FALSINI, MATTEO
 Distribuzione geografica
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Continente #
EU - Europa 157
NA - Nord America 137
OC - Oceania 90
AS - Asia 42
AF - Africa 7
SA - Sud America 1
Totale 434
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Nazione #
US - Stati Uniti d'America 136
AU - Australia 90
IT - Italia 58
IE - Irlanda 25
GB - Regno Unito 19
IN - India 12
JP - Giappone 12
CZ - Repubblica Ceca 11
DE - Germania 10
FR - Francia 7
CN - Cina 6
SE - Svezia 6
EG - Egitto 4
NL - Olanda 4
PL - Polonia 4
VN - Vietnam 4
RU - Federazione Russa 3
FI - Finlandia 2
KR - Corea 2
NO - Norvegia 2
SI - Slovenia 2
TR - Turchia 2
ZA - Sudafrica 2
AT - Austria 1
BG - Bulgaria 1
BR - Brasile 1
HK - Hong Kong 1
HR - Croazia 1
IR - Iran 1
MX - Messico 1
MY - Malesia 1
SG - Singapore 1
TN - Tunisia 1
UA - Ucraina 1
Totale 434
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Città #
Melbourne 89
Florence 30
Dublin 25
Ashburn 11
Gavirate 9
Fairfield 8
Cambridge 7
Seattle 7
Cedar Knolls 6
Las Vegas 6
Santa Cruz 6
Anguillara Sabazia 5
Boardman 5
Buffalo 5
Southampton 5
Tokyo 5
Cairo 4
Delhi 4
Dong Ket 4
Sigtuna 4
Warsaw 4
Wilmington 4
Council Bluffs 3
Hyderabad 3
Los Angeles 3
Madison 3
Mountain View 3
Shanghai 3
University Park 3
Ann Arbor 2
Bengaluru 2
Chicago 2
Eastleigh 2
Helsinki 2
Houston 2
London 2
Mount Joy 2
Nawalgarh 2
Newcastle upon Tyne 2
Prati 2
Southend 2
Woodbridge 2
Wuhan 2
Amsterdam 1
Asenovgrad 1
Beijing 1
Bellevue 1
Berlin 1
Böblingen 1
Castelfranco di Sotto 1
Charlottesville 1
Core 1
Dallas 1
Denver 1
Des Moines 1
Duncan 1
Falkenstein 1
Halesowen 1
Hartford 1
Hong Kong 1
Huntsville 1
Izmir 1
Kitzbühel 1
Laurel 1
Lombard 1
Lund 1
Miami 1
Milan 1
Muizenberg 1
Munich 1
New Orleans 1
Nottingham 1
Providence 1
Recife 1
Reston 1
Rome 1
Santa Clara 1
Seodaemun-gu 1
Singapore 1
Stia 1
Stockholm 1
Sydney 1
Tanjong Malim 1
Trumbull 1
Totale 343
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Nome #
Design and synthesis of new adenosine receptor antagonists as neuroprotective agents, file e398c37d-f2ac-179a-e053-3705fe0a4cff 109
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
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
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
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
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
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
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
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
Development of novel pyridazinone-based adenosine receptor ligands, file e398c37d-d7f3-179a-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
Totale 446
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Categoria #
all - tutte 974
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 974
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202021 0 1 1 2 3 2 1 0 3 5 2 1
2020/202175 6 7 5 2 6 4 3 1 14 12 9 6
2021/202261 3 6 4 2 8 4 5 6 3 9 8 3
2022/2023243 6 4 17 5 12 27 30 10 17 101 14 0
2023/202434 1 0 3 2 0 4 4 5 2 13 0 0
Totale 446