HUP0301167A2 - Neurológiai rendellenességek kezelésére felhasználható szulfonil-pirrolidin-származékok, eljárás az előállításukra, ezeket tartalmazó gyógyszerkészítmények és alkalmazásuk - Google Patents
Neurológiai rendellenességek kezelésére felhasználható szulfonil-pirrolidin-származékok, eljárás az előállításukra, ezeket tartalmazó gyógyszerkészítmények és alkalmazásukInfo
- Publication number
- HUP0301167A2 HUP0301167A2 HU0301167A HUP0301167A HUP0301167A2 HU P0301167 A2 HUP0301167 A2 HU P0301167A2 HU 0301167 A HU0301167 A HU 0301167A HU P0301167 A HUP0301167 A HU P0301167A HU P0301167 A2 HUP0301167 A2 HU P0301167A2
- Authority
- HU
- Hungary
- Prior art keywords
- group
- lower alkyl
- optionally substituted
- halogen atom
- cycloalkyl
- Prior art date
Links
- 208000012902 Nervous system disease Diseases 0.000 title abstract 2
- 208000025966 Neurological disease Diseases 0.000 title abstract 2
- FDAMVVHYWSPPFN-UHFFFAOYSA-N 2-sulfonylpyrrolidine Chemical class O=S(=O)=C1CCCN1 FDAMVVHYWSPPFN-UHFFFAOYSA-N 0.000 title 1
- 238000000034 method Methods 0.000 title 1
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 9
- 150000001875 compounds Chemical class 0.000 abstract 4
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 4
- 125000005843 halogen group Chemical group 0.000 abstract 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 3
- 125000003118 aryl group Chemical group 0.000 abstract 2
- 125000001072 heteroaryl group Chemical group 0.000 abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 2
- 102000016193 Metabotropic glutamate receptors Human genes 0.000 abstract 1
- 108010010914 Metabotropic glutamate receptors Proteins 0.000 abstract 1
- -1 N-hydroxyamidino group Chemical group 0.000 abstract 1
- 230000001154 acute effect Effects 0.000 abstract 1
- 230000001684 chronic effect Effects 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 239000000825 pharmaceutical preparation Substances 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
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- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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- C07D403/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- C07D413/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
Abstract
A találmány (I) általános képletű vegyületekre[mely képletben R1jelentése hidrogénatom vagy adott esetben halogénatommalhelyettesített arilcsoport; R2 jelentése adott esetben halogénatommalvagy kis szénatomszámú alkilcsoporttal helyettesített arilcsoport; R3jelentése -OR', cianocsoport, halogénatom, N-hidroxi-amidino-csoport,C(O)-OR, -C(O)NR'R", -N(R')-C(O)=R4, -N(R')-S(O)2-R, -N(R')-C(S)-NR'Rcsoport, vagy 5- vagy 6-tagú, egy-négy azonos vagy különbözőnitrogénatomot és/vagy oxigénatomot tartalmazó és adott esetben kisszénatomszámú alkil- vagy cikloalkilcsoporttal helyettesítettheteroarilcsoport; R4 jelentése cikloalkilcsoport, fenilcsoport vagyadott esetben halogénatommal helyettesített kis szénatomszámúalkilcsoport; R jelentése kis szénatomszámú alkilcsoport; R' jelentésehidrogénatom, kis szénatomszámú alkil- vagy cikloalkil-(kisszénatomszámú alkil)-csoport, mimellett ha egynél több R' csoport vanjelen, úgy ezek jelentése egymástól független; R< jelentésehidrogénatom, kis szénatomszámú alkilcsoport, vagy 5- vagy 6-tagú,egy-négy azonos vagy különböző nitrogénatomot és/vagy oxigénatomottartalmazó, adott esetben kis szénatomszámú alkil- vagycikloalkilcsoporttal szubsztituált heteroarilcsoporttal helyettesítettkis szénatomszámú alkilcsoport; és n értéke 0-5] és gyógyászatilagalkalmas sóikra, továbbá a fenti vegyületeket tartalmazó gyógyászatikészítményekre és e vegyületek előállítására vonatkozik. A találmányszerinti vegyületek a metabotrop glutamát receptorokhoz affinitástmutatnak és ezért akut és/vagy krónikus neurológiai rendellenességekkezelésére vagy megelőzésére alkalmazhatók. Ó
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP00113894 | 2000-06-30 | ||
PCT/EP2001/007135 WO2002002554A1 (en) | 2000-06-30 | 2001-06-22 | Sulfonyl-pyrrolidine derivatives useful for the treatment of neurological disorders |
Publications (2)
Publication Number | Publication Date |
---|---|
HUP0301167A2 true HUP0301167A2 (hu) | 2003-08-28 |
HUP0301167A3 HUP0301167A3 (en) | 2009-12-28 |
Family
ID=8169121
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HU0301167A HUP0301167A3 (en) | 2000-06-30 | 2001-06-22 | Sulfonyl-pyrrolidine derivatives useful for the treatment of neurological disorders, process for their preparation, pharmaceutical compositions containing them and their use |
Country Status (35)
Country | Link |
---|---|
US (2) | US6589978B2 (hu) |
EP (1) | EP1299383B1 (hu) |
JP (1) | JP3994051B2 (hu) |
KR (1) | KR100529423B1 (hu) |
CN (1) | CN1178936C (hu) |
AR (1) | AR029288A1 (hu) |
AT (1) | ATE286895T1 (hu) |
AU (2) | AU8187701A (hu) |
BR (1) | BR0112093A (hu) |
CA (1) | CA2413243A1 (hu) |
CZ (1) | CZ2003280A3 (hu) |
DE (1) | DE60108394T2 (hu) |
DK (1) | DK1299383T3 (hu) |
EC (1) | ECSP024403A (hu) |
ES (1) | ES2234869T3 (hu) |
HK (1) | HK1058358A1 (hu) |
HR (1) | HRP20021023B1 (hu) |
HU (1) | HUP0301167A3 (hu) |
IL (2) | IL153425A0 (hu) |
JO (1) | JO2384B1 (hu) |
MA (1) | MA26923A1 (hu) |
MX (1) | MXPA02012270A (hu) |
MY (1) | MY126903A (hu) |
NO (1) | NO324218B1 (hu) |
NZ (1) | NZ523025A (hu) |
PE (1) | PE20020103A1 (hu) |
PL (1) | PL360396A1 (hu) |
PT (1) | PT1299383E (hu) |
RU (1) | RU2272026C2 (hu) |
SI (1) | SI1299383T1 (hu) |
TW (1) | TWI265928B (hu) |
UY (1) | UY26812A1 (hu) |
WO (1) | WO2002002554A1 (hu) |
YU (1) | YU99702A (hu) |
ZA (1) | ZA200209966B (hu) |
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TW200302717A (en) | 2002-02-06 | 2003-08-16 | Schering Corp | Novel gamma secretase inhibitors |
DE10240818A1 (de) * | 2002-08-30 | 2004-05-13 | Grünenthal GmbH | Substituierte 2-Pyrrolidin-2-yl-[1,3,4]-oxadiazol-Derivate |
GB0225938D0 (en) * | 2002-11-06 | 2002-12-11 | Glaxo Group Ltd | Novel compounds |
CA2563033A1 (en) * | 2004-04-05 | 2005-10-20 | Schering Corporation | Novel gamma secretase inhibitors |
US20060035884A1 (en) * | 2004-05-20 | 2006-02-16 | Elan Pharmaceuticals, Inc. | N-cyclic sulfonamido inhibitors of gamma secretase |
US7763613B2 (en) | 2004-06-30 | 2010-07-27 | Schering Corporation | Substituted N-arylsulfonylheterocyclic amines as gamma-secretase inhibitors |
US7803802B2 (en) * | 2004-07-22 | 2010-09-28 | Schering Corporation | Substituted amide beta secretase inhibitors |
EP1803709B1 (en) | 2004-09-30 | 2013-01-02 | Takeda Pharmaceutical Company Limited | Proton pump inhibitors |
MY142214A (en) * | 2005-04-04 | 2010-11-15 | Takeda Pharmaceutical | Prophylactic or therapeutic agent for depression or anxiety disorder |
EP1928437A2 (en) | 2005-08-26 | 2008-06-11 | Braincells, Inc. | Neurogenesis by muscarinic receptor modulation |
EP2258359A3 (en) | 2005-08-26 | 2011-04-06 | Braincells, Inc. | Neurogenesis by muscarinic receptor modulation with sabcomelin |
NZ566378A (en) | 2005-08-30 | 2011-03-31 | Takeda Pharmaceutical | 1-Heterocyclylsulfonyl, 2-aminomethyl, 5-(hetero-) aryl substituted 1-H-pyrrole derivatives as acid secretion inhibitors |
EP1940389A2 (en) | 2005-10-21 | 2008-07-09 | Braincells, Inc. | Modulation of neurogenesis by pde inhibition |
EP2314289A1 (en) | 2005-10-31 | 2011-04-27 | Braincells, Inc. | Gaba receptor mediated modulation of neurogenesis |
US20100216734A1 (en) | 2006-03-08 | 2010-08-26 | Braincells, Inc. | Modulation of neurogenesis by nootropic agents |
EP2026813A2 (en) | 2006-05-09 | 2009-02-25 | Braincells, Inc. | 5 ht receptor mediated neurogenesis |
EP2377531A2 (en) | 2006-05-09 | 2011-10-19 | Braincells, Inc. | Neurogenesis by modulating angiotensin |
WO2008030651A1 (en) | 2006-09-08 | 2008-03-13 | Braincells, Inc. | Combinations containing a 4-acylaminopyridine derivative |
US20100184806A1 (en) | 2006-09-19 | 2010-07-22 | Braincells, Inc. | Modulation of neurogenesis by ppar agents |
SI2066659T1 (sl) * | 2006-09-29 | 2013-10-30 | Grunenthal Gmbh | Substituirani sulfonamidni derivati |
US8933105B2 (en) | 2007-02-28 | 2015-01-13 | Takeda Pharmaceutical Company Limited | Pyrrole compounds |
DK2315591T3 (en) * | 2008-08-15 | 2016-06-06 | Nivalis Therapeutics Inc | NOVEL PYRROLE INHIBITORS OF S-nitrosoglutathione-reductase as therapeutic agents |
AR073136A1 (es) | 2008-08-27 | 2010-10-13 | Takeda Pharmaceutical | Compuestos de pirrol |
WO2010099217A1 (en) | 2009-02-25 | 2010-09-02 | Braincells, Inc. | Modulation of neurogenesis using d-cycloserine combinations |
ES2351323B1 (es) * | 2009-06-26 | 2011-10-05 | Institut Univ. De Ciència I Tecnologia, S.A. | Bibliotecas de n-fenil-1-sulfonil-2-pirrolidinacarboxamidas para el descubrimiento de farmacos. |
ES2351452B1 (es) * | 2009-07-01 | 2011-10-05 | Institut Univ. De Ciència I Tecnologia, S.A. | Bibliotecas de n-fenil-1-sulfonil-2-pirrolidinacarboxamidas para la identificacion de actividad biologica y farmacologica. |
WO2022270628A1 (ja) * | 2021-06-25 | 2022-12-29 | 国立大学法人 大分大学 | Rsウイルス感染症の処置および/または予防用医薬としてのヘテロシクロアルキル置換ポリヘテロアゾール誘導体 |
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US6645939B1 (en) * | 1997-11-24 | 2003-11-11 | Merck & Co., Inc. | Substituted β-alanine derivatives as cell adhesion inhibitors |
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WO1999062888A1 (en) | 1998-06-03 | 1999-12-09 | Gpi Nil Holdings, Inc. | Aza-heterocyclic compounds used to treat neurological disorders and hair loss |
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IL144577A0 (en) * | 1999-01-27 | 2002-05-23 | Ortho Mcneil Pharm Inc | Peptidyl heterocyclic ketones useful as tryptase inhibitors |
TW575561B (en) | 1999-03-25 | 2004-02-11 | Hoffmann La Roche | 1-arenesulfonyl-2-aryl-pyrrolidine and piperidine derivatives |
DE60037587T2 (de) * | 1999-05-20 | 2008-04-30 | Dong Wha Pharmaceutical Industrial Co. Ltd. | Optisch aktive quinolin-carbonsäure-derivate mit einem 7-pyrrolidin-substituenten, der die optische aktivität verursacht und ein verfahren zu seiner herstellung |
US6143776A (en) * | 2000-02-02 | 2000-11-07 | Sunesis Pharmaceuticals, Inc. | Tosylproline analogs as thymidylate synthase inhibitors |
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