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This page gives details of CPPsite entry with ID 1763
Primary information
CPPsite ID1763
PEPTIDE SEQUENCEKETWWETWWTEWSQPKKKRKV
PEPTIDE NAMEPN182 (SEQ ID NO: 62)
CHIRALITYL
LINEAR/CYCLICLinear
SOURCESynthetic
CATEGORYUnknown
SUB CELLULAR LOCALIZATIONUnknown
N-TERMINAL MODIFICATIONAcetylation
C-TERMINAL MODIFICATIONAmidation
UPTAKE EFFICIENCYUnknown
PROPOSED UPTAKE MECHANISMUnknown
INVITRO/INVIVOIn vitro
CELL LINE9 L/LacZ cells
CARGONucleic acid (siRNA)
PMID0
PATENTUS 20060035815
LENGTH21
Secondary StructureCCCSTTHHHHGGGCTTTTTCC
SMILESCC(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCC(=O)O)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](CCCC[NH3])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@
Tertiary Structure
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  (PEPstrMOD)