2020

Engineered Ferritin Nanoparticles for the Bioluminescence Tracking of Nanodrug Delivery in Cancer

Bellini, M.| Riva, B.| Tinelli, V.| Rizzuto, M.A.| Salvioni, L.| Colombo, M.| Mingozzi, F.| Visioli, A.| Marongiu, L.| Frascotti, G.| Christodoulou, M.S.| Passarella, D.| Prosperi, D.| Fiandra, L.

Small, 16, 2001450, (2000)

DOI: 10.1002/smll.202001450


Putative SARS-CoV-2 Mpro Inhibitors from an In-House Library of Natural and Nature-Inspired Products: A Virtual Screening and Molecular Docking Study

Mazzini, S.| Musso, L.| Dallavalle, S.| Artali, R.

Molecules25 (16), 3745 (2020)

DOI:10.3390/molecules25163745


Urinary TMAO levels are associated with the taxonomic composition of the gut microbiota and with the choline TMA-lyase gene (cutC) harbored by enterobacteriaceae

Dalla Via, A.| Gargari, G.| Taverniti, V.| Rondini, G.| Velardi, I.| Gambaro, V.| Visconti, G.L.| De Vitis, V.| Gardana, C.| Ragg, E.| Pinto, A.| Riso, P.| Guglielmetti, S.

Nutrients12(1), 62, (2000)

DOI: 10.3390/nu12010062


A small library of chalcones induce liver cancer cell death through Akt phosphorylation inhibition

Sahin, I.D.| Christodoulou, M.S.| Guzelcan, E.A.| Koyas, A.| Karaca, C.| Passarella, D.| Cetin-Atalay, R.

Sci. Rep. 10, 11814 (2020)

DOI: 10.1038/s41598-020-68775-9


Continuous preparation of flavour-active acetate esters by direct biocatalytic esterification

Chiarelli Perdomo, I.| Letizia Contente, M.| Pinto, A.| Romano, D.| Fernandes, P.| Molinari, F.

Flavour Fragr J., 35,190–196 (2020)

DOI: 10.1002/ffj.3552


An enzymatic flow-based preparative route to vidarabine

Tamborini, L.| Previtali, C.| Annunziata, F.| Bavaro, T.| Terreni, M.| Calleri, E.| Rinaldi, F.| Pinto, A.| Speranza, G.| Ubiali, D.| Conti, P.

Molecules , 25(5), 1223 (2020)

DOI:10.3390/molecules25051223


Stilbenoids: A natural arsenal against bacterial pathogens

Mattio, L.M.| Catinella, G.| Dallavalle, S.| Pinto, A.

Antibiotics9(6), 336 (2020)

DOI: 10.3390/antibiotics9060336


Asymmetric hydrogenation of 1-aryl substituted-3,4-dihydroisoquinolines with iridium catalysts bearing different phosphorus-based ligands

Facchetti, G.| Christodoulou, M.S.| Binda, E.| Fusè, M.| Rimoldi, I.

Catalysts10(8), 914, (2020)

DOI: 10.3390/catal10080914


Divergent Conversion of 4-Naphthoquinone-substituted 4 H-Isoxazolones to Different Benzo-fused Indole Derivatives

Christodoulou, M.S.| Giofrè, S.| Beccalli, E.M.| Foschi, F.| Broggini, G.

Org. Lett. 2020, 22, 7, 2735–2739

DOI: 10.1021/acs.orglett.0c00709


Natural and nature-inspired stilbenoids as antiviral agents

Mattio, L.M.| Catinella, G.| Pinto, A.| Dallavalle, S.

Eur. J. Med. Chem., 202 ,112541 (2020)

DOI: 10.1016/j.ejmech.2020.112541


Improvement of conventional anti-cancer drugs as new tools against multidrug resistant tumors

Dallavalle, S.| Dobričić, V.| Lazzarato, L.| Gazzano, E.| Machuqueiro, M.| Pajeva, I.| Tsakovska, I.| Zidar, N.| Fruttero, R.

Drug Resist Updat. 50:100682 (2020)

DOI: 10.1016/j.drup.2020.100682


Embelin as lead compound for new neuroserpin polymerization inhibitors

Visentin, C.| Musso, L.| Broggini, L.| Bonato, F.| Russo, R.| Moriconi, C.| Bolognesi, M.| Miranda, E.| Dallavalle, S.| Passarella, D.| Ricagno, S.

Life, 10(7), 111 (2020)

DOI: 10.3390/life10070111


Structural requirements of benzofuran derivatives dehydro-δ-and dehydro-ε-viniferin for antimicrobial activity against the foodborne pathogen listeria monocytogenes

Catinella, G.| Mattio, L.M.| Musso, L.| Arioli, S.| Mora, D.| Beretta, G.L.| Zaffaroni, N.| Pinto, A.| Dallavalle, S.

Int. J. Mol. Sci.21(6), 2168 (2020)

DOI: 10.3390/ijms21062168


Chiral separation, X-ray structure, and biological evaluation of a potent and reversible dual binding site ache inhibitor

Catto, M.| Pisani, L.| Mora, E.D.L.| Belviso, B.D.| Mangiatordi, G.F.| Pinto, A.| De Palma, A.| Denora, N.| Caliandro, R.| Colletier, J.-P.| Silman, I.| Nicolotti, O.| Altomare, C.D.

ACS Med. Chem. Lett., 11, 5, 869-876

DOI: 10.1021/acsmedchemlett.9b00656


Uncommon overoxidative catalytic activity in a new halo-tolerant alcohol dehydrogenase

Contente, M.L.| Fiore, N.| Cannazza, P.| Roura Padrosa, D.| Molinari, F.| Gourlay, L.| Paradisi, F.

ChemCatChem, 12, 5679 – 5685 (2020)

DOI: 10.1002/cctc.202001112


Use of Immobilized Amine Transaminase from Vibrio fluvialis under Flow Conditions for the Synthesis of (S)-1-(5-Fluoropyrimidin-2-yl)-ethanamine

Semproli, R.| Vaccaro, G.| Ferrandi, E.E.| Vanoni, M.| Bavaro, T.| Marrubini, G.| Annunziata, F.| Conti, P.| Speranza, G.| Monti, D.| Tamborini, L.| Ubiali, D.

ChemCatChem, 12, 1359 – 1367 (2020)

DOI: 10.1002/cctc.201902080


Lipase mediated enzymatic kinetic resolution of phenylethyl halohydrins acetates: A case of study and rationalization

Fonseca, T.D.S.| Vega, K.B.| da Silva, M.R.| de Oliveira, M.D.C.F.| de Lemos, T.L.G.| Contente, M.L.| Molinari, F.| Cespugli, M.| Fortuna, S.| Gardossi, L.| de Mattos, M.C.

Molecular Catalysis, 485, 110819 (2020)

DOI: 10.1016/j.mcat.2020.110819


Biological properties of new chiral 2-Methyl-5,6,7,8-tetrahydroquinolin-8-amine-based compounds

Facchetti, G.| Christodoulou, M.S.| Mendoza, L.B.| Cusinato, F.| Dalla Via, L.| Rimoldi, I.

Molecules, 25(23), 5561 (2020)

DOI: 10.3390/molecules25235561


Advances on whole-cell biocatalysis in flow

Pinto, A.| Contente, M.L.| Tamborini, L.

Current Opinion in Green and Sustainable Chemistry 25:100343 (2020)

DOI: 0.1016/j.cogsc.2020.04.004


Efficient chemo-enzymatic flow synthesis of high value amides and esters

Annunziata, F.| Contente, M.L.| Betti, D.| Pinna, C.| Molinari, F.| Tamborini, L.| Pinto, A.

Catalysts10(8), 939 (2020)

DOI: 10.3390/catal10080939


Novel 3,3-disubstituted oxindole derivatives. Synthesis and evaluation of the anti-proliferative activity

Christodoulou, M.S.| Nicoletti, F.| Mangano, K.| Chiacchio, M.A.| Facchetti, G.| Rimoldi, I.| Beccalli, E.M.| Giofrè, S.

Bioorganic and Medicinal Chemistry Letters, 30, 2, 126845 (2020)

DOI: 10.1016/j.bmcl.2019.126845


Chemoenzymatic synthesis of arabinomannan (AM) glycoconjugates as potential vaccines for tuberculosis

Li, Z.| Bavaro, T.| Tengattini, S.| Bernardini, R.| Mattei, M.| Annunziata, F.| Cole, R.B.| Zheng, C.| Sollogoub, M.| Tamborini, L.| Terreni, M.| Zhang, Y.

European Journal of Medicinal Chemistry 204, 112578 (2020)

DOI: 10.1016/j.ejmech.2020.112578


Palladium-catalyzed benzodiazepines synthesis

Christodoulou, M.S.| Beccalli, E.M.| Giofrè, S.

Catalysts, 10(6), 634 (2020)

DOI: 10.3390/catal10060634


Natural compound-derived cytochrome bc1 complex inhibitors as antifungal agents

Musso, L.| Fabbrini, A.| Dallavalle, S.

Molecules 25(19), 4582 (2020)

DOI:10.3390/molecules25194582


Immobilized enzyme reactors based on nucleoside phosphorylases and 2′-deoxyribosyltransferase for the in-flow synthesis of pharmaceutically relevant nucleoside analogues

Rinaldi, F.| Fernández-Lucas, J.| de la Fuente, D.| Zheng, C.| Bavaro, T.| Peters, B.| Massolini, G.| Annunziata, F.| Conti, P.| de la Mata, I.| Terreni, M.| Calleri, E.

Bioresource Technology 307, 123258 (2020)

DOI: 10.1016/j.biortech.2020.123258


An overview of coumarin as a versatile and readily accessible scaffold with broad-ranging biological activities

Annunziata, F.| Pinna, C.| Dallavalle, S.| Tamborini, L.| Pinto, A.

Int. J. Mol. Sci., 21(13), 4618 (2020)

DOI:10.3390/ijms21134618


Antiproliferative effects of chalcones on T cell acute lymphoblastic leukemia-derived cells: Role of PKCβ

Corsini, E.| Facchetti, G.| Esposito, S.| Maddalon, A.| Rimoldi, I.| Christodoulou, M.S.

Arch Pharm., 353:e2000062 (2020)

DOI: 10.1002/ardp.202000062


Stereoselective Reduction of Prochiral Cyclic 1,3-Diketones Using Different Biocatalysts

Contente, M.L.| Dall’Oglio, F.| Annunziata, F.| Molinari, F.| Rabuffetti, M.| Romano, D.| Tamborini, L.| Rother, D.| Pinto, A

Catal Lett 150, 1176–1185 (2020)

DOI: 10.1007/s10562-019-03015-y


A strategic Ser/Cys exchange in the catalytic triad unlocks an acyltransferase-mediated synthesis of thioesters and tertiary amides

Contente, M.L.| Roura Padrosa, D.| Molinari, F.| Paradisi, F.

Nat Catal 3, 1020–1026 (2020).

DOI: 10.1038/s41929-020-00539-0


Aromas flow: eco-friendly, continuous, and scalable preparation of flavour esters

Contente, M.L.| Tamborini, L.| Molinari, F.| Paradisi, F.

J Flow Chem 10, 235–240 (2020).

DOI:10.1007/s41981-019-00063-8