Chrysophanic acid

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Chrysophanic acid
Chrysophanol.svg
Names
IUPAC name
1,8-Dihydroxy-3-methyl-9,10-anthraquinone
Identifiers
ChEBI CHEBI:3687
ChemSpider 9793
Jmol 3D model Interactive image
PubChem 10208
  • InChI=1S/C15H10O4/c1-7-5-9-13(11(17)6-7)15(19)12-8(14(9)18)3-2-4-10(12)16/h2-6,16-17H,1H3
    Key: LQGUBLBATBMXHT-UHFFFAOYSA-N
  • InChI=1/C15H10O4/c1-7-5-9-13(11(17)6-7)15(19)12-8(14(9)18)3-2-4-10(12)16/h2-6,16-17H,1H3
    Key: LQGUBLBATBMXHT-UHFFFAOYAW
  • CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3O
Properties
C15H10O4
Molar mass 254.24 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).
Infobox references

Chrysophanic acid, also known as chrysophanol, is a fungal isolate and a natural anthraquinone with anti-cancer activity.[1]

Drug action

Chrysophanol induces the necrosis of cancer cells via a reduction in ATP levels.[2] Chrysophanol attentuates the effects of lead exposure in mice by reducing hippocampal neuronal cytoplasmic edema, enhancing mitochondrial crista fusion, significantly increasing memory and learning abilities, reducing lead content in blood, heart, brain, spleen, kidney and liver, promoting superoxide dismutase and glutathione peroxidase activities and reducing malondialdehyde level in the brain, kidney and liver. [3]

Notes

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  3. In lead-exposed neonatal mice, chrysophanol attenuates injury to hippocampal neurons. Zhang et al. (2014) http://www.medicalnewstoday.com/releases/279724.php



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