Acylhydrazones and their biological activity: a review

LI Socea, SF Barbuceanu, EM Pahontu, AC Dumitru… - Molecules, 2022 - mdpi.com
Due to the structure of acylhydrazones both by the pharmacophore–CO–NH–N= group and
by the different substituents present in the molecules of compounds of this class, various …

Anticancer agents incorporating the N‐acylhydrazone scaffold: Progress from 2017 to present

AE Kassab - Archiv der Pharmazie, 2023 - Wiley Online Library
The N‐acylhydrazone motif has been shown to be particularly adaptable and promising in
the area of medicinal chemistry and drug development, due to its significant biological and …

Synthesis, admetSAR predictions, DPPH radical scavenging activity, and potent anti-mycobacterial studies of hydrazones of substituted 4-(anilino methyl) …

VJ Desale, SN Mali, BR Thorat… - … Computer-Aided Drug …, 2021 - ingentaconnect.com
Background: For the past several decades, the presence of tuberculosis (TB) is being
remarked as the most common infectious disease leading to mortality. Objective: Hydrazone …

Synthesis, in silico and in vitro analysis of hydrazones as potential antituberculosis agents

BR Thorat, SN Mali, D Rani… - Current Computer-Aided …, 2021 - ingentaconnect.com
Tuberculosis (TB) is a major cause of mortality and illness as reported by the WHO in 2019.
The WHO report also mentioned the fact that about 10.0 million people fell ill with …

Synthesis and biological evaluation of chalcone derivatives containing aminoguanidine or acylhydrazone moieties

ZY Wei, KQ Chi, ZK Yu, HY Liu, LP Sun… - Bioorganic & medicinal …, 2016 - Elsevier
Three novel series of chalcone derivatives containing an aminoguanidine or acylhydrazone
moiety were designed, synthesized and evaluated in terms of their antibacterial, antifungal …

Spectral studies, thermal investigations, and anticancer activity of some divalent metal complexes derived from 2‐(4‐bromophenylamino) acetohydrazide ligand

EM Emara, WA El‐Sayed… - Applied …, 2022 - Wiley Online Library
A series of biologically active metal complexes was yielded from the reactions of 2‐(4‐
bromophenylamino) acetohydrazide ligand (HL) with Co (II), Ni (II), Cu (II), Cd (II) chlorides …

Synthesis, spectroscopic, in-vitro and computational analysis of hydrazones as potential antituberculosis agents:(part-I)

BR Thorat, D Rani, RS Yamgar… - … Chemistry & High …, 2020 - ingentaconnect.com
Background: Since the last few decades, the healthcare sector is facing the problem of the
development of multidrug-resistant (MDR-TB) and extensively drug-resistant tuberculosis …

[HTML][HTML] Synthesis, cytotoxicity and antifungal activity of 5-nitro-thiophene-thiosemicarbazones derivatives

LN de Araújo Neto, MCA de Lima, JF de Oliveira… - Chemico-biological …, 2017 - Elsevier
In the present work, twelve N-substituted 2-(5-nitro-thiophene)-thiosemicarbazones
derivatives (L1-12) were synthesized, characterized and their in vitro cytotoxic and …

Synthesis and anti-mycobacterium study on halo-substituted 2-aryl oxyacetohydrazones

VJ Desale, SN Mali, HK Chaudhari… - … computer-aided drug …, 2020 - ingentaconnect.com
Background: The treatment of multiple-drug-resistant tuberculosis (MDR-TB) with currently
available marketed drugs remains a global health concern. The cases of resistant …

Design, synthesis, and characterization of cinnamic acid derivatives with two novel acrylohydrazones on HeLa and CHO-1 cancer cell lines: the experimental and …

AD Ogunlakin, MA Sonibare, OE Yeye, A Jabeen… - Chemistry Africa, 2024 - Springer
Purpose To investigate the effect of derivatives of cinnamic acid on the proliferation of CHO-
1 and HeLa cell lines. Methods Three Acrylohydrazones (7–9) derived from cinnamic acid …