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Manniosides G-J, New Ursane- and Lupane-Type Saponins from Schefflera mannii (Hook.f.) Harms
by
Tsopmene, Ulrich Joël
, Poka, Madan
, Ponou, Beaudelaire Kemvoufo
, Dzoyem, Jean Paul
, Antunes, Edith M.
, Siwe-Noundou, Xavier
, Demana, Patrick H.
, Tchegnitegni, Billy Toussie
, Teponno, Rémy Bertrand
, Tapondjou, Léon Azefack
, Beukes, Denzil R.
, Tonga, Simionne Lapoupée Kuitcha
in
Acids
/ Anti-Bacterial Agents - chemistry
/ Anti-Bacterial Agents - isolation & purification
/ Anti-Bacterial Agents - pharmacology
/ antibacterial activity
/ Antifungal agents
/ Antioxidants
/ Araliaceae
/ Araliaceae - chemistry
/ Carbon
/ Metabolites
/ Microbial Sensitivity Tests
/ Molecular Structure
/ Pentacyclic Triterpenes - chemistry
/ Pentacyclic Triterpenes - isolation & purification
/ Pentacyclic Triterpenes - pharmacology
/ Plant Extracts - chemistry
/ Plant Extracts - pharmacology
/ Plant Leaves - chemistry
/ Saponins
/ Saponins - chemistry
/ Saponins - isolation & purification
/ Saponins - pharmacology
/ Schefflera mannii
/ Staphylococcus aureus - drug effects
/ structure elucidation
/ Triterpenes - chemistry
/ Triterpenes - isolation & purification
/ Triterpenes - pharmacology
/ triterpenoid saponins
2024
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Manniosides G-J, New Ursane- and Lupane-Type Saponins from Schefflera mannii (Hook.f.) Harms
by
Tsopmene, Ulrich Joël
, Poka, Madan
, Ponou, Beaudelaire Kemvoufo
, Dzoyem, Jean Paul
, Antunes, Edith M.
, Siwe-Noundou, Xavier
, Demana, Patrick H.
, Tchegnitegni, Billy Toussie
, Teponno, Rémy Bertrand
, Tapondjou, Léon Azefack
, Beukes, Denzil R.
, Tonga, Simionne Lapoupée Kuitcha
in
Acids
/ Anti-Bacterial Agents - chemistry
/ Anti-Bacterial Agents - isolation & purification
/ Anti-Bacterial Agents - pharmacology
/ antibacterial activity
/ Antifungal agents
/ Antioxidants
/ Araliaceae
/ Araliaceae - chemistry
/ Carbon
/ Metabolites
/ Microbial Sensitivity Tests
/ Molecular Structure
/ Pentacyclic Triterpenes - chemistry
/ Pentacyclic Triterpenes - isolation & purification
/ Pentacyclic Triterpenes - pharmacology
/ Plant Extracts - chemistry
/ Plant Extracts - pharmacology
/ Plant Leaves - chemistry
/ Saponins
/ Saponins - chemistry
/ Saponins - isolation & purification
/ Saponins - pharmacology
/ Schefflera mannii
/ Staphylococcus aureus - drug effects
/ structure elucidation
/ Triterpenes - chemistry
/ Triterpenes - isolation & purification
/ Triterpenes - pharmacology
/ triterpenoid saponins
2024
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Manniosides G-J, New Ursane- and Lupane-Type Saponins from Schefflera mannii (Hook.f.) Harms
by
Tsopmene, Ulrich Joël
, Poka, Madan
, Ponou, Beaudelaire Kemvoufo
, Dzoyem, Jean Paul
, Antunes, Edith M.
, Siwe-Noundou, Xavier
, Demana, Patrick H.
, Tchegnitegni, Billy Toussie
, Teponno, Rémy Bertrand
, Tapondjou, Léon Azefack
, Beukes, Denzil R.
, Tonga, Simionne Lapoupée Kuitcha
in
Acids
/ Anti-Bacterial Agents - chemistry
/ Anti-Bacterial Agents - isolation & purification
/ Anti-Bacterial Agents - pharmacology
/ antibacterial activity
/ Antifungal agents
/ Antioxidants
/ Araliaceae
/ Araliaceae - chemistry
/ Carbon
/ Metabolites
/ Microbial Sensitivity Tests
/ Molecular Structure
/ Pentacyclic Triterpenes - chemistry
/ Pentacyclic Triterpenes - isolation & purification
/ Pentacyclic Triterpenes - pharmacology
/ Plant Extracts - chemistry
/ Plant Extracts - pharmacology
/ Plant Leaves - chemistry
/ Saponins
/ Saponins - chemistry
/ Saponins - isolation & purification
/ Saponins - pharmacology
/ Schefflera mannii
/ Staphylococcus aureus - drug effects
/ structure elucidation
/ Triterpenes - chemistry
/ Triterpenes - isolation & purification
/ Triterpenes - pharmacology
/ triterpenoid saponins
2024
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Manniosides G-J, New Ursane- and Lupane-Type Saponins from Schefflera mannii (Hook.f.) Harms
Journal Article
Manniosides G-J, New Ursane- and Lupane-Type Saponins from Schefflera mannii (Hook.f.) Harms
2024
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Overview
Four previously unreported triterpenoid saponins named 3β-hydroxy-23-oxours-12-en-28-oic acid 28-O-β-D-glucopyranosyl ester (mannioside G) (1), 23-O-acetyl-3β-hydroxyurs-12-en-28-oic acid 28-O-β-D-glucopyranosyl ester (mannioside H) (2), ursolic acid 28-O-[α-L-rhamnopyranosyl-(1→4)-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl] ester (mannioside I) (3), and 3β-hydroxy-23-oxolup-20(29)-en-28-oic acid 28-O-β-D-glucopyranosyl ester (mannioside J) (4) were isolated as minor constituents from the EtOAc soluble fraction of the MeOH extract of the leaves of Schefflera mannii along with the known compounds 23-hydroxyursolic acid 28-O-β-D-glucopyranosyl ester (5), ursolic acid 28-O-β-D-glucopyranosyl ester (6), pulsatimmoside B (7) betulinic acid 28-O-[α-L-rhamnopyranosyl-(1→4)-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl] ester (8), 23-hydroxy-3-oxo-urs-12-en-28-oic acid (9), hederagenin (10), ursolic acid (11), betulinic acid (12), and lupeol (13). Their structures were elucidated by a combination of 1D and 2D NMR analysis and mass spectrometry. The MeOH extract, the EtOAc and n-BuOH fractions, and some of the isolated compounds were evaluated for their antibacterial activity against four bacteria: Staphylococcus aureus ATCC1026, Staphylococcus epidermidis ATCC 35984, Escherichia coli ATCC10536, and Klepsiella pnemoniae ATCC13882. They were also screened for their antioxidant properties, but no significant results were obtained.
Publisher
MDPI AG
Subject
/ Anti-Bacterial Agents - chemistry
/ Anti-Bacterial Agents - isolation & purification
/ Anti-Bacterial Agents - pharmacology
/ Carbon
/ Pentacyclic Triterpenes - chemistry
/ Pentacyclic Triterpenes - isolation & purification
/ Pentacyclic Triterpenes - pharmacology
/ Plant Extracts - pharmacology
/ Saponins
/ Saponins - isolation & purification
/ Staphylococcus aureus - drug effects
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