Isojacareubin

Isojacareubin
Names

IUPAC name 6,10,11-Trihydroxy-3,3-dimethyl-1,2-dihydropyrano[2,3-c]xanthen-7-one
Identifiers
3D model (JSmol)	Interactive image
ChemSpider	28514885
PubChem CID	70697351
InChI InChI=1S/C18H16O6/c1-18(2)6-5-8-12(24-18)7-11(20)13-14(21)9-3-4-10(19)15(22)17(9)23-16(8)13/h3-4,7,19-20,22H,5-6H2,1-2H3 Key: NNWFEKLCJFLWGN-UHFFFAOYSA-N
SMILES CC1(CCC2=C3C(=C(C=C2O1)O)C(=O)C4=C(O3)C(=C(C=C4)O)O)C
Properties
Chemical formula	C₁₈H₁₆O₆
Molar mass	328.32 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

Isojacareubin is an antibacterial isolate of Hypericum japonicum.^[1]

References

↑ Zuo, GY; An, J; Han, J; Zhang, YL; Wang, GC; Hao, XY; Bian, ZQ (2012). "Isojacareubin from the Chinese Herb Hypericum japonicum: Potent Antibacterial and Synergistic Effects on Clinical Methicillin-Resistant Staphylococcus aureus (MRSA)". International journal of molecular sciences. 13 (7): 8210–8. PMC 3430230 . PMID 22942699. doi:10.3390/ijms13078210.

Types of xanthonoids
Aglycones	Apetalinone A, B, C and D Bellidifolin Calozeyloxanthone Desoxygambogenin Desoxymorellin Euxanthone Forbesione Gambogellic acid Gambogenic acid Gambogenin Gambogenin dimethyl acetal Gambogic acid Gambogin Gaudichaudiic acid A, B, C, D and E Gaudichaudione A, B, C, D, E, F, G and H Hanburin Isogambogenin Isojacareubin Isomorellin Isomoreollin B Methylswertianin Morellic acid Morellin dimethyl acetal Moreollic acid Norathyriol Psorospermin 2,3′,4,6-tetrahydroxybenzophenone Tomentonone Zeyloxanthonone
Glycosides	Indian yellow Isomangiferin Mangiferin Mangostin-3,6-di-O-glucoside Wubangziside A Wubangziside B
Acetylated	Mangostin
Misc.	Gartanin 8-disoxygartanin Normangostin

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