3D model is for representation purpose only.
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TKPKGTKPKGTKPKGTKPKG | glycolic acid | N-(4-Acetylphenyl)-5-bromo-2-hydroxybenzamide |
Identification | |
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ConjuPepDB ID | cpd00129 |
Smiles | |
Inchi Key | InChIKey=MMYZOAGZZUYPKI-NHFOEDLHSA-N |
Molecular weight | 2450.28 |
Molecular formula | C109H180BrN31O28 |
Chemical name | Peptide information |
Sequence (one letter) | TKPKGTKPKGTKPKGTKPKG |
Length | 20 |
Peptide name | N/A |
External ID | |
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CAS number | 2100270-30-0 |
Other information | |
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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 | |
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LogP | -13.34487 |
Rotatable bonds | 78 |
H bond donor | 31 |
H bond acceptor | 37 |
Polar surface area (PSA) | 949.93000 |
Citations | |||||
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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 |