about
Dinuclear Pt(II)-bisphosphonate complexes: a scaffold for multinuclear or different oxidation state platinum drugs.Ru(III)-based compounds with sulfur donor ligands: synthesis, characterization, electrochemical behaviour and anticancer activity.Chemical and biological profiles of novel copper(II) complexes containing S-donor ligands for the treatment of cancer.Structural characterization, solution studies, and DFT calculations on a series of binuclear gold(III) oxo complexes: relationships to biological properties.A complete family of isostructural cluster compounds with cubane-like M(3)S(4)M' cores (M = Mo, W; M' = Ni, Pd, Pt): comparative crystallography and electrochemistry.Study of ruthenium(II) complexes with anticancer drugs as ligands. Design of metal-based phototherapeutic agents.3,3-Diethyl-and 3,3-dibenzyl-1,2-diferrocenylcyclopropenes.Synthesis, structural characterization, solution chemistry, and preliminary biological studies of the ruthenium(III) complexes [TzH][trans-RuCl4(Tz)2] and [TzH][trans-RuCl4(DMSO)(Tz)].(DMSO), the thiazole analogues of antitumor ICR and NAMI-A.Activity of Rat Cytosolic Thioredoxin Reductase Is Strongly Decreased bytrans-[Bis(2-amino-5- methylthiazole)tetrachlororuthenate(III)]: First Report of Relevant Thioredoxin Reductase Inhibition for a Ruthenium CompoundNew Copper(II)/Cyclic Tetrapeptide System That Easily Oxidizes to Copper(III) under Atmospheric OxygenHomoleptic, mononuclear transition metal complexes of 1,2-dioxolenes: Updating their electrochemical-to-structural (X-ray) propertiesSupramolecular aggregates of complex cations via unusual purine-purine base pairing in a new organorhodium(III) compound containing the antileukemic drug purine-6-thione. Synthesis, X-ray structure of trans(C,N7),trans(S,S),trans(P,N7)-[Rh(C6H5)(H1,Antioxidant Effect of the Castanea sativa Mill. Leaf Extract on Oxidative Stress Induced upon Human Spermatozoa
P50
Q39316883-AC893F61-C325-4531-B232-1A6F382C575EQ39893530-D02E5C2A-0F20-4B68-AFCB-0A8D114D46CEQ39969230-A7A93D38-2CA4-4960-966C-9AF0075A481EQ40006619-4C17AB79-8C14-46C0-BB7D-67C984CC9B8AQ44316375-9AD2E0B3-16BA-4A4F-8DFF-2813FD796EFAQ44665205-693A94A3-664F-48DB-9856-F26EFF824B3AQ44731446-C6DC98F4-FBCE-4115-9E43-27C9FF7B9608Q44944131-7E26F80F-F5CC-4E61-B71C-83879F335DCEQ58856085-B934BE75-0220-4EC0-8D26-C357A45315C6Q58856091-4BC783F2-9306-46DC-9180-3065B5AA5923Q60018892-BFC72AC5-2689-4FEE-A03A-6219C7FF3014Q73381769-75830C2C-9B06-4FD5-9F5D-AC6375461B07Q92619549-E3D352E0-7378-47FA-A9E2-CBA39C9206D2
P50
description
researcher ORCID ID = 0000-0002-5920-5436
@en
wetenschapper
@nl
name
Maddalena Corsini
@ast
Maddalena Corsini
@en
Maddalena Corsini
@es
Maddalena Corsini
@nl
type
label
Maddalena Corsini
@ast
Maddalena Corsini
@en
Maddalena Corsini
@es
Maddalena Corsini
@nl
prefLabel
Maddalena Corsini
@ast
Maddalena Corsini
@en
Maddalena Corsini
@es
Maddalena Corsini
@nl
P106
P1153
7004559920
P21
P31
P496
0000-0002-5920-5436