Cyclo(Arg-Gly-Asp-D-Phe-Val) TFA

Modify Date: 2024-01-07 08:59:12

Cyclo(Arg-Gly-Asp-D-Phe-Val) TFA Structure
Cyclo(Arg-Gly-Asp-D-Phe-Val) TFA structure
Common Name Cyclo(Arg-Gly-Asp-D-Phe-Val) TFA
CAS Number 199807-33-5 Molecular Weight 688.653
Density N/A Boiling Point N/A
Molecular Formula C28H39F3N8O9 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of Cyclo(Arg-Gly-Asp-D-Phe-Val) TFA


Cyclo(Arg-Gly-Asp-D-Phe-Val) (TFA) is an inhibitor of integrin αvβ3, with antitumor activity.

 Names

Name Cyclo(Arg-Gly-Asp-D-Phe-Val) TFA
Synonym More Synonyms

 Cyclo(Arg-Gly-Asp-D-Phe-Val) TFA Biological Activity

Description Cyclo(Arg-Gly-Asp-D-Phe-Val) (TFA) is an inhibitor of integrin αvβ3, with antitumor activity.
Related Catalog
Target

αvβ3[1]

In Vitro Cyclo(Arg-Gly-Asp-D-Phe-Val) (TFA) is an inhibitor of integrin αvβ3. Cyclo(Arg-Gly-Asp-D-Phe-Val) [c(RGDfV); 35 nM] induces disruption of leukemia cell migration and adhesion to leukemia osteoblasts in the 3D and 2D culture systems, affects the leukemia cell cycle and induces apoptosis in leukemia cells[1].
Cell Assay The osteoblasts are cultured in RPMI 1640 medium for 2 days. MV4-11 cells (1.8×105 cells/mL in the 2D culture system and 1×106 cells/mL in the 3D culture system) are co-cultured with leukemia osteoblasts in RPMI 1640 medium. The experiments used two groups: The experimental group received c(RGDfV) (35 nmol/mL) and the control group received an equal volume of phosphate-buffered saline (PBS) only[1].
References

[1]. Shen ZH, et al. Targeting of the leukemia microenvironment by c(RGDfV) overcomes the resistance to chemotherapy in acute myeloid leukemia in biomimetic polystyrene scaffolds. Oncol Lett. 2016 Nov;12(5):3278-3284.

 Chemical & Physical Properties

Molecular Formula C28H39F3N8O9
Molecular Weight 688.653
Exact Mass 688.279236

 Synonyms

Cyclo(L-arginylglycyl-L-α-aspartyl-D-phenylalanyl-L-valyl) trifluoroacetate (1:1)
Acetic acid, 2,2,2-trifluoro-, compd. with cyclo(L-arginylglycyl-L-α-aspartyl-D-phenylalanyl-L-valyl) (1:1)