siaresinolic acid
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2018 ◽  
Vol 13 (11) ◽  
pp. 1934578X1801301
Author(s):  
Suphitcha Limjiasahapong ◽  
Patoomratana Tuchinda ◽  
Vichai Reutrakul ◽  
Manat Pohmakotr ◽  
Radeekorn Akkarawongsapat ◽  
...  

The first phytochemical investigation of the leaves and twigs of Santisukia pagetii (Bignoniaceae) using a bioassay-guided fractionation led to the isolation and identification of seventeen known compounds, including four triterpenoids, 3- O-acetylpomolic acid (1), ursolic acid (2), 3- O-acetylursolic acid (3) and siaresinolic acid (4), three iridoid glycosides, specioside (5), verminoside (6) and ambiguuside (7), three flavonoid glycosides, luteolin-7- O-neohesperidoside (8), apigenin-7- O-neohesperidoside (9) and isoquercitrin (10), two phenolic compounds, p-coumaric acid (11) and caffeic acid (12), one monoterpenoid, ( 6S)-menthiafolic acid (13), together with α-D-glucose (14), β-D-maltose (15), β-sitosterol 3- O-β-D-glucopyranoside (16), a mixture of β-sitosterol (17A) and stigmasterol (17B). Compounds 1–13 were isolated from Santisukia genus for the first time. In addition, compounds 1–7, 9 and 10 were found to be active against HIV-1 in anti-syncytium assay, while only compounds 1 and 3 were found to be active (84.4% and 87.2% inhibition at 200 μg/mL, with IC50 values of 290.96 and 210.34 μM, respectively) against HIV-1 reverse transcriptase. Moreover, anti-HIV-1 activities of compounds 1, 3–8, and 13 were reported for the first time.


2015 ◽  
Vol 69 (2) ◽  
pp. 232-240 ◽  
Author(s):  
Anderson Marques de Oliveira ◽  
Almair Ferreira de Araújo ◽  
Rosangela P. Lyra Lemos ◽  
Lucia M. Conserva ◽  
Jamylle Nunes de Souza Ferro ◽  
...  

2011 ◽  
Vol 89 (10) ◽  
pp. 1277-1282 ◽  
Author(s):  
Guang-Chun Gao ◽  
Zhong-Xian Lu ◽  
Shu-Hong Tao ◽  
Si Zhang ◽  
Fa-Zuo Wang ◽  
...  

Four new triterpenoid saponins, Catunaroside E (1; 3-O-{β-D-glucopyranosyl-(1→2)-[β-D-glucopyranosyl-(1→3)]-β-D-glucopyranosyl}-siaresinolic acid), Catunaroside F (2; 3-O-{α-L-rhamnopyranosyl-(1→2)-[β-D-glucopyranosyl-(1→3)]-β-D-glucopyranosyl}-28-O-(β-D-glucopyranosyl)-oleanolic acid), Catunaroside G (3; 3-O-[α-L-rhamnopyranosyl-(1→2)-β-D-glucopyranosyl]- 28-O-(β-D-glucopyranosyl)-siaresinolic acid), and Catunaroside H (4; 3-O-{β-D-glucopyranosyl-(1→2)-[β-D-glucopyranosyl-(1→3)]-β-D-glucopyranosyl}-28-O-(β-D-glucopyranosyl)-siaresinolic acid), and the known triterpenoid saponin Mussaendoside J (5), were isolated from the stem bark of Catunaregam spinosa . Their structures were elucidated on the basis of their spectral data and chemical evidence.


Author(s):  
D. H. R. Barton ◽  
N. J. Holness ◽  
K. H. Overton ◽  
W. J. Rosenfelder

Author(s):  
Philip Bilham ◽  
George A. R. Kon ◽  
Walter C. J. Ross
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