Design, synthesis and pharmacophoric model building of new 3‐alkoxymethyl/3‐phenyl indole‐2‐carboxamides with potential antiproliferative activity

MH Abdelrahman, AS Aboraia… - Chemical biology & …, 2017 - Wiley Online Library
Novel 3‐alkoxymethyl/3‐phenyl indole‐2‐carboxamide derivatives were synthesized and
evaluated for their anticancer activity. Most of the tested compounds showed moderate to …

Design, synthesis and antiproliferative activity of a novel class of indole-2-carboxylate derivatives

X Ji, S Xue, Y Zhan, J Shen, L Wu, J Jin… - European Journal of …, 2014 - Elsevier
Based on the chemical structure of Pyrroloquinoline quinone (PQQ), a novel class of indole-
2-carboxylate derivatives was designed, synthesized and assayed for antiproliferative …

Synthesis, structure–activity relationship studies and biological evaluation of novel 2, 5‐disubstituted indole derivatives as anticancer agents

H Hu, J Wu, M Ao, H Wang, T Zhou… - Chemical Biology & …, 2016 - Wiley Online Library
Three novel series of 2, 5‐disubstituted indole derivatives were synthesized and evaluated
in vitro for their antiproliferative activity against human cancer cells and HIV‐1 inhibition …

Design, synthesis, molecular docking and biological activity evaluation of some novel indole derivatives as potent anticancer active agents and apoptosis inducers

AMS El-Sharief, YA Ammar, A Belal… - Bioorganic …, 2019 - Elsevier
Abstract Reaction of 5-morphilinosulfonylisatin (1) with acetophenones (2a–e) afforded 3-
hydroxy-3-substituted-2-oxoindoles 3a-e, when treated with acetic acid the expected 3 …

Molecular targets, anti-cancer properties and potency of synthetic indole-3-carbinol derivatives

MN Karimabad, M Mahmoodi… - Mini reviews in …, 2019 - ingentaconnect.com
The indole-3-carbinol (I3C) displays anti-cancer/proliferative activities against human cancer
cells. Cellular proliferation is an event associated with the progress and its continuation. This …

Synthesis of 1-(2, 6-dichlorophenyl)-3-methylene-1, 3-dihydro-indol-2-one derivatives and in vitro anticancer evaluation against SW620 colon cancer cell line

V Virsodia, A Manvar, K Upadhyay, R Loriya… - European journal of …, 2009 - Elsevier
A small library of 2-indolinone derivatives with the 2, 6-dichlorophenyl ring at the N1 position
and with varying substitutions including aryl groups at the 3-position were synthesized, and …

Synthesis and cytotoxicity of 1, 6, 8, 9-substituted α-carboline derivatives

JY Tsai, YC Lin, MH Hsu, SC Kuo, LJ Huang - The Kaohsiung Journal of …, 2010 - Elsevier
α-Carboline (pyrido [2, 3-b] indole) was selected as the basic scaffold for development of
antileukemic agents by structural modification. From the structure-activity study, it was found …

[HTML][HTML] Synthesis, biological evaluation and modeling studies of new pyrido [3, 4-b] indole derivatives as broad-spectrum potent anticancer agents

SA Patil, JK Addo, H Deokar, S Sun… - Drug designing: open …, 2017 - ncbi.nlm.nih.gov
Objective There is an urgent need drugs against particularly difficult to treat solid tumors
such as pancreatic, triple negative breast, lung, colon, metastatic prostate cancers and …

Design, synthesis, and biological evaluation of novel 1-oxo-1, 2, 3, 4-tetrahydropyrazino [1, 2-a] indole-3-carboxamide analogs in MCF-7 and MDA-MB-468 breast …

YJ Kim, JS Pyo, YS Jung, JH Kwak - Bioorganic & Medicinal Chemistry …, 2017 - Elsevier
A series of novel 1-oxo-1, 2, 3, 4-tetrahydropyrazino [1, 2-a] indole-3-carboxamide analogs
were designed and synthesized for developing pyrazinoindolone scaffolds as anti-breast …

Novel indole derivatives as potential anticancer agents: Design, synthesis and biological screening

B Prakash, A Amuthavalli, D Edison… - Medicinal Chemistry …, 2018 - Springer
To prepare the anticancer indoles, a series of substituted heteroannulated indole derivatives
has been synthesized and characterized by spectral and elemental analysis. Subsequently …