JP2011506551A5 - - Google Patents
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- JP2011506551A5 JP2011506551A5 JP2010538692A JP2010538692A JP2011506551A5 JP 2011506551 A5 JP2011506551 A5 JP 2011506551A5 JP 2010538692 A JP2010538692 A JP 2010538692A JP 2010538692 A JP2010538692 A JP 2010538692A JP 2011506551 A5 JP2011506551 A5 JP 2011506551A5
- Authority
- JP
- Japan
- Prior art keywords
- inden
- dihydro
- propanesulfonamide
- oxy
- pyridinyl
- 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.)
- Withdrawn
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- 150000001875 compounds Chemical class 0.000 claims 6
- 150000003839 salts Chemical class 0.000 claims 5
- 239000008194 pharmaceutical composition Substances 0.000 claims 4
- -1 6-methyl-3-pyridinyl Chemical group 0.000 claims 2
- 150000001408 amides Chemical class 0.000 claims 2
- 201000010099 disease Diseases 0.000 claims 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 229910052736 halogen Inorganic materials 0.000 claims 2
- 125000004076 pyridyl group Chemical group 0.000 claims 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 1
- 102000018899 Glutamate Receptors Human genes 0.000 claims 1
- 108010027915 Glutamate Receptors Proteins 0.000 claims 1
- 241000124008 Mammalia Species 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- DAPVXZCXLJGPGR-INIZCTEOSA-N n-[(2s)-5-(2-methylpyridin-3-yl)oxy-2,3-dihydro-1h-inden-2-yl]propane-2-sulfonamide Chemical compound C([C@@H](CC1=C2)NS(=O)(=O)C(C)C)C1=CC=C2OC1=CC=CN=C1C DAPVXZCXLJGPGR-INIZCTEOSA-N 0.000 claims 1
- BJYXPIPVEZLRSL-SFHVURJKSA-N n-[(2s)-5-(2-pyridin-3-ylethoxy)-2,3-dihydro-1h-inden-2-yl]propane-2-sulfonamide Chemical compound C([C@@H](CC1=C2)NS(=O)(=O)C(C)C)C1=CC=C2OCCC1=CC=CN=C1 BJYXPIPVEZLRSL-SFHVURJKSA-N 0.000 claims 1
- HOKNDXYFTLPJGK-IBGZPJMESA-N n-[(2s)-5-(3-pyridin-3-ylpropoxy)-2,3-dihydro-1h-inden-2-yl]propane-2-sulfonamide Chemical compound C([C@@H](CC1=C2)NS(=O)(=O)C(C)C)C1=CC=C2OCCCC1=CC=CN=C1 HOKNDXYFTLPJGK-IBGZPJMESA-N 0.000 claims 1
- XBZNOWAESMBPKI-INIZCTEOSA-N n-[(2s)-5-(4-methylpyridin-2-yl)oxy-2,3-dihydro-1h-inden-2-yl]propane-2-sulfonamide Chemical compound C([C@@H](CC1=C2)NS(=O)(=O)C(C)C)C1=CC=C2OC1=CC(C)=CC=N1 XBZNOWAESMBPKI-INIZCTEOSA-N 0.000 claims 1
- HWIRDBDGDAZUSF-INIZCTEOSA-N n-[(2s)-5-(4-methylpyridin-3-yl)oxy-2,3-dihydro-1h-inden-2-yl]propane-2-sulfonamide Chemical compound C([C@@H](CC1=C2)NS(=O)(=O)C(C)C)C1=CC=C2OC1=CN=CC=C1C HWIRDBDGDAZUSF-INIZCTEOSA-N 0.000 claims 1
- NYZWMVDYYWUUBV-HNNXBMFYSA-N n-[(2s)-5-(5-fluoropyridin-2-yl)oxy-2,3-dihydro-1h-inden-2-yl]propane-2-sulfonamide Chemical compound C([C@@H](CC1=C2)NS(=O)(=O)C(C)C)C1=CC=C2OC1=CC=C(F)C=N1 NYZWMVDYYWUUBV-HNNXBMFYSA-N 0.000 claims 1
- XEKPDKCRFHDZGO-INIZCTEOSA-N n-[(2s)-5-(5-methylpyridin-2-yl)oxy-2,3-dihydro-1h-inden-2-yl]propane-2-sulfonamide Chemical compound C([C@@H](CC1=C2)NS(=O)(=O)C(C)C)C1=CC=C2OC1=CC=C(C)C=N1 XEKPDKCRFHDZGO-INIZCTEOSA-N 0.000 claims 1
- YHPFRPDHQVGPND-INIZCTEOSA-N n-[(2s)-5-(6-methylpyridin-2-yl)oxy-2,3-dihydro-1h-inden-2-yl]propane-2-sulfonamide Chemical compound C([C@@H](CC1=C2)NS(=O)(=O)C(C)C)C1=CC=C2OC1=CC=CC(C)=N1 YHPFRPDHQVGPND-INIZCTEOSA-N 0.000 claims 1
- RPJZNPHGRUNBPZ-INIZCTEOSA-N n-[(2s)-5-(6-methylpyridin-3-yl)oxy-2,3-dihydro-1h-inden-2-yl]propane-2-sulfonamide Chemical compound C([C@@H](CC1=C2)NS(=O)(=O)C(C)C)C1=CC=C2OC1=CC=C(C)N=C1 RPJZNPHGRUNBPZ-INIZCTEOSA-N 0.000 claims 1
- XUYUPGYCAGXEFV-KRWDZBQOSA-N n-[(2s)-5-(pyridin-2-ylmethoxy)-2,3-dihydro-1h-inden-2-yl]propane-2-sulfonamide Chemical compound C([C@@H](CC1=C2)NS(=O)(=O)C(C)C)C1=CC=C2OCC1=CC=CC=N1 XUYUPGYCAGXEFV-KRWDZBQOSA-N 0.000 claims 1
- JHHVJIWYPMDCAS-KRWDZBQOSA-N n-[(2s)-5-(pyridin-3-ylmethoxy)-2,3-dihydro-1h-inden-2-yl]propane-2-sulfonamide Chemical compound C([C@@H](CC1=C2)NS(=O)(=O)C(C)C)C1=CC=C2OCC1=CC=CN=C1 JHHVJIWYPMDCAS-KRWDZBQOSA-N 0.000 claims 1
- UWJLKXSBOMSXSO-KRWDZBQOSA-N n-[(2s)-5-(pyridin-4-ylmethoxy)-2,3-dihydro-1h-inden-2-yl]propane-2-sulfonamide Chemical compound C([C@@H](CC1=C2)NS(=O)(=O)C(C)C)C1=CC=C2OCC1=CC=NC=C1 UWJLKXSBOMSXSO-KRWDZBQOSA-N 0.000 claims 1
- WGZQDXIQHQWHDP-IBGZPJMESA-N n-[(2s)-5-[(2,6-dimethylpyridin-3-yl)methoxy]-2,3-dihydro-1h-inden-2-yl]propane-2-sulfonamide Chemical compound C([C@@H](CC1=C2)NS(=O)(=O)C(C)C)C1=CC=C2OCC1=CC=C(C)N=C1C WGZQDXIQHQWHDP-IBGZPJMESA-N 0.000 claims 1
- AYXKAGSPZCXCNU-SFHVURJKSA-N n-[(2s)-5-[(2-methylpyridin-3-yl)methoxy]-2,3-dihydro-1h-inden-2-yl]propane-2-sulfonamide Chemical compound C([C@@H](CC1=C2)NS(=O)(=O)C(C)C)C1=CC=C2OCC1=CC=CN=C1C AYXKAGSPZCXCNU-SFHVURJKSA-N 0.000 claims 1
- UAHKRWCXIJLXOZ-SFHVURJKSA-N n-[(2s)-5-[(2-methylpyridin-4-yl)methoxy]-2,3-dihydro-1h-inden-2-yl]propane-2-sulfonamide Chemical compound C([C@@H](CC1=C2)NS(=O)(=O)C(C)C)C1=CC=C2OCC1=CC=NC(C)=C1 UAHKRWCXIJLXOZ-SFHVURJKSA-N 0.000 claims 1
- RLASHXSMQMFIRE-SFHVURJKSA-N n-[(2s)-5-[(6-methylpyridin-3-yl)methoxy]-2,3-dihydro-1h-inden-2-yl]propane-2-sulfonamide Chemical compound C([C@@H](CC1=C2)NS(=O)(=O)C(C)C)C1=CC=C2OCC1=CC=C(C)N=C1 RLASHXSMQMFIRE-SFHVURJKSA-N 0.000 claims 1
- CEBJYMAYHIRLRM-FQEVSTJZSA-N n-[(2s)-5-[3-(6-methylpyridin-3-yl)propoxy]-2,3-dihydro-1h-inden-2-yl]propane-2-sulfonamide Chemical compound C([C@@H](CC1=C2)NS(=O)(=O)C(C)C)C1=CC=C2OCCCC1=CC=C(C)N=C1 CEBJYMAYHIRLRM-FQEVSTJZSA-N 0.000 claims 1
- RCVRBPSRLCNRMT-INIZCTEOSA-N n-[(2s)-5-phenoxy-2,3-dihydro-1h-inden-2-yl]propane-2-sulfonamide Chemical compound C([C@@H](CC1=C2)NS(=O)(=O)C(C)C)C1=CC=C2OC1=CC=CC=C1 RCVRBPSRLCNRMT-INIZCTEOSA-N 0.000 claims 1
- GSOHMVNULNXMNY-HNNXBMFYSA-N n-[(2s)-5-pyridin-2-yloxy-2,3-dihydro-1h-inden-2-yl]propane-2-sulfonamide Chemical compound C([C@@H](CC1=C2)NS(=O)(=O)C(C)C)C1=CC=C2OC1=CC=CC=N1 GSOHMVNULNXMNY-HNNXBMFYSA-N 0.000 claims 1
- 230000004770 neurodegeneration Effects 0.000 claims 1
- 208000015122 neurodegenerative disease Diseases 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
Claims (11)
- nが0である、請求項1に記載の化合物。
- R2がHであり、nが1、2または3である、請求項1に記載の化合物。
- R1が、場合によりハロゲンで、または一つもしくは二つのC1−4アルキルで置換されていてもよいピリジルである、請求項1〜3のいずれか一項に記載の化合物。
- N−[(2S)−5−(フェニルオキシ)−2,3−ジヒドロ−1H−インデン−2−イル]−2−プロパンスルホンアミド;
N−{(2S)−5−[(6−メチル−3−ピリジニル)オキシ]−2,3−ジヒドロ−1H−インデン−2−イル}−2−プロパンスルホンアミド;
N−[(2S)−5−(2−ピリジニルオキシ)−2,3−ジヒドロ−1H−インデン−2−イル]−2−プロパンスルホンアミド;
N−{(2S)−5−[(5−フルオロ−2−ピリジニル)オキシ]−2,3−ジヒドロ−1H−インデン−2−イル}−2−プロパンスルホンアミド;
N−{(2S)−5−[(2−メチル−3−ピリジニル)オキシ]−2,3−ジヒドロ−1H−インデン−2−イル}−2−プロパンスルホンアミド;
N−{(2S)−5−[(4−メチル−3−ピリジニル)オキシ]−2,3−ジヒドロ−1H−インデン−2−イル}−2−プロパンスルホンアミド;
N−{(2S)−5−[(6−メチル−2−ピリジニル)オキシ]−2,3−ジヒドロ−1H−インデン−2−イル}−2−プロパンスルホンアミド;
N−{(2S)−5−[(5−メチル−2−ピリジニル)オキシ]−2,3−ジヒドロ−1H−インデン−2−イル}−2−プロパンスルホンアミド;
N−{(2S)−5−[(4−メチル−2−ピリジニル)オキシ]−2,3−ジヒドロ−1H−インデン−2−イル}−2−プロパンスルホンアミド;
である化合物、またはその塩。 - N−{(2S)−5−[(2−ピリジニルメチル)オキシ]−2,3−ジヒドロ−1H−インデン−2−イル}−2−プロパンスルホンアミド;
N−((2S)−5−{[(2−メチル−3−ピリジニル)メチル]オキシ}−2,3−ジヒドロ−1H−インデン−2−イル)−2−プロパンスルホンアミド;
N−((2S)−5−{[(6−メチル−3−ピリジニル)メチル]オキシ}−2,3−ジヒドロ−1H−インデン−2−イル)−2−プロパンスルホンアミド;
N−{(2S)−5−[(3−ピリジニルメチル)オキシ]−2,3−ジヒドロ−1H−インデン−2−イル}−2−プロパンスルホンアミド;
N−((2S)−5−{[3−(3−ピリジニル)プロピル]オキシ}−2,3−ジヒドロ−1H−インデン−2−イル)−2−プロパンスルホンアミド;
N−((2S)−5−{[3−(6−メチル−3−ピリジニル)プロピル]オキシ}−2,3−ジヒドロ−1H−インデン−2−イル)−2−プロパンスルホンアミド;
N−((2S)−5−{[2−(3−ピリジニル)エチル]オキシ}−2,3−ジヒドロ−1H−インデン−2−イル)−2−プロパンスルホンアミド;
N−((2S)−5−{[(2,6−ジメチル−3−ピリジニル)メチル]オキシ}−2,3−ジヒドロ−1H−インデン−2−イル)−2−プロパンスルホンアミド;
N−{(2S)−5−[(4−ピリジニルメチル)オキシ]−2,3−ジヒドロ−1H−インデン−2−イル}−2−プロパンスルホンアミド;
N−((2S)−5−{[(2−メチル−4−ピリジニル)メチル]オキシ}−2,3−ジヒドロ−1H−インデン−2−イル)−2−プロパンスルホンアミド;
N−((2S)−5−{[(1S)−1−(6−メチル−3−ピリジニル)エチル]オキシ}−2,3−ジヒドロ−1H−インデン−2−イル)−2−プロパンスルホンアミド;
N−((2S)−5−{[(1R)−1−(6−メチル−3−ピリジニル)エチル]オキシ}−2,3−ジヒドロ−1H−インデン−2−イル)−2−プロパンスルホンアミド;
である化合物、またはその塩。 - 請求項1〜6のいずれか一項に記載の化合物、またはその薬学上許容可能な塩。
- 請求項7に記載の化合物またはその薬学上許容可能な塩を含んでなる医薬組成物。
- 少なくとも一種の薬学上許容可能な担体または希釈剤をさらに含有する、請求項8に記載の医薬組成物。
- 哺乳動物におけるグルタミン酸受容体機能の低下または不均衡に起因する疾患または状態の治療における使用のための、請求項8または9に記載の医薬組成物。
- 疾患が神経変性疾患である、請求項10に記載の医薬組成物。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB0724783A GB0724783D0 (en) | 2007-12-19 | 2007-12-19 | Compounds |
GB0818068A GB0818068D0 (en) | 2008-10-02 | 2008-10-02 | Compounds |
PCT/EP2008/067681 WO2009080637A1 (en) | 2007-12-19 | 2008-12-17 | Compounds which potentiate the ampa receptor and uses thereof in medicine |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2011506551A JP2011506551A (ja) | 2011-03-03 |
JP2011506551A5 true JP2011506551A5 (ja) | 2012-02-02 |
Family
ID=40566351
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2010538692A Withdrawn JP2011506551A (ja) | 2007-12-19 | 2008-12-17 | Ampa受容体増強化合物および医薬におけるその使用 |
Country Status (9)
Country | Link |
---|---|
US (1) | US8173820B2 (ja) |
EP (1) | EP2222632A1 (ja) |
JP (1) | JP2011506551A (ja) |
AR (1) | AR069781A1 (ja) |
CL (1) | CL2008003773A1 (ja) |
PE (1) | PE20091086A1 (ja) |
TW (1) | TW200940491A (ja) |
UY (1) | UY31544A1 (ja) |
WO (1) | WO2009080637A1 (ja) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009018657A1 (en) | 2007-08-03 | 2009-02-12 | Boehringer Ingelheim International Gmbh | Viral polymerase inhibitors |
WO2009076747A1 (en) | 2007-12-19 | 2009-06-25 | Boehringer Ingelheim International Gmbh | Viral polymerase inhibitors |
TW201012803A (en) * | 2008-06-06 | 2010-04-01 | Organon Nv | Heterocyclic derivatives |
GB0821166D0 (en) * | 2008-11-19 | 2008-12-24 | Glaxo Group Ltd | Compounds |
EP2417101B1 (en) | 2009-04-09 | 2013-10-23 | Merck Sharp & Dohme B.V. | Indane derivatives |
US9527807B2 (en) | 2011-04-05 | 2016-12-27 | Takeda Pharmaceutical Company Limited | Sulfonamide derivative and use thereof |
JP6319805B2 (ja) * | 2014-10-08 | 2018-05-09 | 田岡化学工業株式会社 | スピロビフルオレン骨格を有するジオール化合物およびその製造方法 |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU5235599A (en) * | 1998-07-31 | 2000-02-21 | Eli Lilly And Company | N-substituted sulfonamide derivatives |
GB0417709D0 (en) | 2004-08-09 | 2004-09-08 | Glaxo Group Ltd | Compounds |
DE602005021407D1 (de) * | 2004-08-09 | 2010-07-01 | Glaxo Group Ltd | Verbindungen zur Verstärkung der Glutamatrezeptorwirkung und deren Verwendung in der Medizin |
-
2008
- 2008-12-17 US US12/808,197 patent/US8173820B2/en not_active Expired - Fee Related
- 2008-12-17 JP JP2010538692A patent/JP2011506551A/ja not_active Withdrawn
- 2008-12-17 UY UY31544A patent/UY31544A1/es unknown
- 2008-12-17 EP EP08864027A patent/EP2222632A1/en not_active Withdrawn
- 2008-12-17 CL CL2008003773A patent/CL2008003773A1/es unknown
- 2008-12-17 TW TW097149086A patent/TW200940491A/zh unknown
- 2008-12-17 WO PCT/EP2008/067681 patent/WO2009080637A1/en active Application Filing
- 2008-12-17 AR ARP080105496A patent/AR069781A1/es not_active Application Discontinuation
- 2008-12-17 PE PE2008002104A patent/PE20091086A1/es not_active Application Discontinuation
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