about
Antiproliferative and Pro-Apoptotic Effect of Novel Nitro-Substituted Hydroxynaphthanilides on Human Cancer Cell Lines.The Chemical Composition of Achillea wilhelmsii C. Koch and Its Desirable Effects on Hyperglycemia, Inflammatory Mediators and Hypercholesterolemia as Risk Factors for Cardiometabolic Disease.Synthesis and Biological Evaluation of N-Alkoxyphenyl-3-hydroxynaphthalene-2-carboxanilides.Preparation and biological properties of ring-substituted naphthalene-1-carboxanilides.Investigating the spectrum of biological activity of substituted quinoline-2-carboxamides and their isosteres.Flavonoid 4'-O-Methylkuwanon E from Morus alba Induces the Differentiation of THP-1 Human Leukemia CellsAntibacterial and herbicidal activity of ring-substituted 2-hydroxynaphthalene-1-carboxanilides.Proline-Based Carbamates as Cholinesterase Inhibitors.Synthesis and Spectrum of Biological Activities of Novel N-arylcinnamamidesBioactivity of Methoxylated and Methylated 1-Hydroxynaphthalene-2-Carboxanilides: Comparative Molecular Surface AnalysisRing-Substituted 1-Hydroxynaphthalene-2-Carboxanilides Inhibit Proliferation and Trigger Mitochondria-Mediated Apoptosis
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Q37209901-8E476D3D-B928-4B39-A725-AF4D82BCF145Q38782616-41E0F350-001E-476C-B597-0F3B6AB504B7Q38869654-F02A109B-C1FB-4692-AD5D-BCC3C6CA173EQ38974385-8E20BADE-F915-4FF6-A39B-0B2560E8AF79Q39414401-DB79EB8B-5BA7-42BB-AC3F-7C6C31163F49Q42096403-3A6C1240-D8B3-42AD-82D0-45EEB55D9247Q42709982-B3DB68B4-3DC2-47E6-819B-A03B79C729C9Q47600197-DC95B9D4-B2D4-4B84-98CF-47BAD685EB45Q58796788-DCB874E0-473E-4120-AEE8-1719CFB5A9EDQ92703483-CD38228E-26C2-4F0D-BC0C-66ABBA0C309BQ94681287-D5243F11-6E6D-4672-9D9B-5E3EEBA14666
P50
description
investigador
@es
researcher
@en
name
Peter Kollar
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type
label
Peter Kollar
@en
prefLabel
Peter Kollar
@en
P31
P496
0000-0003-2265-1528