The
sesquiterpenoid
compound abelsaginol (
AS
) was
successfully isolated from
Abelmoschus sagittifolius
for the first time. The compound was identified using NMR and MS
data. The antioxidant activity of
AS
was also evaluated
both theoretically and experimentally.
AS
was found to
be a weak HOO
•
radical scavenger in organic solvents
such as pentyl ethanoate and dimethyl sulfoxide (
k
overall
= ∼ 10
2
M
–1
s
–1
), in a good agreement with the results of
the 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid)
assay. However,
AS
exhibited good HOO
•
antiradical activity in water at pH 7.40 (
k
overall
= 9.00 × 10
6
M
–1
s
–1
) through the single-electron transfer mechanism of
the anion state. Further calculations also demonstrated that
AS
could exert good to moderate activity against CH
3
O
•
, CH
3
OO
•
, CCl
3
OO
•
, NO
2
, and SO
4
•–
radicals, with
k
f
values from 4.00 × 10
3
to 1.52 × 10
7
M
–1
s
–1
. However,
AS
exerted much lower activity against HO
•
, CCl
3
O
•
, NO, O
2
•–
, and N
3
•
radicals under the studied
conditions. In general, the activity of
AS
in water at
pH 7.40 is higher than that of Trolox or butylated hydroxytoluene,
which are common reference antioxidants. Thus, in an aqueous physiological
milieu,
AS
is a promising natural antioxidant.