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公开(公告)号:HRP20010512A2
公开(公告)日:2002-08-31
申请号:HRP20010512
申请日:2001-07-10
Applicant: ABBOTT LAB
Inventor: LINK JAMES , LIU GANG , PEI ZHONGHUA , GELDERN THOMAS W VON , WINN MARTIN , XIN ZHILI , BOYD STEVEN A , JAE HWAN-SOO , LYNCH JOHN K , ZHU GUI-DONG , FREEMAN JENNIFER C , GUNAWARDANA INDRANI W , STAEGER MICHAEL A
IPC: C07D295/12 , A61K31/16 , A61K31/164 , A61K31/165 , A61K31/167 , A61K31/40 , A61K31/4015 , A61K31/404 , A61K31/407 , A61K31/417 , A61K31/438 , A61K31/44 , A61K31/443 , A61K31/445 , A61K31/4465 , A61K31/4468 , A61K31/45 , A61K31/453 , A61K31/454 , A61K31/472 , A61K31/495 , A61K31/496 , A61K31/506 , A61K31/5375 , A61K31/5377 , A61K31/54 , A61K31/541 , A61P29/00 , A61P37/02 , C07C323/00 , C07C323/62 , C07C323/63 , C07D207/08 , C07D207/09 , C07D207/12 , C07D207/14 , C07D207/20 , C07D207/22 , C07D207/26 , C07D207/263 , C07D207/27 , C07D207/273 , C07D207/34 , C07D207/36 , C07D209/08 , C07D209/12 , C07D209/14 , C07D209/18 , C07D211/22 , C07D211/26 , C07D211/42 , C07D211/44 , C07D211/46 , C07D211/54 , C07D211/60 , C07D211/62 , C07D211/66 , C07D211/74 , C07D213/74 , C07D213/75 , C07D213/81 , C07D213/82 , C07D215/04 , C07D215/36 , C07D217/06 , C07D233/61 , C07D235/26 , C07D239/42 , C07D241/04 , C07D241/18 , C07D241/24 , C07D243/08 , C07D265/30 , C07D295/13 , C07D295/16 , C07D295/18 , C07D295/185 , C07D295/205 , C07D295/215 , C07D295/26 , C07D295/32 , C07D307/52 , C07D307/68 , C07D317/58 , C07D317/62 , C07D319/18 , C07D319/20 , C07D401/04 , C07D401/06 , C07D401/12 , C07D403/04 , C07D403/12 , C07D405/06 , C07D405/12 , C07D405/14 , C07D411/04 , C07D413/04 , C07D413/12 , C07D413/14 , C07D417/12 , C07D471/10 , C07D487/08 , C07D491/10 , C07D295/20 , A61K31/10 , A61K31/33
Abstract: The present invention relates to novel cinnamide compounds that are useful for treating inflammatory and immune diseases, to pharmaceutical compositions comprising these compounds, and to methods of inhibiting inflammation or suppressing immune response in a mammal.
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52.
公开(公告)号:CZ20013522A3
公开(公告)日:2002-05-15
申请号:CZ20013522
申请日:2000-04-03
Applicant: ABBOTT LAB
Inventor: LINK JAMES , LIU GANG , PEI ZHONGHUA , VON GELDERN THOMAS W , WINN MARTIN , XIN ZHILI , WANG SHELDON , BOYD STEVEN A , ZHU GUI-DONG , FREEMAN JENNIFER C , GUNAWARDANA INDRANI W , STAEGER MICHAEL A , JAE HWAN-SOO , LYNCH JOHN K
IPC: C07D243/08 , A61K20060101 , A61K31/10 , A61K31/165 , A61K31/33 , A61K31/40 , A61K31/4015 , A61K31/41 , A61K31/417 , A61K31/438 , A61K31/44 , A61K31/4427 , A61K31/445 , A61K31/4468 , A61K31/451 , A61K31/453 , A61K31/454 , A61K31/4545 , A61K31/472 , A61K31/496 , A61K31/4965 , A61K31/506 , A61K31/5375 , A61K31/5377 , A61K31/54 , A61K31/541 , A61K31/55 , A61K31/551 , A61P20060101 , A61P29/00 , A61P37/06 , C07C20060101 , C07C323/60 , C07C323/62 , C07D20060101 , C07D205/04 , C07D207/09 , C07D207/12 , C07D207/14 , C07D207/16 , C07D207/26 , C07D207/27 , C07D207/273 , C07D209/08 , C07D209/12 , C07D211/20 , C07D211/22 , C07D211/46 , C07D211/60 , C07D211/62 , C07D211/64 , C07D211/66 , C07D211/70 , C07D213/40 , C07D213/74 , C07D213/81 , C07D215/24 , C07D217/02 , C07D217/04 , C07D217/06 , C07D233/61 , C07D239/42 , C07D241/04 , C07D241/24 , C07D257/04 , C07D279/12 , C07D295/18 , C07D295/185 , C07D295/20 , C07D295/205 , C07D295/22 , C07D295/26 , C07D307/24 , C07D307/52 , C07D307/68 , C07D317/58 , C07D317/66 , C07D319/18 , C07D401/04 , C07D401/12 , C07D405/12 , C07D417/12 , C07D471/20 , C07D487/04 , C07D491/113 , C07D521/00
Abstract: The present invention relates to cinnamide compounds of formula (I), in which at least one of R1 to R5 is a "cis-cinnamide" (a) or a "trans-cinnamide" (b) and the other variables are as defined in the claims, that are useful for treating inflammatory and immune diseases, to pharmaceutical compositions containing these compounds and to methods of inhibiting inflammation or suppressing immune response in a mammal.
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53.
公开(公告)号:CZ20012412A3
公开(公告)日:2002-04-17
申请号:CZ20012412
申请日:1999-12-29
Applicant: ABBOTT LAB
Inventor: LINK JAMES , LIU GANG , PEI ZHONGHUA , VON GELDERN TOM , WINN MARTIN , XIN ZHILI , BOYD STEVEN A , JAE HWAN-SOO , LYNCH JOHN K , ZHU GUI-DONG , FREEMAN JENNIFER C , GUNAWARDANA INDRANI W , STAEGER MICHAEL A
IPC: C07D295/12 , A61K31/16 , A61K31/164 , A61K31/165 , A61K31/167 , A61K31/40 , A61K31/4015 , A61K31/404 , A61K31/407 , A61K31/417 , A61K31/438 , A61K31/44 , A61K31/443 , A61K31/445 , A61K31/4465 , A61K31/4468 , A61K31/45 , A61K31/453 , A61K31/454 , A61K31/472 , A61K31/495 , A61K31/496 , A61K31/506 , A61K31/5375 , A61K31/5377 , A61K31/54 , A61K31/541 , A61P29/00 , A61P37/02 , C07C323/00 , C07C323/62 , C07C323/63 , C07D207/08 , C07D207/09 , C07D207/12 , C07D207/14 , C07D207/20 , C07D207/22 , C07D207/26 , C07D207/263 , C07D207/27 , C07D207/273 , C07D207/34 , C07D207/36 , C07D209/08 , C07D209/12 , C07D209/14 , C07D209/18 , C07D211/22 , C07D211/26 , C07D211/42 , C07D211/44 , C07D211/46 , C07D211/54 , C07D211/60 , C07D211/62 , C07D211/66 , C07D211/74 , C07D213/74 , C07D213/75 , C07D213/81 , C07D213/82 , C07D215/04 , C07D215/36 , C07D217/06 , C07D233/61 , C07D235/26 , C07D239/42 , C07D241/04 , C07D241/18 , C07D241/24 , C07D243/08 , C07D265/30 , C07D295/13 , C07D295/16 , C07D295/18 , C07D295/185 , C07D295/205 , C07D295/215 , C07D295/26 , C07D295/32 , C07D307/52 , C07D307/68 , C07D317/58 , C07D317/62 , C07D319/18 , C07D319/20 , C07D401/04 , C07D401/06 , C07D401/12 , C07D403/04 , C07D403/12 , C07D405/06 , C07D405/12 , C07D405/14 , C07D411/04 , C07D413/04 , C07D413/12 , C07D413/14 , C07D417/12 , C07D471/10 , C07D487/08 , C07D491/10 , C07D311/22 , C07D209/38 , C07D209/30 , C07D239/88 , C07D295/20 , A61K31/095 , A61K31/33 , A61P37/00
Abstract: The present invention relates to novel cinnamide compounds that are useful for treating inflammatory and immune diseases, to pharmaceutical compositions comprising these compounds, and to methods of inhibiting inflammation or suppressing immune response in a mammal.
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公开(公告)号:NO20013241D0
公开(公告)日:2001-06-28
申请号:NO20013241
申请日:2001-06-28
Applicant: ABBOTT LAB
Inventor: LINK JAMES , LIU GANG , PEI ZHONGHUA , GELDERN TOM VON , WINN MARTIN , XIN ZHILI , BOYD STEVEN A , JAE HWAN-SOO , LYNCH JOHN K , ZHU GUI-DONG , FREEMAN JENNIFER C , GUNAWARDANA INDRANI W , STAEGER MICHAEL A
IPC: C07D295/12 , A61K31/16 , A61K31/164 , A61K31/165 , A61K31/167 , A61K31/40 , A61K31/4015 , A61K31/404 , A61K31/407 , A61K31/417 , A61K31/438 , A61K31/44 , A61K31/443 , A61K31/445 , A61K31/4465 , A61K31/4468 , A61K31/45 , A61K31/453 , A61K31/454 , A61K31/472 , A61K31/495 , A61K31/496 , A61K31/506 , A61K31/5375 , A61K31/5377 , A61K31/54 , A61K31/541 , A61P29/00 , A61P37/02 , C07C323/00 , C07C323/62 , C07C323/63 , C07D207/08 , C07D207/09 , C07D207/12 , C07D207/14 , C07D207/20 , C07D207/22 , C07D207/26 , C07D207/263 , C07D207/27 , C07D207/273 , C07D207/34 , C07D207/36 , C07D209/08 , C07D209/12 , C07D209/14 , C07D209/18 , C07D211/22 , C07D211/26 , C07D211/42 , C07D211/44 , C07D211/46 , C07D211/54 , C07D211/60 , C07D211/62 , C07D211/66 , C07D211/74 , C07D213/74 , C07D213/75 , C07D213/81 , C07D213/82 , C07D215/04 , C07D215/36 , C07D217/06 , C07D233/61 , C07D235/26 , C07D239/42 , C07D241/04 , C07D241/18 , C07D241/24 , C07D243/08 , C07D265/30 , C07D295/13 , C07D295/16 , C07D295/18 , C07D295/185 , C07D295/205 , C07D295/215 , C07D295/26 , C07D295/32 , C07D307/52 , C07D307/68 , C07D317/58 , C07D317/62 , C07D319/18 , C07D319/20 , C07D401/04 , C07D401/06 , C07D401/12 , C07D403/04 , C07D403/12 , C07D405/06 , C07D405/12 , C07D405/14 , C07D411/04 , C07D413/04 , C07D413/12 , C07D413/14 , C07D417/12 , C07D471/10 , C07D487/08 , C07D491/10 , C07C
Abstract: The present invention relates to novel cinnamide compounds that are useful for treating inflammatory and immune diseases, to pharmaceutical compositions comprising these compounds, and to methods of inhibiting inflammation or suppressing immune response in a mammal.
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公开(公告)号:AU4194400A
公开(公告)日:2000-10-23
申请号:AU4194400
申请日:2000-04-03
Applicant: ABBOTT LAB
Inventor: LINK JAMES , LIU GANG , PEI ZHONGHUA , GELDERN THOMAS W VON , WINN MARTIN , XIN ZHILI , WANG SHELDON , BOYD STEVEN A , ZHU GUI-DONG , FREEMAN JENNIFER C , GUNAWARDANA INDRANI W , STAEGER MICHAEL A , JAE HWAN-SOO , LYNCH JOHN K
IPC: C07D243/08 , A61K20060101 , A61K31/10 , A61K31/165 , A61K31/33 , A61K31/40 , A61K31/4015 , A61K31/41 , A61K31/417 , A61K31/438 , A61K31/44 , A61K31/4427 , A61K31/445 , A61K31/4468 , A61K31/451 , A61K31/453 , A61K31/454 , A61K31/4545 , A61K31/472 , A61K31/496 , A61K31/4965 , A61K31/506 , A61K31/5375 , A61K31/5377 , A61K31/54 , A61K31/541 , A61K31/55 , A61K31/551 , A61P20060101 , A61P29/00 , A61P37/06 , C07C20060101 , C07C323/60 , C07C323/62 , C07D20060101 , C07D205/04 , C07D207/09 , C07D207/12 , C07D207/14 , C07D207/16 , C07D207/26 , C07D207/27 , C07D207/273 , C07D209/08 , C07D209/12 , C07D211/20 , C07D211/22 , C07D211/46 , C07D211/60 , C07D211/62 , C07D211/64 , C07D211/66 , C07D211/70 , C07D213/40 , C07D213/74 , C07D213/81 , C07D215/24 , C07D217/02 , C07D217/04 , C07D217/06 , C07D233/61 , C07D239/42 , C07D241/04 , C07D241/24 , C07D257/04 , C07D279/12 , C07D295/18 , C07D295/185 , C07D295/20 , C07D295/205 , C07D295/22 , C07D295/26 , C07D307/24 , C07D307/52 , C07D307/68 , C07D317/58 , C07D317/66 , C07D319/18 , C07D401/04 , C07D401/12 , C07D405/12 , C07D417/12 , C07D471/20 , C07D487/04 , C07D491/113 , C07D521/00
Abstract: The present invention relates to cinnamide compounds of formula (I), in which at least one of R1 to R5 is a "cis-cinnamide" (a) or a "trans-cinnamide" (b) and the other variables are as defined in the claims, that are useful for treating inflammatory and immune diseases, to pharmaceutical compositions containing these compounds and to methods of inhibiting inflammation or suppressing immune response in a mammal.
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公开(公告)号:ES2421326T3
公开(公告)日:2013-08-30
申请号:ES07854765
申请日:2007-11-26
Applicant: ABBOTT LAB , ABBVIE INC
Inventor: SOUERS ANDREW J , GAO JU , HANSEN TODD MATTHEW , IYENGAR RAJESH R , KYM PHILIP R , LIU BO X , PEI ZHONGHUA , YEH VINCE , ZHAO GANG , XIN ZHILI
IPC: A61K31/17 , A61P1/16 , A61P3/00 , C07C229/40 , C07D231/20 , C07D263/48 , C07D277/38 , C07D403/04 , C07D405/04 , C07D487/04
Abstract: Un compuesto que tiene la fórmula (I), o una sal farmacéuticamente aceptable del mismo donde Q es fenilo o un heteroarilo monocíclico, opcionalmente sustituido con 1, 2 o 3 sustituyentes como se representan por T, donde cada T es independientemente alquilo, alquenilo, alquinilo, halógeno, -CN, -NO2, -OR1, -C) C (O) (R2), -N (Rw) (R1), -N (Rw) C (O) (R1), -N (Rw) -C (O) O (R1), -N (Rw) -C (O) N (R1) 2, -N (Rw) -S (O) 2 (R2), -C (O) O (R1), C (O) N (Rw) (R1), -CCO) R1, -SR1, -S (O) R2, -S (O) 2R2, -S (O) 2N (Rw) (R1), - (CRgRh) t-CN, - (CRgRh) t-NO2, - (CRgRh) t-OR1, - (CRgRh) t-OC (O) (R2) s - (CRgRh) t-N (Rw) (R1), - (CRgRh) t-N (Rw) C (O) (R1), - (CRgRh) t-N (Rw) -C (O) O (R1), - (CRgRh) tN (Rw) -C (O) N (R1) 2, - (CRgRh) t-N (Rw) -S (O) 2 (R2), - (CRgRh) t-C (O) O (R1), - (CRgRh) t-C (O) N (Rw) (R1), - (CRgRh) t-C (O) R1, (CRgRh) t-SR1, - (CRgRh) t-S (O) R2, - (CRgRh) t-S (O) 2R2, - (CRgRh) t-S (O) 2N (Rw) (R1) o haloalquilo; como alternativa, dos de los sustituyentes T adyacentes, junto con los átomos de carbono a los que están unidos, forman un anillo monocíclico seleccionados entre el grupo que consiste en fenilo, heterociclo y heteroarilo, donde opcionalmente cada anillo está opcionalmente sustituido adicionalmente con 1, 2 o 3 sustituyentes seleccionados entre el grupo que consiste en oxo, alquilo, alquenilo, alquinilo, halógeno, -CN, -NO2, -OR1-OC (O) (R2), -N (Rw) (R1), N (Rw) C (O) (R1), -N (Rw) -C (O) O (R1), -N (Rw) -C (O) N (R1) 2, -N (Rw) -S (O) 2 (R2), -C (O) O (R1), -C (O) N (Rw) (R1), -C (O) R1, -SR1, -S (O) R2, -S (O) 2R2, -S (O) 2N (Rw) (R1), - (CRgRh) t-CN, - (CRgRh) t-NO2, - (CRgRh) t-OR1, - (CRgRh) -OC (O) (R2), (CRgRh) t-N (Rw) (R1), - (CRgRh) t-N (RwC (O) (R1), - (CRgRh) t-N (Rw) -C (O) O (R1), - (CRgRh) t-N (Rw) -C (O) N (R1) 2, - (CRgRh) tN (Rw) -S (O) 2 (R2), - (CRgRh) t-C (O) O (R1), - (CRgRh) t-C (O) N (Rw) (R1), - (CRgRh) t-C (O) R1, - (CRgRh) t-SR1, - (CRgRh) tS (O) R2, - (CRgRh) t-S (O) 2R2, - (CRgRh) t-S (O) 2N (Rw) (R1) y haloalquilo; A es pirazolilo o triazolilo, donde cada A está independientemente sin sustituir o sustituido adicionalmente con 1, 2, 3, 4 o sustituyentes representados por Ra, y Ra se selecciona entre el grupo que consiste en oxo, -N (Rw) C (O) H, alquilo, alquenilo, alquinilo, halógeno, -NO2, -CN, haloalquilo, G1, - (CReRf) q-G1, -Y1-Y3, -Y1- (CReRf) q-Y3, -Y1 (CReRf) q-Y2-Y3 y -Y1- (CReRf) q-Y2- (CReRf) q-Y3; o A es la fórmula (a) donde Va es C (R4), Vb es N o C (R5) y Vc es N; o Va es N, Vb es C (R5) y Vc es N o C (R6); R4 es hidrógeno, halógeno, alquilo, haloalquilo, -CN, -ORb, -SRb, -S (O) Rc, -S (O) 2Rc, -N (Rb) (Rd) o heterociclo, R5 es hidrógeno, alquilo, halógeno, haloalquilo, -CN, -ORb, -SRb, -S (O) Rc, -S (O) 2Rc, arilo, heteroarilo, cicloalquilo, cicloalquenilo o heterociclo; R6 es hidrógeno, alquilo, halógeno, haloalquilo, arilo, heteroarilo, cicloalquilo, cicloalquenilo o heterociclo; o R4 y R5, junto con los átomos de carbono a los que están unidos, forman un anillo fenilo que está adicionalmente sin sustituir o sustituido con 1, 2, 3 o 4 sustituyentes seleccionados entre el grupo que consiste en alquilo, halógeno, -CN, -ORb, -SRb y haloalquilo; R7 es hidrógeno, alquilo, halógeno, -CN o haloalquilo; G1 es cicloalquilo, cicloalquenilo, heterociclo, heteroarilo o arilo; cada uno de Y1 e Y2 es, en cada caso, independientemente O, S, S (O), S (O) 2, N (Rw), -C (O), -OC (O) -, N (Rw) C (O) -, -N (Rw) S (O) 2-, -N (Rw) C (O) N (Rw) -, -OC (O) N (Rw) -, -N (Rw) C (O) O-, -C (O) O-, -C (O) N (Rw) -o S (O) 2N (Rw) -; donde el lado derecho de los restos -OC (O) -, -N (Rw) C (O) -, -N (Rw) S (O) 2 , -N (Rw) C (O) N (Rw) -, -OC (O) N (Rw) -, -N (Rw) C (O) O-, -C (O) O-, -C (O) N (Rw) -y -S (O) 2 (Rw) -está conectado con - (CReRf) q-o Y3; Y3, en cada caso, es independientemente hidrógeno, alquilo, haloalquilo, cicloalquilo, cicloalquenilo, heterociclo, heteroarilo o arilo; r y s son independientemente 1 o 2; X es X1, - (CRkRm) u-X1, - (CRkRm) u-C (O) -X2 o -C (O) -X2, X1, en cada caso, es independientemente heterociclo o heteroarilo; X2, en cada caso, es independientemente heteroarilo, heterociclo, -OR11, -N (Rw) (R3), -N (Rw) - (CRnRq) w-C (O) OR11, -N (Rw) - (CRnRq) w-OR11 o -N (Rw) - (CRnRq) w-S (O) 2R12; R11, en cada caso, es independientemente hidrógeno, alquilo, haloalquilo, arilalquilo o heteroarilalquilo; R12, en cada caso, es alquilo, haloalquilo, arilalquilo o heteroarilalquilo; donde el cicloalquenilo, cicloalquilo, heterociclo, heteroarilo, arilo, el resto arilo del arilalquilo y el resto heteroarilo del heteroarilalquilo como se representan por G1, Y3, X1, X2, R4, R5, R6, R11 y R12, está cada uno opcionalmente sustituido adicionalmente con 1, 2, 3, 4 o 5 sustituyentes seleccionados entre el grupo que consiste en alquilo, alquenilo, alquinilo, halógeno, oxo, etilendioxi, metilendioxi, -CN, -NO2, -OR1, -OC (O) (R2), -N (Rw) (R1), N (Rw) C (O) (R1), -M (Rw) -C (O) O (R1), -N (Rw) -S (O) 2 (R2), -C (O) O (R1), -C (O) N (Rw) (R1), -C (O) R1, -SR1, -S (O) R2, S (O) 2R2, -S (O) 2N (Rw) (R1), haloalquilo, - (CRgRh) t-CN, - (CRgRh) v-NO2, - (CRgRh) v-OR1, - (CRgRh) v-OC (O) (R2), (CRgRh) -N (Rw) (R1), - (CRgRh) v-N (Rw) C (O) (R1), - (CRgRh) w-N (Rw) -C (O) O (R1), - (CRgRh) v-N (Rw) -S (O) 2 (R2), - (CRgRh) vC (O) O (R1), - (CRgRh) v-C (O) N (Rw) (R1), - (CRgRh) v-C (O) R1, - (CRgRh) v-SR1, - (CRgRh) v-S (O) R2, - (CRgRh) v-S (O) 2R2 (CRgRh) v-S (O) 2N (Rw) (R1) y haloalquilo, cada uno de q, t, u, ν y w, en cada caso, es independientemente 1, 2, 3, 4, 5 o 6; R3 es hidrógeno, alquilo, haloalquilo, -OH, -S (O) 2R1, -C (O) OR1, heterociclo o heteroarilo, donde el heteroarilo está conectado al átomo de nitrógeno a través del átomo de carbono del anillo, y el heterociclo y el heteroarilo están opcionalmente sustituidos adicionalmente con 1 o 2 sustituyentes seleccionados entre el grupo que consiste en alquilo, halógeno, haloalquilo, -C (O) OR1, -OR1 y -N (Rw) (R1); Rb, Rd, Rx, Ry, Rza, Rzb, Rw, Re, Rg, Rh, Rk, Rm, Rn, Rq y R1, en cada caso, son independientemente hidrógeno, alquilo o haloalquilo; Re y R2, en cada caso, son independientemente alquilo o haloalquilo; y Rf, en cada caso, es independientemente hidrógeno, alquilo, halógeno, haloalquilo, -OH, -O (alquilo) o O (haloalquilo).
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公开(公告)号:CA2705987A1
公开(公告)日:2009-05-28
申请号:CA2705987
申请日:2008-11-20
Applicant: ABBOTT LAB
Inventor: VON GELDERN THOMAS W , BURKALOW JUFANG H , BARNES DAVID M , HAIGHT ANGHONY R , HENGEVELD JOHN E , LI XIAOFENG , MCLAUGHLIN MAUREEN A , NOONAN WILLIAM T , PEI ZHONGHUA , WU-WONG JINSHYUN RUTH
IPC: C07C401/00
Abstract: The invention relates to compounds that are vitamin D receptor activators, compositions comprising such compounds, methods of using such compounds and compositions, processes for preparing such compounds, and intermediates obtained during such processes.
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公开(公告)号:CZ296726B6
公开(公告)日:2006-05-17
申请号:CZ20012412
申请日:1999-12-29
Applicant: ABBOTT LAB
Inventor: LINK JAMES , LIU GANG , PEI ZHONGHUA , VON GELDERN TOM , WINN MARTIN , XIN ZHILI , BOYD STEVEN A , JAE HWAN-SOO , LYNCH JOHN K , ZHU GUI-DONG , FREEMAN JENNIFER C , GUNAWARDANA INDRANI W , STAEGER MICHAEL A
IPC: C07C323/62 , C07D295/12 , A61K31/095 , A61K31/16 , A61K31/164 , A61K31/165 , A61K31/167 , A61K31/33 , A61K31/40 , A61K31/4015 , A61K31/404 , A61K31/407 , A61K31/417 , A61K31/438 , A61K31/44 , A61K31/443 , A61K31/445 , A61K31/4465 , A61K31/4468 , A61K31/45 , A61K31/453 , A61K31/454 , A61K31/472 , A61K31/495 , A61K31/496 , A61K31/506 , A61K31/5375 , A61K31/5377 , A61K31/54 , A61K31/541 , A61P29/00 , A61P37/00 , A61P37/02 , C07C323/00 , C07C323/63 , C07D207/08 , C07D207/09 , C07D207/12 , C07D207/14 , C07D207/20 , C07D207/22 , C07D207/26 , C07D207/263 , C07D207/27 , C07D207/273 , C07D207/34 , C07D207/36 , C07D209/08 , C07D209/12 , C07D209/14 , C07D209/18 , C07D209/30 , C07D209/38 , C07D211/22 , C07D211/26 , C07D211/42 , C07D211/44 , C07D211/46 , C07D211/54 , C07D211/60 , C07D211/62 , C07D211/66 , C07D211/74 , C07D213/74 , C07D213/75 , C07D213/81 , C07D213/82 , C07D215/04 , C07D215/36 , C07D217/06 , C07D233/61 , C07D235/26 , C07D239/42 , C07D239/88 , C07D241/04 , C07D241/18 , C07D241/24 , C07D243/08 , C07D265/30 , C07D295/13 , C07D295/16 , C07D295/18 , C07D295/185 , C07D295/20 , C07D295/205 , C07D295/215 , C07D295/26 , C07D295/32 , C07D307/52 , C07D307/68 , C07D311/22 , C07D317/58 , C07D317/62 , C07D319/18 , C07D319/20 , C07D401/04 , C07D401/06 , C07D401/12 , C07D403/04 , C07D403/12 , C07D405/06 , C07D405/12 , C07D405/14 , C07D411/04 , C07D413/04 , C07D413/12 , C07D413/14 , C07D417/12 , C07D471/10 , C07D487/08 , C07D491/10
Abstract: Predlozené resení se týká urcitých aryl - nebo heteroarylthiofenylcinnamidu, tedy sloucenin na báziamidu kyseliny skoricové, obec. vzorce I, kde alespon jedna ze skupin R.sub.1.n. nebo R.sub.3.n. jsou cis-cinnamid vzorce a nebo trans-cinnamid vzorce b, které jsou vhodné pro lécení zánetlivých a imunních onemocnení, farmaceutických prostredku obsahujících tyto slouceniny. Dále se týká zpusobu výroby techto sloucenin a jejich pouzití pro výrobu léciv.
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公开(公告)号:HRP20010512B1
公开(公告)日:2006-02-28
申请号:HRP20010512
申请日:2001-07-10
Applicant: ABBOTT LAB
Inventor: LINK JAMES , LIU GANG , PEI ZHONGHUA , GELDERN TOM VON , WINN MARTIN , XIN ZHILI , BOYD STEVEN A , JAE HWAN-SOO , LYNCH JOHN K , ZHU GUI-DONG , FREEMAN JENNIFER C , GUNAWARDANA INDRANI W , STAEGER MICHAEL A
IPC: C07C323/62 , C07D295/12 , A61K31/10 , A61K31/16 , A61K31/164 , A61K31/165 , A61K31/167 , A61K31/33 , A61K31/40 , A61K31/4015 , A61K31/404 , A61K31/407 , A61K31/417 , A61K31/438 , A61K31/44 , A61K31/443 , A61K31/445 , A61K31/4465 , A61K31/4468 , A61K31/45 , A61K31/453 , A61K31/454 , A61K31/472 , A61K31/495 , A61K31/496 , A61K31/506 , A61K31/5375 , A61K31/5377 , A61K31/54 , A61K31/541 , A61P29/00 , A61P37/02 , C07C323/00 , C07C323/63 , C07D207/08 , C07D207/09 , C07D207/12 , C07D207/14 , C07D207/20 , C07D207/22 , C07D207/26 , C07D207/263 , C07D207/27 , C07D207/273 , C07D207/34 , C07D207/36 , C07D209/08 , C07D209/12 , C07D209/14 , C07D209/18 , C07D211/22 , C07D211/26 , C07D211/42 , C07D211/44 , C07D211/46 , C07D211/54 , C07D211/60 , C07D211/62 , C07D211/66 , C07D211/74 , C07D213/74 , C07D213/75 , C07D213/81 , C07D213/82 , C07D215/04 , C07D215/36 , C07D217/06 , C07D233/61 , C07D235/26 , C07D239/42 , C07D241/04 , C07D241/18 , C07D241/24 , C07D243/08 , C07D265/30 , C07D295/13 , C07D295/16 , C07D295/18 , C07D295/185 , C07D295/20 , C07D295/205 , C07D295/215 , C07D295/26 , C07D295/32 , C07D307/52 , C07D307/68 , C07D317/58 , C07D317/62 , C07D319/18 , C07D319/20 , C07D401/04 , C07D401/06 , C07D401/12 , C07D403/04 , C07D403/12 , C07D405/06 , C07D405/12 , C07D405/14 , C07D411/04 , C07D413/04 , C07D413/12 , C07D413/14 , C07D417/12 , C07D471/10 , C07D487/08 , C07D491/10
Abstract: The present invention relates to novel cinnamide compounds that are useful for treating inflammatory and immune diseases, to pharmaceutical compositions comprising these compounds, and to methods of inhibiting inflammation or suppressing immune response in a mammal.
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公开(公告)号:GEP20053657B
公开(公告)日:2005-11-10
申请号:GEAP2000004605
申请日:2000-04-03
Applicant: ABBOTT LAB
Inventor: JAE WOO PARK , LINK JAMES , LIU GANG , PEI ZHONGHUA , VON GELDERN TOM , WINN MARTIN , XIN ZHILI , WANG SHELDON , BOYD STEVEN A , ZHU GUI-DONG , FREEMAN JENNIFER C , GUNAWARDANA ; INDRANI W , STAEGER MICHAEL A , JAE HWAN-SOO , LYNCH JOHN K
IPC: C07C323/62 , C07D243/08 , A61K20060101 , A61K31/10 , A61K31/165 , A61K31/33 , A61K31/40 , A61K31/4015 , A61K31/41 , A61K31/417 , A61K31/438 , A61K31/44 , A61K31/4427 , A61K31/445 , A61K31/4468 , A61K31/451 , A61K31/453 , A61K31/454 , A61K31/4545 , A61K31/472 , A61K31/496 , A61K31/4965 , A61K31/506 , A61K31/5375 , A61K31/5377 , A61K31/54 , A61K31/541 , A61K31/55 , A61K31/551 , A61P20060101 , A61P29/00 , A61P37/06 , C07C20060101 , C07C323/60 , C07D20060101 , C07D205/04 , C07D207/09 , C07D207/12 , C07D207/14 , C07D207/16 , C07D207/26 , C07D207/27 , C07D207/273 , C07D209/08 , C07D209/12 , C07D211/20 , C07D211/22 , C07D211/46 , C07D211/60 , C07D211/62 , C07D211/64 , C07D211/66 , C07D211/70 , C07D213/40 , C07D213/74 , C07D213/81 , C07D215/24 , C07D217/02 , C07D217/04 , C07D217/06 , C07D233/61 , C07D239/42 , C07D241/04 , C07D241/24 , C07D257/04 , C07D279/12 , C07D295/18 , C07D295/185 , C07D295/20 , C07D295/205 , C07D295/22 , C07D295/26 , C07D307/24 , C07D307/52 , C07D307/68 , C07D317/58 , C07D317/66 , C07D319/18 , C07D401/04 , C07D401/12 , C07D405/12 , C07D417/12 , C07D471/20 , C07D487/04 , C07D491/113 , C07D521/00
Abstract: 1. Technical Result Increase in treatment efficiency of inflamma¬tory and immune diseases. 2. Essence The present invention relates to compounds that are useful for treating inflammatory and immune diseases, to pharmaceutical compositions containing these compounds and to methods of inhibiting inflammation or suppressing immune response in a mammal. 3. Field of Application Medicine.
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