| dc.contributor.advisor | Glover, George I. | |
| dc.creator | Kelley, Kristine | |
| dc.date.accessioned | 2022-04-04T13:38:43Z | |
| dc.date.available | 2022-04-04T13:38:43Z | |
| dc.date.issued | 1977 | |
| dc.identifier.uri | https://hdl.handle.net/1969.1/CAPSTONE-DuBoisR_1977 | |
| dc.description | Program year: 1976/1977 | en |
| dc.description | Digitized from print original stored in HDR | en |
| dc.description.abstract | Naturally occuring peptides with C-terminal aldehyde functions have been shown to inhibit serine and thiol proteases possibly by reacting with the hydroxyl or sulfhydryl group in the active site. Tri-peptides were synthesized containing a C-terminal leucine residue with the aldehyde moiety to mimic the action of these natural inhibitors. | en |
| dc.format.extent | 10 pages | en |
| dc.format.medium | electronic | en |
| dc.format.mimetype | application/pdf | |
| dc.subject | C-terminal aldehyde functions | en |
| dc.subject | natural inhibitors | en |
| dc.subject | serine and thiol proteases | en |
| dc.subject | Tri-peptides | en |
| dc.title | Synthesis of a Tripeptide Containing a C-Terminal Aldehyde Moiety | en |
| dc.type | Thesis | en |
| thesis.degree.department | Biochemistry | en |
| thesis.degree.grantor | University Undergraduate Fellow | en |
| thesis.degree.level | Undergraduate | en |
| dc.type.material | text | en |
