This study aims to
identify the major phytochemical constituents
in
Aquilaria malaccensis
(Thymelaeaceae) ethanolic
leaf extract (ALEX-M) and elucidate their ability to suppress nitric
oxide (NO) production from a murine macrophage-like cell line (RAW
264.7) stimulated by lipopolysaccharide (LPS) and interferon-γ
(IFN-γ). Dichloromethane (DCM) and ethyl acetate (EtOAc) fractions
of ALEX-M were subjected to column chromatography. Eight known compounds
were isolated for the first time from this species. Compounds were
identified using spectroscopic techniques (IR, UV, HRESIMS, and 1D
and 2D NMR). Anti-inflammatory activity of both extract and isolated
compounds were investigated in vitro. The fractions offered the isolation
of epifriedelanol (
1
), 5-hydroxy-7,4′-dimethoxyflavone
(
2
), luteolin-7,3′,4′-trimethyl ether (
3
), luteolin-7,4′-dimethyl ether (
4
),
acacetin (
5
), aquilarinenside E (
6
), iriflophenone-2-
O
-α-
l
-rhamnopyranoside (
7
),
and iriflophenone-3-
C
-β-glucoside (
8
). The findings suggest the pharmacological potential of the crude
extract (ALEX-M) and its isolates as natural anti-inflammatory agents,
capable of suppressing NO production in RAW 264.7 cells stimulated
by LPS/IFN-γ.