18 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Novel 3-Substituted 7-Phenylpyrrolo[3,2-f]quinolin-9(6H)-ones as Single Entities with Multitarget Antiproliferative Activity.
University of Padova
Novel 9'-substituted-noscapines: synthesis with Suzuki cross-coupling, structure elucidation and biological evaluation.
University of Padova
Design, synthesis, and structure-activity relationships of azolylmethylpyrroloquinolines as nonsteroidal aromatase inhibitors.
University of Padova
Quinazoline-based multi-tyrosine kinase inhibitors: synthesis, modeling, antitumor and antiangiogenic properties.
University of Padova
8-Hydroxynaphthalene-1,4-dione derivative as novel compound for glioma treatment.
University of Padova
Hypericins and thioredoxin reductase: Biochemical and docking studies disclose the molecular basis for effective inhibition by naphthodianthrones.
University of Padova
Side chain cyclization based on serine residues: synthesis, structure, and activity of a novel cyclic analogue of the parathyroid hormone fragment 1-11.
University of Padova
Anthracene based compounds as new L-type Ca2+ channel blockers: design, synthesis, and full biological profile.
University of Padova
Aminoacyl-anthraquinone conjugates as telomerase inhibitors: synthesis, biophysical and biological evaluation.
University of Padova
Tri-, tetra- and heptacyclic perylene analogues as new potential antineoplastic agents based on DNA telomerase inhibition.
University of Padova
Scaffold Repurposing of in-House Chemical Library toward the Identification of New Casein Kinase 1 ? Inhibitors.
University of Padova
Third-generation CDK inhibitors: A review on the synthesis and binding modes of Palbociclib, Ribociclib and Abemaciclib.
University of Padova
Evaluating the effects of fluorine on biological properties and metabolic stability of some antitubulin 3-substituted 7-phenyl-pyrroloquinolinones.
University of Padova
Novel polyamine analogues: from substrates towards potential inhibitors of monoamine oxidases.
University of Padova
Targeting RORs nuclear receptors by novel synthetic steroidal inverse agonists for autoimmune disorders.
University of Padova
Tetraiodobenzimidazoles are potent inhibitors of protein kinase CK2.
University of Padova
Biochemical and three-dimensional-structural study of the specific inhibition of protein kinase CK2 by [5-oxo-5,6-dihydroindolo-(1,2-a)quinazolin-7-yl]acetic acid (IQA).
University of Padova