Template:Did you know nominations/Apparicine
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Revision as of 20:23, 7 February 2017 by imported>Cwmhiraeth (Passed for DYK)
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Apparicine
- ... that establishing the structure of apparicine was a notable early use of nuclear magnetic resonance decoupling to determine a chemical structure? Saxton, J. Edwin, ed. (1983). "Indoles: Part Four: The Monoterpenoid Indole Alkaloids". The Chemistry of Heterocyclic Compound. 25. John Wiley & Sons. ISBN 0470188448., page 287
- ALT1:... that the chemical structure of apparicine was established by nuclear magnetic resonance decoupling using the 1H isotope of hydrogen? Phillipson, John David; Zenk, M.H., eds. (1980). Indole and Biogenetically Related Alkaloids. Annual proceedings of the Phytochemical Society of Europe. 17. Phytochemical Society of Europe. Academic Press. ISBN 0125544502. ISSN 0309-9393., page 230
- ALT2:... that the alkaloid apparicine has moderate to strong activity against some human pathogens? Schmelzer, G.H.; Gurib-Fakim, A., eds. (2008). Medicinal Plants. 1. PROTA Foundation, Backhuys Publishers. ISBN 9789057822049. ISSN 1877-430X., page 590
- ALT3:... that the alkaloid apparicine exhibits strong activity against poliovirus type 3? Schmelzer, G.H.; Gurib-Fakim, A., eds. (2008). Medicinal Plants. 1. PROTA Foundation, Backhuys Publishers. ISBN 9789057822049. ISSN 1877-430X., page 592
- ALT4:... that the alkaloid apparicine exhibits cytotoxicity against an experimental lymphocytic leukemia cell line? Schmelzer, G.H.; Gurib-Fakim, A., eds. (2008). Medicinal Plants. 1. PROTA Foundation, Backhuys Publishers. ISBN 9789057822049. ISSN 1877-430X., page 592
- Reviewed: Template:Did you know nominations/The Transactor (see my DYK tracker)
Created by Mindmatrix (talk). Self-nominated at 17:18, 1 January 2017 (UTC).
This article is new enough and long enough. The image is in the public domain and any of the hooks could be used, although I like ALT0 best. The article is neutral and neither Earwig nor I detected any policy issues. Cwmhiraeth (talk) 20:22, 7 February 2017 (UTC)