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Hitoshi Ban

Tyrosine Bioconjugation through Aqueous Ene-Type Reactions: A Click-Like Reaction for Tyrosine
2010 · Hitoshi Ban, Julia Gavrilyuk, et al. · Journal of the American Chemical Society · 351
Facile and Stabile Linkages through Tyrosine: Bioconjugation Strategies with the Tyrosine-Click Reaction
2013 · Hitoshi Ban, Masanobu Nagano, et al. · Bioconjugate Chemistry · 206
Rate Enhancement of the Pauson–Khand Reaction by Primary Amines
1997 · Takumichi Sugihara, Mamiko Yamada, et al. · Angewandte Chemie International Edition in English · 137
Formylbenzene Diazonium Hexafluorophosphate Reagent for Tyrosine-Selective Modification of Proteins and the Introduction of a Bioorthogonal Aldehyde
2012 · Julia Gavrilyuk, Hitoshi Ban, et al. · Bioconjugate Chemistry · 116
An Efficient Method for Generation of α-Oxoketenes: Cycloreversion of Enolized Meldrum's Acid Derivatives
1997 · Masayuki Sato, Hitoshi Ban, et al. · Tetrahedron Letters · 44
Novel decomplexation method for alkyne–Co2(CO)6 complexes
1998 · Takumichi Sugihara, Hitoshi Ban, et al. · Journal of Organometallic Chemistry · 29
A convenient synthesis of 4-aryl-1,8-naphthyridin-2(1H)-ones by the Suzuki coupling
2003 · Hitoshi Ban, Masami Muraoka, et al. · Tetrahedron Letters · 26
Antibody Conjugation Approach Enhances Breadth and Potency of Neutralization of Anti-HIV-1 Antibodies and CD4-IgG
2013 · Julia Gavrilyuk, Hitoshi Ban, et al. · Journal of Virology · 24
Beschleunigung der Pauson‐Khand‐Reaktion durch primäre Amine
1997 · Takumichi Sugihara, Mamiko Yamada, et al. · Angewandte Chemie · 23
Targeting Tumor-Associated Macrophages with the Immune-Activating Nanomedicine for Achieving Strong Antitumor Activity with Rapid Clearance from the Body
2024 · Yosuke Ota, Ryosaku Inagaki, et al. · ACS Nano · 21
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Synthesis and biological activity of novel 4-phenyl-1,8-naphthyridin-2(1H)-on-3-yl ureas: Potent acyl-CoA:cholesterol acyltransferase inhibitor with improved aqueous solubility
2005 · Hitoshi Ban, Masami Muraoka, et al. · Bioorganic & Medicinal Chemistry Letters · 20
Synthesis of SMP-797: a new potent ACAT inhibitor
2005 · Hitoshi Ban, Masami Muraoka, et al. · Tetrahedron · 16
Thermal cycloreversion of 4H-1,3-dioxine-4-thiones to acyl thioketenes:a general synthesis of β-keto thioic O-acid derivatives
1996 · Masayuki Sato, Hitoshi Ban, et al. · Chemical Communications · 12
Preclinical Evaluation of a Novel Orally Bioavailable Menin-MLL Interaction Inhibitor, DSP-5336, for the Treatment of Acute Leukemia Patients with MLL-Rearrangement or NPM1 Mutation
2021 · Ken Eguchi, Takafumi Shimizu, et al. · Blood · 11
In vivo programming of endogenous antibodies via oral administration of adaptor ligands
2017 · Masanobu Nagano, Nancy Carrillo, et al. · Bioorganic & Medicinal Chemistry · 9
Mechanism of action of DSP-7888 (adegramotide/nelatimotide) Emulsion, a peptide-based therapeutic cancer vaccine with the potential to turn up the heat on non-immunoreactive tumors
2022 · Natsuko Suginobe, Megumi Nakamura, et al. · Clinical & Translational Oncology · 8
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DSP-7888, a Novel Cocktail Design of WT1 Peptide Vaccine, and Its Combinational Immunotherapy with Immune Checkpoint-Blocking Antibody Against PD-1
2016 · Masashi Goto, Megumi Nakamura, et al. · Blood · 6
Novel 1,4-diarylpiperidine-4-methylureas as anti-hyperlipidemic agents: Dual effectors on acyl-CoA:cholesterol O-acyltransferase and low-density lipoprotein receptor expression
2009 · Shigehiro Asano, Hitoshi Ban, et al. · Bioorganic & Medicinal Chemistry Letters · 6
A Novel Class of Antihyperlipidemic Agents with Low Density Lipoprotein Receptor Up-Regulation via the Adaptor Protein Autosomal Recessive Hypercholesterolemia
2010 · Shigehiro Asano, Hitoshi Ban, et al. · Journal of Medicinal Chemistry · 5
A Convenient One-Pot Preparation of N-Substituted 4-Phenylpiperidines
2008 · Hitoshi Ban, Shigehiro Asano · Heterocycles · 4
A Practical Synthesis of 1-Alkyl-3-amino-4-aryl-1,8-naphthyridin-2-(1H)-one, a Partial Structure of ACAT Inhibitor SMP-797
2005 · Hitoshi Ban, Masami Muraoka, et al. · Heterocycles · 3
Abstract 5724: Preclinical evaluation of a novel CHK1 inhibitor encapsulated within the liposome, SMP-3124, for the treatment of solid cancer
2024 · Yuka Kumagai, Ryosaku Inagaki, et al. · Cancer Research · 2
Abstract 2903: Evaluation of SMP-3124, a novel liposome-encapsulated CHK1 inhibitor, in patient-derived preclinical models of treatment-resistant ovarian cancer
2025 · Yuka Kumagai, Junzo Hamanishi, et al. · Cancer Research · 1
Abstract 3595: DSP-0692, a selective SCD inhibitor, enhances the anti-tumor activity of anti-PD1 antibody
2019 · Eiji Sugaru, Yudai Furuta, et al. · Molecular and Cellular Biology / Genetics · 1
Synthesis and structure–activity relationships of N-(4-amino-2,6-diisopropylphenyl)-N’-(1,4-diarylpiperidine-4-yl)methylureas as anti-hyperlipidemic agents
2009 · Shigehiro Asano, Hitoshi Ban, et al. · Bioorganic & Medicinal Chemistry · 1
Works count: 35
Citation count: 1,083
H-index: 12
I10-index: 14
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