PE20060426A1 - DERIVADOS DE ACIDO TARTARICO COMO INHIBIDORES DE MMPs, ADAMs, TACE Y TNF-alfa - Google Patents

DERIVADOS DE ACIDO TARTARICO COMO INHIBIDORES DE MMPs, ADAMs, TACE Y TNF-alfa

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Publication number
PE20060426A1
PE20060426A1 PE2005000615A PE2005000615A PE20060426A1 PE 20060426 A1 PE20060426 A1 PE 20060426A1 PE 2005000615 A PE2005000615 A PE 2005000615A PE 2005000615 A PE2005000615 A PE 2005000615A PE 20060426 A1 PE20060426 A1 PE 20060426A1
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PE
Peru
Prior art keywords
tace
alkyl
mmps
adams
inhibitors
Prior art date
Application number
PE2005000615A
Other languages
English (en)
Inventor
Zhuyan Guo
Peter Orth
Zhaoning Zhu
Tin Yau Chan
Brian Mckittrick
Brian Lavey
Sunil Paliwal
Neng-Yang Shih
Kristin E Rosner
Shipps
Lianyun Zhao
Wensheng Yu
Janeta Popovici-Muller
Vinay M Girijavallabhan
Dansu Li
Chaoyang Dai
David B Belanger
M Arshad Siddiqui
Pauline C Ting
Shing-Chun Wong
Guowei Zhou
Joseph A Kozlowski
Henry A Vaccaro
Robert D Mazzola
Original Assignee
Schering Corp
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Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=35355800&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PE20060426(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Schering Corp filed Critical Schering Corp
Publication of PE20060426A1 publication Critical patent/PE20060426A1/es

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Abstract

SE REFIERE A COMPUESTOS DE FORMULA (I), EN DONDE A ES (R1)(R2)NCO-, (R1)(R2)NCS-, ENTRE OTROS; J Y E SON O, S O NR5; T ES O U S; R1 Y R2 SON INDEPENDIENTEMENTE H, ALQUILO, CICLOALQUILO, ENTRE OTROS, O JUNTOS CON EL N AL CUAL ESTAN UNIDOS FORMAN UN HETEROCICLO DE 4 A 8 MIEMBROS CON 1 A 3 HETEROATOMOS DE N OPCIONALMENTE SUSTITUIDOS POR R70 U OPCIONALMENTE FUSIONADO CON ARILO, HETEROARILO, ENTRE OTROS; OPCIONALMENTE SUSTITUIDOS; R10, R20, R30, R40 Y R50 SON INDEPENDIENTEMENTE H, ALQUILO, ENTRE OTROS; W ES -(CR(13)2)n- O UN ENLACE COVALENTE; X ESTA PRESENTE O NO, ES ALQUILO, ARILO TAL COMO, FENILO, AZETIDINO, PIRIDINILO, PIRROLIDINO, PIPERIDINILO, TIENILO, OXAZOLILO, IMIDAZOLILO, ENTRE OTROS; Y ESTA PRESENTE O NO, ES UN ENLACE COVALENTE O -C(R6)2]n-; Z ES H, ARILO O HETEROARILO, TAL COMO FENILO, INDOLILO, BENZOIMIDAZOLILO, PIRAZOLILO, TIENILO, PIRIDINILO, IMIDAZOLILO, ENTRE OTROS, OPCIONALMENTE SUSTITUIDOS POR CIANO, ALCOXI, HALOGENO, ALQUILO, ENTRE OTROS. ESTOS COMPUESTOS SON INHIBIDORES DE LAS MALOPROTEINASAS DE MATRIZ (MMPS), UNA DESINTEGRINA Y METALOPROTEASAS (ADAMs) Y/O A LA ENZIMA CONVERTIDORA DEL FACTOR DE NECROSIS TUMORAL ALFA (TACE) POR LO QUE EVITAN LA LIBERACION DEL FACTOR DE NECROSIS TUMORAL ALFA (TNF-a), POR LO QUE SON UTILES EN EL TRATAMIENTO DE OSTEOARTRITIS Y ARTRITIS REUMATOIDEA Y OTRAS ENFERMEDADES AUTOINMUNES
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IL179674A0 (en) 2007-05-15
US20100145048A1 (en) 2010-06-10
US7652020B2 (en) 2010-01-26
MXPA06014054A (es) 2007-01-31
KR20070103671A (ko) 2007-10-24
AR051172A1 (es) 2006-12-27
US8039467B2 (en) 2011-10-18
CA2569111A1 (en) 2005-12-22
JP2008501691A (ja) 2008-01-24
WO2005121130A2 (en) 2005-12-22
EP1773821A2 (en) 2007-04-18
CN101027295A (zh) 2007-08-29
AU2005252201A1 (en) 2005-12-22
US20060252778A1 (en) 2006-11-09

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