RSC Advances,
Journal Year:
2024,
Volume and Issue:
14(43), P. 31850 - 31860
Published: Jan. 1, 2024
Novel
complexes
of
Cd(
ii
)
and
Ag(
i
derived
from
TPT
ligand
have
been
synthesized.
The
silver
showed
great
potential
as
a
therapeutic
candidate
for
treating
breast
cancer.
Reviews in Inorganic Chemistry,
Journal Year:
2020,
Volume and Issue:
40(4), P. 193 - 232
Published: Aug. 7, 2020
Abstract
In
wake
of
emerging
applications
organotellurium
compounds
in
biological
and
material
science
avenues,
the
current
review
describes
their
key
synthetic
methodologies
while
focusing
synthesis
through
five
ligand-to-metal
linkages
including
carbon;
carbon-oxygen;
carbon-nitrogen;
carbon-metal;
carbon-sulfur
to
tellurium.
all
these
whether
tellurium
links
with
ligands
a
complicated
or
simple
pathways,
it
is
often
governed
electrophilic
substitution
reactions.
The
present
study
encompasses
major
routes
so
as
acquire
comprehensive
understanding
compounds.
JBIC Journal of Biological Inorganic Chemistry,
Journal Year:
2024,
Volume and Issue:
29(5), P. 499 - 509
Published: June 26, 2024
Encephalitozoon
intestinalis
is
an
opportunistic
microsporidian
parasite
that
primarily
infects
immunocompromised
individuals,
such
as
those
with
HIV/AIDS
or
undergoing
organ
transplantation.
Leishmaniasis
responsible
for
parasitic
infections,
particularly
in
developing
countries.
The
disease
has
not
been
effectively
controlled
due
to
the
lack
of
effective
vaccine
and
affordable
treatment
options.
Current
options
E.
infection
leishmaniasis
are
limited
often
associated
adverse
side
effects.
There
no
previous
study
literature
on
antimicrosporidial
activities
Ag(I)-N-heterocyclic
carbene
compounds.
In
this
study,
vitro
previously
synthesized
complexes
were
evaluated
using
spores
cultured
human
renal
epithelial
cell
lines
(HEK-293).
Inhibition
replication
was
determined
by
spore
counting.
addition,
effects
compounds
Leishmania
major
promastigotes
assessed
measuring
metabolic
activity
viability
a
tetrazolium
reaction.
Statistical
analysis
performed
determine
significant
differences
between
treated
control
groups.
Our
results
showed
growth
L.
inhibited
tested
concentration-dependent
manner.
A
decrease
observed
at
highest
concentrations.
These
suggest
have
potential
anti-microsporidial
anti-leishmanial
activity.
Further
research
required
elucidate
underlying
mechanisms
action
evaluate
efficacy
animal
models
clinical
trials.
Macedonian Journal of Chemistry and Chemical Engineering,
Journal Year:
2020,
Volume and Issue:
39(1), P. 1 - 1
Published: May 30, 2020
Two
new
organoselenium
analogs,
(3,3'-(1,2-phenylenebis(methylene))bis(2-selenoxo-2,3-dihydro-1H-imidazole-3,1-diyl))bis(methylene)
dibenzoate
(III)
and
3,3'-(1,2-phenylenebis(methylene))bis(1-benzyl-1H-imidazole-2(3H)-selenone)
(V),
were
derived
from
newly
synthesized
organic
salts
1,1'-(1,2-phenylenebis(methylene))bis(3-(2-phenoxyacetyl)-1H-imidazol-3-ium)
chloride
(II)
1,1'-(1,2-phenylenebis(methylene))bis(3-benzyl-1H-imidazol-3-ium)
(IV),
each
was
characterized
by
various
analytical
techniques,
such
as
Fourier-Transform
Infrared
Spectroscopy
(FT-IR),
UV–visible,
Nuclear
Magnetic
Resonance
(NMR)
spectroscopy,
well
Ultra-high
performance
liquid
chromatography
mass
spectrometry/Photodiode
array
(UHPL-MS/PDA).
All
compounds
tested
for
their
antioxidant
anticancer
potential.
Very
good
radical
scavenging
results
obtained
II
IV,
with
cell
viability
values
of
84.6±3.5
56.7±5.5%,
respectively,
compared
to
adducts.
products
showed
significant
activity
against
MCF-7
breast
cancer
cells,
but
III
better
results,
40.5±2.0%
34.4±1.5%,
respectively.
Journal of Coordination Chemistry,
Journal Year:
2023,
Volume and Issue:
76(7-8), P. 847 - 861
Published: April 18, 2023
The
discovery
of
cisplatin
antitumor
properties
in
1969
encouraged
researchers
to
design
metal-based
anticancer
drugs.
Recently,
research
on
N-heterocyclic
carbene-based
metal
complexes
was
successful
due
their
excellent
potency
and
other
biological
activities,
for
example
antitubercular,
antiviral,
anti-ulcerogenic,
antifungal,
antiglycation
antimalarial,
anti-inflammatory,
antineuropathic,
antihypertensive,
antioxidant,
anti-obesity,
antibacterial,
analgesic
activity.
These
have
even
higher
than
cisplatin.
Herein,
we
summarize
the
activities
carbene
(NHC)
based
Au(I),
Ag(I),
Cu(I).
Further,
mechanism
action
possible
structure-activity
relationships
(SAR)
are
discussed.
We
hope
this
article
will
help
designing
highly
potent
Cu(I)-N-heterocyclic
treatment
various
types
cancer.
Inorganics,
Journal Year:
2024,
Volume and Issue:
12(11), P. 283 - 283
Published: Oct. 30, 2024
A
number
of
N-heterocyclic
carbene–silver
compounds
(NHCs)AgX
were
tested
in
the
direct
carboxylation
terminal
alkynes
using
carbon
dioxide
as
C1
feedstock.
The
reactions
proceed
at
a
pressure
1
atm
CO2
room
temperature,
presence
Cs2CO3,
and
silver–NHC
complexes
catalysts.
Thus,
phenylacetylene
several
are
converted
to
corresponding
propiolic
acids
good
high
conversions.
activity
catalysts
is
strongly
influenced
by
substituents
on
NHC
backbone
nature
counterion.
Specifically,
most
active
compound
exhibits
iodide
counterion
stabilized
benzimidazole
derivative.
After
24
h
reaction,
quantitative
conversion
obtained
utilizing
DMF
solvent
substrate.
Drug Development Research,
Journal Year:
2021,
Volume and Issue:
82(7), P. 907 - 926
Published: May 12, 2021
Abstract
Because
of
the
continuous
need
for
efficient
therapeutic
agents
against
various
kinds
cancers
and
infectious
diseases,
pharmaceutical
industry
has
to
find
new
candidates
strategies
develop
novel
drugs.
They
increasingly
use
computational
tools
in
R&D
stages
screening
extensive
sets
drug
before
starting
pre‐clinical
clinical
trials.
N‐Heterocyclic
carbenes
(NHCs)
can
be
evaluated
as
good
because
they
offer
both
anti‐cancer
anti‐inflammatory
features
with
their
general
low‐toxicity
profiles.
To
date,
different
NHCs
(Cu,
Co,
Ni,
Au,
Ag,
Ru,
etc.)
have
been
synthesized
uses
shown.
Here,
we
reviewed
recent
studies
focused
on
Ag(I)‐NHC
complexes
activities.
Also,
existing
examples
usage
density
functional
theory
structure–activity
relationship
evaluated.