This page gives details of CPPsite entry with ID 2673 |
| Primary information | |
|---|---|
| CPPsite ID | 2673 |
| PEPTIDE SEQUENCE | rrrrrrrrrrrrGC |
| PEPTIDE NAME | r12 |
| CHIRALITY | D |
| LINEAR/CYCLIC | Linear |
| SOURCE | Synthetic |
| CATEGORY | Cationic |
| C-TERMINAL MODIFICATION | Amidation |
| UPTAKE EFFICIENCY | High accumulation of r12 was also observed, but it was similar to that of R8 and significantly less than that of r8 |
| INVITRO/INVIVO | In vivo |
| In VIVO MODEL | Tumor-xenografted nude mice |
| CARGO | Fluorophore (Alexa660) |
| PMID | 22285548 |
| PATENT | Unknown |
| LENGTH | 14 |
| Secondary Structure | CGGGGHHHHTTCCC |
| SMILES | N[C@H](CCCNC(=[NH2])N)C(=O)N[C@H](CCCNC(=[NH2])N)C(=O)N[C@H](CCCNC(=[NH2])N)C(=O)N[C@H](CCCNC(=[NH2])N)C(=O)N[C@H](CCCNC(=[NH2])N)C(=O)N[C@H](CCCNC(=[NH2])N)C(=O)N[C@H](CCCNC(=[NH2])N)C(=O)N[C@H](CCCNC(=[NH2])N)C(=O)N[C@H](CCCNC(=[NH2])N)C(=O)N[C@H](CCCNC(=[NH2])N)C(=O)N[C@H](CCCNC(=[NH2])N)C(=O)N[C@H](CCCNC(=[NH2])N)C(=O)NCC(=O)N[C@@H](CS)C(=O)N |
| Tertiary Structure (Technique) | View in Jmol  OR Download Structure (PEPstrMOD) |