Cyclo(-RGDfK)
CAS No. 161552-03-0
Cyclo(-RGDfK)( Cyclo(RGDfK) peptide | Cyclic RGDfK peptide )
Catalog No. M12350 CAS No. 161552-03-0
A RGD pipetide, potent and selective αvβ3 integrin inhibitor with Kd of 41.7 nM.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 50 | In Stock |
|
| 5MG | 90 | In Stock |
|
| 10MG | 163 | In Stock |
|
| 25MG | 308 | In Stock |
|
| 50MG | 494 | In Stock |
|
| 100MG | 577 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameCyclo(-RGDfK)
-
NoteResearch use only, not for human use.
-
Brief DescriptionA RGD pipetide, potent and selective αvβ3 integrin inhibitor with Kd of 41.7 nM.
-
DescriptionA RGD pipetide, potent and selective αvβ3 integrin inhibitor with Kd of 41.7 nM; shows strong inhibitory effect on the proliferation of T-24 cells; induces less tumor progression, less tumor metabolic activity, fewer intratumoral vessels in mice model.(In Vitro):Cyclo(-RGDfK) is a potent and selective inhibitor of the αvβ3 integrin, with a IC50 of 0.94 nM. [66Ga]DOTA-E-[c(RGDfK)]2 can be prepared with high radiochemical purity (>97%), specific activity (36-67GBq/μM), in vitro stability, and moderate protein binding. MicroPET imaging up to 24 post-injection showed contrasting tumors reflecting αvβ3-targeted tracer accumulation.
-
In VitroCyclo(-RGDfK) is a potent and selective inhibitor of the αvβ3 integrin, with a IC50 of 0.94 nM. [66Ga]DOTA-E-[c(RGDfK)]2 can be prepared with high radiochemical purity (>97%), specific activity (36-67GBq/μM), in vitro stability, and moderate protein binding. MicroPET imaging up to 24 post-injection showed contrasting tumors reflecting αvβ3-targeted tracer accumulation.
-
In Vivo——
-
SynonymsCyclo(RGDfK) peptide | Cyclic RGDfK peptide
-
PathwayCell Cycle/DNA Damage
-
TargetIntegrin
-
RecptorαVβ3integrin
-
Research AreaCancer
-
Indication——
Chemical Information
-
CAS Number161552-03-0
-
Formula Weight603.6705
-
Molecular FormulaC27H41N9O7
-
Purity>98% (HPLC)
-
SolubilityDMSO: ≥150 mg/mL
-
SMILESC1C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N1)CCCN=C(N)N)CCCCN)CC2=CC=CC=C2)CC(=O)O
-
Chemical NameCyclo(L-arginylglycyl-L-α-aspartyl-D-phenylalanyl-L-lysyl)
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Sancey L, et al. Mol Ther. 2009, 17(5), 837-843.
2. Zhou D, et al. J Control Release. 2013, 169(3), 204-210.
3. Vilchis-Juarez A, et al. J Biomed Nanotechnol. 2014 Mar;10(3):393-404.
molnova catalog
related products
-
Fibronectin CS1 Pept...
he connecting segment 1 (CS-1) is a cell attachment domain located in the type III homology connecting segment (IIICS) of fibronectin. CS1 peptide of fibronectin, which lacks the Arg-Gly-Asp-containing domain, actively inhibits tumor metastases in spontaneous and experimental metastasis models. The use of Fibronectin CS1 Peptide might offer a promising therapeutic approach for combating and preventing cancer metastasis.
-
Elarofiban TFA
Elarofiban TFA (RWJ-53308 TFA) is a novel and orally active and selective GPIIb/IIIa antagonist for the study of cardiovascular disease.
-
TBC3486
A potent, selective, non-peptidic integrin α4β1 (VLA-4) antagonist with IC50 of 9 nM.
Cart
sales@molnova.com