Research and development of N, N'-diarylureas as anti-tumor agents

X Sun, Z Xie, X Lei, S Huang, G Tang… - RSC Medicinal …, 2023 - pubs.rsc.org
Tumor neovascularization provides abundant nutrients for the occurrence and development
of tumors, and is also an important factor in tumor invasion and metastasis, which has …

Novel multi-target angiogenesis inhibitors as potential anticancer agents: Design, synthesis and preliminary activity evaluation

Q Zhang, Z Li, J Zhang, Y Li, X Pan, J Qu, J Zhang - Bioorganic Chemistry, 2024 - Elsevier
Based on the crucial role of histone deacetylase (HDAC) and receptor tyrosine kinase in
angiogenesis, in situ assembly, skeletal transition, molecular hybridization, and …

An overview of imidazole and its analogues as potent anticancer agents

S Abdullah, S Ganguly - Future Medicinal Chemistry, 2023 - Future Science
The quest for novel, physiologically active imidazoles remains an exciting topic of research
among medicinal chemists. The imidazole ring is a five-membered aromatic heterocycle that …

[PDF][PDF] Selecting protein structure/s for docking-based virtual screening: A case study on type II inhibitors of VEGFR-2 kinase

HR Bhojwani, UJ Joshi - Int. J. Pharm. Sci. Res, 2019 - researchgate.net
In this study, 36 crystal structures available with type IV inhibitors of VEGFR-2 kinase in the
RCSB PDB were classified into DFG-in/-out conformation using visual analysis and KLIFS …

Selectivity studies towards the synthesis of novel biaryl ureas by (hetero) nanocatalysis: Size control and support effects

JD Senra, GM Viana, LFB Malta, ABC Simas… - …, 2016 - Wiley Online Library
A series of novel biaryl ureas containing different structural patterns have been prepared in
good yields in the presence of palladium nanoparticles (PdNPs) with narrow particle size …

Part-1: Design, synthesis and biological evaluation of novel bromo-pyrimidine analogs as tyrosine kinase inhibitors

CS Munikrishnappa, SB Puranik, GVS Kumar… - European Journal of …, 2016 - Elsevier
A novel series of 5-bromo-pyrimidine derivatives (5a-l, 6a-h, 9a-m and 10a-d) were
synthesized through multi step reactions starting from 5-bromo-2, 4-dichloro pyrimidine. The …

Search for novel histone deacetylase inhibitors. Part II: design and synthesis of novel isoferulic acid derivatives

W Lu, F Wang, T Zhang, J Dong, H Gao, P Su… - Bioorganic & Medicinal …, 2014 - Elsevier
Previously, we described the discovery of potent ferulic acid-based histone deacetylase
inhibitors (HDACIs) with halogeno-acetanilide as novel surface recognition moiety (SRM). In …

The imperatorin derivative OW1, a new vasoactive compound, inhibits VSMC proliferation and extracellular matrix hyperplasia

N Zhou, Y Zhang, T Wang, J He, H He, L He - Toxicology and applied …, 2015 - Elsevier
Chronic hypertension induces vascular remodeling. The most important factor for
hypertension treatment is reducing the risk of cardiovascular disease. OW1 is a novel …

Inhibitors of angiogenesis in cancer therapy–synthesis and biological activity

M Gensicka, A Glowacka, K Dzierzbicka… - Current Medicinal …, 2015 - ingentaconnect.com
Angiogenesis is the process of formation of new capillaries from preexisting blood vessels.
Angiogenesis is involved in normal physiological processes, and plays an important role in …

Thiazole‐tethered biaryls as fluorescent chemosensors for the selective detection of Fe3+ ions

B Mariammal, A Shylaja, SV Kumar… - Journal of …, 2020 - Wiley Online Library
Amino‐5‐(thiazol‐2‐yl)‐[1, 1′‐biaryl]‐2, 4‐dicarbonitriles have been synthesized
employing a facile one‐pot pseudo four‐component domino strategy. All these thiazole …