Micrococcin P1 is a macrocyclic peptide antibiotic and is a potent hepatitis C virus (HCV) inhibitor with an EC 50 range of 0.1-0.5 μM Micrococcin P1 has in vitro antibacterial activity against Gram-positive bacterial strains. The MIC values of Micrococcin P1 against S. aureus 1974149, E. faecalis 1674621 and S. pyogenes 1744264 are 2 μg/mL, 1 μg/mL and 1 μg/mL, respectively Micrococcin P1 is also a potent inhibitor of the malaria parasite Plasmodium falciparum In Vitro Dose-response assays reveales Micrococcin P1 to be very potent with a minimal inhibitory concentration (MIC) of 32-63 nM. Cytotoxicity assays reveales no significant impairment on cell line growth ( Form:Solid IC50& Target:HCV,Bacterial,Parasite
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Micrococcin P1
CAS number:67401-56-3 molecular formula:C48H49N13O9S6
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Specs
| Chinese alias | 微球菌素P1 | ||
| English alias | Micrococcin P, 13',19'-didehydro-19'-deoxy-28,44-dihydro-44-hydroxy- | BRN 1070340 | Micrococcin P1 | ||
| CAS number | 67401-56-3 | molecular formula | C48H49N13O9S6 |
| molecular weight | 1144.37 g/mol | Exact mass | ≥95% |
| PSA | - | logp | - |
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