Nom:Taltiréline
Autre nom: PAREMENT 0910;Taltiréline;Taltiréline;Cérédiste, PAREMENT-0910;Acétate de Taltiréline;PAREMENT-0910, taltiréline;Taltirelin intermédiaire;INTERMÉDIAIRES TALTIRELINE;Acétate de Taltiréline,PAREMENT-0910;L-Prolinamide,(4S)-hexahydro-1-méthyle-
Formule moléculaire: C17H23N7O5
Poids moléculaire: 405.41
Numéro de cas: 103300-74-9
Pureté:98%
Apparence: poudre blanche
Source: synthétique
Taltiréline (marketed under the tradename Ceredist) is a thyrotropin-releasing hormone (TRH) analogique, which mimics the physiological actions of TRH, but with a much longer half-life and duration of effects,and little development of tolerance following prolonged dosing.It has nootropic,neuroprotective and analgesic effects.
Taltirelin is primarily being researched for the treatment of spinocerebellar ataxia; limited research has also been carried out with regard to other neurodegenerative disorders
Taltiréline (TAL) is a thyrotropin-releasing hormone (TRH) analog that is approved for use in humans in Japan. In this study, we characterized TAL binding to and signaling by the human TRH receptor (TRH-R) in a model cell system. We found that TAL exhibited lower binding affinities than TRH and lower signaling potency via the inositol-1,4,5-trisphosphate/calcium pathway than TRH. Cependant, TAL exhibited higher intrinsic efficacy than TRH in stimulating inositol-1,4,5-trisphosphate second messenger generation. This is the first study that elucidates the pharmacology of TAL at TRH-R and shows that TAL is a superagonist at TRH-R. We suggest the superagonism exhibited by TAL may in part explain its higher activity in mediating central nervous system effects in humans compared to TRH.