Octreotide acetate

CAS No. 79517-01-4

Octreotide acetate( SMS-201995 )

Catalog No. M15977 CAS No. 79517-01-4

An octapeptide that mimics natural somatostatin pharmacologically, that is 200 times more potent than somatostatin.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 27 In Stock
10MG 42 In Stock
25MG 63 In Stock
50MG 84 In Stock
100MG 123 In Stock
200MG 177 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Octreotide acetate
  • Note
    Research use only, not for human use.
  • Brief Description
    An octapeptide that mimics natural somatostatin pharmacologically, that is 200 times more potent than somatostatin.
  • Description
    An octapeptide that mimics natural somatostatin pharmacologically, that is 200 times more potent than somatostatin; has also been shown to produce analgesic effects, most probably acting as a partial agonist at the mu opioid receptor.(In Vivo):Octreotide-treated groups show a significant reduction in the tumor volume when compared with saline group. Octreotide-PPSG (1.4 mg/kg, i.p.) shows greater antitumor effect than Octreotide-soln (100 μg/kg, i.p.). Octreotide-treatments results in significant inhibitory effect on the expression levels of SSTR2 and SSTR5 in primary HCC-bearing rats compared with the saline group. Octreotide-PPSG appears to inhibit the expression of SSTR2 and SSTR5 to a greater extent than that of Octreotide-soln treated group. A test dose of octreotide acetate significantly decreases the serum gastrin level to approximately one third of the baseline in 2 hr and the effect lasted approximately for 6 hr. On day 21, treatment with sustained-release formulation of octreotide acetatea (5 mg intramuscular, q 4 wk) is initiated.
  • In Vitro
    ——
  • In Vivo
    Octreotide-treated groups show a significant reduction in the tumor volume when compared with saline group. Octreotide-PPSG (1.4 mg/kg, i.p.) shows greater antitumor effect than Octreotide-soln (100 μg/kg, i.p.). Octreotide-treatments results in significant inhibitory effect on the expression levels of SSTR2 and SSTR5 in primary HCC-bearing rats compared with the saline group. Octreotide-PPSG appears to inhibit the expression of SSTR2 and SSTR5 to a greater extent than that of Octreotide-soln treated group. A test dose of octreotide acetate significantly decreases the serum gastrin level to approximately one third of the baseline in 2 hr and the effect lasted approximately for 6 hr. On day 21, treatment with sustained-release formulation of octreotide acetatea (5 mg intramuscular, q 4 wk) is initiated.
  • Synonyms
    SMS-201995
  • Pathway
    GPCR/G Protein
  • Target
    Somatostatin Receptor
  • Recptor
    SomatostatinReceptor|Somatostatin
  • Research Area
    Other Indications
  • Indication
    Other Disease

Chemical Information

  • CAS Number
    79517-01-4
  • Formula Weight
    1079.291
  • Molecular Formula
    C51H70N10O12S2
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: ≥ 29 mg/mL
  • SMILES
    CC(C1C(=O)NC(CSSCC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N1)CCCCN)CC2=CNC3=CC=CC=C32)CC4=CC=CC=C4)NC(=O)C(CC5=CC=CC=C5)N)C(=O)NC(CO)C(C)O)O
  • Chemical Name
    L-Cysteinamide, D-phenylalanyl-L-cysteinyl-L-phenylalanyl-D-tryptophyl-L-lysyl-L-threonyl-N-[(1R,2R)-2-hydroxy-1-(hydroxymethyl)propyl]-, cyclic (2→7)-disulfide, acetate (1:?)

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Maurer R, et al. Proc Natl Acad Sci U S A. 1982 Aug;79(15):4815-7. 2. Allen MP, et al. Bioorg Med Chem Lett. 2000 Mar 20;10(6):523-6.
molnova catalog
related products
  • Pasireotide L-aspart...

    A potent, stable cyclohexapeptide somatostatin mimic that exhibits unique high-affinity binding to human somatostatin receptors.

  • L-803087

    L-803087 is a potent and selective agonist of the growth inhibitor sst4 receptor with a Ki value of 0.7 nM for sst4, demonstrating over 280-fold selectivity compared to other growth inhibitory receptors.

  • Cortistatin-14

    Cortistatin 14 is a neuropeptide expressed in inhibitory neurons of the cerebral cortex. Depresses neuronal activity, and induces slow-wave sleep, likely through antagonism of acetylcholine. It is structurally and functionally similar to somatostatin 14. Competes with somatostatin 14 for binding of somatostatin receptors (IC50s=5, 0.09, 0.3, 0.2, and 0.3nM for receptors sst1-5, respectively).