Abstract:
The present invention relates to compounds such as those of formula (I-A) inhibitors of voltage-gated sodium channels. The invention also provides pharmaceutically acceptable compositions comprising the compounds of the invention and methods of using the compositions in the treatment of various disorders, such as pain.
Abstract:
The present invention relates to compounds such as those of formula (I-A) inhibitors of voltage-gated sodium channels. The invention also provides pharmaceutically acceptable compositions comprising the compounds of the invention and methods of using the compositions in the treatment of various disorders, such as pain.
Abstract:
The present invention relates to compounds such as those of formula (I-A) inhibitors of voltage-gated sodium channels. The invention also provides pharmaceutically acceptable compositions comprising the compounds of the invention and methods of using the compositions in the treatment of various disorders, such as pain.
Abstract:
The present invention relates to heterocyclic derivatives useful as inhibitors of ion channels. The invention also provides pharmaceutically acceptable compositions comprising the compounds of the invention and methods of using the compositions in the treatment of various disorders.
Abstract:
REFERIDA A UN COMPUESTO DE FORMULA I-A DONDE RN ES H, C1-C4 ALIIFATICO OPCIONALMENTE SUSTITUIDO; X1 ES O, S O NRX; X2 ES C1-C3 ALIFATICO OPCIONALMENTE SUSTITUIDO; p ES 0-1; Z ES i, ii, ENTRE OTROS; T ES ANILLO BICICLICO O TRICICLICO, AROMATICO O NO, DE 8-14 MIEMBROS TAL COMO NAFTILO, TETRALINA, O DECALINA. SON COMPUESTOS PREFERIDOS: 4-(2,4-DICLOROFENOXI)-BUTIRATO DE ETILO; 5,7-DICLORO-INDOL-2-IL-N-[4-(TIADIAZOL-2-ILSULFAMOIL)-FENIL]AMIDA Y N-[4-(TIAZOL-2-ILSULFAMOIL)-FENIL]-2-(4-FLUOROFENOXI)-ACETAMIDA; ENTRE OTROS. TAMBIEN REFERIDO A COMPOSICIONES FARMACEUTICAS QUE COMPRENDEN DICHOS COMPUESTOS QUE SON UTILES PARA EL TRATAMIENTO DE DOLORES NEUROPATICOS E INTRATABLES
Abstract:
The present invention relates to compounds of formula (I) useful as inhibito rs of voltage-gated sodium channels. The invention also provides pharmaceutical ly acceptable compositions comprising the compounds of the invention and method s of using the compositions in the treatment of various disorders. Wherein R1, R2, X1-X4, P, and ring A are as defined in the present application.
Abstract:
Compounds of formula I, wherein the substituents are as defined in the specification, are useful for inhibiting sodium and calcium channels, and for treating acute, chronic, neuropathic, or inflammatory pain, arthritis, migraine, cluster headaches, trigeminal neuralgia, herpetic neuralgia, general neuralgias, epilepsy or epileptic conditions, neurodegenerative disorders, psychiatric disorders, anxiety, depression, myotonia, arrhythmia, movement disorders, neuroendocrine disorders, ataxia, multiple sclerosis, irritable bowel syndrome, incontinence, visceral pain, osteoarthritis pain, postherpetic neuralgia, diabetic neuropathy, radicular pain, sciatica, back pain, head or neck pain, severe or intractable pain, nociceptive pain, breakthrough pain, postsurgical pain, and cancer pain. Novel compounds of formula I-A are also disclosed.
Abstract:
REFERIDA A UN COMPUESTO DE FORMULA I O A UNA DE SUS SALES DONDE p ES 0-2; X1, X2, X3 Y X4 SON CADA UNO C=O, S, O, ENTRE OTROS; R1 Y R2 SON CADA UNO, H, UN GRUPO ALIFATICO C1-C6; ARILO DE 5-6 MIEMBROS, ENTRE OTROS; A ES ANILLO MONOCICLICO DE 5-6 MIEMBROS O BICICLICO DE 8-10 MIEMBROS, ANILLO SATURADO DE 3-7 MIEMBROS, ENTRE OTROS. ADICIONALMENTE, ESTOS COMPUESTOS RESULTANTES QUE SON UTILES COMO INHIBIDORES DE LOS CANALES DE SODIO REGULADOS POR VOLTAJE FORMAN COMPOSICIONES FARMACEUTICAS PARA EL TRATAMIENTO DE DOLOR AGUDO, ARTRITIS, EPILEPSIA, ENTRE OTROS
Abstract:
The present invention relates to compounds useful as inhibitors of voltage-gated sodium channels. The invention also provides pharmaceutically acceptable compositions comprising the compounds of the invention and methods of using the compositions in the treatment of various disorders.
Abstract:
Disclosed are compounds of formula III, wherein the substituents are as defined in the specification, their properties as inhibitors of voltage-gated sodium or calcium channel blockers and their utility in the treatment of pain. Also disclosed is a broader class of voltage-gated sodium/calcium channel blockers having formula T-L1-A-L2-Z wherein the substituents are as defined in the specification. (62) Divided Out of 545710