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This page gives details of CPPsite entry with ID 2667
Primary information
CPPsite ID2667
PEPTIDE SEQUENCERQIKIWFQNRRMKWKKGC
PEPTIDE NAMEPen
CHIRALITYL
LINEAR/CYCLICLinear
SOURCESynthetic
CATEGORYCationic
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
LENGTH18
Secondary StructureCCCCCCCSSCCCSSSTTC
SMILESN[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CCCC[NH3])C(=O)NCC(=O)N[C@@H](CS)C(=O)N
Tertiary Structure
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  (PEPstrMOD)