Cyclo (-RGDfK) 2,2,2-Trifluoroacetic acid

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Cyclo (-RGDfK) 2,2,2-Trifluoroacetic acid manufacturers

Cyclo (-RGDfK) 2,2,2-Trifluoroacetic acid Basic information
Product Name:Cyclo (-RGDfK) 2,2,2-Trifluoroacetic acid
Synonyms:Cyclo (-RGDfK) 2,2,2-Trifluoroacetic acid;Cyclo(-RGDfK) Trifluoroacetate;2-((2S,5R,8S,11S)-8-(4-Aminobutyl)-5-benzyl-11-(3-guanidinopropyl)-3,6,9,12,15-pentaoxo-1,4,7,10,13-pentaazacyclopentadecan-2-yl)acetic acid Trifluoroacetate (1:1);Cyclo(-RGDfK) TFA, 10 mM in DMSO;Cyclo(-Arg-Gly-Asp-D-Phe-Lys) trifluoroacetate;2,2,2-trifluoroacetic acid--2-((2S,5R,8S,11S)-8-(4-aminobutyl)-5-benzyl-11-(3-guanidinopropyl)-3,6,9,12,15-pentaoxo-1,4,7,10,13-pentaazacyclopentadecan-2-yl)acetic acid (1/1)
CAS:500577-51-5
MF:C29H42F3N9O9
MW:717.6938896
EINECS:
Product Categories:
Mol File:500577-51-5.mol
Cyclo (-RGDfK) 2,2,2-Trifluoroacetic acid Structure
Cyclo (-RGDfK) 2,2,2-Trifluoroacetic acid Chemical Properties
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
solubility DMSO: 100 mg/mL (139.34 mM)
form Solid
color White to off-white
Water Solubility Water: 33.33 mg/mL (46.44 mM)
SequenceCyclo(Arg-Gly-Asp-Phe-Lys)
Safety Information
MSDS Information
Cyclo (-RGDfK) 2,2,2-Trifluoroacetic acid Usage And Synthesis
UsesCyclo(-RGDfK) TFA is a potent and selective inhibitor of the αvβ3 integrin, with an IC50 of 0.94 nM[1]. Cyclo(-RGDfK) TFA potently targets tumor microvasculature and cancer cells through the specific binding to the αvβ3 integrin on the cell surface[3].
IC 50αvβ3: 0.94 nM (IC50)
References[1] Simecek J, et al. Benefits of NOPO as chelator in gallium-68 peptides, exemplified by preclinical characterization of (68)Ga-NOPO-c(RGDfK). Mol Pharm. 2014 May 5;11(5):1687-95. DOI:10.1021/mp5000746
[2] Lopez-Rodriguez V, et al. Preparation and preclinical evaluation of (66)Ga-DOTA-E(c(RGDfK))2 as a potential theranostic radiopharmaceutical. Nucl Med Biol. 2015 Feb;42(2):109-14. DOI:10.1016/j.nucmedbio.2014.09.010
Cyclo (-RGDfK) 2,2,2-Trifluoroacetic acid Preparation Products And Raw materials
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