Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C17H12O5 |
| Molecular Weight | 296.2742 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC1=C(C(=O)O\C1=C/C2=CC=C(O)C=C2)C3=CC=C(O)C=C3
InChI
InChIKey=BNNVVTQUWNGKPH-ZROIWOOFSA-N
InChI=1S/C17H12O5/c18-12-5-1-10(2-6-12)9-14-16(20)15(17(21)22-14)11-3-7-13(19)8-4-11/h1-9,18-20H/b14-9-
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Cross-Chemistry Leads to Product Diversity from Atromentin Synthetases in Aspergilli from Section Nigri. | 2019-02-21 |
|
| A Non-canonical Melanin Biosynthesis Pathway Protects Aspergillus terreus Conidia from Environmental Stress. | 2016-05-19 |
|
| Induction of secondary metabolism of Aspergillus terreus ATCC 20542 in the batch bioreactor cultures. | 2016-04 |
|
| Spatial regulation of a common precursor from two distinct genes generates metabolite diversity. | 2015-10-01 |
|
| Aspulvinones from a mangrove rhizosphere soil-derived fungus Aspergillus terreus Gwq-48 with anti-influenza A viral (H1N1) activity. | 2013-03-15 |
|
| Effects of high salt stress on secondary metabolite production in the marine-derived fungus Spicaria elegans. | 2011 |
|
| A new group of aromatic prenyltransferases in fungi, catalyzing a 2,7-dihydroxynaphthalene 3-dimethylallyl-transferase reaction. | 2010-05-28 |
|
| Purification and characterization of dimethylallyl pyrophosphate: aspulvinone dimethylallyltransferase from Aspergillus terreus. | 1978-06-27 |
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49637-60-7
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17704
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DTXSID201317721
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54675753
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SUBSTANCE RECORD
