Catalogo dei prodotti della ricerca

ARTICO, Marino
 Distribuzione geografica
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Continente #
NA - Nord America 4.640
EU - Europa 1.423
AS - Asia 774
AF - Africa 115
SA - Sud America 53
OC - Oceania 4
Continente sconosciuto - Info sul continente non disponibili 1
Totale 7.010
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Nazione #
US - Stati Uniti d'America 4.584
IT - Italia 466
SG - Singapore 304
SE - Svezia 301
IN - India 261
UA - Ucraina 229
CN - Cina 197
FI - Finlandia 138
TG - Togo 110
DE - Germania 101
CA - Canada 55
AR - Argentina 47
GB - Regno Unito 47
RU - Federazione Russa 29
RO - Romania 27
IE - Irlanda 21
BG - Bulgaria 18
BE - Belgio 11
DK - Danimarca 10
NL - Olanda 5
CH - Svizzera 3
CO - Colombia 3
EE - Estonia 3
FR - Francia 3
IR - Iran 3
AU - Australia 2
CL - Cile 2
HU - Ungheria 2
NZ - Nuova Zelanda 2
ZA - Sudafrica 2
AE - Emirati Arabi Uniti 1
AT - Austria 1
BR - Brasile 1
CY - Cipro 1
CZ - Repubblica Ceca 1
ES - Italia 1
EU - Europa 1
GH - Ghana 1
GR - Grecia 1
HK - Hong Kong 1
HR - Croazia 1
ID - Indonesia 1
KR - Corea 1
MA - Marocco 1
ME - Montenegro 1
MX - Messico 1
MY - Malesia 1
NO - Norvegia 1
PK - Pakistan 1
PL - Polonia 1
SC - Seychelles 1
SK - Slovacchia (Repubblica Slovacca) 1
TR - Turchia 1
TW - Taiwan 1
Totale 7.010
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Città #
Fairfield 716
Chandler 445
Woodbridge 379
Ashburn 321
Houston 259
Seattle 231
Cambridge 216
Wilmington 213
Singapore 206
Fasano 163
Ann Arbor 155
Princeton 133
Dearborn 129
Plano 127
Lomé 110
Rome 100
Jacksonville 93
Beijing 74
Boston 73
Lawrence 69
Santa Clara 68
San Paolo di Civitate 64
Millbury 61
San Diego 49
Des Moines 46
Federal 46
Fremont 42
Boardman 41
Ottawa 33
Andover 28
Grafing 25
Dublin 21
Toronto 19
Norwalk 18
Sofia 18
New York 17
Kunming 16
Falls Church 15
Nanjing 15
Bremen 14
Hefei 14
Los Angeles 13
Moscow 13
Helsinki 12
Mannheim 12
Brussels 11
Frankfurt am Main 11
Copenhagen 10
Salerno 9
Washington 9
Bühl 7
Falkenstein 7
Galdo 7
Garching 7
Shenyang 7
Guangzhou 6
London 6
Indiana 5
Jinan 5
Nanchang 5
Shanghai 5
Dallas 4
Milan 4
Redmond 4
Redwood City 4
Weihai 4
Xian 4
Auburn Hills 3
Bern 3
Changsha 3
Chengdu 3
Fisciano 3
Hangzhou 3
Philadelphia 3
San Mateo 3
Stockholm 3
Tallinn 3
Zhongxin 3
Auckland 2
Besana In Brianza 2
Bogotá 2
Chicago 2
Delhi 2
Florence 2
Fuzhou 2
Herndon 2
Kiskunhalas 2
Las Vegas 2
Minturno 2
Mumbai 2
Munich 2
Nanning 2
Napoli 2
Nuremberg 2
San Francisco 2
Trumbull 2
Villeneuve 2
Wuhan 2
Zhengzhou 2
Amsterdam 1
Totale 5.149
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Nome #
Potential Antitumor Agents. IV. Pyrrole Analogues of Oncodazole. 113
1-[(3-Aryloxy-3-aryl)propyl]-2H-imidazoles, new imidazoles with potent activity against Candida albicans and dermatophytes. Synthesis, structure-activity relationship, and molecular modeling studies 104
Bovine Serum Amine Oxidase: Half-Site Reactivity with Phenylhydrazine, Semicarbazide and Aromatic Hydrazides. 96
5-Alkyl-6-benzyl-2-(2-oxo-2-phenylethylsulfanyl)pyrimidin-4(3H)-ones, a series of anti-HIV-1 agents of the dihydro-alkoxy-benzyl-oxopyrimidine family with peculiar structure-activity relationship profile. 95
(((thienylcarbonyl)alkyl)oxy)phenyl)- and (((pyrrylcarbonyl)alkyl)oxy)phenyl)oxazoline derivatives with potent and selective antihuman rhinovirus activity 93
Novel 1-[2-(Diarylmethoxy)ethyl]-2-methyl-5-nitroimidazoles as HIV-1 Non-Nucleoside Reverse Transcriptase Inhibitors. A Structure-Activity Relationship Investigation. 93
Arylthioindole Inhibitors of Tubulin Polymerization. 3. Biological Evaluation, Structure−Activity Relationships and Molecular Modeling Studies 92
Research on antibacterial and antifungal agents. 16. Synthesis and antifungal activities of 1-[α-(1-naphthyl)benzyl]imidazole derivatives and related 2-naphthyl isomers 85
5-Alkyl-2-alkylamino-6-(2,6-difluorophenylalkyl)-3,4-dihydropyrimidin-4(3H)-ones, a new series of potent, broad-spectrum non-nucleoside reverse transcriptase inhibitors belonging to the DABO family 85
THE USE OF COPPER-(II) BROMIDE AND N-BROMOSUCCINIMIDE IN THE BROMINATION OF 1-(1-METHYL-1H-PYRROL-2-YL)-2-PHENYLETHANONE 84
6-(3-methylbenzyl)-2-(2-methylpropyl)thio-4(3h)-pyrimidinone (dabo 622) 83
3-(1H-Pyrrol-2-yl)-2-oxazolidinones as novel monoamine oxidase type A inhibitors. 83
5-alkyl-2-(alkylthio)-6-(2,6-dihalophenylmethyl)-3,4-dihydropyrimidin-4(3h)-ones: novel potent and selective dihydro-alkoxy-benzyl-oxopyrimidine derivatives 83
Arylthiopyrrole (ATP) Derivatives as Non-Nucleoside HIV-1 Reverse Transcriptase Inhibitors 82
3,4-Dihydro-2-alkoxy-6-benzyl-oxopyrimidines (DABOs): Development of a Potent Class of Non-nucleoside Reverse Transcriptase Inhibitors 82
Analoghi azolici della fluoxetina, una nuova classe di agenti antifungini 81
Antimycobacterial Pyrroles: Synthesis, Anti-Mycobacterium tuberculosis Activity and QSAR Studies. 81
HIV-1 Integrase Inhibitors that Block HIV-1 Replication in Infected Cells. Planning Synthetic Derivatives from Natural Products 81
Design, molecular modeling, synthesis, and anti-HIV-1 activity of new indolyl aryl sulfones. Novel derivatives of the indole-2-carboxamide 79
Arylthioindoles, potent inhibitors of tubulin polymerization. 76
N-Benzil e N-Propargil 1H-Pirrolo-2-carbossiamidi, Semplici ed Efficaci Inibitori delle Monoamino Ossidasi. 75
Antibacterial and antifungal agents. XV. Synthesis and antifungal activity of structural analogues of bifonazole and ketoconazole. 74
6-Aryl-2,4-dioxo-5-hexenoic Acids, Novel Integrase Inhibitors Active Against HIV-1 Multiplication in Cell-Based Assays. 74
Arylthioindoles, Potent Inhibitors of Tubulin Polymerization. 73
Indole nucleus as a selected pharmacophore for the design of novel highly anti-HIV RT inhibitors and also capable to inhibit tumor cell replication. 72
1-[4-(4-Chlorophenyl)-1H-pyrrol-3-yl](2,4-dichlorophenyl)methyl-1H-imidazole (RDS 416) 72
2,6-Bis(3,4,5-trihydroxybenzylydene) derivatives of cyclohexanone: novel potent HIV-1 integrase inhibitors that prevent HIV-1 multiplication in cell-based assays 70
New 6-nitroquinolones: synthesis and antimicrobial activities 70
Potential Antitumor Agents. III. Synthesis of Pyrazolo[3,4-e]pyrrolo[3,4-g]indolizine and 1H-Pyrazolo[3,4-e]indolizine Derivatives. 70
N-[4-(1,1'-Biphenyl)methyl]-4-(4-thiomorpholinylmethyl)benzenamines as non-oxazolidinone analogues of antimycobacterial U-100480. 69
Imidazole Analogues of Fluoxetine, a Novel Class of Anti-Candida Agents. 69
Structure-activity relationship studies on potential non-nucleoside DABO-like inhibitors of HIV-1 reverse transcriptase. 69
AROMATIC HYDRAZIDES AS SPECIFIC INHIBITORS OF BOVINE SERUM AMINE OXIDASE 68
Synthesis and biochemical evaluation of (R)-5-acyloxymethyl- and (S)-5-acylaminomethyl-3-(1H-pyrrol-1-yl)-2-oxazolidinones as new anti-monoamine oxidase (anti-MAO) agents. 68
Docking and 3-D QSAR Studies on Indolyl Aryl Sulfones. Binding Mode Exploration at the HIV-1 Reverse Transcriptase Non-Nucleoside Binding Site and Design of Highly Active N-(2-Hydroxyethyl)carboxamide and N-(2-Hydroxyethyl)carbohydrazide Derivatives. 68
Anti-HIV-1 Activity of Pyrryl Aryl Sulfone (PAS) Derivatives: Synthesis and SAR Studies of Novel Esters and Amides at the Position 2 of the Pyrrole Nucleus. 67
Arylketotetramethylene analogues of disoxaril with anti-human rhinovirus 14 activity 67
Synthesis and biological properties of novel 2-aminopyrimidin-4(3H)-ones highly potent against HIV-1 mutant strains 67
Pyrrolnitrin and Related Pyrroles Endowed with Antibacterial Activities against Mycobacterium Tuberculosis. 66
Arylthiopyrrole (AThP) Derivatives as Non-Nucleoside HIV-1 Reverse Transcriptase Inhibitors. Synthesis, Structure-Activity Relationships and Docking Studies. Part 1. 66
Computer-Aided Design, Synthesis, and Anti-HIV-1 Activity in Vitro of 2-Alkylamino-6-[1-(2,6-difluorophenyl)alkyl]-3,4-dihydro-5-alkylpyrimidin-4(3H)-ones as Novel Potent Non-Nucleoside Reverse Transcriptase Inhibitors, Also Active Against the Y181C Variant 66
High potency of indolyl aryl sulfone nonnucleoside inhibitors towards drug-resistant human immunodeficiency virus type 1 reverse transcriptase mutants is due to selective targeting of different mechanistic forms of the enzyme 66
Methyl-2-thienylketopolymethyleneoxyphenyl derivatives of alkyl-substituted 4,5-dihydro-oxazoles with anti-human picornavirus activity. 66
6-[1-(2,6-difluorophenyl)ethyl]pyrimidinones antagonize cell proliferation and induce cell differentiation by inhibiting (a nontelomeric) endogenous reverse transcriptase 66
6-Alkylthio-4-[1-(2,6-difluorophenyl)alkyl]-1H-[1,3,5]triazin-2-ones (ADATs): Novel Regulators of Cell Differentiation and Proliferation 65
Enantioselective liquid Chromatography of C3-chiral 2,3-dihydro-1,2,5-benzothiadiazepin-4(5H)-one and thione 1,1-dioxides on polyacrylamide- and polysaccaride-based chiral stationary phases 64
Antifungal estrogen-like imidazoles. Synthesis and antifungal activities of thienyl and 1H-pyrrolyl derivatives of 1-aryl-2-(1H-imidazol-1-yl)ethane. 64
Geometrically and Conformationally Restrained Cinnamoyl-Compounds as Inhibitors of HIV-1 Integrase: Synthesis, Biological Evaluation and Molecular Modeling 64
synthesis and antiviral activity of new 3,4-dihydro-2-alkoxy-6-benzyl-4-oxopyrimidines (DABOs), specific inhibitors of human immunodeficiency virus type 1 64
Pyrrolobenzodiazepines with antinociceptive activity: synthesis and pharmacological activities. 63
HIV-1 Integrase Inhibitors That Block HIV-1 Replication in Infected Cells: Planning Synthetic Derivatives from Natural Products. 62
Structure based design, synthesis and biological evaluation of novel pyrrolyl aryl sulfones (PASs) active at nanomolar concentration as HIV-1 non nucleoside reverse transcriptase inhibitors. 62
Simple but highly effective three-dimensional chemical-feature-based pharmacophore model for diketo acid derivatives as hepatitis C virus RNA-dependent RNA polymerase inhibitors 62
Does the 2-methylthiomethyl substituent really confer high anti-HIV-1 activity to S-DABOs ? 61
New Arylthioindoles: Potent Inhibitors of Tubulin Polymerization. 2. Structure-Activity Relationships and Molecular Modeling Studies. 61
Anti-HIV-1 NNRT Agents: Acylamino Pyrryl Aryl Sulfones (APASs) as Truncated Analogues of Tricyclic PBTDs. 61
Synthesis of Biologically Active Azoles via TosMIC 61
Indolyl Aryl Sulfones as HIV-1 Non-Nucleoside Reverse Transcriptase Inhibitors: Role of Two Halogen Atoms at the Indole Ring in Developing New Analogues with Improved Antiviral Activity 61
ricerche su composti antibatterici ed antifungini. Nota VIII - sintesi ed attività antifungina di derivati pirrolici correlati con la tricostatina A 60
Reactions of 6-benzyl-5-methyl-2-(methylsulfanyl)pyrimidin-4(3H)-one with aliphatic and aliphatic-aromatic amines 60
Pyrrolo[1,2-b][1,2,5]benzothiadiazepines (PBTDs): A New Class of Agents with High Apoptotic Activity in Chronic Myelogenous Leukemia K562 Cells and in Cells from Patients at Onset and Who Were Imatinib-Resistant. 60
Novel Indolyl Aryl Sulfones Active against HIV-1 Carrying NNRTI Resistance Mutations: Synthesis and SAR Studies. 60
Structure-Based Design, Synthesis and Biological Evaluation of Conformationally Restricted Novel 2-Alkylthio-6-[1-(2,6-difluorophenyl)alkyl]-3,4-dihydro-5-alkylpyrimidin-4(3H)-ones as Non-nucleoside Inhibitors of HIV-1 Reverse Transcriptase 58
Investigation on QSAR and Binding Mode of a New Class of Human Rhinovirus-14 Inhibitors by CoMFA and Docking Experiments. 58
Chiral resolution and binding study of 1,3,4,14b-tetrahydro-2,10-dimethyl-2H,10H-pyrazino[2,1-d]pyrrolo[1,2-b] [1,2,5]benzotriazepine (10-methyl-10-azaaptazepine) and 2-methyl-1,3,4,14b-tetrahydro-2H-pyrazino[2,1-d]pyrrolo[1,2-b][1,2,5]-benzothiadiazepine 10,10-dioxide (tiaaptazepine). 58
Iso-miconazole and related derivatives: synthesis and antifungal activities. 56
New pyrrole inhibitors of monoamine oxidase: synthesis, biological evaluation, and structural determinants of MAO-A and MAO-B selectivity. 56
Substrate-induced stable enzyme-inhibitor complex formation allows tight binding of novel 2-aminopyrimidin-4(3H)-ones to drug-resistant HIV-1 reverse transcriptase mutants. 56
Synthesis and in vitro antimycobacterial activity of novel 3-(1H-pyrrol-1-yl)-2-oxazolidinone analogues of PNU-100480 56
The specific character of the reaction of derivatives of 2-thioxo-2,3-dihydropyrimidin-4(1H)-one with iodomethane and alkyl chloromethyl sulfides. 55
Agenti anti-HIV-1: Acilamino Pirril Aril Solfoni (APAS), Analoghi Troncati delle PBTD Tricicliche. 53
1-[(Aril)(4-aril-1H-pirrol-3-il)metil]-1H-imidazoli: Effetti della Sostituzione all'Azoto Pirrolico sull'Attività anti-Candida. 52
Indolyl aryl Sulfones (IASs): Development of highly potent NNRTIs active against wt-HIV-1 and clinically relevant drug resistant mutants 52
Synthetic approaches to difluoroindolecarboxylic acid ethyl esters. 52
Arylthioindoles, Potent Inhibitors of Tubulin Polymerization. 51
Design, Synthesis and Biological Evaluation of New Pyrrole MAO-B Inhibitors. 50
Synthesis and biological evaluation of enantiomerically pure pyrrolyl- oxazolidinones as a new class of potent and selective monoamine oxidase type A inhibitors. 50
Synthesis, biological evaluation, and binding mode of novel 1-[2-(diarylmethoxy)ethyl]-2-methyl-5-nitroimidazoles targeted at the HIV-1 reverse transcriptase 50
Substituted phenylindoles for treatment of HIV. 49
Studies on Novel Agents for Depression and Parkinson’s Disease. Potent Pyrrole and Indole Monoamine Oxidase Inhibitors. 49
Nuovi Indolil Aril Solfoni 2-Sostituiti Attivi su HIV-1 WT e su Altri Mutanti Resistenti. 49
Molecular Modeling of Azole Antifungal Agents Active.Againts Candida Albicans.I: a CoMFA Study. 47
Anti-HIV-1 NNRT Agents: Acylamino Pyrryl Aryl Sulfones (APASs) as Truncated Analogues of Tricyclic PBTDs. 47
3-(1H-pyrrol-2- and –3-yl)-2-oxazolidinones as novel potent and selective monoamine oxidase type A inhibitors. 47
Nitroquinolones with Broad-Spectrum Antimycobacterial Activity in Vitro. 47
Potenti Inibitori delle Monoamino Ossidasi a Struttura Pirrolica ed Indolica. 46
N-Benzyl and N-propargyl 1H-pyrrole-2-carboxyamides, as simple and effective monoamine oxidase inhibitors. 46
Azole Analogues of Fluoxetine, a Novel Class of anti-Candida Agents. 45
3-(1H-pyrrol-2- and –3-yl)-2-oxazolidinones as novel potent and selective monoamine oxidase type A inhibitors. 44
N-Benzyl and N-Propargyl 1H-Pyrrole-2-carboxyamides, as Simple and Potent MAO Inhibitors. 44
Synthesis and Biological Evaluation of Enantiomerically Pure 3-(1H-Pyrrol-1-yl)-2-oxazolidinones as a New Class of Potent and Selective Monoamine Oxidase Type A Inhibitors 43
Pyrrolo[1,2-b]benzothiadiazepines (PBTDs) induce Apoptosis in Chronic Myelogenous K562 Leucemic Cells 42
1-[Aril-(1-aril-1H-pirrol-3-il)metil]-1H-imidazoli, una Nuova Classe di Potenti Inibitori della Farnesiltrasferasi 42
Stereoselective synthesis of 2-substituted 6-[1-(2,6-difluorophenyl)ethyl]-5-methylpyrimidin-4(3H)-ones. 42
Derivati del 2H-pirrolo[3,4-c]chinolin-4(5H)-one: Nuovi Potenziali Agonisti dei Recettori 5-HT3 41
1[(Aryl)(4-aryl-1H-pyrrol-3-yl)methyl]-1H-imidazoles: a Class of Potent Antifungal Agents. SAR Studies of N-1 Substituted Derivatives. 41
CRYSTAL STRUCTURE OF 2-[5-(4-CARBETOXYPHENOXY)PENTANOYL]-5-CHLOROTHIOPHENE, C18H19O4ClS 39
Derivati Imidazolici Isomeri dell’Econazolo ad Azione Anti-Candida. 38
Quinolinyl 2,4-dioxobutanoic Acids, Conformationally Restrained Analogues of Aryldioxohexenoic Acids as HIV-1 Integrase Inhibitors. 37
Docking and 3-D QSAR Studies on Indolyl Aryl Solfones (IASs). Binding Mode Exploration at the HIV-1 RT NNBS and Structure Based Drug Design. 37
Totale 6.349
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Categoria #
all - tutte 20.815
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 501
selected - selezionate 0
volume - volumi 0
Totale 21.316
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020761 0 0 0 0 0 0 241 174 163 94 43 46
2020/2021708 72 66 18 49 13 99 14 52 57 59 77 132
2021/20221.322 6 91 110 121 157 19 20 154 102 98 160 284
2022/20231.520 231 347 42 205 195 174 31 97 116 22 49 11
2023/2024440 34 82 24 31 20 48 7 23 4 81 41 45
2024/2025371 80 61 59 22 78 71 0 0 0 0 0 0
Totale 7.143