JP2017535586A5 - - Google Patents
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- JP2017535586A5 JP2017535586A5 JP2017528154A JP2017528154A JP2017535586A5 JP 2017535586 A5 JP2017535586 A5 JP 2017535586A5 JP 2017528154 A JP2017528154 A JP 2017528154A JP 2017528154 A JP2017528154 A JP 2017528154A JP 2017535586 A5 JP2017535586 A5 JP 2017535586A5
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- JP
- Japan
- Prior art keywords
- substituted
- unsubstituted
- hydrogen
- compound
- alkyl
- 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.)
- Granted
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- 229910052739 hydrogen Inorganic materials 0.000 claims description 115
- 239000001257 hydrogen Substances 0.000 claims description 115
- 150000001875 compounds Chemical class 0.000 claims description 95
- 125000000217 alkyl group Chemical group 0.000 claims description 80
- 125000001072 heteroaryl group Chemical group 0.000 claims description 62
- 125000006706 (C3-C6) carbocyclyl group Chemical group 0.000 claims description 60
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 57
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 55
- 150000002431 hydrogen Chemical group 0.000 claims description 54
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 53
- 125000003118 aryl group Chemical group 0.000 claims description 52
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 25
- 208000035475 disorder Diseases 0.000 claims description 23
- 229910052736 halogen Inorganic materials 0.000 claims description 23
- 150000002367 halogens Chemical group 0.000 claims description 23
- 125000000623 heterocyclic group Chemical group 0.000 claims description 20
- 150000003839 salts Chemical class 0.000 claims description 15
- 239000003795 chemical substances by application Substances 0.000 claims description 11
- 210000003169 central nervous system Anatomy 0.000 claims description 10
- 229910052757 nitrogen Inorganic materials 0.000 claims description 10
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 10
- 125000004432 carbon atom Chemical group C* 0.000 claims description 9
- 239000002575 chemical warfare agent Substances 0.000 claims description 7
- 230000006378 damage Effects 0.000 claims description 6
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 6
- 239000008194 pharmaceutical composition Substances 0.000 claims description 6
- 206010010904 Convulsion Diseases 0.000 claims description 5
- 239000003691 GABA modulator Substances 0.000 claims description 5
- 150000003431 steroids Chemical class 0.000 claims description 5
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 4
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims description 4
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims description 4
- BTCSSZJGUNDROE-UHFFFAOYSA-N gamma-aminobutyric acid Chemical group NCCCC(O)=O BTCSSZJGUNDROE-UHFFFAOYSA-N 0.000 claims description 4
- 208000019022 Mood disease Diseases 0.000 claims description 3
- 208000016285 Movement disease Diseases 0.000 claims description 3
- 208000002193 Pain Diseases 0.000 claims description 3
- 208000007271 Substance Withdrawal Syndrome Diseases 0.000 claims description 3
- 208000009205 Tinnitus Diseases 0.000 claims description 3
- 208000030886 Traumatic Brain injury Diseases 0.000 claims description 3
- 206010048010 Withdrawal syndrome Diseases 0.000 claims description 3
- 208000029560 autism spectrum disease Diseases 0.000 claims description 3
- 208000010877 cognitive disease Diseases 0.000 claims description 3
- 230000036461 convulsion Effects 0.000 claims description 3
- 230000036407 pain Effects 0.000 claims description 3
- 208000022821 personality disease Diseases 0.000 claims description 3
- 201000000980 schizophrenia Diseases 0.000 claims description 3
- 208000019116 sleep disease Diseases 0.000 claims description 3
- 208000020685 sleep-wake disease Diseases 0.000 claims description 3
- 238000001228 spectrum Methods 0.000 claims description 3
- 201000009032 substance abuse Diseases 0.000 claims description 3
- 231100000736 substance abuse Toxicity 0.000 claims description 3
- 208000011117 substance-related disease Diseases 0.000 claims description 3
- 231100000886 tinnitus Toxicity 0.000 claims description 3
- 230000009529 traumatic brain injury Effects 0.000 claims description 3
- 208000026139 Memory disease Diseases 0.000 claims description 2
- 201000009916 Postpartum depression Diseases 0.000 claims description 2
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 claims description 2
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 claims description 2
- 125000004429 atom Chemical group 0.000 claims description 2
- 125000004452 carbocyclyl group Chemical group 0.000 claims description 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
- 201000010099 disease Diseases 0.000 claims description 2
- 125000001624 naphthyl group Chemical group 0.000 claims description 2
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 229930192474 thiophene Natural products 0.000 claims description 2
- 150000003852 triazoles Chemical class 0.000 claims description 2
- 230000002792 vascular Effects 0.000 claims description 2
- 125000003342 alkenyl group Chemical group 0.000 claims 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 6
- 239000000203 mixture Substances 0.000 claims 6
- 125000000304 alkynyl group Chemical group 0.000 claims 3
- 235000020083 shōchū Nutrition 0.000 claims 1
- 238000000034 method Methods 0.000 description 40
- 0 C[C@@]1(CC[C@@](C)([C@@]2CC3)[C@]4(C)C3CC(C)(C)CC4)C(C(c(cccc3)c3F)=O)=*C[C@]12I Chemical compound C[C@@]1(CC[C@@](C)([C@@]2CC3)[C@]4(C)C3CC(C)(C)CC4)C(C(c(cccc3)c3F)=O)=*C[C@]12I 0.000 description 16
- 229910052799 carbon Inorganic materials 0.000 description 7
- 206010002091 Anaesthesia Diseases 0.000 description 5
- 206010039897 Sedation Diseases 0.000 description 5
- 230000037005 anaesthesia Effects 0.000 description 5
- 210000005036 nerve Anatomy 0.000 description 5
- 230000036280 sedation Effects 0.000 description 5
- 208000027418 Wounds and injury Diseases 0.000 description 4
- 208000014674 injury Diseases 0.000 description 4
- 239000003814 drug Substances 0.000 description 3
- 229940124597 therapeutic agent Drugs 0.000 description 3
- 239000003053 toxin Substances 0.000 description 3
- 231100000765 toxin Toxicity 0.000 description 3
- 108700012359 toxins Proteins 0.000 description 3
- FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical compound C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 description 2
- 208000009575 Angelman syndrome Diseases 0.000 description 2
- 208000001914 Fragile X syndrome Diseases 0.000 description 2
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 2
- 208000006289 Rett Syndrome Diseases 0.000 description 2
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 2
- 230000001939 inductive effect Effects 0.000 description 2
- 238000001990 intravenous administration Methods 0.000 description 2
- 208000005809 status epilepticus Diseases 0.000 description 2
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 1
- 108010066676 Abrin Proteins 0.000 description 1
- LKPVDGWWWXFWJJ-ROOJVTFQSA-N CC(CC1)(C(CC2)C(c(cc3)cc(C)c3F)O)[C@@H]2C(CC2)[C@H]1[C@@](C)(CC1)[C@@H]2C[C@]1(C)O Chemical compound CC(CC1)(C(CC2)C(c(cc3)cc(C)c3F)O)[C@@H]2C(CC2)[C@H]1[C@@](C)(CC1)[C@@H]2C[C@]1(C)O LKPVDGWWWXFWJJ-ROOJVTFQSA-N 0.000 description 1
- SKKKXWBZVMFJFJ-YSDXZOGCSA-N CC(CC1)([C@@H](CC2)C(CC3)[C@H]1C(C)(CC1)[C@@H]3C[C@]1(C)O)C2C(c1cc(C)c(C)cc1)=O Chemical compound CC(CC1)([C@@H](CC2)C(CC3)[C@H]1C(C)(CC1)[C@@H]3C[C@]1(C)O)C2C(c1cc(C)c(C)cc1)=O SKKKXWBZVMFJFJ-YSDXZOGCSA-N 0.000 description 1
- SEVLRZGBSQUYHK-PPGGWLFVSA-N CC(CC1)([C@@H](CC2)C(CC3)[C@H]1[C@@](C)(CC1)C3C[C@]1(C)O)[C@H]2C(c(cc1)ccc1OC(F)(F)F)=O Chemical compound CC(CC1)([C@@H](CC2)C(CC3)[C@H]1[C@@](C)(CC1)C3C[C@]1(C)O)[C@H]2C(c(cc1)ccc1OC(F)(F)F)=O SEVLRZGBSQUYHK-PPGGWLFVSA-N 0.000 description 1
- OYCAXWJZOXEPRE-SKCDODSBSA-N CC1C(C)=CC(C([C@@H](CC2)[C@@](C)(CC3)[C@@H]2C(CC2)[C@H]3[C@@](C)(CC3)[C@@H]2C[C@]3(C)O)=O)=CC1 Chemical compound CC1C(C)=CC(C([C@@H](CC2)[C@@](C)(CC3)[C@@H]2C(CC2)[C@H]3[C@@](C)(CC3)[C@@H]2C[C@]3(C)O)=O)=CC1 OYCAXWJZOXEPRE-SKCDODSBSA-N 0.000 description 1
- QUECWXYHZYXRNL-AKMKAEOHSA-N CCC(CC1)([C@](C)(CC2)C(C)(CC3)C2C(C2C(C4)C4C(N(C)C)=CC2)=O)[C@@]3(C)C(C)(CC2)[C@H]1C[C@]2(C)O Chemical compound CCC(CC1)([C@](C)(CC2)C(C)(CC3)C2C(C2C(C4)C4C(N(C)C)=CC2)=O)[C@@]3(C)C(C)(CC2)[C@H]1C[C@]2(C)O QUECWXYHZYXRNL-AKMKAEOHSA-N 0.000 description 1
- LBMMGQNKAKKYFQ-INLHBMBJSA-N CCC(CC[C@](C)(C1)[O]=C)(C(C)CC2)[C@@]1(C)CCC[C@H](CC1)[C@@]2(C)C1C(c(cc1)cc(C)c1F)=O Chemical compound CCC(CC[C@](C)(C1)[O]=C)(C(C)CC2)[C@@]1(C)CCC[C@H](CC1)[C@@]2(C)C1C(c(cc1)cc(C)c1F)=O LBMMGQNKAKKYFQ-INLHBMBJSA-N 0.000 description 1
- PSLHTBSZNHOGDF-JYQNWREZSA-N C[C@@H](CC1)C[C@@H](CC2)[C@H]1[C@@H](CC1)[C@@H]2[C@H](CC2)[C@@]1(C)[C@H]2C(c1ccc(C)cc1)=N Chemical compound C[C@@H](CC1)C[C@@H](CC2)[C@H]1[C@@H](CC1)[C@@H]2[C@H](CC2)[C@@]1(C)[C@H]2C(c1ccc(C)cc1)=N PSLHTBSZNHOGDF-JYQNWREZSA-N 0.000 description 1
- SHQUFCQNCSMJHQ-LAWOIKPDSA-N C[C@@H](CCC1(C)[C@@H]2C(CC3)CCC[C@H](C(c4ccc(C)c(F)c4)O)C(C)CC2)C[C@@]13N Chemical compound C[C@@H](CCC1(C)[C@@H]2C(CC3)CCC[C@H](C(c4ccc(C)c(F)c4)O)C(C)CC2)C[C@@]13N SHQUFCQNCSMJHQ-LAWOIKPDSA-N 0.000 description 1
- NJZLRUALCFJKFJ-SUSYSVFISA-N C[C@@](CC[C@@H](C1CC2)C(CC[C@](C)(C3)O)C23N)(C(CC2)C(c3ccccc3I)=C)[C@]12N Chemical compound C[C@@](CC[C@@H](C1CC2)C(CC[C@](C)(C3)O)C23N)(C(CC2)C(c3ccccc3I)=C)[C@]12N NJZLRUALCFJKFJ-SUSYSVFISA-N 0.000 description 1
- JDJYBSSMKXYWBA-ROEXDCMRSA-N C[C@H](CC1)[C@](C)(CC[C@@H](CCC2)[C@@H](CC3)[C@@H]2C[C@]3(C)O)[C@H]1C(c(cc1)ccc1OC)=O Chemical compound C[C@H](CC1)[C@](C)(CC[C@@H](CCC2)[C@@H](CC3)[C@@H]2C[C@]3(C)O)[C@H]1C(c(cc1)ccc1OC)=O JDJYBSSMKXYWBA-ROEXDCMRSA-N 0.000 description 1
- BOBXFKPVTXBFDX-XKKDOOBNSA-N C[C@](CC1)([C@@H](CC2)C(CC3)[C@H]1[C@@H]1[C@H]3CC(C)(C)CC1)[C@H]2C(c1cnc[nH]1)=[U] Chemical compound C[C@](CC1)([C@@H](CC2)C(CC3)[C@H]1[C@@H]1[C@H]3CC(C)(C)CC1)[C@H]2C(c1cnc[nH]1)=[U] BOBXFKPVTXBFDX-XKKDOOBNSA-N 0.000 description 1
- YDUKUYRDNOIQBA-LSBZSBGNSA-N C[C@](CC1)([C@@H](CC2)[C@H](CC3)[C@H]1[C@@](C)(CC1)[C@@H]3C[C@]1(C)O)[C@H]2C(c(cc1)ccc1Cl)=O Chemical compound C[C@](CC1)([C@@H](CC2)[C@H](CC3)[C@H]1[C@@](C)(CC1)[C@@H]3C[C@]1(C)O)[C@H]2C(c(cc1)ccc1Cl)=O YDUKUYRDNOIQBA-LSBZSBGNSA-N 0.000 description 1
- UXTNTNONGLSRPS-RGYBDQPCSA-N C[C@](CC1)([C@@H](CC2)[C@H](CC3)[C@H]1[C@@](C)(CC1)[C@H]3C[C@]1(C)O)[C@H]2C(c(cc1)cc(cc2)c1cc2OC)=O Chemical compound C[C@](CC1)([C@@H](CC2)[C@H](CC3)[C@H]1[C@@](C)(CC1)[C@H]3C[C@]1(C)O)[C@H]2C(c(cc1)cc(cc2)c1cc2OC)=O UXTNTNONGLSRPS-RGYBDQPCSA-N 0.000 description 1
- IOSGZVVLXFCLDP-SCNDPVEVSA-N C[C@](CC1)([C@@H](CC2)[C@H](CC3)[C@H]1[C@@](C)(CC1)[C@H]3C[C@]1(C)O)[C@H]2C(c1cccc([I]=C)c1)=O Chemical compound C[C@](CC1)([C@@H](CC2)[C@H](CC3)[C@H]1[C@@](C)(CC1)[C@H]3C[C@]1(C)O)[C@H]2C(c1cccc([I]=C)c1)=O IOSGZVVLXFCLDP-SCNDPVEVSA-N 0.000 description 1
- LEOLRQXBZFHWNP-XIGAYJBWSA-N C[C@](CC1)([C@@H](CC2)[C@H](CC3)[C@H]1[C@@](C)(CC[C@](C)(C1)O)[C@]31N)[C@H]2C(c1ccc(C)cc1)=C Chemical compound C[C@](CC1)([C@@H](CC2)[C@H](CC3)[C@H]1[C@@](C)(CC[C@](C)(C1)O)[C@]31N)[C@H]2C(c1ccc(C)cc1)=C LEOLRQXBZFHWNP-XIGAYJBWSA-N 0.000 description 1
- SIUDUIXAPIRZAZ-BFNNADBGSA-N C[C@](CC1)([C@@H](CC2)[C@H](CC3)[C@H]1[C@@](C)(CC[C@](C)(C1)[N+]([O-])=O)[C@]31N)[C@H]2C(c1c(C)cccc1)=O Chemical compound C[C@](CC1)([C@@H](CC2)[C@H](CC3)[C@H]1[C@@](C)(CC[C@](C)(C1)[N+]([O-])=O)[C@]31N)[C@H]2C(c1c(C)cccc1)=O SIUDUIXAPIRZAZ-BFNNADBGSA-N 0.000 description 1
- 208000028698 Cognitive impairment Diseases 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical group [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 108010039491 Ricin Proteins 0.000 description 1
- DYAHQFWOVKZOOW-UHFFFAOYSA-N Sarin Chemical compound CC(C)OP(C)(F)=O DYAHQFWOVKZOOW-UHFFFAOYSA-N 0.000 description 1
- GRXKLBBBQUKJJZ-UHFFFAOYSA-N Soman Chemical compound CC(C)(C)C(C)OP(C)(F)=O GRXKLBBBQUKJJZ-UHFFFAOYSA-N 0.000 description 1
- 208000005392 Spasm Diseases 0.000 description 1
- 206010044565 Tremor Diseases 0.000 description 1
- PJVJTCIRVMBVIA-JTQLQIEISA-N [dimethylamino(ethoxy)phosphoryl]formonitrile Chemical compound CCO[P@@](=O)(C#N)N(C)C PJVJTCIRVMBVIA-JTQLQIEISA-N 0.000 description 1
- RFRXIWQYSOIBDI-UHFFFAOYSA-N benzarone Chemical compound CCC=1OC2=CC=CC=C2C=1C(=O)C1=CC=C(O)C=C1 RFRXIWQYSOIBDI-UHFFFAOYSA-N 0.000 description 1
- 125000002619 bicyclic group Chemical group 0.000 description 1
- 206010015037 epilepsy Diseases 0.000 description 1
- 201000006517 essential tremor Diseases 0.000 description 1
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 description 1
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 description 1
- 206010027175 memory impairment Diseases 0.000 description 1
- 230000002151 myoclonic effect Effects 0.000 description 1
- 230000001537 neural effect Effects 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- RPQXVSUAYFXFJA-HGRQIUPRSA-N saxitoxin Chemical compound NC(=O)OC[C@@H]1N=C(N)N2CCC(O)(O)[C@@]22N=C(N)N[C@@H]12 RPQXVSUAYFXFJA-HGRQIUPRSA-N 0.000 description 1
- RPQXVSUAYFXFJA-UHFFFAOYSA-N saxitoxin hydrate Natural products NC(=O)OCC1N=C(N)N2CCC(O)(O)C22NC(N)=NC12 RPQXVSUAYFXFJA-UHFFFAOYSA-N 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 208000019553 vascular disease Diseases 0.000 description 1
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2021090965A JP7186259B2 (ja) | 2014-11-27 | 2021-05-31 | Cns障害を処置するための組成物および方法 |
| JP2022189056A JP2023022187A (ja) | 2014-11-27 | 2022-11-28 | Cns障害を処置するための組成物および方法 |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN2014092369 | 2014-11-27 | ||
| CNPCT/CN2014/092369 | 2014-11-27 | ||
| PCT/CN2015/095765 WO2016082789A1 (en) | 2014-11-27 | 2015-11-27 | Compositions and methods for treating cns disorders |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2021090965A Division JP7186259B2 (ja) | 2014-11-27 | 2021-05-31 | Cns障害を処置するための組成物および方法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2017535586A JP2017535586A (ja) | 2017-11-30 |
| JP2017535586A5 true JP2017535586A5 (cg-RX-API-DMAC7.html) | 2019-01-10 |
| JP6893173B2 JP6893173B2 (ja) | 2021-06-23 |
Family
ID=56073637
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017528154A Active JP6893173B2 (ja) | 2014-11-27 | 2015-11-27 | Cns障害を処置するための組成物および方法 |
| JP2021090965A Active JP7186259B2 (ja) | 2014-11-27 | 2021-05-31 | Cns障害を処置するための組成物および方法 |
| JP2022189056A Pending JP2023022187A (ja) | 2014-11-27 | 2022-11-28 | Cns障害を処置するための組成物および方法 |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2021090965A Active JP7186259B2 (ja) | 2014-11-27 | 2021-05-31 | Cns障害を処置するための組成物および方法 |
| JP2022189056A Pending JP2023022187A (ja) | 2014-11-27 | 2022-11-28 | Cns障害を処置するための組成物および方法 |
Country Status (16)
| Country | Link |
|---|---|
| US (4) | US10774108B2 (cg-RX-API-DMAC7.html) |
| EP (2) | EP3719029A1 (cg-RX-API-DMAC7.html) |
| JP (3) | JP6893173B2 (cg-RX-API-DMAC7.html) |
| CY (1) | CY1123200T1 (cg-RX-API-DMAC7.html) |
| DK (1) | DK3224269T3 (cg-RX-API-DMAC7.html) |
| ES (1) | ES2793237T3 (cg-RX-API-DMAC7.html) |
| HR (1) | HRP20200840T1 (cg-RX-API-DMAC7.html) |
| HU (1) | HUE049014T2 (cg-RX-API-DMAC7.html) |
| LT (1) | LT3224269T (cg-RX-API-DMAC7.html) |
| ME (1) | ME03749B (cg-RX-API-DMAC7.html) |
| PL (1) | PL3224269T3 (cg-RX-API-DMAC7.html) |
| PT (1) | PT3224269T (cg-RX-API-DMAC7.html) |
| RS (1) | RS60343B1 (cg-RX-API-DMAC7.html) |
| SI (1) | SI3224269T1 (cg-RX-API-DMAC7.html) |
| SM (1) | SMT202000276T1 (cg-RX-API-DMAC7.html) |
| WO (1) | WO2016082789A1 (cg-RX-API-DMAC7.html) |
Families Citing this family (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2014528485A (ja) | 2011-10-14 | 2014-10-27 | セージ セラピューティクス, インコーポレイテッド | 3,3−二置換19−ノルプレグナン化合物およびその使用 |
| IL294306B2 (en) | 2012-08-21 | 2024-01-01 | Sage Therapeutics Inc | Methods of treating epilepsy or status epilepticus |
| WO2014169836A1 (en) | 2013-04-17 | 2014-10-23 | Sage Therapeutics, Inc. | 19-nor neuroactive steroids and methods of use thereof |
| WO2014169831A1 (en) | 2013-04-17 | 2014-10-23 | Sage Therapeutics, Inc. | 19-nor c3,3-disubstituted c21-c-bound heteroaryl steroids and methods of use thereof |
| AU2014256228C1 (en) | 2013-04-17 | 2017-09-14 | Sage Therapeutics, Inc. | 19-nor neuroactive steroids and methods of use thereof |
| RS58297B1 (sr) | 2013-04-17 | 2019-03-29 | Sage Therapeutics Inc | 19-nor c3,3-disupstituisani c21-n-pirazolil steroidi i postupci za njihovu upotrebu |
| BR112016000975B1 (pt) | 2013-07-19 | 2020-10-06 | Sage Therapeutics, Inc. | Compostos esteróides neuroativos e composições compreendendo os mesmos |
| RS61370B1 (sr) | 2013-08-23 | 2021-02-26 | Sage Therapeutics Inc | Neuroaktivni steroidi, njihove kompozicije i upotreba |
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| AU2018392093B2 (en) | 2017-12-22 | 2024-02-01 | Sage Therapeutics, Inc. | Compositions and methods for treating CNS disorders |
| MA51568A (fr) | 2018-01-12 | 2021-04-21 | Sage Therapeutics Inc | Composés aza-, oxa et thia-pregnan-20-one-3.alpha.-ol s'utilisant dans le traitement de troubles du système nerveux central |
| JP2021527092A (ja) | 2018-06-12 | 2021-10-11 | セージ セラピューティクス, インコーポレイテッド | 19−ノルc3,3−二置換c21−n−ピラゾリルステロイドおよびその使用方法 |
| DK3864022T3 (da) | 2018-10-12 | 2023-12-18 | Sage Therapeutics Inc | Neuroaktive steroider substitueret i Position 10 med en cyklisk gruppe til anvendelse til behandlingen af CNS-lidelser |
| CA3116892A1 (en) | 2018-10-19 | 2020-04-23 | Sage Therapeutics, Inc. | 9(11)-unsaturated neuroactive steroids and their methods of use |
| IL312610A (en) | 2018-12-05 | 2024-07-01 | Sage Therapeutics Inc | Neuroactive steroids and methods of using them |
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| TW202523658A (zh) | 2019-05-24 | 2025-06-16 | 美商賽吉醫療公司 | 化合物、組合物及使用方法 |
| BR112021024033A2 (pt) | 2019-05-31 | 2022-02-08 | Sage Therapeutics Inc | Esteroides neuroativos e suas composições |
| CA3144701A1 (en) | 2019-06-27 | 2020-12-30 | Sage Therapeutics, Inc. | Compositions and methods for treating cns disorders |
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| KR20220038680A (ko) | 2019-06-27 | 2022-03-29 | 세이지 테라퓨틱스, 인크. | Cns 장애를 치료하기 위한 조성물 및 방법 |
| EP4069250A1 (en) | 2019-12-05 | 2022-10-12 | Sage Therapeutics, Inc. | A 19-nor c3,3-disubstituted c21-n-pyrazolyl steroid and methods of use thereof |
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| US20230414636A1 (en) | 2020-03-25 | 2023-12-28 | Sage Therapeutics, Inc. | Use of gabaa modulators for treatment of respiratory conditions |
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| CN116367827A (zh) | 2020-07-20 | 2023-06-30 | 萨奇治疗股份有限公司 | 19-去甲-c3,3-二取代-c21-n-吡唑基类固醇的制剂及其使用方法 |
| WO2022115381A1 (en) | 2020-11-25 | 2022-06-02 | Sage Therapeutics, Onc. | Compositions and methods for treating cns disorders cross reference to related application |
| KR20230136599A (ko) | 2021-01-28 | 2023-09-26 | 세이지 테라퓨틱스, 인크. | 성 기능장애의 치료를 위한 신경활성 스테로이드의용도 |
| US20240148756A1 (en) | 2021-02-18 | 2024-05-09 | Sage Therapeutics, Inc. | Use of neuroactive steroid for treatment of sexual dysfunction |
| KR20230158033A (ko) | 2021-03-17 | 2023-11-17 | 세이지 테라퓨틱스, 인크. | 주요 우울 장애의 치료를 위한 19-노르 c3,3-이치환된 c21-n-피라졸릴 스테로이드 |
| JP2024513581A (ja) | 2021-04-12 | 2024-03-26 | セージ セラピューティクス, インコーポレイテッド | 本態性振戦の治療 |
| CN117580580A (zh) | 2021-04-29 | 2024-02-20 | 萨奇治疗股份有限公司 | 用于在哺乳期女性中治疗重度抑郁障碍和产后抑郁症的神经活性类固醇 |
| TW202308654A (zh) | 2021-04-29 | 2023-03-01 | 美商賽吉醫療公司 | 19-nor-c3,3-二取代c21-n-吡唑基類固醇及其使用方法 |
-
2015
- 2015-11-27 SI SI201531219T patent/SI3224269T1/sl unknown
- 2015-11-27 HU HUE15862506A patent/HUE049014T2/hu unknown
- 2015-11-27 HR HRP20200840TT patent/HRP20200840T1/hr unknown
- 2015-11-27 EP EP20159317.5A patent/EP3719029A1/en not_active Ceased
- 2015-11-27 PT PT158625061T patent/PT3224269T/pt unknown
- 2015-11-27 US US15/531,313 patent/US10774108B2/en active Active
- 2015-11-27 ES ES15862506T patent/ES2793237T3/es active Active
- 2015-11-27 ME MEP-2020-105A patent/ME03749B/me unknown
- 2015-11-27 RS RS20200610A patent/RS60343B1/sr unknown
- 2015-11-27 SM SM20200276T patent/SMT202000276T1/it unknown
- 2015-11-27 LT LTEP15862506.1T patent/LT3224269T/lt unknown
- 2015-11-27 PL PL15862506T patent/PL3224269T3/pl unknown
- 2015-11-27 WO PCT/CN2015/095765 patent/WO2016082789A1/en not_active Ceased
- 2015-11-27 EP EP15862506.1A patent/EP3224269B1/en active Active
- 2015-11-27 DK DK15862506.1T patent/DK3224269T3/da active
- 2015-11-27 JP JP2017528154A patent/JP6893173B2/ja active Active
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2020
- 2020-02-25 US US16/800,053 patent/US20210017218A1/en not_active Abandoned
- 2020-05-26 CY CY20201100480T patent/CY1123200T1/el unknown
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2021
- 2021-05-31 JP JP2021090965A patent/JP7186259B2/ja active Active
-
2022
- 2022-10-04 US US17/959,592 patent/US11945836B2/en active Active
- 2022-11-28 JP JP2022189056A patent/JP2023022187A/ja active Pending
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2024
- 2024-02-20 US US18/581,595 patent/US20250042934A1/en active Pending
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