IRIS
MASSA, SILVIO
 Distribuzione geografica
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Continente #
NA - Nord America 649
EU - Europa 422
AS - Asia 70
OC - Oceania 2
Continente sconosciuto - Info sul continente non disponibili 1
Totale 1.144
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Nazione #
US - Stati Uniti d'America 647
GB - Regno Unito 108
IE - Irlanda 91
CN - Cina 59
UA - Ucraina 48
IT - Italia 47
SE - Svezia 37
FR - Francia 31
DE - Germania 25
FI - Finlandia 13
ES - Italia 7
BE - Belgio 6
RU - Federazione Russa 4
CZ - Repubblica Ceca 3
HK - Hong Kong 3
SG - Singapore 3
TR - Turchia 3
AU - Australia 2
CA - Canada 2
AE - Emirati Arabi Uniti 1
EU - Europa 1
IN - India 1
LV - Lettonia 1
SI - Slovenia 1
Totale 1.144
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Città #
Southend 99
Fairfield 97
Dublin 91
Menlo Park 74
Woodbridge 53
Wilmington 48
Ashburn 47
Seattle 41
Chandler 40
Houston 40
Jacksonville 40
Siena 39
Cambridge 35
Ann Arbor 29
Beijing 15
Princeton 12
San Diego 9
Fremont 8
Nanchang 8
Nanjing 8
Málaga 7
Shanghai 7
Brussels 6
New York 6
Shenyang 6
San Mateo 5
Düsseldorf 4
Boardman 3
Brno 3
Helsinki 3
Izmir 3
Moscow 3
Venezia 3
Changsha 2
Hangzhou 2
Hong Kong 2
Jiaxing 2
Kilburn 2
Lappeenranta 2
Los Angeles 2
Singapore 2
Tianjin 2
Toronto 2
Canberra 1
Curno 1
Delhi 1
Florence 1
Glasgow 1
Guangzhou 1
Hebei 1
Islington 1
Jinan 1
Kunming 1
Lanzhou 1
Leawood 1
Locri 1
London 1
Monmouth Junction 1
Norwalk 1
Redwood City 1
Riga 1
Saint Petersburg 1
San Francisco 1
Signa 1
Sydney 1
Vace 1
Washington 1
Zhengzhou 1
Totale 937
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Nome #
Antifungal agents. 10. New derivatives of 1-[(Aryl)[4-aryl-1H-pyrrol-3-yl]methyl]-1H-imidazole, synthesis, anti-Candida activity and Quantitative Structure-Analysis Relationship studies 163
Dihydro-alkylthio-benzyl-oxopyrimidines as Inhibitors of Reverse Transcriptase: Synthesis and Rationalization of the Biological Data on Both Wild-Type Enzyme and Relevant Clinical Mutants 159
Exploration of novel thiobarbituric acid- rhodanine- and thiohydantoin-based HIV-1 integrase inhibitors 144
Toward novel HIV-1 integrase binding inhibitors: molecular modeling, synthesis, and biological studies 133
A Versatile Route to C-6 Arylmethyl-Functionalized S-DABO and Related Analogues 132
A combination of molecular dynamics and docking calculations to explore the binding mode of ADS-J1, a polyanionic compound endowed with anti-HIV-1 activity 130
Solution-phase parallel synthesis of S-DABO analogues 127
Novel virtual screening protocol based on the combined use of molecular modeling and electron-ion interaction potential techniques to design HIV-1 integrase inhibitors. 121
Discovery of uracil-based histone deacetylase inhibitors able to reduce acquired antifungal resistance and trailing growth in Candida albicans 8
Aroyl-Pyrrolyl Hydroxyamides: Influence of Pyrrole C4-Phenylacetyl Substitution on Histone Deacetylase Inhibition. 4
3-D QSAR StudieS on Histone Deacetylase Inhibitors. A GOLPE/GRID Approach on Different Series of Compounds 4
5-Alkyl-2-alkylamino-6-(2,6-difluorophenylalkyl)-3,4-dihydropyrimidin-4(3H)-ones, a new series of potent, broad-spectrum non-nucleoside reverse transcriptase inhibitors belonging to the DABO family. 3
5-Alkyl-2-alkylthio-6-(2,6-dihalophenylmethyl)-3,4dihydropyrimidin-4(3H)ones: novel DABO derivatives active at nanomolar concentrations 3
3-(1H-pyrrol-1-yl)-2-oxazolidinones as reversibile, highly potent, and selective inhibitors of monoamine oxidase type A 2
1,2,5-Benzothiazepine and pyrrolo[1,2-d][1,2,5]benzothiazepine derivatives with specific anti-human immunodeficiency virus tipe 1 activity; 2
) 2,6-Bis(3,4,5-trihydroxybenzylydene) derivatives of cyclohexanone novel potent HIV-1 integrase inhibitors that prevent HIV-1 multiplication in cell-based assays. 2
3-(4-Aroyl-1H-pyrrol-1-yl)-N-hydroxy-2-propenamides, a new class of synthetic histone deacetylase inhibitors 2
1-[2-(Diphenhylmethoxy)ethyl]-2methyl-5nitroimidazole: a potent lead for the design of novel NNRTIs. 2
3-(4-Aroyl-1-methyl-1H-2-pyrrolyl)-N-hydroxy-2-propenamides as a New Class of Synthetic Histone Deacetylase Inhibitors. 2. Effect of Pyrrole-C2 and/or -C4 Substitutions on Biological Activity. 2
3-(4-Aroyl-1-methyl-1H-2-pyrrolyl)-N-hydroxy-2-alkylamides as a New Class of Synthetic Histone Deacetylase Inhibitors. 1. Design, Synthesis, Biological Evaluation, and Binding Mode Studies Performed through Three Different Docking Procedures. 2
181) Synthesis and biological properties of novel, uracil-containing histone deacetylase inhibitors 1
Totale 1.146
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Categoria #
all - tutte 3.292
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 3.292
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020245 31 9 14 43 18 20 21 28 21 20 6 14
2020/2021169 11 16 1 18 7 26 13 27 21 6 16 7
2021/2022106 7 27 6 3 5 1 7 1 7 14 7 21
2022/2023161 11 10 28 18 14 34 2 16 14 9 2 3
2023/2024129 6 1 5 10 6 35 53 3 1 2 1 6
2024/20255 5 0 0 0 0 0 0 0 0 0 0 0
Totale 1.146