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Katsuhiro Imaki
Observed names:
K Imaki,
K. IMAKI,
K. Imaki,
KATSUHIRO IMAKI
Institution:
Ono Pharmaceutical (Japan)
Observed institution:
Ono Pharmaceutical (Japan)
OpenAlex ID:
A5035461005
ONO-5046, a novel inhibitor of human neutrophil elastase
1991
·
Kazuhito Kawabata
, Mayumi Suzuki
, et al.
·
Biochemical and Biophysical Research Communications
·
358
Non-peptidic inhibitors of human neutrophil elastase: The design and synthesis of sulfonanilide-containing inhibitors
1996
·
Katsuhiro Imaki
, Takanori Okada
, et al.
·
Bioorganic & Medicinal Chemistry
·
36
Radioimmunoassays of prostaglandin F2α and prostaglandin F2α-main urinary metabolite with prostaglandin-125I-tyrosine methylester amide
1974
·
Shiro Ohki
, Katsuhiro Imaki
, et al.
·
Prostaglandins
·
24
Gas chromatographic — Mass spectrometric quantitation of 16,16-dimethyl-trans-Δ2-PGE1
1983
·
V. Dimov
, K. Gréen
, et al.
·
Prostaglandins
·
17
Radioimmunoassay of main urinary metabolite of prostaglandin F2α
1975
·
Shiro Ohki
, Katsuhiro Imaki
, et al.
·
Prostaglandins
·
17
Inhibitory Effects of ONO-3307 on Various Proteases and Tissue Thromboplastin In Vitro and on Experimental Thrombosis In Vivo
1989
·
Syozo Matsuoka
, Mayumi Futagami
, et al.
·
The Japanese Journal of Pharmacology
·
16
Potent orally active inhibitors of angiotensin-converting enzyme (ACE).
1981
·
KATSUHIRO IMAKI
, SHIGERU SAKUYAMA
, et al.
·
Chemical and Pharmaceutical Bulletin
·
16
PDF
Simplified immunoassays of prostaglandin E main metabolite in human urine.
1983
·
T Inagawa
, K Imaki
, et al.
·
PubMed
·
15
The levels of main urinary metabolite of prostaglandin F1α and F2α in human subjects measured by radioimmunoassay
1976
·
Shiro Ohki
, Yoshimasa Nishigaki
, et al.
·
Prostaglandins
·
10
An Efficient Method for the Synthesis of a Novel Leukotriene B4 Receptor Antagonist, ONO-4057, via Michael Reaction of Dihydroresorcinol
2000
·
Mitoshi Konno
, Takahiko Nakae
, et al.
·
Synlett
·
9
A convenient preparation of N-acylpyroglutamic acid.
1981
·
KATSUHIRO IMAKI
, HARUKI NIWA
, et al.
·
Chemical and Pharmaceutical Bulletin
·
8
PDF
ChemInform Abstract: An Efficient Method for the Synthesis of a Novel Leukotriene B4 Receptor Antagonist, ONO‐4057, via Michael Reaction of Dihydroresorcinol.
1998
·
M. KONNO
, T. NAKAE
, et al.
·
ChemInform
Stereochemistry-activity studies in 6-keto-prostaglandin-E1 (6-keto-PGE1) analogs.
1989
·
K Imaki
, M Kawamura
, et al.
·
PubMed
ChemInform Abstract: A CONVENIENT PREPARATION OF N‐ACYLPYROGLUTAMIC ACID
1982
·
K. IMAKI
, H. NIWA
, et al.
·
ChemInform
ChemInform Abstract: POTENT ORALLY ACTIVE INHIBITORS OF ANGIOTENSIN‐CONVERTING ENZYME (ACE)
1982
·
K. IMAKI
, S. SAKUYAMA
, et al.
·
ChemInform
ChemInform Abstract: SYNTHESIS AND RESOLUTION OF (3RS)‐4‐AMINO‐3‐HYDROXYBUTANANILIDE
1979
·
SH. MIYAMOTO
, S. SHIGEOKA
, et al.
·
ChemInform
Radioimmunoassays of prostaglandin F/sub 2$alpha$/ and prostaglandin F/sub 2$alpha$/-main urinary metabolite with prostaglandin-$sup 125$I-tyrosine methylester amide
1974
·
Shiro Ohki
, Toshio Hanyu
, et al.
·
OSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information)
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Works count:
17
Citation count:
526
H-index:
9
I10-index:
9
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