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  3. Octreotide dihydrochloride

Octreotide dihydrochloride  (Synonyms: SMS 201-995 dihydrochloride)

Cat. No.: HY-P0036A
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Octreotide (SMS 201-995) hydrochloride is a somatostatin receptor agonist and synthetic octapeptide endogenous somatostatin analogue. Octreotide hydrochloride can bind to the somatostatin receptors which are mainly subtypes 2, 3 and 5. Octreotide hydrochloride increases Gi activity and reduces intracellular cAMP production. Octreotide hydrochloride has antitumor activity, mediates apoptosis and may also be used in disease studies in acromegaly.

For research use only. We do not sell to patients.

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Octreotide dihydrochloride

Octreotide dihydrochloride Chemical Structure

CAS No. : 1607842-55-6

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Description

Octreotide (SMS 201-995) hydrochloride is a somatostatin receptor agonist and synthetic octapeptide endogenous somatostatin analogue. Octreotide hydrochloride can bind to the somatostatin receptors which are mainly subtypes 2, 3 and 5. Octreotide hydrochloride increases Gi activity and reduces intracellular cAMP production. Octreotide hydrochloride has antitumor activity, mediates apoptosis and may also be used in disease studies in acromegaly[1][2].

In Vitro

Octreotide hydrochloride (10‑8mM, 6 hours) induces phosphorylated‑glycogen synthase kinase 3β (GSK3β) phosphorylation and increases glycogen synthase (GS) activity[3].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Western Blot Analysis[3]

Cell Line: Human hepatoblastoma HepG2 cell line
Concentration: 10‑8mM
Incubation Time: 6 hours
Result: Increased the protein expression levels of phosphorylated‑Akt and GSK3β by 140.8% and 12.2%, respectively and the mRNA level of GS also increased.
In Vivo

Octreotide hydrochloride (subcutaneous injection, 30 mg/kg, once, 8 weeks) can inhibit tumor growth significantly with no effect on body weight[1].
Octreotide hydrochloride (intramuscular injection, 60 mg/kg, every 21 days, 42 days) inhibits serum insulin-like growth factor (IGF-I) without toxicity in dogs with appendicular osteosarcoma (OSA)[2].
Octreotide hydrochloride (subcutaneous injection, 40 μg/kg, Every 12 hours, 8 days) improves hepatic glycogen synthesis in obese male Sprague‑Dawley (SD) rats[3].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Female nude mice (nu/nu Balbc-A weighing 19-22 g)[1]
Dosage: 30 mg/kg
Administration: Subcutaneous injection; once; 8 weeks
Result: Showed that the average volume of tumors treated was 25.8% of the control group and no effect on body weight.
Animal Model: Dogs with appendicular OSA[2]
Dosage: 60 mg/kg
Administration: Intramuscular injection; Every 21 days; 42 days
Result: Resulted in a 43% decrease in mean serum IGF-I compared with mean baseline concentrations.
Animal Model: Male Sprague‑Dawley (SD) rats (3 weeks; 40-60 g)[3]
Dosage: 40 μg/kg
Administration: Subcutaneous injection; Every 12 hours; 8 days
Result: Significantly improved fat deposition and reduced lipid infiltration.
Molecular Weight

1092.16

Formula

C49H68Cl2N10O10S2

CAS No.
Sequence

{d-Phe}-cyclo(Cys-Phe-{d-Trp}-Lys-Thr-Cys-{d-Threoninol}) (Disulfide bridge: Cys2-Cys7)

Sequence Shortening

{d-Phe}-cyclo(CF{d-Trp}-KTC)-{d-Threoninol} (Disulfide bridge: Cys2-Cys7)

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Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Product Name:
Octreotide dihydrochloride
Cat. No.:
HY-P0036A
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