HK1087702A1 - Arylmethylamine derivatives for use as tryptase inhibitors - Google Patents

Arylmethylamine derivatives for use as tryptase inhibitors

Info

Publication number
HK1087702A1
HK1087702A1 HK06107891.9A HK06107891A HK1087702A1 HK 1087702 A1 HK1087702 A1 HK 1087702A1 HK 06107891 A HK06107891 A HK 06107891A HK 1087702 A1 HK1087702 A1 HK 1087702A1
Authority
HK
Hong Kong
Prior art keywords
tryptase
tryptase inhibitors
arylmethylamine
derivatives
arylmethylamine derivatives
Prior art date
Application number
HK06107891.9A
Other languages
English (en)
Inventor
Peter C Astles
Paul R Eastwood
Olivier Houille
Julian Levell
Heinz Pauls
Mark Czekaj
Guyan Liang
Yong Gong
James Pribish
Kent Neuenschwander
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
Publication of HK1087702A1 publication Critical patent/HK1087702A1/xx

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    • C07D401/02—Heterocyclic 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
    • C07D401/06—Heterocyclic 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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    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16—Drugs 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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    • A61P19/00—Drugs for skeletal disorders
    • A61P19/06—Antigout agents, e.g. antihyperuricemic or uricosuric agents
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    • C07D211/18—Heterocyclic 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
    • C07D211/30—Heterocyclic 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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    • C07D211/36—Heterocyclic 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
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    • C07D401/10—Heterocyclic 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 aromatic rings
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    • C07D401/02—Heterocyclic 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
    • C07D401/12—Heterocyclic 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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HK06107891.9A 2000-05-22 2006-07-14 Arylmethylamine derivatives for use as tryptase inhibitors HK1087702A1 (en)

Applications Claiming Priority (2)

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

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HK1087702A1 true HK1087702A1 (en) 2006-10-20

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

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DE602005017471D1 (xx) * 2004-03-02 2009-12-17 Aventis Pharma Inc
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
US9611230B2 (en) 2004-10-13 2017-04-04 Ptc Therapeutics, Inc. 1,3,4-oxadiazole benzoic acid compounds and their use for nonsense suppression and the treatment of disease
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