Veldoreotide TFA

For research use only. Not for therapeutic Use.

  • CAT Number: I040060
  • CAS Number: 2126831-23-8
  • Molecular Formula: C62H75F3N12O12
  • Molecular Weight: 1237.33
  • Purity: ≥95%
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Veldoreotide TFA (Cat No.: I040060) is a somatostatin analog with potent inhibitory effects on growth hormone (GH) secretion, making it a promising candidate for endocrine disease research. It exhibits high affinity for somatostatin receptors, particularly in conditions like acromegaly and neuroendocrine tumors. The trifluoroacetate (TFA) salt enhances its stability and solubility for in vitro and in vivo studies. Veldoreotide TFA is valuable in developing targeted therapies for hormone-related disorders, offering potential benefits in metabolic and endocrine disease research.


CAS Number 2126831-23-8
Synonyms

2-[(3S,6S,9S,12R,15S,18S)-9-(4-aminobutyl)-3,18-dibenzyl-6-[(1R)-1-hydroxyethyl]-12,15-bis(1H-indol-3-ylmethyl)-2,5,8,11,14,17,20,25-octaoxo-1,4,7,10,13,16,19,24-octazacyclooctacos-1-yl]acetamide;2,2,2-trifluoroacetic acid

Molecular Formula C62H75F3N12O12
Purity ≥95%
InChI InChI=1S/C60H74N12O10.C2HF3O2/c1-37(73)54-59(81)70-50(31-39-18-6-3-7-19-39)60(82)72(36-51(62)74)29-15-26-52(75)63-28-14-25-53(76)66-47(30-38-16-4-2-5-17-38)56(78)68-49(33-41-35-65-45-23-11-9-21-43(41)45)58(80)69-48(32-40-34-64-44-22-10-8-20-42(40)44)57(79)67-46(55(77)71-54)24-12-13-27-61;3-2(4,5)1(6)7/h2-11,16-23,34-35,37,46-50,54,64-65,73H,12-15,24-33,36,61H2,1H3,(H2,62,74)(H,63,75)(H,66,76)(H,67,79)(H,68,78)(H,69,80)(H,70,81)(H,71,77);(H,6,7)/t37-,46+,47+,48-,49+,50+,54+;/m1./s1
InChIKey KMXURQSBSDDSPX-NTYYTJCMSA-N
SMILES CC(C1C(=O)NC(C(=O)N(CCCC(=O)NCCCC(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N1)CCCCN)CC2=CNC3=CC=CC=C32)CC4=CNC5=CC=CC=C54)CC6=CC=CC=C6)CC(=O)N)CC7=CC=CC=C7)O.C(=O)(C(F)(F)F)O
Reference

[1]. Dasgupta P, et al. Pharmacological Characterization of Veldoreotide as a Somatostatin Receptor 4 Agonist. Life (Basel). 2021 Oct 12;11(10):1075.
[Content Brief]

[2]. Plöckinger U, et al. DG3173 (somatoprim), a unique somatostatin receptor subtypes 2-, 4- and 5-selective analogue, effectively reduces GH secretion in human GH-secreting pituitary adenomas even in Octreotide non-responsive tumours. Eur J Endocrinol. 2012 Feb;166(2):223-34.
[Content Brief]

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