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1.
公开(公告)号:EA034587B1
公开(公告)日:2020-02-25
申请号:EA201890123
申请日:2016-06-22
Applicant: SERVIER LAB , VERNALIS R&D LTD
Inventor: SZLAVIK ZOLTAN , SZABO ZOLTAN , CSEKEI MARTON , PACZAL ATTILA , KOTSCHY ANDRAS , BRUNO ALAIN , GENESTE OLIVIER , CHEN I-JEN , DAVIDSON JAMES EDWARD PAUL , MURRAY JAMES BROOKE , ONDI LEVENTE , RADICS GABOR , SIPOS SZABOLCS , PROSZENYAK AGNES , PERRON-SIERRA FRANCOISE , BALINT BALAZS
IPC: C07D495/04 , A61K31/519 , A61P35/00 , A61P37/00
Abstract: Соединенияформулы (I)где R, R, R, R, R, R, X, Y, A, E и n являютсятакими, какопределенов описании. Лекарственныесредства.
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公开(公告)号:JO3430B1
公开(公告)日:2019-10-20
申请号:JOP20160126
申请日:2016-06-22
Applicant: SERVIER LAB , VERNALIS R&D LTD
Inventor: DAVIDSON JAMES EDWARD PAUL , PERRON-SIERRA FRANCOISE , PROSZENYAK AGNES , BRUNO ALAIN , SZLAVIK ZOLTAN , PACZAL ATTILA , KOTSCHY ANDRAS , ONDI LEVENTE , CSEKEI MARTON , GENESTE OLIVIER , MURRAY JAMES BROOKE , SZABO ZOLTAN , CHEN I-JEN , BALINT BALAZS , SIPOS SZABOLCS , RADICS GABOR
IPC: A61K31/519 , A61P35/00 , A61P37/00 , C07D495/04
Abstract: يتعلقالاختراعالحاليبمركباتلهاالصيغة ( I ) : حيثتكون R 1 ، R 2 ، R 5 ، R 6 ، R 7 ، R 12 ، X ، Y ، A ، E و n مثلماتمتحديدهفيالوصف. الأدوية.
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公开(公告)号:AU2016280806A1
公开(公告)日:2018-01-04
申请号:AU2016280806
申请日:2016-06-16
Applicant: INTERCEPT PHARMACEUTICALS INC , SERVIER LAB
Inventor: PELLICCIARI ROBERTO , GIOIELLO ANTIMO , MACCHIARULO ANTONIO , PERRON-SIERRA FRANCOISE , SEEDORF KLAUS
IPC: A61K31/575 , A61K31/58 , A61P1/16 , A61P3/06 , A61P3/10 , A61P9/00 , A61P13/12 , A61P29/00 , A61P35/00 , A61P37/06 , C07J9/00 , C07J41/00 , C07J43/00
Abstract: The application relates to compounds of formula (A): or a salt, solvate, ester, tautomer, amino acide conjugate, or metabolite thereof. The compounds of formula A are TGR5 modulators useful for the treatment of various diseases, including metabolic disease, inflammatory disease, autoimmune disease, cardiac disease, kidney disease, cancer, and gastrointestinal disease.
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公开(公告)号:CA2990089A1
公开(公告)日:2016-12-29
申请号:CA2990089
申请日:2016-06-22
Applicant: VERNALIS (R&D) LTD , SERVIER LAB
Inventor: SZLAVIK ZOLTAN , SZABO ZOLTAN , CSEKEI MARTON , PACZAL ATTILA , KOTSCHY ANDRAS , BRUNO ALAIN , GENESTE OLIVIER , CHEN I-JEN , DAVIDSON JAMES EDWARD PAUL , MURRAY JAMES BROOKE , ONDI LEVENTE , RADICS GABOR , SIPOS SZABOLCS , PROSZENYAK AGNES , PERRON-SIERRA FRANCOISE , BALINT BALAZS
IPC: C07D495/04 , A61K31/519 , A61P35/00 , A61P37/00
Abstract: Compounds of formula (I): wherein R1, R2, R5, R6, R7, R12, X, Y, A, E and n are as defined in the description. Medicaments.
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公开(公告)号:DOP2014000282A
公开(公告)日:2016-06-30
申请号:DO2014000282
申请日:2014-12-15
Applicant: SERVIER LAB , VERNALIS R&D LTD
Inventor: MURRAY JAMES BROOKE , GENESTE OLIVIER , KOTSCHY ANDRAS , SZLAVIK ZOLTAN , CSEKEI MARTON , PACZAL ATTILA , SZABO ZOLTAN , SIPOS SZABOLCS , RADICS GABOR , PROSZENYAK AGNES , BELINT BALAZS , BRUNO ALAIN , DAVIDSON JAMES EDWARD PAUL , CHEN I-JEN , PERRON-SIERRA FRANCOISE
IPC: A61K31/505 , A61K31/513 , A61P35/00
Abstract: Compuestos de fórmula (I): en la que R1, R2, R3, R4, R5, R6, R7, R12, X, A y n son como se definen en la descripción. Medicamentos.
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公开(公告)号:MD20140137A2
公开(公告)日:2015-06-30
申请号:MD20140137
申请日:2014-12-22
Applicant: SERVIER LAB , VERNALIS R & D LTD
Inventor: ANDRAS KOTSCHY , ZOLTAN SZLAVIK , MARTON CSEKEI , ATTILA PACZAL , ZOLTAN SZABO , SZABOLCS SIPOS , GABOR RADICS , AGNES PROSZENYAK , BALAZS BALINT , ALAIN BRUNO , OLIVIER GENESTE , DAVIDSON JAMES EDWARD PAUL , MURRAY JAMES BROOKE , CHEN I-JEN , PERRON-SIERRA FRANCOISE
IPC: C07D495/04 , A61K31/519
Abstract: Invenţia se referă la derivaţi noi de tienopirimidină cu formula (I):în care R1, R2, R3, R4, R5, R6, R7, R12, X, A şi n au semnificaţiile definite în descriere. Invenţia se mai referă la un procedeu de preparare a acestora şi la compoziţii farmaceutice care îi conţin.Compuşii menţionaţi au caracteristici farmacologice valoroase în domeniul apoptozei şi oncologiei.
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公开(公告)号:CA2402686C
公开(公告)日:2008-02-05
申请号:CA2402686
申请日:2001-03-06
Applicant: SERVIER LAB
Inventor: CASARA PATRICK , TUCKER GORDON , ATASSI GHANEM , PERRON-SIERRA FRANCOISE , SAINT-DIZIER DOMINIQUE
IPC: C07D213/74 , C07D233/24 , A61K31/4164 , A61K31/4168 , A61K31/417 , A61K31/4184 , A61K31/426 , A61K31/4375 , A61K31/44 , A61K31/4402 , A61K31/505 , A61K31/55 , A61P9/00 , A61P19/10 , A61P27/02 , A61P29/00 , A61P33/14 , A61P35/00 , A61P43/00 , C07D213/36 , C07D223/04 , C07D223/12 , C07D233/48 , C07D233/54 , C07D235/10 , C07D235/14 , C07D235/30 , C07D239/14 , C07D277/18 , C07D277/20 , C07D277/42 , C07D401/12 , C07D403/12 , C07D471/04
Abstract: L'invention concerne de nouveaux composés répondant à la formule (I) : dans laquelle G représente un groupement phényle; G1 et G2 représentent un atome de carbone; T1 représente un groupement -CH2-CH2-, -CH=CH- ou =CH-CH2-, et -T2- représen te une liaison, R5 représente un groupement -(CH2)m-COOR6 dans lequel m est un enti er compris entre 1 et 6 inclusivement; R6 représentent un atome d'hydrogène ou un groupement alkyle, aryle ou arylalkyle; W représente un groupement -CH-, =C- ou -C= et A représente un groupement -CH2- ou =CH-; X représente un groupement choisi parmi -CO-X1-, - CO- NR6- X1-, -NR6-CO-X1-, -O-X1-, -SO2-NR6-X1- et -S(O)n-X1-, dans lesquels n est compris entre 0 et 2 inclusivement, et X1 représente un groupement alkylène; Y représente un groupement choisi parmi -Y1-, -Y2-Y1- et -Y1-Y2-Y1-, dans lesquels Y1 représente un groupement alkylène, alkénylène ou alkynylène, et Y2 représente un groupemen t arylène, hétéroarylène, cycloalkylène ou hétérocycloalkylène; Z représente un groupement choisi parmi Z1-, Z10-NR6- et Z10-NR6-CO-, dans lesquels Z10 représente un groupeme nt alkyle ou Z1, et Z1 représente un groupement choisi parmi Z2, Z2O-(C=NR6)-, Z20-NR6- e t Z20-NR6- CO-, dans lesquels Z20 représente un groupement alkyle, hétéroalkyle ou Z2, et Z2 représente ungroupement hétéroaryle, hétérocycloalkyle, hétéroarylalkyle, hétérocycloalkylalkyle, arylhétéroaryle fusionné, arylhétérocycloalkyle fusionné, hétéroarylhétérocycloalkyle fusionné, hétérocycloalkyl-hétéroaryle fusionné, hétéroarylhétéroaryle fusionné ou cycloalkylhétérocycloalkyle fusionné. L'invention vise également les énantiomères et diastéréoisomères des composés de formule (I), ainsi que leurs sels d'addition à un acide ou à une base pharmaceutiquement acceptable . Les composés selon l'invention sont utiles à titre de médicaments pour le traitement des maladies cardiovasculaires, des maladies inflammatoires, du cancer, de l'ostéoporose, de l'arthrite rhumatoïde, du psoriasis, des rétinopathies et des cancers.
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公开(公告)号:AU2001293374B2
公开(公告)日:2005-02-17
申请号:AU2001293374
申请日:2001-03-06
Applicant: SERVIER LAB
Inventor: CASARA PATRICK , PERRON-SIERRA FRANCOISE , ATASSI GHANEM , TUCKER GORDON , SAINT-DIZIER DOMINIQUE
IPC: C07D233/24 , A61K31/4164 , A61K31/4168 , A61K31/417 , A61K31/4184 , A61K31/426 , A61K31/4375 , A61K31/44 , A61K31/4402 , A61K31/505 , A61K31/55 , A61P9/00 , A61P19/10 , A61P27/02 , A61P29/00 , A61P33/14 , A61P35/00 , A61P43/00 , C07D213/36 , C07D213/74 , C07D223/04 , C07D223/12 , C07D233/48 , C07D233/54 , C07D235/10 , C07D235/14 , C07D235/30 , C07D239/14 , C07D277/18 , C07D277/20 , C07D277/42 , C07D401/12 , C07D403/12 , C07D471/04 , A61P009/00 , A61K031/55 , A61K031/44 , A61K031/4184 , A61K031/4164
Abstract: Compounds of formula (1):wherein:G represents an optionally substituted phenyl or optionally substituted heterocycle, G1 and G2 being N or C,T1 represents -CH2-CH2-, -CH=CH- or =CH-CH2-, and T2 is a bond, or T1 represents -CH2- or =CH- and T2 is -CH2-, =CH-,R5 represents -(CH2)m-COOR6,R6 and R6' represent hydrogen, alkyl, optionally substituted aryl or optionally substituted arylalkyl,A represents -CO-, -CH2-, =CH- or -CH= and W represents -CH-, =C- or -C=, or A represents -CO- or -CH2- and W represents N,X represents -CO-X1-, -CO-NR6-X1-, -NR6-CO-X1-, -O-X1-, -SO2-NR6-X1- or -S(O)n-X1-,Y represents -Y1-, -Y2-Y1- or -Y1-Y2-Y1-, Y1 being an alkylene, alkenylene or alkynylene, and Y2 being an arylene, heteroarylene, cycloalkylene or heterocycloalkylene,Z represents -Z1-, -Z10-NR6-, and -Z10-NR6-CO-, Z1 being a heteroaryl, heterocycloalkyl, heteroarylalkyl, heterocycloalkylalkyl, fused arylheteroaryl, fused arylheterocycloalkyl, fused heteroarylheterocycloalkyl, fused heterocycloalkylheteroaryl or fused heteroarylheteroaryl, each of which is optionally substituted, or a group,Z2-NR6 or Z2-NR6-CO, Z2 being a group Z1, alkyl or heteroalkyl, andZ10 represents Z1 or an alkyl,its enantiomers, diastereoisomers, and addition salts thereof with a pharmaceutically acceptable acid or base,and medicinal products containing the same which are useful as vitronectin receptor antagonists.
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公开(公告)号:NZ520805A
公开(公告)日:2004-12-24
申请号:NZ52080501
申请日:2001-03-06
Applicant: SERVIER LAB
Inventor: CASARA PATRICK , PERRON-SIERRA FRANCOISE , ATASSI GHANEM , TUCKER GORDON , SAINT-DIZIER DOMINIQUE
IPC: A61K31/4164 , A61K31/4168 , A61K31/417 , A61K31/4184 , A61K31/426 , A61K31/4375 , A61K31/44 , A61K31/4402 , A61K31/505 , A61K31/55 , A61P9/00 , C07D233/24 , A61P19/10 , A61P27/02 , A61P29/00 , A61P33/14 , A61P35/00 , A61P43/00 , C07D213/36 , C07D213/74 , C07D223/04 , C07D223/12 , C07D233/48 , C07D233/54 , C07D235/10 , C07D235/14 , C07D235/30 , C07D239/14 , C07D277/18 , C07D277/20 , C07D277/42 , C07D401/12 , C07D403/12 , C07D471/04
Abstract: A bicyclic compound of formula (I); the preparation thereof; and use of the compound as vitronectin receptor antagonists is disclosed, wherein the variables are as defined in the specification.
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10.
公开(公告)号:SK12702002A3
公开(公告)日:2003-03-04
申请号:SK12702002
申请日:2001-03-06
Applicant: SERVIER LAB
Inventor: CASARA PATRICK , PERRON-SIERRA FRANCOISE , ATASSI GHANEM , TUCKER GORDON , SAINT-DIZIER DOMINIQUE
IPC: A61K31/4164 , A61K31/4168 , A61K31/417 , A61K31/4184 , A61K31/426 , A61K31/4375 , A61K31/44 , A61K31/4402 , A61K31/505 , A61K31/55 , A61P9/00 , C07D233/24 , A61P19/10 , A61P27/02 , A61P29/00 , A61P33/14 , A61P35/00 , A61P43/00 , C07D213/36 , C07D213/74 , C07D223/04 , C07D223/12 , C07D233/48 , C07D233/54 , C07D235/10 , C07D235/14 , C07D235/30 , C07D239/14 , C07D277/18 , C07D277/20 , C07D277/42 , C07D401/12 , C07D403/12 , C07D471/04
Abstract: Compounds of formula (1):wherein:G represents an optionally substituted phenyl or optionally substituted heterocycle, G1 and G2 being N or C,T1 represents -CH2-CH2-, -CH=CH- or =CH-CH2-, and T2 is a bond, or T1 represents -CH2- or =CH- and T2 is -CH2-, =CH-,R5 represents -(CH2)m-COOR6,R6 and R6' represent hydrogen, alkyl, optionally substituted aryl or optionally substituted arylalkyl,A represents -CO-, -CH2-, =CH- or -CH= and W represents -CH-, =C- or -C=, or A represents -CO- or -CH2- and W represents N,X represents -CO-X1-, -CO-NR6-X1-, -NR6-CO-X1-, -O-X1-, -SO2-NR6-X1- or -S(O)n-X1-,Y represents -Y1-, -Y2-Y1- or -Y1-Y2-Y1-, Y1 being an alkylene, alkenylene or alkynylene, and Y2 being an arylene, heteroarylene, cycloalkylene or heterocycloalkylene,Z represents -Z1-, -Z10-NR6-, and -Z10-NR6-CO-, Z1 being a heteroaryl, heterocycloalkyl, heteroarylalkyl, heterocycloalkylalkyl, fused arylheteroaryl, fused arylheterocycloalkyl, fused heteroarylheterocycloalkyl, fused heterocycloalkylheteroaryl or fused heteroarylheteroaryl, each of which is optionally substituted, or a group,Z2-NR6 or Z2-NR6-CO, Z2 being a group Z1, alkyl or heteroalkyl, andZ10 represents Z1 or an alkyl,its enantiomers, diastereoisomers, and addition salts thereof with a pharmaceutically acceptable acid or base,and medicinal products containing the same which are useful as vitronectin receptor antagonists.
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