9-Dehydroxyeurotinone
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Category | Others |
Catalog number | BBF-04450 |
CAS | 1360606-85-4 |
Molecular Weight | 272.25 |
Molecular Formula | C15H12O5 |
Purity | 98.0% |
Ordering Information
Catalog Number | Size | Price | Stock | Quantity |
---|---|---|---|---|
BBF-04450 | 1 mg | $629 | In stock |
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Add to cartDescription
9-Dehydroxyeurotinone is produced from the endophyte of Suaeda glauca.
Specification
Synonyms | Dibenz[b,e]oxepin-6(11H)-one, 2,4,7-trihydroxy-9-methyl- |
Storage | Store at -20°C |
IUPAC Name | 2,4,7-trihydroxy-9-methyl-11H-benzo[c][1]benzoxepin-6-one |
Canonical SMILES | CC1=CC(=C2C(=C1)CC3=CC(=CC(=C3OC2=O)O)O)O |
InChI | InChI=1S/C15H12O5/c1-7-2-8-4-9-5-10(16)6-12(18)14(9)20-15(19)13(8)11(17)3-7/h2-3,5-6,16-18H,4H2,1H3 |
InChI Key | JVEWVOQVOXHEQA-UHFFFAOYSA-N |
Properties
Appearance | Powder |
Boiling Point | 578.8±50.0°C (Predicted) |
Density | 1.488±0.06 g/cm3 (Predicted) |
Solubility | Soluble in Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone |
Reference Reading
1. Natural anthraquinone derivatives from a marine mangrove plant-derived endophytic fungus Eurotium rubrum: structural elucidation and DPPH radical scavenging activity
Dong-Li Li, Xiao-Ming Li, Bin-Gui Wang J Microbiol Biotechnol. 2009 Jul;19(7):675-80.
There is considerable interest in the isolation of potent radical scavenging compounds from natural resources to treat diseases involving oxidative stress. In this report, four new fungal metabolites including one new bisdihydroanthracenone derivative (1, eurorubrin), two new seco-anthraquinone derivatives [3, 2-O-methyl-9-dehydroxyeurotinone and 4, 2-Omethyl- 4-O-(alpha-D-ribofuranosyl)-9-dehydroxyeurotinone], and one new anthraquinone glycoside [6, 3-O-(alpha-D-ribofuranosyl)- questin], were isolated and identified from Eurotium rubrum, an endophytic fungal strain that was isolated from the inner tissue of the stem of the marine mangrove plant Hibiscus tiliaceus. In addition, three known compounds including asperflavin (2), 2-O-methyleurotinone (5), and questin (7) were also isolated and identified. Their structures were elucidated on the basis of spectroscopic analysis. All of the isolated compounds were evaluated for 1,1-diphenyl-2-picrylhydrazyl(DPPH) radical scavenging activity.
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Bio Calculators
* Our calculator is based on the following equation:
Concentration (start) x Volume (start) = Concentration (final) x Volume (final)
It is commonly abbreviated as: C1V1 = C2V2
* Total Molecular Weight:
g/mol
Tip: Chemical formula is case sensitive. C22H30N4O √ c22h30n40 ╳