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Somatostatin Receptor

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Somatostatin Receptor

Chemical Structure Cat. No. Product Name CAS No.
Lutetium Lu177 edotreotide Chemical Structure
 BCP49208 Lutetium Lu177 edotreotide 321835-55-6
Lutetium Lu 177-Edotreotide is a radioconjugate consisting of the somatostatin analogue edotreotide labeled with lutetium Lu 177 with potential antineoplastic activities.
Paltusotine Chemical Structure
 BCP47002 Paltusotine 2172870-89-0
Paltusotine, also known as CRN00808, is a somatostatin receptor agonist.
Octreotide D8 Chemical Structure
 BCP31200 Octreotide D8 1240797-41-4
Octreotide D8 is a labeled Octreotide, intended for use as an internal standard for the quantification of Octreotide by GC- or LC-mass spectrometry.
TT 232 Chemical Structure
 BCP12430 TT 232 147159-51-1
TT2-32 induces a biphasic activation of phosphotyrosine phosphatase activity in human colon tumor cell line, SW620.
Somatostatin Chemical Structure
 BCP04492 Somatostatin 51110-01-1
Somatostatin is a tetradecapeptide which can suppress the growth hormone (GH) secretion and control the pituitary hormone secretion in human CNS.
Somatostatin Acetate Chemical Structure
 BCP02048 Somatostatin Acetate 38916-34-6
Somatostatin Acetate is a peptide hormone that regulates the endocrine system and affects neurotransmission and cell proliferation via interaction with G protein-coupled somatostatin receptors and inhibition of the release of numerous secondary hormones.
Pasireotide Chemical Structure
 BCP28075 Pasireotide 396091-73-9
Pasireotide(SOM 230) is a stable cyclohexapeptide somatostatin mimic that exhibits unique high-affinity binding to human somatostatin receptors (subtypes sst1/2/3/4/5, pKi=8.2/9.0/9.1/<7.0/9.9 respectively).
Octreotide acetate Chemical Structure
 BCP04661 Octreotide acetate 79517-01-4
Octreotide acetate(SMS 201995 acetate) is a long-acting octapeptide with pharmacologic actions mimicking those of the natural hormone somatostatin.
Octreotide Chemical Structure
 BCP28870 Octreotide 83150-76-9
Octreotide is a somatostatin analog that binds to the somatostatin receptor, mainly subtypes 2, 3, and 5, increases Gi activity, and reduces intracellular cAMP production.
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