| Name | cyclo(arg-gly-asp-d-phe-val) |
|---|---|
| Synonyms |
Cyclog-Gls-Asp-D-Phe-Val)
CYCLOG-GLY-ASP-D-PHE-VAL) Cyclo(L-ginylglycyl-L-α-asptyl-D-phenylalanyl-L-valyl) EMD 66203, c(RGDfV) cyclo(RGD-DPhe-V) RGDFV PTIDE, CYCLIC Cyclog-Gly-Asp-D-Phe-Val) - - Calbiochem CYCLO(RGDD-FV) RGDFV PEPTIDE,CYCLIC cRGDfV Cyclo(-g-Gly-Asp-D-Phe-Val) trifluoroacetate salt Cyclo(Arg-Gly-Asp-D-Phe-Val) |
| Description | Cyclo(Arg-Gly-Asp-D-Phe-Val) is an integrin αvβ3 inhibitor. Cyclo(Arg-Gly-Asp-D-Phe-Val) has antitumor activity. Cyclo(Arg-Gly-Asp-D-Phe-Val) can be used for the research of acute myeloid leukemia[1]. |
|---|---|
| Related Catalog | |
| Target |
αvβ3[1] |
| In Vitro | Cyclo(Arg-Gly-Asp-d-Phe-Val) (c(RGDfV)) (35 nM, 4-24 h) disruptes the adhesion and migration between the tumor cells and the matrix, induces the leukemia cells to leave the protective microenvironment and increases their sensitivity to cell cycle-dependent agents[1]. Cell Cycle Analysis[1] Cell Line: MV4–11 cells Concentration: 35 nM Incubation Time: 24 h Result: Affected the leukemia cell cycle, decreased the G0/G1 phase of leukemia cells in the 3D and 2D culture systems and increased the S phase of leukemia cells in the 3D and 2D culture systems. Apoptosis Analysis[1] Cell Line: MV4–11 cells Concentration: 35 nM Incubation Time: 24 h Result: Increased the apoptosis rates. |
| Molecular Formula | C26H38N8O7 |
|---|---|
| Molecular Weight | 574.62900 |
| Exact Mass | 574.28600 |
| PSA | 244.70000 |
| LogP | 0.52700 |