Ines Bruno - Publications

Affiliations: 
University of Salerno 

78 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
2023 Gazzillo E, Pierri M, Colarusso E, Chini MG, Ferraro MG, Piccolo M, Irace C, Bruno I, Bifulco G, Terracciano S, Lauro G. Exploring the chemical space of functionalized [1,2,4]triazolo[4,3-a]quinoxaline-based compounds targeting the bromodomain of BRD9. Bioorganic Chemistry. 139: 106677. PMID 37352721 DOI: 10.1016/j.bioorg.2023.106677  0.792
2023 Morretta E, Ruggiero D, Belvedere R, Petrella A, Bruno I, Terracciano S, Monti MC. A multidisciplinary functional proteomics-aided strategy as a tool for the profiling of a novel cytotoxic thiadiazolopyrimidone. Bioorganic Chemistry. 138: 106620. PMID 37229937 DOI: 10.1016/j.bioorg.2023.106620  0.714
2022 Potenza M, Giordano A, Chini MG, Saviano A, Kretzer C, Raucci F, Russo M, Lauro G, Terracciano S, Bruno I, Iorizzi M, Hofstetter RK, Pace S, Maione F, Werz O, et al. Identification of 2-Aminoacyl-1,3,4-thiadiazoles as Prostaglandin E and Leukotriene Biosynthesis Inhibitors. Acs Medicinal Chemistry Letters. 14: 26-34. PMID 36655121 DOI: 10.1021/acsmedchemlett.2c00343  0.761
2022 Colarusso E, Ceccacci S, Monti MC, Gazzillo E, Giordano A, Chini MG, Ferraro MG, Piccolo M, Ruggiero D, Irace C, Terracciano S, Bruno I, Bifulco G, Lauro G. Identification of 2,4,5-trisubstituted-2,4-dihydro-3H-1,2,4-triazol-3-one-based small molecules as selective BRD9 binders. European Journal of Medicinal Chemistry. 247: 115018. PMID 36577218 DOI: 10.1016/j.ejmech.2022.115018  0.779
2022 Di Micco S, Terracciano S, Pierri M, Cantone V, Liening S, König S, Garscha U, Hofstetter RK, Koeberle A, Werz O, Bruno I, Bifulco G. Identification of 2,4-Dinitro-Biphenyl-Based Compounds as MAPEG Inhibitors. Chemmedchem. PMID 36111583 DOI: 10.1002/cmdc.202200327  0.775
2022 Gazzillo E, Terracciano S, Ruggiero D, Potenza M, Chini MG, Lauro G, Fischer K, Hofstetter RK, Giordano A, Werz O, Bruno I, Bifulco G. Repositioning of Quinazolinedione-Based Compounds on Soluble Epoxide Hydrolase (sEH) through 3D Structure-Based Pharmacophore Model-Driven Investigation. Molecules (Basel, Switzerland). 27. PMID 35744994 DOI: 10.3390/molecules27123866  0.766
2022 Ruggiero D, Terracciano S, Lauro G, Pecoraro M, Franceschelli S, Bifulco G, Bruno I. Structural Refinement of 2,4-Thiazolidinedione Derivatives as New Anticancer Agents Able to Modulate the BAG3 Protein. Molecules (Basel, Switzerland). 27. PMID 35163936 DOI: 10.3390/molecules27030665  0.754
2022 Pierri M, Gazzillo E, Chini MG, Ferraro MG, Piccolo M, Maione F, Irace C, Bifulco G, Bruno I, Terracciano S, Lauro G. Introducing structure-based three-dimensional pharmacophore models for accelerating the discovery of selective BRD9 binders. Bioorganic Chemistry. 118: 105480. PMID 34823196 DOI: 10.1016/j.bioorg.2021.105480  0.772
2021 Di Micco S, Terracciano S, Ruggiero D, Potenza M, Vaccaro MC, Fischer K, Werz O, Bruno I, Bifulco G. Identification of 2-(thiophen-2-yl)acetic Acid-Based Lead Compound for mPGES-1 Inhibition. Frontiers in Chemistry. 9: 676631. PMID 34046398 DOI: 10.3389/fchem.2021.676631  0.763
2020 Nemati F, Salehi P, Bararjanian M, Hadian N, Mohebbi M, Lauro G, Ruggiero D, Terracciano S, Bifulco G, Bruno I. Discovery of noscapine derivatives as potential β-tubulin inhibitors. Bioorganic & Medicinal Chemistry Letters. 30: 127489. PMID 32784088 DOI: 10.1016/J.Bmcl.2020.127489  0.776
2020 Chini MG, Giordano A, Potenza M, Terracciano S, Fischer K, Vaccaro MC, Colarusso E, Bruno I, Riccio R, Koeberle A, Werz O, Bifulco G. Targeting mPGES-1 by a Combinatorial Approach: Identification of the Aminobenzothiazole Scaffold to Suppress PGE Levels. Acs Medicinal Chemistry Letters. 11: 783-789. PMID 32435385 DOI: 10.1021/Acsmedchemlett.9B00618  0.775
2020 Lauro G, Terracciano S, Cantone V, Ruggiero D, Fischer K, Pace S, Werz O, Bruno I, Bifulco G. A Combinatorial Virtual Screening Approach Driving the Synthesis of 2,4-Thiazolidinedione-Based Molecules as New Dual mPGES-1/5-LO Inhibitors. Chemmedchem. PMID 32022480 DOI: 10.1002/Cmdc.201900694  0.791
2020 Vita SD, Terracciano S, Bruno I, Chini MG. From natural compounds to bioactive molecules by way of NMR and in silico methodologies European Journal of Organic Chemistry. DOI: 10.1002/Ejoc.202000469  0.727
2019 Giordano A, Forte G, Terracciano S, Russo A, Sala M, Scala MC, Johansson C, Oppermann U, Riccio R, Bruno I, Di Micco S. Identification of the 2-Benzoxazol-2-yl-phenol Scaffold as New Hit for JMJD3 Inhibition. Acs Medicinal Chemistry Letters. 10: 601-605. PMID 30996803 DOI: 10.1021/Acsmedchemlett.8B00589  0.792
2019 Schettini R, Costabile C, Della Sala G, Buirey J, Tosolini M, Tecilla P, Vaccaro MC, Bruno I, De Riccardis F, Izzo I. Tuning the biomimetic performances of 4-hydroxyproline-containing cyclic peptoids. Organic & Biomolecular Chemistry. 16: 6708-6717. PMID 30182115 DOI: 10.1039/C8Ob01522H  0.32
2019 Terracciano S, Chini MG, Vaccaro MC, Strocchia M, Foglia A, Vassallo A, Saturnino C, Riccio R, Bifulco G, Bruno I. Correction: Identification of the key structural elements of a dihydropyrimidinone core driving toward more potent Hsp90 C-terminal inhibitors. Chemical Communications (Cambridge, England). 52: 13515. PMID 27805204 DOI: 10.1039/C6Cc90506D  0.771
2018 Khalfaoui A, Chini MG, Bouheroum M, Belaabed S, Lauro G, Terracciano S, Vaccaro MC, Bruno I, Benayache S, Mancini I, Bifulco G. Glucopyranosylbianthrones from the Algerian Asphodelus tenuifolius: Structural Insights and Biological Evaluation on Melanoma Cancer Cells. Journal of Natural Products. PMID 30063349 DOI: 10.1021/Acs.Jnatprod.8B00234  0.761
2018 Di Micco S, Pulvirenti L, Bruno I, Terracciano S, Russo A, Vaccaro MC, Ruggiero D, Muccilli V, Cardullo N, Tringali C, Riccio R, Bifulco G. Identification by Inverse Virtual Screening of magnolol-based scaffold as new tankyrase-2 inhibitors. Bioorganic & Medicinal Chemistry. PMID 29934219 DOI: 10.1016/J.Bmc.2018.06.019  0.807
2018 Terracciano S, Lauro G, Russo A, Vaccaro MC, Vassallo A, De Marco M, Ranieri B, Rosati A, Turco MC, Riccio R, Bifulco G, Bruno I. Discovery and synthesis of the first selective BAG domain modulator of BAG3 as an attractive candidate for the development of a new class of chemotherapeutics. Chemical Communications (Cambridge, England). PMID 29926854 DOI: 10.1039/C8Cc03399D  0.771
2018 Terracciano S, Russo A, Chini MG, Vaccaro MC, Potenza M, Vassallo A, Riccio R, Bifulco G, Bruno I. Discovery of new molecular entities able to strongly interfere with Hsp90 C-terminal domain. Scientific Reports. 8: 1709. PMID 29374167 DOI: 10.1038/S41598-017-14902-Y  0.786
2018 Terracciano S, Chini MG, Vaccaro MC, Strocchia M, Foglia A, Vassallo A, Saturnino C, Riccio R, Bifulco G, Bruno I. Identification of the key structural elements of a dihydropyrimidinone core driving toward more potent Hsp90 C-terminal inhibitors. Chemical Communications (Cambridge, England). 52: 12857-12860. PMID 27731433 DOI: 10.1039/c6cc06379a  0.694
2017 Di Micco S, Terracciano S, Cantone V, Fischer K, Koeberle A, Foglia A, Riccio R, Werz O, Bruno I, Bifulco G. Discovery of new potent molecular entities able to inhibit mPGES-1. European Journal of Medicinal Chemistry. PMID 29133047 DOI: 10.1016/J.Ejmech.2017.10.039  0.808
2017 D'Amato A, Volpe R, Vaccaro MC, Terracciano S, Bruno I, Tosolini M, Tedesco C, Pierri G, Tecilla P, Costabile C, Della Sala G, Izzo I, De Riccardis F. Cyclic Peptoids as Mycotoxin Mimics: An Exploration of Their Structural and Biological Properties. The Journal of Organic Chemistry. 82: 8848-8863. PMID 28763612 DOI: 10.1021/Acs.Joc.7B00965  0.692
2016 Lauro G, Tortorella P, Bertamino A, Ostacolo C, Koeberle A, Fischer K, Bruno I, Terracciano S, Gomez-Monterrey IM, Tauro M, Loiodice F, Novellino E, Riccio R, Werz O, Campiglia P, et al. Structure-Based Design of Microsomal Prostaglandin E2 Synthase-1 (mPGES-1) Inhibitors using a Virtual Fragment Growing Optimization Scheme. Chemmedchem. PMID 26915684 DOI: 10.1002/Cmdc.201500598  0.824
2016 Terracciano S, Foglia A, Chini MG, Vaccaro MC, Russo A, Dal Piaz F, Saturnino C, Riccio R, Bifulco G, Bruno I. New dihydropyrimidin-2(1H)-one based Hsp90 C-terminal inhibitors Rsc Advances. 6: 82330-82340. DOI: 10.1039/C6Ra17235K  0.799
2015 Picaud S, Strocchia M, Terracciano S, Lauro G, Mendez J, Daniels DL, Riccio R, Bifulco G, Bruno I, Filippakopoulos P. 9H-purine scaffold reveals induced-fit pocket plasticity of the BRD9 bromodomain. Journal of Medicinal Chemistry. 58: 2718-36. PMID 25703523 DOI: 10.1021/Jm501893K  0.809
2015 Terracciano S, Lauro G, Strocchia M, Fischer K, Werz O, Riccio R, Bruno I, Bifulco G. Structural Insights for the Optimization of Dihydropyrimidin-2(1H)-one Based mPGES-1 Inhibitors. Acs Medicinal Chemistry Letters. 6: 187-91. PMID 25699159 DOI: 10.1021/Ml500433J  0.802
2015 Strocchia M, Terracciano S, Chini MG, Vassallo A, Vaccaro MC, Dal Piaz F, Leone A, Riccio R, Bruno I, Bifulco G. Targeting the Hsp90 C-terminal domain by the chemically accessible dihydropyrimidinone scaffold. Chemical Communications (Cambridge, England). 51: 3850-3. PMID 25656927 DOI: 10.1039/C4Cc10074C  0.792
2015 Chini MG, Ferroni C, Cantone V, Dambruoso P, Varchi G, Pepe A, Fischer K, Pergola C, Werz O, Bruno I, Riccio R, Bifulco G. Elucidating new structural features of the triazole scaffold for the development of mPGES-1 inhibitors Medchemcomm. 6: 75-79. DOI: 10.1039/C4Md00319E  0.703
2015 Terracciano S, Lauro G, Strocchia M, Fischer K, Werz O, Riccio R, Bruno I, Bifulco G. Structural insights for the optimization of dihydropyrimidin-2(1 H)-one based mPGES-1 inhibitors Acs Medicinal Chemistry Letters. 6: 187-191. DOI: 10.1021/ml500433j  0.659
2014 Lauro G, Strocchia M, Terracciano S, Bruno I, Fischer K, Pergola C, Werz O, Riccio R, Bifulco G. Exploration of the dihydropyrimidine scaffold for the development of new potential anti-inflammatory agents blocking prostaglandin E₂ synthase-1 enzyme (mPGES-1). European Journal of Medicinal Chemistry. 80: 407-15. PMID 24794772 DOI: 10.1016/J.Ejmech.2014.04.061  0.798
2014 Berlinck RG, Braekman JC, Daloze D, Bruno I, Riccio R, Rogeau D, Amade P. Crambines C1 and C2: Two Further Ichthyotoxic Guanidine Alkaloids from the Sponge Crambe crambe. Journal of Natural Products. 55: 528-32. PMID 24697558 DOI: 10.1021/Np50082A026  0.495
2013 Terracciano S, Chini MG, Piaz FD, Vassallo A, Riccio R, Bruno I, Bifulco G. Dimeric and trimeric triazole based molecules as a new class of Hsp90 molecular chaperone inhibitors. European Journal of Medicinal Chemistry. 65: 464-76. PMID 23770448 DOI: 10.1016/J.Ejmech.2013.05.016  0.819
2013 Di Micco S, Chini MG, Terracciano S, Bruno I, Riccio R, Bifulco G. Structural basis for the design and synthesis of selective HDAC inhibitors. Bioorganic & Medicinal Chemistry. 21: 3795-807. PMID 23693069 DOI: 10.1016/J.Bmc.2013.04.036  0.8
2012 De Simone R, Bruno I, Riccio R, Stadler K, Bauer J, Schaible AM, Laufer S, Werz O. Identification of new γ-hydroxybutenolides that preferentially inhibit the activity of mPGES-1. Bioorganic & Medicinal Chemistry. 20: 5012-6. PMID 22795900 DOI: 10.1016/J.Bmc.2012.06.032  0.612
2012 Chini MG, De Simone R, Bruno I, Riccio R, Dehm F, Weinigel C, Barz D, Werz O, Bifulco G. Design and synthesis of a second series of triazole-based compounds as potent dual mPGES-1 and 5-lipoxygenase inhibitors. European Journal of Medicinal Chemistry. 54: 311-23. PMID 22683242 DOI: 10.1016/J.Ejmech.2012.05.014  0.727
2012 Terracciano S, Chini MG, Riccio R, Bruno I, Bifulco G. Design, synthesis, and biological activity of hydroxamic tertiary amines as histone deacetylase inhibitors. Chemmedchem. 7: 694-702. PMID 22278987 DOI: 10.1002/Cmdc.201100531  0.805
2011 De Simone R, Chini MG, Bruno I, Riccio R, Mueller D, Werz O, Bifulco G. Structure-based discovery of inhibitors of microsomal prostaglandin E2 synthase-1, 5-lipoxygenase and 5-lipoxygenase-activating protein: promising hits for the development of new anti-inflammatory agents. Journal of Medicinal Chemistry. 54: 1565-75. PMID 21323313 DOI: 10.1021/Jm101238D  0.745
2010 De Simone R, Andrés RM, Aquino M, Bruno I, Guerrero MD, Terencio MC, Paya M, Riccio R. Toward the discovery of new agents able to inhibit the expression of microsomal prostaglandin E synthase-1 enzyme as promising tools in drug development. Chemical Biology & Drug Design. 76: 17-24. PMID 20492447 DOI: 10.1111/J.1747-0285.2010.00984.X  0.651
2010 Terracciano S, Di Micco S, Bifulco G, Gallinari P, Riccio R, Bruno I. Synthesis and biological activity of cyclotetrapeptide analogues of the natural HDAC inhibitor FR235222. Bioorganic & Medicinal Chemistry. 18: 3252-60. PMID 20381359 DOI: 10.1016/J.Bmc.2010.03.022  0.827
2010 Terracciano S, Chini MG, Bifulco G, D'Amico E, Marzocco S, Riccio R, Bruno I. Synthesis of new mono and bis amides projected as potential histone deacetylase (HDAC) inhibitors Tetrahedron. 66: 2520-2528. DOI: 10.1016/J.Tet.2010.01.061  0.81
2009 Guerrero MD, Aquino M, Bruno I, Riccio R, Terencio MC, Payá M. Anti-inflammatory and analgesic activity of a novel inhibitor of microsomal prostaglandin E synthase-1 expression. European Journal of Pharmacology. 620: 112-9. PMID 19686718 DOI: 10.1016/J.Ejphar.2009.08.007  0.573
2008 Aquino M, Guerrero MD, Bruno I, Terencio MC, Paya M, Riccio R. Development of a second generation of inhibitors of microsomal prostaglandin E synthase 1 expression bearing the gamma-hydroxybutenolide scaffold. Bioorganic & Medicinal Chemistry. 16: 9056-64. PMID 18790649 DOI: 10.1016/J.Bmc.2008.08.001  0.641
2008 Di Micco S, Terracciano S, Bruno I, Rodriquez M, Riccio R, Taddei M, Bifulco G. Molecular modeling studies toward the structural optimization of new cyclopeptide-based HDAC inhibitors modeled on the natural product FR235222. Bioorganic & Medicinal Chemistry. 16: 8635-42. PMID 18715788 DOI: 10.1016/J.Bmc.2008.08.003  0.83
2008 Terracciano S, Bruno I, D'Amico E, Bifulco G, Zampella A, Sepe V, Smith CD, Riccio R. Synthetic and pharmacological studies on new simplified analogues of the potent actin-targeting Jaspamide. Bioorganic & Medicinal Chemistry. 16: 6580-8. PMID 18508272 DOI: 10.1016/J.Bmc.2008.05.019  0.799
2008 Petrella A, D'Acunto CW, Rodriquez M, Festa M, Tosco A, Bruno I, Terracciano S, Taddei M, Paloma LG, Parente L. Effects of FR235222, a novel HDAC inhibitor, in proliferation and apoptosis of human leukaemia cell lines: role of annexin A1. European Journal of Cancer (Oxford, England : 1990). 44: 740-9. PMID 18295477 DOI: 10.1016/J.Ejca.2008.01.023  0.676
2007 Gomez-Paloma L, Bruno I, Cini E, Khochbin S, Rodriquez M, Taddei M, Terracciano S, Sadoul K. Design and synthesis of cyclopeptide analogues of the potent histone deacetylase inhibitor FR235222. Chemmedchem. 2: 1511-9. PMID 17694590 DOI: 10.1002/Cmdc.200700095  0.757
2007 Guerrero MD, Aquino M, Bruno I, Terencio MC, Paya M, Riccio R, Gomez-Paloma L. Synthesis and pharmacological evaluation of a selected library of new potential anti-inflammatory agents bearing the gamma-hydroxybutenolide scaffold: a new class of inhibitors of prostanoid production through the selective modulation of microsomal prostaglandin E synthase-1 expression. Journal of Medicinal Chemistry. 50: 2176-84. PMID 17407277 DOI: 10.1021/Jm0700823  0.649
2007 Aquino M, Bruno I, Riccio R, Gomez-Paloma L. Regioselective entry to bromo-gamma-hydroxybutenolides: useful building blocks for assemblying natural product-like libraries. Organic Letters. 8: 4831-4. PMID 17020314 DOI: 10.1021/OL0618611  0.493
2007 Bruno I, Dambruoso P, Terracciano S, Bifulco G. Total Synthesis of Natural Products Cheminform. 38. DOI: 10.1002/chin.200716255  0.626
2006 Rodriquez M, Aquino M, Bruno I, De Martino G, Taddei M, Gomez-Paloma L. Chemistry and biology of chromatin remodeling agents: state of art and future perspectives of HDAC inhibitors. Current Medicinal Chemistry. 13: 1119-39. PMID 16719774 DOI: 10.2174/092986706776360905  0.402
2006 Rodriquez M, Bruno I, Cini E, Marchetti M, Taddei M, Gomez-Paloma L. Synthesis of 2-amino-8-oxodecanoic acids (Aodas) present in natural hystone deacetylase inhibitors. The Journal of Organic Chemistry. 71: 103-7. PMID 16388624 DOI: 10.1021/Jo0518250  0.347
2006 Rodriquez M, Terracciano S, Cini E, Settembrini G, Bruno I, Bifulco G, Taddei M, Gomez-Paloma L. Total synthesis, NMR solution structure, and binding model of the potent histone deacetylase inhibitor FR235222. Angewandte Chemie (International Ed. in English). 45: 423-7. PMID 16311994 DOI: 10.1002/Anie.200501995  0.748
2005 Terracciano S, Bruno I, Bifulco G, Avallone E, Smith CD, Gomez-Paloma L, Riccio R. Synthesis, solution structure, and bioactivity of six new simplified analogues of the natural cyclodepsipeptide jaspamide. Bioorganic & Medicinal Chemistry. 13: 5225-39. PMID 16023351 DOI: 10.1016/J.Bmc.2005.05.042  0.805
2005 Napolitano A, Bruno I, Riccio R, Gomez-Paloma L. Synthesis, structure, and biological aspects of cyclopeptides related to marine phakellistatins 7–9 Tetrahedron. 61: 6808-6815. DOI: 10.1016/J.Tet.2005.04.067  0.605
2004 Terracciano S, Bruno I, Bifulco G, Copper JE, Smith CD, Gomez-Paloma L, Riccio R. Synthesis, conformational analysis, and cytotoxicity of new analogues of the natural cyclodepsipeptide jaspamide. Journal of Natural Products. 67: 1325-31. PMID 15332850 DOI: 10.1021/Np049955B  0.804
2003 Napolitano A, Rodriquez M, Bruno I, Marzocco S, Autore G, Riccio R, Gomez-Paloma L. Synthesis, structural aspects and cytotoxicity of the natural cyclopeptides yunnanins A, C and phakellistatins 1, 10 Tetrahedron. 59: 10203-10211. DOI: 10.1016/J.Tet.2003.10.073  0.582
2002 Napolitano A, Bruno I, Rovero P, Lucas R, Peris MP, Gomez-Paloma L, Riccio R. Synthesis and biological properties of the seven alanine-modified analogues of the marine cyclopeptide hymenamide C. Journal of Peptide Science : An Official Publication of the European Peptide Society. 8: 407-17. PMID 12212804 DOI: 10.1002/Psc.396  0.614
2001 Casapullo A, Cutignano A, Bruno I, Bifulco G, Debitus C, Gomez-Paloma L, Riccio R. Makaluvamine P, a new cytotoxic pyrroloiminoquinone from Zyzzya cf. fuliginosa. Journal of Natural Products. 64: 1354-6. PMID 11678667 DOI: 10.1021/Np010053+  0.756
2001 Cimino P, Bifulco G, Casapullo A, Bruno I, Gomez-Paloma L, Riccio R. Isolation and NMR characterization of rosacelose, a novel sulfated polysaccharide from the sponge Mixylla rosacea. Carbohydrate Research. 334: 39-47. PMID 11470249 DOI: 10.1016/S0008-6215(01)00141-0  0.737
2001 Grassia A, Bruno I, Debitus C, Marzocco S, Pinto A, Gomez-Paloma L, Riccio R. Spongidepsin, a new cytotoxic macrolide from Spongia sp. Tetrahedron. 57: 6257-6260. DOI: 10.1016/S0040-4020(01)00587-7  0.594
2001 Napolitano A, Bruno I, Rovero P, Lucas R, Peris MP, Gomez-Paloma L, Riccio R. Synthesis, structural aspects and bioactivity of the marine cyclopeptide hymenamide C Tetrahedron. 57: 6249-6255. DOI: 10.1016/S0040-4020(01)00579-8  0.608
2001 Cutignano A, Bruno I, Bifulco G, Casapullo A, Debitus C, Gomez-Paloma L, Riccio R. Dactylolide, a New Cytotoxic Macrolide from the Vanuatu SpongeDactylospongia sp. European Journal of Organic Chemistry. 2001: 775-778. DOI: 10.1002/1099-0690(200102)2001:4<775::Aid-Ejoc775>3.0.Co;2-Z  0.761
2000 Casapullo A, Bifulco G, Bruno I, Riccio R. New bisindole alkaloids of the topsentin and hamacanthin classes from the Mediterranean marine sponge Rhaphisia lacazei. Journal of Natural Products. 63: 447-51. PMID 10785411 DOI: 10.1021/Np9903292  0.789
2000 Cutignano A, Bifulco G, Bruno I, Casapullo A, Gomez-Paloma L, Riccio R. Dragmacidin F: A New Antiviral Bromoindole Alkaloid from the Mediterranean Sponge Halicortex sp. Tetrahedron. 56: 3743-3748. DOI: 10.1016/S0040-4020(00)00281-7  0.769
2000 Cutignano A, Bifulco G, Bruno I, Casapullo A, Gomez-Paloma L, Riccio R. ChemInform Abstract: Dragmacidin F: A New Antiviral Bromoindole Alkaloid from the Mediterranean Sponge Halicortex sp. Cheminform. 31: no-no. DOI: 10.1002/CHIN.200041175  0.573
1995 Bifulco G, Bruno I, Minale L, Riccio R, Calignano A, Debitus C. (+/-)-Gelliusines A and B, two diastereomeric brominated tris-indole alkaloids from a deep water new caledonian marine sponge (Gellius or Orina sp.). Journal of Natural Products. 57: 1294-9. PMID 7798965 DOI: 10.1021/Np50111A020  0.675
1995 Bifulco G, Bruno I, Riccio R, Lavayre J, Bourdy G. Further brominated bis- and tris-indole alkaloids from the deep-water New Caledonian marine sponge Orina Sp. Journal of Natural Products. 58: 1254-60. PMID 7595591 DOI: 10.1021/Np50122A017  0.682
1995 Bifulco G, Bruno I, Minale L, Riccio R, Debitus C, Bourdy G, Vassas A, Lavayre J. Bioactive Prenylhydroquinone Sulfates and a Novel C31Furanoterpene Alcohol Sulfate from the Marine Sponge, Ircinia Sp. Journal of Natural Products. 58: 1444-1449. DOI: 10.1021/Np50123A017  0.594
1994 Bifulco G, Bruno I, Minale L, Riccio R. Novel HIV-inhibitory halistanol sulfates F-H from a marine sponge, Pseudoaxinissa digitata. Journal of Natural Products. 57: 164-7. PMID 8158159 DOI: 10.1021/Np50103A026  0.613
1993 Bruno I, Minale L, Riccio R, Cariello L, Higa T, Tanaka J. Starfish saponins, Part 50. Steroidal glycosides from the Okinawan starfish Nardoa tuberculata. Journal of Natural Products. 56: 1057-64. PMID 8377014 DOI: 10.1021/Np50097A008  0.557
1993 Berlinck RG, Braekman JC, Daloze D, Bruno I, Riccio R, Ferri S, Spampinato S, Speroni E. Polycyclic guanidine alkaloids from the marine sponge Crambe crambe and Ca++ channel blocker activity of crambescidin 816. Journal of Natural Products. 56: 1007-15. PMID 8377012 DOI: 10.1021/Np50097A004  0.576
1993 Bifulco G, Bruno I, Paloma LG, Riccio R. Edwardsolides A, B and C. New Sesquiterpenoid Lactones from the Mediterranean OctocoralMaasella edwardsi Natural Product Letters. 3: 167-171. DOI: 10.1080/10575639308043857  0.658
1992 Bruno I, D'Auria MV, Iorizzi M, Minale L, Riccio R. Marine eicosanoids: Occurrence of 8,11,12-trihydroxylated eicosanoic acids in starfishes Experientia. 48: 114-115. DOI: 10.1007/Bf01923622  0.487
1990 Bruno I, Minale L, Riccio R. Starfish Saponins, Part 43. Structures of Two New Sulfated Steroidal Fucofuranosides (Imbricatosides A and B) and Six New Polyhydroxysteroids from the Starfish Dermasterias imbricata Journal of Natural Products. 53: 366-374. DOI: 10.1021/Np50068A015  0.567
1990 Berlinck RGS, Braekman JC, Daloze D, Hallenga K, Ottinger R, Bruno I, Riccio R. Two new guanidine alkaloids from the mediterranean sponge crambe crambe. Tetrahedron Letters. 31: 6531-6534. DOI: 10.1016/S0040-4039(00)97109-0  0.564
1989 Bruno I, Minale L, Riccio R. Statfish Saponins, 38. Steroidal Glycosides from the Starfish Pycnopodia heliantboides Journal of Natural Products. 52: 1022-1026. DOI: 10.1021/Np50065A017  0.532
1984 Bruno I, Minale L, Pizza C, Zollo F, Riccio R, Mellon FM. Starfish saponins. Part 14. Structures of the steroidal glycoside sulphates from the starfish Marthasterias glacialis Journal of the Chemical Society-Perkin Transactions 1. 15: 1875-1883. DOI: 10.1039/P19840001875  0.476
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