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This page gives details of CPPsite entry with ID 2343
Primary information
CPPsite ID2343
PEPTIDE SEQUENCERRRRRRRRK
PEPTIDE NAMER8
CHIRALITYL
LINEAR/CYCLICLinear
SOURCESynthetic
CATEGORYCationic
N-TERMINAL MODIFICATIONConjugation with 5-carboxyfluorescein via a lysine residue
C-TERMINAL MODIFICATIONFree
UPTAKE EFFICIENCYLower uptake efficiency
INVITRO/INVIVOIn vitro and in vivo
CELL LINEWong-Kilbourne-derived human conjunctival epithelial cells (NHC)
In VIVO MODELMale SpragueDawley rats and male albino rabbits
CARGOFluorophore [5-carboxyfluorescein (FAM)]
PMID24521351
PATENTUnknown
LENGTH9
Secondary StructureCGGGTCSCC
SMILESN[C@@H](CCCNC(=[NH2])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)N[C@@H](CCCNC(=[NH2])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)N[C@@H](CCCC[NH3])C=O
Tertiary Structure
(Technique)
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 (PEPstrMOD)