JP2004520290A5 - - Google Patents

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Publication number
JP2004520290A5
JP2004520290A5 JP2002546515A JP2002546515A JP2004520290A5 JP 2004520290 A5 JP2004520290 A5 JP 2004520290A5 JP 2002546515 A JP2002546515 A JP 2002546515A JP 2002546515 A JP2002546515 A JP 2002546515A JP 2004520290 A5 JP2004520290 A5 JP 2004520290A5
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JP
Japan
Prior art keywords
compound
pharmaceutically acceptable
acceptable salt
condition
compound according
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.)
Granted
Application number
JP2002546515A
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English (en)
Japanese (ja)
Other versions
JP2004520290A (ja
JP4177101B2 (ja
Filing date
Publication date
Priority claimed from SE0004458A external-priority patent/SE0004458D0/xx
Priority claimed from SE0100965A external-priority patent/SE0100965D0/xx
Priority claimed from SE0101239A external-priority patent/SE0101239D0/xx
Priority claimed from SE0102921A external-priority patent/SE0102921D0/xx
Application filed filed Critical
Priority claimed from PCT/SE2001/002657 external-priority patent/WO2002044145A1/en
Publication of JP2004520290A publication Critical patent/JP2004520290A/ja
Publication of JP2004520290A5 publication Critical patent/JP2004520290A5/ja
Application granted granted Critical
Publication of JP4177101B2 publication Critical patent/JP4177101B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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JP2002546515A 2000-12-01 2001-11-30 新規マンデル酸誘導体とそれらのトロンビン阻害剤としての使用 Expired - Fee Related JP4177101B2 (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
SE0004458A SE0004458D0 (sv) 2000-12-01 2000-12-01 Pharmaceutically useful compounds
SE0100965A SE0100965D0 (sv) 2001-03-19 2001-03-19 Pharmaceutically-useful compounds
SE0101239A SE0101239D0 (sv) 2001-04-06 2001-04-06 Pharmaceutically useful compounds
SE0102921A SE0102921D0 (sv) 2001-08-30 2001-08-30 Pharmaceutically useful compounds
PCT/SE2001/002657 WO2002044145A1 (en) 2000-12-01 2001-11-30 New mandelic acid derivatives and their use as throbin inhibitors

Related Child Applications (2)

Application Number Title Priority Date Filing Date
JP2008006611A Division JP2008138009A (ja) 2000-12-01 2008-01-16 新規マンデル酸誘導体とそれらのトロンビン阻害剤としての使用
JP2008006608A Division JP2008156362A (ja) 2000-12-01 2008-01-16 新規マンデル酸誘導体とそれらのトロンビン阻害剤としての使用

Publications (3)

Publication Number Publication Date
JP2004520290A JP2004520290A (ja) 2004-07-08
JP2004520290A5 true JP2004520290A5 (enExample) 2008-03-06
JP4177101B2 JP4177101B2 (ja) 2008-11-05

Family

ID=27484527

Family Applications (3)

Application Number Title Priority Date Filing Date
JP2002546515A Expired - Fee Related JP4177101B2 (ja) 2000-12-01 2001-11-30 新規マンデル酸誘導体とそれらのトロンビン阻害剤としての使用
JP2008006611A Pending JP2008138009A (ja) 2000-12-01 2008-01-16 新規マンデル酸誘導体とそれらのトロンビン阻害剤としての使用
JP2008006608A Pending JP2008156362A (ja) 2000-12-01 2008-01-16 新規マンデル酸誘導体とそれらのトロンビン阻害剤としての使用

Family Applications After (2)

Application Number Title Priority Date Filing Date
JP2008006611A Pending JP2008138009A (ja) 2000-12-01 2008-01-16 新規マンデル酸誘導体とそれらのトロンビン阻害剤としての使用
JP2008006608A Pending JP2008156362A (ja) 2000-12-01 2008-01-16 新規マンデル酸誘導体とそれらのトロンビン阻害剤としての使用

Country Status (29)

Country Link
US (4) US20070218136A1 (enExample)
EP (2) EP2186800A1 (enExample)
JP (3) JP4177101B2 (enExample)
KR (4) KR100914535B1 (enExample)
CN (1) CN1291975C (enExample)
AR (2) AR035216A1 (enExample)
AT (1) ATE461171T1 (enExample)
AU (2) AU2007203520B2 (enExample)
BG (1) BG66261B1 (enExample)
BR (1) BR0115861A (enExample)
CA (1) CA2436220C (enExample)
CY (1) CY1113487T1 (enExample)
CZ (1) CZ303708B6 (enExample)
DE (1) DE60141603D1 (enExample)
DK (1) DK1347955T3 (enExample)
EE (1) EE05382B1 (enExample)
ES (1) ES2341318T3 (enExample)
HU (1) HU228814B1 (enExample)
IL (1) IL156096A0 (enExample)
IS (1) IS2755B (enExample)
MX (1) MXPA03004794A (enExample)
MY (1) MY136133A (enExample)
NO (3) NO325228B1 (enExample)
NZ (1) NZ526205A (enExample)
PL (1) PL207045B1 (enExample)
PT (1) PT1347955E (enExample)
SI (1) SI1347955T1 (enExample)
SK (1) SK287692B6 (enExample)
WO (1) WO2002044145A1 (enExample)

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LT2766346T (lt) 2011-10-14 2017-06-12 Bristol-Myers Squibb Company Pakeistieji tetrahidroizochinolino junginiai, kaip faktoriaus xia inhibitoriai
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CA2880898A1 (en) 2012-08-03 2014-02-06 Bristol-Myers Squibb Company Dihydropyridone p1 as factor xia inhibitors
GB2510407A (en) 2013-02-04 2014-08-06 Kalvista Pharmaceuticals Ltd Aqueous suspensions of kallikrein inhibitors for parenteral administration
JP6479763B2 (ja) 2013-03-25 2019-03-06 ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company 第xia因子阻害剤としての置換アゾール含有のテトラヒドロイソキノリン
NO2760821T3 (enExample) 2014-01-31 2018-03-10
JP6505727B2 (ja) 2014-01-31 2019-04-24 ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company ヘテロ環式p2’基を有する第xia因子阻害剤としてのマクロ環
NO2721243T3 (enExample) 2014-10-01 2018-10-20
US10160750B2 (en) 2015-06-19 2018-12-25 Bristol-Myers Squibb Company Diamide macrocycles as factor XIa inhibitors
ES2871111T3 (es) 2015-07-29 2021-10-28 Bristol Myers Squibb Co Inhibidores macrocíclicos del factor XIa que contienen un grupo P2' no aromático
US10336730B2 (en) 2015-08-05 2019-07-02 Bristol-Myers Squibb Company Substituted glycine derived FXIA inhibitors
CN105294520A (zh) * 2015-11-23 2016-02-03 大连九信生物化工科技有限公司 一种2-(2’,2’-二氟乙氧基)-6-三氟甲基苯基丙基硫醚的合成工艺
CN109195973A (zh) 2016-03-02 2019-01-11 百时美施贵宝公司 具有因子xia抑制活性的二酰胺大环类化合物
CN106674085B (zh) * 2016-12-20 2020-06-23 苏州汉德创宏生化科技有限公司 N-1,3-二氟异丙基-4-氨基哌啶类化合物的合成方法
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