Table 2: S. aureus (KCTC 1621) MIC = 4 μM for BP100.
- Measure
- MIC
- Value
- 4.0 μM
- Target
- Staphylococcus aureus
- Assay
- Not reported by source
Molecules · 2024
Sequence evidence
KKLFKKILKYLNH
KKLFKKILKYL-NH2
Experimental observations
Table 2: S. aureus (KCTC 1621) MIC = 4 μM for BP100.
Table 2: S. epidermidis (KCTC 1917) MIC = 4 μM for BP100.
Table 2: B. subtilis (KCTC 3068) MIC = 8 μM for BP100.
Table 2: MRSA (CCARM 3089) MIC = 32 μM for BP100.
Table 2: MRSA (CCARM 3090) MIC = 64 μM for BP100.
Table 2: E. coli (KCTC 1682) MIC = 4 μM for BP100.
Table 2: P. aeruginosa (KCTC 1637) MIC = 16 μM for BP100.
Table 2: S. typhimurium (KCTC 1926) MIC = 4 μM for BP100.
Table 2: MDRPA (CCARM 2095) MIC = 32 μM for BP100.
Table 2: MDRPA (CCARM 2109) MIC = 16 μM for BP100.
Table 2: HC10 >256 μM for BP100 (no detectable hemolysis at 256 μM).
Table 3: BP100 MBIC50 = 4–8 μM against MDRPA.
Table 3: BP100 MBIC90 = 8 μM against MDRPA.
Table 3: BP100 MBEC50 = 16–32 μM against MDRPA.
Table 3: BP100 MBEC90 = 32 μM against MDRPA.
Table 4: E. coli control MIC = 4 μM for BP100.
Table 4: E. coli MIC = 16 μM for BP100 in 150 mM NaCl.
Table 4: E. coli MIC = 16 μM for BP100 in 4.5 mM KCl.
Table 4: E. coli MIC = 16 μM for BP100 in 6 μM NH4Cl.
Table 4: E. coli MIC = 16 μM for BP100 in 1 mM MgCl2.
Table 4: E. coli MIC = 16 μM for BP100 in 2.5 mM CaCl2.
Table 4: E. coli MIC = 16 μM for BP100 in 4 μM FeCl3.
Table 4: E. coli MIC = 16 μM for BP100 in 10% human serum.
Table 4: S. aureus control MIC = 4 μM for BP100.
Table 4: S. aureus MIC = 16 μM for BP100 in 150 mM NaCl.
Table 4: S. aureus MIC = 16 μM for BP100 in 4.5 mM KCl.
Table 4: S. aureus MIC = 16 μM for BP100 in 6 μM NH4Cl.
Table 4: S. aureus MIC = 16 μM for BP100 in 1 mM MgCl2.
Table 4: S. aureus MIC = 16 μM for BP100 in 2.5 mM CaCl2.
Table 4: S. aureus MIC = 16 μM for BP100 in 4 μM FeCl3.
Table 4: S. aureus MIC = 32 μM for BP100 in 10% human serum.
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.