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17878-69-2 | 7H-Furo[3',2':4,5]furo[2,3-c]xanthen-7-one, 3a,12c-dihydro-6,8-dimethoxy-, (3aR,12cS)-
CAS No: 17878-69-2 Catalog No: AG0026B0 MDL No:
Product Description
Catalog Number:
AG0026B0
Chemical Name:
7H-Furo[3',2':4,5]furo[2,3-c]xanthen-7-one, 3a,12c-dihydro-6,8-dimethoxy-, (3aR,12cS)-
CAS Number:
17878-69-2
Molecular Formula:
C19H14O6
Molecular Weight:
338.3109
IUPAC Name:
(3S,7R)-11,15-dimethoxy-6,8,20-trioxapentacyclo[10.8.0.02,9.03,7.014,19]icosa-1,4,9,11,14(19),15,17-heptaen-13-one
InChI:
InChI=1S/C19H14O6/c1-21-10-4-3-5-11-15(10)17(20)16-12(22-2)8-13-14(18(16)24-11)9-6-7-23-19(9)25-13/h3-9,19H,1-2H3/t9-,19+/m0/s1
InChI Key:
JKUJKKGMOZDDJV-ZRNGKTOUSA-N
SMILES:
COc1cc2O[C@@H]3[C@H](c2c2c1c(=O)c1c(o2)cccc1OC)C=CO3
Properties
Complexity:
576
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
2
Defined Bond Stereocenter Count:
0
Exact Mass:
338.079g/mol
Formal Charge:
0
Heavy Atom Count:
25
Hydrogen Bond Acceptor Count:
6
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
338.315g/mol
Monoisotopic Mass:
338.079g/mol
Rotatable Bond Count:
2
Topological Polar Surface Area:
63.2A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.1
Literature
| Title | Journal |
|---|---|
| Functional and phylogenetic analysis of the Aspergillus ochraceoroseus aflQ (ordA) gene ortholog. | Mycologia 20120101 |
| Spiroethers of German chamomile inhibit production of aflatoxin G and trichothecene mycotoxin by inhibiting cytochrome P450 monooxygenases involved in their biosynthesis. | FEMS microbiology letters 20080701 |
| Biochemical analysis of oxidative stress in the production of aflatoxin and its precursor intermediates. | Mycopathologia 20060901 |
| Kinetics of the oxidoreductase involved in the conversion of O-methylsterigmatocystin to aflatoxin B1. | Preparative biochemistry & biotechnology 20060101 |
| Taxonomic comparison of three different groups of aflatoxin producers and a new efficient producer of aflatoxin B1, sterigmatocystin and 3-O-methylsterigmatocystin, Aspergillus rambellii sp. nov. | Systematic and applied microbiology 20050701 |
| Metal ion enhancement of fungal growth, gene expression and aflatoxin synthesis in Aspergillus flavus: RT-PCR characterization. | Journal of applied microbiology 20030101 |
| Synthesis of 11-hydroxyl O-methylsterigmatocystin and the role of a cytochrome P-450 in the final step of aflatoxin biosynthesis. | Journal of the American Chemical Society 20020515 |
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