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Octreotide acetate

  • Chemical raw materials, non-pharmaceuticals.
  • Product Name: Octreotide acetate
  • CasNo: 83150-76-9
  • Purity:
  • Appearance: white powder

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CasNo: 83150-76-9

Molecular Formula: C49H66N10O10S2

Appearance: white powder

Purity 99% Min Octreotide acetate 83150-76-9 Spot Supply with Safe Transportation

  • Molecular Formula:C49H66N10O10S2
  • Molecular Weight:1019.26
  • Appearance/Colour:white powder 
  • Vapor Pressure:0mmHg at 25°C 
  • Refractive Index:1.673 
  • Boiling Point:1447.228°C at 760 mmHg 
  • PKA:12.60±0.70(Predicted) 
  • Flash Point:829.053 C 
  • PSA:382.82000 
  • Density:1.395 g/cm3 
  • LogP:3.02100 

Octreotide acetate(Cas 83150-76-9) Usage

Indications

Octreotide acetate (Sandostatin) is a synthetic peptide analogue of the hormone somatostatin. Its actions include inhibition of the pituitary secretion of growth hormone and an inhibition of pancreatic islet cell secretion of insulin and glucagon. Unlike somatostatin, which has a plasma half-life of a few minutes, octreotide has a plasma elimination half-life of 1 to 2 hours. Excretion of the drug is primarily renal.

Therapeutic Function

Antiulcer, Growth hormone inhibitor

Biological Functions

Octreotide acetate, a long-acting octapeptide analogue of somatostatin, has a half-life of approximately 100 minutes. A comparison of the primary structures of octreotide and somatostatin suggests little similarity, but from earlier work at the Salk Institute it was known that not all the residues in somatostatin were necessary to elicit its full biological activity. Other studies suggested that the essential fragment for its activity was the tetrapeptide Phe7-Trp8- Lys9-Thr10. These earlier studies helped in the design of the potent drug now known as octreotide acetate. This drug suppresses the secretion of gastroenteropancreatic peptides, such as gastrin, vasoactive intestinal peptide (VIP), insulin, and glucagon, as well as pituitary GH. Furthermore, it is more potent than natural somatostatin in inhibiting the release of glucagon, insulin, and GH.

Biochem/physiol Actions

Octreotide is three times more potent than the native hormone in inhibiting the secretion of growth hormone glucagon and insulin in vivo. Octreotide regulates serum prolactin levels and resolves galactorrhea or (secondary) amenorrhea in acromegaly patients. Hence, this peptide can be considered as a potent therapeutic for acromegaly treatment.

Veterinary Drugs and Treatments

Octreotide may be useful in the adjunctive treatment of hyperinsulinemia in patients with insulinomas (especially dogs, ferrets). Response is variable, presumably dependent on whether the tumor cells have receptors for somatostatin. Octreotide may also be useful in the diagnosis and symptomatic treatment of gastrinomas in dogs or cats. It may be of use in the treatment of acute pancreatitis, but more research is needed before it can be recommended for this use in veterinary patients.

Mode of action

Octreotide acetate is a synthetic somatostatin analogue with similar pharmacologic effects to naturally occurring somatostatin, but with a prolonged duration of action. It inhibits pathologically increased secretion of growth hormone, thyroid stimulating hormone, and serotonin, insulin, glucagon, and other peptides produced within the gastro-entero-pancreatic endocrine system. Somatostatin is cell cycle phase-specific, mediating arrest at the G1- phase. Long acting somatostatin analogues have been shown to inhibit tumour growth.

Brand name

Sandostatin (Novartis).

General Description

Octreotide is a somatostatin analogue with D-Phe-Cys-Phe-D-Trp-Lys-ThrCys-Thr-OH amino acid sequence.

InChI:InChI=1/C49H66N10O10S2.C2H4O2/c1-28(61)39(25-60)56-48(68)41-27-71-70-26-40(57-43(63)34(51)21-30-13-5-3-6-14-30)47(67)54-37(22-31-15-7-4-8-16-31)45(65)55-38(23-32-24-52-35-18-10-9-17-33(32)35)46(66)53-36(19-11-12-20-50)44(64)59-42(29(2)62)49(69)58-41;1-2(3)4/h3-10,13-18,24,28-29,34,36-42,52,60-62H,11-12,19-23,25-27,50-51H2,1-2H3,(H,53,66)(H,54,67)(H,55,65)(H,56,68)(H,57,63)(H,58,69)(H,59,64);1H3,(H,3,4)/t28-,29-,34-,36+,37+,38-,39-,40+,41+,42+;/m1./s1

83150-76-9 Relevant articles

Use of trichloroacetimidate linker in solid-phase peptide synthesis

Yan, Liang Zeng,Mayer, John P.

, p. 1161 - 1162 (2003)

A solid-phase method for the preparation...

Rapid Photolysis-Mediated Folding of Disulfide-Rich Peptides

Patil, Nitin A.,Karas, John A.,Wade, John D.,Hossain, Mohammed Akhter,Tailhades, Julien

, p. 8599 - 8603 (2019/06/04)

Structure–activity relationship studies ...

METHOD FOR PRODUCTION OF OCTREOTIDE

-

Paragraph 0060, (2016/10/08)

PROBLEM TO BE SOLVED: To provide a metho...

Synthesis of peptide alcohols on the basis of an O-N acyl-transfer reaction

Tailhades, Julien,Gidel, Marie-Aude,Grossi, Benjamin,Lecaillon, Jennifer,Brunel, Luc,Subra, Gilles,Martinez, Jean,Amblard, Muriel

experimental part, p. 117 - 120 (2010/04/04)

(Figure Presented) Getting the better of...

Electrophilic S-trifluoromethylation of cysteine side chains in α- and β-peptides: Isolation of trifluoromethylated sandostatin (octreotide) derivatives

Caponea, Stefania,Kieltschb, Iris,Floegela, Oliver,Lelaisa, Gerald,Togni, Antonio,Seebach, Dieter

body text, p. 2035 - 2056 (2009/02/08)

The new electrophilic trifluoromethylati...

83150-76-9 Process route

H-D-Phe-Cys-Phe-D-Trp-Lys-Thr-Cys-Thr-OH

H-D-Phe-Cys-Phe-D-Trp-Lys-Thr-Cys-Thr-OH

octreotide
83150-76-9

octreotide

Conditions
Conditions Yield
With ammonium acetate; pyrographite; In tetrahydrofuran; water; at 20 ℃;
85.6%
D-Phe-Cys-Phe-D-Trp-Lys-Thr-Cys-Thr(ol)

D-Phe-Cys-Phe-D-Trp-Lys-Thr-Cys-Thr(ol)

octreotide
83150-76-9

octreotide

Conditions
Conditions Yield
In water; at 20 ℃; for 47.5h; pH=7.4; aq. phosphate buffer;
80%
With phosphate buffer; air; at 25 ℃; for 48h; Yield given;
With ammonium acetate; for 48h; pH=7.0;
With air;

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    Togni's reagent II

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