IRIS
SPALLAROSSA, ANDREA
 Distribuzione geografica
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Continente #
EU - Europa 426
Totale 426
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Nazione #
IT - Italia 426
Totale 426
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Città #
Genova 186
Genoa 147
Rapallo 77
Bordighera 16
Totale 426
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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 75
Potent and Broad-Spectrum Bactericidal Activity of a Nanotechnologically Manipulated Novel Pyrazole, file e268c4ce-9e73-a6b7-e053-3a05fe0adea1 30
The three-dimensional structure of NK cell receptor NKp44, a triggering partner in natural cytotoxicity, file e268c4c5-f615-a6b7-e053-3a05fe0adea1 28
One-Pot Synthesis and Antiproliferative Activity of Highly Functionalized Pyrazole Derivatives, file e268c4ce-5006-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
Valorization and Potential Antimicrobial Use of Olive Mill Wastewater (OMW) from Italian Olive Oil Production, file e268c4ce-aafc-a6b7-e053-3a05fe0adea1 24
Regioselective Synthesis, Structural Characterization, and Antiproliferative Activity of Novel Tetra-Substituted Phenylaminopyrazole Derivatives, file 44c8cd5e-379b-47ca-9f19-a11476b2ab73 18
Characterization data of water-soluble hydrophilic and amphiphilic dendrimers prodrugs for delivering bioactive chemical entities otherwise non soluble., file e268c4cd-06a6-a6b7-e053-3a05fe0adea1 16
Successful Dendrimer and Liposome-Based Strategies to Solubilize an Antiproliferative Pyrazole Otherwise Not Clinically Applicable, file e268c4ce-41e8-a6b7-e053-3a05fe0adea1 16
Characterization data of water-soluble hydrophilic and amphiphilic dendrimers prodrugs for delivering bioactive chemical entities otherwise non soluble., file e268c4cd-1be9-a6b7-e053-3a05fe0adea1 15
Mono- and di-acylated imidazolidine-2-thione derivatives: synthesis, cytotoxicity evaluation and computational studies, file ad10fded-ff5d-4e23-b294-a244f8c00ef1 14
Insights into the Pharmacological Activity of the Imidazo-Pyrazole Scaffold, file 8bc05cf3-6592-4327-bb53-a412ed1452ca 12
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
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 11
The Development of FAK Inhibitors: A Five-Year Update, file e268c4cf-1054-a6b7-e053-3a05fe0adea1 10
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
Novel insights on the molecular mechanism of action of the anti-angiogenic pyrazolyl-urea GeGe-3 by functional proteomics, file e268c4cd-fd3f-a6b7-e053-3a05fe0adea1 8
The Development of BTK Inhibitors: A Five-Year Update, file e268c4ce-506d-a6b7-e053-3a05fe0adea1 7
Bicyclic basic merbarone analogues as antiproliferative agents, file e268c4cd-e052-a6b7-e053-3a05fe0adea1 6
Nanotechnology of tyrosine kinase inhibitors in cancer therapy: A perspective, file e268c4ce-1c3a-a6b7-e053-3a05fe0adea1 5
Microbiological Screening of 5-Functionalized Pyrazoles for the Future Development of Optimized Pyrazole-Based Delivery Systems, file 908da7f4-f189-478f-b4f4-c67f430071ff 4
Novel 5-aminopyrazoles endowed with anti-angiogenetic properties: Design, synthesis and biological evaluation, file da1afdc8-a4b6-4a3a-a972-627648705ad9 4
Nanotechnology for Pediatric Retinoblastoma Therapy, file baf0e4e7-9de8-4c2d-913b-89e383f49504 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
Successful Dendrimer and Liposome-Based Strategies to Solubilize an Antiproliferative Pyrazole Otherwise Not Clinically Applicable, file e268c4ce-41e9-a6b7-e053-3a05fe0adea1 3
Amino-Pyrazoles in Medicinal Chemistry: A Review, file 0d2ba286-53e1-4a45-8f66-190bc60cb531 2
STRUCTURAL FUNCTIONALIZATION OF TRI-SUBSTITUTED PYRAZOLE DERIVATIVES AND PRELIMINARY EVALUATION OF THEIR ANTIMALARIAL ACTIVITY, file 6cea32e9-5f94-4a98-907c-b3a5313a5c0c 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
Synthesis, functional proteomics and biological evaluation of new 5-pyrazolyl ureas as potential anti-angiogenic compounds, file e268c4ce-3c88-a6b7-e053-3a05fe0adea1 2
Btk inhibitors: a medicinal chemistry and drug delivery perspective, file e268c4ce-4563-a6b7-e053-3a05fe0adea1 2
Synthesis, Antiproliferative, and Antioxidant Properties of Highly Functionalized Pyrazoles, file 3fd2c0b3-8a8d-4293-868a-67db2d3bea07 1
Antimalarial Activity of Tri- and Tetra-Substituted Anilino Pyrazoles, file 53c2f15a-1e3f-4bd1-9d8b-4b42ad0f9943 1
Cyclic diacyl thioureas enhance activity of corrector Lumacaftor on F508del‐CFTR, file 540753d0-420b-46f1-be28-a06164b35b06 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
Exploring the binding features of rimonabant analogues and acyclic CB1 antagonists: docking studies and QSAR analysis, 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
Synthesis and biological evaluation of new pyrazole carbohydrazides as antiproliferative and antioxidant agents., file e268c4ce-5357-a6b7-e053-3a05fe0adea1 1
Totale 426
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Categoria #
all - tutte 1.692
article - articoli 1.543
book - libri 0
conference - conferenze 149
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 3.384
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/20192 0 0 0 0 0 0 0 0 0 1 0 1
2019/202010 0 0 3 0 2 0 3 0 0 0 2 0
2020/202126 0 0 0 0 5 1 0 1 0 6 4 9
2021/202261 4 3 7 1 11 1 3 1 9 4 16 1
2022/202399 4 5 9 12 10 13 6 9 5 5 15 6
2023/2024141 7 6 17 20 8 10 38 21 5 9 0 0
Totale 426