IRIS
AGNELLO, STEFANO
 Distribuzione geografica
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Continente #
EU - Europa 488
NA - Nord America 430
AS - Asia 111
Totale 1029
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Nazione #
US - Stati Uniti d'America 430
IE - Irlanda 188
SE - Svezia 127
VN - Vietnam 62
UA - Ucraina 50
CN - Cina 47
DE - Germania 37
GB - Regno Unito 25
FI - Finlandia 20
IT - Italia 20
BE - Belgio 17
RU - Federazione Russa 2
AT - Austria 1
HU - Ungheria 1
IR - Iran 1
SG - Singapore 1
Totale 1029
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Città #
Dublin 188
Jacksonville 107
Chandler 103
Nyköping 96
Dong Ket 62
Dearborn 40
Beijing 28
Princeton 21
Cambridge 20
Medford 20
Lancaster 18
Brussels 17
Des Moines 17
Boardman 12
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
Taiyuan 2
Alghero 1
Ardabil 1
Barlassina 1
Brooklyn 1
Budapest 1
Kunming 1
Ningbo 1
Vienna 1
Totale 805
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Nome #
1-Aryl-6,7-dimethoxy-3,4-dihydroisoquinoline-2(1H)-sulfonamide derivatives: synthesis and biological evaluation 119
Small molecules targeting the interaction between HIV-1 integrase and LEDGF/p75 cofactor. 58
Identification of 3,4-Dihydroisoquinoline-2(1H)-sulfonamides as Potent Carbonic Anhydrase Inhibitors: Synthesis, Biological Evaluation, and Enzyme−Ligand X-ray Studies 57
Synthesis and structure-active relationship of 1-aryl-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline anticonvulsants 56
Small Molecules Targeting Protein–Protein Interactions: A Promising Anti-HIV Strategy 55
Discovery of potent and selective inhibitors of druggable carbonic anhydrase isoforms 54
Identification of isoquinoline-sulfonamides as potent and selective carbonic anhydrase inhibitors 54
Synthesis of new pyridazine derivatives as potential anti-HIV-1 agents 51
PROGETTAZIONE E SINTESI DI NUOVI DERIVATI ISOCHINOLINICI COME AGENTI ANTICONVULSIVANTI MULTITARGET 48
Structural basis for the interaction between carbonic anhydrase and 1,2,3,4-tetrahydroisoquinolin-2-ylsulfonamides 48
PROGETTAZIONE E SINTESI DI NUOVI DKA ANALOGHI COME POTENZIALI INIBITORI DELL’INTEGRASI DELL’HIV-1 47
Identification of Potent and Selective Human Carbonic Anhydrase VII (hCA VII) Inhibitors 46
PROGETTAZIONE E SINTESI DI NUOVI DKA ANALOGHI COME POTENZIALI INIBITORI DELL'INTEGRASI DELL'HIV-1 45
From 3D-pharmacophore models to synthetic route towards anti-HIV agents 45
A structure-based approach to ligand discovery for inhibition of HIV-1 IN-LEDGF/p75 interaction: a new target for anti-AIDS therapy 45
Discovery of HIV-1 Integrase and cellular cofactor LEDGF/p75 interaction inhibitors 43
Novel targets for HIV therapy: small molecules blocking IN-LEDGF/p75 interaction 41
New potent and selective carbonic anhydrase inhibitors: synthesis, biological evaluation and X-ray studies 41
Synthesis and evaluation of pharmacological profile of 1-aryl-6,7-dimethoxy-3,4-dihydroisoquinoline-2(1H)-sulfonamides. 41
Identification of potent carbonic anhydrase inhibitors: synthesis, biological evaluation and enzyme-ligand x-ray studies 37
Totale 1031
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Categoria #
all - tutte 2115
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 2115
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2017/20181 0000 00 00 0001
2018/201934 3100 214 40 1000
2019/2020180 291208 038 2623 022220
2020/2021165 200227 119 011 08869
2021/202297 3845 13 21 602044
2022/2023468 39662316 2545 230 2080140
Totale 1031