IRIS
SORBA, Giovanni
 Distribuzione geografica
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Continente #
EU - Europa 1.345
NA - Nord America 1.225
AS - Asia 287
Continente sconosciuto - Info sul continente non disponibili 6
SA - Sud America 2
Totale 2.865
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Nazione #
US - Stati Uniti d'America 1.219
IE - Irlanda 405
SE - Svezia 221
DE - Germania 215
IT - Italia 187
UA - Ucraina 154
CN - Cina 121
FI - Finlandia 95
IN - India 61
HK - Hong Kong 52
TR - Turchia 32
CZ - Repubblica Ceca 20
GB - Regno Unito 17
BE - Belgio 13
IR - Iran 13
RU - Federazione Russa 10
CA - Canada 6
EU - Europa 6
VN - Vietnam 6
FR - Francia 3
GR - Grecia 3
CL - Cile 1
IQ - Iraq 1
KR - Corea 1
LT - Lituania 1
NO - Norvegia 1
PE - Perù 1
Totale 2.865
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Città #
Dublin 405
Jacksonville 296
Dearborn 156
Ann Arbor 106
Chandler 87
Piemonte 76
Wilmington 76
Hong Kong 52
Lawrence 51
Princeton 51
Beijing 49
San Mateo 49
Andover 35
Ashburn 25
Bremen 20
Brno 20
Ankara 17
Brussels 13
Hefei 9
Kunming 9
Milan 9
Nanjing 9
Helsinki 8
Kocaeli 8
Norwalk 8
Woodbridge 8
Grignasco 7
Kecioeren 7
Nanchang 7
Dong Ket 6
Formigine 6
Monmouth Junction 6
Toronto 6
Jinan 5
Noicattaro 5
Torino 5
Turin 5
Berlin 4
Chengdu 4
Fairfield 4
Houston 4
Shenyang 4
Zanjan 4
Ardabil 3
Athens 3
Düsseldorf 3
Hebei 3
Leawood 3
Xian 3
Augusta 2
Boardman 2
Cambridge 2
Cassano Magnago 2
Cerano 2
Gunzenhausen 2
Montesarchio 2
Novara 2
Occimiano 2
Pavia 2
Philadelphia 2
Redmond 2
St Petersburg 2
Wachtberg 2
Absecon 1
Albano Laziale 1
Baghdad 1
Bangalore 1
Baotou 1
Borgomanero 1
Changchun 1
Changsha 1
Chelyabinsk 1
Como 1
Des Moines 1
Falkenstein 1
Fuzhou 1
Gravedona 1
Guangzhou 1
Henderson 1
Imola 1
Jincheng 1
Kaunas 1
Kurgan 1
La Canada Flintridge 1
Las Vegas 1
Lima 1
Malakoff 1
Nanning 1
Nanping 1
Novokuznetsk 1
Quzhou 1
Sacramento 1
San Diego 1
Shanghai 1
Shaoxing 1
Simi Valley 1
Strasbourg 1
Tehran 1
Trento 1
Urbino 1
Totale 1.824
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Nome #
Inhibitors of Nicotinamide Phosphoribosyltransferase, compositions, products and uses thereof. 103
Design, synthesis, and biological evaluation of combretabenzodiazepines: a novel class of anti-tubulin agents 94
Identification of Novel Triazole-Based Nicotinamide Phosphoribosyltransferase (NAMPT) Inhibitors Endowed with Antiproliferative and Antiinflammatory Activity 94
Targeting Transient Receptor Potential Vanilloid 1 (TRPV1) Channel Softly: The Discovery of Passerini Adducts as a Topical Treatment for Inflammatory Skin Disorders 86
Capitolo 23. Istamina e agenti antistaminici 84
Synthesis and pharmacological characterization of new H2-antagonists containing NO-donor moieties, endowed with mixed antisecretory and gastroprotective activities 78
A Concise Synthesis of Pyrazole Analogues of Combretastatin A1 as Potent Antitubulin Agents 77
The Guareschi Pyridine Scaffold as a Valuable Platform for the Identification of Selective PI3K Inhibitors 76
Anti-Helicobacter pylori agents endowed with H2-antagonist properties 75
Identification of a Potent Phosphoinositide 3-Kinase Pan Inhibitor Displaying a Strategic Carboxylic Acid Group and Development of Its Prodrugs 75
In silico-driven multicomponent synthesis of 4,5- and 1,5-disubstituted imidazoles as indoleamine 2,3-dioxygenase inhibitors 74
Quinolin-4 (1h) -one derivatives as inhibitors of phosphatidylinositol 3-kinases 70
A multicomponent approach in the discovery of indoleamine 2,3-dioxygenase 1 inhibitors: Synthesis, biological investigation and docking studies 70
Groebke multicomponent reaction and subsequent nucleophilic aromatic substitution for a convenient synthesis of 3,8-diaminoimidazo[1,2-a]pyrazines as potential kinase inhibitors 69
Are 1,4- and 1,5-Disubstituted 1,2,3-Triazoles Good Pharmacophoric Groups? 69
Pyrtriazoles, a Novel Class of Store-Operated Calcium Entry Modulators: Discovery, Biological Profiling, and in Vivo Proof-of-Concept Efficacy in Acute Pancreatitis 69
A novel potent nicotinamide phosphoribosyltransferase inhibitor synthesized via click chemistry 65
Replacement of the double bond of antitubulin chalcones with triazoles and tetrazoles: synthesis and biological evaluation 63
Estrogenic analogues synthesized by click chemistry 62
Identification of a sirtuin 3 inhibitor that displays selectivity over sirtuin 1 and 2 61
Synthesis and biological evaluation of isosteric analogues of FK866, an inhibitor of NAD salvage 59
Design, synthesis, and biological evaluation of new (2E,6E)-10-(dimethylamino)-3,7-dimethyl-2,6-decadien-1-ol ethers as inhibitors of human and Trypanosoma cruzi oxidosqualene cyclase 58
Click chemistry reactions in medicinal chemistry: applications of the 1,3-dipolar cycloaddition between azides and alkynes 57
Replacement of the lactone moiety on podophyllotoxin and steganacin analogues with a 1,5-disubstituted 1,2,3-triazole via ruthenium-catalyzed click chemistry 56
Computer-aided identification, design and synthesis of a novel series of compounds with selective antiviral activity against chikungunya virus 56
Solution-phase parallel synthesis and biological evaluation of combretatriazoles 54
A new furoxan NO-donor rabeprazole derivative and related compounds 54
Essential role of the p110β subunit of phosphoinositide 3-OH kinase in male fertility 52
Triazole-modified histone deacetylase inhibitors as a rapid route to drug discovery 52
Synthesis and cytotoxic evaluation of combretafurans, potential scaffolds for dual-action antitumoral agents 52
ZINClick: A Database of 16 Million Novel, Patentable, and Readily Synthesizable 1,4-Disubstituted Triazoles 52
Synthesis and cytotoxic evaluation of combretafurazans 50
“Identification of the first selective Sirt3 inhibitor”, 49
[3-(1H-Imidazol-4-yl)propyl]guanidines containing furoxan moieties: a New Class of H3-Antagonists endowed with NO-Donor properties 47
De novo computer-aided design of novel antiviral agents 47
“Synthesis and in vitro evaluation of tetrasubstituted pyridines as potential PI3Ks inhibitors” 46
Furoxan Analogues of the Histamine H3 receptor antagonist imoproxifan and related furazan derivatives 45
Synthesis, biological evaluation, and molecular docking of Ugi products containing a zinc-chelating moiety as novel inhibitors of histone deacetylase 45
A practical synthesis of 5-aroyl-1-aryltetrazoles using an Ugi-like 4-component reaction followed by a biomimetic transamination 45
Molecular Field Analysis and 3D-Quantitative Structure-Activity Relationship Studies (MFA 3D-QSAR) of Bile Acids and Fexaramine Derivatives as Agonists of Farnesoid X Receptor (FXR) 43
Medicinal chemistry of combretastatin A4: present and future directions 42
Synthesis and anti-Helicobacter pylori properties of NO-donor/metronidazole hybrids and related compounds 42
The tubulin colchicine domain: a molecular modelling perspective 42
In search of novel antitubulin agents: synthesis of 1-aryl-5-aroyl tetrazoles by an Ugi 4-CR/hydrogenolysis/transamination reaction 40
Role of the nicotinic acid group in NAADP receptor selectivity 37
Synthesis and antimalarial activities of some furoxan sulfones and related furazans 37
Synthesis and biological evaluation of combretatriazoles 37
NO-donors: focus on furoxan derivatives 35
Rapid synthesis of triazole-modified resveratrol analogues via click chemistry 34
Icilio Guareschi and his amazing “1897 reaction” 34
Unsymmetrically substituted furoxans. Part 18. Smiles rearrangement in furoxan systems and in related furazans 33
Totale 2.946
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Categoria #
all - tutte 12.448
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 12.448
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201910 0 0 0 0 0 0 0 0 0 0 7 3
2019/2020641 2 3 56 5 97 93 143 34 58 83 67 0
2020/2021399 57 3 52 8 51 30 53 5 56 25 53 6
2021/2022376 23 6 44 48 19 1 40 8 20 22 50 95
2022/2023869 59 40 64 17 60 87 29 51 416 3 23 20
2023/2024181 22 16 23 13 45 0 54 4 1 0 3 0
Totale 2.946