Structure-Activity Relationships and Molecular Docking of Novel Dihydropyrimidine-Based Mitotic Eg5 Inhibitors-Reference-Cited by-同舟云学术

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Structure-Activity Relationships and Molecular Docking of Novel Dihydropyrimidine-Based Mitotic Eg5 Inhibitors

Published:2010-08-24 Issue:10 Volume:5 Page:1760-1769
ISSN:1860-7179
Container-title:ChemMedChem
language:en
Short-container-title:ChemMedChem

Author:

Prokopcová Hana,Dallinger Doris,Uray Georg,Kaan Hung Yi Kristal,Ulaganathan Venkatasubramanian,Kozielski Frank,Laggner Christian,Kappe C. Oliver

Publisher

Wiley

Subject

Organic Chemistry,General Pharmacology, Toxicology and Pharmaceutics,Molecular Medicine,Drug Discovery,Biochemistry,Pharmacology

Reference48 articles.

1. Targeted anti-mitotic therapies: can we improve on tubulin agents?

2. Kinesin motor proteins as targets for cancer therapy

3. UA62784, a novel inhibitor of centromere protein E kinesin-like protein

4. Mammalian mitotic centromere-associated kinesin (MCAK)

5. BTB-1, ein niedermolekularer Inhibitor des mitotischen Motorproteins Kif18A

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3. Precision in stereochemistry: the integral role of catalytic asymmetric Biginelli reaction in crafting enantiomerically pure dihydropyrimidinones;Molecular Diversity;2024-03-27

4. Synthesis, evaluation of the cytotoxicity, apoptosis induction in AGS cell line and gene expression and molecular modeling studies of novel tetrahydropyrimidine derivatives;Arabian Journal of Chemistry;2024-01

5. Sulfo-Biginelli reaction: an insight into interaction between sulfamides and enolizable ketones;Chemistry of Heterocyclic Compounds;2023-07

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