C. ThebtaranonthY. ThebtaranonthS. WanauppathamkulY. YuthavongThailand National Science and Technology Development AgencyMahidol UniversityThailand National Center for Genetic Engineering and Biotechnology2018-07-042018-07-041995-01-01Phytochemistry. Vol.40, No.1 (1995), 125-128003194222-s2.0-0029360451https://repository.li.mahidol.ac.th/handle/20.500.14594/17232Activity-guided investigation of Cyperus rotundus tubers led to the isolation of patchoulenone, caryophyllene α-oxide, 10,12-peroxycalamenene and 4,7-dimethyl-1-tetralone. The antimalarial activities of these compounds are in the range of EC5010-4-10-6M, with the novel endoperoxide sesquiterpene, 10,12-peroxycalamenene, exhibiting the strongest effect at EC502.33 × 10-6M. © 1995.Mahidol UniversityAgricultural and Biological SciencesBiochemistry, Genetics and Molecular BiologyChemistryPharmacology, Toxicology and PharmaceuticsAntimalarial sesquiterpenes from tubers of Cyperus rotundus: structure of 10,12-Peroxycalamenene, a sesquiterpene endoperoxideArticleSCOPUS10.1016/0031-9422(95)00260-E