NO20073098L - Substituerte biarylforbindelser som faktor XIa-Inhibitorer - Google Patents

Substituerte biarylforbindelser som faktor XIa-Inhibitorer

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Publication number
NO20073098L
NO20073098L NO20073098A NO20073098A NO20073098L NO 20073098 L NO20073098 L NO 20073098L NO 20073098 A NO20073098 A NO 20073098A NO 20073098 A NO20073098 A NO 20073098A NO 20073098 L NO20073098 L NO 20073098L
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Norway
Prior art keywords
compounds
factor
factor xia
inhibitors
xia inhibitors
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Application number
NO20073098A
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English (en)
Inventor
James R Corte
Mimi L Quan
Joanne M Smallheer
Donald J Pinto
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Bristol Myers Squibb Co
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Application filed by Bristol Myers Squibb Co filed Critical Bristol Myers Squibb Co
Publication of NO20073098L publication Critical patent/NO20073098L/no

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    • C07C255/00Carboxylic acid nitriles
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    • C07C255/32Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring
    • C07C255/42Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring the carbon skeleton being further substituted by singly-bound nitrogen atoms, not being further bound to other hetero atoms
    • C07C255/44Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring the carbon skeleton being further substituted by singly-bound nitrogen atoms, not being further bound to other hetero atoms at least one of the singly-bound nitrogen atoms being acylated
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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    • A61P7/02Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
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    • C07C237/00Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
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    • C07C271/28Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atom of at least one of the carbamate groups bound to a carbon atom of a six-membered aromatic ring to a carbon atom of a non-condensed six-membered aromatic ring
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    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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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    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom 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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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Pyrrole Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Heterocyclic Compounds Containing Sulfur Atoms (AREA)
  • Quinoline Compounds (AREA)
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Abstract

Foreliggende oppfinnelse tilveiebringer forbindelser med formel (I): (I) eller en stereoisomer, tautomer, farmasøytisk akseptabelt salt eller solvat form derav, hvor variablene A, L, Z, R3 og ring B er som definert her. Forbindelsene med formel (I) er anvendelige som selektive inhibitorer av serinprotease enzymer av koaguleringskaskaden og/eller kontaktaktiveringsystemet; for eksempel trombin, faktor Xa, faktor XIa, faktor IXa, faktor VIIa og/eller plasma kallikrein. Spesielt angår den forbindelser som er selektiv faktor XIa inhibitorer. Foreliggende oppfinnelse angår også farmasøytiske preparater omfattende disse forbindelser og fremgangsmåter for behandling av tromboemboliske og/eller inflammatoriske lidelser ved anvendelse av samme.
NO20073098A 2005-01-13 2007-06-18 Substituerte biarylforbindelser som faktor XIa-Inhibitorer NO20073098L (no)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US64375905P 2005-01-13 2005-01-13
PCT/US2006/001224 WO2006076575A2 (en) 2005-01-13 2006-01-12 Substituted biaryl compounds as factor xia inhibitors
US11/330,528 US7459564B2 (en) 2005-01-13 2006-01-12 Substituted biaryl compounds as factor XIa inhibitors

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NO20073098L true NO20073098L (no) 2007-07-19

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NO20073098A NO20073098L (no) 2005-01-13 2007-06-18 Substituerte biarylforbindelser som faktor XIa-Inhibitorer

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US (2) US7459564B2 (no)
EP (1) EP1841504B1 (no)
JP (1) JP5236293B2 (no)
CN (1) CN101137412B (no)
NO (1) NO20073098L (no)
WO (1) WO2006076575A2 (no)

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