IRIS
MOR, Marco
 Distribuzione geografica
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Continente #
EU - Europa 384
AS - Asia 136
NA - Nord America 134
AF - Africa 14
OC - Oceania 14
SA - Sud America 4
Totale 686
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Nazione #
IT - Italia 188
US - Stati Uniti d'America 130
IE - Irlanda 53
CN - Cina 46
IN - India 30
FR - Francia 26
DE - Germania 18
VN - Vietnam 15
AU - Australia 14
UA - Ucraina 14
CZ - Repubblica Ceca 11
CH - Svizzera 9
GB - Regno Unito 9
NL - Olanda 9
ES - Italia 8
JP - Giappone 8
ET - Etiopia 7
KR - Corea 7
RU - Federazione Russa 7
IR - Iran 6
HU - Ungheria 5
FI - Finlandia 4
RO - Romania 4
HK - Hong Kong 3
ID - Indonesia 3
IL - Israele 3
MX - Messico 3
MY - Malesia 3
NG - Nigeria 3
RS - Serbia 3
TR - Turchia 3
TW - Taiwan 3
AT - Austria 2
BE - Belgio 2
BR - Brasile 2
DK - Danimarca 2
NO - Norvegia 2
PL - Polonia 2
SG - Singapore 2
ZA - Sudafrica 2
AR - Argentina 1
BO - Bolivia 1
CA - Canada 1
EE - Estonia 1
EG - Egitto 1
GR - Grecia 1
KW - Kuwait 1
KZ - Kazakistan 1
MK - Macedonia 1
MU - Mauritius 1
PK - Pakistan 1
PT - Portogallo 1
SI - Slovenia 1
SK - Slovacchia (Repubblica Slovacca) 1
TH - Thailandia 1
Totale 686
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Città #
Parma 62
Dublin 53
Beijing 32
Canberra 14
Ashburn 9
Dong Ket 9
Reggio Nell'emilia 8
Council Bluffs 7
Hangzhou 7
Milan 7
New York 7
Hanoi 6
New Delhi 6
Mumbai 5
Naples 5
Tehran 5
Ann Arbor 4
Boardman 4
Bomporto 4
Brescia 4
Chicago 4
Florence 4
Hamden 4
Helsinki 4
Shanghai 4
Almere 3
Berkeley 3
Bologna 3
Frankfurt am Main 3
Grandate 3
Lake Forest 3
London 3
Mainz 3
Marseille 3
Mcallen 3
Rome 3
San Jose 3
Szeged 3
Waterville 3
Amsterdam 2
Athens 2
Austin 2
Bangalore 2
Belgrade 2
Brookeville 2
Brookline 2
Cambridge 2
Chennai 2
Concord 2
Delhi 2
Ekimaedori 2
Gladbeck 2
Higashifukai 2
Houghton 2
Kansas City 2
Kowloon 2
Livorno 2
Los Angeles 2
Manchester 2
Mantin 2
Monserrat 2
Mountain View 2
Newcastle Upon Tyne 2
Paris 2
Piacenza 2
Ponte Lambro 2
Port Harcourt 2
Ramla 2
Redmond 2
Ruvo di Puglia 2
Salerno 2
San Francisco 2
San Genesio Ed Uniti 2
Seville 2
Taipei 2
Tappahannock 2
Thun 2
Vadodara 2
Venice 2
Vienna 2
Washington 2
Écublens 2
Ahmedabad 1
Andra 1
Barcelona 1
Bedford 1
Bengaluru 1
Beograd 1
Bethesda 1
Boston 1
Boydton 1
Bremen 1
Buffalo 1
Casina 1
Castellón 1
Castenaso 1
Cato Ridge 1
Central 1
Chengdu 1
Cislago 1
Totale 424
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Nome #
Complex product composition generates risks for generic substitution also with dosage forms for intravenous administration, file e177fbc4-3d91-50b0-e053-d805fe0adaee 87
Δ5-Cholenoyl-amino acids as selective and orally available antagonists of the Eph-ephrin system, file e177fbc5-0615-50b0-e053-d805fe0adaee 62
Steps towards sustainable solid phase peptide synthesis: use and recovery ofN-octyl pyrrolidone, file e177fbc7-69b7-50b0-e053-d805fe0adaee 54
N-Acylethanolamine Acid Amidase (NAAA): Mechanism of Palmitoylethanolamide Hydrolysis Revealed by Mechanistic Simulations, file e177fbc7-19cd-50b0-e053-d805fe0adaee 48
Metadynamics Simulations Distinguish Short- and Long-Residence-Time Inhibitors of Cyclin-Dependent Kinase 8., file e177fbc7-4f83-50b0-e053-d805fe0adaee 47
Long-lasting inhibition of EGFR autophosphorylation in A549 tumor cells by intracellular accumulation of non-covalent inhibitors, file e177fbc4-3b54-50b0-e053-d805fe0adaee 42
Antidepressant-like activity and cardioprotective effects of fatty acid amide hydrolase inhibitor URB694 in socially stressed Wistar Kyoto rats, file e177fbc4-9e46-50b0-e053-d805fe0adaee 30
Quantum mechanics/molecular mechanics modeling of covalent addition between EGFR-cysteine 797 and N -(4-Anilinoquinazolin-6-yl) acrylamide, file e177fbc4-f1bc-50b0-e053-d805fe0adaee 30
The autocrine fgf/fgfr system in both skin and uveal melanoma: Fgf trapping as a possible therapeutic approach, file e177fbc6-c46d-50b0-e053-d805fe0adaee 28
Epidermal growth factor receptor tyrosine kinase inhibitors: current status and future perspectives in the development of novel irreversible inhibitors for the treatment of mutant non-small cell lung cancer, file e177fbc4-374a-50b0-e053-d805fe0adaee 26
Chiral Recognition of Flexible Melatonin Receptor Ligands Induced by Conformational Equilibria, file e177fbc6-e219-50b0-e053-d805fe0adaee 25
Clinical perspective for irreversible tyrosine kinase inhibitors in cancer, file e177fbc4-3212-50b0-e053-d805fe0adaee 23
Antidepressant-like effects of pharmacological inhibition of FAAH activity in socially isolated female rats, file 2151183d-783c-44f5-b775-8048aaf4993a 19
Highly Potent and Selective MT2 Melatonin Receptor Full Agonists from Conformational Analysis of 1-Benzyl-2-acylaminomethyl-tetrahydroquinolines, file e177fbc7-5fec-50b0-e053-d805fe0adaee 18
Expanding the Arsenal of FGFR Inhibitors: A Novel Chloroacetamide Derivative as a New Irreversible Agent With Anti-proliferative Activity Against FGFR1-Amplified Lung Cancer Cell Lines., file e177fbc6-8938-50b0-e053-d805fe0adaee 14
Novel Benzazole Derivatives Endowed with Potent Antiheparanase Activity, file e177fbc7-4ff7-50b0-e053-d805fe0adaee 14
L718Q Mutation as New Mechanism of Acquired Resistance to AZD9291 in EGFR-Mutated NSCLC, file e177fbc7-4f23-50b0-e053-d805fe0adaee 12
Fatty Acid Amide Hydrolase, file e177fbc4-2f5a-50b0-e053-d805fe0adaee 11
Long-Pentraxin 3 Derivative as a Small-Molecule FGF Trap for Cancer Therapy, file e177fbc4-a06d-50b0-e053-d805fe0adaee 9
Fatty Acid Amide Hydrolase (FAAH), Acetylcholinesterase (AChE), and Butyrylcholinesterase (BuChE): Networked Targets for the Development of Carbamates as Potential Anti-Alzheimer's Disease Agents, file e177fbc7-578e-50b0-e053-d805fe0adaee 9
Computer-Aided Design of Novel Antagonists of the EphA2 Receptor, file e177fbc4-4481-50b0-e053-d805fe0adaee 8
The Hippo Pathway and YAP/TAZ-TEAD Protein-Protein Interaction as Targets for Regenerative Medicine and Cancer Treatment, file e177fbc7-4eb4-50b0-e053-d805fe0adaee 8
N-tert-butyloxycarbonyl-Phe-Leu-Phe-Leu-Phe (BOC2) inhibits the angiogenic activity of heparin-binding growth factors., file e177fbc7-a6be-50b0-e053-d805fe0adaee 8
Fatty acid amide hydrolase inhibitors: a patent review (2009 - 2014), file e177fbc7-5175-50b0-e053-d805fe0adaee 6
Free-Energy Simulations Support a Lipophilic Binding Route for Melatonin Receptors, file 677189cf-719f-481f-8b52-ae464b9d7aa6 5
Novel Irreversible Epidermal Growth Factor Receptor Inhibitors by Chemical Modulation of the Cysteine-Trap Portion, file e177fbc4-1fa1-50b0-e053-d805fe0adaee 5
Modulation of Anxiety Through Blockade of Anandamide Hydrolysis, file e177fbc4-2c7c-50b0-e053-d805fe0adaee 5
Modular Approach toward the Construction of the Core Motifs of Annonaceous Acetogenins and Variants Thereof, file e177fbc4-2419-50b0-e053-d805fe0adaee 3
N-(Anilinoethyl)amide Melatonergic Ligands with Improved Water Solubility and Metabolic Stability, file e177fbc7-4ff4-50b0-e053-d805fe0adaee 3
L718Q mutant EGFR escapes covalent inhibition by stabilizing a non-reactive conformation of the lung cancer drug osimertinib, file e177fbc7-a8b4-50b0-e053-d805fe0adaee 3
2-Arylmelatonin analogues: Probing the 2-phenyl binding pocket of melatonin MT1 and MT2 receptors, file 64aaf389-c974-40b2-9d3c-0c0b4144998c 2
Functional characterization of gefitinib uptake in non-small cell lung cancer cell lines, file e177fbc4-1f39-50b0-e053-d805fe0adaee 2
Synthesis and characterization of new bivalent agents as melatonin- and histamine h3-ligands., file e177fbc4-3d4b-50b0-e053-d805fe0adaee 2
270 Discovery, development and optimization of low molecular weight EPH–ephrin protein–protein inhibitors, file e177fbc4-8d3c-50b0-e053-d805fe0adaee 2
Combining ligand- and structure-based approaches for the discovery of new inhibitors of the EPHA2-ephrin-A1 interaction, file e177fbc4-a2da-50b0-e053-d805fe0adaee 2
Antidepressant-like effects of pharmacological inhibition of FAAH activity in socially isolated female rats, file e177fbc6-f848-50b0-e053-d805fe0adaee 2
Metadynamics Simulations Distinguish Short- and Long-Residence-Time Inhibitors of Cyclin-Dependent Kinase 8., file e177fbc7-13bc-50b0-e053-d805fe0adaee 2
Pushing the Boundaries of Vinylogous Reactivity: Catalytic Enantioselective Mukaiyama Aldol Reactions of Highly Unsaturated 2-Silyloxyindoles, file e177fbc7-4f93-50b0-e053-d805fe0adaee 2
A sulfonyl fluoride derivative inhibits EGFR L858R/T790M/C797S by covalent modification of the catalytic lysine, file e177fbc7-9c8b-50b0-e053-d805fe0adaee 2
Amino acid conjugates of lithocholic acid as antagonists of the EphA2 receptor., file e177fbc4-37d7-50b0-e053-d805fe0adaee 1
Synthesis and Structure-Activity Relationships of Amino Acid Conjugates of Cholanic Acid as Antagonists of the EphA2 Receptor., file e177fbc4-3cbb-50b0-e053-d805fe0adaee 1
Comparative Analysis of Virtual Screening Approaches in the Search for Novel EphA2 Receptor Antagonists, file e177fbc4-950f-50b0-e053-d805fe0adaee 1
Quantum mechanics/molecular mechanics modeling of fatty acid amide hydrolase reactivation distinguishes substrate from irreversible covalent inhibitors., file e177fbc4-bd1d-50b0-e053-d805fe0adaee 1
Different roles for the acyl chain and the amine leaving group in the substrate selectivity of N-Acylethanolamine acid amidase, file e177fbc7-6bc7-50b0-e053-d805fe0adaee 1
FGF trapping inhibits multiple myeloma growth through c-Myc degradation–induced mitochondrial oxidative stress, file e177fbc7-7404-50b0-e053-d805fe0adaee 1
N-Acylethanolamine Acid Amidase (NAAA): Structure, Function, and Inhibition, file e177fbc7-9804-50b0-e053-d805fe0adaee 1
N-Acylethanolamine Acid Amidase (NAAA): Structure, Function, and Inhibition, file e177fbc7-9c94-50b0-e053-d805fe0adaee 1
Fibroblast growth factor receptor inhibitors: patent review (2015–2019), file e177fbc7-a59a-50b0-e053-d805fe0adaee 1
Benzisothiazolinone Derivatives as Potent Allosteric Monoacylglycerol Lipase Inhibitors That Functionally Mimic Sulfenylation of Regulatory Cysteines, file e177fbc7-a889-50b0-e053-d805fe0adaee 1
Balancing reactivity and antitumor activity: heteroarylthioacetamide derivatives as potent and time-dependent inhibitors of EGFR, file e177fbc7-ab25-50b0-e053-d805fe0adaee 1
Drug-gut microbiota metabolic interactions: the case of UniPR1331, selective antagonist of the Eph-ephrin system, in mice, file e177fbc7-afda-50b0-e053-d805fe0adaee 1
The GABAB receptor positive allosteric modulator COR659: In vitro metabolism, in vivo pharmacokinetics in rats, synthesis and pharmacological characterization of metabolically protected derivatives, file e177fbc8-06d9-50b0-e053-d805fe0adaee 1
Mechanistic Modeling of Lys745 Sulfonylation in EGFR C797S Reveals Chemical Determinants for Inhibitor Activity and Discriminates Reversible from Irreversible Agents, file fa9700a7-6a41-4982-b8ca-bd332e575dd9 1
Totale 694
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Categoria #
all - tutte 1.555
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 1.555
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201 0 1 0 0 0 0 0 0 0 0 0 0
2020/202113 0 0 0 0 0 0 0 0 3 0 1 9
2021/2022139 1 10 1 23 7 3 42 8 10 7 22 5
2022/2023274 9 6 14 21 20 20 41 31 72 15 22 3
2023/202437 5 2 3 3 1 0 10 5 1 7 0 0
Totale 694