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Potential of synthetic endoperoxides against Trichomonas vaginalis in vitro

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dc.contributor.authorSeo, Min-Young-
dc.contributor.authorRyu, Jae-Sook-
dc.contributor.authorSato, Akira-
dc.contributor.authorKurosaki, Yuji-
dc.contributor.authorChang, Kyung-Soo-
dc.contributor.authorKim, Hye-Sook-
dc.date.accessioned2022-07-13T04:35:38Z-
dc.date.available2022-07-13T04:35:38Z-
dc.date.issued2017-10-
dc.identifier.issn1383-5769-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/151483-
dc.description.abstractMetronidazole is well known for medicine against Trichomonas vaginalis infection, but it has side effects though it is effective, and especially because reports of metronidazole-tolerant species are increasing, the development of new medicine is being required. Here, we noticed the killing effects of endoperoxide compounds, N-89 and N-251 as new antimalarial drug candidates, on T. vaginalis and searched the possibility of development of new medicine. We added each of metronidazole, artemisinin, and two of new endoperoxides (N-89 and N-251) to metronidazole-resistant and -sensitive species and compared its anti-trichomonal efficacy. For metronidazole, IC50 value, 50% of killing concentration for T. vaginalis, was very low for metronidazole-sensitive isolates (11.7 to 22.8 mu M), but was high for metronidazole-resistant ones (182.9 to 730.4 mu M). The IC50 values of N-89 and N-251 were 41.0 to 60.0 mu M, and 82.0 to 300.0 mu M for metronidazole-sensitive and-resistant isolates, respectively. In conclusion, we found the endoperoxides, N-89 and N-251, have anti-trichomonal effect against metronidazole-resistant T. vaginalis as well as metronidazole-sensitive ones. These results indicate that the anti-richomonal effects for our endoperoxides are equivalent or better in metronidazole-resistant T. vaginalis in comparison to metronidazole.-
dc.format.extent3-
dc.language영어-
dc.language.isoENG-
dc.publisherElsevier BV-
dc.titlePotential of synthetic endoperoxides against Trichomonas vaginalis in vitro-
dc.typeArticle-
dc.publisher.location아일랜드-
dc.identifier.doi10.1016/j.parint.2017.05.008-
dc.identifier.scopusid2-s2.0-85021863511-
dc.identifier.wosid000409154000019-
dc.identifier.bibliographicCitationParasitology International, v.66, no.5, pp 619 - 621-
dc.citation.titleParasitology International-
dc.citation.volume66-
dc.citation.number5-
dc.citation.startPage619-
dc.citation.endPage621-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaParasitology-
dc.relation.journalWebOfScienceCategoryParasitology-
dc.subject.keywordPlusANTIMALARIAL ACTIVITY-
dc.subject.keywordPlusPLASMODIUM-FALCIPARUM-
dc.subject.keywordPlusMETRONIDAZOLE-
dc.subject.keywordPlusPREVALENCE-
dc.subject.keywordPlusRESISTANT-
dc.subject.keywordPlusSTAGE-
dc.subject.keywordPlusN-251-
dc.subject.keywordPlusRISK-
dc.subject.keywordPlusN-89-
dc.subject.keywordAuthorTrichomonas vaginalis-
dc.subject.keywordAuthor1,2,6,7-tetraoxaspiro[7.11]nonadecane (N-89)-
dc.subject.keywordAuthor6-(1,2,6,7-Tetraoxaspiro[7.11]nonadec-4-yl)hexan-1-ol (N-251)-
dc.subject.keywordAuthorAnti-trichomonal activity-
dc.subject.keywordAuthorEndoperoxides-
dc.subject.keywordAuthorMetronidazole-resistant isolate-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S1383576917301824?via%3Dihub-
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서울 의과대학 > 서울 환경의생물학교실 > 1. Journal Articles

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