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|---|---|---|---|---|
| GFLGTKPKG | glycolic acid | N-(4-Acetylphenyl)-5-bromo-2-hydroxybenzamide |
| Identification | |
|---|---|
| ConjuPepDB ID | cpd00113 |
| Smiles | |
| Inchi Key | InChIKey=PQCOSSUJNLHVGP-POYMZKDISA-N |
| Molecular weight | 1291.52 |
| Molecular formula | C59H82BrN13O15 |
| Chemical name | Peptide information |
| Sequence (one letter) | GFLGTKPKG |
| Length | 9 |
| Peptide name | N/A |
| External ID | |
|---|---|
| CAS number | 2100270-46-8 |
| Other information | |
|---|---|
| Application | Antimicrobial therapy, anti-tuberculosis |
| Additional function | Target cell-directed delivery and fluorescent labeling |
| Pharmacological class | antimicrobial, antibacterial |
| Conjugate type | amide |
| Linker | N/A |
| Linker Type | glycolic acid |
| Small molecule | N-(4-Acetylphenyl)-5-bromo-2-hydroxybenzamide |
| Small molecule CAS | 1007653-77-1 |
| Small molecule structure | |
| Structure method | 1H- and 13C-NMR |
| Calculated properties | |
|---|---|
| LogP | -5.93475 |
| Rotatable bonds | 36 |
| H bond donor | 14 |
| H bond acceptor | 18 |
| Polar surface area (PSA) | 433.60000 |
| Citations | |||||
|---|---|---|---|---|---|
| ID | Title | Year | Authors | Journal | DOI |
In vitro biological evaluation of new antimycobacterial salicylanilide-tuftsin conjugates | 2017 | European Journal of Medicinal Chemistry | European Journal of Medicinal Chemistry | ||