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Furanochromone

Names
Preferred IUPAC name 5H-Furobenzopyran-5-one
Identifiers
CAS Number	67777-61-1
3D model (JSmol)	Interactive image
ChemSpider	114232
PubChem CID	128913
UNII	9KW282SZD5
CompTox Dashboard (EPA)	DTXSID30987113
InChI InChI=1S/C11H6O3/c12-9-2-4-14-11-6-10-7(1-3-13-10)5-8(9)11/h1-6HKey: QBCCGEPNFFWJOU-UHFFFAOYSA-N InChI=1/C11H6O3/c12-9-2-4-14-11-6-10-7(1-3-13-10)5-8(9)11/h1-6HKey: QBCCGEPNFFWJOU-UHFFFAOYAV
SMILES O=C\1c3c(O/C=C/1)cc2occc2c3
Properties
Chemical formula	C11H6O3
Molar mass	186.166 g·mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references

Furanochromone is a chemical compound which is a derivative of chromone (1,4-benzopyrone) and furan.

Some chemical derivatives of furanochromone show strong interaction with DNA. Furanochromones can be produced in callus cultures of Ammi visnaga or in Pimpinella monoica.

References

1. Pereira, David M.; Valentão, Patrícia; Pereira, José A.; Andrade, Paula B. (2009). "Phenolics: From Chemistry to Biology". Molecules. 14 (6): 2202–2211. doi:10.3390/molecules14062202. PMC 6254163. S2CID 5489895.
2. Niccolai, Neri; Bovalini, Lucia; Martelli, Paola (1986). "The mechanisms of interaction between furanochromones and dna". Biophysical Chemistry. 24 (3): 217–20. doi:10.1016/0301-4622(86)85027-X. PMID 3768467.
3. Krolicka A.; Staniszewska I.; Malinski E.; Szafranek J.; Łojkowska E. (2003). "Stimulation of furanochromone accumulation in callus cultures of Ammi visnaga L. by addition of elicitors". Pharmazie. 58 (8): 590–592. PMID 12967041.
4. Luthria, D.L.; Banerji, A. (1994). "Biosynthesis of furanochromones in Pimpinella monoica" (PDF). Proceedings of the Indian Academy of Sciences – Chemical Sciences. 106 (5): 1149–1156. doi:10.1007/BF02841922. S2CID 93321002.

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