1. Cytoskeleton Apoptosis
  2. Integrin Apoptosis
  3. Cyclo(Arg-Gly-Asp-D-Phe-Val)

Cyclo(Arg-Gly-Asp-D-Phe-Val)  (Synonyms: Cyclo(RGDfV); C(RGDfV))

目录号: HY-P1613
产品使用指南 技术支持

Cyclo(Arg-Gly-Asp-D-Phe-Val) (Cyclo(RGDfV)) 是一种整合素 αvβ3 抑制剂。Cyclo(Arg-Gly-Asp-D-Phe-Val) 具有抗肿瘤活性。Cyclo(Arg-Gly-Asp-D-Phe-Val) 可用于急性髓系白血病的研究。

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Custom Peptide Synthesis

Cyclo(Arg-Gly-Asp-D-Phe-Val) Chemical Structure

Cyclo(Arg-Gly-Asp-D-Phe-Val) Chemical Structure

CAS No. : 137813-35-5

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Cyclo(Arg-Gly-Asp-D-Phe-Val) 的其他形式现货产品:

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Other Forms of Cyclo(Arg-Gly-Asp-D-Phe-Val):

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

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].

IC50 & Target

αvβ3[1]

细胞效力
(Cellular Effect)
Cell Line Type Value Description References
A549 IC50
3.25 x 10-1 μM
Compound: 6, c(RGDfV)
Displacement of [125I]echistatin from human integrin alpha5beta3 expressed in human A549 cells by binding assay
Displacement of [125I]echistatin from human integrin alpha5beta3 expressed in human A549 cells by binding assay
[PMID: 21349709]
HUVEC IC50
0.53 μM
Compound: CycloRGDfV
Inhibition of HUVEC migration after 4 hrs
Inhibition of HUVEC migration after 4 hrs
[PMID: 19081719]
HUVEC IC50
3.1 μM
Compound: CycloRGDfV
Inhibition of FGF-induced HUVEC proliferation after 48 hrs
Inhibition of FGF-induced HUVEC proliferation after 48 hrs
[PMID: 19081719]
HUVEC IC50
4.5 μM
Compound: CycloRGDfV
Inhibition of VEGF-induced HUVEC proliferation after 48 hrs
Inhibition of VEGF-induced HUVEC proliferation after 48 hrs
[PMID: 19081719]
HUVEC IC50
9.6 μM
Compound: c[RGDfV]
Inhibition of alphavbeta3 integrin-mediated cell adhesion in HUVEC on vitronectin coated plate after 30 mins
Inhibition of alphavbeta3 integrin-mediated cell adhesion in HUVEC on vitronectin coated plate after 30 mins
[PMID: 20055426]
K562 IC50
34.7 μM
Compound: cyclo-Arg-Gly-Asp-D-Phe-Val
Antagonist activity at alpha5beta1 integrin in human K562 cells assessed as inhibition of fibronectin-mediated cell adhesion after 30 mins by fluorescence assay
Antagonist activity at alpha5beta1 integrin in human K562 cells assessed as inhibition of fibronectin-mediated cell adhesion after 30 mins by fluorescence assay
[PMID: 24973662]
K562 IC50
34.7 μM
Compound: c[RGDfV]
Inhibition of alpha5beta1 integrin-mediated cell adhesion in human K562 cells on fibronectin coated plate after 30 mins
Inhibition of alpha5beta1 integrin-mediated cell adhesion in human K562 cells on fibronectin coated plate after 30 mins
[PMID: 20055426]
WM-115 IC50
0.5 μM
Compound: c-(-Arg-Gly-Asp-D-Phe-Val-)
Binding affinity to integrin in human WM-115 cells after 30 mins by immobilized vitronectin-based competitive cell adhesion assay
Binding affinity to integrin in human WM-115 cells after 30 mins by immobilized vitronectin-based competitive cell adhesion assay
[PMID: 23387527]
体外研究
(In Vitro)

Cyclo(Arg-Gly-Asp-d-Phe-Val) (Cyclo(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].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

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.
分子量

574.63

Formula

C26H38N8O7

CAS 号
Sequence Shortening

Cyclo(RGD-{d-Phe}-V)

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

纯度 & 产品资料
参考文献
  • 摩尔计算器

  • 稀释计算器

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

质量   浓度   体积   分子量 *
= × ×

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start) × 体积 (start) = 浓度 (final) × 体积 (final)
× = ×
C1   V1   C2   V2
Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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产品名称:
Cyclo(Arg-Gly-Asp-D-Phe-Val)
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HY-P1613
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