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Satoshi Iwayama
Observed names:
S. IWAYAMA,
S. Iwayama,
Satoshi IWAYAMA,
岩山, 聡
Institution:
Ajinomoto (Japan)
Observed institutions:
Tokyo Medical and Dental University,
Ajinomoto (Japan)
OpenAlex ID:
A5031845518
Synthesis and Antiviral Activity of Novel Acyclic Nucleosides: Discovery of a Cyclopropyl Nucleoside with Potent Inhibitory Activity against Herpesviruses
1998
·
Takaaki Sekiyama
, Satoshi Hatsuya
, et al.
·
Journal of Medicinal Chemistry
·
123
Intracellular localization and DNA-binding activity of a class of viral early phosphoproteins in human fibroblasts infected with human cytomegalovirus (Towne strain)
1994
·
S. Iwayama
, T. Yamamoto
, et al.
·
Journal of General Virology
·
49
Synthesis and Antiviral Activity of Novel Anti-VZV 5-Substituted Uracil Nucleosides with a Cyclopropane Sugar Moiety
1999
·
Tomoyuki Onishi
, Chika Mukai
, et al.
·
Journal of Medicinal Chemistry
·
36
Antiherpesvirus Activities of (1′ S ,2′ R )-9-{[1′,2′-Bis(hydroxymethyl)cycloprop-1′-yl]methyl}guanine (A-5021) in Cell Culture
1998
·
Satoshi Iwayama
, Nobukazu Ono
, et al.
·
Antimicrobial Agents and Chemotherapy
·
35
PDF
Neuronal Ca2+ Channel Blocking Action of an Antihypertensive Drug, Cilnidipine, in IMR-32 Human Neuroblastoma Cells
2003
·
Akira TAKAHARA
, Shin-ichi FUJITA
, et al.
·
Hypertension Research
·
33
PDF
Synthesis and evaluation of isoxazole derivatives as lysophosphatidic acid (LPA) antagonists
2007
·
Takashi Yamamoto
, Koichi Fujita
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
32
Mode of Action of (1′ S ,2′ R )-9-{[1′,2′-Bis(hydroxymethyl) cycloprop-1′-yl]methyl}guanine (A-5021) against Herpes Simplex Virus Type 1 and Type 2 and Varicella-Zoster Virus
1998
·
Nobukazu Ono
, Satoshi Iwayama
, et al.
·
Antimicrobial Agents and Chemotherapy
·
31
Discovery, structure–activity relationship study, and oral analgesic efficacy of cyproheptadine derivatives possessing N-type calcium channel inhibitory activity
2006
·
Takashi Yamamoto
, Seiji Niwa
, et al.
·
Bioorganic & Medicinal Chemistry
·
27
Asymmetric synthesis and biological evaluations of (+)- and (−)-6-dimethoxymethyl-1,4-dihydropyridine-3-carboxylic acid derivatives blocking N-type calcium channels
2011
·
Takashi Yamamoto
, Seiji Ohno
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
19
Evaluation of anti-herpesvirus activity of (1′S,2′R)-9-[[1′,2′-bis(hydroxymethyl)cycloprop-1′-yl]methyl]guanine (A-5021) in mice
1999
·
Satoshi Iwayama
, Yuko Ohmura
, et al.
·
Antiviral Research
·
16
Discovery and evaluation of selective N-type calcium channel blockers: 6-Unsubstituted-1,4-dihydropyridine-5-carboxylic acid derivatives
2012
·
Takashi Yamamoto
, Seiji Niwa
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
14
The effect of risedronate (17.5 mg/week) treatment on quality of life in Japanese women with osteoporosis: a prospective observational study
2012
·
Toshitaka Nakamura
, Mitsuharu Osawa
, et al.
·
Journal of Bone and Mineral Metabolism
·
8
ChemInform Abstract: Synthesis and Antiviral Activity of Novel Acyclic Nucleosides: Discovery of a Cyclopropyl Nucleoside with Potent Inhibitory Activity Against Herpes Viruses.
1998
·
T. SEKIYAMA
, S. HATSUYA
, et al.
·
ChemInform
·
5
Intracellular localization and DNA-binding activity of a class of viral early phosphoproteins in human fibroblasts infected with @@S ' human cytomegalovirus (Towne strain)
1994
·
Satoshi Iwayama
, Takako Yamamoto
, et al.
·
Collected papers from the Institute of Immunological Science Hokkaido University
新規ヌクレオシド誘導体の抗ヘルペスウイルス活性の特徴に関する研究
·
岩山, 聡
·
Institutional Repositories DataBase (IRDB)
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Works count:
16
Citation count:
428
H-index:
11
I10-index:
11
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