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Mizuki Takahashi

Observed names: M Takahashi, M. Takahashi, Mizuki TAKAHASHI
Observed institutions: Hitotsubashi University, Tokyo Institute of Technology, University of Tsukuba, Shiga University of Medical Science, Keio University, Niigata Prefectural Shibata Hospital, Daiichi-Sankyo (Japan), National Institutes for Quantum Science and Technology, Tsukuba Medical Center Hospital, Japanese Foundation For Cancer Research, University of Toyama, National Institute of Radiological Sciences, Yuri Kumiai General Hospital, Daiichi Sankyo RD Novare (Japan), Proton Medical Research Center, University of Tsukuba, Institute for Radiological Science, Ibaraki University, Kindai University, Meijo University
ORCID: 0000-0002-6238-9838
Observed ORCID: 0000-0002-6238-9838
OpenAlex ID: A5015284443
Vibrational spectra and structures of zinc carboxylates I. Zinc acetate dihydrate
1998 · Tsutomu Ishioka, Youko Shibata, et al. · Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy · 94
Construction of a Protein-Detection System Using a Loop Peptide Library with a Fluorescence Label
2003 · Mizuki Takahashi, Kiyoshi Nokihara, et al. · Chemistry & Biology · 83
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Vibrational spectra and structures of zinc carboxylates II. Anhydrous zinc acetate and zinc stearate
1998 · Tsutomu Ishioka, Youko Shibata, et al. · Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy · 53
Identification of the fused bicyclic 4-amino-2-phenylpyrimidine derivatives as novel and potent PDE4 inhibitors
2013 · Taiji Goto, Akiko Shiina, et al. · Bioorganic & Medicinal Chemistry Letters · 41
Crystal structure of the mineralocorticoid receptor ligand‐binding domain in complex with a potent and selective nonsteroidal blocker, esaxerenone (CS‐3150)
2020 · Mizuki Takahashi, Osamu Ubukata, et al. · FEBS Letters · 40
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Peptide arrays with designed α-helical structures for characterization of proteins from FRET fingerprint patterns
2004 · Kenji Usui, Mizuki Takahashi, et al. · Molecular Diversity · 40
Peptide arrays with designed secondary structures for protein characterization using fluorescent fingerprint patterns
2004 · Kenji Usui, Tetsunori Ojima, et al. · Biopolymers · 40
Discovery of DS-9300: A Highly Potent, Selective, and Once-Daily Oral EP300/CBP Histone Acetyltransferase Inhibitor
2022 · Ryutaro Kanada, Yoshiko Kagoshima, et al. · Journal of Medicinal Chemistry · 37
Identification of the 5,5-dioxo-7,8-dihydro-6H-thiopyrano[3,2-d]pyrimidine derivatives as highly selective PDE4B inhibitors
2013 · Taiji Goto, Akiko Shiina, et al. · Bioorganic & Medicinal Chemistry Letters · 35
Colletoic Acid, a Novel 11β-Hydroxysteroid Dehydrogenase Type 1 Inhibitor from Colletotrichum gloeosporioides SANK 21404
2008 · Azusa Aoyagi, Mariko Ito-Kobayashi, et al. · The Journal of Antibiotics · 33
GZD824 Inhibits GCN2 and Sensitizes Cancer Cells to Amino Acid Starvation Stress
2020 · Yu Kato, Kazuhiro Kunimasa, et al. · Molecular Pharmacology · 32
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Structure-based drug design of tricyclic 8H-indeno[1,2-d][1,3]thiazoles as potent FBPase inhibitors
2009 · Tomoharu Tsukada, Mizuki Takahashi, et al. · Bioorganic & Medicinal Chemistry Letters · 32
Peptide Design Based on an Antibody Complementarity-Determining Region (CDR): Construction of Porphyrin-Binding Peptides and Their Affinity Maturation by a Combinatorial Method
2000 · Mizuki Takahashi, Akihiko Ueno, et al. · Chemistry - A European Journal · 32
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Synthesis, SAR, and X-ray structure of tricyclic compounds as potent FBPase inhibitors
2009 · Tomoharu Tsukada, Mizuki Takahashi, et al. · Bioorganic & Medicinal Chemistry Letters · 30
Preclinical Development of U3-1784, a Novel FGFR4 Antibody Against Cancer, and Avoidance of Its On-target Toxicity
2019 · René Bartz, Keisuke Fukuchi, et al. · Molecular Cancer Therapeutics · 24
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Discovery of EP300/CBP histone acetyltransferase inhibitors through scaffold hopping of 1,4-oxazepane ring
2022 · Ryutaro Kanada, Yoshiko Kagoshima, et al. · Bioorganic & Medicinal Chemistry Letters · 23
Synthesis and biological evaluation of 5-carbamoyl-2-phenylpyrimidine derivatives as novel and potent PDE4 inhibitors
2013 · Taiji Goto, Akiko Shiina, et al. · Bioorganic & Medicinal Chemistry · 19
Design of novel porphyrin-binding peptides based on antibody CDR
1998 · Mizuki Takahashi, Akihiko Ueno, et al. · Bioorganic & Medicinal Chemistry Letters · 19
A covalent fragment-based strategy targeting a novel cysteine to inhibit activity of mutant EGFR kinase
2023 · Naoki Kuki, David L. Walmsley, et al. · RSC Medicinal Chemistry · 15
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11P Preclinical evaluation of DS-2087b, a novel and selective inhibitor of EGFR/HER2 exon 20 insertions
2020 · Y. Nagamoto, M. Miyamoto, et al. · Annals of Oncology · 15
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Discovery of DS-8108b, a Novel Orally Bioavailable Renin Inhibitor
2012 · Yuji Nakamura, Teppei Fujimoto, et al. · ACS Medicinal Chemistry Letters · 14
Design and optimization of novel (2S,4S,5S)-5-amino-6-(2,2-dimethyl-5-oxo-4-phenylpiperazin-1-yl)-4-hydroxy-2-isopropylhexanamides as renin inhibitors
2012 · Yuji Nakamura, Chie Sugita, et al. · Bioorganic & Medicinal Chemistry Letters · 14
Proton beam therapy for hepatocellular carcinoma with bile duct invasion
2023 · Takashi Iizumi, Toshiyuki Okumura, et al. · BMC Gastroenterology · 12
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Activating Mutations in EGFR and PI3k Promote ATF4 Induction for NSCLC Cell Survival During Amino Acid Deprivation
2022 · Mizuki Takahashi, Yuka Okamoto, et al. · Heliyon · 11
Revisiting biomolecular NMR spectroscopy for promoting small-molecule drug discovery
2020 · Hiroyuki Hanzawa, Takashi Shimada, et al. · Journal of Biomolecular NMR · 11
Works count: 63
Citation count: 883
H-index: 18
I10-index: 27
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