Bioactive Fused Pyrazoles Inspired by the Adaptability of 5-Aminopyrazole Derivatives: Recent Review
Dana M. Odeh,
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Mohanad Odeh,
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Taghrid S. Hafez
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et al.
Molecules,
Journal Year:
2025,
Volume and Issue:
30(2), P. 366 - 366
Published: Jan. 17, 2025
Heterocyclic
compounds,
especially
those
containing
the
pyrazole
moiety,
are
highly
significant
in
organic
chemistry
and
possess
remarkable
diverse
biological
properties.
The
5-aminopyrazole
derivatives
key
starting
materials
for
synthesis
of
numerous
bioactive
compounds
such
as
pyrazolopyridine,
pyrazolopyrimidine,
pyrazoloquinazoline,
pyrazolotriazine
derivatives.
Many
inspired
by
a
wide
spectrum
activities
medicinal
applications
antioxidants,
anticancer
agents,
enzyme
inhibitors,
antimicrobials,
anti-tuberculosis
activities.
This
review
summarizes
recently
reported
methods
fused
pyrazole-based
based
on
within
last
5
years
(2020
to
present).
One
important
goals
this
is
illustrate
future
strategies
design,
development,
utilization
products
potent
drugs.
Language: Английский
Emerging synthetic Strategies and Pharmacological Insights of 1,3,4-Thiadiazole Derivatives: A Comprehensive Review
Davinder Kumar,
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Navidha Aggarwal,
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Virender Kumar
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et al.
Future Medicinal Chemistry,
Journal Year:
2024,
Volume and Issue:
16(6), P. 563 - 581
Published: Feb. 14, 2024
This
review
meticulously
examines
the
synthesis
techniques
for
1,3,4-thiadiazole
derivatives,
focusing
on
cyclization,
condensation
reactions
and
functional
group
transformations.
It
enhances
understanding
of
these
chemical
methods
that
re
crucial
tailoring
derivative
properties
functionalities.
study
is
considered
to
be
vital
researchers,
detailing
established
effects
such
as
antioxidant,
antimicrobial
anticancer
activities,
revealing
emerging
pharmacological
potentials
neuroprotective,
antiviral
antidiabetic
properties.
also
discusses
molecular
mechanisms
underlying
effects.
In
addition,
this
article
covers
structure–activity
relationship
studies
computational
modelling
are
essential
designing
potent,
selective
compounds.
work
lays
a
foundation
future
research
targeted
therapeutic
development.
Language: Английский
Molecular modeling and antimicrobial activity of newly synthesized benzothiazole-thiazole conjugates
Arwa Alharbi,
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Mansoor Alsahag,
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Ali Alisaac
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et al.
Journal of Photochemistry and Photobiology A Chemistry,
Journal Year:
2024,
Volume and Issue:
456, P. 115852 - 115852
Published: June 22, 2024
Language: Английский
Azole Derivatives: Cutting‐Edge Agents in Cancer Therapy
Anuradha Mehra,
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Amit Mittal,
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Rekha Sangwan
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et al.
ChemistrySelect,
Journal Year:
2024,
Volume and Issue:
9(43)
Published: Nov. 1, 2024
Abstract
Monocyclic
5‐membered
heterocycles
including
imidazoles,
thiazoles,
oxazoles,
and
their
related
compounds
have
gained
significant
attention
in
medicinal
chemistry
because
of
potent
anticancerous
activity.
These
small
heterocyclic
molecules
possess
versatile
properties,
biological
activity,
absorption,
distribution,
metabolism,
excretion,
chemical
diversity
that
give
them
immense
potential
as
anticancer
agents.
It
is
also
a
fact
inherent
characteristic
azoles
to
combine
with
many
through
hydrogen
bond,
stacking,
hydrophobic
interaction
makes
effective
against
almost
all
cancer
types.
In
the
present
paper
author
discusses
way
which
connected
structure
monocyclic
activity
namely
ability
these
intercalate
DNA,
inhibit
some
enzymes
interfere
cellular
signaling
pathways.
Interestingly,
several
azole
derivatives
been
seen
be
preclinical
efficacy
studies
well
clinical
trials
are
considered
overcoming
problem
resistance
side
effects
common
As
synthetic
progresses,
structural
system
has
diversified
development
pharmacology
become
more
specific.
This
helped
enhancing
formation
new
class
improved
selectivity
efficacy.
Furthermore,
comprehensive
review
explains
how
computational
structure‐activity
relationship
(SAR)
approaches
applied
design
future‐generation
compounds.
light
facts,
this
article
designed
broad
overview
current
state
azole‐based
agents
an
attempt
further
assert
its
therapeutic
promise
spur
attempts
at
infusing
said
into
therapeutics
fray.
The
discoveries
made
study
may
allow
radical
different
approaches,
could
lead
targeted
treatment
cancer.
Language: Английский