Lanreotide diTFA

Modify Date: 2025-07-26 17:23:17

Lanreotide diTFA Structure
Lanreotide diTFA structure
Common Name Lanreotide diTFA
CAS Number 1024499-83-9 Molecular Weight 1324.37
Density N/A Boiling Point N/A
Molecular Formula C58H71F6N11O14S2 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of Lanreotide diTFA


Lanreotide (BIM 23014) diTFA is a somatostatin analogue with antineoplastic activity. Lanreotide diTFA can be used for the research of carcinoid syndrome[1][2].

 Names

Name Lanreotide diTFA

 Lanreotide diTFA Biological Activity

Description Lanreotide (BIM 23014) diTFA is a somatostatin analogue with antineoplastic activity. Lanreotide diTFA can be used for the research of carcinoid syndrome[1][2].
Related Catalog
In Vitro Lanreotide (BIM 23014) (100  nM; 0-48 h) enhanced radiation-induced apoptosis[1]. Lanreotide results in a dose-dependent decrease in GH3 cell colony forming units. Lanreotide at concentrations of 1, 10, 100, and 1000 nM results in cell survival rates of 75, 56, 39 and 27% respectively. The IC50 is 57 nM[1]. Lanreotide inhibits GH-secreting pituitary adenoma cell proliferation and hormone release in vitro[2]. Apoptosis Analysis[1] Cell Line: GH3 Concentration: 100 nM Incubation Time: 48 h, 24 h, or immediately (0 h) before radiation Result: Increased apoptotic sub-G1 proportion compared with radiation alone.
In Vivo Lanreotide (2.5-10mg/kg; s.c.; daily for 5 days) results in tumor growth inhibition[1]. Animal Model: Male nude mice, 8 weeks old and 20–25 g in body weight (GH3 tumor-bearing nude mice)[1] Dosage: 2.5, 5, 10 mg/kg Administration: Subcutaneous; daily for 5 days Result: Produced tumor growth inhibition.
References

[1]. Ning S, et al. Lanreotide promotes apoptosis and is not radioprotective in GH3 cells.Endocr Relat Cancer. 2009 Sep;16(3):1045-55.

[2]. Florio T, et al. Characterization of the intracellular mechanisms mediating somatostatin and lanreotide inhibition of DNA synthesis and growth hormone release from dispersed human GH-secreting pituitary adenoma cells in vitro.Clin Endocrinol (Oxf). 2003 Jul;59(1):115-28.

 Chemical & Physical Properties

Molecular Formula C58H71F6N11O14S2
Molecular Weight 1324.37
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