AR061744A1 - Metodo para identificar proteinas mediadoras de respuesta a colapsina - Google Patents

Metodo para identificar proteinas mediadoras de respuesta a colapsina

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Publication number
AR061744A1
AR061744A1 ARP070102916A ARP070102916A AR061744A1 AR 061744 A1 AR061744 A1 AR 061744A1 AR P070102916 A ARP070102916 A AR P070102916A AR P070102916 A ARP070102916 A AR P070102916A AR 061744 A1 AR061744 A1 AR 061744A1
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AR
Argentina
Prior art keywords
alkyl
aryl
heterocyclic
group
crmp
Prior art date
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ARP070102916A
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English (en)
Inventor
Bettina Beyreuther
Thomas Stohr
Joachim Freitag
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Sanol Arznei Schwarz Gmbh
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Priority claimed from EP06013655A external-priority patent/EP1873527A1/en
Priority claimed from EP06021470A external-priority patent/EP1920780A1/en
Priority claimed from EP06024241A external-priority patent/EP1925314A1/en
Application filed by Sanol Arznei Schwarz Gmbh filed Critical Sanol Arznei Schwarz Gmbh
Publication of AR061744A1 publication Critical patent/AR061744A1/es

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Abstract

Reivindicacion 1: Un método para identificar un modulador de CRMP adecuado para la prevencion, alivio y/o tratamiento de una enfermedad asociada con CRMP, caracterizado porque comprende los pasos de: (a) seleccionar una sustancia; b) poner en contacto la sustancia seleccionada en el paso (a) con CRMP, y c) determinar si la CRMP interactua con la sustancia, en donde la sustancia que interactua con CRMP es un modulador de CRMP. Reivindicacion 37: Un complejo caracterizado porque comprende CRMP y un compuesto formula general (1) en donde R es hidrogeno, alquilo, alquenilo, alquinilo, arilo, aril alquilo heterocíclico, heterocíclico alquilo, alquilo heterocíclico, cicloalquilo o cicloalquil alquilo, y R está insustituido o está sustituido con al menos un grupo aceptor de electrones, y/o al menos un grupo donante de electrones; R1 es hidrogeno o alquilo, alquenilo, alquinilo, aril alquilo, arilo, heterocíclico alquilo, alquilo heterocíclico, heterocíclico, cicloalquilo, cicloalquil alquilo, cada uno insustituido o sustituido con al menos un grupo donante de electrones y/o al menos un grupo aceptor de electrones; R2 y R3 son independientemente hidrogeno, alquilo, alquenilo, alquinilo, alcoxi, alcoxialquilo, aril alquilo, arilo, halo, heterocíclico, heterocíclico alquilo, alquilo heterocíclico, cicloalquilo, cicloalquil alquilo, o Z-Y en donde R2 y R3 pueden estar insustituidos o sustituidos con al menos un grupo aceptor de electrones y/o al menos un grupo donante de electrones; Z es O, S, S(O)a, NR4, NR'6, PR4 o un enlace químico; Y es hidrogeno, alquilo, arilo, aril alquilo, alquenilo, alquinilo, halo, heterocíclico, heterocíclico alquilo, alquil heterocíclico e Y puede estar insustituido o sustituido con al menos un grupo donante de electrones y/o al menos un grupo aceptor de electrones, con la condicion de que, cuando Y es halo, Z es un enlace químico, o ZY conjuntamente son NR4NR5R7, NR4OR5, ONR4R7, OPR4R5, PR4OR5, SNR4R7, NR4SR7, SPR4R5, PR4SR7, NR4PR5R6, PR4NR5R7, N+R5R6R7, NR4C(=O)R5, SC(=O)R5, NR4C(=O)OR5, SC(=O)OR5 o NR4NR5-C(=O)OR6; R'6 es hidrogeno, alquilo, alquenilo o alquinilo y que puede estar insustituido o sustituido con al menos un grupo aceptor de electrones y/o al menos un grupo donante de electrones; R4, R5 y R6 son independientemente hidrogeno, alquilo, arilo, aril alquilo, alquenilo, o alquinilo, en donde R4, R5 y R6 pueden estar independientemente insustituidos o sustituidos con al menos un grupo aceptor de electrones y/o al menos un grupo donante de electrones; R7 es R6 o COOR8 o COR8, en donde R7 puede estar insustituido o sustituido con al menos un grupo aceptor de electrones y/o al menos un grupo donante de electrones; R8 es hidrogeno o alquilo, o aril alquilo, y el grupo arilo o alquilo puede estar insustituido o sustituido con al menos un grupo aceptor de electrones y/o al menos un grupo donante de electrones; y n es 1-4; o una sal farmacéuticamente aceptable o metabolito del mismo, en donde el compuesto, sal farmacéuticamente aceptable del mismo o metabolito del mismo, exhibe afinidad con CRMP distinguida por un KD inferior a aproximadamente 5 mM.
ARP070102916A 2006-06-30 2007-06-29 Metodo para identificar proteinas mediadoras de respuesta a colapsina AR061744A1 (es)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
EP06013655A EP1873527A1 (en) 2006-06-30 2006-06-30 Method for identifying CRMP modulators
EP06021469 2006-10-12
EP06021470A EP1920780A1 (en) 2006-10-12 2006-10-12 Peptide compounds for the treatment of hyperexcitability disorders
EP06024241A EP1925314A1 (en) 2006-11-22 2006-11-22 Pharmaceutical composition with synergistic anticonvulsant effect

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Publication Number Publication Date
AR061744A1 true AR061744A1 (es) 2008-09-17

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Family Applications (2)

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ARP070102915A AR061743A1 (es) 2006-06-30 2007-06-29 Compuestos peptidicos para el tratamiento de trastornos de hiperexcitabilidad y trastornos asociados con disfuncion del canal de hierro
ARP070102916A AR061744A1 (es) 2006-06-30 2007-06-29 Metodo para identificar proteinas mediadoras de respuesta a colapsina

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ARP070102915A AR061743A1 (es) 2006-06-30 2007-06-29 Compuestos peptidicos para el tratamiento de trastornos de hiperexcitabilidad y trastornos asociados con disfuncion del canal de hierro

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US (3) US9308183B2 (es)
EP (3) EP2038659A2 (es)
JP (1) JP2009541397A (es)
KR (1) KR20090030329A (es)
CN (2) CN101466390B (es)
AR (2) AR061743A1 (es)
AU (1) AU2007263936A1 (es)
BR (1) BRPI0713994A2 (es)
CA (1) CA2654652C (es)
EA (1) EA200900098A1 (es)
ES (1) ES2569333T3 (es)
MX (1) MX2009000249A (es)
TW (2) TW200819744A (es)
WO (2) WO2008000512A2 (es)

Families Citing this family (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE60100055T2 (de) * 2001-03-21 2003-07-24 Sanol Arznei Schwarz Gmbh Neue Verwendung einer Klasse von Peptidverbindungen zur Behandlung von Allodynie oder andere Arten von chronischen oder Phantomschmerzen
US20100256179A1 (en) * 2004-03-26 2010-10-07 Ucb Pharma Gmbh Combination therapy for pain in painful diabetic neuropathy
CA2562937A1 (en) * 2004-04-16 2005-10-27 Schwarz Pharma Ag Use of peptidic compounds for the prophylaxis and treatment of chronic headache
EP1604655A1 (en) 2004-06-09 2005-12-14 Schwarz Pharma Ag Novel use of peptide compounds for treating pain in trigeminal neuralgia
AU2005276634B2 (en) * 2004-08-27 2011-03-24 Ucb Pharma Gmbh Use of peptide compounds for treating bone cancer pain, chemotherapy-and nucleoside-induced pain
EP1642889A1 (en) * 2004-10-02 2006-04-05 Schwarz Pharma Ag Improved synthesis scheme for lacosamide
EP1754476A1 (en) * 2005-08-18 2007-02-21 Schwarz Pharma Ag Lacosamide (SPM 927) for treating myalgia, e.g. fibromyalgia
US20070043120A1 (en) * 2005-08-18 2007-02-22 Bettina Beyreuther Therapeutic combination for painful medical conditions
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