Recent advances on anticancer activity of benzodiazine heterocycles through kinase inhibition
RSC Advances,
Journal Year:
2025,
Volume and Issue:
15(7), P. 5597 - 5638
Published: Jan. 1, 2025
This
is
an
updated
review
for
the
anticancer
activity
of
benzodiazine
heterocyclic
derivatives
through
kinase
inhibition.
Language: Английский
In silico exploration of Aloe Vera leaf compounds as dual AChE and BChE inhibitors for Alzheimer’s disease therapy
Meriem Khedraoui,
No information about this author
Fatima Zahra Guerguer,
No information about this author
El Mehdi Karim
No information about this author
et al.
Current Pharmaceutical Analysis,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 1, 2025
Language: Английский
Rationale, in silico docking, ADMET profile, design, synthesis and cytotoxicity evaluations of phthalazine derivatives as VEGFR-2 inhibitors and apoptosis inducers
Hatem Hussein Bayoumi,
No information about this author
Mohamed‐Kamal Ibrahim,
No information about this author
Mohammed A. Dahab
No information about this author
et al.
RSC Advances,
Journal Year:
2024,
Volume and Issue:
14(37), P. 27110 - 27121
Published: Jan. 1, 2024
New
phthalazine
derivatives
as
vascular
endothelial
growth
factor
receptor-2
(VEGFR-2)
inhibitors
were
synthesized
joined
to
different
spacers
including
pyrazole,
α,β-unsaturated
ketonic
fragment,
pyrimidinone
and/or
pyrimidinthione.
Language: Английский
Phthalazine Derivatives as VEGFR‐2 Inhibitors: Docking, ADMET, Synthesis, Design, Anticancer Evaluations, and Apoptosis Inducers
Hatem Hussein Bayoumi,
No information about this author
Mohamed‐Kamal Ibrahim,
No information about this author
Mohammed A. Dahab
No information about this author
et al.
Drug Development Research,
Journal Year:
2024,
Volume and Issue:
86(1)
Published: Dec. 24, 2024
New
phthalazine-derived
inhibitors
for
VEGFR-2
were
synthesized
anticancer
evaluations.
Also,
docking
studies
performed
to
explore
the
suggested
binding
orientations
of
novel
derivatives
inside
site
VEGFR-2.
The
achieved
biological
data
extremely
interrelated
that
study.
In
specific,
derivative
3f
was
greatest
effective
compound
against
HepG2
and
MCF-7
cancer
cell
lines
with
IC
Language: Английский