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Balanophonin

From Wikipedia, the free encyclopedia
Balanophonin
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
  • InChI=1S/C20H20O6/c1-24-17-10-13(5-6-16(17)23)19-15(11-22)14-8-12(4-3-7-21)9-18(25-2)20(14)26-19/h3-10,15,19,22-23H,11H2,1-2H3/b4-3+/t15-,19+/m0/s1
    Key: GWCSSLSMGCFIFR-LNFBDUAVSA-N
  • COC1=CC(=CC2=C1O[C@@H]([C@H]2CO)C3=CC(=C(C=C3)O)OC)/C=C/C=O
Properties
C20H20O6
Molar mass 356.37 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Balanophonin is a neo-lignan. It is a bioactive compound which can be isolated from Dipteryx odorata[2] and Balanophora japonica.[3]

References

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  1. "KNApSAcK Metabolite Information - C00033656". www.knapsackfamily.com.
  2. Jang, DS; Park, EJ; Hawthorne, ME; Vigo, JS; Graham, JG; Cabieses, F; Santarsiero, BD; Mesecar, AD; Fong, HH; Mehta, RG; Pezzuto, JM; Kinghorn, AD (2003). "Potential cancer chemopreventive constituents of the seeds of Dipteryx odorata (tonka bean)". J Nat Prod. 66 (5): 583–7. Bibcode:2003JNAtP..66..583J. doi:10.1021/np020522n. PMID 12762787.
  3. Balanophonin, a new neo-lignan from Balanophora japonica Makino, Haruna Mitsumasa, Koube Tomoko, Ito Kazuo and Murata Hiroyuki, Chemical & Pharmaceutical Bulletin, 25-04-1982, 30(4), pages 1525-1527 (abstract)
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