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Cyclosomatostatin

Catalog No.GC15495

La cyclosomatostatine est un puissant antagoniste des récepteurs de la somatostatine (SST). La cyclosomatostatine peut inhiber la signalisation du récepteur de la somatostatine de type 1 (SSTR1) et diminuer la prolifération cellulaire, la taille de la population de cellules ALDH+ et la formation de sphères dans les cellules du cancer colorectal (CRC).

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Cyclosomatostatin Chemical Structure

Cas No.: 84211-54-1

Taille Prix Stock Qté
1mg
259,00 $US
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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents Related Products

IC50: N/A

Cyclosomatostatin is a non-selective somatostatin receptor antagonist.

Somatostatin is a regulatory hormone or tissue factor playing an inhibitory role in the normal regulation of several organ systems including hypothalamus and pituitary gland, central nervous system, gastrointestinal tract as well as pancreas.

In vitro: Although cyclosomatostatin could fully block the effect of somatostatin, it only partially reversed the inhibitory effect of cortistatin, a new anti-inflammatory peptide. This observation was further supported by the fact that cyclosomatostatin reversed the antiinfl ammatory effect of somatostatin and octreotide in vitro completely, while only partially reversing the effect of cortistatin [1].

In vivo: The effect of cortistatin was found to be dose dependent, with dose as low as 0.5 nmol (50 μg/kg) being partially protective. In contrast, cyclosomatostatin, somatostatin as well as octreotide were not protective [1].

Clinical trial: As the precursor of cyclosomatostatin, somatostatin has already been introduced in the clinical practice in some macrophage populations. Somatostatin shows protective effect in certain inflammatory disorders including pancreatitis and liver injury. However, somatostatin is not protective in lethal septic shock [1].

Reference:
[1] Gonzalez-Rey E,Chorny A,Robledo G,Delgado M.  Cortistatin, a new antiinflammatory peptide with therapeutic effect on lethal endotoxemia. J Exp Med.2006 Mar 20;203(3):563-71.

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