Compounds derived from indole and azaindol as inhibitors of FAAH； Pharmaceutical composition that is useful for the Treatment or prevention of Pain, autoimmune disorders, inflammation, pruritus, Gastrointestinal Diseases, Substance Abuse related disease S, among other diseases.
The present disclosure relates to compounds useful as inhibitors of the enzyme Fatty Acid Amide Hydrolase (FAAH). The disclosure also provides pharmaceutically acceptable compositions comprising the compounds of the disclosure and methods of using the compositions in the treatment or prevention of various disorders. Compounds of the invention are described in Table 1.COMPUESTOS DERIVADOS DE HETREOCICLOS NITROGENADOS CON ACTIVIDAD INHIBIDORA DE FAAH； COMPOSCION FARMACEUTICA QUE LOS COMPRENBDE； UTILES EN EL TRATAMIENTO DEL DOLOR, INFLAMACION, ENFERMEDADES NEUROLOGICAS, ENFERMEDADES AUTOINMUNE, ENTRE OTROS.
