Paper · 2013 · Planta Medica

Antiparasitic and Antimicrobial Constituents from Terminalia brownii

F Machumi; J Zhang; JO Midiwo; et al.

5
claims
10
verbatim quotes
2
citations
2
research areas
—
Not open access

Abstract

Terminalia brownii is an African medicinal plant used to treat parasitic and microbial infections. A new oleanane-type triterenoid was isolated from its stem bark extract by bioassay-guided fractionation using the method of chromatographic separations and was identified as 3,24-O-ethylidenyl-2,19-dihydroxyolean-12-en-28-oic acid (1), along with seven known oleanane-type triterpenoids and seven ellagic acid derivatives. The compounds were evaluated for their antiplasmodial, antileishmanial and antimicrobial activities giving the most potent antiplasmodial activity with IC50 values of 2.76 µg/mL for 23-galloylarjunolic acid (2) against P. falciparum W2 strain and the most potent antimicrobial activity with IC50 values of 0.32 µg/mL for diellagic lactone (3) against C. glabrata.

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Claims 5

Observationobservedoriginal resultpositivemeasured

Claim · model-written summary

A new oleanane-type triterenoid was isolated and identified from stem bark extract.

Taxon
Terminalia browniiTerminalia browniie0
Organ / stage
stem barke1
Outcome
identified as 3,24-O-ethylidenyl-2,19-dihydroxyolean-12-en-28-oic acid (1)e1

Verbatim

e0

“Terminalia brownii”

✓ located verbatim in the source · abstract, characters 0–18 · show in text ↑
e1

“A new oleanane-type triterenoid was isolated from its stem bark extract by bioassay-guided fractionation using the method of chromatographic separations and was identified as 3,24-O-ethylidenyl-2,19-dihydroxyolean-12-en-28-oic acid (1)”

✓ located verbatim in the source · abstract, characters 99–334 · show in text ↑
Observationobservedoriginal resultpositivemeasured

Claim · model-written summary

Seven known oleanane-type triterpenoids were identified with the new constituent.

Taxon
Terminalia browniiTerminalia browniie0
Outcome
seven known oleanane-type triterpenoidse1

Not reportedValue

Verbatim

e0

“Terminalia brownii”

✓ located verbatim in the source · abstract, characters 0–18 · show in text ↑
e1

“along with seven known oleanane-type triterpenoids and seven ellagic acid derivatives”

✓ located verbatim in the source · abstract, characters 336–421 · show in text ↑
Observationobservedoriginal resultpositivemeasured

Claim · model-written summary

Seven ellagic acid derivatives were identified with the new constituent.

Taxon
Terminalia browniiTerminalia browniie0
Outcome
seven ellagic acid derivativese1

Verbatim

e0

“Terminalia brownii”

✓ located verbatim in the source · abstract, characters 0–18 · show in text ↑
e1

“seven ellagic acid derivatives”

✓ located verbatim in the source · abstract, characters 391–421 · show in text ↑
Observationobservedoriginal resultpositivemeasured

Claim · model-written summary

23-galloylarjunolic acid had the most potent antiplasmodial activity against P. falciparum W2, with IC50 of 2.76 µg/mL.

Taxon
Terminalia browniiTerminalia browniie0
Outcome
antiplasmodial activitye1
Direction
most potente1
Value
2.76 µg/mLe1
Qualifier
23-galloylarjunolic acid (2) against P. falciparum W2 straine1

Not reportedMaterial

Verbatim

e0

“Terminalia brownii”

✓ located verbatim in the source · abstract, characters 0–18 · show in text ↑
e1

“most potent antiplasmodial activity with IC50 values of 2.76 µg/mL for 23-galloylarjunolic acid (2) against P. falciparum W2 strain”

✓ located verbatim in the source · abstract, characters 534–665 · show in text ↑
Observationobservedoriginal resultpositivemeasured

Claim · model-written summary

Diellagic lactone had the most potent antimicrobial activity against C. glabrata, with IC50 of 0.32 µg/mL.

Taxon
Terminalia browniiTerminalia browniie0
Outcome
antimicrobial activitye1
Direction
most potente1
Value
0.32 µg/mLe1
Qualifier
diellagic lactone (3) against C. glabratae1

Verbatim

e0

“Terminalia brownii”

✓ located verbatim in the source · abstract, characters 0–18 · show in text ↑
e1

“most potent antimicrobial activity with IC50 values of 0.32 µg/mL for diellagic lactone (3) against C. glabrata”

✓ located verbatim in the source · abstract, characters 674–785 · show in text ↑