{"refrec":{"BRefID":113279,"RR":"<b>Wattanadilok, R.; Sawangwong, P.; Rodrigues, C.; Cidade, H.; Pinto, M.; Pinto, E.; Silva, A.; Kijjoa, A.</b> (2007). Antifungal activity evaluation of the constituents of <i>Haliclona baeri</i> and <i>Haliclona cymaeformis</i>, collected from the Gulf of Thailand. <i>Mar. Drugs 5(2)</i>: 40-51. <a href=\"https://dx.doi.org/10.3390/md502040\" target=\"_blank\">https://dx.doi.org/10.3390/md502040</a>","BEntID":107731,"PublicFlag":1,"CheckedFlag":0,"wosflag":1,"vabbflag":0,"RefStringPartII":". <i>Mar. Drugs 5(2)</i>: 40-51. <a href=\"https://dx.doi.org/10.3390/md502040\" target=\"_blank\">https://dx.doi.org/10.3390/md502040</a>","DocTypID":8,"DocType":"Journal article","MarineFlag":1,"FreshFlag":0,"BrackishFlag":0,"TerrestrialFlag":0,"Authorstring":"Wattanadilok, R.; Sawangwong, P.; Rodrigues, C.; Cidade, H.; Pinto, M.; Pinto, E.; Silva, A.; Kijjoa, A.","OrigTitleTranslFlag":0,"Authorstringtrunc":"Wattanadilok, R. <i>et al.</i>","Englishabstract":"A new compound maleimide-5-oxime was isolated, together with 3,4-dihydroxybenzoic acid, tetillapyrone, from the ethyl acetate extract of the marine sponge <i>Haliclona baeri </i>while tetillapyrone, nortetillapyrone, p-hydroxybenzaldehyde and phenylacetic acid were isolated from the ethyl acetate extract of <i>Haliclona cymaeformis</i>, collected from the Gulf of Thailand. The structures of tetillapyrone and nortetillapyrone were re-examined using HMBC correlations. Maleimide-5-oxime, tetillapyrone and nortetillapyrone were found to be inactive against three human tumor cell lines (the estrogen-dependent ER(+) MCF-7, the estrogen-independent ER(-) MDA-MB-231 and NCI-H460. Maleimide-5-oxime, p-hydroxybenzaldehyde, phenylacetic acid, tetillapyrone and nortetillapyrone were evaluated for their growth inhibitory effect against seven yeasts and eight filamentous fungi. Only nortetillapyrone showed antifungal activity, with a preponderance on the dermatophytic filamentous fungi. 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