IRIS
DE LUCA, Laura
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
EU - Europa 552
AS - Asia 182
NA - Nord America 132
AF - Africa 20
OC - Oceania 12
SA - Sud America 10
Totale 908
Salva come PNG Salva come JPEG
Nazione #
PL - Polonia 275
IT - Italia 131
US - Stati Uniti d'America 102
IQ - Iraq 56
IE - Irlanda 39
PK - Pakistan 26
FR - Francia 23
DE - Germania 22
IN - India 21
CA - Canada 20
GB - Regno Unito 20
TR - Turchia 18
IR - Iran 16
AU - Australia 12
EG - Egitto 11
NL - Olanda 9
VN - Vietnam 8
ES - Italia 7
HK - Hong Kong 7
JP - Giappone 6
MX - Messico 6
BR - Brasile 5
CN - Cina 5
KR - Corea 5
DO - Repubblica Dominicana 4
DZ - Algeria 4
MY - Malesia 4
NG - Nigeria 4
FI - Finlandia 3
LT - Lituania 3
PE - Perù 3
PT - Portogallo 3
AR - Argentina 2
CH - Svizzera 2
DK - Danimarca 2
GR - Grecia 2
HU - Ungheria 2
ID - Indonesia 2
IL - Israele 2
JO - Giordania 2
MK - Macedonia 2
SG - Singapore 2
BD - Bangladesh 1
BE - Belgio 1
CZ - Repubblica Ceca 1
LV - Lettonia 1
MT - Malta 1
RU - Federazione Russa 1
SE - Svezia 1
SI - Slovenia 1
TW - Taiwan 1
UG - Uganda 1
Totale 908
Salva come PNG Salva come JPEG
Città #
Częstochowa 218
Messina 55
Dublin 39
Duhok 34
Francofonte 18
Warsaw 17
Ashburn 11
Delhi 8
Dong Ket 8
Redmond 8
Walluf 8
Bear 7
Damanhur 7
Baghdad 6
Islamabad 6
Paris 6
Philadelphia 6
Waco 6
Niagara Falls 5
Reggio Calabria 5
Riesi 5
Al Hillah 4
Brzesko 4
Catania 4
Council Bluffs 4
Elâzığ 4
Frankfurt am Main 4
Gazi 4
Krakow 4
Lahore 4
London 4
Rawalpindi 4
Tehran 4
Bengaluru 3
Borghetto Santo Spirito 3
Florence 3
Gdynia 3
Izmir 3
Lagos 3
Lima 3
Lisbon 3
Los Angeles 3
New York 3
Olsztyn 3
Perth 3
Pollença 3
Putrajaya 3
Santo Domingo 3
Sydney 3
Aberdeen 2
Amman 2
Amsterdam 2
Ankara 2
Bloomington 2
Brooklyn 2
Cairns 2
Cairo 2
Carini 2
Ciudad Juárez 2
Clifton 2
Columbus 2
Gwalior 2
Gwangjin-gu 2
Hamburg 2
Ichikawa 2
Istanbul 2
Katowice 2
Kolkata 2
Kongens Lyngby 2
Lodz 2
Louisville 2
Lublin 2
Melbourne 2
Milan 2
Murcia 2
Oran 2
Piazza Armerina 2
Piotrkow Trybunalski 2
Pittsburgh 2
Prilep 2
Rome 2
Roth 2
Syracuse 2
Tampere 2
The Bronx 2
The Hague 2
Thessaloniki 2
Toluca 2
Viagrande 2
Wilmington 2
Woking 2
Wroclaw 2
Zurich 2
's-Gravenzande 1
Anping District 1
Antalya 1
Bad Griesbach 1
Barcelona 1
Basrah 1
Bayan Lepas 1
Totale 674
Salva come PNG Salva come JPEG
Nome #
Vitamin D: a steroid hormone with progesterone-like activity, file de3e52b4-b460-762d-e053-3705fe0a30e0 637
Rational design of small molecules able to inhibit α-synuclein amyloid aggregation for the treatment of Parkinson’s disease, file de3e52b5-2e73-762d-e053-3705fe0a30e0 42
Synthesis and biological evaluation of sulfonamide-based compounds as inhibitors of carbonic anhydrase from Vibrio cholerae, file a073709c-1d2b-43da-a48a-8957f90d8e18 41
Seeking new approach for therapeutic treatment of cholera disease via inhibition of bacterial carbonic anhydrases: experimental and theoretical studies for sixteen benzenesulfonamide derivatives, file de3e52b2-1d3c-762d-e053-3705fe0a30e0 20
In Silico-Guided Identification of New Potent Inhibitors of Carbonic Anhydrases Expressed in Vibrio cholerae, file 48c1a758-16a7-41a3-aa91-c44b499a2dc7 19
N-acylhydrazone inhibitors of influenza virus PA endonuclease with versatile metal binding modes, file de3e52b0-4224-762d-e053-3705fe0a30e0 19
Synthesis, computational studies and assessment of in vitro inhibitory activity of umbelliferon-based compounds against tumour-associated carbonic anhydrase isoforms IX and XII, file de3e52b3-50c0-762d-e053-3705fe0a30e0 19
Looking toward the Rim of the Active Site Cavity of Druggable Human Carbonic Anhydrase Isoforms, file bb71dea4-5919-4977-95c5-c66fbd10e415 16
Searching for indole derivatives as potential mushroom tyrosinase inhibitors, file de3e52b4-9788-762d-e053-3705fe0a30e0 12
Effetto in vitro di derivati di 1-(1H-indol-3-il) etanone e propan-1-one su Candida spp. and Aspergillus niger, file de3e52b4-bf2d-762d-e053-3705fe0a30e0 7
The in vitro potential of novel carbonic anhydrase Inhibitors against candida spp, file 0d9115ab-e71d-42ca-8664-8faaec89a331 6
Graphene Quantum Dots Based Systems As HIV Inhibitors, file de3e52b1-9612-762d-e053-3705fe0a30e0 6
Structural optimization and in vitro evaluation of new 1-(4-fluorobenzyl)piperazine derivatives as inhibitors of Tyrosinase from Agaricus bisporus, file de3e52b4-ba9f-762d-e053-3705fe0a30e0 6
NOVEL N1-ARYL-2- ARYLTHIOACETAMIDOBENZIMIDAZOLES WERE EFFECTIVE AGAINST HERPES SIMPLEX VIRUS 1 (HSV-1) REPLICATION IN VITRO, file de3e52b1-3470-762d-e053-3705fe0a30e0 5
Novel 3-(4-benzylpiperidin-1-yl)-1-(1H-indol-3-yl)propan-1-one derivates were effective in vitro against clinical isolates of Candida spp. and Aspergillus niger, file de3e52b1-a688-762d-e053-3705fe0a30e0 5
A Combination of Pharmacophore and Docking-based Virtual Screening to Discover new Tyrosinase Inhibitors, file de3e52b4-d904-762d-e053-3705fe0a30e0 4
The SIRT2 Pathway Is Involved in the Antiproliferative Effect of Flavanones in Human Leukemia Monocytic THP-1 Cells, file 248843af-9f2c-41aa-8067-b8a54fe7d04d 3
Evaluation of the In Vitro Antifungal Activity of Novel Arylsulfonamides against Candida spp, file bf0695b8-4862-4531-8b1d-73eae380ef16 3
Targeting Tyrosinase: Development and Structural Insights of Novel Inhibitors Bearing Arylpiperidine and Arylpiperazine Fragments, file de3e52b4-1ede-762d-e053-3705fe0a30e0 3
AMPA receptor antagonists: Synthesis and pharmacological evaluation, file de3e52b4-e060-762d-e053-3705fe0a30e0 3
Discovery of a new potent inhibitor of mushroom tyrosinase (Agaricus bisporus) containing 4-(4-hydroxyphenyl)piperazin-1-yl moiety, file de3e52b4-eefe-762d-e053-3705fe0a30e0 3
The In Vitro Potential of 1-(1H-indol-3-yl) Derivatives against Candida spp. and Aspergillus niger as Tyrosinase Inhibitors, file de3e52b4-fc75-762d-e053-3705fe0a30e0 3
The 1-(4-fluorobenzyl)piperazine fragment for the development of novel tyrosinase inhibitors, file de3e52b5-2416-762d-e053-3705fe0a30e0 3
Efficient 3D Database screening for novel HIV-1 IN inhibitors, file de3e52ae-a8ba-762d-e053-3705fe0a30e0 2
Computational Studies to Discover a New NR2B/NMDA Receptor Antagonist and Evaluation of Pharmacological Profile, file de3e52ae-b83d-762d-e053-3705fe0a30e0 2
Discovery of benzimidazole-based Leishmania mexicana cysteine protease CPB2.8ΔCTE inhibitors as potential therapeutics for leishmaniasis, file de3e52b3-33b1-762d-e053-3705fe0a30e0 2
Exploiting the 1-(4-fluorobenzyl)piperazine fragment for the development of novel tyrosinase inhibitors as anti-melanogenic agents: Design, synthesis, structural insights and biological profile, file de3e52b4-2c0e-762d-e053-3705fe0a30e0 2
Design, synthesis and in vitro evaluation of 4-fluorobenzyl- and 4-hydroxyphenyl-based compounds targeting tyrosinases, file de3e52b5-3ac2-762d-e053-3705fe0a30e0 2
Discovery of a novel class of Tyrosinase inhibitors as antimelanogenic agents, file de3e52b5-4461-762d-e053-3705fe0a30e0 2
Exploring the chemical space of 3-chloro-4-fluorophenyl-based compounds as tyrosinase inhibitors, file 50ce6b10-9708-43ed-ab12-5bb86de3b12e 1
In silico approach to select new natural-based compounds targeting tyrosinase, file ad726307-312f-4599-8a13-ed0827195430 1
Design and synthesis of N1-aryl-benzimidazoles 2-substituted as novel HIV-1 non-nucleoside reverse transcriptase inhibitors, file de3e52ae-ef4f-762d-e053-3705fe0a30e0 1
null, file de3e52b1-9366-762d-e053-3705fe0a30e0 1
Simulated human digestion of N1-aryl-2-arylthioacetamidobenzimidazoles and their activity against Herpes-simplex virus 1 in vitro, file de3e52b2-63b5-762d-e053-3705fe0a30e0 1
The link between the AMPK/SIRT1 axis and a flavonoid-rich extract of Citrus bergamia juice: A cell-free, in silico, and in vitro study, file de3e52b2-98b6-762d-e053-3705fe0a30e0 1
Inhibitory effects and structural insights for a novel series of coumarin-based compounds that selectively target human CA IX and CA XII carbonic anhydrases, file de3e52b2-e8eb-762d-e053-3705fe0a30e0 1
Structural optimization of N1-aryl-benzimidazoles for the discovery of new non-nucleoside reverse transcriptase inhibitors active against wild-type and mutant HIV-1 strains, file de3e52b3-0102-762d-e053-3705fe0a30e0 1
Structure-guided design of new indoles as negative allosteric modulators (NAMs) of N-methyl-d-aspartate receptor (NMDAR) containing GluN2B subunit, file de3e52b3-36be-762d-e053-3705fe0a30e0 1
Probing Molecular Interactions between Human Carbonic Anhydrases (hCAs) and a Novel Class of Benzenesulfonamides, file de3e52b3-5adf-762d-e053-3705fe0a30e0 1
null, file de3e52b3-cb22-762d-e053-3705fe0a30e0 1
Chemical exploration of 4-(4-fluorobenzyl)piperidine fragment for the development of new tyrosinase inhibitors, file de3e52b4-1070-762d-e053-3705fe0a30e0 1
Exploring structural properties of potent human carbonic anhydrase inhibitors bearing a 4-(cycloalkylamino-1-carbonyl)benzenesulfonamide moiety, file de3e52b4-3bfb-762d-e053-3705fe0a30e0 1
Carbonic anhydrase inhibitors: Design, synthesis and structural characterization of new heteroaryl-N-carbonylbenzenesulfonamides targeting druggable human carbonic anhydrase isoforms, file de3e52b4-b101-762d-e053-3705fe0a30e0 1
1-Benzylpiperidine derivatives: design and synthesis of new compounds as tyrosinase inhibitors from Agaricus bisporus, file de3e52b5-1778-762d-e053-3705fe0a30e0 1
Structure- and Ligand-based optimization of fragment binding tyrosinase from Agaricus bisporus to develop anti-melanogenic agents, file e1b6e188-1f58-4f26-bfd2-36146a4ede39 1
Totale 913
Salva come PNG Salva come JPEG
Categoria #
all - tutte 1.626
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 1.626
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/20192 0 0 0 0 0 0 0 0 0 0 2 0
2019/20204 0 0 0 0 0 0 0 0 0 2 1 1
2020/202155 1 0 0 0 2 0 1 6 20 13 2 10
2021/2022157 9 0 0 0 0 2 22 19 34 25 16 30
2022/2023373 39 20 32 28 33 18 18 29 75 32 35 14
2023/2024319 32 25 27 42 23 34 51 29 28 19 9 0
Totale 913