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Yokomatsu, T
Takechi, H
Akiyama, T
Shibuya, S
Kominato, T
Soeda, S
Shimeno, H
Citation: T. Yokomatsu et al., Synthesis and evaluation of a difluoromethylene analogue of sphingomyelin as an inhibitor of sphingomyelinase, BIOORG MED, 11(10), 2001, pp. 1277-1280
Citation: S. Soeda et al., Deficient release of plasminogen activator inhibitor-1 from astrocytes triggers apoptosis in neuronal cells, MOL BRAIN R, 91(1-2), 2001, pp. 96-103
Citation: S. Soeda et al., Daunorubicin attenuates tumor necrosis factor-alpha-induced biosynthesis of plasminogen activator inhibitor-1 in human umbilical vein endothelial cells, BBA-MOL CEL, 1538(2-3), 2001, pp. 234-241
Authors:
Soeda, S
Ochiai, T
Paopong, L
Tanaka, H
Shoyama, Y
Shimeno, H
Citation: S. Soeda et al., Crocin suppresses tumor necrosis factor-alpha-induced cell death of neuronally differentiated PC-12 cells, LIFE SCI, 69(24), 2001, pp. 2887-2898
Authors:
Yokomatsu, T
Hayakawa, Y
Kihara, T
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Soeda, S
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Citation: T. Yokomatsu et al., Synthesis and evaluation of multisubstrate analogue inhibitors of purine nucleoside phosphorylases, BIO MED CH, 8(11), 2000, pp. 2571-2579
Authors:
Kimura, M
Soeda, S
Oda, M
Ochiai, T
Kihara, T
Ono, N
Shimeno, H
Citation: M. Kimura et al., Release of plasminogen activator inhibitor-1 from human astrocytes is regulated by intracellular ceramide, J NEUROSC R, 62(6), 2000, pp. 781-788
Citation: S. Soeda et al., Oversulfated fucoidan inhibits the basic fibroblast growth factor-induced tube formation by human umbilical vein endothelial cells: its possible mechanism of action, BBA-MOL CEL, 1497(1), 2000, pp. 127-134
Authors:
Terao, T
Nakamura, J
Yoshimura, R
Ohmori, O
Takahashi, N
Kojima, H
Soeda, S
Shinkai, T
Nakano, H
Okuno, T
Citation: T. Terao et al., Relationship between serum cholesterol levels and meta-chlorophenylpiperazine-induced cortisol responses in healthy men and women, PSYCHIAT R, 96(2), 2000, pp. 167-173
Authors:
Yokomatsu, T
Yamagishi, T
Suemune, K
Abe, H
Kihara, T
Soeda, S
Shimeno, H
Shibuya, S
Citation: T. Yokomatsu et al., Stereoselective reduction of cyclopropylalkaones possessing a difluoromethylenephosphonate group at the ring: Application to stereoselective synthesis of novel cyclopropane nucleotide analogues, TETRAHEDRON, 56(37), 2000, pp. 7099-7108
Authors:
Yokomatsu, T
Murano, T
Umesue, I
Soeda, S
Shimeno, H
Shibuya, S
Citation: T. Yokomatsu et al., Synthesis and biological evaluation of alpha,alpha-difluorobenzylphosphonic acid derivatives as small molecular inhibitors of protein-tyrosine phosphatase 1B, BIOORG MED, 9(4), 1999, pp. 529-532
Authors:
Yokomatsu, T
Hayakawa, Y
Suemune, K
Kihara, T
Soeda, S
Shimeno, H
Shibuya, S
Citation: T. Yokomatsu et al., Synthesis and biological evaluation of 1,1-difluoro-2-(tetrahydro-3-furanyl)ethylphosphonic acids possessing a N9-purinylmethyl functional group at the ring. A new class of inhibitors for purine nucleoside phosphorylases, BIOORG MED, 9(19), 1999, pp. 2833-2836
Authors:
Yokomatsu, T
Abe, H
Sato, M
Suemune, K
Kihara, T
Soeda, S
Shimeno, H
Shibuya, S
Citation: T. Yokomatsu et al., Synthesis of 1,1-difluoro-5-(1H-9-purinyl)-2-pentenylphosphonic acids and the related methano analogues. Remarkable effect of the nucleobases and thecyclopropane rings on inhibitory activity toward purine nucleoside phosphorylase, BIO MED CH, 6(12), 1998, pp. 2495-2505