MICALE, Nicola
 Distribuzione geografica
Continente #
EU - Europa 165
NA - Nord America 25
AS - Asia 15
Totale 205
Nazione #
IT - Italia 97
IE - Irlanda 36
US - Stati Uniti d'America 25
FR - Francia 17
VN - Vietnam 10
PL - Polonia 8
RU - Federazione Russa 3
IQ - Iraq 2
PK - Pakistan 2
AZ - Azerbaigian 1
DE - Germania 1
DK - Danimarca 1
GB - Regno Unito 1
NL - Olanda 1
Totale 205
Città #
Messina 53
Dublin 36
Dong Ket 10
Warsaw 8
Ashburn 7
Catania 6
Troina 6
Floridia 5
Francofonte 5
Moscow 3
Redmond 3
Reggio Calabria 3
Richmond 3
Borghetto Santo Spirito 2
Augusta 1
Copenhagen 1
Council Bluffs 1
Fiorenzuola D'arda 1
Fleming Island 1
Houston 1
Mountain View 1
Nakhchivan 1
Nashville 1
Nuremberg 1
Oxford 1
Piazza Armerina 1
San Diego 1
Sargodha 1
Varese 1
Totale 165
Nome #
Hydroxamic Acid-Based Histone Deacetylase (HDAC) Inhibitors Bearing a Pyrazole Scaffold and a Cinnamoyl Linker, file de3e52b1-d64c-762d-e053-3705fe0a30e0 20
Antimicrobial peptide capsids of de novo design, file de3e52b1-378d-762d-e053-3705fe0a30e0 19
A hyaluronic acid–pentamidine bioconjugate as a macrophage mediated drug targeting delivery system for the treatment of leishmaniasis, file de3e52b4-4742-762d-e053-3705fe0a30e0 19
Synthesis of C3/C1-Substituted Tetrahydroisoquinolines, file de3e52af-4599-762d-e053-3705fe0a30e0 17
Hydrogels for the Delivery of Plant-Derived (Poly)Phenols, file de3e52b3-2c31-762d-e053-3705fe0a30e0 14
Antiproliferative properties of a few auranofin-related gold(I) and silver(I) complexes in leukemia cells and their interferences with the ubiquitin proteasome system, file de3e52b3-7227-762d-e053-3705fe0a30e0 14
Targeting of the Leishmania Mexicana cysteine protease CPB2.8 ΔCTE by decorated fused benzo[b] thiophene scaffold., file de3e52b4-090e-762d-e053-3705fe0a30e0 14
Some new antimicrobial/antioxidant nanostructure zinc complexes: Synthesis, crystal structure, Hirshfeld surface analyses and thermal behavior, file 36125917-ecd1-454e-bd70-ef22832f24db 4
Mono and binuclear cadmium complexes: X-ray crystal structures, Hirshfeld surface analysis and antimicrobial/antioxidant studies, file d631c9ff-4222-4cd9-8713-c88bb654f71f 4
Development of peptidomimetic boronates as proteasome inhibitors, file de3e52ae-dd09-762d-e053-3705fe0a30e0 4
Silibinin-conjugated graphene nanoplatform: Synthesis, characterization and biological evaluation, file de3e52b1-1b95-762d-e053-3705fe0a30e0 4
Development of Novel Peptidomimetics Containing a VinylSulfone Moiety as Proteasome Inhibitors, file de3e52ae-d95c-762d-e053-3705fe0a30e0 3
Glutamate Binding-Site Ligands of NMDA Receptors, file de3e52ae-dc0a-762d-e053-3705fe0a30e0 3
Optimization of peptidomimetic boronates bearing a P3 bicyclic scaffold as proteasome inhibitors, file de3e52ae-f362-762d-e053-3705fe0a30e0 3
Identification of a new series of amides as non-covalent proteasome inhibitors., file de3e52af-00e9-762d-e053-3705fe0a30e0 3
Cross-Metathesis Reactions in the Synthesis of Constrained Dipeptide Mimics as Potent Falcipain-2 Inhibitors, file de3e52af-6ce7-762d-e053-3705fe0a30e0 3
Synthesis of Nanoterapeutics based on G/HA platforms for osteosarcoma targeting., file de3e52af-d45d-762d-e053-3705fe0a30e0 3
null, file de3e52b2-76d9-762d-e053-3705fe0a30e0 3
Fluorine-based pseudopeptides from halocarbene transfer reaction: synthesis and biological perspectives, file de3e52b3-99a4-762d-e053-3705fe0a30e0 3
null, file de3e52b5-75ea-762d-e053-3705fe0a30e0 3
Synthesis, chiral resolution and enantiopharmacology of a potent 2,3-benzodiazepine as noncompetitive AMPA receptor antagonist, file de3e52ae-ab36-762d-e053-3705fe0a30e0 2
Subunit-specific agonist activity at NR2A, NR2B, NR2C, and NR2D containing N-methyl-D-aspartate glutamate receptors., file de3e52ae-b544-762d-e053-3705fe0a30e0 2
Synthesis of benzothiazole derivatives and their biological evaluation as anticancer agents, file de3e52ae-da17-762d-e053-3705fe0a30e0 2
Development of peptidomimetic boronates as proteasome inhibitors, file de3e52ae-e3a1-762d-e053-3705fe0a30e0 2
Recent advances and perspectives on tropical diseases: Malaria, file de3e52ae-e699-762d-e053-3705fe0a30e0 2
Gold compounds as cysteine protease inhibitors: perspectives for pharmaceutical application as antiparasitic agents, file de3e52b0-db46-762d-e053-3705fe0a30e0 2
Physicochemical properties of inclusion complexes of highly soluble β-cyclodextrins with highly hydrophobic testosterone propionate, file de3e52b1-1de6-762d-e053-3705fe0a30e0 2
"Click" on PLGA-PEG and hyaluronic acid: Gaining access to anti-leishmanial pentamidine bioconjugates, file de3e52b1-9c2a-762d-e053-3705fe0a30e0 2
Synthesis, solution behaviour and potential anticancer activity of new trinuclear organometallic palladium(II) complex of S-1-phenylethyl dithiooxamide: Comparison with the trinuclear heterobimetallic platinum(II) analogue, file de3e52b1-f35b-762d-e053-3705fe0a30e0 2
Anticancer study of heterobimetallic platinum(II)-ruthenium(II) and platinum(II)-rhodium(III) complexes with bridging dithiooxamide ligand, file de3e52b2-6155-762d-e053-3705fe0a30e0 2
Discovery of benzimidazole-based Leishmania mexicana cysteine protease CPB2.8ΔCTE inhibitors as potential therapeutics for leishmaniasis, file de3e52b3-33b1-762d-e053-3705fe0a30e0 2
Cyrene: A Green Solvent for the Synthesis of Bioactive Molecules and Functional Biomaterials, file 28ce8a49-954c-43fe-beb7-c0a1abcd38c3 1
Supramolecular assembly of pentamidine and polymeric cyclodextrin bimetallic core–shell nanoarchitectures, file 4572d97c-0a8e-4f76-be73-216c972ddf9a 1
null, file 517110ce-2158-4999-a59f-5ac83fc8b9a3 1
Novel Peptidomimetics Containing a Vinyl Ester Moiety as Highly Potent and Selective Falcipain-2 Inhibitors, file de3e52ae-adaa-762d-e053-3705fe0a30e0 1
Enantioseparation, absolute configuration determination, and anticonvulsant activity of (+/-)-1-(4-aminophenyl)-7,8-methylenedioxy-1,2,3,5-tetrahydro)-4H-2,3-be nzodiazepin-4-one, file de3e52ae-ae6f-762d-e053-3705fe0a30e0 1
Chloro-substituted Hoveyda-Grubbs ruthenium carbene: Investigation of electronic effects, file de3e52ae-bc11-762d-e053-3705fe0a30e0 1
Synthesis of novel peptidomimetics as inhibitors of protozoan cysteine proteases falcipain-2 and rhodesain, file de3e52ae-c3d0-762d-e053-3705fe0a30e0 1
Synthesis and anti-HIV activity evaluation of new phenyl ethyl thiourea (PET) derivatives, file de3e52ae-c3d1-762d-e053-3705fe0a30e0 1
Peptidomimetics containing a vinyl ketone warhead as falcipain-2 inhibitors, file de3e52ae-d95b-762d-e053-3705fe0a30e0 1
Mechanism of Inhibition of the GluA2 AMPA Receptor Channel Opening: The Role of 4-Methyl versus 4-Carbonyl Group on the Diazepine Ring of 2,3-Benzodiazepine Derivatives, file de3e52ae-d95d-762d-e053-3705fe0a30e0 1
Selected gold compounds cause pronounced inhibition of Falcipain 2 and effectively block P. falciparum growth in vitro, file de3e52ae-da18-762d-e053-3705fe0a30e0 1
Development of Novel Selective Peptidomimetics Containing a Boronic Acid Moiety, Targeting the 20S Proteasome as Anticancer Agents, file de3e52ae-ec01-762d-e053-3705fe0a30e0 1
Synthesis and biological evaluation of new 2-amino-6-(trifluoromethoxy)benzoxazole derivatives, analogues of riluzole., file de3e52ae-f8a8-762d-e053-3705fe0a30e0 1
Inhibition of Rhodesain as a Novel Therapeutic Modality for Human African Trypanosomiasis, file de3e52af-01d2-762d-e053-3705fe0a30e0 1
null, file de3e52af-d32d-762d-e053-3705fe0a30e0 1
Silibinin conjugated graphene and hyaluronic acid platforms for osteosarcoma targeting, file de3e52b0-0379-762d-e053-3705fe0a30e0 1
Mechanism of falcipain-2 inhibition by α,β-unsaturated benzo[1,4]diazepin-2-one methyl ester, file de3e52b0-0df3-762d-e053-3705fe0a30e0 1
Development of targeting drug delivery systems based on hyaluronic acid bioconjugates., file de3e52b0-7c10-762d-e053-3705fe0a30e0 1
Ensemble-based ADME-Tox profiling and virtual screening for the discovery of new inhibitors of the Leishmania mexicana cysteine protease CPB2.8ΔCTE, file de3e52b1-3bc0-762d-e053-3705fe0a30e0 1
Target-based drug design and development of drug delivery systems to tackle leishmaniasis, file de3e52b1-a3a8-762d-e053-3705fe0a30e0 1
Gold compounds as cysteine protease inhibitors: perspectives for pharmaceutical application as antiparasitic agents, file de3e52b3-3972-762d-e053-3705fe0a30e0 1
Copper(II) complexes with tridentate halogen‐substituted Schiff base ligands: synthesis, crystal structures and investigating the effect of halogenation, leaving group and ligand flexibility on antiproliferative activities, file de3e52b4-a28e-762d-e053-3705fe0a30e0 1
Totale 205
Categoria #
all - tutte 583
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 583

Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202019 0 0 0 1 0 1 0 0 5 4 5 3
2020/202131 0 1 0 0 0 3 1 1 1 14 0 10
2021/202214 0 0 0 4 0 3 5 1 0 0 1 0
2022/202360 0 2 1 0 3 4 3 4 37 0 3 3
2023/202439 4 0 1 7 2 0 17 0 8 0 0 0
Totale 205