Zearalanone

From Wikipedia, the free encyclopedia
Jump to navigation Jump to search
Zearalanone
Zearalanone.svg
Names
Preferred IUPAC name
(3S)-14,16-Dihydroxy-3-methyl-3,4,5,6,9,10,11,12-octahydro-1H-2-benzoxacyclotetradecine-1,7(8H)-dione
Other names
Mycotoxin, ZAN
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.165.079 Edit this at Wikidata
KEGG
UNII
  • InChI=1S/C18H24O5/c1-12-6-5-9-14(19)8-4-2-3-7-13-10-15(20)11-16(21)17(13)18(22)23-12/h10-12,20-21H,2-9H2,1H3/t12-/m0/s1
    Key: APJDQUGPCJRQRJ-LBPRGKRZSA-N
  • O=C1O[C@H](CCCC(=O)CCCCCc2cc(O)cc(O)c12)C
Properties
C18H24O5
Molar mass 320.385 g·mol−1
Hazards
GHS pictograms GHS07: HarmfulGHS08: Health hazard
GHS Signal word Warning
H302, H312, H315, H319, H332, H335, H351
P201, P202, P261, P264, P270, P271, P280, P281, P301+312, P302+352, P304+312, P304+340, P305+351+338, P308+313, P312, P321, P322, P330, P332+313, P337+313, P362, P363, P403+233, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Zearalanone (ZAN) is a semi-synthetic mycoestrogen that is a derivative of zearalenone (ZEN).[1] Zearalanone is extracted from medical herbs and edible herbs alone with other substance called aflatoxins in the same time by a specific immunoaffinity column. Zearalanone has six analog. They are ZEN, zearalanone, α-zeralanol, β-zeralanol, α-zearalenol, and β-zearalenol.[2]

See also[edit]

References[edit]

  1. ^ Drzymala; et al. (April 28, 2012). "(3S)-14,16-Dihydroxy-3-methyl-3,4,5,6,9,10,11,12-octahydro-1H-2-benzoxacyclotetradecine-1,7(8H)-dione (zearalanone) monohydrate". Acta Crystallogr E. 68 (5): o1577. doi:10.1107/S1600536812018168. PMC 3344672. PMID 22590434.
  2. ^ Sun, Shujuan (August 2018). "Determination of aflatoxin and zearalenone analogs in edible and medicinal herbs using a group-specific immunoaffinity column coupled to ultra-high-performance liquid chromatography with tandem mass spectrometry". Journal of Chromatography B. 1092: 228–236. doi:10.1016/j.jchromb.2018.06.012. PMID 29909149.