Multi-target anti-inflammatory and cytotoxic activities of flavonoids from Varthemia iphionoides Boiss. & C. I. Blanche
Amal Al‐Aboudi,
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Musa Abu Zarga,
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Wafa Hourani
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et al.
Natural Product Research,
Journal Year:
2025,
Volume and Issue:
unknown, P. 1 - 9
Published: May 2, 2025
Chronic
inflammation
plays
a
central
role
in
the
onset
of
many
diseases,
whereas
long-term
use
anti-inflammatory
drugs
is
often
associated
with
harmful
side
effects.
This
study
examined
and
cytotoxic
effects
seven
flavonoids
isolated
from
Varthemia
iphionoides
Boiss.
&
C.
I.
Blanche:
jaceidin
(1),
kumatakenin
(2),
4'-hydroxy-3,5,6,7-tetramethoxyflavone
(3),
santin
(4),
quercetin-3,3'-dimethyl
ether
(5),
viscosine
(6),
isokaempferide
(7).
Compounds
1,
5
6
showed
potent
inhibition
ROS
(IC50
µM:
1.0,
1.7,
11.4
whole
blood;
7.4,
<0.3,
9.9
PMNs,
respectively).
All
compounds,
except
compound
2,
reduced
NO•
production
(IC50:
9.1-26.9
µM).
3,
selectively
inhibited
COX-1.
Most
compounds
exhibited
low
toxicity
BJ
fibroblasts,
selective
cytotoxicity
against
HeLa
cancer
cells.
These
findings
highlight
multi-targeted
potential
flavonoids,
particularly
5,
as
promising
lead
for
research
inflammation-related
including
cancer.
Language: Английский
Dammarane-Type 3,4-seco-Triterpenoid from Silver Birch (Betula pendula Roth) Buds Induces Melanoma Cell Death by Promotion of Apoptosis and Autophagy
Molecules,
Journal Year:
2024,
Volume and Issue:
29(17), P. 4091 - 4091
Published: Aug. 29, 2024
Despite
unquestionable
advances
in
therapy,
melanoma
is
still
characterized
by
a
high
mortality
rate.
For
years,
expectations
have
been
raised
compounds
of
natural
origin
as
component
pharmacotherapy,
particularly
triterpenes
found
the
bark
birch
trees.
In
this
study,
3,4-
Language: Английский