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

Names

[ CAS No. ]:
199807-33-5

[ Name ]:
Cyclo(Arg-Gly-Asp-D-Phe-Val) TFA

[Synonym ]:
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)

Biological Activity

[Description]:

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

[Related Catalog]:

Signaling Pathways >> Cytoskeleton >> Integrin
Peptides
Research Areas >> Cancer

[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.


[Related Small Molecules]

Cilengitide | Cyclo(-Arg-Gly-Asp-D-Phe-Lys) trifluoroacetate salt | Arg-Gly-Asp-Ser | CWHM-12 | OSU-T315 | E 7820 | GLPG 0187 | Firategrast | ATN-161 trifluoroacetate salt | Cucurbitacin B | Eptifibatide acetate salt | iRGD peptide | Lifitegrast | Zaurategrast | Integrin Antagonist 1 (hydrochloride)

Chemical & Physical Properties

[ Molecular Formula ]:
C28H39F3N8O9

[ Molecular Weight ]:
688.653

[ Exact Mass ]:
688.279236


Related Compounds