Sulochrin
Sulochrin structure
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Common Name | Sulochrin | ||
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| CAS Number | 519-57-3 | Molecular Weight | 332.30500 | |
| Density | 1.378g/cm3 | Boiling Point | 576.3ºC at 760 mmHg | |
| Molecular Formula | C17H16O7 | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | 212.6ºC | |
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New chlorinated diphenyl ethers from an Aspergillus species.
J. Nat. Prod. 65(1) , 7-10, (2002) Two new chlorinated diphenyl ethers (5, 6) have been isolated from the culture broth of an Aspergillus species obtained from leaf litter, together with the known benzophenone sulochrin (1), the grisandiene geodin (2), and the diphenyl ether asterric acid (3).... |
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Physiological, morphological and kinetic aspects of lovastatin biosynthesis by Aspergillus terreus.
Biotechnol. J. 4(5) , 647-64, (2009) This review focuses on selected aspects of lovastatin biosynthesis by Aspergillus terreus. Biochemical issues concerning this process are presented to introduce polyketide metabolites, in particular lovastatin. The formation of other than lovastatin polyketid... |
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A liquid chromatography/tandem mass spectrometric multi-mycotoxin method for the quantification of 87 analytes and its application to semi-quantitative screening of moldy food samples.
Anal. Bioanal. Chem 389(5) , 1505-23, (2007) This paper describes the extension of a previously published method based on liquid chromatography/electrospray ionization tandem mass spectrometry (HPLC/ESI-MS/MS) from 39 to currently 87 analytes. Besides the mycotoxins for which regulated concentrations ex... |
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Sulochrin inhibits eosinophil degranulation.
J. Antibiot. 50(11) , 972-4, (1997)
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Effects of ortho-substituent groups of sulochrin on inhibitory activity to eosinophil degranulation.
Bioorg. Med. Chem. Lett. 9(14) , 1945-8, (1999) Sulochrin, a metabolite of fungi, has been shown to have an inhibitory activity to eosinophil degranulation. A series of sulochrin derivatives substituted at ortho-positions to the 10-carbonyl group was examined the activity. The importance of alkylester at C... |
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Aspergillus fumigatus CY018, an endophytic fungus in Cynodon dactylon as a versatile producer of new and bioactive metabolites.
J. Biotechnol. 114(3) , 279-87, (2004) Aspergillus fumigatus CY018 was recognized as an endophytic fungus for the first time in the leaf of Cynodon dactylon. By bioassay-guided fractionation, the EtOAc extract of a solid-matrix steady culture of this fungus afforded two new metabolites, named aspe... |
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Rational elimination of Aspergillus terreus sulochrin production.
J. Biotechnol. 108(2) , 171-8, (2004) Elimination of undesirable co-metabolites from industrial fermentations is often required due to the toxicities associated with the contaminants and/or due to difficulties in removing the contaminants during downstream processing. Sulochrin is a co-metabolite... |
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Specific inhibition of hepatitis C virus entry into host hepatocytes by fungi-derived sulochrin and its derivatives
Biochem. Biophys. Res. Commun. 440(4) , 515-20, (2013) • Chemical screening identified sulochrin as a natural product reducing HCV infection. • Sulochrin inhibited HCV entry. • The anti-HCV activity of sulochrin was conserved in different HCV genotypes. • Cotreatment of sulochrin with IFNα or telaprevir showed a ... |
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Hydroxysulochrin, a tea pollen growth inhibitor from the fungus Aureobasidium sp.
Biosci. Biotechnol. Biochem. 67(2) , 442-4, (2003) A new plant growth regulator, hydroxysulochrin (1), together with sulochrin (2) was isolated from the culture filtrate of Aureobasidium sp. grown on a malt extract medium. The structures of 1 and 2 were established by spectroscopic methods. 1 and 2 inhibited ... |