Vapreotide

For research use only. Not for therapeutic Use.

  • CAT Number: I000190
  • CAS Number: 103222-11-3
  • Molecular Formula: C57H70N12O9S2
  • Molecular Weight: 1131.37
  • Purity: ≥95%
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Vapreotide(Cat No.:I000190)is a synthetic octapeptide that acts as a somatostatin analogue, mimicking the effects of the naturally occurring hormone somatostatin. It works by binding to somatostatin receptors, particularly SST2 and SST5, to inhibit the secretion of several hormones, including growth hormone, insulin, glucagon, and serotonin. Vapreotide is primarily investigated for treating conditions like acromegaly, neuroendocrine tumors, and variceal bleeding in cirrhosis. It has been shown to reduce hormone-related symptoms and improve patient outcomes. Ongoing clinical trials are evaluating its safety, efficacy, and potential for broader therapeutic applications in endocrinological and gastrointestinal disorders.


Catalog Number I000190
CAS Number 103222-11-3
Molecular Formula C57H70N12O9S2
Purity ≥95%
Target Neuronal Signaling
Solubility H2O
Storage Store at -20°C
IUPAC Name 10-(4-aminobutyl)-N-[1-amino-3-(1H-indol-3-yl)-1-oxopropan-2-yl]-19-[(2-amino-3-phenylpropanoyl)amino]-16-[(4-hydroxyphenyl)methyl]-13-(1H-indol-3-ylmethyl)-6,9,12,15,18-pentaoxo-7-propan-2-yl-1,2-dithia-5,8,11,14,17-pentazacycloicosane-4-carboxamide
InChI InChI=1S/C57H70N12O9S2/c1-32(2)49-57(78)68-48(55(76)64-44(50(60)71)26-35-28-61-41-16-8-6-14-38(35)41)31-80-79-30-47(67-51(72)40(59)24-33-12-4-3-5-13-33)56(77)65-45(25-34-19-21-37(70)22-20-34)53(74)66-46(27-36-29-62-42-17-9-7-15-39(36)42)54(75)63-43(52(73)69-49)18-10-11-23-58/h3-9,12-17,19-22,28-29,32,40,43-49,61-62,70H,10-11,18,23-27,30-31,58-59H2,1-2H3,(H2,60,71)(H,63,75)(H,64,76)(H,65,77)(H,66,74)(H,67,72)(H,68,78)(H,69,73)
InChIKey SWXOGPJRIDTIRL-UHFFFAOYSA-N
SMILES CC(C)C1C(=O)NC(CSSCC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N1)CCCCN)CC2=CNC3=CC=CC=C32)CC4=CC=C(C=C4)O)NC(=O)C(CC5=CC=CC=C5)N)C(=O)NC(CC6=CNC7=CC=CC=C76)C(=O)N
Reference

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<br>[1]. Spitsin S et al. Analog of somatostatin vapreotide exhibits biological effects in vitro via interaction with neurokinin-1 receptor. Neuroimmunomodulation. 2013;20(5):247-55.

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