Indole: A privileged scaffold for the design of anti-cancer agents

Y Wan, Y Li, C Yan, M Yan, Z Tang - European journal of medicinal …, 2019 - Elsevier
In general, heterocyclic compounds are a significant source of pharmacologically active
compounds. Among them, the indole scaffold widely distributes in natural products and …

Indoles as therapeutics of interest in medicinal chemistry: Bird's eye view

N Chadha, O Silakari - European Journal of Medicinal Chemistry, 2017 - Elsevier
Indoles constitute extensively explored heterocyclic ring systems with wide range of
applications in pathophysiological conditions that is, cancer, microbial and viral infections …

Indole in the target-based design of anticancer agents: A versatile scaffold with diverse mechanisms

S Dadashpour, S Emami - European journal of medicinal chemistry, 2018 - Elsevier
The indole scaffold is one of the most widespread heterocycles in the naturally occurring
and synthetic bioactive compounds including anticancer agents. Due to its biodiversity and …

Indole-based derivatives as potential antibacterial activity against methicillin-resistance Staphylococcus aureus (MRSA)

HL Qin, J Liu, WY Fang, L Ravindar… - European journal of …, 2020 - Elsevier
Antibacterial-resistance speaks to an overall alarm, particularly in regards to the flare-up of
methicillin-resistance Staphylococcus aureus (MRSA), a classic reason for genuine skin and …

Recent development in indole derivatives as anticancer agent: A mechanistic approach

N Devi, K Kaur, A Biharee… - Anti-Cancer Agents in …, 2021 - ingentaconnect.com
Background: Cancer accounts for several deaths each year. There are multiple FDA
approved drugs for cancer treatments. Due to the severe side effects and multiple drug …

[HTML][HTML] Indole derivatives as potential anticancer agents: A review

H Sachdeva, J Mathur, A Guleria - Journal of the Chilean Chemical …, 2020 - SciELO Chile
Heterocyclic moiety serve as perfect framework on which pharmacophores can be effectively
attached to produce novel drugs. Among various heterocyclic compounds, nitrogen-based …

Switchable Synthesis of 2-Methylene-3-aminoindolines and 2-Methyl-3-aminoindoles Using Calcium Carbide as a Solid Alkyne Source

Z Wang, Z Zhang, Z Li - Organic Letters, 2022 - ACS Publications
The one-pot three-component method for the switchable synthesis of 2-methylene-3-
aminoindolines and 2-methyl-3-aminoindoles by reactions of N-(2-formylaryl) sulfonamides …

[HTML][HTML] 2-methylindole analogs as cholinesterases and glutathione S-transferase inhibitors: Synthesis, biological evaluation, molecular docking, and pharmacokinetic …

A Cetin, E Bursal, F Türkan - Arabian Journal of Chemistry, 2021 - Elsevier
In this study, we aimed to (i) synthesize new 2-methylindole analogs containing various
amino structures, pyrrolidine, piperidine, morpholine, and substituted phenyl groups through …

Identification of 1, 3, 4-oxadiazoles as tubulin-targeted anticancer agents: a combined field-based 3D-QSAR, pharmacophore model-based virtual screening …

A Das, M Sarangi, K Jangid, V Kumar… - Journal of …, 2023 - Taylor & Francis
Cancer is one of the most prominent causes of death worldwide and tubulin is a crucial
protein of cytoskeleton that maintains essential cellular functions including cell division as …

Organocatalytic asymmetric synthesis of cyclic compounds bearing a trifluoromethylated stereogenic center: recent developments

XH He, YL Ji, C Peng, B Han - Advanced Synthesis & Catalysis, 2019 - Wiley Online Library
The broad prospects of trifluoromethylated compounds in materials science, agricultural
chemistry, and pharmaceutical chemistry have stimulated the rapid development of …