Synthesis and Metal-Catalyzed Reactions of gem-Dihalovinyl Systems

G Chelucci - Chemical Reviews, 2012 - ACS Publications
1, 1-Dihalo-1-alkenes are valuable synthetic tools in organic chemistry and serve as
interesting synthetic intermediates in a variety of non-metal-assisted chemical …

Developments of isoCombretastatin A-4 derivatives as highly cytotoxic agents

A Hamze, M Alami, O Provot - European journal of medicinal chemistry, 2020 - Elsevier
Abstract Combretastatin A-4 (CA-4) is a natural anti-cancer agent isolated in 1989 from the
African willow tree, Combretum caffrum. Due to its chemical simplicity, this (Z)-stilbene has …

Design, synthesis and bioevaluation of novel trifluoromethylquinoline derivatives as tubulin polymerization inhibitors

S Zhang, M Mo, M Lv, W Xia, K Liu, G Yu… - Future Medicinal …, 2023 - Taylor & Francis
Aim: A series of novel trifluoromethylquinoline derivatives were designed, synthesized and
evaluated for antitumor activities. Methodology: All compounds were evaluated for …

Ultrasound-promoted two-step synthesis of 3-arylselenylindoles and 3-arylthioindoles as novel combretastatin A-4 analogues

Z Wen, X Li, D Zuo, B Lang, Y Wu, M Jiang, H Ma… - Scientific reports, 2016 - nature.com
Abstract A series of 3-(3′-hydroxy-4′-methoxyphenyl) selenyl-5, 6, 7-trimethoxy-1 H-
indoles and 3-(3′-hydroxy-4′-methoxyphenyl) thio-5, 6, 7-trimethoxy-1 H-indoles were …

Carbohydrate-based peptidomimetics targeting neuropilin-1: Synthesis, molecular docking study and in vitro biological activities

M Richard, A Chateau, C Jelsch, C Didierjean… - Bioorganic & Medicinal …, 2016 - Elsevier
Abstract Neuropilin-1 (NRP-1), a transmembrane glycoprotein acting as a co-receptor of
VEGF-A, is expressed by cancer and angiogenic endothelial cells and is involved in the …

Stereoselective Synthesis of Ribofuranoid exo-Glycals by One-Pot Julia Olefination Using Ribofuranosyl Sulfones

N Oka, A Mori, K Suzuki, K Ando - The Journal of Organic …, 2020 - ACS Publications
One-pot Julia olefination using ribofuranosyl sulfones is described. The α-anomers of the
ribofuranosyl sulfones were synthesized with complete α-selectivity via the glycosylation of …

The trimethoxyphenyl (TMP) functional group: a versatile pharmacophore

MA Langarizadeh, A Ameri, MR Tavakoli… - Medicinal Chemistry …, 2023 - Springer
The Trimethoxyphenyl (TMP) group serves as a pharmacophore in numerous potent agents
exhibiting diverse bioactivity effects. This moiety is prominently present in the molecular …

New ligands of the tubulin colchicine site based on X-ray structures

R Alvarez, M Medarde, R Pelaez - Current topics in medicinal …, 2014 - ingentaconnect.com
Colchicine site ligands have proved to be potent inhibitors of tubulin polymerization, which
leads them not only to display cytotoxic effects but also vascular disrupting effects on tumour …

Synthesis of Unprecedented Sulfonylated Phosphono‐exo‐Glycals Designed as Inhibitors of the Three Mycobacterial Galactofuranose Processing Enzymes

CJM Frédéric, A Tikad, J Fu, W Pan… - … A European Journal, 2016 - Wiley Online Library
This study reports a new methodology to synthesize exo‐glycals bearing both a sulfone and
a phosphonate. This synthetic strategy provides a way to generate exo‐glycals displaying …

Dual-arm nanocapsule targets neuropilin-1 receptor and microtubule: A potential nanomedicine platform

S Barman, G Das, V Gupta, P Mondal… - Molecular …, 2019 - ACS Publications
A multiarm nanomedicine template has been designed following bottom-up approach, which
target neuropilin-1 (Nrp-1) receptor of cancer cells. Through this venture, we discovered that …