IRIS
MASSA, SILVIO
 Distribuzione geografica
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Continente #
NA - Nord America 693
EU - Europa 458
AS - Asia 86
OC - Oceania 2
AF - Africa 1
Continente sconosciuto - Info sul continente non disponibili 1
Totale 1.241
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Nazione #
US - Stati Uniti d'America 690
GB - Regno Unito 109
IE - Irlanda 91
CN - Cina 59
UA - Ucraina 48
IT - Italia 47
SE - Svezia 37
RU - Federazione Russa 35
FR - Francia 32
DE - Germania 26
SG - Singapore 19
FI - Finlandia 14
ES - Italia 7
BE - Belgio 6
CA - Canada 3
CZ - Repubblica Ceca 3
HK - Hong Kong 3
TR - Turchia 3
AU - Australia 2
AE - Emirati Arabi Uniti 1
EU - Europa 1
IN - India 1
LT - Lituania 1
LV - Lettonia 1
MA - Marocco 1
SI - Slovenia 1
Totale 1.241
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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
Santa Clara 34
Ann Arbor 29
Singapore 17
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
Helsinki 4
Los Angeles 4
Boardman 3
Brno 3
Izmir 3
Moscow 3
Toronto 3
Venezia 3
Changsha 2
Hangzhou 2
Hong Kong 2
Jiaxing 2
Kilburn 2
Lappeenranta 2
Tianjin 2
Canberra 1
Curno 1
Delhi 1
Florence 1
Frankfurt am Main 1
Glasgow 1
Guangzhou 1
Hebei 1
Islington 1
Jinan 1
Kunming 1
Lanzhou 1
Leawood 1
Locri 1
London 1
Monmouth Junction 1
Newark 1
Norwalk 1
Paris 1
Redwood City 1
Riga 1
Saint Petersburg 1
San Francisco 1
Signa 1
Sydney 1
Vace 1
Washington 1
Zhengzhou 1
Totale 993
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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 177
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 173
Exploration of novel thiobarbituric acid- rhodanine- and thiohydantoin-based HIV-1 integrase inhibitors 156
Toward novel HIV-1 integrase binding inhibitors: molecular modeling, synthesis, and biological studies 146
A Versatile Route to C-6 Arylmethyl-Functionalized S-DABO and Related Analogues 142
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 142
Solution-phase parallel synthesis of S-DABO analogues 137
Novel virtual screening protocol based on the combined use of molecular modeling and electron-ion interaction potential techniques to design HIV-1 integrase inhibitors 133
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 1.243
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Categoria #
all - tutte 3.694
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 3.694
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020130 0 0 0 0 0 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
2024/2025102 6 10 34 7 33 12 0 0 0 0 0 0
Totale 1.243