SPALLAROSSA, ANDREA
 Distribuzione geografica
Continente #
EU - Europa 240
Totale 240
Nazione #
IT - Italia 240
Totale 240
Città #
Genova 186
Rapallo 46
Genoa 8
Totale 240
Nome #
Iterative design and optimization of initially inactive Proteolysis Targeting Chimeras (PROTACs) identify VZ185 as a potent, fast and selective von Hippel-Lindau (VHL)-based dual degrader probe of BRD9 and BRD7, file e268c4cd-b3ba-a6b7-e053-3a05fe0adea1 57
The three-dimensional structure of NK cell receptor NKp44, a triggering partner in natural cytotoxicity, file e268c4c5-f615-a6b7-e053-3a05fe0adea1 28
Synthesis of N-substituted-N-acylthioureas of 4-substituted piperazines endowed with local anaesthetic, antihyperlipidemic, antiproliferative activities and antiarrythmic, analgesic, antiaggregating actions, file e268c4c5-f6c4-a6b7-e053-3a05fe0adea1 25
Structure-based Design, Parallel Synthesis, SAR and Molecular Modelling Studies of Thiocarbamates, New Potent Non-Nucleoside HIV-1 Reverse Transcriptase Inhibitor Isosteres of Phenethylthiazolylthiourea (PETT) Derivatives., file e268c4c5-eab5-a6b7-e053-3a05fe0adea1 12
Expression and crystallographic characterization of the extracellular domain of human Natural Killer cell triggering receptor NKp46, file e268c4c5-ec82-a6b7-e053-3a05fe0adea1 9
Structure of the human NK cell triggering receptor NKp46 ectodomain, file e268c4c5-fd98-a6b7-e053-3a05fe0adea1 9
Characterization data of water-soluble hydrophilic and amphiphilic dendrimers prodrugs for delivering bioactive chemical entities otherwise non soluble., file e268c4cd-06a6-a6b7-e053-3a05fe0adea1 9
Characterization data of water-soluble hydrophilic and amphiphilic dendrimers prodrugs for delivering bioactive chemical entities otherwise non soluble., file e268c4cd-1be9-a6b7-e053-3a05fe0adea1 9
null, file e268c4ce-41e8-a6b7-e053-3a05fe0adea1 9
null, file e268c4ce-9e73-a6b7-e053-3a05fe0adea1 9
Non-PAMAM amino acids-modified dendrimers nanoparticles for enhancing water-solubility of insoluble bioactive molecules: our state of the art, file e268c4cc-9619-a6b7-e053-3a05fe0adea1 6
The Development of FAK Inhibitors: A Five-Year Update, file e268c4cf-1054-a6b7-e053-3a05fe0adea1 6
Parallel synthesis, molecular modelling and further structure-activity relationship studies of new acylthiocarbamates as potent non-nucleoside HIV-1 reverse transcriptase inhibitors, file e268c4c9-3c90-a6b7-e053-3a05fe0adea1 4
Successful Dendrimer and Liposome-Based Strategies to Solubilize an Antiproliferative Pyrazole Otherwise Not Clinically Applicable, file e268c4ce-c714-a6b7-e053-3a05fe0adea1 4
Regioselective Synthesis, Structural Characterization, and Antiproliferative Activity of Novel Tetra-Substituted Phenylaminopyrazole Derivatives, file 44c8cd5e-379b-47ca-9f19-a11476b2ab73 3
Rational design, synthesis and biological evaluation of new 1,5-diarylpyrazole derivatives as CB1 receptor antagonists, structurally related to rimonabant,, file e268c4c9-5d38-a6b7-e053-3a05fe0adea1 3
Hydrophilic and amphiphilic water-soluble dendrimer formulations of a not-soluble thiocarbamate derivative with moderate anti HIV activity for biomedical applications., file e268c4c9-61c6-a6b7-e053-3a05fe0adea1 3
Mono- and di-acylated imidazolidine-2-thione derivatives: synthesis, cytotoxicity evaluation and computational studies, file ad10fded-ff5d-4e23-b294-a244f8c00ef1 2
Synthesis and antiproliferative activity of basic thioanalogues of merbarone, file e268c4c6-01d3-a6b7-e053-3a05fe0adea1 2
Identification of novel pyrazolo[3,4-d]pyrimidine able to inhibit cell proliferation of a human osteogenic sarcoma in vitro and in a xenograft model in mice, file e268c4c6-14e2-a6b7-e053-3a05fe0adea1 2
Hydrophilic and amphiphilic water-soluble dendrimer prodrugs suitable for parenteral administration of a non-soluble non-nucleoside HIV-1 reverse transcriptase inhibitor thiocarbamate derivative, file e268c4c9-dd68-a6b7-e053-3a05fe0adea1 2
Nanotechnology of tyrosine kinase inhibitors in cancer therapy: A perspective, file e268c4ce-1c3a-a6b7-e053-3a05fe0adea1 2
null, file e268c4ce-3c88-a6b7-e053-3a05fe0adea1 2
Valorization and Potential Antimicrobial Use of Olive Mill Wastewater (OMW) from Italian Olive Oil Production, file e268c4ce-aafc-a6b7-e053-3a05fe0adea1 2
Synthesis, Antiproliferative, and Antioxidant Properties of Highly Functionalized Pyrazoles, file 3fd2c0b3-8a8d-4293-868a-67db2d3bea07 1
Design, synthesis and biological evaluation of novel 5-amino pyrazoles with antiangiogenic properties, file 82f11d62-a6df-48f5-859d-e79b1892e0d3 1
The "Rhodanese" fold and catalytic mechanism of 3-mercaptopyruvate sulfurtransferases: Crystal structure of SseA from Escherichia coli, file e268c4c5-ee33-a6b7-e053-3a05fe0adea1 1
Thiocarbamates as non-nucleoside HIV-1 reverse transcriptase inhibitors. Part 2: parallel synthesis, molecular modelling and structure-activity relationship studies on analogues of O-(2-phenylethyl)-N-phenylthiocarbamate, file e268c4c5-f610-a6b7-e053-3a05fe0adea1 1
Parallel one-pot synthesis and structure-activity relationship study of symmetric formimidoester disulfides as a novel class of potent non-nucleoside HIV-1 reverse transcriptase inhibitors, file e268c4c5-f73f-a6b7-e053-3a05fe0adea1 1
null, file e268c4c5-f7b4-a6b7-e053-3a05fe0adea1 1
6-amino-4-oxo-1,3-diphenyl-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carbonyl derivatives as a new class of potent inhibitors of Interleukin-8-induced neutrophil chemotaxis, file e268c4c5-f8c9-a6b7-e053-3a05fe0adea1 1
Hydrophilic and amphiphilic water-soluble dendrimer prodrugs suitable for parenteral administration of a non-soluble non-nucleoside HIV-1 reverse transcriptase inhibitor thiocarbamate derivative, file e268c4c9-2a51-a6b7-e053-3a05fe0adea1 1
Characterization of water soluble dendrimer formulations of an insoluble thiocarbamate derivative with moderate anti HIV-1 activity: an overview, file e268c4c9-6939-a6b7-e053-3a05fe0adea1 1
Characterization data of water-soluble hydrophilic and amphiphilic dendrimers prodrugs for delivering bioactive chemical entities otherwise non soluble., file e268c4c9-a29f-a6b7-e053-3a05fe0adea1 1
Non-PAMAM amino acids-modified dendrimers nanoparticles for enhancing water-solubility of insoluble bioactive molecules: our state of the art, file e268c4c9-a2a1-a6b7-e053-3a05fe0adea1 1
Characterization data of water-soluble hydrophilic and amphiphilic dendrimers prodrugs for delivering bioactive chemical entities otherwise non soluble., file e268c4c9-d4b8-a6b7-e053-3a05fe0adea1 1
Synthesis and biological evaluation of (acyl)hydrazones and thiosemicarbazones obtained via in situ condensation of iminium salts with nitrogen-containing nucleophiles, file e268c4ca-0729-a6b7-e053-3a05fe0adea1 1
HIGHLY-FUNCTIONALIZED AMINO PYRAZOLES AS ANTIOXIDANT AGENTS: A PRELIMINARY SYNTHETIC ACCESSIBILITY STUDY, file e268c4cd-ddb4-a6b7-e053-3a05fe0adea1 1
Bicyclic basic merbarone analogues as antiproliferative agents, file e268c4cd-e052-a6b7-e053-3a05fe0adea1 1
null, file e268c4cd-fd3f-a6b7-e053-3a05fe0adea1 1
Btk inhibitors: a medicinal chemistry and drug delivery perspective, file e268c4ce-4563-a6b7-e053-3a05fe0adea1 1
One-Pot Synthesis and Antiproliferative Activity of Highly Functionalized Pyrazole Derivatives, file e268c4ce-5006-a6b7-e053-3a05fe0adea1 1
The Development of BTK Inhibitors: A Five-Year Update, file e268c4ce-506d-a6b7-e053-3a05fe0adea1 1
Synthesis and biological evaluation of new pyrazole carbohydrazides as antiproliferative and antioxidant agents., file e268c4ce-5357-a6b7-e053-3a05fe0adea1 1
Potent and Broad-Spectrum Bactericidal Activity of a Nanotechnologically Manipulated Novel Pyrazole, file e268c4ce-f567-a6b7-e053-3a05fe0adea1 1
Totale 240
Categoria #
all - tutte 390
article - articoli 334
book - libri 0
conference - conferenze 56
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 780


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201989 0010 072 122 0101
2019/202010 0030 20 30 0020
2020/202126 0000 51 01 0649
2021/202261 4371 111 31 94161
2022/202354 781013 142 00 0000
Totale 240