PEG-DOX-c(RADfK)

General Information


DRACP ID  DRACP05899

Peptide Name   PEG-DOX-c(RADfK)

Sequence  XRADfK

Sequence Length  6

UniProt ID  Not available

PubChem CID  Not available

Origin  Synthetic

Type  Synthetic peptide

Classification

  

Targeted peptide conjugates Antiangiogenic αvβ3 Inhibitor



Activity Information


Cell Line Disease Cancer Classified Activity Assay Testing Time Literature
U87 Glioblastoma Blastoma IC50=900 nM MTT assay 72 h 1

Hemolytic Activity  Not available

Normal (non-cancerous) Cytotoxicity  HUVEC: IC50=50 nM

Target  αvβ3

Affinity  Not available

Mechanism  Not available

Nature  Anticancer



Structure Information


PDB ID  Not available

Predicted Structure  Not available

Helicity  Not available

Linear/Cyclic  Cyclic

Disulfide/Other Bond  NCB: Arg1<--->Lys5

N-terminal Modification  PEG, Poly ethylene glycol

C-terminal Modification  Free

Other Modification  X=DOX, Doxorubicin

Chiral  Mix



Physicochemical Information


Formula  C19H32N8O5

Absent amino acids  CEFGHILMNPQSTVWY

Common amino acids  ADKRX

Mass  65188

Pl  9.69

Basic residues  2

Acidic residues  1

Hydrophobic residues  1

Net charge  1

Boman Index  -2738

Hydrophobicity  -168.33

Aliphatic Index  16.67

Half Life 
  /

Extinction Coefficient cystines  0

Absorbance 280nm  0

Polar residues  0

Amino acid distribution



Literature Information


Literature 1

Pubmed ID Not available

Title  Development of PEGylated doxorubicin-E-[c(RGDfK)2] conjugate for integrin-targeted cancer therapy

Doi 10.1002/pat.1731

Year  2010

Patent

Patent ID Not available

Patent Title  Not available

Other Iinformation  Not available

Other Published ID  Not available




DRACP is developed by Dr.Zheng's team.