Details of SAPdb ID 1638 |
Primary information | ||
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SAPdb_ID | 1638 | |
PMID | 29164193 | |
Year | 2017 | |
Name | FF-MNT | |
Sequence | FF | |
N-Terminal Modification | Free | |
C-Terminal Modification | Free | |
Non-terminal Modication | None | |
Length | 2 | |
Peptide/Conjugate/Mixture | peptide | |
Conjugate Partner | None | |
Technique | confocal micro-Raman spectrometer | |
Solvent | 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) | |
Method | Lyophilized form of L-diphenylalanine (FF) was purchased from Bachem and 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) solvent from Sigma Aldrich. A FF:HFIP solution was prepared (100mg/ml concentration). Then, an aliquot of 2 μl of solution wasplaced onto a glass slide. Due to the solvent evaporation under ambient conditions (typically T = 20oC and relative humidity of about 20%) a transparent amorphous film was obtained in few seconds. | |
Concentration | 100 mg/ml | |
pH | NA | |
Temperature | 20°C | |
Incubation Period | 0- 20 s | |
Self-Assembly Formation | Yes | |
Type of Self-Assembly | microtube | |
Size of Self-Assembled structure | d=1443nm | |
Linear/Cyclic | Linear | |
Stability of Nanostructure | Stable | |
Comment | NA | |
Secondary information | ||
Physico-Chemical properties |
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STRUCTURE |
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SMILES | N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O |