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   <subfield code="a">Antileishmanial polyphenols from Corymbia maculata</subfield>
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   <subfield code="c">[JASMEEN SIDANA, DINESH NEERADI, ALKA CHOUDHARY, SUSHMA SINGH, WILLIAM FOLEY, INDER SINGH]</subfield>
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   <subfield code="a">An activity-guided fractionation was used to identify the antileishmanial compounds of Corymbia maculata. The hexane, ethyl acetate and methanol extracts were active in in vitro antileishmanial assay. Twelve polyphenols including 8-demethyl eucalyptin (1), eucalyptin (2), myrciaphenone A (3), myrciaphenone B (4), quercetin-3-O-β-d-xylopyranoside (5), myricetin-3-O-α-l-rhamnopyranoside (6), quercetin-3-O-β-d-galactopyranoside (7), quercetin-3-O-β-d-glucopyranoside (8), quercetin-3-O-α-l-rhamnopyranoside (9), syringic acid (10), gallic acid-3-methyl ether (11), gallic acid-4-methyl ether (12) and gallic acid (13) were isolated from the active extracts. All the tested compounds except 8-demethyleucalyptin and myrciaphenone B showed strong to moderate (6.9-24.5 $\upmu$ M) antileishmanial activity against Leishmania donovani promastigotes. An HPLC-PDA method has been developed to detect/quantify 29 compounds in the extracts of C. maculata leaves. This validated method allows simultaneous quantitation of seven flavonoids, fourteen phloroglucinols and eight other polyphenols and can be applied for qualitative as well as quantitative determination of phytoconstituents in Eucalyptus matrices. Graphical Abstract Phytochemical screening of Corymbia maculata resulted in the isolation of thirteen compounds from hexane and methanol extracts of the dried leaves. Flavonoid glycosides and a phloroglucinol glycoside were the active antileishmanial compounds. An HPLC-PDA method was developed and applied to detect and quantify twelve compounds in the extracts of C. maculata leaves.</subfield>
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