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This page gives details of CPPsite entry with ID 2013
Primary information
CPPsite ID2013
PEPTIDE SEQUENCEGALFLGFLGAAGSTMGAWSQPKSKRKV
PEPTIDE NAMEMPGNLS
CHIRALITYL
LINEAR/CYCLICLinear
SOURCESynthetic
N-TERMINAL MODIFICATIONAcetylation
C-TERMINAL MODIFICATIONCysteamide group
INVITRO/INVIVOIn vitro and in vivo
CELL LINEHDFs
In VIVO MODELfemale Sprague-Dawley rats
CARGONucleic acid (siRNA)
PMID23036951
PATENTUnknown
LENGTH27
Secondary StructureCCCSSGGGGTTTTTCSTTTSSSCSCCC
SMILESNCC(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CC(C)C)C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CC(C)C)C(=O)NCC(=O)N[C@@H](C)C(=O)N[C@@H](C)C(=O)NCC(=O)N[C@@H](CO)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCSC)C(=O)NCC(=O)N[C@@H](C)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCC(=O)N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](C(C)C)C=O
Tertiary Structure
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  (PEPstrMOD)