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This page gives details of CPPsite entry with ID 2550
Primary information
CPPsite ID2550
PEPTIDE SEQUENCERGGRLSYSRRRFSTSTGRA
PEPTIDE NAMESynB1-ELP-H1
CHIRALITYL
LINEAR/CYCLICLinear
SOURCEProtein derived
CATEGORYAmphipathic
N-TERMINAL MODIFICATIONFree
C-TERMINAL MODIFICATIONConjugation with ELP-Rho
UPTAKE EFFICIENCYSignificantly enhancing brain tumor deposition of the ELP carrier
INVITRO/INVIVOIn vitro and in vivo
CELL LINEHuman U-87-MG and D54 glioma cells along with the rat C6 glioma cells
In VIVO MODELFemale Sprague Dawley rats
CARGOPeptide (Rhodamine labeled ELP)
PMID23372821
PATENTUnknown
LENGTH19
Secondary StructureCCSCCTTSCCSSSSSSSCC
SMILESN[C@@H](CCCNC(=[NH2])N)C(=O)NCC(=O)NCC(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CO)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](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CO)C(=O)N[C@@H]([C@@H](C)O)C(=O)NCC(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](C)C=O
Tertiary Structure
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  (PEPstrMOD)