Quinalizarin

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Quinalizarin
Skeletal formula of quinalizarin
Ball-and-stick model
Names
IUPAC name
1,2,5,8-Tetrahydroxyanthracene-9,10-dione
Identifiers
81-61-8 YesY
ChEMBL ChEMBL29898 N
ChemSpider 4829 N
Jmol 3D model Interactive image
PubChem 5004
  • InChI=1S/C14H8O6/c15-6-3-4-7(16)11-10(6)12(18)5-1-2-8(17)13(19)9(5)14(11)20/h1-4,15-17,19H N
    Key: VBHKTXLEJZIDJF-UHFFFAOYSA-N N
  • InChI=1/C14H8O6/c15-6-3-4-7(16)11-10(6)12(18)5-1-2-8(17)13(19)9(5)14(11)20/h1-4,15-17,19H
    Key: VBHKTXLEJZIDJF-UHFFFAOYAM
  • C1=CC(=C(C2=C1C(=O)C3=C(C=CC(=C3C2=O)O)O)O)O
Properties
C14H8O6
Molar mass 272.21 g·mol−1
Vapor pressure {{{value}}}
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

Quinalizarin or 1,2,5,8-tetrahydroxyanthraquinone is an organic compound with formula C
14
H
8
O
6
. It is one of many tetrahydroxyanthraquinone isomers, formally derived from anthraquinone by replacement of four hydrogen atoms by hydroxyl (OH) groups.

Quinalizarin is an inhibitor of the enzyme protein kinase CK2. It is more potent and selective than emodin.[1]

See also

References

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