-[n]1nnc(C)c1C2)=O Chemical compound CCOC(c(nc1)c2[n]1-c(ccc(F)c1)c1-[n]1nnc(C)c1C2)=O ZYZQIAZMXMKALR-UHFFFAOYSA-N 0.000 description 1
- NZVBOTSQXACVLJ-UHFFFAOYSA-N CCOC(c(nc1)c2[n]1-c(ccc(OC)c1)c1-[n]1ncc(C)c1C2)=O Chemical compound CCOC(c(nc1)c2[n]1-c(ccc(OC)c1)c1-[n]1ncc(C)c1C2)=O NZVBOTSQXACVLJ-UHFFFAOYSA-N 0.000 description 1
- XKPJKXNBLXDANJ-UHFFFAOYSA-N CCOC(c(nc1)c2[n]1-c(ccc(OC)c1)c1-[n]1nnc(-c3ccccc3)c1C2)=O Chemical compound CCOC(c(nc1)c2[n]1-c(ccc(OC)c1)c1-[n]1nnc(-c3ccccc3)c1C2)=O XKPJKXNBLXDANJ-UHFFFAOYSA-N 0.000 description 1
- QWKWDGUSFIUGAR-UHFFFAOYSA-N CCOC(c(nc1)c2[n]1-c(ccc(OC)c1)c1-[n]1nnc(I)c1C2)=O Chemical compound CCOC(c(nc1)c2[n]1-c(ccc(OC)c1)c1-[n]1nnc(I)c1C2)=O QWKWDGUSFIUGAR-UHFFFAOYSA-N 0.000 description 1
- SYNDRZZAKOPOIS-UHFFFAOYSA-N CC[O](C)c(cc1)cc(-[n]2nnc(C(NN)=O)c2C2)c1NC2=O Chemical compound CC[O](C)c(cc1)cc(-[n]2nnc(C(NN)=O)c2C2)c1NC2=O SYNDRZZAKOPOIS-UHFFFAOYSA-N 0.000 description 1
- JPGZNAVHTLGORQ-UHFFFAOYSA-N COc(cc1)cc(-[n]2nnc(C=O)c2C2)c1-[n]1c2c(C#N)nc1 Chemical compound COc(cc1)cc(-[n]2nnc(C=O)c2C2)c1-[n]1c2c(C#N)nc1 JPGZNAVHTLGORQ-UHFFFAOYSA-N 0.000 description 1
- MTYQHNLELGYPLI-UHFFFAOYSA-N COc(cc1)cc(-[n]2nnc(COc(cc3)ccc3F)c2C2)c1-[n]1c2c(C#N)nc1 Chemical compound COc(cc1)cc(-[n]2nnc(COc(cc3)ccc3F)c2C2)c1-[n]1c2c(C#N)nc1 MTYQHNLELGYPLI-UHFFFAOYSA-N 0.000 description 1
- DEAGPJXNWWQNLG-UHFFFAOYSA-N COc(cc1)cc(-[n]2nnc(N)c2C2)c1NC2=O Chemical compound COc(cc1)cc(-[n]2nnc(N)c2C2)c1NC2=O DEAGPJXNWWQNLG-UHFFFAOYSA-N 0.000 description 1
- MRPKDIIWJWWHSI-UHFFFAOYSA-N COc1cc(OC)c(CN(CC(Nc(c2c3)ccc3Cl)=O)C2=O)cc1 Chemical compound COc1cc(OC)c(CN(CC(Nc(c2c3)ccc3Cl)=O)C2=O)cc1 MRPKDIIWJWWHSI-UHFFFAOYSA-N 0.000 description 1
- NONSIZWRHUUUTJ-MRVPVSSYSA-N C[C@H](CNNc(cc(cc1)OC)c1N)OC Chemical compound C[C@H](CNNc(cc(cc1)OC)c1N)OC NONSIZWRHUUUTJ-MRVPVSSYSA-N 0.000 description 1
- GSZGQBUPNMMNLN-UHFFFAOYSA-N Cc1c(CC(Nc2c-3cccc2)=O)[n]-3nn1 Chemical compound Cc1c(CC(Nc2c-3cccc2)=O)[n]-3nn1 GSZGQBUPNMMNLN-UHFFFAOYSA-N 0.000 description 1
- QGLIGNDLHDFWRD-UHFFFAOYSA-N Cc1c(Cc([n](cn2)-c(cc3)c-4cc3F)c2S(c2ccc(C)cc2)(=O)=O)[n]-4nn1 Chemical compound Cc1c(Cc([n](cn2)-c(cc3)c-4cc3F)c2S(c2ccc(C)cc2)(=O)=O)[n]-4nn1 QGLIGNDLHDFWRD-UHFFFAOYSA-N 0.000 description 1
- TXTFDYFURDPKJN-UHFFFAOYSA-N Cc1c(Cc2c(-c3ccccc3)nc[n]2-c(cc2)c-3cc2F)[n]-3nn1 Chemical compound Cc1c(Cc2c(-c3ccccc3)nc[n]2-c(cc2)c-3cc2F)[n]-3nn1 TXTFDYFURDPKJN-UHFFFAOYSA-N 0.000 description 1
- JBUHHHOXISISNK-UHFFFAOYSA-N Cc1c(Cc2c(-c3ccnc(C)c3)nc[n]2-c(cc2)c-3cc2F)[n]-3nn1 Chemical compound Cc1c(Cc2c(-c3ccnc(C)c3)nc[n]2-c(cc2)c-3cc2F)[n]-3nn1 JBUHHHOXISISNK-UHFFFAOYSA-N 0.000 description 1
- YAVKIAYTJNRPJB-UHFFFAOYSA-N Cc1c(Cc2c(-c3n[o]cn3)nc[n]2-c(cc2)c-3cc2F)[n]-3nn1 Chemical compound Cc1c(Cc2c(-c3n[o]cn3)nc[n]2-c(cc2)c-3cc2F)[n]-3nn1 YAVKIAYTJNRPJB-UHFFFAOYSA-N 0.000 description 1
- SLROMPQLSJFHFX-UHFFFAOYSA-N Cc1c(Cc2c(-c3nc(C)n[o]3)nc[n]2-c(cc2)c-3cc2OC)[n]-3nn1 Chemical compound Cc1c(Cc2c(-c3nc(C)n[o]3)nc[n]2-c(cc2)c-3cc2OC)[n]-3nn1 SLROMPQLSJFHFX-UHFFFAOYSA-N 0.000 description 1
- SIGLWYRKUDLWNS-UHFFFAOYSA-N Cc1c(Cc2c(-c3nc(C)n[o]3)nc[n]2-c2c-3cccc2)[n]-3nn1 Chemical compound Cc1c(Cc2c(-c3nc(C)n[o]3)nc[n]2-c2c-3cccc2)[n]-3nn1 SIGLWYRKUDLWNS-UHFFFAOYSA-N 0.000 description 1
- CXDHTFIQVLVLGA-UHFFFAOYSA-N Cc1c(Cc2c(C(Cl)=O)nc[n]2-c(cc2)c-3cc2F)[n]-3nn1 Chemical compound Cc1c(Cc2c(C(Cl)=O)nc[n]2-c(cc2)c-3cc2F)[n]-3nn1 CXDHTFIQVLVLGA-UHFFFAOYSA-N 0.000 description 1
- PDZJFPWVQWIJQH-UHFFFAOYSA-N Cc1c(Cc2c(C(N)=C=CO)nc[n]2-c2c-3cccc2)[n]-3nn1 Chemical compound Cc1c(Cc2c(C(N)=C=CO)nc[n]2-c2c-3cccc2)[n]-3nn1 PDZJFPWVQWIJQH-UHFFFAOYSA-N 0.000 description 1
- UPNGTIFLDCGAJP-UHFFFAOYSA-N Cc1c(Cc2c(C(O)=O)nc[n]2-c(cc2)c-3cc2F)[n]-3nn1 Chemical compound Cc1c(Cc2c(C(O)=O)nc[n]2-c(cc2)c-3cc2F)[n]-3nn1 UPNGTIFLDCGAJP-UHFFFAOYSA-N 0.000 description 1
- LPZFPHRTKOOKLX-UHFFFAOYSA-N Cc1nnc(C)[n]1C Chemical compound Cc1nnc(C)[n]1C LPZFPHRTKOOKLX-UHFFFAOYSA-N 0.000 description 1
- NNRDXBRBXKDKFH-UHFFFAOYSA-N N#Cc(nc1)c(C[n]2c(-c3c4)nnc2COc2ccccc2)[n]1-c3ccc4F Chemical compound N#Cc(nc1)c(C[n]2c(-c3c4)nnc2COc2ccccc2)[n]1-c3ccc4F NNRDXBRBXKDKFH-UHFFFAOYSA-N 0.000 description 1
- MYQFJMYJVJRSGP-UHFFFAOYSA-N O=C(c(cc(cc1)Cl)c1N1)OC1=O Chemical compound O=C(c(cc(cc1)Cl)c1N1)OC1=O MYQFJMYJVJRSGP-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
- C07D487/12—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 three hetero rings
- C07D487/14—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
- A61K31/13—Amines
-
- 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
- A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
- A61K31/27—Esters, e.g. nitroglycerine, selenocyanates of carbamic or thiocarbamic acids, meprobamate, carbachol, neostigmine
-
- 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
- A61K31/445—Non condensed piperidines, e.g. piperocaine
-
- 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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- 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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
-
- 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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
-
- 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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
- A61K31/5513—1,4-Benzodiazepines, e.g. diazepam or clozapine
- A61K31/5517—1,4-Benzodiazepines, e.g. diazepam or clozapine condensed with five-membered rings having nitrogen as a ring hetero atom, e.g. imidazobenzodiazepines, triazolam
-
- 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
- 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
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- 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
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- 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
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- 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
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Organic Chemistry (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Psychiatry (AREA)
- Emergency Medicine (AREA)
- Hospice & Palliative Care (AREA)
- Psychology (AREA)
- Addiction (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU2021200164A AU2021200164B2 (en) | 2015-06-19 | 2021-01-13 | Benzodiazepine derivatives, compositions, and methods for treating cognitive impairment |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201562182336P | 2015-06-19 | 2015-06-19 | |
| US62/182,336 | 2015-06-19 | ||
| PCT/US2016/038224 WO2016205739A1 (en) | 2015-06-19 | 2016-06-17 | Benzodiazepine derivatives, compositions, and methods for treating cognitive impairment |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2021200164A Division AU2021200164B2 (en) | 2015-06-19 | 2021-01-13 | Benzodiazepine derivatives, compositions, and methods for treating cognitive impairment |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AU2016279052A1 true AU2016279052A1 (en) | 2018-02-15 |
Family
ID=57546444
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2016279052A Abandoned AU2016279052A1 (en) | 2015-06-19 | 2016-06-17 | Benzodiazepine derivatives, compositions, and methods for treating cognitive impairment |
| AU2021200164A Active AU2021200164B2 (en) | 2015-06-19 | 2021-01-13 | Benzodiazepine derivatives, compositions, and methods for treating cognitive impairment |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2021200164A Active AU2021200164B2 (en) | 2015-06-19 | 2021-01-13 | Benzodiazepine derivatives, compositions, and methods for treating cognitive impairment |
Country Status (12)
| Country | Link |
|---|---|
| US (3) | US10815242B2 (enExample) |
| EP (1) | EP3310785B1 (enExample) |
| JP (2) | JP6987384B2 (enExample) |
| CN (2) | CN113264939A (enExample) |
| AU (2) | AU2016279052A1 (enExample) |
| CA (1) | CA2990004C (enExample) |
| EA (1) | EA036844B1 (enExample) |
| IL (1) | IL256354B (enExample) |
| MA (1) | MA42624A (enExample) |
| MX (2) | MX392119B (enExample) |
| WO (1) | WO2016205739A1 (enExample) |
| ZA (1) | ZA201800360B (enExample) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP4032889B1 (en) | 2013-12-20 | 2026-05-06 | Agenebio, Inc. | Benzodiazepine derivatives, compositions, and methods for treating cognitive impairment |
| EP3310785B1 (en) | 2015-06-19 | 2024-11-20 | Agenebio, Inc. | Benzodiazepine derivatives, compositions, and methods for treating cognitive impairment |
| US20180170941A1 (en) | 2016-12-19 | 2018-06-21 | Agenebio, Inc. | Benzodiazepine derivatives, compositions, and methods for treating cognitive impairment |
| AU2019288382B2 (en) * | 2018-06-19 | 2024-07-25 | Agenebio, Inc. | Benzodiazepine derivatives, compositions, and methods for treating cognitive impairment |
| US12636291B2 (en) * | 2019-02-13 | 2026-05-26 | Centre For Addiction And Mental Health | Compositions and methods relating to use of agonists of ALPHA5-containing GABAA receptors |
| IL294031A (en) * | 2019-12-19 | 2022-08-01 | Agenebio Inc | History of benzodiazepines, preparations and methods for the treatment of cognitive impairment |
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