Alpinumisoflavone

Alpinumisoflavone
Names

IUPAC name 5-hydroxy-3-(4-hydroxyphenyl)-8,8-dimethylpyrano[3,2-g]chromen-4-one
Other names 5-hydroxy-7-(p-hydroxyphenyl)-2,2-dimethyl-2H-6H-benzodipyran-6-one
Identifiers
CAS Number	34086-50-5
ChEMBL	ChEMBL238628^Y
ChemSpider	4590280^Y
Jmol interactive 3D	Image Image
PubChem	5490139
InChI InChI=1S/C20H16O5/c1-20(2)8-7-13-15(25-20)9-16-17(18(13)22)19(23)14(10-24-16)11-3-5-12(21)6-4-11/h3-10,21-22H,1-2H3^Y Key: RQAMSFTXEFSBPK-UHFFFAOYSA-N^Y InChI=1/C20H16O5/c1-20(2)8-7-13-15(25-20)9-16-17(18(13)22)19(23)14(10-24-16)11-3-5-12(21)6-4-11/h3-10,21-22H,1-2H3 Key: RQAMSFTXEFSBPK-UHFFFAOYAG
SMILES CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C(=CO3)C4=CC=C(C=C4)O)C O=C2/C(c1ccc(O)cc1)=C\Oc4c2c(O)c3\C=C/C(Oc3c4)(C)C
Properties
Chemical formula	C₂₀H₁₆O₅
Molar mass	336.33 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y verify (what is ^YN ?)
Infobox references

Alpinumisoflavone is a pyranoisoflavone, a type of isoflavone. It can be found in the bark of Rinorea welwitschii.^[1] It can also be found in the molluscicide plant Millettia thonningii and is thought to be an antischistosomal agent^[2] since it has been shown to kill the snails which transmit the schistosomiasis and also the larvae of the parasite itself.^[3]

References

↑ Pyranoisoflavones from Rinorea welwitschii. M. Stewart, B. Bartholomew, F. Currie, D. K. Abbiw, Z. Latif, S. D. Sarker and R. J. Nash, Fitoterapia, Volume 71, Issue 5, 1 September 2000, Pages 595-597, doi:10.1016/S0367-326X(00)00210-0
↑ The plant molluscicide Millettia thonningii (Leguminosae) as a topical antischistosomal agent. S. Perrett, P. J. Whitfield, L. Sanderson and A. Bartlett, Journal of Ethnopharmacology, Volume 47, Issue 1, 23 June 1995, Pages 49-54
↑ Aqueous degradation of isoflavonoids in an extract of Millettia thonningii (Leguminosae) which is larvicidal towards schistosomes. Perrett S. and Whitfield P. J., PTR. Phytotherapy, 1995, vol. 9, no6, pp. 401-404

Isoflavones and their glycosides

Isoflavones	Daidzein Genistein Irilone Orobol Pseudobaptigenin Anagyroidisoflavone A and B

O-methylated isoflavones	Biochanin A Calycosin Formononetin Glycitein Irigenin 5-O-methylgenistein Pratensein Prunetin Psi-tectorigenin Retusin Tectorigenin

Glycosides	Daidzin Genistin Iridin Ononin Puerarin Sophoricoside Tectoridin

Prenylated isoflavones	Bidwillol A Derrubone Luteone 7-O-Methylluteone Wighteone

Pyranoisoflavones	Alpinumisoflavone Barbigerone Di-O-methylalpinumisoflavone 4'-methyl-alpinumisoflavone

Misc	Rotenoids

Synthetic	Ipriflavone

This article is issued from Wikipedia - version of the Saturday, October 31, 2015. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.