COLOTTA, VITTORIA
 Distribuzione geografica
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Continente #
NA - Nord America 341
EU - Europa 249
OC - Oceania 111
AS - Asia 99
AF - Africa 7
SA - Sud America 4
Totale 811
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Nazione #
US - Stati Uniti d'America 337
AU - Australia 111
IT - Italia 80
IE - Irlanda 39
VN - Vietnam 30
CN - Cina 29
GB - Regno Unito 23
DE - Germania 22
FR - Francia 21
IN - India 14
CZ - Repubblica Ceca 12
JP - Giappone 11
PL - Polonia 10
IR - Iran 8
NL - Olanda 8
RU - Federazione Russa 8
EG - Egitto 6
SE - Svezia 6
BR - Brasile 4
FI - Finlandia 4
UA - Ucraina 4
AT - Austria 3
CA - Canada 3
ID - Indonesia 2
IQ - Iraq 2
LT - Lituania 2
AE - Emirati Arabi Uniti 1
BE - Belgio 1
BG - Bulgaria 1
BY - Bielorussia 1
CH - Svizzera 1
GR - Grecia 1
HK - Hong Kong 1
MX - Messico 1
MY - Malesia 1
NO - Norvegia 1
PT - Portogallo 1
ZA - Sudafrica 1
Totale 811
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Città #
Melbourne 111
Florence 46
Dublin 39
Santa Cruz 34
Dong Ket 28
Houston 23
Buffalo 21
Fairfield 21
Ashburn 20
Ann Arbor 18
Cambridge 15
Woodbridge 15
Seattle 12
Wilmington 12
Shanghai 10
Warsaw 10
Gavirate 9
Las Vegas 9
Beijing 8
Los Angeles 7
Anguillara Sabazia 6
Cedar Knolls 6
Chicago 6
Mountain View 6
Tokyo 5
Wuhan 5
Atherstone 4
Bengaluru 4
Boardman 4
Helsinki 4
Sigtuna 4
Amsterdam 3
Dallas 3
Kumar 3
Manchester 3
Rome 3
Videira 3
Arbil 2
Columbus 2
Council Bluffs 2
Denver 2
Guangzhou 2
Hangzhou 2
Jakarta 2
Madison 2
Montpellier 2
Mount Joy 2
Newcastle upon Tyne 2
Northvale 2
Prati 2
Providence 2
San Jose 2
Southend 2
Toronto 2
University Park 2
Vienna 2
Asenovgrad 1
Atlanta 1
Austin 1
Bad Vilbel 1
Bellevue 1
Berlin 1
Brescia 1
Brighton 1
Böblingen 1
Central 1
Centrale 1
Charlottesville 1
Costa Mesa 1
Des Moines 1
Duncan 1
Falkenstein 1
Geneva 1
Ghent 1
Gurgaon 1
Halesowen 1
Hartford 1
Herndon 1
Ho Chi Minh City 1
Homewood 1
Huntsville 1
Indore 1
Kitzbühel 1
Kota Kinabalu 1
Laurel 1
Leiden 1
Lombard 1
Los Altos 1
Lucca 1
Lund 1
Miami 1
Milan 1
Minsk 1
Montréal 1
Moscow 1
Muizenberg 1
Munich 1
Mysore 1
New Albany 1
New Orleans 1
Totale 622
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Nome #
The identification of the 2-phenylphthalazin-1(2H)-one scaffold as a new decorable core skeleton for the design of potent and selective human A3 adenosine receptor antagonists., file e398c378-b0a4-179a-e053-3705fe0a4cff 247
The role of 5-arylalkylamino- and 5-piperazino- moieties on the 7-aminopyrazolo[4,3-d]pyrimidine core in affecting adenosine A1 and A2A receptor affinity and selectivity profiles, file e398c37b-af0f-179a-e053-3705fe0a4cff 82
Inhibition of A2Aadenosine receptor signaling in cancer cells proliferation by the novel antagonist TP455, file e398c37c-c0e3-179a-e053-3705fe0a4cff 68
Synthesis and biological evaluation of novel 9-heteroaryl substituted 7-chloro-4,5-dihydro-4-oxo-1,2,4-triazolo[1,5-a]quinoxaline-2-carboxylates (TQX) as AMPA receptor antagonists., file e398c378-9380-179a-e053-3705fe0a4cff 48
Exploring the 2- and 5-positions of the pyrazolo[4,3-d]pyrimidin-7-amino scaffold to target human A1 and A2A adenosine receptors, file e398c380-f07f-179a-e053-3705fe0a4cff 43
Modifications on the Amino-3,5-dicyanopyridine Core To Obtain Multifaceted Adenosine Receptor Ligands with Antineuropathic Activity, file e398c382-4cb9-179a-e053-3705fe0a4cff 43
Structure-activity relationship studies and pharmacological characterization of N5-heteroarylalkyl-substituted-2-(2-furanyl)thiazolo[5,4-d]pyrimidine-5,7-diamine-based derivatives as inverse agonists at human A2Aadenosine receptor, file e398c381-1eee-179a-e053-3705fe0a4cff 39
Adenosine A2B receptors stimulation inhibits oligodendrocyte maturation by interacting with sphingosine kinase/sphingosine 1-phosphate signalling axis in primary purified oligodendrocyte cultures, file e398c37c-ed32-179a-e053-3705fe0a4cff 36
1,2,4-Triazolo[1,5-a]quinoxaline derivatives and their simplified analogues as adenosine A3 receptor antagonists. Synthesis, structure–affinity relationships and molecular modeling studies, file e398c380-ce88-179a-e053-3705fe0a4cff 35
Antioxidant-Conjugated 1,2,4-Triazolo[4,3-a]pyrazin-3-one Derivatives: Highly Potent and Selective Human A2A Adenosine Receptor Antagonists Possessing Protective Efficacy in Neuropathic Pain, file e398c382-5144-179a-e053-3705fe0a4cff 35
null, file e398c380-e7c8-179a-e053-3705fe0a4cff 24
The aminopyridine-3,5-dicarbonitrile core for the design of new non-nucleoside-like agonists of the human adenosine A2Breceptor, file e398c380-f64e-179a-e053-3705fe0a4cff 20
4-Heteroaryl Substituted Amino-3,5-Dicyanopyridines as New Adenosine Receptor Ligands: Novel Insights on Structure-Activity Relationships and Perspectives, file e398c382-21d1-179a-e053-3705fe0a4cff 17
Structural investigations on coumarins leading to chromeno[4,3-c]pyrazol-4-ones and pyrano[4,3-c]pyrazol-4-ones: New scaffolds for the design of the tumor-associated carbonic anhydrase isoforms IX and XII, file e398c380-cb02-179a-e053-3705fe0a4cff 15
3-Hydroxy-1H-quinazoline-2,4-dione as a New Scaffold to Develop Potent and Selective Inhibitors of the Tumor-Associated Carbonic Anhydrases IX and XII, file e398c382-2dd7-179a-e053-3705fe0a4cff 11
Imidazo[1,2-a]pyrazin-8-amine core for the design of new adenosine receptor antagonists: Structural exploration to target the A3 and A2A subtypes, file e398c380-d129-179a-e053-3705fe0a4cff 10
Design, synthesis, and pharmacological characterization of 2‑(2- furanyl)thiazolo[5,4‑d]pyrimidine-5,7-diamine derivatives: new highly potent A2A adenosine receptor inverse agonists with antinociceptive activity, file e398c382-4df5-179a-e053-3705fe0a4cff 8
Imidazo[1,2-a]pyrazin-8-amine core for the design of new adenosine receptor antagonists: Structural exploration to target the A3 and A2A subtypes, file e398c37a-d04e-179a-e053-3705fe0a4cff 6
Pharmacological Characterization of P626, a Novel Dual Adenosine A2A/A2B Receptor Antagonist, on Synaptic Plasticity and during an Ischemic-like Insult in CA1 Rat Hippocampus, file 4813175c-5712-4969-9cf0-c2fb3faf102d 5
Structural investigations on coumarins leading to chromeno[4,3-c]pyrazol-4-ones and pyrano[4,3-c]pyrazol-4-ones: New scaffolds for the design of the tumor-associated carbonic anhydrase isoforms IX and XII, file e398c37c-e83b-179a-e053-3705fe0a4cff 4
Adenosine A2B receptors inhibit K+ currents and cell differentiation in cultured oligodendrocyte precursor cells and modulate sphingosine-1-phosphate signaling pathway, file e398c37f-422e-179a-e053-3705fe0a4cff 4
A comprehensive strategy in the development of a cyclodextrin-modified microemulsion electrokinetic chromatographic method for the assay of diclofenac and its impurities: Mixture-process variable experiments and quality by design, file e398c37a-a39c-179a-e053-3705fe0a4cff 3
3-Hydroxy-1H-quinazoline-2,4-dione as a New Scaffold to Develop Potent and Selective Inhibitors of the Tumor-Associated Carbonic Anhydrases IX and XII, file e398c37c-220c-179a-e053-3705fe0a4cff 3
The 1,2,4-Triazolo[4,3-a]pyrazin-3-one as a Versatile Scaffold for the Design of Potent Adenosine Human Receptor Antagonists. Structural Investigations to Target the A2A Receptor Subtype, file e398c37c-259f-179a-e053-3705fe0a4cff 3
The aminopyridine-3,5-dicarbonitrile core for the design of new non-nucleoside-like agonists of the human adenosine A2Breceptor, file e398c37d-1433-179a-e053-3705fe0a4cff 3
Modifications on the Amino-3,5-dicyanopyridine Core To Obtain Multifaceted Adenosine Receptor Ligands with Antineuropathic Activity, file e398c37e-8a35-179a-e053-3705fe0a4cff 3
Antioxidant-Conjugated 1,2,4-Triazolo[4,3-a]pyrazin-3-one Derivatives: Highly Potent and Selective Human A2A Adenosine Receptor Antagonists Possessing Protective Efficacy in Neuropathic Pain, file e398c37e-c446-179a-e053-3705fe0a4cff 3
Design, synthesis, and pharmacological characterization of 2‑(2- furanyl)thiazolo[5,4‑d]pyrimidine-5,7-diamine derivatives: new highly potent A2A adenosine receptor inverse agonists with antinociceptive activity, file e398c380-ce91-179a-e053-3705fe0a4cff 3
7-Amino-2-phenylpyrazolo[4,3-d]pyrimidine derivatives: Structural investigations at the 5-position to target human A1 and A2A adenosine receptors. Molecular modeling and pharmacological studies, file e398c378-eea2-179a-e053-3705fe0a4cff 2
null, file e398c378-f0d4-179a-e053-3705fe0a4cff 2
Discovery of first-in-class multi-target adenosine A2A receptor antagonists-carbonic anhydrase IX and XII inhibitors. 8-Amino-6-aryl-2-phenyl-1,2,4-triazolo [4,3-a]pyrazin-3-one derivatives as new potential antitumor agents, file e398c37f-bbe1-179a-e053-3705fe0a4cff 2
Piperazine-and piperidine-containing thiazolo[5,4-d]pyrimidine derivatives as new potent and selective adenosine a2a receptor inverse agonists, file e398c380-0c4c-179a-e053-3705fe0a4cff 2
“Dual Anta-Inhibitors” of the A2A Adenosine Receptor and Casein Kinase CK1delta: Synthesis, Biological Evaluation, and Molecular Modeling Studies, file 6a5b9472-d6d8-40c3-afd3-e5dd408fd470 1
Exploring the 7-oxo-thiazolo[5,4-d]pyrimidine core for the design of new human adenosine A3 receptor antagonists. Synthesis, molecular modeling studies and pharmacological evaluation, file e398c378-f0d5-179a-e053-3705fe0a4cff 1
Exploring the 2- and 5-positions of the pyrazolo[4,3-d]pyrimidin-7-amino scaffold to target human A1 and A2A adenosine receptors, file e398c37b-3a34-179a-e053-3705fe0a4cff 1
Pharmacological characterization of new highly potent A2a adenosine receptor inverse agonissts with antinociceptive activity, file e398c37c-9d25-179a-e053-3705fe0a4cff 1
Development of novel pyridazinone-based adenosine receptor ligands, file e398c37d-d7f3-179a-e053-3705fe0a4cff 1
Functional characterization of a novel adenosine A2B receptor agonist on short-term plasticity and synaptic inhibition during oxygen and glucose deprivation in the rat CA1 hippocampus, file e398c37e-560d-179a-e053-3705fe0a4cff 1
Structure-activity relationship studies and pharmacological characterization of N5-heteroarylalkyl-substituted-2-(2-furanyl)thiazolo[5,4-d]pyrimidine-5,7-diamine-based derivatives as inverse agonists at human A2Aadenosine receptor, file e398c380-ccd4-179a-e053-3705fe0a4cff 1
Design and Synthesis of Novel Thiazolo[5,4-d]pyrimidine Derivatives with High Affinity for Both the Adenosine A1 and A2A Receptors, and Efficacy in Animal Models of Depression, file e398c381-8121-179a-e053-3705fe0a4cff 1
Totale 837
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Categoria #
all - tutte 1.907
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 1.907
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201914 0 0 0 0 0 0 0 0 0 0 5 9
2019/202077 7 6 4 7 6 6 3 6 12 9 7 4
2020/2021126 7 8 4 8 8 5 4 5 18 12 20 27
2021/2022162 17 7 10 25 24 8 12 5 3 9 34 8
2022/2023336 13 10 43 15 21 34 40 10 16 127 6 1
2023/202444 2 1 3 0 5 3 7 8 4 7 4 0
Totale 837