Justicidin A

Justicidin A
Names
	Preferred IUPAC name 9-(2H-1,3-Benzodioxol-5-yl)-4,6,7-trimethoxynaptho[2,3-c]furan-1(3H)-one
	Other names Diphyllin methyl ether
Identifiers
CAS Number	25001-57-4 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:6093;
ChEMBL	ChEMBL508532;
ChemSpider	140644;
KEGG	C10633;
PubChem CID	159982;
UNII	Q58EXN1G4M ;
CompTox Dashboard (EPA)	DTXSID40179709 ;
	InChI InChI=1S/C22H18O7/c1-24-16-7-12-13(8-17(16)25-2)21(26-3)14-9-27-22(23)20(14)19(12)11-4-5-15-18(6-11)29-10-28-15/h4-8H,9-10H2,1-3H3 Key: ANFSXHKDCKWWDB-UHFFFAOYSA-N;
	SMILES COC1=C(C=C2C(=C1)C(=C3C(=C2OC)COC3=O)C4=CC5=C(C=C4)OCO5)OC;
Properties
Chemical formula	C22H18O7
Molar mass	394.379 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Justicidin A is an organic compound isolated from Justicia procumbens. It is classified as a lignan.^[1]^[2] The compound may possess cytotoxic effects.^[3]

References

^ Umezawa, Toshiaki (2003). "Diversity in lignan biosynthesis". Phytochemistry Reviews. 2 (3): 371–390. Bibcode:2003PChRv...2..371U. doi:10.1023/B:PHYT.0000045487.02836.32. S2CID 6276953.
^ Xiong, Lu; Bi, Ming-Gang; Wu, Song; Tong, Yuan-Feng (2012). "Total synthesis of 6′-hydroxyjusticidin A". Journal of Asian Natural Products Research. 14 (4): 322–6. doi:10.1080/10286020.2011.653561. PMID 22375869. S2CID 26689006.
^ Fukamiya, Narihiko; Lee, Kuo-Hsiung (1986). "Antitumor Agents, 81. Justicidin-A and Diphyllin, Two Cytotoxic Principles from Justicia procumbens". Journal of Natural Products. 49 (2): 348–50. doi:10.1021/np50044a030. PMID 3734816.

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