Bacillomycin
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Preferred IUPAC name
3-[3,9-Bis(2-amino-2-oxo-ethyl)-16-(1-hydroxyethyl)-19-(hydroxymethyl)-6-[(4-hydroxyphenyl)methyl]-13-octyl-2,5,8,11,15,18,21,24-octaoxo-1,4,7,10,14,17,20,23-octazabicyclo[23.3.0]octacosan-22-yl]propanoic acid | |
Systematic IUPAC name
3-[16,22-Bis(carbamoylmethyl)-9-(1-hydroxyethyl)-6-(hydroxymethyl)-19-[(4-hydroxyphenyl)methyl]-12-octyl-1,4,7,10,14,17,20,23-octaoxo-hexacosahydro-1H-pyrrolo[1,2-j]1,4,7,10,13,16,19,22-octaazacyclopentacosan-3-yl]propanoic acid | |
Other names
3-[16,22-bis(carbamoylmethyl)-9-(1-hydroxyethyl)-6-(hydroxymethyl)-19-[(4-hydroxyphenyl)methyl]-12-octyl-1,4,7,10,14,17,20,23-octaoxo-octadecahydro-2H-pyrrolo[1,2-j]1,4,7,10,13,16,19,22-octaazacyclopentacosan-3-yl]propanoic acid
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Identifiers | |
3D model (JSmol)
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ChemSpider | |
PubChem CID
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Properties | |
C45H68N10O15 | |
Molar mass | 989.094 g·mol−1 |
Density | 1.4g/cm3 |
Hazards | |
Flash point | 883.1 °C (1,621.6 °F; 1,156.2 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Bacillomycins are a group of antifungal polypeptide antibiotics isolated from Bacillus subtilis.
Examples include:
- Bacillomycin A (fungosin, structure unknown)[1][2]
- Bacillomycin C (structure unknown)[2]
- Bacillomycin D (C45H68N10O15)[3]
- Bacillomycin F (C52H84N12O14)[4]
- Bacillomycin Fc (C52H84N12O14)[5]
- Bacillomycin L (Landy substance)[2][6]
- Bacillomycin S (structure unknown)[2]
References
- ^ Bacillomycin A
- ^ a b c d John Buckingham (ed.). Dictionary of Natural Products. pp. 590–591.
- ^ . PMID 7285926.
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(help) - ^ CID 3086138 from PubChem
- ^ CID 3086563 from PubChem
- ^ . PMID 24043450.
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