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Peptides pharmaceutiques

» Peptides » Peptides pharmaceutiques

  • Caractéristiques
  • Description du produit
  • Utilisation du produit

Nom:Taltirelin
Autre nom: TA 0910;Taltirelin;Taltireline;Ceredist, TA-0910;Taltirelin Acetate;TA-0910, taltirelin;Taltirelin interMediate;TALTIRELIN INTERMEDIATES;Taltirelin Acetate,TA-0910;L-Prolinamide,(4S)-hexahydro-1-methyl-
Formule moléculaire: C17H23N7O5
Poids moléculaire: 405.41
Numéro de cas: 103300-74-9
Pureté:98%
Apparence: poudre blanche
Source: synthétique

Taltirelin (marketed under the tradename Ceredist) is a thyrotropin-releasing hormone (TRH) analog, 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

Taltirelin (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.

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