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Schematic representation of peptide, linker and drug in the peptide-drug conjugates
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|---|---|---|---|---|
| CVKRGLKLRHVRPRVTRMDV | 4-maleimidobutyric acid | Doxorubicin |
| Identification | |
|---|---|
| ConjuPepDB ID | cpd01248 |
| Smiles | |
| Molecular weight | 3126.62 |
| Molecular formula | C138H223N41O38S2 |
| Chemical name | Peptide information |
| Sequence (one letter) | CVKRGLKLRHVRPRVTRMDV |
| Length | 20 |
| Peptide name | N/A |
| External ID | |
|---|---|
| CAS number | 916443-75-9 |
| Other information | |
|---|---|
| Application | Antitumor therapy, colon and breast tumors |
| Additional function | improved efficacy and circumventing resistance |
| Pharmacological class | anticancer |
| Conjugate type | sulfide |
| Linker | N/A |
| Linker Type | 4-maleimidobutyric acid |
| Small molecule | Doxorubicin |
| Small molecule CAS | 23214-92-8 |
| Structure method | 1H NMR, HPLC |
| NMR solvent | DMSO-d6 |
| Calculated properties | |
|---|---|
| LogP | -13.64516 |
| Rotatable bonds | 96 |
| H bond donor | 45 |
| H bond acceptor | 57 |
| Polar surface area (PSA) | 1304.70000 |
| Citations | |||||
|---|---|---|---|---|---|
| ID | Title | Year | Authors | Journal | DOI |
Improved Therapeutic Efficacy of Doxorubicin through Conjugation with a Novel Peptide Drug Delivery Technology (Vectocell) | 2006 | Meyer-Losic, Florence; Quinonero, Jerome; Dubois, Vincent; Alluis, Bertrand; Dechambre, Mireille; Michel, Matthieu; Cailler, Francoise; Fernandez, Anne-Marie; Trouet, Andre; Kearsey, Jonathan | Journal of Medicinal Chemistry | ||
