CYCLO(ARG-GLY-ASP-D-PHE-VAL)
CYCLO(ARG-GLY-ASP-D-PHE-VAL) Basic information
- Product Name:
- CYCLO(ARG-GLY-ASP-D-PHE-VAL)
- Synonyms:
-
- RGDFV PEPTIDE, CYCLIC
- Cyclo(Arg-Gls-Asp-D-Phe-Val)
- EMD 66203, c(RGDfV)
- CYCLO(ARG-GLY-ASP-D-PHE-VAL)
- CYCLO(RGDD-FV)
- Cyclo(-Arg-Gly-Asp-D-Phe-Val) trifluoroacetate salt
- Cyclo(Arg-Gly-Asp-D-Phe-Val) - CAS 137813-35-5 - Calbiochem
- cRGDfV
- CAS:
- 137813-35-5
- MF:
- C26H38N8O7
- MW:
- 574.63
- Mol File:
- 137813-35-5.mol
CYCLO(ARG-GLY-ASP-D-PHE-VAL) Chemical Properties
- Density
- 1.45±0.1 g/cm3(Predicted)
- storage temp.
- −20°C
- solubility
- 1 N acetic acid: 5mg/mL
- form
- White solid
- pka
- 4.01±0.10(Predicted)
- color
- white
MSDS
- Language:English Provider:SigmaAldrich
CYCLO(ARG-GLY-ASP-D-PHE-VAL) Usage And Synthesis
Uses
Cyclo(Arg-Gly-Asp-D-Phe-Val) (Cyclo(RGDfV)) 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].
General Description
Potent inhibitor of cell adhesion. Inhibits tumor cell adhesion to laminin and vitronectin substrates. In vivo investigations in rats showed it to be useful in the amelioration of ischemic acute renal failure in rats. Also inhibits tubular obstruction by preventing cell-cell adhesion. Inhibits the redistribution of c-Src into focal adhesions, thereby leading to impaired MAP Kinase activation.
Biochem/physiol Actions
Primary Targetinhibits tumor cell adhesion to laminin and vitronectin substrates
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. DOI:10.3892/ol.2016.5042
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