IRIS
AGNELLO, STEFANO
 Distribuzione geografica
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Continente #
NA - Nord America 512
EU - Europa 485
AS - Asia 156
Totale 1.153
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Nazione #
US - Stati Uniti d'America 512
IE - Irlanda 176
SE - Svezia 127
VN - Vietnam 62
CN - Cina 52
UA - Ucraina 50
DE - Germania 40
IN - India 34
GB - Regno Unito 26
FI - Finlandia 23
IT - Italia 21
BE - Belgio 11
SG - Singapore 7
CZ - Repubblica Ceca 6
RU - Federazione Russa 2
AT - Austria 1
FR - Francia 1
HU - Ungheria 1
IR - Iran 1
Totale 1.153
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Città #
Dublin 175
Jacksonville 107
Chandler 103
Nyköping 96
Dong Ket 62
Dearborn 40
Ashburn 38
Beijing 28
Princeton 21
Cambridge 20
Medford 20
Pune 19
Lancaster 18
Des Moines 17
Boardman 12
Brussels 11
Hyderabad 11
Ann Arbor 10
Brno 6
Woodbridge 6
Los Angeles 4
Nanjing 4
San Mateo 4
Brugherio 3
Haikou 3
Lappeenranta 3
Messina 3
Shenyang 3
Singapore 3
Wilmington 3
Zhengzhou 3
Catania 2
Jinan 2
Munich 2
New York 2
Taiyuan 2
Alghero 1
Ardabil 1
Barlassina 1
Brooklyn 1
Budapest 1
Korba 1
Kunming 1
London 1
Longford 1
Milan 1
Ningbo 1
Nuremberg 1
Tappahannock 1
Vienna 1
Washington 1
Totale 881
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Nome #
1-Aryl-6,7-dimethoxy-3,4-dihydroisoquinoline-2(1H)-sulfonamide derivatives: synthesis and biological evaluation 136
Small molecules targeting the interaction between HIV-1 integrase and LEDGF/p75 cofactor. 64
Identification of 3,4-Dihydroisoquinoline-2(1H)-sulfonamides as Potent Carbonic Anhydrase Inhibitors: Synthesis, Biological Evaluation, and Enzyme−Ligand X-ray Studies 62
Synthesis and structure-active relationship of 1-aryl-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline anticonvulsants 62
Small Molecules Targeting Protein–Protein Interactions: A Promising Anti-HIV Strategy 62
Synthesis of new pyridazine derivatives as potential anti-HIV-1 agents 61
Discovery of potent and selective inhibitors of druggable carbonic anhydrase isoforms 60
Identification of isoquinoline-sulfonamides as potent and selective carbonic anhydrase inhibitors 58
Identification of Potent and Selective Human Carbonic Anhydrase VII (hCA VII) Inhibitors 57
PROGETTAZIONE E SINTESI DI NUOVI DERIVATI ISOCHINOLINICI COME AGENTI ANTICONVULSIVANTI MULTITARGET 55
PROGETTAZIONE E SINTESI DI NUOVI DKA ANALOGHI COME POTENZIALI INIBITORI DELL’INTEGRASI DELL’HIV-1 54
From 3D-pharmacophore models to synthetic route towards anti-HIV agents 52
A structure-based approach to ligand discovery for inhibition of HIV-1 IN-LEDGF/p75 interaction: a new target for anti-AIDS therapy 50
PROGETTAZIONE E SINTESI DI NUOVI DKA ANALOGHI COME POTENZIALI INIBITORI DELL'INTEGRASI DELL'HIV-1 48
Discovery of HIV-1 Integrase and cellular cofactor LEDGF/p75 interaction inhibitors 48
Structural basis for the interaction between carbonic anhydrase and 1,2,3,4-tetrahydroisoquinolin-2-ylsulfonamides 47
Synthesis and evaluation of pharmacological profile of 1-aryl-6,7-dimethoxy-3,4-dihydroisoquinoline-2(1H)-sulfonamides. 46
Novel targets for HIV therapy: small molecules blocking IN-LEDGF/p75 interaction 45
New potent and selective carbonic anhydrase inhibitors: synthesis, biological evaluation and X-ray studies 45
Identification of potent carbonic anhydrase inhibitors: synthesis, biological evaluation and enzyme-ligand x-ray studies 43
Totale 1.155
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Categoria #
all - tutte 4.236
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 4.236
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020151 0 12 0 8 0 38 26 23 0 22 22 0
2020/2021165 20 0 22 7 1 19 0 11 0 8 8 69
2021/202297 3 8 4 5 1 3 2 1 6 0 20 44
2022/2023448 39 66 23 16 25 45 2 29 187 0 14 2
2023/2024127 7 19 4 26 10 34 0 0 0 14 5 8
2024/202517 8 9 0 0 0 0 0 0 0 0 0 0
Totale 1.155