Supporting Information
Supporting Information File 1: Spectroscopic data and other relevant information for compounds 1–4. | ||
Format: PDF | Size: 1.3 MB | Download |
Cite the Following Article
Bioactive selaginellins from Selaginella tamariscina (Beauv.) Spring
Chao Yang, Yutian Shao, Kang Li and Wujiong Xia
Beilstein J. Org. Chem. 2012, 8, 1884–1889.
https://doi.org/10.3762/bjoc.8.217
How to Cite
Yang, C.; Shao, Y.; Li, K.; Xia, W. Beilstein J. Org. Chem. 2012, 8, 1884–1889. doi:10.3762/bjoc.8.217
Download Citation
Citation data can be downloaded as file using the "Download" button or used for copy/paste from the text window
below.
Citation data in RIS format can be imported by all major citation management software, including EndNote,
ProCite, RefWorks, and Zotero.
Citations to This Article
Up to 20 of the most recent references are displayed here.
Scholarly Works
- Ferenczi, E.; Keglevich, P.; Tayeb, B. A.; Minorics, R.; Papp, D.; Schlosser, G.; Zupkó, I.; Hazai, L.; Csámpai, A. Synthesis and Antiproliferative Effect of New Alkyne-Tethered Vindoline Hybrids Containing Pharmacophoric Fragments. International journal of molecular sciences 2024, 25, 7428. doi:10.3390/ijms25137428
- Murthy, H. N.; Yadav, G. G.; Bhat, M. A. Bioactive Compounds of Pteridophytes. Reference Series in Phytochemistry; Springer International Publishing, 2023; pp 185–282. doi:10.1007/978-3-031-23243-5_10
- Murthy, H. N.; Yadav, G. G.; Bhat, M. A. Bioactive Compounds of Pteridophytes. Reference Series in Phytochemistry; Springer International Publishing, 2023; pp 1–98. doi:10.1007/978-3-030-97415-2_10-1
- Murányi, J.; Duró, C.; Gurbi, B.; Móra, I.; Varga, A.; Németh, K.; Simon, J.; Csala, M.; Csámpai, A. Novel Erlotinib-Chalcone Hybrids Diminish Resistance in Head and Neck Cancer by Inducing Multiple Cell Death Mechanisms. International journal of molecular sciences 2023, 24, 3456. doi:10.3390/ijms24043456
- Hughes, N. M.; Lev-Yadun, S. Review: Why do some plants have leaves with red or purple undersides?. Environmental and Experimental Botany 2023, 205, 105126. doi:10.1016/j.envexpbot.2022.105126
- Reginaldo, F. P. S.; Bueno, P. C. P.; Lourenço, E. M. G.; de Matos Costa, I. C.; Moreira, L. G. L.; de Araújo Roque, A.; Barbosa, E. G.; Fett-Neto, A. G.; Cavalheiro, A. J.; Giordani, R. B. Methyl jasmonate induces selaginellin accumulation in Selaginella convoluta. Metabolomics : Official journal of the Metabolomic Society 2022, 19, 2. doi:10.1007/s11306-022-01966-9
- Li, G.-H.; Zhang, Y.; Wu, J.-P.; Wang, Y.-Y.; Deng, G.-M.; Zeng, H.-L.; He, X.-A.; Long, H.-P.; Zhu, G.-Z.; Chen, Z.-H.; Cheng, F.; Xu, K.-P. Two New C21 Steroidal Glycosides from Selaginella Braunii Baker. Chemistry & biodiversity 2022, 19, e202200767. doi:10.1002/cbdv.202200767
- Wang, S.; Wang, X.; Shao, Y.; Shao, K.; Wang, Y.; Xiuhan, G.; Dong, H.; Zhao, W.; Li, Y.; Li, G. Synthesis and evaluation of 3-(phenylethynyl)-1,1'-biphenyl-2-carboxylate derivatives as new HIF-1 inhibitors. Bioorganic chemistry 2021, 116, 105298. doi:10.1016/j.bioorg.2021.105298
- Li, W.; Tang, G.-H.; Yin, S. Selaginellins from the genus Selaginella: isolation, structure, biological activity, and synthesis. Natural product reports 2021, 38, 822–842. doi:10.1039/d0np00065e
- Kumar, R.; Viktorova, J.; Krizkovska, B.; Lipov, J.; Ruml, T. Structural diversity and biological activities of secondary metabolites isolated from the genus Selaginella. Phytochemistry Reviews 2021, 20, 1–35.
- Kumar, R.; Viktorova, J.; Krizkovska, B.; Lipov, J.; Ruml, T. Structural diversity and biological activities of secondary metabolites isolated from the genus Selaginella. Phytochemistry Reviews 2021, 20, 1209–1243. doi:10.1007/s11101-021-09743-7
- Gupta, S.; Lee, D. Aryne-mediated construction of fluorene skeletons and its applications to total synthesis of selaginpulvilins. Strategies and Tactics in Organic Synthesis; Elsevier, 2021; Vol. 15, pp 149–175. doi:10.1016/b978-0-12-822212-6.00009-6
- Křížkovská, B.; Kumar, R.; Řehořová, K.; Sýkora, D.; Dobiasová, S.; Kučerová, D.; Tan, M. C. S.; Linis, V. C.; Oyong, G. G.; Ruml, T.; Lipov, J.; Viktorova, J. Comparison of Chemical Composition and Biological Activities of Eight Selaginella Species. Pharmaceuticals (Basel, Switzerland) 2020, 14, 16. doi:10.3390/ph14010016
- Reginaldo, F. P. S.; Bueno, P. C. P.; de, I. C. C.; de, A. R.; Fett-Neto, A. G.; Cavalheiro, A. J.; Giordani, R. B. Molecular Networking Discloses the Chemical Diversity of Flavonoids and Selaginellins in Selaginella convoluta. Planta medica 2020, 87, 113–123. doi:10.1055/a-1315-0666
- Chu, P.; Wang, S.; Zhu, X.; Yang, Y.; Li, H.; Tesfaldet, T.; Shopit, A.; Yang, Y.; Ma, X.; Peng, J.; Tang, Z.; Sun, Z. Selaginellin B induces apoptosis and autophagy in pancreatic cancer cells via the JAK2/STAT3 signaling pathway. American journal of translational research 2020, 12, 7127–7143.
- Xie, Y.; Xu, P.-S.; Xu, K.-P.; Zou, Z.-X.; Zhou, G.; Li, D.; Li, D.; Li, X.-M.; Li, J.; Tan, G.-S. Two new biflavanoids from Selaginella trichoclada Alsto. Natural product research 2019, 35, 3410–3416. doi:10.1080/14786419.2019.1700506
- He, X.-R.; Xu, L.-Y.; Jin, C.; Yue, P.-F.; Zhou, Z.-W.; Liang, X.-L. Tamariscinols U–W, new dihydrobenzofuran-type norneolignans with tyrosinase inhibitory activity from Selaginella tamariscina. Phytochemistry Letters 2019, 34, 79–83. doi:10.1016/j.phytol.2019.08.013
- Kojom, J. J. W.; Nguemfo, E. L.; Djouatsa, Y. N. N.; Bogning, C. Z.; Azebaze, A. G. B.; Llorent-Martínez, E. J.; Córdova, M. L. F.-d.; Dongmo, A. B. Phytochemical, antihypertensive and nephroprotective study of aqueous extract of the stems and roots of Selaginella vogelii Mett (Selaginellaceae) in rats. South African Journal of Botany 2019, 127, 256–264. doi:10.1016/j.sajb.2019.08.030
- Tuan, N. D.; Thuy, T.; Quan, P. M.; Hung, N. P. Inhibitory Selaginellins from Selaginella tamariscina against LPS-induced NO production in RAW264.7 cells. Vietnam Journal of Chemistry 2019, 57, 324–327. doi:10.1002/vjch.201900025
- Wang, S.; Liu, L.; Xiuhan, G.; Li, G.; Wang, X.; Huijuan, D.; Li, Y.; Zhao, W. Synthesis of novel natural product-like diaryl acetylenes as hypoxia inducible factor-1 inhibitors and antiproliferative agents. RSC advances 2019, 9, 13878–13886. doi:10.1039/c9ra02525a