ROMAGNOLI, Romeo
 Distribuzione geografica
Continente #
EU - Europa 365
NA - Nord America 303
AS - Asia 60
AF - Africa 17
OC - Oceania 2
SA - Sud America 1
Totale 748
Nazione #
US - Stati Uniti d'America 286
IT - Italia 233
SE - Svezia 63
CA - Canada 17
CZ - Repubblica Ceca 12
EG - Egitto 12
IN - India 12
HK - Hong Kong 10
PL - Polonia 10
RU - Federazione Russa 10
BE - Belgio 7
DE - Germania 7
KR - Corea 7
VN - Vietnam 7
CH - Svizzera 5
IR - Iran 5
FR - Francia 3
GB - Regno Unito 3
ID - Indonesia 3
NG - Nigeria 3
NL - Olanda 3
TJ - Tagikistan 3
AU - Australia 2
DK - Danimarca 2
IL - Israele 2
IQ - Iraq 2
MO - Macao, regione amministrativa speciale della Cina 2
MY - Malesia 2
TR - Turchia 2
CN - Cina 1
GR - Grecia 1
HR - Croazia 1
HU - Ungheria 1
IE - Irlanda 1
IS - Islanda 1
JP - Giappone 1
MA - Marocco 1
NO - Norvegia 1
PE - Perù 1
SI - Slovenia 1
TH - Thailandia 1
ZA - Sudafrica 1
Totale 748
Città #
Ferrara 97
Stockholm 63
Santa Cruz 32
Fairfield 24
Palermo 24
Ashburn 19
Ferrara di Monte Baldo 17
Mistretta 14
Boardman 12
Seattle 11
Camerino 10
Chicago 9
Des Moines 9
Beauharnois 8
Buffalo 8
Houston 8
Dong Ket 7
Cairo 6
Central 6
Lake Forest 6
Los Angeles 6
Warsaw 6
Ann Arbor 5
Padova 5
Saint Petersburg 5
Bologna 4
Bracebridge 4
Crugers 4
Henderson 4
Messancy 4
New York 4
Sesto Fiorentino 4
Trento 4
Alexandria 3
Central District 3
Clearwater 3
Dallas 3
Dehradun 3
Fleming Island 3
Las Vegas 3
Parsippany 3
Somoniyon 3
Wilmington 3
Ahmedabad 2
Ahoada 2
Castelraimondo 2
Catania 2
Council Bluffs 2
Delhi 2
Este 2
Giza 2
Jakarta 2
Lebbeke 2
Legnica 2
Lille 2
Lincoln 2
Ludhiana 2
Macao 2
Melbourne 2
Milan 2
Montreal 2
Reston 2
Rome 2
Saint Louis 2
San Francisco 2
Seoul 2
Amsterdam 1
Athens 1
Atlanta 1
Baghdad 1
Bagno a Ripoli 1
Ballyhaise 1
Ban Chan 1
Bassano Del Grappa 1
Bellevue 1
Bethesda 1
Brooklyn 1
Cambridge 1
Casablanca 1
Chambéry 1
Chignolo d'Isola 1
Clarks Summit 1
Copenhagen 1
Damietta 1
Denver 1
Falkenstein 1
Geneva 1
Guarda Veneta 1
Hatfield 1
Herndon 1
Iesi 1
Irvine 1
Isfahan 1
Istanbul 1
Izmir 1
Jinhua 1
Kashan 1
Koedijk 1
Kongens Lyngby 1
Kuala Lumpur 1
Totale 559
Nome #
A3 Adenosine Receptors as Modulators of Inflammation: From Medicinal Chemistry to Therapy, file e309ade2-c09e-3969-e053-3a05fe0a2c94 132
Effects of Pimozide Derivatives on pSTAT5 in K562 Cells, file e309ade3-a2a0-3969-e053-3a05fe0a2c94 66
Design and Synthesis of Potent in Vitro and in Vivo Anticancer Agents Based on 1-(3’,4’,5’-Trimethoxyphenyl)-2-Aryl-1H-Imidazole, file e309ade0-d8e0-3969-e053-3a05fe0a2c94 54
Design, synthesis, in vitro antiproliferative activity and apoptosis-inducing studies of 1-(3',4',5'-trimethoxyphenyl)-3-(2'-alkoxycarbonylindolyl)-2-propen-1-one derivatives obtained by a molecular hybridisation approach, file e309ade1-e366-3969-e053-3a05fe0a2c94 51
Synthesis and Biological Evaluation of 2-Methyl-4,5-Disubstituted Oxazoles as a Novel Class of Highly Potent Antitubulin Agents, file e309ade1-5591-3969-e053-3a05fe0a2c94 49
Synthesis and biological evaluation of alpha-bromoacryloylamido indolyl pyridinyl propenones as potent apoptotic inducers in human leukaemia cells, file e309ade1-ce26-3969-e053-3a05fe0a2c94 37
Design, synthesis and biological evaluation of 3-substituted-2-oxindole hybrid derivatives as novel anticancer agents, file e309ade3-9be9-3969-e053-3a05fe0a2c94 35
Design, synthesis and antiproliferative activity of novel heterobivalent hybrids based on imidazo[2,1-b][1,3,4]thiadiazole and imidazo[2,1-b][1,3]thiazole scaffolds, file e309ade3-94ea-3969-e053-3a05fe0a2c94 22
Design, synthesis and biological evaluation of novel vicinal diaryl-substituted 1H-Pyrazole analogues of combretastatin A-4 as highly potent tubulin polymerization inhibitors, file e309ade5-37c9-3969-e053-3a05fe0a2c94 22
Current status of A1 adenosine receptor allosteric enhancers, file e309ade3-dddf-3969-e053-3a05fe0a2c94 16
Design, Synthesis, and Biological Evaluation of 6-Substituted Thieno[3,2-d]pyrimidine Analogues as Dual Epidermal Growth Factor Receptor Kinase and Microtubule Inhibitors, file e309ade4-e60b-3969-e053-3a05fe0a2c94 14
Positive allosteric modulation of A1 adenosine receptors as a novel and promising therapeutic strategy for anxiety, file e309ade3-b282-3969-e053-3a05fe0a2c94 12
Design, synthesis, in vitro, and in vivo anticancer and antiangiogenic activity of novel 3-arylaminobenzofuran derivatives targeting the colchicine site on tubulin, file e309ade3-956d-3969-e053-3a05fe0a2c94 11
Design, synthesis and biological evaluation of 2-alkoxycarbonyl-3-anilinoindoles as a new class of potent inhibitors of tubulin polymerization, file e309ade2-8100-3969-e053-3a05fe0a2c94 9
Synthesis and biological evaluation of new antitubulin agents containing 2-(30,40,50-trimethoxyanilino)-3,6-disubstituted-4,5,6,7-tetrahydrothieno[2,3-c]pyridine Scaffold, file e309ade2-9b91-3969-e053-3a05fe0a2c94 9
Design, synthesis, and biological evaluation of novel 2-((2-(4-(substituted)phenylpiperazin-1-yl)ethyl)amino)-5'-N-ethylcarboxamidoadenosines as potent and selective agonists of the A2A adenosine receptor, file e309ade3-cfd0-3969-e053-3a05fe0a2c94 9
Design, synthesis, in vitro and in vivo biological evaluation of 2-amino-3-aroylbenzo[b]furan derivatives as highly potent tubulin polymerization inhibitors, file 2ffd3d25-7e35-4ed6-981b-d7480817070d 8
null, file e309ade0-cb9c-3969-e053-3a05fe0a2c94 8
The new iodoacetamidobenzofuran derivative TR120 decreases STAT5 expression and induces antitumor effects in imatinib-sensitive and imatinib-resistant BCR-ABL-expressing leukemia cells, file e309ade1-530f-3969-e053-3a05fe0a2c94 8
2-Alkoxycarbonyl-3-arylamino-5-substituted thiophenes as a novel class of antimicrotubule agents: Design, synthesis, cell growth and tubulin polymerization inhibition, file e309ade3-9385-3969-e053-3a05fe0a2c94 8
Design, synthesis, in vitro and in vivo biological evaluation of 2-amino-3-aroylbenzo[b]furan derivatives as highly potent tubulin polymerization inhibitors, file 8195c995-8220-43c0-9993-5063de1a7e9e 7
Positive allosteric modulation of A1 adenosine receptors as a novel and promising therapeutic strategy for anxiety, file e309ade1-1c25-3969-e053-3a05fe0a2c94 7
Anticancer activity of novel hybrid molecules containing 5-benzylidene thiazolidine-2,4-dione, file e309ade0-46f7-3969-e053-3a05fe0a2c94 6
A3 Adenosine Receptors as Modulators of Inflammation: From Medicinal Chemistry to Therapy, file e309ade1-fb1d-3969-e053-3a05fe0a2c94 6
The Detrimental Action of Adenosine on Glutamate-Induced Cytotoxicity in PC12 Cells Can Be Shifted towards a Neuroprotective Role through A1AR Positive Allosteric Modulation, file e309ade3-0748-3969-e053-3a05fe0a2c94 6
Novel iodoacetamido benzoheterocyclic derivatives with potent antileukemic activity are inhibitors of STAT5 phosphorylation, file e309ade3-8d6b-3969-e053-3a05fe0a2c94 6
Synthesis and biological evaluation of a new series of 2-amino-3-aroyl thiophene derivatives as agonist allosteric modulators of the A1 adenosine receptor. A position-dependent effect study, file e309ade3-ffd2-3969-e053-3a05fe0a2c94 6
Design, synthesis, in vitro, and in vivo anticancer and antiangiogenic activity of novel 3-arylaminobenzofuran derivatives targeting the colchicine site on tubulin, file e309ade0-5d19-3969-e053-3a05fe0a2c94 5
One-pot reaction to obtain N,N'-disubstituted guanidines of pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyrimidine scaffold as human A3 adenosine receptor antagonists, file e309ade0-7e5c-3969-e053-3a05fe0a2c94 5
7-Oxo-[1,4]oxazino[2,3,4-ij]quinoline-6-carboxamides as Selective CB2 Cannabinoid Receptor Ligands: Structural Investigations around a Novel Class of Full Agonists, file e309ade0-ccd8-3969-e053-3a05fe0a2c94 5
A3 adenosine receptor antagonists: History and future perspectives, file e309ade1-88ae-3969-e053-3a05fe0a2c94 5
Synthesis and biological evaluation of 2-substituted benzyl-/phenylethylamino-4-amino-5-aroylthiazoles as apoptosis-inducing anticancer agents, file e309ade2-9d61-3969-e053-3a05fe0a2c94 5
Thioridazine requires calcium influx to induce MLL-AF6-rearranged AML cell death, file e309ade2-b269-3969-e053-3a05fe0a2c94 5
Synthesis and biological effects of novel 2-amino-3-(4-chlorobenzoyl)-4- substituted thiophenes as allosteric enhancers of the A1 adenosine receptor, file e309ade2-bea4-3969-e053-3a05fe0a2c94 5
3-Aryl/Heteroaryl-5-amino-1-(3′,4′,5′-trimethoxybenzoyl)-1,2,4-triazoles as antimicrotubule agents. Design, synthesis, antiproliferative activity and inhibition of tubulin polymerization, file e309ade5-0e62-3969-e053-3a05fe0a2c94 5
Thioridazine requires calcium influx to induce MLL-AF6-rearranged AML cell death, file bfee7d23-bb98-448f-90ef-5c2ad2dc254a 4
Allosteric modulation of A1-adenosine receptor: A review, file e309ade0-4035-3969-e053-3a05fe0a2c94 4
Design, synthesis, and biological evaluation of novel 2-((2-(4-(substituted)phenylpiperazin-1-yl)ethyl)amino)-5'-N-ethylcarboxamidoadenosines as potent and selective agonists of the A2A adenosine receptor, file e309ade0-cb8b-3969-e053-3a05fe0a2c94 4
7-Substituted-pyrrolo[3,2-d]pyrimidine-2,4-dione derivatives as antagonists of the transient receptor potential ankyrin 1 (TRPA1) channel: A promising approach for treating pain and inflammation, file e309ade0-cb90-3969-e053-3a05fe0a2c94 4
Synthesis and Biological Evaluation of 2-(Alkoxycarbonyl)-3-Anilinobenzo[b]thiophenes and Thieno[2,3-b]pyridines as New Potent Anticancer Agents, file e309ade2-beae-3969-e053-3a05fe0a2c94 4
Synthesis and Biological Evaluation of Highly Active 7-Anilino Triazolopyrimidines as Potent Antimicrotubule Agents, file e309ade5-675e-3969-e053-3a05fe0a2c94 4
Water-Soluble Pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyrimidines as Human A3 Adenosine Receptor Antagonists, file e309ade0-2fe0-3969-e053-3a05fe0a2c94 3
Synthesis and biological evaluation of 2-amino-3-(4-chlorobenzoyl)-4-[(4- arylpiperazin-1-yl)methyl]-5-substituted-thiophenes. Effect of the 5-modification on allosteric enhancer activity at the A1 adenosine receptor, file e309ade0-3ba0-3969-e053-3a05fe0a2c94 3
null, file e309ade0-a439-3969-e053-3a05fe0a2c94 3
The Novel Antitubulin Agent TR-764 Strongly Reduces Tumor Vasculature and Inhibits HIF-1α Activation, file e309ade1-2364-3969-e053-3a05fe0a2c94 3
null, file e309ade1-2d29-3969-e053-3a05fe0a2c94 3
2-Alkoxycarbonyl-3-arylamino-5-substituted thiophenes as a novel class of antimicrotubule agents: Design, synthesis, cell growth and tubulin polymerization inhibition, file e309ade1-8e8e-3969-e053-3a05fe0a2c94 3
Design, synthesis and biological evaluation of novel vicinal diaryl-substituted 1H-Pyrazole analogues of combretastatin A-4 as highly potent tubulin polymerization inhibitors, file e309ade2-4421-3969-e053-3a05fe0a2c94 3
Synergistic effects of the combined treatment of U251 and T98G glioma cells with an anti-tubulin tetrahydrothieno[2,3-c]pyridine derivative and a peptide nucleic acid targeting miR-221-3p, file e309ade4-d2eb-3969-e053-3a05fe0a2c94 3
Synthesis and Biological Evaluation of Novel Allosteric Enhancers of the A1 Adenosine Receptor Based on 2-Amino-3-(4’-Chlorobenzoyl)-4-Substituted-5-Arylethynyl Thiophene, file e309ade0-415a-3969-e053-3a05fe0a2c94 2
Concise Synthesis and Biological Evaluation of 2-Aroyl-5-Amino Benzo[b]thiophene Derivatives As a Novel Class of Potent Antimitotic Agents, file e309ade0-45e8-3969-e053-3a05fe0a2c94 2
null, file e309ade0-46ea-3969-e053-3a05fe0a2c94 2
Synthesis and biological evaluation of a new series of 2-amino-3-aroyl thiophene derivatives as agonist allosteric modulators of the A1 adenosine receptor. A position-dependent effect study, file e309ade0-6f37-3969-e053-3a05fe0a2c94 2
Current status of A1 adenosine receptor allosteric enhancers, file e309ade0-7edc-3969-e053-3a05fe0a2c94 2
Pyrazole phenylcyclohexylcarbamates as inhibitors of human fatty acid amide hydrolases (FAAH), file e309ade0-c408-3969-e053-3a05fe0a2c94 2
null, file e309ade0-c45d-3969-e053-3a05fe0a2c94 2
Synthesis and growth inhibition activity of alpha-bromoacrylic heterocyclic and benzoheterocyclic derivatives of distamycin A modified on the amidino moiety, file e309ade0-f557-3969-e053-3a05fe0a2c94 2
Design, synthesis and biological evaluation of 3-substituted-2-oxindole hybrid derivatives as novel anticancer agents, file e309ade1-582b-3969-e053-3a05fe0a2c94 2
TR-644 a novel potent tubulin binding agent induces impairment of endothelial cells function and inhibits angiogenesis, file e309ade2-c480-3969-e053-3a05fe0a2c94 2
A Facile Synthesis of Diaryl Pyrroles Led to the Discovery of Potent Colchicine Site Antimitotic Agents, file e309ade3-5f05-3969-e053-3a05fe0a2c94 2
Effects of Pimozide Derivatives on pSTAT5 in K562 Cells, file e309ade3-99a9-3969-e053-3a05fe0a2c94 2
Apoptosis Pathways Triggered by a Potent Antiproliferative Hybrid Chalcone on Human Melanoma Cells, file e309ade4-f1dc-3969-e053-3a05fe0a2c94 2
Cinnamic acid derivatives linked to arylpiperazines as novel potent inhibitors of tyrosinase activity and melanin synthesis, file e309ade5-401c-3969-e053-3a05fe0a2c94 2
Synergistic Effects of A Combined Treatment of Glioblastoma U251 Cells with An Anti-miR-10b-5p Molecule and An AntiCancer Agent Based on 1-(3',4',5'-Trimethoxyphenyl)-2-Aryl-1H-Imidazole Scaffold, file f887e2be-398f-43ba-b843-928abdb89536 2
Design, Synthesis and Biological Investigation of 2-Anilino Triazolopyrimidines as Tubulin Polymerization Inhibitors with Anticancer Activities, file 649693de-449a-45ff-b25c-9e1f5e793355 1
Design, synthesis, in vitro and in vivo biological evaluation of 2-amino-3-aroylbenzo[b]furan derivatives as highly potent tubulin polymerization inhibitors, file 76b1ec24-1e88-4d08-aded-41e6b2c8aca9 1
null, file e309ade0-4754-3969-e053-3a05fe0a2c94 1
null, file e309ade0-47e1-3969-e053-3a05fe0a2c94 1
null, file e309ade0-485d-3969-e053-3a05fe0a2c94 1
Novel iodoacetamido benzoheterocyclic derivatives with potent antileukemic activity are inhibitors of STAT5 phosphorylation, file e309ade0-a3bb-3969-e053-3a05fe0a2c94 1
null, file e309ade0-d506-3969-e053-3a05fe0a2c94 1
Inhibition of NF-kB/DNA Interactions and HIV-1 LTR Directed Transcription by Hybrid Molecules Containing Pyrrolo [2,1-c] [1,4] Benzodiazepine (PBD) and Oligopyrrole Carriers, file e309ade0-eb05-3969-e053-3a05fe0a2c94 1
Binding of hybrid molecules containing pyrrolo [2,1-c][1,4]benzodiazepine (PBD) and oligopyrrole carriers to the human immunodeficiency type 1 virus TAR-RNA, file e309ade0-eb86-3969-e053-3a05fe0a2c94 1
Design, synthesis and biological activity of 5-fluorouracil-distamycin hybrids, file e309ade0-ec0a-3969-e053-3a05fe0a2c94 1
Design, synthesis and growth inhibition activity of bis-epoxyethyl derivatives of stallimycin modified on the amidino moiety, file e309ade0-edcf-3969-e053-3a05fe0a2c94 1
Bis-epoxyethyl derivatives of distamycin A modified on the amidino moiety: Induction of production of fetal hemoglobin in human erythroid precursor cells, file e309ade0-f42c-3969-e053-3a05fe0a2c94 1
Benzoyl nitrogen mustard derivatives of benzoheterocyclic analogues of netropsin: Synthesis and biological activity, file e309ade0-f559-3969-e053-3a05fe0a2c94 1
3-Aryl/Heteroaryl-5-amino-1-(3′,4′,5′-trimethoxybenzoyl)-1,2,4-triazoles as antimicrotubule agents. Design, synthesis, antiproliferative activity and inhibition of tubulin polymerization, file e309ade1-d9a9-3969-e053-3a05fe0a2c94 1
Design, Synthesis, and Biological Evaluation of 6-Substituted Thieno[3,2-d]pyrimidine Analogues as Dual Epidermal Growth Factor Receptor Kinase and Microtubule Inhibitors, file e309ade2-2424-3969-e053-3a05fe0a2c94 1
A Facile Synthesis of Diaryl Pyrroles Led to the Discovery of Potent Colchicine Site Antimitotic Agents, file e309ade3-5f06-3969-e053-3a05fe0a2c94 1
Concise synthesis and biological evaluation of 2-Aryl-3-Anilinobenzo[b]thiophene derivatives as potent apoptosis-inducing agents, file e309ade4-2979-3969-e053-3a05fe0a2c94 1
Antimicrobial and antitumor activity of N-heteroimmine-1,2,3-dithiazoles and their transformation in triazolo-, imidazo-, and pyrazolopirimidines, file e309ade4-f1bd-3969-e053-3a05fe0a2c94 1
Totale 760
Categoria #
all - tutte 2502
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 5
Totale 2507


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2017/20182 0000 00 00 2000
2018/20191 0000 00 10 0000
2019/20207 0000 05 00 0200
2020/202171 0005 10 213 11101217
2021/2022205 181215 1117 2411 1575133
2022/2023418 40495929 6147 2282 29000
Totale 760