DK1296972T3 - Arylmethylamin-derivater til anvendelse som tryptaseinhibitorer - Google Patents

Arylmethylamin-derivater til anvendelse som tryptaseinhibitorer

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Publication number
DK1296972T3
DK1296972T3 DK01930925.1T DK01930925T DK1296972T3 DK 1296972 T3 DK1296972 T3 DK 1296972T3 DK 01930925 T DK01930925 T DK 01930925T DK 1296972 T3 DK1296972 T3 DK 1296972T3
Authority
DK
Denmark
Prior art keywords
tryptase
tryptase inhibitors
arylmethylamine
derivatives
arylmethylamine derivatives
Prior art date
Application number
DK01930925.1T
Other languages
English (en)
Inventor
Mark Czekaj
Peter C Astles
Paul R Eastwood
Olivier Houille
Julian Levell
Guyan Liang
Yong Gong
James Pribish
Kent Neuenschwander
Heinz Pauls
Original Assignee
Aventis Pharma Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Aventis Pharma Inc filed Critical Aventis Pharma Inc
Priority claimed from PCT/US2001/013811 external-priority patent/WO2001090101A1/en
Application granted granted Critical
Publication of DK1296972T3 publication Critical patent/DK1296972T3/da

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    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/06Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/02Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
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    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A61P29/02Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID] without antiinflammatory effect
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    • C07D211/30Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by doubly bound oxygen or sulfur atoms or by two oxygen or sulfur atoms singly bound to the same carbon atom
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    • C07D211/06Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D211/56Nitrogen atoms
    • C07D211/58Nitrogen atoms attached in position 4
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    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • C07D513/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
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DK01930925.1T 2000-05-22 2001-04-27 Arylmethylamin-derivater til anvendelse som tryptaseinhibitorer DK1296972T3 (da)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GBGB0012362.0A GB0012362D0 (en) 2000-05-22 2000-05-22 Chemical compounds
US09/843,126 US6977263B2 (en) 2000-05-22 2001-04-26 Chemical compounds
PCT/US2001/013811 WO2001090101A1 (en) 2000-05-22 2001-04-27 Arylmethylamine derivatives for use as tryptase inhibitors

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DK1296972T3 true DK1296972T3 (da) 2010-04-26

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US (1) US6977263B2 (da)
JP (1) JP4796732B2 (da)
CN (1) CN1740169B (da)
AT (1) ATE452884T1 (da)
CR (1) CR6824A (da)
DE (1) DE60140871D1 (da)
DK (1) DK1296972T3 (da)
EA (1) EA006687B1 (da)
ES (1) ES2337550T3 (da)
GB (1) GB0012362D0 (da)
HK (1) HK1087702A1 (da)
IL (1) IL152830A (da)
ME (1) MEP54608A (da)
PT (1) PT1296972E (da)
RS (1) RS51751B (da)
UA (1) UA74579C2 (da)
ZA (1) ZA200209484B (da)

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DOP2005000039A (es) * 2004-03-26 2005-10-31 Aventis Pharma Inc Hidrocloruro de [4-(5-aminometil-2-fluoro-fenil)- piperidin-1-il]-(4-bomo-3-metil-5-propoxi-tiofen-2-il)-metanona como un inhibidor de la triptasa de mastocitos
US7423176B2 (en) * 2004-04-13 2008-09-09 Cephalon, Inc. Bicyclic aromatic sulfinyl derivatives
BRPI0516110A (pt) 2004-10-13 2008-08-26 Ptc Therapeutics Inc compostos para supressão sem sentido e métodos para seu uso
WO2006105035A2 (en) * 2005-03-28 2006-10-05 Vertex Pharmaceuticals Incorporated Muscarinic modulators
JP5019768B2 (ja) * 2006-03-23 2012-09-05 独立行政法人科学技術振興機構 新規低分子化合物およびその製造方法
SG177920A1 (en) * 2007-01-10 2012-02-28 Sanofi Aventis Method for determining the stability of organic methyleneamines in the presence of semicarbazide-sensitive amine oxidase
US8703119B2 (en) * 2007-10-05 2014-04-22 Polygene Ltd. Injectable biodegradable polymer compositions for soft tissue repair and augmentation
ES2469824T3 (es) * 2007-11-21 2014-06-20 Janssen Pharmaceutica N.V. Espiropiperidinas para su uso como inhibidores de la triptasa
CN102149705B (zh) * 2008-08-22 2013-08-07 赛诺菲-安万特 作为肥大细胞类胰蛋白酶抑制剂的[4-(5-氨基甲基-2-氟苯基)-哌啶-1-基]-[7-氟-1-(2-甲氧基乙基)-4-三氟甲氧基-1h-吲哚-3-基]-甲酮
FR2955324A1 (fr) * 2010-01-15 2011-07-22 Sanofi Aventis [4-(5-aminomethyl-phenyl)-piperidin-1-yl]-1h-indol-3-yl]-methanones disubstituees
KR20120112600A (ko) 2009-12-23 2012-10-11 사노피 [4[4?(5?아미노메틸?2?플루오로?페닐)?피페리딘?1?일]?(1h?피롤로?피리딘?일)?메탄온들 및 이들의 합성
AR079662A1 (es) * 2009-12-23 2012-02-08 Sanofi Aventis Indolil-piperidinil bencilaminas como inhibidores de beta-triptasa
PL2516418T3 (pl) 2009-12-23 2014-10-31 Sanofi Sa Proleki [4-[4-(5-aminometylo-2-fluoro-fenylo)-piperydyn-1-ylo]-(1H-pirolo-pirydynylo)-metanonów oraz ich synteza
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US6977263B2 (en) 2005-12-20
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DE60140871D1 (de) 2010-02-04
PT1296972E (pt) 2010-03-03
RS51751B (sr) 2011-12-31
MEP54608A (en) 2011-05-10
ATE452884T1 (de) 2010-01-15
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