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Found 1 organism. Displayed organism 1
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1. (Organism ID: 10860)

Beauveria bassiana ATCC 7159

(Ancestor NCBI TaxID 176275, species name lookup)

Previously named: Botrytis bassiana ATCC 7159
Taxonomic group: fungi
Phylum: Ascomycota

The following compound(s) are assigned to this organism:

Compound ID: 18492

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Structure type: monomer ; 448
C22H24O10

Chemical and Pharmaceutical Bulletin 2011, "Microbial metabolism. Part 12. Isolation, characterization and bioactivity evaluation of eighteen microbial metabolites of 4'-hydroxyflavanone"
CSDB ID 43463 (all data & tools)
Compound ID: 18493

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Structure type: monomer ; 455.1277 [M+Na]+
C22H24O9

Chemical and Pharmaceutical Bulletin 2011, "Microbial metabolism. Part 12. Isolation, characterization and bioactivity evaluation of eighteen microbial metabolites of 4'-hydroxyflavanone"
CSDB ID 43464 (all data & tools)
Compound ID: 18510

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Structure type: monomer ; 413.1267 [M-H]+
C22H22O8

Chemical and Pharmaceutical Bulletin 2006, "Microbial metabolism. Part 6. Metabolites of 3- and 7-hydroxyflavones"
CSDB ID 43484 (all data & tools)
Compound ID: 18511

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Structure type: monomer ; 429.1212 [M-H]+
C22H22O9

Chemical and Pharmaceutical Bulletin 2006, "Microbial metabolism. Part 6. Metabolites of 3- and 7-hydroxyflavones"
CSDB ID 43485 (all data & tools)
Compound ID: 19182

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Structure type: monomer
Compound class: glycoside

Brazilian Journal of Microbiology 2008, "Selection of filamentous fungi of the Beauveria genus able to metabolize quercetin like mammalian cells"
CSDB ID 44371 (all data & tools)

Biotechnology Advances 2015, "Microbial biotransformation of bioactive flavonoids"
CSDB ID 48695 (all data & tools)
Compound ID: 19255

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Structure type: monomer ; 417.1626 [M+H]+
C21H22O8
Compound class: glycoside

Chemical and Pharmaceutical Bulletin 2012, "Bioconversion of 7-hydroxyflavanone: Isolation, characterization and bioactivity evaluation of twenty-one phase I and phase II microbial metabolites"
CSDB ID 44488 (all data & tools)
Compound ID: 19256

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Structure type: monomer ; 433.1517 [M+H]+
C21H22O9
Compound class: glycoside

Chemical and Pharmaceutical Bulletin 2012, "Bioconversion of 7-hydroxyflavanone: Isolation, characterization and bioactivity evaluation of twenty-one phase I and phase II microbial metabolites"
CSDB ID 44489 (all data & tools)
Compound ID: 19910

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Structure type: monomer ; 545.2021 [M+H]+
C28H32O1
Compound class: glycoside

Natural Product Communications 2010, "4'-O-methylglycosylation of curcumin by Beauveria bassiana"
CSDB ID 45970 (all data & tools)
Compound ID: 20746

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Structure type: monomer ; 479.1196 [M+H]+
C22H22O12

Biocatalysis and Biotransformation 2006, "Selective 4′-O-methylglycosylation of the pentahydroxy-flavonoid quercetin by Beauveria bassiana ATCC 7159"
CSDB ID 46665 (all data & tools)
Compound ID: 18504

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Structure type: monomer
C22H22O9
Compound class: glycoside, flavonoid glycoside

Chemical and Pharmaceutical Bulletin 2015, "Eleven microbial metabolites of 6-hydroxyflavanone"
CSDB ID 47949 (all data & tools)
Compound ID: 21246

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Structure type: monomer
Compound class: glucoside, glycoside

Molecules 2018, "Glycosylation of 3-hydroxyflavone, 3-methoxyflavone, quercetin and baicalein in fungal cultures of the genus Isaria"
CSDB ID 48670 (all data & tools)

Polish Journal of Microbiology 2016, "Microbial glycosylation of flavonoids"
CSDB ID 48942 (all data & tools)
Compound ID: 21247

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Structure type: monomer
Trivial name: quercimeritrin
Compound class: glucoside, glycoside, flavonoid glycoside
Reference(s) to other database(s): PubChem: 5282160

Molecules 2018, "Glycosylation of 3-hydroxyflavone, 3-methoxyflavone, quercetin and baicalein in fungal cultures of the genus Isaria"
CSDB ID 48671 (all data & tools)
Compound ID: 22367

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Structure type: monomer ; 431.1332 [M+H]+
Compound class: glycoside, anthraquinone glycoside

Phytochemistry Letters 2020, "Isolation and selective glycosylation of antisalmonellal anthraquinones from the stem bark of Morinda lucida Benth. (Rubiaceae)"
CSDB ID 50439 (all data & tools)
Compound ID: 22368

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Structure type: monomer ; 491.1543 [M+H]+
Compound class: glycoside, anthraquinone glycoside

Phytochemistry Letters 2020, "Isolation and selective glycosylation of antisalmonellal anthraquinones from the stem bark of Morinda lucida Benth. (Rubiaceae)"
CSDB ID 50440 (all data & tools)

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