2016
DOI: 10.1016/j.bmc.2016.04.020
|View full text |Cite|
|
Sign up to set email alerts
|

Antiplasmodial phloroglucinol derivatives from Syncarpia glomulifera

Abstract: Bioassay guided fractionation of a MeOH extract of the stem bark of Syncarpia glomulifera (Myrtaceae) led to the isolation of the two new phloroglucinol derivatives (±)-rhodomyrtosone F (1) and (±)-calliviminone C (2), the three known triterpenes, betulinic acid (3), ursolic acid-3-acetate (4), and ursolic acid (5), and 1-(2,4,6-trihydroxyphenyl)-1-hexanone (6). Compound 1 exhibited strong antiplasmodial activity, while compounds 2 – 4 were moderately active and 5 and 6 were inactive in this assay. The structu… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

0
5
1

Year Published

2016
2016
2024
2024

Publication Types

Select...
7
2

Relationship

0
9

Authors

Journals

citations
Cited by 13 publications
(8 citation statements)
references
References 23 publications
0
5
1
Order By: Relevance
“…The combinations of 35 µg/mL luteolin-5- O -β-d-glucoside and 5 µg/mL verbenoside, and 25 µg/mL luteolin-5- O -β-d-glucoside and 10 μg/mL verbenoside had the strongest antagonistic effects. 30 The antiedematogenic 31 and antiplasmodial 32 activities of betulinic acid, and the antioxidant activity of quercetin 3- O -rhamnoside 33, 34 have been reported in medical herbs, but showed no significant effect in the present study.…”
Section: Discussioncontrasting
confidence: 51%
“…The combinations of 35 µg/mL luteolin-5- O -β-d-glucoside and 5 µg/mL verbenoside, and 25 µg/mL luteolin-5- O -β-d-glucoside and 10 μg/mL verbenoside had the strongest antagonistic effects. 30 The antiedematogenic 31 and antiplasmodial 32 activities of betulinic acid, and the antioxidant activity of quercetin 3- O -rhamnoside 33, 34 have been reported in medical herbs, but showed no significant effect in the present study.…”
Section: Discussioncontrasting
confidence: 51%
“…A new phloroglucinol β-triketone rhodomyrtosone F ( 380 ) (Fig. 51) from Syncarpia glomulifera (Myrtaceae) stem bark extract, displayed sub-micromolar inhibition of Dd2 P. falciparum and only inhibited HEK293 cells by 58% at 50 µM, suggesting selective toxicity to parasites [235]. Likewise, rhodomyrtone ( 381 ), from the flower extract of Angophora woodsiana (Myrtaceae), was active against 3D7 and Dd2 parasites but moderately cytotoxic [236].…”
Section: Polyphenolsmentioning
confidence: 99%
“…It is interesting to note that a number of phloroglucinol derivatives reportedly possess antiparasitic activity. (±)-Rhodomyrtosone F from Syncarpia glomulifera (Myrtaceae), mallatojaponin C from Mallotus oppositifolius (Euphorbiaceae), and tomentosone A from Rhodomyrtus tomentosa (Myrtaceae) are examples of antiplasmodial phloroglucinol derivatives, while antileishmanial activity has been described for lindbergins E and F from Elaphoglossum lindbergii (Dryopteridaceae), and spiranthenones A and B from Spiranthera odoratissima (Rutaceae) …”
Section: Resultsmentioning
confidence: 99%