albocycline
albocycline structure
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Common Name | albocycline | ||
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| CAS Number | 25129-91-3 | Molecular Weight | 308.41300 | |
| Density | 1.04g/cm3 | Boiling Point | 465.7ºC at 760 mmHg | |
| Molecular Formula | C18H28O4 | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | 161.2ºC | |
| Symbol |
GHS06 |
Signal Word | Danger | |
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Computational identification and analysis of orphan assembly-line polyketide synthases.
J. Antibiot. 67(1) , 89-97, (2014) The increasing availability of DNA sequence data offers an opportunity for identifying new assembly-line polyketide synthases (PKSs) that produce biologically active natural products. We developed an automated method to extract and consolidate all multimodula... |
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Albocycline: structure determination by x-ray crystallography.
J. Antibiot. 35(12) , 1658-64, (1982) The structure and absolute configuration of the macrolide antibiotic albocycline (1a) has been determined by X-ray crystallographic analysis on the derived p-bromobenzoate (1b). The absolute configuration of albocycline is 4R, 7S, 12S, 13R. |
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Studies on an antibiotic, albocycline VII. Minor components of albocycline.
J. Antibiot. 37(10) , 1187-97, (1984) As an approach to the search for new potentially useful macrolide antibiotics, we explored the minor components of albocycline (ALB) from the culture broth of Streptomyces bruneogriseus. Eight minor components were isolated and their structures were confirmed... |
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Albocycline- and carbomycin-type macrolides, inhibitors of human prolyl endopeptidases.
J. Antibiot. 51(3) , 368-71, (1998)
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Biosynthesis of albocycline: origin of the carbon skeleton.
J. Antibiot. 50(6) , 526-8, (1997)
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A new inhibitor of melanogenesis, albocycline K3, produced by Streptomyces sp. OH-3984.
J. Antibiot. 49(5) , 485-6, (1996)
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