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Minghong Ni

Observed names: M. H. NI, Ming Hong Ni, Ming-Hong Ni, Ming‐Hong Ni
ORCID: 0000-0001-6118-3750
Observed ORCID: 0000-0001-6118-3750
OpenAlex ID: A5039874007
Novel tumor-targeted RGD peptide–camptothecin conjugates: Synthesis and biological evaluation
2009 · Alma Dal Pozzo, Ming-Hong Ni, et al. · Bioorganic & Medicinal Chemistry · 58
Chemical Modification of Glycosaminoglycan Polysaccharides
2021 · Lais C. G. F. Palhares, James A. London, et al. · Molecules · 43
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Conjugates of a Novel 7-Substituted Camptothecin with RGD-Peptides as αvβ3 Integrin Ligands: An Approach to Tumor-Targeted Therapy
2010 · Alma Dal Pozzo, Emiliano Esposito, et al. · Bioconjugate Chemistry · 29
Incorporation of the Unusual Cα-Fluoroalkylamino Acids into Cyclopeptides: Synthesis of Arginine−Glycine−Aspartate (RGD) Analogues and Study of Their Conformational and Biological Behavior
2006 · Alma Dal Pozzo, Minghong Ni, et al. · Journal of Medicinal Chemistry · 25
Amino Acid Bromides: Their N-Protection and Use in the Synthesis of Peptides with Extremely Difficult Sequences
2002 · Alma DalPozzo, Minghong Ni, et al. · The Journal of Organic Chemistry · 23
New macrocyclic analogs of the natural histone deacetylase inhibitor FK228; design, synthesis and preliminary biological evaluation
2015 · Minghong Ni, Emiliano Esposito, et al. · Bioorganic & Medicinal Chemistry · 22
A new synthesis of carboxyterfenadine (fexofenadine) and its bioisosteric tetrazole analogs
1999 · Barbara Di Giacomo, Donato Coletta, et al. · Il Farmaco · 21
Investigating Glycol-Split-Heparin-Derived Inhibitors of Heparanase: A Study of Synthetic Trisaccharides
2016 · Minghong Ni, Stefano Elli, et al. · Molecules · 18
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Evidence for Multiple Binding Modes in the Initial Contact Between SARS‐CoV‐2 Spike S1 Protein and Cell Surface Glycans**
2022 · Michela Parafioriti, Minghong Ni, et al. · Chemistry - A European Journal · 17
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N-Protected amino acid bromides: efficient reagents for the incorporation into peptides of extremely hindered α,α-dialkyl- and α-fluoroalkyl-amino acids
2001 · Alma DalPozzo, Roberto Bergonzi, et al. · Tetrahedron Letters · 17
Efficient selective deacetylation of complex oligosaccharides using the neutral organotin catalyst [tBu2SnOH(Cl)]2
2020 · Minghong Ni, Marco Guerrini, et al. · Carbohydrate Research · 9
Amino acid bromides: their utilization for difficult couplings in solid-phase peptide synthesis
2005 · Minghong Ni, Emiliano Esposito, et al. · Tetrahedron Letters · 7
Synthetic glycol-split heparin tri- and tetrasaccharides provide new insights into structural peculiarities for antiheparanase activity
2024 · Minghong Ni, Michela Parafioriti, et al. · Bioorganic & Medicinal Chemistry · 6
A novel biomimetic probe for galectin‐3 recognition: Chemical synthesis and structural characterization of a β‐galactose branched sodium hyaluronate
2024 · Sofia Nizzolo, Emiliano Esposito, et al. · Proteoglycan Research · 3
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Synthesis and Conformational Studies of Novel, Side-Chain Protected, L-(aMe)Ser Homo-Peptides
2009 · Fernando Formaggio, Cristina Peggion, et al. · Advances in experimental medicine and biology · 1
Amino Acid Bromides: Their N-Protection and Use in the Synthesis of Peptides with Extremely Difficult Sequences.
2003 · Alma DalPozzo, Minghong Ni, et al. · The Journal of Organic Chemistry · 1
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Amino Acid Bromides: A Convenient Choice for Very Difficult Couplings
2001 · Alma DalPozzo, Roberto Bergonzi, et al. · Springer eBooks · 1
Interaction Between Heparan Sulfate Oligosaccharide and the Receptor-Binding Domain of the Wild-Type and Omicron Variant of the SARS-CoV-2 Spike Protein
2025 · Mandalari Marco, Michela Parafioriti, et al. · Biomolecules
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Chemoenzymatic Synthesis of D‐Glucaro‐δ‐lactam Containing Oligosaccharides as Putative Heparanase Inhibitors
2021 · Minghong Ni, Eduardo Stancanelli, et al. · ChemistrySelect
Amino Acid Bromides: A Convenient Choice for Very Difficult Couplings
2003 · Alma DalPozzo, Roberto Bergonzi, et al. · ChemInform
ChemInform Abstract: N‐Protected Amino Acid Bromides: Efficient Reagents for the Incorporation into Peptides of Extremely Hindered α,α‐Dialkyl‐ and α‐Fluoroalkyl‐amino Acids.
2001 · Alma DalPozzo, Roberto Bergonzi, et al. · ChemInform
ChemInform Abstract: A New Synthesis of Carboxyterfenadine (Fexofenadine) and Its Bioisosteric Tetrazole Analogues.
2000 · Barbara Di Giacomo, Donato Coletta, et al. · ChemInform
ChemInform Abstract: Synthesis and Biological Evaluation of 6‐Carboxy‐3,4‐methanoprolines, New Rigid Glutamate Analogues.
1995 · M. MARINOZZI, B. NATALINI, et al. · ChemInform
Works count: 23
Citation count: 301
H-index: 10
I10-index: 10
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