β-Lactams as promising anticancer agents: Molecular hybrids, structure activity relationships and potential targets

DJ Fu, YF Zhang, AQ Chang, J Li - European Journal of Medicinal …, 2020 - Elsevier
Abstract β-Lactam, commonly referred as azetidin-2-one, is a multifunctional building block
for synthesizing β-amino ketones, γ-amino alcohols, and other compounds. Besides its well …

Structure-activity relationships of HDAC8 inhibitors: Non-hydroxamates as anticancer agents

SA Amin, N Adhikari, T Jha - Pharmacological Research, 2018 - Elsevier
Histone deacetylase inhibitors (HDACIs) have a paramount importance in the acetylation
process of histone and non-histone proteins that are crucial players in the cellular epigenetic …

Synthesis, biological evaluation, and computational studies of 6-fluoro-3-(piperidin-4-yl)-1, 2-benzisoxazole sulfonamide conjugates

JT Kilbile, Y Tamboli, SA Ansari… - Polycyclic Aromatic …, 2023 - Taylor & Francis
Herein, the synthesis and biological evaluation of 6-fluoro-3-(piperidin-4-yl) benzo [d]
isoxazole sulfonamide hybrids are discussed. All the synthesized molecules were assessed …

Synthesis of quinoline acetohydrazide-hydrazone derivatives evaluated as DNA gyrase inhibitors and potent antimicrobial agents

P Sridhar, M Alagumuthu, S Arumugam, SR Reddy - RSC advances, 2016 - pubs.rsc.org
The (E)-N′-(substituted-benzylidene)-2-(7-fluoro-2-methoxyquinolin-8-yl) acetohydrazide-
hydrazone derivatives reported in this manuscript represent a new series of antibacterial …

Structure-Activity Relationship Studies of β-Lactam-azide Analogues as Orally Active Antitumor Agents Targeting the Tubulin Colchicine Site

DJ Fu, L Fu, YC Liu, JW Wang, YQ Wang, BK Han… - Scientific Reports, 2017 - nature.com
We have synthesized a series of new β-lactam-azide derivatives as orally active anti-tumor
agents by targeting tubulin colchicine binding site and examined their structure activity …

Recent advances in the synthesis of organic chloramines and their insights into health care

GG Victoria, SR Reddy - New Journal of Chemistry, 2021 - pubs.rsc.org
Nitrogen–chlorine compounds and their derivatives are regarded as important heterocyclic
motifs, exhibiting a wide range of synthetic and pharmaceutical applications, such as N …

Synthesis, Biological Evaluation, Molecular Docking, and Acid Dissociation Constant of New Bis‐1, 2, 3‐triazole Compounds

Y Nural, S Ozdemir, MS Yalcin, B Demir… - …, 2021 - Wiley Online Library
In this study, new bis‐1, 2, 3‐triazole derivatives, N, N′‐(1, 3‐phenylene) bis (2‐(4‐R‐1H‐
1, 2, 3‐triazol‐1‐yl) acetamide), were synthesized by copper‐catalyzed azide‐alkyne …

Hybrid Pyrazole‐Tetrazole Derivatives with High α‐Amylase Inhibition Activity: Synthesis, Biological Evaluation and Docking Study

T Harit, M Cherfi, N Elhouda Daoudi, J Isaad… - …, 2022 - Wiley Online Library
The elaboration of some N‐alkylated pyrazole‐tetrazole derivatives is reported. The
structures of the newly ones are verified using NMR and FTIR spectroscopies, mass …

Research advances in the use of histone deacetylase inhibitors for epigenetic targeting of cancer

Y Bai, D Ahmad, T Wang, G Cui… - Current topics in medicinal …, 2019 - ingentaconnect.com
The causes and progression of cancer are controlled by epigenetic processes. The
mechanisms involved in epigenetic regulation of cancer development, gene expression, and …

Recent advances in β-lactam derivatives as potential anticancer agents

X Zhang, Y Jia - Current Topics in Medicinal Chemistry, 2020 - ingentaconnect.com
Cancer, accounts for around 10 million deaths annually, is the second leading cause of
death globally. The continuous emergency of drug-resistant cancers and the low specificity …