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| Product | Description | |
|---|---|---|
| Micrococcin P1 | It is a thiopeptide antibiotic isolated from the culture broth of Bacillus pumilus as a main component of the micrococcin P complex. Synonyms: 2'-[(11S, 14Z, 21S, 28S)-14-ethylidene-9, 10, 11, 12, 13, 14, 20, 21, 27, 28-decahydro-28-[(1R)-1-hydroxyethyl]-11-[(1R)-1-hydroxyethyl]-21-(1-methylethyl)-9, 12, 19, 26-tetraoxo-19H, 26H-8, 5:18, 15:25, 22:32, 29-tetranitrilo-5H, 15H-pyrido[3, 2-m][1, 11, 17, 24, 4, 7, 20, 27]tetrathiatetraazacyclotriacontin-2-yl]-N-[(1Z)-1-[[[(2R)-2-hydroxypropyl]amino]carbonyl]-1-propen-1-yl]-[2, 4'-bithiazole]-4-carboxamide; 13',19'-Didehydro-19'-deoxy-28,44-dihydro-44-hydroxymicrococcin P. Grades: >95% by HPLC. CAS No. 67401-56-3. Molecular formula: C48H49N13O9S6. Mole weight: 1144.37. |  |
| Micrococcin P1 | 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 [1]. 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 [2]. Micrococcin P1 is also a potent inhibitor of the malaria parasite Plasmodium falciparum [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 67401-56-3. Pack Sizes: 500 μg; 1 mg. Product ID: HY-125728. |  |
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