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This page gives details of CPPsite entry with ID 2719
Primary information
CPPsite ID2719
PEPTIDE SEQUENCEGLWWKAWWKAWWKSLWWRKRKRKA
PEPTIDE NAMECADY-1
CHIRALITYL
LINEAR/CYCLICLinear
SOURCESynthetic
CATEGORYAmphipathic
UPTAKE EFFICIENCYCompared to free doxorubicin, the CADY-1/doxorubicin complex exhibited remarkable cell death activity
INVITRO/INVIVOIn vitro and in vivo
CELL LINEThe HeLa cells
In VIVO MODELHuman tumour xenograft female DBA/2 mice
CARGOSmall molecule drug (Doxorubicin)
PMID22688249
PATENTUnknown
LENGTH24
Secondary StructureCCCTTTTHHHHHHHHHHHHHHHCC
SMILESNCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](C)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](C)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCCC[NH3])C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CCC
Tertiary Structure
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