Welcome to Entry Card of Peptide


This page gives details of CPPsite entry with ID 2014
Primary information
CPPsite ID2014
PEPTIDE SEQUENCEGLWRALWRLLRSLWRLLWRA
PEPTIDE NAMECADY
CHIRALITYL
LINEAR/CYCLICLinear
SOURCESynthetic
CATEGORYAmphipathic
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
LENGTH20
Secondary StructureCTHHHHHHHHHHHHHHHTTC
SMILESNCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(=[NH2])N)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](CCCNC(=[NH2])N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O)N[C@@H](C)C=O
Tertiary Structure
(Technique)		View in Jmol  OR Download Structure
  (PEPstrMOD)