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Haruaki Kurasaki
Institution:
Peptidream (Japan)
Observed institutions:
Tokyo University of Science,
Peptidream (Japan),
Showa Pharmaceutical University
ORCID:
0000-0003-4276-0545
Observed ORCID:
0000-0003-4276-0545
OpenAlex ID:
A5029399800
Total Synthesis of Grandisine D
2009
·
Haruaki Kurasaki
, Iwao Okamoto
, et al.
·
Organic Letters
·
43
Sulfonamide-based non-alkyne LpxC inhibitors as Gram-negative antibacterial agents
2016
·
Tetsuya Kawai
, Iwase Kazuhiko
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
36
LpxC Inhibitors: Design, Synthesis, and Biological Evaluation of Oxazolidinones as Gram-negative Antibacterial Agents
2016
·
Haruaki Kurasaki
, Kosuke Tsuda
, et al.
·
ACS Medicinal Chemistry Letters
·
36
A Flexible Approach to Grandisine Alkaloids: Total Synthesis of Grandisines B, D, and F
2009
·
Haruaki Kurasaki
, Iwao Okamoto
, et al.
·
Chemistry - A European Journal
·
33
Synthesis and in vitro antitumor activity of novel 2-alkyl-5-methoxycarbonyl-11-methyl-6H-pyrido[4,3-b]carbazol-2-ium and 2-alkylellipticin-2-ium chloride derivatives
2014
·
Ryota Mori
, Asako Kato
, et al.
·
European Journal of Medicinal Chemistry
·
23
Structure activity relationship of C-2 ether substituted 1,5-naphthyridine analogs of oxabicyclooctane-linked novel bacterial topoisomerase inhibitors as broad-spectrum antibacterial agents (Part-5)
2015
·
Sheo B. Singh
, David E. Kaelin
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
19
Isostearyl Mixed Anhydrides for the Preparation ofN-Methylated Peptides UsingC-Terminally UnprotectedN-Methylamino Acids
2020
·
Haruaki Kurasaki
, Akihiro Nagaya
, et al.
·
Organic Letters
·
18
Structure activity relationship of substituted 1,5-naphthyridine analogs of oxabicyclooctane-linked novel bacterial topoisomerase inhibitors as broad-spectrum antibacterial agents (Part-4)
2015
·
Sheo B. Singh
, David E. Kaelin
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
17
ODP353 Sustained Suppression of IGF1 with AZP-3813, a Bicyclic 16-Amino Acid Peptide Antagonist of the Human Growth Hormone Receptor and a Potential New Treatment for Acromegaly
2022
·
Michael Culler
, Stephane Milano
, et al.
·
Journal of the Endocrine Society
·
9
PDF
Extended Solution-phase Peptide Synthesis Strategy Using Isostearyl-Mixed Anhydride Coupling and a New C-Terminal Silyl Ester-Protecting Group for N-Methylated Cyclic Peptide Production
2021
·
Akihiro Nagaya
, Shota Murase
, et al.
·
Organic Process Research & Development
·
9
Synthesis and evaluation of opioid receptor-binding affinity of elaeocarpenine and its analogs
2010
·
Haruaki Kurasaki
, Iwao Okamoto
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
8
Determination of binding modes and binding constants for the complexes of 6H-pyrido[4,3-b]carbazole derivatives with DNA
2016
·
Akihito Shimazu
, Masashi Kawagoshi
, et al.
·
Bioorganic & Medicinal Chemistry
·
7
Additive effects of ALXN2420, a GH receptor antagonist, and octreotide on IGF1 suppression in vivo
2025
·
Guillaume Ravel
, Xavier Gaume
, et al.
·
European Journal of Endocrinology
·
6
PDF
THU046 Repeated Treatment With AZP-3813, A Bicyclic, 16-Amino Acid Peptide Antagonist Of The Human Growth Hormone Receptor, Induces Enhanced Suppression Of IGF1 In Beagle Dogs
2023
·
Guillaume Ravel
, Clémentine Chalmey
, et al.
·
Journal of the Endocrine Society
·
4
AZP-3813, a bicyclic 16-amino acid peptide antagonist of the human growth hormone receptor as a potential new treatment for acromegaly
2022
·
Stephane Milano
, Haruaki Kurasaki
, et al.
·
Endocrine Abstracts
·
4
Enantioselective Ring Opening of Meso-Epoxide —Scope of Halohydrination—
2009
·
Haruaki Kurasaki
·
Journal of Synthetic Organic Chemistry Japan
·
4
PDF
Additive effect of combined treatment with the small peptide GH receptor antagonist, AZP-3813, and the somatostatin analog, octreotide, in decreasing IGF1 levels in the rat
2024
·
Guillaume Ravel
, Corentin Berardet
, et al.
·
Endocrine Abstracts
·
1
2524. Safety and Pharmacokinetics of PA-001, a New Potential COVID-19 Drug That Targets the S2 Subunit of SARS-CoV-2 Spike Protein, in Healthy Subjects
2023
·
Haruaki Kurasaki
, Masaki Ohuchi
, et al.
·
Open Forum Infectious Diseases
·
1
PDF
2141. Preclinical Evaluation of PA-001: A Novel, Potential Macrocyclic Peptide-Based Treatment for COVID-19 Which Binds to the S2 Subunit of SARS-CoV-2 Spike Protein
2023
·
Tatsuro Kawamura
, Masaki Ohuchi
, et al.
·
Open Forum Infectious Diseases
·
1
PDF
A macrocyclic peptide-based fusion inhibitor targeting SARS-CoV-2 Spike S2 subunit
2026
·
Hirofumi Ohashi
, Tatsuro Kawamura
, et al.
·
bioRxiv (Cold Spring Harbor Laboratory)
7145 Enhanced Ability of the Small Peptide GH Receptor Antagonist, AZP-3813, to Decrease IGF1 When Combined with the Somatostatin Analog, Octreotide
2024
·
Guillaume Ravel
, Corentin Berardet
, et al.
·
Journal of the Endocrine Society
Exploring Innovative Liquid-Phase Peptide Synthesis Strategies with Silane-Containing Molecules
2024
·
Naoki Nishizawa
, Akihiro Nagaya
, et al.
·
European Peptide Symposium (EPS)
PDF
AZP-3813, a bicyclic, 16-amino acid peptide antagonist of the human growth hormone receptor, effectively suppresses IGF1 in beagle dogs
2023
·
Guillaume Ravel
, Clementine Chalmey
, et al.
·
Endocrine Abstracts
DNAと6H‐ピリド[4,3‐b]カルバゾール誘導体との複合体の結合様式および結合定数の決定
2017
·
Shimazu Akihito
, Masashi Kawagoshi
, et al.
·
Bioorganic & Medicinal Chemistry
ChemInform Abstract: Total Synthesis of Grandisine D (I).
2009
·
Haruaki Kurasaki
, Iwao Okamoto
, et al.
·
ChemInform
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Works count:
25
Citation count:
279
H-index:
9
I10-index:
8
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