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This page gives details of CPPsite entry with ID 2666
Primary information
CPPsite ID2666
PEPTIDE SEQUENCEGRKKRRQRRRPPQC
PEPTIDE NAMETAT
CHIRALITYL
LINEAR/CYCLICLinear
SOURCESynthetic
CATEGORYCationic and amphipathic
C-TERMINAL MODIFICATIONAmidation
UPTAKE EFFICIENCYAccumulations were only slightly different from that of the control GC peptide in tumors
INVITRO/INVIVOIn vivo
In VIVO MODELTumor-xenografted nude mice
CARGOFluorophore (Alexa660)
PMID22285548
PATENTUnknown
LENGTH14
Secondary StructureCCTTCCCCCCSSCC
SMILESNCC(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H](CS)C(=O)N
Tertiary Structure
(Technique)		View in Jmol  OR Download Structure
  (PEPstrMOD)