Table 1.
Target protein | Peptide Name | Sequence | Derived from | IC50 | Assay Format Tested | Phase | Reference |
---|---|---|---|---|---|---|---|
HA | LL-37 | LLGDFFRKSKEKIGKEFKRIVQRIKDFLRNLVPRTES | Cathelicidin | 0.9−11.3 μM | Neutralization assay | Pre-clinical | [197] |
GI-20 | GIKEFKRIVQRIKDFLRNLV | AMP (LL-37) | 1.6−3.2 μM | Neutralization assay | Pre-clinical | ||
P1, P2, P3 | SKHSSLDCVLRP (1), AGDDQGLDKCVPNSKEK (2), and NGESSADWAKN (3) | Lactoferrin | PM-FM | Neutralization assay | Pre-clinical | [7] | |
Tetrapeptides | Peptide 14 (VLRP) | Lactoferrin | fM range | Neutralization assay | Pre-clinical | [184] | |
Peptide 15 (SLDC) and | SKHSSLDCVLRP (1), | ||||||
Peptide 17 (SKHS) | |||||||
P9 | NGAICWGPCPTAFRQIGNCGHFKVRCCKIR | mouse β-defensin-4 | 1.5−4.8 μg/mL | plaque reduction assay | Pre-clinical | [231] | |
EB | RRKKAAVALLPAVLLALLAP | fibroblast growth factor 4 | 3−10 μM | hemagglutination inhibition assay | Pre-clinical | [106] | |
FP-4 | RRKKWLVFFVIFYFFR | Tyrosine kinase inhibitor peptide | 0.05−0.13 μM | plaque-reduction assay | Pre-clinical | [5] | |
Flufirvitide-3 | - * | fusion initiation region | nM range | plaque inhibition assay | Phase 1 | [67] | |
P7 | (Nva-Orn-meLEYchlFEWLS-βAla | Neutralizing antibodies | 30−70 nM | AlphaLisa competition binding assay | Pre-clinical | [108] | |
C-18-s2(1−5) | C17H35CO-ARLPR-NH | Phage library | 1.6−1.9 μM | plaque inhibition assay | Pre-clinical | [137] | |
NA | peptide P | PGEKGPSGEAGTAGPPGTPGPQGL | Cod skin hydrolysates | 3.5 mg/mL | NA inhibitory assay | Pre-clinical | [118] |
P2 | errKPAQP | Binding pockets of oseltamivir in NA | 4.25 μM | NA inhibitory assay Cytopathic effect (CPE) assay | Pre-clinical | [34] |
*not available in the literature.