3D model is for representation purpose only.
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LARKFEAFARAG | Coumarine, 7-Methoxy-2-oxo-2H-1-benzopyran-3-carboxylic acid |
Identification | |
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ConjuPepDB ID | cpd00613 |
Smiles | |
Inchi Key | InChIKey=ZROWSJALYKHNOA-GXIPQKELSA-N |
Molecular weight | 1794.83 |
Molecular formula | C84H113F3N20O21 |
Chemical name | Peptide information |
Sequence (one letter) | LARKFEAFARAG |
Length | 12 |
Peptide name | dodecapeptide |
External ID | |
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CAS number | 1370726-95-6 |
Other information | |
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Application | Synthesis |
Additional function | Assembling functional peptide bioconjugates |
Conjugate type | amide |
Linker | no |
Small molecule | Coumarine, 7-Methoxy-2-oxo-2H-1-benzopyran-3-carboxylic acid |
Small molecule CAS | 20300-59-8 |
Small molecule structure | |
Small molecule 2 | 1-(2,4,5-trifluorophenol) hexanedioic acid ester |
Small molecule CAS 2 | 1370726-86-5 |
Structure method | 1H-, 13C- and 19F-NMR |
Calculated properties | |
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LogP | -3.76694 |
Rotatable bonds | 55 |
H bond donor | 19 |
H bond acceptor | 25 |
Polar surface area (PSA) | 649.32000 |
Citations | |||||
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ID | Title | Year | Authors | Journal | DOI |
Efficient formation of heterodimers from peptides and proteins using unsymmetrical polyfluorophenyl esters of dicarboxylic acids | 2012 | Slosarczyk, Adam T.; Baltzer, Lars | Journal of Peptide Science |