Parvifloranines A and B, two 11-carbon alkaloids from Geijera parviflora

Journal of Natural Products

Volumn 76, Issue 7, 2013, Pages 1384-1387

  Shou, Qingyao ^a   Banbury, Linda K ^a   Renshaw, Dane E ^a   Smith, Joshua E ^a   He, Xiaoxiang ^a   Dowell, Ashley ^a   Griesser, Hans J ^b   Heinrich, Michael ^a,c   Wohlmuth, Hans ^a  

^a SOUTHERN CROSS UNIVERSITY   (Australia)

^b UNIVERSITY OF SOUTH AUSTRALIA   (Australia)

^c UNIVERSITY OF LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ALKALOID DERIVATIVE; GEIPARVARIN; NITRIC OXIDE; PARVIFLORANINE A; PARVIFLORANINE B; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; BIOSYNTHESIS; CHEMOTAXONOMY; ENANTIOMER; GEIJERA PARVIFLORA; IC 50; IN VITRO STUDY; MACROPHAGE; MICHAEL ADDITION; MOUSE; NONHUMAN; PLANT LEAF; RUTACEAE;

ALKALOIDS; ANIMALS; AUSTRALIA; INHIBITORY CONCENTRATION 50; LIPOPOLYSACCHARIDES; MACROPHAGES; MICE; MOLECULAR STRUCTURE; NITRIC OXIDE; NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR; STEREOISOMERISM;

EID: 84880892028     PISSN: 01633864     EISSN: 15206025     Source Type: Journal    
DOI: 10.1021/np400376r     Document Type: Article

References (12)

1. Mabberley, D. J. Mabberley's Plant-book: A Portable Dictionary of Plants, Their Classification and Uses, 3 rd ed.; Cambridge Press University: Cambridge, USA, 2008; p 353.
2. Duretto, M., F. Rutaceae. In Flora of Victoria, 4 th ed.; Walsh, N. G., Entwisle, T. J., Eds.; Inkata Press: Melbourne, Australia, 1999; p 153.
3. Lahey, F.; Macleod, J. Aust. J. Chem. 1967, 20, 1943
4. Dreyer, D. L.; Lee, A. Phytochemistry 1972, 11, 763
5. Jones, R. V. H.; Sutherland, M. D. Aust. J. Chem. 1968, 21, 2255
6. Brophy, J. J.; Goldsack, R. J.; Forster, P. I. J. Essent. Oil Res. 2005, 17, 169
7. Chimichi, S.; Boccalini, M.; Salvador, A.; Dall'Acqua, F.; Basso, G.; Viola, G. ChemMedChem. 2009, 4, 769
8. Frisch, M. J.; Trucks, G. W.; Schlegel, H. B.; Scuseria, G. E.; Robb, M. A.; Cheeseman, J. R.; Montgomery, J. A., Jr.; Vreven, T.; Kudin, K. N.; Burant, J. C.; Millam, J. M.; Iyengar, S. S.; Tomasi, J.; Barone, V.; Mennucci, B.; Cossi, M.; Scalmani, G.; Rega, N.; Petersson, G. A.; Nakatsuji, H.; Hada, M.; Ehara, M.; Toyota, K.; Fukuda, R.; Hasegawa, J.; Ishida, M.; Nakajima, T.; Honda, Y.; Kitao, O.; Nakai, H.; Klene, M.; Li, X.; Knox, J. E.; Hratchian, H. P.; Cross, J. B.; Adamo, C.; Jaramillo, J.; Gomperts, R.; Stratemann, R. E.; Yazyev, O.; Austin, A. J.; Cammi, R.; Pomelli, C.; Ochterski, J. W.; Ayala, P. Y.; Morokuma, K.; Voth, G. A.; Salvador, P.; Dannenberg, J. J.; Zakrzewski, V. G.; Dapprich, S.; Daniels, A. D.; Strain, M. C.; Farkas, O.; Malick, D. K.; Rabuk, A. D.; Raghavachari, K.; Foresman, J. B.; Ortiz, J. V.; Cui, Q.; Baboul, A. G.; Clifford, S.; Cioslowski, J.; Stefanov, B. B.; Liu, G.; Liashenko, A.; Piskorz, P.; Komaromi, I.; Martin, R. L.; Fox, D. J.; Keith, T.; Al-Laham, M. A.; Peng, C. Y.; Nanayakkara, A.; Challacombe, M.; Gill, P. M. W.; Johnson, B.; Chen, W.; Wong, M. W.; Gonzalez, C.; Pople, J. A. Gaussian 09 User's Reference; Gaussian Inc.: Carnegie, PA, USA, 2009.
9. Dewick, P. M. Medicinal Natural Products. A Biosynthetic Approach, 2 nd ed.; John Wiley & Sons, Ltd: London, UK, 2002; p 349.
10. Tsikas, D. J. Chromatogr. B 2007, 851, 51
11. Zhu, H. J. Modern Organic Stereochemistry; Science Presses of China: Beijing, 2009; Chapters 1 and 6.
12. Shou, Q.; Banbury, L. K.; Renshaw, D. E.; Lambley, E. H.; Mon, H.; Macfarlane, G. A.; Griesser, H. J.; Heinrich, M.; Wohlmuth, H. J. Nat. Prod. 2012, 75, 1612