Qingyao Shou
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Qingyao Shou has a total of 16 co-authors. Here are the top co-authors by number of shared publications:
- Hans Joerg Griesser
Future Industries Institute University of South Australia Mawson Lakes South Australia Australia
2 shared publications - Alan T. Maccarone
School of Chemistry, University of Wollongong, Wollongong, NSW 2522, Australia
1 shared publication - Ashley Dowell
Southern Cross Plant Science, Southern Cross University, Lismore, NSW 2480, Australia
1 shared publication Dane E. Renshaw
Southern Cross Plant Science, Southern Cross University, PO Box 157, Lismore NSW 2480, Australia
1 shared publication- Dane E. Renshaw
Southern Cross Plant Science, Southern Cross University, PO Box 157, Lismore, NSW 2480, Australia
1 shared publication Hans Wohlmuth
Southern Cross Plant Science, Southern Cross University, PO Box 157, Lismore NSW 2480, Australia
1 shared publication
Latest Publications
- 1 March 2014
- Published by Elsevier in Fitoterapia
- Vol. 93, 62-66
Antibacterial anthranilic acid derivatives from Geijera parviflora
- 1 March 2014
- Published by Elsevier in Fitoterapia
- Vol. 93, 62-66
Antibacterial anthranilic acid derivatives from Geijera parviflora
- 12 July 2013
- Published by American Chemical Society (ACS) in Journal of Natural Products
- Vol. 76 (7) , 1384-1387
Parvifloranines A and B, Two 11-Carbon Alkaloids from Geijera parviflora
Two novel alkaloids (parvifloranines A and B), possessing an unusual 11-carbon skeleton linked with amino acids, were isolated from Geijera parviflora, an endemic Australian Rutaceae. Their structures were elucidated by extensive spectroscopic measurements including 2D NMR analyses. Parvifloranine A was found to be a mixture of two enantiomers, (S)-1 and (R)-1, in a ratio of 1:4, based on their separation using a chiral column. Parvifloranine B is also believed to be a mixture of enantiomers. Proposed biosynthetic pathways are discussed. Parvifloranine A inhibited the synthesis of nitric oxide in LPS-stimulated RAW 264.7 macrophages with an IC50 value of 23.4 μM.
- 12 July 2013
- Published by American Chemical Society (ACS) in Journal of Natural Products
- Vol. 76 (7) , 1384-1387
Parvifloranines A and B, Two 11-Carbon Alkaloids from Geijera parviflora
Two novel alkaloids (parvifloranines A and B), possessing an unusual 11-carbon skeleton linked with amino acids, were isolated from Geijera parviflora, an endemic Australian Rutaceae. Their structures were elucidated by extensive spectroscopic measurements including 2D NMR analyses. Parvifloranine A was found to be a mixture of two enantiomers, (S)-1 and (R)-1, in a ratio of 1:4, based on their separation using a chiral column. Parvifloranine B is also believed to be a mixture of enantiomers. Proposed biosynthetic pathways are discussed. Parvifloranine A inhibited the synthesis of nitric oxide in LPS-stimulated RAW 264.7 macrophages with an IC50 value of 23.4 μM.