ToxicityCytotoxicNegative / threshold
Record detail RV-23 was not cytotoxic up to the highest dose (50 μM). Figure 1 shows cell viability at 50–3.125 μM.
- Measure
- CC50
- Value
- >50 μM
- Target
- Vero
- Assay
- Not reported by source
Microorganisms · 2023
Sequence evidence
RIGVLLARLPKLFSLFKLMGKKV
RIGVLLARLPKLFSLFKLMGKKV
Experimental observations
RV-23 was not cytotoxic up to the highest dose (50 μM). Figure 1 shows cell viability at 50–3.125 μM.
RV-23 was found to be more active than AR-23, with an inhibitory concentration of 50% (IC50) at 10 μM ... in co-treatment.
RV-23 ... IC50 at ... 6.25 μM ... in virus pre-treatment assays.
On the contrary, no activity was observed after the viral adsorption step (post-treatment), indicating that the peptides did not interfere later in the infection.
Local peptide labels such as P1, PEP1, or peptide 1 are grouped only within this paper and are not assumed to represent the same molecule across publications.