Giuseppe Campiani - Publications

Affiliations: 
University of Siena, Italy, Siena, Toscana, Italy 
Area:
MedChem

165 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2022 Papa A, Pasquini S, Galvani F, Cammarota M, Contri C, Carullo G, Gemma S, Ramunno A, Lamponi S, Gorelli B, Saponara S, Varani K, Mor M, Campiani G, Boscia F, et al. Development of potent and selective FAAH inhibitors with improved drug-like properties as potential tools to treat neuroinflammatory conditions. European Journal of Medicinal Chemistry. 246: 114952. PMID 36462439 DOI: 10.1016/j.ejmech.2022.114952  0.305
2020 Guidi A, Prasanth Saraswati A, Relitti N, Gimmelli R, Saccoccia F, Sirignano C, Taglialatela-Scafati O, Campiani G, Ruberti G, Gemma S. (+)-(R)- and (-)-(S)-Perhexiline maleate: Enantioselective synthesis and functional studies on Schistosoma mansoni larval and adult stages. Bioorganic Chemistry. 102: 104067. PMID 32663671 DOI: 10.1016/J.Bioorg.2020.104067  0.309
2020 Frydenvang K, Pickering DS, Kshirsagar GU, Chemi G, Gemma S, Sprogøe D, Kærn AM, Brogi S, Campiani G, Butini S, Kastrup JS. The ionotropic glutamate receptor GluA2 in complex with bicyclic pyrimidinedione-based compounds: when small compound modifications have distinct effects on binding interactions. Acs Chemical Neuroscience. PMID 32437601 DOI: 10.1021/Acschemneuro.0C00195  0.361
2020 Sirous H, Campiani G, Brogi S, Calderone V, Chemi G. Computer-Driven Development of an in Silico Tool for Finding Selective Histone Deacetylase 1 Inhibitors. Molecules (Basel, Switzerland). 25. PMID 32331470 DOI: 10.3390/Molecules25081952  0.345
2020 Relitti N, Saraswati AP, Federico S, Khan T, Brindisi M, Zisterer D, Brogi S, Gemma S, Butini S, Campiani G. Telomerase-based Cancer Therapeutics: A Review on their Clinical Trials. Current Topics in Medicinal Chemistry. 20: 433-457. PMID 31894749 DOI: 10.2174/1568026620666200102104930  0.303
2019 Battah B, Chemi G, Butini S, Campiani G, Brogi S, Delogu G, Gemma S. A Repurposing Approach for Uncovering the Anti-Tubercular Activity of FDA-Approved Drugs with Potential Multi-Targeting Profiles. Molecules (Basel, Switzerland). 24. PMID 31795400 DOI: 10.3390/Molecules24234373  0.315
2019 Saccoccia F, Brindisi M, Gimmelli R, Relitti N, Guidi A, Saraswati AP, Cavella C, Brogi S, Chemi G, Butini S, Papoff G, Senger J, Herp D, Jung M, Campiani G, et al. Screening and phenotypical characterization of Schistosoma mansoni histone deacetylase 8 (SmHDAC8) inhibitors as multi-stage antischistosomal agents. Acs Infectious Diseases. PMID 31661956 DOI: 10.1021/Acsinfecdis.9B00224  0.356
2019 Grillo A, Chemi G, Brogi S, Brindisi M, Relitti N, Fezza F, Fazio D, Castelletti L, Perdona E, Wong A, Lamponi S, Pecorelli A, Benedusi M, Fantacci M, Valoti M, ... ... Campiani G, et al. Development of novel multipotent compounds modulating endocannabinoid and dopaminergic systems. European Journal of Medicinal Chemistry. 183: 111674. PMID 31518969 DOI: 10.1016/J.Ejmech.2019.111674  0.392
2019 Sirous H, Chemi G, Campiani G, Brogi S. An integrated in silico screening strategy for identifying promising disruptors of p53-MDM2 interaction. Computational Biology and Chemistry. 83: 107105. PMID 31473433 DOI: 10.1016/J.Compbiolchem.2019.107105  0.378
2019 Sirous H, Chemi G, Gemma S, Butini S, Debyser Z, Christ F, Saghaie L, Brogi S, Fassihi A, Campiani G, Brindisi M. Identification of Novel 3-Hydroxy-pyran-4-One Derivatives as Potent HIV-1 Integrase Inhibitors Using Structure-Based Combinatorial Library Design Approach. Frontiers in Chemistry. 7: 574. PMID 31457006 DOI: 10.3389/Fchem.2019.00574  0.304
2019 D'Alessandro S, Alfano G, Di Cerbo L, Brogi S, Chemi G, Relitti N, Brindisi M, Lamponi S, Novellino E, Campiani G, Gemma S, Basilico N, Taramelli D, Baratto MC, Pogni R, et al. Bridged bicyclic 2,3-dioxabicyclo[3.3.1]nonanes as antiplasmodial agents: Synthesis, structure-activity relationships and studies on their biomimetic reaction with Fe(II). Bioorganic Chemistry. 89: 103020. PMID 31185392 DOI: 10.1016/J.Bioorg.2019.103020  0.363
2019 Saraswati AP, Relitti N, Brindisi M, Gemma S, Zisterer D, Butini S, Campiani G. Raising the bar in anticancer therapy: recent advances in, and perspectives on, telomerase inhibitors. Drug Discovery Today. 24: 1370-1388. PMID 31136800 DOI: 10.1016/J.Drudis.2019.05.015  0.326
2019 da Silva ER, Brogi S, Lucon-Júnior JF, Campiani G, Gemma S, Maquiaveli CDC. Dietary polyphenols rutin, taxifolin and quercetin related compounds target Leishmania amazonensis arginase. Food & Function. PMID 31134235 DOI: 10.1039/C9Fo00265K  0.337
2018 Brindisi M, Ulivieri C, Alfano G, Gemma S, de Asís Balaguer F, Khan T, Grillo A, Chemi G, Menchon G, Prota AE, Olieric N, Lucena-Agell D, Barasoain I, Diaz JF, Nebbioso A, ... ... Campiani G, et al. Structure-activity relationships, biological evaluation and structural studies of novel pyrrolonaphthoxazepines as antitumor agents. European Journal of Medicinal Chemistry. 162: 290-320. PMID 30448418 DOI: 10.1016/J.Ejmech.2018.11.004  0.412
2018 da Silva ER, Brogi S, Grillo A, Campiani G, Gemma S, Vieira PC, do Carmo Maquiaveli C. Cinnamic acids derived compounds with antileishmanial activity target Leishmania amazonensis arginase. Chemical Biology & Drug Design. PMID 30216691 DOI: 10.1111/Cbdd.13391  0.365
2018 Janssen APA, Van der Vliet D, Bakker AT, Jiang M, Grimm SH, Campiani G, Butini S, van der Stelt M. Development of a multiplexed activity-based protein profiling assay to evaluate activity of endocannabinoid hydrolase inhibitors. Acs Chemical Biology. PMID 30199617 DOI: 10.1021/Acschembio.8B00534  0.329
2018 Brindisi M, Senger J, Cavella C, Grillo A, Chemi G, Gemma S, Cucinella DM, Lamponi S, Sarno F, Iside C, Nebbioso A, Novellino E, Shaik TB, Romier C, Herp D, ... ... Campiani G, et al. Novel spiroindoline HDAC inhibitors: Synthesis, molecular modelling and biological studies. European Journal of Medicinal Chemistry. 157: 127-138. PMID 30092367 DOI: 10.1016/J.Ejmech.2018.07.069  0.429
2018 Brindisi M, Borrelli G, Brogi S, Grillo A, Maramai S, Paolino M, Benedusi M, Pecorelli A, Valacchi G, Di Cesare Mannelli L, Ghelardini C, Allarà M, Ligresti A, Minetti P, Campiani G, et al. Development of Potent Inhibitors of Fatty Acid Amide Hydrolase Useful for the Treatment of Neuropathic Pain. Chemmedchem. 13: 2090-2103. PMID 30085402 DOI: 10.1002/Cmdc.201800397  0.416
2018 Vallone A, D'Alessandro S, Brogi S, Brindisi M, Chemi G, Alfano G, Lamponi S, Lee SG, Jez JM, Koolen KJM, Dechering KJ, Saponara S, Fusi F, Gorelli B, Taramelli D, ... ... Campiani G, et al. Antimalarial agents against both sexual and asexual parasites stages: structure-activity relationships and biological studies of the Malaria Box compound 1-[5-(4-bromo-2-chlorophenyl)furan-2-yl]-N-[(piperidin-4-yl)methyl]methanamine (MMV019918) and analogues. European Journal of Medicinal Chemistry. 150: 698-718. PMID 29571157 DOI: 10.1016/J.Ejmech.2018.03.024  0.357
2018 Brogi S, Brindisi M, Butini S, Kshirsagar GU, Maramai S, Chemi G, Gemma S, Campiani G, Novellino E, Fiorenzani P, Pinassi J, Aloisi AM, Gynther M, Venskutonyte R, Han L, et al. (S)-2-Amino-3-(5-methyl-3-hydroxyisoxazol-4-yl)propanoic Acid (AMPA) and Kainate Receptor Ligands: Further Exploration of Bioisosteric Replacements, Structural and Biological Investigation. Journal of Medicinal Chemistry. PMID 29451794 DOI: 10.1021/Acs.Jmedchem.8B00099  0.341
2018 Paolino M, Brindisi M, Vallone A, Butini S, Campiani G, Nannicini C, Giuliani G, Anzini M, Lamponi S, Giorgi G, Sbardella D, Ferraris DM, Marini S, Coletta M, Palucci I, et al. Development of potent inhibitors of the Mycobacterium tuberculosis virulence factor Zmp1 and evaluation of their effect on mycobacterial survival inside macrophages. Chemmedchem. PMID 29334428 DOI: 10.1002/Cmdc.201700759  0.325
2018 Chouha N, Hammoud H, Brogi S, Campiani G, Welsch C, Robert C, Vagner S, Cresteil T, Bentouhami E, Désaubry L. Discovery of Iminobenzimidazole Derivatives as Novel Cytotoxic Agents The Open Medicinal Chemistry Journal. 12: 74-83. DOI: 10.2174/1874104501812010074  0.338
2018 Federico S, Khan T, Relitti N, Chemi G, Brindisi M, Brogi S, Novellino E, Zisterer DM, Campiani G, Gemma S, Butini S. A Jocic-type approach for a practical and scalable synthesis of pyrrolonaphthoxazepine (PNOX)-based potent proapoptotic agents Tetrahedron Letters. 59: 4466-4470. DOI: 10.1016/J.Tetlet.2018.11.005  0.335
2018 Gemma S, Cerbo Ld, Relitti N, Vallone A, Brindisi M, Brogi S, Chemi G, Novellino E, Campiani G, Butini S. Synthetic studies toward bicyclic endoperoxides presenting polar side chains Tetrahedron Letters. 59: 4330-4333. DOI: 10.1016/J.Tetlet.2018.10.059  0.339
2017 Brogi S, Maramai S, Brindisi M, Chemi G, Porcari V, Corallo C, Gennari L, Novellino E, Ramunno A, Butini S, Campiani G, Gemma S. Activation of the Wnt Pathway by Small Peptides: Rational Design, Synthesis and Biological Evaluation. Chemmedchem. 12: 2074-2085. PMID 29131552 DOI: 10.1002/Cmdc.201700551  0.345
2017 Brogi S, Ramunno A, Savi L, Chemi G, Alfano G, Pecorelli A, Pambianchi E, Galatello P, Compagnoni G, Focher F, Biamonti G, Valacchi G, Butini S, Gemma S, Campiani G, et al. First dual AK/GSK-3β inhibitors endowed with antioxidant properties as multifunctional, potential neuroprotective agents. European Journal of Medicinal Chemistry. 138: 438-457. PMID 28689095 DOI: 10.1016/J.Ejmech.2017.06.017  0.415
2017 Chemi G, Gemma S, Campiani G, Brogi S, Butini S, Brindisi M. Computational Tool for Fast Evaluation of ERG K Channel Affinity. Frontiers in Chemistry. 5: 7. PMID 28503546 DOI: 10.3389/Fchem.2017.00007  0.317
2017 Brogi S, Fiorillo A, Chemi G, Butini S, Lalle M, Ilari A, Gemma S, Campiani G. Structural characterization of Giardia duodenalis thioredoxin reductase (gTrxR) and computational analysis of its interaction with NBDHEX. European Journal of Medicinal Chemistry. 135: 479-490. PMID 28477573 DOI: 10.1016/J.Ejmech.2017.04.057  0.364
2017 Zaccagnini L, Brogi S, Brindisi M, Gemma S, Chemi G, Legname G, Campiani G, Butini S. Identification of novel fluorescent probes preventing PrP replication in prion diseases. European Journal of Medicinal Chemistry. 127: 859-873. PMID 27842893 DOI: 10.1016/J.Ejmech.2016.10.064  0.317
2017 Ismaili L, Refouvelet B, Benchekroun M, Brogi S, Brindisi M, Gemma S, Campiani G, Filipic S, Agbaba D, Esteban G, Unzeta M, Nikolic K, Butini S, Marco-Contelles J. Multitarget compounds bearing tacrine- and donepezil-like structural and functional motifs for the potential treatment of Alzheimer's disease. Progress in Neurobiology. 151: 4-34. PMID 26797191 DOI: 10.1016/J.Pneurobio.2015.12.003  0.326
2016 Greene LM, Butini S, Campiani G, Williams DC, Zisterer DM. Pre-clinical evaluation of a novel class of anti-cancer agents, the Pyrrolo-1, 5-benzoxazepines. Journal of Cancer. 7: 2367-2377. PMID 27994676 DOI: 10.7150/Jca.16616  0.35
2016 Maramai S, Gemma S, Brogi S, Campiani G, Butini S, Stark H, Brindisi M. Dopamine D3 Receptor Antagonists as Potential Therapeutics for the Treatment of Neurological Diseases. Frontiers in Neuroscience. 10: 451. PMID 27761108 DOI: 10.3389/Fnins.2016.00451  0.332
2016 Brindisi M, Cavella C, Brogi S, Nebbioso A, Senger J, Maramai S, Ciotta A, Iside C, Butini S, Lamponi S, Novellino E, Altucci L, Jung M, Campiani G, Gemma S. Phenylpyrrole-based HDAC inhibitors: synthesis, molecular modeling and biological studies. Future Medicinal Chemistry. PMID 27556815 DOI: 10.4155/Fmc-2016-0068  0.338
2016 Lennon JC, Butini S, Campiani G, O'Meara A, Williams DC, Zisterer DM. Involvement of AMP-activated protein kinase in mediating pyrrolo-1,5-benzoxazepine-induced apoptosis in neuroblastoma cells. Investigational New Drugs. PMID 27334143 DOI: 10.1007/S10637-016-0366-3  0.382
2016 Butini S, Nikolic K, Kassel S, Brückmann H, Filipic S, Agbaba D, Gemma S, Brogi S, Brindisi M, Campiani G, Stark H. Polypharmacology of dopamine receptor ligands Progress in Neurobiology. 142: 68-103. PMID 27234980 DOI: 10.1016/J.Pneurobio.2016.03.011  0.309
2016 Nathwani SM, Greene LM, Butini S, Campiani G, Williams DC, Samali A, Szegezdi E, Zisterer DM. The pyrrolo-1,5-benzoxazepine, PBOX-15, enhances TRAIL‑induced apoptosis by upregulation of DR5 and downregulation of core cell survival proteins in acute lymphoblastic leukaemia cells. International Journal of Oncology. PMID 27176505 DOI: 10.3892/Ijo.2016.3518  0.345
2016 Brindisi M, Maramai S, Brogi S, Fanigliulo E, Butini S, Guarino E, Casagni A, Lamponi S, Bonechi C, Nathwani SM, Finetti F, Ragonese F, Arcidiacono P, Campiglia P, Valenti S, ... ... Campiani G, et al. Development of novel cyclic peptides as pro-apoptotic agents. European Journal of Medicinal Chemistry. 117: 301-320. PMID 27150036 DOI: 10.1016/J.Ejmech.2016.04.001  0.302
2016 Brindisi M, Brogi S, Giovani S, Gemma S, Lamponi S, De Luca F, Novellino E, Campiani G, Docquier JD, Butini S. Targeting clinically-relevant metallo-β-lactamases: from high-throughput docking to broad-spectrum inhibitors. Journal of Enzyme Inhibition and Medicinal Chemistry. 1-12. PMID 27121013 DOI: 10.3109/14756366.2016.1172575  0.306
2016 Maquiaveli CC, Lucon-Júnior JF, Brogi S, Campiani G, Gemma S, Vieira PC, Silva ER. Verbascoside Inhibits Promastigote Growth and Arginase Activity of Leishmania amazonensis. Journal of Natural Products. 79: 1459-63. PMID 27096224 DOI: 10.1021/Acs.Jnatprod.5B00875  0.363
2016 Brindisi M, Maramai S, Gemma S, Brogi S, Grillo A, Di Cesare Mannelli L, Gabellieri E, Lamponi S, Saponara S, Gorelli B, Tedesco D, Bonfiglio T, Landry C, Jung KM, Armirotti A, ... ... Campiani G, et al. Development and Pharmacological Characterization of Selective Blockers of 2-Arachidonoyl Glycerol Degradation with Efficacy in Rodent Models of Multiple Sclerosis and Pain. Journal of Medicinal Chemistry. PMID 26888301 DOI: 10.1021/Acs.Jmedchem.5B01812  0.335
2016 Kinsella P, Greene LM, Bright SA, Pollock JK, Butini S, Campiani G, Bauer S, Williams DC, Zisterer DM. The novel pyrrolo-1,5-benzoxazepine, PBOX-15, synergistically enhances the apoptotic efficacy of imatinib in gastrointestinal stromal tumours; suggested mechanism of action of PBOX-15. Investigational New Drugs. 34: 159-67. PMID 26885657 DOI: 10.1007/S10637-016-0331-1  0.368
2016 Brogi S, Giovani S, Brindisi M, Gemma S, Novellino E, Campiani G, Blackman MJ, Butini S. In silico study of subtilisin-like protease 1 (SUB1) from different Plasmodium species in complex with peptidyl-difluorostatones and characterization of potent pan-SUB1 inhibitors. Journal of Molecular Graphics & Modelling. 64: 121-30. PMID 26826801 DOI: 10.1016/J.Jmgm.2016.01.005  0.333
2016 Brindisi M, Brogi S, Maramai S, Grillo A, Borrelli G, Butini S, Novellino E, Allarà M, Ligresti A, Campiani G, Marzo VD, Gemma S. Harnessing the pyrroloquinoxaline scaffold for FAAH and MAGL interaction: definition of the structural determinants for enzyme inhibition Rsc Advances. 6: 64651-64664. DOI: 10.1039/C6Ra12524G  0.359
2015 Wu MY, Esteban G, Brogi S, Shionoya M, Wang L, Campiani G, Unzeta M, Inokuchi T, Butini S, Marco-Contelles J. Donepezil-like multifunctional agents: Design, synthesis, molecular modeling and biological evaluation. European Journal of Medicinal Chemistry. PMID 26471320 DOI: 10.1016/J.Ejmech.2015.10.001  0.363
2015 Brogi S, Brindisi M, Joshi BP, Sanna Coccone S, Parapini S, Basilico N, Novellino E, Campiani G, Gemma S, Butini S. Exploring clotrimazole-based pharmacophore: 3D-QSAR studies and synthesis of novel antiplasmodial agents. Bioorganic & Medicinal Chemistry Letters. 25: 5412-8. PMID 26428874 DOI: 10.1016/J.Bmcl.2015.09.007  0.368
2015 Fiore D, Proto MC, Pisanti S, Picardi P, Pagano Zottola AC, Butini S, Gemma S, Casagni A, Laezza C, Vitale M, Ligresti A, Di Marzo V, Zisterer DM, Nathwani S, Williams DC, ... Campiani G, et al. Antitumor effect of pyrrolo-1,5-benzoxazepine-15 and its synergistic effect with Oxaliplatin and 5-FU in colorectal cancer cells. Cancer Biology & Therapy. 0. PMID 26392056 DOI: 10.1080/15384047.2015.1078028  0.369
2015 Spallarossa A, Caneva C, Caviglia M, Alfei S, Butini S, Campiani G, Gemma S, Brindisi M, Zisterer DM, Bright SA, Williams CD, Crespan E, Maga G, Sanna G, Delogu I, et al. Unconventional Knoevenagel-type indoles: Synthesis and cell-based studies for the identification of pro-apoptotic agents. European Journal of Medicinal Chemistry. 102: 648-60. PMID 26320088 DOI: 10.1016/J.Ejmech.2015.08.009  0.401
2015 Savi L, Brindisi M, Alfano G, Butini S, La Pietra V, Novellino E, Marinelli L, Lossani A, Focher F, Cavella C, Campiani G, Gemma S. Site-directed Mutagenesis of Key Residues Unveiled a Novel Allosteric Site on Human Adenosine Kinase for Pyrrolobenzoxa(thia)zepinone Non-Nucleoside Inhibitors. Chemical Biology & Drug Design. PMID 26242695 DOI: 10.1111/Cbdd.12630  0.341
2015 O'Callaghan K, Palagano E, Butini S, Campiani G, Williams DC, Zisterer DM, O'Sullivan J. Induction of apoptosis in oral squamous carcinoma cells by pyrrolo-1,5-benzoxazepines. Molecular Medicine Reports. PMID 26005189 DOI: 10.3892/Mmr.2015.3832  0.339
2015 Brindisi M, Brogi S, Relitti N, Vallone A, Butini S, Gemma S, Novellino E, Colotti G, Angiulli G, Di Chiaro F, Fiorillo A, Ilari A, Campiani G. Structure-based discovery of the first non-covalent inhibitors of Leishmania major tryparedoxin peroxidase by high throughput docking. Scientific Reports. 5: 9705. PMID 25951439 DOI: 10.1038/Srep09705  0.407
2015 Giovani S, Penzo M, Butini S, Brindisi M, Gemma S, Novellino E, Campiani G, Blackman MJ, Brogi S. Plasmodium falciparum subtilisin-like protease 1: discovery of potent difluorostatone-based inhibitors Rsc Advances. 5: 22431-22448. DOI: 10.1039/C5Ra01170A  0.325
2015 Brindisi M, Gemma S, Kunjir SA, Cerbo LD, Brogi S, Parapini S, D'Alessandro S, Taramelli D, Habluetzel A, Tapanelli S, Lamponi S, Novellino E, Campiani G, Butini S. Synthetic spirocyclic endoperoxides: new antimalarial scaffolds Medchemcomm. 6: 357-362. DOI: 10.1039/C4Md00454J  0.335
2014 Brogi S, Butini S, Maramai S, Colombo R, Verga L, Lanni C, De Lorenzi E, Lamponi S, Andreassi M, Bartolini M, Andrisano V, Novellino E, Campiani G, Brindisi M, Gemma S. Disease-modifying anti-Alzheimer's drugs: inhibitors of human cholinesterases interfering with β-amyloid aggregation. Cns Neuroscience & Therapeutics. 20: 624-32. PMID 24935788 DOI: 10.1111/Cns.12290  0.326
2014 Giovani S, Penzo M, Brogi S, Brindisi M, Gemma S, Novellino E, Savini L, Blackman MJ, Campiani G, Butini S. Rational design of the first difluorostatone-based PfSUB1 inhibitors. Bioorganic & Medicinal Chemistry Letters. 24: 3582-6. PMID 24909083 DOI: 10.1016/J.Bmcl.2014.05.044  0.394
2014 Castriconi F, Paolino M, Giuliani G, Anzini M, Campiani G, Mennuni L, Sabatini C, Lanza M, Caselli G, De Rienzo F, Menziani MC, Sbraccia M, Molinari P, Costa T, Cappelli A. Synthesis and structure-activity relationship studies in serotonin 5-HT4 receptor ligands based on a benzo[de][2,6]naphthridine scaffold. European Journal of Medicinal Chemistry. 82: 36-46. PMID 24871995 DOI: 10.1016/J.Ejmech.2014.05.015  0.359
2014 Lennon JC, Bright SA, Carroll E, Butini S, Campiani G, O'Meara A, Williams DC, Zisterer DM. The novel pyrrolo-1,5-benzoxazepine, PBOX-6, synergistically enhances the apoptotic effects of carboplatin in drug sensitive and multidrug resistant neuroblastoma cells. Biochemical Pharmacology. 87: 611-24. PMID 24406249 DOI: 10.1016/J.Bcp.2013.12.017  0.378
2014 Gemma S, Brogi S, Patil PR, Giovani S, Lamponi S, Cappelli A, Novellino E, Brown A, Higgins MK, Mustafa K, Szestak T, Craig AG, Campiani G, Butini S, Brindisi M. From (+)-epigallocatechin gallate to a simplified synthetic analogue as a cytoadherence inhibitor for P. falciparum Rsc Adv.. 4: 4769-4781. DOI: 10.1039/C3Ra45933K  0.353
2013 Butini S, Brindisi M, Brogi S, Maramai S, Guarino E, Panico A, Saxena A, Chauhan V, Colombo R, Verga L, De Lorenzi E, Bartolini M, Andrisano V, Novellino E, Campiani G, et al. Multifunctional cholinesterase and amyloid Beta fibrillization modulators. Synthesis and biological investigation. Acs Medicinal Chemistry Letters. 4: 1178-82. PMID 24900626 DOI: 10.1021/Ml4002908  0.316
2013 Butini S, Gabellieri E, Brindisi M, Giovani S, Maramai S, Kshirsagar G, Guarino E, Brogi S, La Pietra V, Giustiniano M, Marinelli L, Novellino E, Campiani G, Cappelli A, Gemma S. A stereoselective approach to peptidomimetic BACE1 inhibitors. European Journal of Medicinal Chemistry. 70: 233-47. PMID 24158015 DOI: 10.1016/J.Ejmech.2013.09.056  0.395
2013 Butini S, Brogi S, Novellino E, Campiani G, Ghosh AK, Brindisi M, Gemma S. The structural evolution of β-secretase inhibitors: a focus on the development of small-molecule inhibitors. Current Topics in Medicinal Chemistry. 13: 1787-807. PMID 23931442 DOI: 10.2174/15680266113139990137  0.337
2013 Gangemi G, Gazzerro P, Fiore D, Proto MC, Butini S, Gemma S, Casagni A, Laezza C, Vitale M, Ligresti A, Di Marzo V, Zisterer DM, Nathwani S, Clive Williams D, Campiani G, et al. PBOX-15 induces apoptosis and improves the efficacy of oxaliplatin in human colorectal cancer cell lines. European Journal of Pharmacology. 714: 379-87. PMID 23872382 DOI: 10.1016/J.Ejphar.2013.07.011  0.374
2013 Cappelli A, Manini M, Valenti S, Castriconi F, Giuliani G, Anzini M, Brogi S, Butini S, Gemma S, Campiani G, Giorgi G, Mennuni L, Lanza M, Giordani A, Caselli G, et al. Synthesis and structure-activity relationship studies in serotonin 5-HT(1A) receptor agonists based on fused pyrrolidone scaffolds. European Journal of Medicinal Chemistry. 63: 85-94. PMID 23466604 DOI: 10.1016/J.Ejmech.2013.01.044  0.352
2013 Butini S, Gemma S, Brindisi M, Maramai S, Minetti P, Celona D, Napolitano R, Borsini F, Cabri W, Fezza F, Merlini L, Dallavalle S, Campiani G, Maccarrone M. Identification of a novel arylpiperazine scaffold for fatty acid amide hydrolase inhibition with improved drug disposition properties. Bioorganic & Medicinal Chemistry Letters. 23: 492-5. PMID 23237837 DOI: 10.1016/J.Bmcl.2012.11.035  0.395
2013 Butini S, Gabellieri E, Brindisi M, Casagni A, Guarino E, Huleatt PB, Relitti N, La Pietra V, Marinelli L, Giustiniano M, Novellino E, Campiani G, Gemma S. Novel peptidomimetics as BACE-1 inhibitors: synthesis, molecular modeling, and biological studies. Bioorganic & Medicinal Chemistry Letters. 23: 85-9. PMID 23218605 DOI: 10.1016/J.Bmcl.2012.11.011  0.415
2013 Lysaght J, Verma NK, Maginn EN, Ryan JM, Campiani G, Zisterer DM, Williams DC, Browne PV, Lawler MP, McElligott AM. The microtubule targeting agent PBOX-15 inhibits integrin-mediated cell adhesion and induces apoptosis in acute lymphoblastic leukaemia cells. International Journal of Oncology. 42: 239-46. PMID 23135704 DOI: 10.3892/Ijo.2012.1688  0.313
2013 Brindisi M, Gemma S, Alfano G, Kshirsagar G, Novellino E, Campiani G, Butini S. A stereoselective route to 6-substituted pyrrolo-1,5-benzoxazepinones and their analogues Tetrahedron Letters. 54: 5387-5390. DOI: 10.1016/J.Tetlet.2013.07.115  0.305
2013 Gemma S, Kunjir S, Brindisi M, Novellino E, Campiani G, Butini S. A synthetic strategy to bridged 2,3,8-trioxabicyclo[3,3,1]nonane endoperoxides Tetrahedron Letters. 54: 1233-1235. DOI: 10.1016/J.Tetlet.2012.12.075  0.314
2012 Gemma S, Camodeca C, Brindisi M, Brogi S, Kukreja G, Kunjir S, Gabellieri E, Lucantoni L, Habluetzel A, Taramelli D, Basilico N, Gualdani R, Tadini-Buoninsegni F, Bartolommei G, Moncelli MR, ... ... Campiani G, et al. Mimicking the intramolecular hydrogen bond: synthesis, biological evaluation, and molecular modeling of benzoxazines and quinazolines as potential antimalarial agents. Journal of Medicinal Chemistry. 55: 10387-404. PMID 23145816 DOI: 10.1021/Jm300831B  0.367
2012 Gemma S, Giovani S, Brindisi M, Tripaldi P, Brogi S, Savini L, Fiorini I, Novellino E, Butini S, Campiani G, Penzo M, Blackman MJ. Quinolylhydrazones as novel inhibitors of Plasmodium falciparum serine protease PfSUB1. Bioorganic & Medicinal Chemistry Letters. 22: 5317-21. PMID 22796182 DOI: 10.1016/J.Bmcl.2012.06.023  0.404
2012 Gemma S, Camodeca C, Sanna Coccone S, Joshi BP, Bernetti M, Moretti V, Brogi S, Bonache de Marcos MC, Savini L, Taramelli D, Basilico N, Parapini S, Rottmann M, Brun R, Lamponi S, ... ... Campiani G, et al. Optimization of 4-aminoquinoline/clotrimazole-based hybrid antimalarials: further structure-activity relationships, in vivo studies, and preliminary toxicity profiling. Journal of Medicinal Chemistry. 55: 6948-67. PMID 22783984 DOI: 10.1021/Jm300802S  0.348
2012 Butini S, Brindisi M, Gemma S, Minetti P, Cabri W, Gallo G, Vincenti S, Talamonti E, Borsini F, Caprioli A, Stasi MA, Di Serio S, Ros S, Borrelli G, Maramai S, ... ... Campiani G, et al. Discovery of potent inhibitors of human and mouse fatty acid amide hydrolases Journal of Medicinal Chemistry. 55: 6898-6915. PMID 22779702 DOI: 10.1021/Jm300689C  0.398
2011 Patil PR, Gemma S, Campiani G, Craig AG. Broad inhibition of plasmodium falciparum cytoadherence by (+)-epigallocatechin gallate. Malaria Journal. 10: 348. PMID 22132804 DOI: 10.1186/1475-2875-10-348  0.32
2011 Gemma S, Kunjir S, Coccone SS, Brindisi M, Moretti V, Brogi S, Novellino E, Basilico N, Parapini S, Taramelli D, Campiani G, Butini S. Synthesis and antiplasmodial activity of bicyclic dioxanes as simplified dihydroplakortin analogues. Journal of Medicinal Chemistry. 54: 5949-53. PMID 21761935 DOI: 10.1021/Jm200686D  0.388
2011 Butini S, Gemma S, Brindisi M, Borrelli G, Fiorini I, Samuele A, Karytinos A, Facchini M, Lossani A, Zanoli S, Campiani G, Novellino E, Focher F, Maga G. Enantioselective binding of second generation pyrrolobenzoxazepinones to the catalytic ternary complex of HIV-1 RT wild-type and L100I and K103N drug resistant mutants. Bioorganic & Medicinal Chemistry Letters. 21: 3935-8. PMID 21636271 DOI: 10.1016/J.Bmcl.2011.05.020  0.303
2011 Gemma S, Colombo L, Forloni G, Savini L, Fracasso C, Caccia S, Salmona M, Brindisi M, Joshi BP, Tripaldi P, Giorgi G, Taglialatela-Scafati O, Novellino E, Fiorini I, Campiani G, et al. Pyrroloquinoxaline hydrazones as fluorescent probes for amyloid fibrils. Organic & Biomolecular Chemistry. 9: 5137-48. PMID 21629961 DOI: 10.1039/C1Ob05288H  0.31
2011 Venskutonyte R, Butini S, Coccone SS, Gemma S, Brindisi M, Kumar V, Guarino E, Maramai S, Valenti S, Amir A, Valadés EA, Frydenvang K, Kastrup JS, Novellino E, Campiani G, et al. Selective kainate receptor (GluK1) ligands structurally based upon 1H-cyclopentapyrimidin-2,4(1H,3H)-dione: synthesis, molecular modeling, and pharmacological and biostructural characterization. Journal of Medicinal Chemistry. 54: 4793-805. PMID 21619066 DOI: 10.1021/Jm2004078  0.354
2011 Butini S, Gemma S, Brindisi M, Borrelli G, Lossani A, Ponte AM, Torti A, Maga G, Marinelli L, La Pietra V, Fiorini I, Lamponi S, Campiani G, Zisterer DM, Nathwani SM, et al. Non-nucleoside inhibitors of human adenosine kinase: Synthesis, molecular modeling, and biological studies Journal of Medicinal Chemistry. 54: 1401-1420. PMID 21319802 DOI: 10.1021/Jm101438U  0.378
2011 Maginn EN, Browne PV, Hayden P, Vandenberghe E, MacDonagh B, Evans P, Goodyer M, Tewari P, Campiani G, Butini S, Williams DC, Zisterer DM, Lawler MP, McElligott AM. PBOX-15, a novel microtubule targeting agent, induces apoptosis, upregulates death receptors, and potentiates TRAIL-mediated apoptosis in multiple myeloma cells. British Journal of Cancer. 104: 281-9. PMID 21179037 DOI: 10.1038/Sj.Bjc.6606035  0.314
2011 Gemma S, Butini S, Campiani G, Brindisi M, Zanoli S, Romano MP, Tripaldi P, Savini L, Fiorini I, Borrelli G, Novellino E, Maga G. Discovery of potent nucleotide-mimicking competitive inhibitors of hepatitis C virus NS3 helicase. Bioorganic & Medicinal Chemistry Letters. 21: 2776-9. PMID 20880703 DOI: 10.1016/J.Bmcl.2010.09.002  0.306
2010 Nathwani SM, Cloonan SM, Stronach M, Campiani G, Lawler M, Williams DC, Zisterer DM. Novel microtubule-targeting agents, pyrrolo-1,5-benzoxazepines, induce cell cycle arrest and apoptosis in prostate cancer cells. Oncology Reports. 24: 1499-507. PMID 21042745 DOI: 10.3892/Or_00001011  0.34
2010 Gemma S, Travagli V, Savini L, Novellino E, Campiani G, Butini S. Malaria chemotherapy: recent advances in drug development. Recent Patents On Anti-Infective Drug Discovery. 5: 195-225. PMID 20738242 DOI: 10.2174/157489110793348776  0.308
2010 Butini S, Campiani G, Franceschini S, Trotta F, Kumar V, Guarino E, Borrelli G, Fiorini I, Novellino E, Fattorusso C, Persico M, Orteca N, Sandager-Nielsen K, Jacobsen TA, Madsen K, et al. Discovery of bishomo(hetero)arylpiperazines as novel multifunctional ligands targeting dopamine D(3) and serotonin 5-HT(1A) and 5-HT(2A) receptors. Journal of Medicinal Chemistry. 53: 4803-7. PMID 20481570 DOI: 10.1021/Jm100294B  0.31
2010 Bright SA, McElligott AM, O'Connell JW, O'Connor L, Carroll P, Campiani G, Deininger MW, Conneally E, Lawler M, Williams DC, Zisterer DM. Novel pyrrolo-1,5-benzoxazepine compounds display significant activity against resistant chronic myeloid leukaemia cells in vitro, in ex vivo patient samples and in vivo. British Journal of Cancer. 102: 1474-82. PMID 20407438 DOI: 10.1038/Sj.Bjc.6605670  0.339
2010 Bright SA, Campiani G, Deininger MW, Lawler M, Williams DC, Zisterer DM. Sequential treatment with flavopiridol synergistically enhances pyrrolo-1,5-benzoxazepine-induced apoptosis in human chronic myeloid leukaemia cells including those resistant to imatinib treatment. Biochemical Pharmacology. 80: 31-8. PMID 20206141 DOI: 10.1016/J.Bcp.2010.02.019  0.393
2010 Nathwani SM, Butler S, Fayne D, McGovern NN, Sarkadi B, Meegan MJ, Lloyd DG, Campiani G, Lawler M, Williams DC, Zisterer DM. Novel microtubule-targeting agents, pyrrolo-1,5-benzoxazepines, induce apoptosis in multi-drug-resistant cancer cells. Cancer Chemotherapy and Pharmacology. 66: 585-96. PMID 20020128 DOI: 10.1007/S00280-009-1200-9  0.334
2010 Nathwani SM, Butler S, Meegan MJ, Campiani G, Lawler M, Williams DC, Zisterer DM. Dual targeting of tumour cells and host endothelial cells by novel microtubule-targeting agents, pyrrolo-1,5-benzoxazepines. Cancer Chemotherapy and Pharmacology. 65: 289-300. PMID 19479253 DOI: 10.1007/S00280-009-1033-6  0.341
2010 Bartolommei G, Tadini-Buoninsegni F, Gemma S, Camodeca C, Butini S, Campiani G, Moncelli MR. Inhibition of SERCA1 by a Novel Antimalarial Compound Biophysical Journal. 98: 5-5. DOI: 10.1016/J.Bpj.2009.12.2751  0.335
2009 Butini S, Budriesi R, Hamon M, Morelli E, Gemma S, Brindisi M, Borrelli G, Novellino E, Fiorini I, Ioan P, Chiarini A, Cagnotto A, Mennini T, Fracasso C, Caccia S, ... Campiani G, et al. Novel, potent, and selective quinoxaline-based 5-HT(3) receptor ligands. 1. Further structure-activity relationships and pharmacological characterization. Journal of Medicinal Chemistry. 52: 6946-50. PMID 19831400 DOI: 10.1021/Jm901126M  0.35
2009 McElligott AM, Maginn EN, Greene LM, McGuckin S, Hayat A, Browne PV, Butini S, Campiani G, Catherwood MA, Vandenberghe E, Williams DC, Zisterer DM, Lawler M. The novel tubulin-targeting agent pyrrolo-1,5-benzoxazepine-15 induces apoptosis in poor prognostic subgroups of chronic lymphocytic leukemia. Cancer Research. 69: 8366-75. PMID 19826055 DOI: 10.1158/0008-5472.Can-09-0131  0.36
2009 Ferlini C, Cicchillitti L, Raspaglio G, Bartollino S, Cimitan S, Bertucci C, Mozzetti S, Gallo D, Persico M, Fattorusso C, Campiani G, Scambia G. Paclitaxel directly binds to Bcl-2 and functionally mimics activity of Nur77. Cancer Research. 69: 6906-14. PMID 19671798 DOI: 10.1158/0008-5472.Can-09-0540  0.34
2009 Gemma S, Savini L, Altarelli M, Tripaldi P, Chiasserini L, Coccone SS, Kumar V, Camodeca C, Campiani G, Novellino E, Clarizio S, Delogu G, Butini S. Development of antitubercular compounds based on a 4-quinolylhydrazone scaffold. Further structure-activity relationship studies. Bioorganic & Medicinal Chemistry. 17: 6063-72. PMID 19620006 DOI: 10.1016/J.Bmc.2009.06.051  0.362
2009 Butini S, Brindisi M, Cosconati S, Marinelli L, Borrelli G, Coccone SS, Ramunno A, Campiani G, Novellino E, Zanoli S, Samuele A, Giorgi G, Bergamini A, Di Mattia M, Lalli S, et al. Specific targeting of highly conserved residues in the HIV-1 reverse transcriptase primer grip region. 2. Stereoselective interaction to overcome the effects of drug resistant mutations. Journal of Medicinal Chemistry. 52: 1224-8. PMID 19170521 DOI: 10.1021/Jm801395V  0.369
2009 Gemma S, Campiani G, Butini S, Joshi BP, Kukreja G, Coccone SS, Bernetti M, Persico M, Nacci V, Fiorini I, Novellino E, Taramelli D, Basilico N, Parapini S, Yardley V, et al. Combining 4-aminoquinoline- and clotrimazole-based pharmacophores toward innovative and potent hybrid antimalarials. Journal of Medicinal Chemistry. 52: 502-13. PMID 19113955 DOI: 10.1021/Jm801352S  0.394
2009 Bright SA, Greene LM, Greene TF, Campiani G, Butini S, Brindisi M, Lawler M, Meegan MJ, Williams DC, Zisterer DM. The novel pyrrolo-1,5-benzoxazepine, PBOX-21, potentiates the apoptotic efficacy of STI571 (imatinib mesylate) in human chronic myeloid leukaemia cells. Biochemical Pharmacology. 77: 310-21. PMID 19014913 DOI: 10.1016/J.Bcp.2008.10.008  0.355
2009 Gemma S, Martí F, Gabellieri E, Campiani G, Novellino E, Butini S. Synthetic studies toward 1,2-dioxanes as precursors of potential endoperoxide-containing antimalarials Tetrahedron Letters. 50: 5719-5722. DOI: 10.1016/J.Tetlet.2009.07.137  0.33
2008 Butini S, Gabellieri E, Huleatt PB, Campiani G, Franceschini S, Brindisi M, Ros S, Coccone SS, Fiorini I, Novellino E, Giorgi G, Gemma S. An efficient approach to chiral C8/C9-piperazino-substituted 1,4-benzodiazepin-2-ones as peptidomimetic scaffolds. The Journal of Organic Chemistry. 73: 8458-68. PMID 18844418 DOI: 10.1021/Jo8015456  0.328
2008 Butini S, Pickering DS, Morelli E, Coccone SS, Trotta F, Angelis MD, Guarino E, Fiorini I, Campiani G, Novellino E, Schousboe A, Christensen JK, Gemma S. 1H-cyclopentapyrimidine-2,4(1H,3H)-dione-related ionotropic glutamate receptors ligands. structure-activity relationships and identification of potent and Selective iGluR5 modulators. Journal of Medicinal Chemistry. 51: 6614-6618. PMID 18811139 DOI: 10.1021/Jm800865A  0.346
2008 Butini S, Guarino E, Campiani G, Brindisi M, Coccone SS, Fiorini I, Novellino E, Belinskaya T, Saxena A, Gemma S. Tacrine based human cholinesterase inhibitors: synthesis of peptidic-tethered derivatives and their effect on potency and selectivity. Bioorganic & Medicinal Chemistry Letters. 18: 5213-6. PMID 18786825 DOI: 10.1016/J.Bmcl.2008.08.076  0.354
2008 Zanoli S, Gemma S, Butini S, Brindisi M, Joshi BP, Campiani G, Fattorusso C, Persico M, Crespan E, Cancio R, Spadari S, Hübscher U, Maga G. Selective targeting of the HIV-1 reverse transcriptase catalytic complex through interaction with the ''primer grip'' region by pyrrolobenzoxazepinone non-nucleoside inhibitors correlates with increased activity towards drug-resistant mutants Biochemical Pharmacology. 76: 156-168. PMID 18541223 DOI: 10.1016/J.Bcp.2008.04.009  0.331
2008 Butini S, Campiani G, Borriello M, Gemma S, Panico A, Persico M, Catalanotti B, Ros S, Brindisi M, Agnusdei M, Fiorini I, Nacci V, Novellino E, Belinskaya T, Saxena A, et al. Exploiting protein fluctuations at the active-site gorge of human cholinesterases: further optimization of the design strategy to develop extremely potent inhibitors. Journal of Medicinal Chemistry. 51: 3154-70. PMID 18479118 DOI: 10.1021/Jm701253T  0.346
2008 Gemma S, Campiani G, Butini S, Kukreja G, Coccone SS, Joshi BP, Persico M, Nacci V, Fiorini I, Novellino E, Fattorusso E, Taglialatela-Scafati O, Savini L, Taramelli D, Basilico N, et al. Clotrimazole scaffold as an innovative pharmacophore towards potent antimalarial agents: design, synthesis, and biological and structure-activity relationship studies. Journal of Medicinal Chemistry. 51: 1278-94. PMID 18278860 DOI: 10.1021/Jm701247K  0.404
2008 Fattorusso C, Campiani G, Kukreja G, Persico M, Butini S, Romano MP, Altarelli M, Ros S, Brindisi M, Savini L, Novellino E, Nacci V, Fattorusso E, Parapini S, Basilico N, et al. Design, synthesis, and structure-activity relationship studies of 4-quinolinyl- and 9-acrydinylhydrazones as potent antimalarial agents. Journal of Medicinal Chemistry. 51: 1333-43. PMID 18278859 DOI: 10.1021/Jm7012375  0.408
2008 Verma NK, Dempsey E, Conroy J, Olwell P, Mcelligott AM, Davies AM, Kelleher D, Butini S, Campiani G, Williams DC, Zisterer DM, Lawler M, Volkov Y. A new microtubule-targeting compound PBOX-15 inhibits T-cell migration via post-translational modifications of tubulin. Journal of Molecular Medicine (Berlin, Germany). 86: 457-69. PMID 18270678 DOI: 10.1007/S00109-008-0312-8  0.323
2008 Greene LM, Campiani G, Lawler M, Williams DC, Zisterer DM. BubR1 is required for a sustained mitotic spindle checkpoint arrest in human cancer cells treated with tubulin-targeting pyrrolo-1,5-benzoxazepines. Molecular Pharmacology. 73: 419-30. PMID 17991869 DOI: 10.1124/Mol.107.039024  0.32
2007 Gemma S, Kukreja G, Campiani G, Butini S, Bernetti M, Joshi BP, Savini L, Basilico N, Taramelli D, Yardley V, Bertamino A, Novellino E, Persico M, Catalanotti B, Fattorusso C. Development of piperazine-tethered heterodimers as potent antimalarials against chloroquine-resistant P. falciparum strains. Synthesis and molecular modeling. Bioorganic & Medicinal Chemistry Letters. 17: 3535-3539. PMID 17493808 DOI: 10.1016/J.Bmcl.2007.04.077  0.36
2007 Gemma S, Campiani G, Butini S, Kukreja G, Joshi BP, Persico M, Catalanotti B, Novellino E, Fattorusso E, Nacci V, Savini L, Taramelli D, Basilico N, Morace G, Yardley V, et al. Design and synthesis of potent antimalarial agents based on clotrimazole scaffold: exploring an innovative pharmacophore. Journal of Medicinal Chemistry. 50: 595-8. PMID 17263523 DOI: 10.1021/Jm061429P  0.398
2007 Greene LM, Kelly L, Onnis V, Campiani G, Lawler M, Williams DC, Zisterer DM. STI-571 (imatinib mesylate) enhances the apoptotic efficacy of pyrrolo-1,5-benzoxazepine-6, a novel microtubule-targeting agent, in both STI-571-sensitive and -resistant Bcr-Abl-positive human chronic myeloid leukemia cells. The Journal of Pharmacology and Experimental Therapeutics. 321: 288-97. PMID 17202400 DOI: 10.1124/Jpet.106.116640  0.339
2006 Fattorusso C, Campiani G, Catalanotti B, Persico M, Basilico N, Parapini S, Taramelli D, Campagnuolo C, Fattorusso E, Romano A, Taglialatela-Scafati O. Endoperoxide derivatives from marine organisms: 1,2-dioxanes of the plakortin family as novel antimalarial agents. Journal of Medicinal Chemistry. 49: 7088-7094. PMID 17125261 DOI: 10.1021/Jm060899G  0.354
2006 Gemma S, Kukreja G, Fattorusso C, Persico M, Romano MP, Altarelli M, Savini L, Campiani G, Fattorusso E, Basilico N, Taramelli D, Yardley V, Butini S. Synthesis of N1-arylidene-N2-quinolyl- and N2-acrydinylhydrazones as potent antimalarial agents active against CQ-resistant P. falciparum strains. Bioorganic & Medicinal Chemistry Letters. 16: 5384-5388. PMID 16890433 DOI: 10.1016/J.Bmcl.2006.07.060  0.322
2006 Gemma S, Gabellieri E, Huleatt P, Fattorusso C, Borriello M, Catalanotti B, Butini S, De Angelis M, Novellino E, Nacci V, Belinskaya T, Saxena A, Campiani G. Discovery of huperzine A-tacrine hybrids as potent inhibitors of human cholinesterases targeting their midgorge recognition sites. Journal of Medicinal Chemistry. 49: 3421-5. PMID 16722663 DOI: 10.1021/Jm060257T  0.363
2006 Mulligan JM, Greene LM, Cloonan S, Mc Gee MM, Onnis V, Campiani G, Fattorusso C, Lawler M, Williams DC, Zisterer DM. Identification of tubulin as the molecular target of proapoptotic pyrrolo-1,5-benzoxazepines. Molecular Pharmacology. 70: 60-70. PMID 16571652 DOI: 10.1124/Mol.105.021204  0.409
2005 Fattorusso C, Gemma S, Butini S, Huleatt P, Catalanotti B, Persico M, De Angelis M, Fiorini I, Nacci V, Ramunno A, Rodriquez M, Greco G, Novellino E, Bergamini A, Marini S, ... ... Campiani G, et al. Specific targeting highly conserved residues in the HIV-1 reverse transcriptase primer grip region. Design, synthesis, and biological evaluation of novel, potent, and broad spectrum NNRTIs with antiviral activity. Journal of Medicinal Chemistry. 48: 7153-65. PMID 16279773 DOI: 10.1021/Jm050257D  0.361
2005 Maga G, Gemma S, Fattorusso C, Locatelli GA, Butini S, Persico M, Kukreja G, Romano MP, Chiasserini L, Savini L, Novellino E, Nacci V, Spadari S, Campiani G. Specific targeting of hepatitis C virus NS3 RNA helicase. Discovery of the potent and selective competitive nucleotide-mimicking inhibitor QU663. Biochemistry. 44: 9637-44. PMID 16008349 DOI: 10.1021/Bi047437U  0.302
2005 Mc Gee MM, Gemma S, Butini S, Ramunno A, Zisterer DM, Fattorusso C, Catalanotti B, Kukreja G, Fiorini I, Pisano C, Cucco C, Novellino E, Nacci V, Williams DC, Campiani G. Pyrrolo[1,5]benzoxa(thia)zepines as a new class of potent apoptotic agents. Biological studies and identification of an intracellular location of their drug target. Journal of Medicinal Chemistry. 48: 4367-77. PMID 15974589 DOI: 10.1021/Jm049402Y  0.398
2005 Ferlini C, Raspaglio G, Mozzetti S, Cicchillitti L, Filippetti F, Gallo D, Fattorusso C, Campiani G, Scambia G. The seco-taxane IDN5390 is able to target class III beta-tubulin and to overcome paclitaxel resistance. Cancer Research. 65: 2397-2405. PMID 15781655 DOI: 10.1158/0008-5472.Can-04-3065  0.304
2005 Campiani G, Fattorusso C, Butini S, Gaeta A, Agnusdei M, Gemma S, Persico M, Catalanotti B, Savini L, Nacci V, Novellino E, Holloway HW, Greig NH, Belinskaya T, Fedorko JM, et al. Development of molecular probes for the identification of extra interaction sites in the mid-gorge and peripheral sites of butyrylcholinesterase (BuChE). Rational design of novel, selective, and highly potent BuChE inhibitors. Journal of Medicinal Chemistry. 48: 1919-29. PMID 15771436 DOI: 10.1021/Jm049510K  0.355
2005 Campiani G, Butini S, Fattorusso C, Trotta F, Gemma S, Catalanotti B, Nacci V, Fiorini I, Cagnotto A, Mereghetti I, Mennini T, Minetti P, Di Cesare MA, Stasi MA, Di Serio S, et al. Novel atypical antipsychotic agents: Rational design, an efficient palladium-catalyzed route, and pharmacological studies Journal of Medicinal Chemistry. 48: 1705-1708. PMID 15771414 DOI: 10.1021/Jm049629T  0.341
2005 Frandsen A, Pickering DS, Vestergaard B, Kasper C, Nielsen BB, Greenwood JR, Campiani G, Fattorusso C, Gajhede M, Schousboe A, Kastrup JS. Tyr702 is an important determinant of agonist binding and domain closure of the ligand-binding core of GluR2. Molecular Pharmacology. 67: 703-13. PMID 15591246 DOI: 10.1124/Mol.104.002931  0.314
2005 Rogers A, Schmuck G, Scholz G, Griffiths R, Meredith C, Schousboe A, Campiani G, Williams DC. Improvements in an in-vitro assay for excitotoxicity by measurement of early gene (c-fos mRNA) levels. Archives of Toxicology. 79: 129-139. PMID 15565427 DOI: 10.1007/S00204-004-0617-5  0.328
2005 Greene LM, Fleeton M, Mulligan J, Gowda C, Sheahan BJ, Atkins GJ, Campiani G, Nacci V, Lawler M, Williams DC, Zisterer DM. The pyrrolo-1,5-benzoxazepine, PBOX-6, inhibits the growth of breast cancer cells in vitro independent of estrogen receptor status and inhibits breast tumour growth in vivo. Oncology Reports. 14: 1357-1363. DOI: 10.3892/Or.14.5.1357  0.342
2004 Lloyd DG, Hughes RB, Zisterer DM, Williams DC, Fattorusso C, Catalanotti B, Campiani G, Meegan MJ. Benzoxepin-derived estrogen receptor modulators: a novel molecular scaffold for the estrogen receptor. Journal of Medicinal Chemistry. 47: 5612-5. PMID 15509159 DOI: 10.1021/Jm0495834  0.317
2004 Mc Gee MM, Greene LM, Ledwidge S, Campiani G, Nacci V, Lawler M, Williams DC, Zisterer DM. Selective induction of apoptosis by the pyrrolo-1,5-benzoxazepine 7-[[dimethylcarbamoyl]oxy]-6-(2-naphthyl)pyrrolo-[2,1-d] (1,5)-benzoxazepine (PBOX-6) in Leukemia cells occurs via the c-Jun NH2-terminal kinase-dependent phosphorylation and inactivation of Bcl-2 and Bcl-XL. The Journal of Pharmacology and Experimental Therapeutics. 310: 1084-95. PMID 15143129 DOI: 10.1124/Jpet.104.067561  0.323
2004 Locatelli GA, Campiani G, Cancio R, Morelli E, Ramunno A, Gemma S, Hübscher U, Spadari S, Maga G. Effects of Drug Resistance Mutations L100I and V106A on the Binding of Pyrrolobenzoxazepinone Nonnucleoside Inhibitors to the Human Immunodeficiency Virus Type 1 Reverse Transcriptase Catalytic Complex Antimicrobial Agents and Chemotherapy. 48: 1570-1580. PMID 15105107 DOI: 10.1128/Aac.48.5.1570-1580.2004  0.352
2004 Campiani G, Butini S, Fattorusso C, Catalanotti B, Gemma S, Nacci V, Morelli E, Cagnotto A, Mereghetti I, Mennini T, Carli M, Minetti P, Di Cesare MA, Mastroianni D, Scafetta N, et al. Pyrrolo[1,3]benzothiazepine-Based Seroonin and Dopamine Receptor Antagonists. Molecular Modeling, Further Structure-Activity Relationship Studies, and Identification of Novel Atypical Antipsychotic Agents Journal of Medicinal Chemistry. 47: 143-157. PMID 14695828 DOI: 10.1021/Jm0309811  0.393
2003 Mennini T, Fumagalli E, Gobbi M, Fattorusso C, Catalanotti B, Campiani G. Substrate inhibitors and blockers of excitatory amino acid transporters in the treatment of neurodegeneration: Critical considerations European Journal of Pharmacology. 479: 291-296. PMID 14612159 DOI: 10.1016/J.Ejphar.2003.08.078  0.308
2003 Mulligan JM, Campiani G, Ramunno A, Nacci V, Zisterer DM. Inhibition of G1 cyclin-dependent kinase activity during growth arrest of human astrocytoma cells by the pyrrolo-1,5-benzoxazepine, PBOX-21. Biochimica Et Biophysica Acta. 1639: 43-52. PMID 12943967 DOI: 10.1016/S0925-4439(03)00128-5  0.303
2003 Campiani G, Butini S, Trotta F, Fattorusso C, Catalanotti B, Aiello F, Gemma S, Nacci V, Novellino E, Stark JA, Cagnotto A, Fumagalli E, Carnovali F, Cervo L, Mennini T. Synthesis and pharmacological evaluation of potent and highly selective D3 receptor ligands: Inhibition of cocaine-seeking behavior and the role of dopamine D3/D2 receptors Journal of Medicinal Chemistry. 46: 3822-3839. PMID 12930145 DOI: 10.1021/Jm0211220  0.334
2003 Sinclair C, Reavy H, Grieve A, Schousboe A, Morelli E, Novellino E, Campiani G, Griffiths R. Inherent desensitisation-preventing properties of a novel, subtype-selective AMPA receptor agonist, (S)-CPW 399, as a possible explanation for its excitotoxic action in cultured cerebellar granule cells. Neurochemistry International. 42: 499-510. PMID 12547649 DOI: 10.1016/S0197-0186(02)00141-9  0.323
2003 Savini L, Gaeta A, Fattorusso C, Catalanotti B, Campiani G, Chiasserini L, Pellerano C, Novellino E, McKissic D, Saxena A. Specific targeting of acetylcholinesterase and butyrylcholinesterase recognition sites. Rational design of novel, selective, and highly potent cholinesterase inhibitors. Journal of Medicinal Chemistry. 46: 1-4. PMID 12502352 DOI: 10.1021/Jm0255668  0.35
2003 Butini S, Campiani G, Angelis MD, Fattorusso C, Nacci V, Fiorini I. Novel antipsychotic agents: recent advances in the drug treatment of schizophrenia Expert Opinion On Therapeutic Patents. 13: 425-448. DOI: 10.1517/13543776.13.4.425  0.311
2003 Gemma S, Butini S, Fattorusso C, Fiorini I, Nacci V, Bellebaum K, McKissic D, Saxena A, Campiani G. A palladium-catalyzed synthetic approach to new Huperzine A analogues modified at the pyridone ring Tetrahedron. 59: 87-93. DOI: 10.1016/S0040-4020(02)01449-7  0.311
2002 Campiani G, Ramunno A, Fiorini I, Nacci V, Morelli E, Novellino E, Goegan M, Mennini T, Sullivan S, Zisterer DM, Williams CD. Synthesis of new molecular probes for investigation of steroid biosynthesis induced by selective interaction with peripheral type benzodiazepine receptors (PBR). Journal of Medicinal Chemistry. 45: 4276-81. PMID 12213069 DOI: 10.1021/Jm020849L  0.381
2002 Campiani G, Ramunno A, Maga G, Nacci V, Fattorusso C, Catalanotti B, Morelli E, Novellino E. Non-nucleoside HIV-1 reverse transcriptase (RT) inhibitors: past, present, and future perspectives. Current Pharmaceutical Design. 8: 615-57. PMID 11945162 DOI: 10.2174/1381612024607207  0.353
2002 Mc Gee MM, Campiani G, Ramunno A, Nacci V, Lawler M, Williams DC, Zisterer DM. Activation of the c-Jun N-terminal kinase (JNK) signaling pathway is essential during PBOX-6-induced apoptosis in chronic myelogenous leukemia (CML) cells. The Journal of Biological Chemistry. 277: 18383-9. PMID 11856743 DOI: 10.1074/Jbc.M112058200  0.318
2002 Campiani G, Butini S, Gemma S, Nacci V, Fattorusso C, Catalanotti B, Giorgi G, Cagnotto A, Goegan M, Mennini T, Minetti P, Di Cesare MA, Mastroianni D, Scafetta N, Galletti B, et al. Pyrrolo[1,3]benzothiazepine-based atypical antipsychotic agents. Synthesis, structure - Activity relationship, molecular modeling, and biological studies Journal of Medicinal Chemistry. 45: 344-359. PMID 11784139 DOI: 10.1021/Jm010982Y  0.358
2002 Gemma S, Campiani G, Butini S, Morelli E, Minetti P, Tinti O, Nacci V. Polycondensed heterocycles. Part 12: An approach to the synthesis of 2-acetyl-1′-methyl-1,2,3,4-tetrahydrospiro[isoquinoline-1,4′-pyrrolidine]-2′-one Tetrahedron. 58: 3689-3692. DOI: 10.1016/S0040-4020(02)00333-2  0.313
2001 Campiani G, Morelli E, Nacci V, Fattorusso C, Ramunno A, Novellino E, Greenwood J, Liljefors T, Griffiths R, Sinclair C, Reavy H, Kristensen AS, Pickering DS, Schousboe A, Cagnotto A, et al. Characterization of the 1H-cyclopentapyrimidine-2,4(1H,3H)-dione derivative (S)-CPW399 as a novel, potent, and subtype-selective AMPA receptor full agonist with partial desensitization properties. Journal of Medicinal Chemistry. 44: 4501-4. PMID 11741469 DOI: 10.1021/Jm015552M  0.355
2001 Zisterer DM, McGee MM, Campiani G, Ramunno A, Fattorusso C, Nacci V, Lawler M, Williams DC. Pyrrolo-1,5-benzoxazepines: a new class of apoptotic agents. Biochemical Society Transactions. 29: 704-6. PMID 11709059 DOI: 10.1042/0300-5127:0290704  0.368
2001 Maga G, Ramunno A, Nacci V, Locatelli GA, Spadari S, Fiorini I, Baldanti F, Paolucci S, Zavattoni M, Bergamini A, Galletti B, Muck S, Hubscher U, Giorgi G, Guiso G, ... ... Campiani G, et al. The stereoselective targeting of a specific enzyme-substrate complex is the molecular mechanism for the synergic inhibition of HIV-1 reverse transcriptase by (R)-(-)-PPO464: a novel generation of nonnucleoside inhibitors. The Journal of Biological Chemistry. 276: 44653-62. PMID 11572864 DOI: 10.1074/Jbc.M106702200  0.304
2001 Campiani G, De Angelis M, Armaroli S, Fattorusso C, Catalanotti B, Ramunno A, Nacci V, Novellino E, Grewer C, Ionescu D, Rauen T, Griffiths R, Sinclair C, Fumagalli E, Mennini T. A rational approach to the design of selective substrates and potent nontransportable inhibitors of the excitatory amino acid transporter EAAC1 (EAAT3). new glutamate and aspartate analogues as potential neuroprotective agents. Journal of Medicinal Chemistry. 44: 2507-10. PMID 11472204 DOI: 10.1021/Jm015509Z  0.369
2001 Savini L, Campiani G, Gaeta A, Pellerano C, Fattorusso C, Chiasserini L, Fedorko JM, Saxena A. Novel and potent tacrine-related hetero- and homobivalent ligands for acetylcholinesterase and butyrylcholinesterase Bioorganic & Medicinal Chemistry Letters. 11: 1779-1782. PMID 11425559 DOI: 10.1016/S0960-894X(01)00294-3  0.366
1999 Campiani G, Morelli E, Fabbrini M, Nacci V, Greco G, Novellino E, Ramunno A, Maga G, Spadari S, Caliendo G, Bergamini A, Faggioli E, Uccella I, Bolacchi F, Marini S, et al. Pyrrolobenzoxazepinone derivatives as non-nucleoside HIV-1 RT inhibitors: further structure-activity relationship studies and identification of more potent broad-spectrum HIV-1 RT inhibitors with antiviral activity. Journal of Medicinal Chemistry. 42: 4462-70. PMID 10543890 DOI: 10.1021/Jm990150O  0.409
1999 Campiani G, Morelli E, Gemma S, Nacci V, Butini S, Hamon M, Novellino E, Greco G, Cagnotto A, Goegan M, Cervo L, Dalla Valle F, Fracasso C, Caccia S, Mennini T. Pyrroloquinoxaline derivatives as high-affinity and selective 5-HT(3) receptor agonists: synthesis, further structure-activity relationships, and biological studies. Journal of Medicinal Chemistry. 42: 4362-79. PMID 10543880 DOI: 10.1021/Jm990151G  0.347
1999 Neamati N, Turpin JA, Winslow HE, Christensen JL, Williamson K, Orr A, Rice WG, Pommier Y, Garofalo A, Brizzi A, Campiani G, Fiorini I, Nacci V. Thiazolothiazepine inhibitors of HIV-1 integrase. Journal of Medicinal Chemistry. 42: 3334-41. PMID 10464020 DOI: 10.1021/Jm990047Z  0.363
1999 Campiani G, Kozikowski AP, Wang S, Ming L, Nacci V, Saxena A, Doctor BP. Synthesis and anticholinesterase activity of huperzine A analogues containing phenol and catechol replacements for the pyridone ring. Bioorganic & Medicinal Chemistry Letters. 8: 1413-8. PMID 9871776 DOI: 10.1016/S0960-894X(98)00229-7  0.355
1999 Garofalo A, Campiani G, Fiorini I, Nacci V. Polycondensed heterocycles. X. A new method for the preparation of pyrrolo[2,1-c][1,4]benzothiazepines by intramolecular mitsunobu cyclisation Tetrahedron. 55: 1479-1490. DOI: 10.1016/S0040-4020(98)01127-2  0.309
1998 Campiani G, Nacci V, Bechelli S, Ciani SM, Garofalo A, Fiorini I, Wikström H, de Boer P, Liao Y, Tepper PG, Cagnotto A, Mennini T. New antipsychotic agents with serotonin and dopamine antagonist properties based on a pyrrolo[2,1-b][1,3]benzothiazepine structure. Journal of Medicinal Chemistry. 41: 3763-72. PMID 9748351 DOI: 10.1021/Jm9706832  0.335
1998 Zisterer DM, Hance N, Campiani G, Garofalo A, Nacci V, Williams DC. Antiproliferative action of pyrrolobenzoxazepine derivatives in cultured cells: absence of correlation with binding to the peripheral-type benzodiazepine binding site. Biochemical Pharmacology. 55: 397-403. PMID 9514073 DOI: 10.1016/S0006-2952(97)00500-5  0.308
1997 Campiani G, Cappelli A, Nacci V, Anzini M, Vomero S, Hamon M, Cagnotto A, Fracasso C, Uboldi C, Caccia S, Consolo S, Mennini T. Novel and highly potent 5-HT3 receptor agonists based on a pyrroloquinoxaline structure. Journal of Medicinal Chemistry. 40: 3670-8. PMID 9357534 DOI: 10.1021/Jm970376W  0.356
1997 Corelli F, Manetti F, Tafi A, Campiani G, Nacci V, Botta M. Diltiazem-like calcium entry blockers: a hypothesis of the receptor-binding site based on a comparative molecular field analysis model. Journal of Medicinal Chemistry. 40: 125-31. PMID 9016337 DOI: 10.1021/Jm9605647  0.351
1997 Campiani G, Nacci V, Fiorini I, Filippis MD, Garofalo A, Ciani S, Greco G, Novellino E, Manzoni C, Mennini T. New pyrrolobenzothiazepine derivatives as molecular probes of the ‘peripheral-type’ benzodiazepine receptor (PBR) binding site European Journal of Medicinal Chemistry. 32: 241-251. DOI: 10.1016/S0223-5234(97)83975-X  0.352
1996 Campiani G, Nacci V, Fiorini I, De Filippis MP, Garofalo A, Ciani SM, Greco G, Novellino E, Williams DC, Zisterer DM, Woods MJ, Mihai C, Manzoni C, Mennini T. Synthesis, biological activity, and SARs of pyrrolobenzoxazepine derivatives, a new class of specific "peripheral-type" benzodiazepine receptor ligands. Journal of Medicinal Chemistry. 39: 3435-50. PMID 8784441 DOI: 10.1021/Jm960251B  0.35
1996 Campiani G, Fiorini I, De Filippis MP, Ciani SM, Garofalo A, Nacci V, Giorgi G, Sega A, Botta M, Chiarini A, Budriesi R, Bruni G, Romeo MR, Manzoni C, Mennini T. Cardiovascular characterization of pyrrolo[2,1-d][1,5]benzothiazepine derivatives binding selectively to the peripheral-type benzodiazepine receptor (PBR): from dual PBR affinity and calcium antagonist activity to novel and selective calcium entry blockers. Journal of Medicinal Chemistry. 39: 2922-38. PMID 8709127 DOI: 10.1021/Jm960162Z  0.355
1996 Campiani G, Nacci V, Fiorini I, De Filippis MP, Garofalo A, Greco G, Novellino E, Altamura S, Di Renzo L. Pyrrolobenzothiazepinones and pyrrolobenzoxazepinones: novel and specific non-nucleoside HIV-1 reverse transcriptase inhibitors with antiviral activity. Journal of Medicinal Chemistry. 39: 2672-80. PMID 8709096 DOI: 10.1021/Jm950702C  0.344
1996 Kozikowski AP, Campiani G, Nacci V, Sega A, Saxena A, Doctor BP. An approach to modified heterocyclic analogues of huperzine A and isohuperzine A. Synthesis of the pyrimidone and pyrazole analogues, and their anticholinesterase activity Journal of the Chemical Society-Perkin Transactions 1. 1287-1297. DOI: 10.1039/P19960001287  0.351
1996 Kozikowski AP, Campiani G, Sun §L, Wang S, Saxena aA, Doctor BP. Identification of a more potent analogue of the naturally occurring alkaloid huperzine A. Predictive molecular modeling of its interaction with AChE Journal of the American Chemical Society. 118: 11357-11362. DOI: 10.1021/Ja9622822  0.385
1995 Dalpiaz A, Bertolasi V, Borea PA, Nacci V, Fiorini I, Campiani G, Mennini T, Manzoni C, Novellino E, Greco G. A concerted study using binding measurements, X-ray structural data, and molecular modeling on the stereochemical features responsible for the affinity of 6-arylpyrrolo[2,1-d][1,5]benzothiazepines toward mitochondrial benzodiazepine receptors. Journal of Medicinal Chemistry. 38: 4730-8. PMID 7473601 DOI: 10.1021/Jm00023A013  0.305
1995 Campiani G, Garofalo A, Fiorini I, Botta M, Nacci V, Tafi A, Chiarini A, Budriesi R, Bruni G, Romeo MR. Pyrrolo[2,1-c][1,4]benzothiazines: synthesis, structure-activity relationships, molecular modeling studies, and cardiovascular activity. Journal of Medicinal Chemistry. 38: 4393-410. PMID 7473567 DOI: 10.1021/Jm00022A005  0.379
1995 Kozikowski AP, Campiani G, Saxena A, Doctor BP. Synthesis and acetylcholinesterase inhibitory activity of several pyrimidone analogues of huperzine A Journal of the Chemical Society, Chemical Communications. 283-285. DOI: 10.1039/C39950000283  0.37
1994 Fiorini I, Nacci V, Ciani SM, Garofalo A, Campiani G, Savini L, Novellino E, Greco G, Bernasconi P, Mennini T. Novel ligands specific for mitochondrial benzodiazepine receptors: 6-arylpyrrolo[2,1-d][1,5]benzothiazepine derivatives. Synthesis, structure-activity relationships, and molecular modeling studies. Journal of Medicinal Chemistry. 37: 1427-38. PMID 8182701 DOI: 10.1021/Jm00036A007  0.394
1994 Greco G, Novellino E, Fiorini I, Nacci V, Campiani G, Ciani SM, Garofalo A, Bernasconi P, Mennini T. A comparative molecular field analysis model for 6-arylpyrrolo[2,1-d] [1,5]benzothiazepines binding selectively to the mitochondrial benzodiazepine receptor. Journal of Medicinal Chemistry. 37: 4100-8. PMID 7990110 DOI: 10.1021/Jm00050A007  0.32
1994 Campiani G, Garofalo A, Fiorini I, Nacci V, Botta M, Tafi A, Chiarini A, Budriesi R, Bruni G, Romeo M. Synthesis and “in vitro” cardiovascular activity of 4-aryl-2,3,3a,4-tetrahydro-1h-pyrrolo[2,1-c][1,4]benzothiazin-1-ones and 7-acetoxy-6-phenyl-7a,8,9,10-tetrahydropyrrolo [2,1,-d][1,5]benzothiazepin-10-one. Bioorganic & Medicinal Chemistry Letters. 4: 1235-1240. DOI: 10.1016/S0960-894X(01)80337-1  0.325
1992 Campiani G, Nacci V, Garofalo A, Botta M, Fiorini I, Tafi A, Bruni G, Romeo M, Peres A, Bertollini L. Synthesis and preliminary biological evaluation of 1-aminomethyl-4-substituted-4-H-pyrrolo[2,1-C][1,4] benzothiazines, a new class of calcium antagonists. Bioorganic & Medicinal Chemistry Letters. 2: 1193-1198. DOI: 10.1016/S0960-894X(00)80212-7  0.311
1990 Nacci V, Campiani G, Garofalo A. Polycondensed Heterocycles.VI. A new efficient synthesis of 4H-pyrrolo [2,1-c][1, 4] Benzothiazines Synthetic Communications. 20: 3019-3029. DOI: 10.1080/00397919008051521  0.302
1990 Nacci V, Campiani G, Garofalo A. Polycondensed heterocycles. IV. synthesis of 1,4-dioxo-2,3,3a,4-tetrahydro-1H-pyrrolo[2,1-c][1,4]benzothiazine† Journal of Heterocyclic Chemistry. 27: 1329-1335. DOI: 10.1002/Jhet.5570270528  0.313
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