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Results: 1-12 |
Results: 12
Synthesis and evaluation of a difluoromethylene analogue of sphingomyelin as an inhibitor of sphingomyelinase
Authors: 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
Deficient release of plasminogen activator inhibitor-1 from astrocytes triggers apoptosis in neuronal cells
Authors: Soeda, S Oda, M Ochiai, T Shimeno, H
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
Daunorubicin attenuates tumor necrosis factor-alpha-induced biosynthesis of plasminogen activator inhibitor-1 in human umbilical vein endothelial cells
Authors: Soeda, S Iwata, K Hosoda, Y Shimeno, H
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
Crocin suppresses tumor necrosis factor-alpha-induced cell death of neuronally differentiated PC-12 cells
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
Synthesis and evaluation of multisubstrate analogue inhibitors of purine nucleoside phosphorylases
Authors: Yokomatsu, T Hayakawa, Y Kihara, T Koyanagi, S Soeda, S Shimeno, H Shibuya, S
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
Release of plasminogen activator inhibitor-1 from human astrocytes is regulated by intracellular ceramide
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
Oversulfated fucoidan inhibits the basic fibroblast growth factor-induced tube formation by human umbilical vein endothelial cells: its possible mechanism of action
Authors: Soeda, S Kozako, T Iwata, K Shimeno, H
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
Stereoselective reduction of cyclopropylalkaones possessing a difluoromethylenephosphonate group at the ring: Application to stereoselective synthesis of novel cyclopropane nucleotide analogues
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
Hepatic heme metabolism in rats with fever induced by interleukin 1 beta
Authors: Kihara, T Umesue, I Soeda, S Toda, A Ono, N Shigematsu, H Shimeno, H
Citation: T. Kihara et al., Hepatic heme metabolism in rats with fever induced by interleukin 1 beta, RES COM M P, 104(2), 1999, pp. 115-126
Synthesis and biological evaluation of alpha,alpha-difluorobenzylphosphonic acid derivatives as small molecular inhibitors of protein-tyrosine phosphatase 1B
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
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
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
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
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
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