Cite
Direct semi-synthesis of the anticancer lead-drug protoapigenone from apigenin, and synthesis of further new cytotoxic protoflavone derivatives.
MLA
Hunyadi, Attila, et al. “Direct Semi-Synthesis of the Anticancer Lead-Drug Protoapigenone from Apigenin, and Synthesis of Further New Cytotoxic Protoflavone Derivatives.” PloS One, vol. 6, no. 8, 2011, p. e23922. EBSCOhost, https://doi.org/10.1371/journal.pone.0023922.
APA
Hunyadi, A., Chuang, D.-W., Danko, B., Chiang, M. Y., Lee, C.-L., Wang, H.-C., Wu, C.-C., Chang, F.-R., & Wu, Y.-C. (2011). Direct semi-synthesis of the anticancer lead-drug protoapigenone from apigenin, and synthesis of further new cytotoxic protoflavone derivatives. PloS One, 6(8), e23922. https://doi.org/10.1371/journal.pone.0023922
Chicago
Hunyadi, Attila, Da-Wei Chuang, Balazs Danko, Michael Y Chiang, Chia-Lin Lee, Hui-Chun Wang, Chin-Chung Wu, Fang-Rong Chang, and Yang-Chang Wu. 2011. “Direct Semi-Synthesis of the Anticancer Lead-Drug Protoapigenone from Apigenin, and Synthesis of Further New Cytotoxic Protoflavone Derivatives.” PloS One 6 (8): e23922. doi:10.1371/journal.pone.0023922.