IRIS
AGNELLO, STEFANO
 Distribuzione geografica
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Continente #
NA - Nord America 507
EU - Europa 473
AS - Asia 132
Totale 1.112
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Nazione #
US - Stati Uniti d'America 507
IE - Irlanda 176
SE - Svezia 127
VN - Vietnam 62
UA - Ucraina 50
CN - Cina 49
DE - Germania 37
GB - Regno Unito 26
FI - Finlandia 21
IT - Italia 21
IN - India 19
BE - Belgio 11
RU - Federazione Russa 2
AT - Austria 1
HU - Ungheria 1
IR - Iran 1
SG - Singapore 1
Totale 1.112
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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
Ann Arbor 10
Woodbridge 6
Nanjing 4
San Mateo 4
Brugherio 3
Haikou 3
Messina 3
Shenyang 3
Wilmington 3
Zhengzhou 3
Catania 2
Jinan 2
New York 2
Taiyuan 2
Alghero 1
Ardabil 1
Barlassina 1
Brooklyn 1
Budapest 1
Kunming 1
Lappeenranta 1
London 1
Longford 1
Los Angeles 1
Milan 1
Ningbo 1
Tappahannock 1
Vienna 1
Washington 1
Totale 852
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Nome #
1-Aryl-6,7-dimethoxy-3,4-dihydroisoquinoline-2(1H)-sulfonamide derivatives: synthesis and biological evaluation 127
Small molecules targeting the interaction between HIV-1 integrase and LEDGF/p75 cofactor. 62
Identification of 3,4-Dihydroisoquinoline-2(1H)-sulfonamides as Potent Carbonic Anhydrase Inhibitors: Synthesis, Biological Evaluation, and Enzyme−Ligand X-ray Studies 61
Synthesis and structure-active relationship of 1-aryl-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline anticonvulsants 61
Discovery of potent and selective inhibitors of druggable carbonic anhydrase isoforms 59
Small Molecules Targeting Protein–Protein Interactions: A Promising Anti-HIV Strategy 59
Synthesis of new pyridazine derivatives as potential anti-HIV-1 agents 57
Identification of isoquinoline-sulfonamides as potent and selective carbonic anhydrase inhibitors 54
PROGETTAZIONE E SINTESI DI NUOVI DKA ANALOGHI COME POTENZIALI INIBITORI DELL’INTEGRASI DELL’HIV-1 53
PROGETTAZIONE E SINTESI DI NUOVI DERIVATI ISOCHINOLINICI COME AGENTI ANTICONVULSIVANTI MULTITARGET 52
From 3D-pharmacophore models to synthetic route towards anti-HIV agents 51
Identification of Potent and Selective Human Carbonic Anhydrase VII (hCA VII) Inhibitors 51
Discovery of HIV-1 Integrase and cellular cofactor LEDGF/p75 interaction inhibitors 48
A structure-based approach to ligand discovery for inhibition of HIV-1 IN-LEDGF/p75 interaction: a new target for anti-AIDS therapy 48
PROGETTAZIONE E SINTESI DI NUOVI DKA ANALOGHI COME POTENZIALI INIBITORI DELL'INTEGRASI DELL'HIV-1 47
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 44
Identification of potent carbonic anhydrase inhibitors: synthesis, biological evaluation and enzyme-ligand x-ray studies 42
Totale 1.114
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Categoria #
all - tutte 3.619
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 3.619
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020180 29 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
2023/2024103 7 19 4 26 10 34 0 0 0 3 0 0
Totale 1.114