Publication:
Bioactive deoxypreussomerins and dimeric naphthoquinones from Diospyros ehretioides fruits: Deoxypreussomerins may not be plant metabolites but may be from fungal epiphytes or endophytes

dc.contributor.authorAreerat Prajoubklangen_US
dc.contributor.authorBusaban Sirithunyalugen_US
dc.contributor.authorPanarat Charoenchaien_US
dc.contributor.authorRapheephat Suvannakaden_US
dc.contributor.authorNongluksna Sriubolmasen_US
dc.contributor.authorSirivipa Piyamongkolen_US
dc.contributor.authorPalangpon Kongsaereeen_US
dc.contributor.authorPrasat Kittakoopen_US
dc.contributor.otherChiang Mai Universityen_US
dc.contributor.otherThailand National Center for Genetic Engineering and Biotechnologyen_US
dc.contributor.otherChulalongkorn Universityen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-06-21T08:07:40Z
dc.date.available2018-06-21T08:07:40Z
dc.date.issued2005-11-28en_US
dc.description.abstractDeoxypreussomerin derivatives, palmarumycins JC1 (1) and JC2 (2), and two dimeric naphthoquinones, isodiospyrin (3) and its new derivative isodiospyrol A (4), were isolated from dried fruits of Diospyros ehretioides. Structures of the isolated compounds were elucidated by spectroscopic analyses. Palmarumycins were not found in the extract of freshly collected fruits; however, they were present in dried fruit extract. The absence of palmarumycins in fresh fruits of D. ehretioides, together with the chemotaxonomic point of view, we proposed that palmarumycins JC1 (1) and JC2 (2) are more likely to be fungal metabolites, i.e., endophytes or epiphytes. The isolation of palmarumycins 1 and 2 from dried D. ehretioides fruits could be reproducible; both plant samples collected in the years 2002 and 2004 provided the same result, and, therefore, symbiont fungal strains should be specific to the plant host, D. ehretioides, and they can grow on the fruits during drying the sample. Palmarumycin JC1 (1) did not exhibit antimalarial, antifungal, antimycobacterial, and cytotoxic activities. Palmarumycin JC2 (2) exhibited antimalarial (IC50 4.5 μg/ml), antifungal (IC50 12.5 μg/ml), antimycobacterial (MIC 6.25 μg/ml), and cytotoxic (IC50 11.0 μg/ml for NCI-H187 cell line) activities. In our bioassay systems, isodiospyrin (3) did not exhibit antimycobacterial, antifungal, antimalarial, and cytotoxic activities. Isodiospyrol A (4) exhibited antimalarial (IC50 2.7 μg/ml) and antimycobacterial (MIC 50 μg/ml) activities, but was inactive towards Candida albicans. Compound 4 also exhibited cytotoxicity against BC cells (IC50 12.3 μg/ml), but not towards KB and Vero cell lines. © 2005 Verlag Helvetica Chimica Acta AG, Zürich.en_US
dc.identifier.citationChemistry and Biodiversity. Vol.2, No.10 (2005), 1358-1367en_US
dc.identifier.doi10.1002/cbdv.200590108en_US
dc.identifier.issn16121880en_US
dc.identifier.issn16121872en_US
dc.identifier.other2-s2.0-27844439394en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/16272
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=27844439394&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemical Engineeringen_US
dc.subjectChemistryen_US
dc.titleBioactive deoxypreussomerins and dimeric naphthoquinones from Diospyros ehretioides fruits: Deoxypreussomerins may not be plant metabolites but may be from fungal epiphytes or endophytesen_US
dc.typeReviewen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=27844439394&origin=inwarden_US

Files

Collections