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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