-
1
-
-
5444258731
-
Antiparasitic agents produced by microorganisms
-
Shiomi K, Ōmura S. Antiparasitic agents produced by microorganisms. Proc Jpn Acad, Ser B 80: 245-258 (2004)
-
(2004)
Proc Jpn Acad, Ser B
, vol.80
, pp. 245-258
-
-
Shiomi, K.1
Omura, S.2
-
2
-
-
14244263615
-
Carbohydrate and energy metabolism in parasitic helminths
-
Ed. J. J. Marr, et al. Academic Press, London
-
Komuniecki R, Tielens AGM. Carbohydrate and energy metabolism in parasitic helminths. In Molecular Medical Parasitology. Ed. J. J. Marr, et al., pp. 339-358. Academic Press, London (2003)
-
(2003)
Molecular Medical Parasitology
, pp. 339-358
-
-
Komuniecki, R.1
Tielens, A.G.M.2
-
3
-
-
0242687126
-
Parasite mitochondria as drug target: Diversity and dynamic changes during the life cycle
-
Kita K, Nihei C, Tomitsuka E. Parasite mitochondria as drug target: diversity and dynamic changes during the life cycle. Curr Med Chem 10: 2535-2548 (2003)
-
(2003)
Curr Med Chem
, vol.10
, pp. 2535-2548
-
-
Kita, K.1
Nihei, C.2
Tomitsuka, E.3
-
4
-
-
0035793109
-
An anthelmintic compound, nafuredin, shows selective inhibition of complex I in helminth mitochondria
-
Omura S, Miyadera H, Ui H, Shiomi K, Yamaguchi Y, Masuma R, Nagamitsu T, Takano D, Sunazuka T, Harder A, Kölbl H, Namikoshi M. Miyoshi H, Sakamoto K, Kita K. An anthelmintic compound, nafuredin, shows selective inhibition of complex I in helminth mitochondria. Proc Natl Acad Sci USA 98: 60-62 (2001)
-
(2001)
Proc Natl Acad Sci USA
, vol.98
, pp. 60-62
-
-
Omura, S.1
Miyadera, H.2
Ui, H.3
Shiomi, K.4
Yamaguchi, Y.5
Masuma, R.6
Nagamitsu, T.7
Takano, D.8
Sunazuka, T.9
Harder, A.10
Kölbl, H.11
Namikoshi, M.12
Miyoshi, H.13
Sakamoto, K.14
Kita, K.15
-
5
-
-
0035028342
-
Nafuredin, a novel inhibitor of NADH-fumarate reductase, produced by Aspergillus niger FT-0554
-
Ui H, Shiomi K, Yamaguchi Y, Masuma R, Nagamitsu T, Takano D, Sunazuka T, Namikoshi M, Ōmura S. Nafuredin, a novel inhibitor of NADH-fumarate reductase, produced by Aspergillus niger FT-0554. J Antibiot 54: 234-238 (2001)
-
(2001)
J Antibiot
, vol.54
, pp. 234-238
-
-
Ui, H.1
Shiomi, K.2
Yamaguchi, Y.3
Masuma, R.4
Nagamitsu, T.5
Takano, D.6
Sunazuka, T.7
Namikoshi, M.8
Omura, S.9
-
6
-
-
0037457881
-
Atpenins, potent and specific inhibitors of mitochondrial complex II (succinate-ubiquinone oxidoreductase)
-
Miyadera H, Shiomi K, Ui H, Yamaguchi Y, Masuma R, Tomoda H, Miyoshi H, Osanai A, Kita K, Ōmura S. Atpenins, potent and specific inhibitors of mitochondrial complex II (succinate-ubiquinone oxidoreductase). Proc Natl Acad Sci USA 100: 473-477 (2003)
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, pp. 473-477
-
-
Miyadera, H.1
Shiomi, K.2
Ui, H.3
Yamaguchi, Y.4
Masuma, R.5
Tomoda, H.6
Miyoshi, H.7
Osanai, A.8
Kita, K.9
Omura, S.10
-
8
-
-
24344432396
-
2-Amino-14,16-dimethyloctadecan-3-ol, a new sphingosine analogue toxin in the fungal genus
-
Uhlig S, Petersen D, Flåøyen A, Wilkins A. 2-Amino-14,16-dimethyloctadecan-3-ol, a new sphingosine analogue toxin in the fungal genus Fusarium. Toxicon 46: 513-522 (2005)
-
(2005)
Fusarium. Toxicon
, vol.46
, pp. 513-522
-
-
Uhlig, S.1
Petersen, D.2
Flåøyen, A.3
Wilkins, A.4
-
9
-
-
0027324028
-
Comparison of the structures of the quinone-binding sites in beef heart mitochondria
-
Tan AK, Ramsay RR, Singer TP, Miyoshi H. Comparison of the structures of the quinone-binding sites in beef heart mitochondria. J Biol Chem 268: 19328-19333 (1993)
-
(1993)
J Biol Chem
, vol.268
, pp. 19328-19333
-
-
Tan, A.K.1
Ramsay, R.R.2
Singer, T.P.3
Miyoshi, H.4
-
10
-
-
0023758278
-
Fumonisins-novel mycotoxins with cancer-promoting activity produced by Fusarium moniliforme
-
Gelderblom WCA, Jaskiewicz K, Marasas WFO, Thiel PG, Horak RM, Vleggaar R, Kriek NPJ. Fumonisins-novel mycotoxins with cancer-promoting activity produced by Fusarium moniliforme. Appl Envir Microbiol 54: 1806-1811 (1988)
-
(1988)
Appl Envir Microbiol
, vol.54
, pp. 1806-1811
-
-
Gelderblom, W.C.A.1
Jaskiewicz, K.2
Marasas, W.F.O.3
Thiel, P.G.4
Horak, R.M.5
Vleggaar, R.6
Kriek, N.P.J.7
-
11
-
-
0025173142
-
Novel marine sponge amino acids, 10. Xestoaminols from Xestospongia sp.
-
Jiménez C, Crews P. Novel marine sponge amino acids, 10. Xestoaminols from Xestospongia sp. J Nat Prod 53: 978-982 (1990)
-
(1990)
J Nat Prod
, vol.53
, pp. 978-982
-
-
Jiménez, C.1
Crews, P.2
-
12
-
-
0033403203
-
Oceanapiside, an antifungal bis-α,ω̇-amino alcohol glycoside from the marine sponge Oceanapia phillipensis
-
Nicholas GM, Hong TW, Molinski TF, Lerch ML, Cancilla MT, Lebrilla CB. Oceanapiside, an antifungal bis-α,ω̇-amino alcohol glycoside from the marine sponge Oceanapia phillipensis. J Nat Prod 62: 1678-1681 (1999)
-
(1999)
J Nat Prod
, vol.62
, pp. 1678-1681
-
-
Nicholas, G.M.1
Hong, T.W.2
Molinski, T.F.3
Lerch, M.L.4
Cancilla, M.T.5
Lebrilla, C.B.6
-
13
-
-
0037245381
-
Inhibition and kinetics of Mycobacterium tuberculosis and Mycobacterium smegmatis mycothiol-S-conjugate amidase by natural product inhibitors
-
Nicholas GM, Eckman LL, Newton GL, Fahey RC, Ray S, Bewley CA. Inhibition and kinetics of Mycobacterium tuberculosis and Mycobacterium smegmatis mycothiol-S-conjugate amidase by natural product inhibitors. Bioorg Med Chem 11: 601-608 (2003)
-
(2003)
Bioorg Med Chem
, vol.11
, pp. 601-608
-
-
Nicholas, G.M.1
Eckman, L.L.2
Newton, G.L.3
Fahey, R.C.4
Ray, S.5
Bewley, C.A.6
-
14
-
-
0034725101
-
The marine compound spisulosine, an inhibitor of cell proliferation, promotes the disassembly of actin stress fibers
-
Cuadros R, Montejo de Garcini E, Wandosell F, Faircloth G, Fernandez-Sousa JM, Avila J. The marine compound spisulosine, an inhibitor of cell proliferation, promotes the disassembly of actin stress fibers. Cancer Lett 152: 23-29 (2000)
-
(2000)
Cancer Lett
, vol.152
, pp. 23-29
-
-
Cuadros, R.1
Montejo De Garcini, E.2
Wandosell, F.3
Faircloth, G.4
Fernandez-Sousa, J.M.5
Avila, J.6
-
15
-
-
0027358029
-
Fumonisins and other inhibitors of de novo sphingolipid biosynthesis
-
Ed. R. M. Bell, et al., Academic Press, San Diego
-
Merrill AH Jr, Wang E, Gilchrist DG, Riley RT. Fumonisins and other inhibitors of de novo sphingolipid biosynthesis. In Advances in Lipid Research Vol. 26. Sphingolipids. Part B: Regulation and Function of Metabolism. Ed. R. M. Bell, et al., pp. 215-234. Academic Press, San Diego (1993)
-
(1993)
Advances in Lipid Research Vol. 26. Sphingolipids. Part B: Regulation and Function of Metabolism
, pp. 215-234
-
-
Merrill Jr., A.H.1
Wang, E.2
Gilchrist, D.G.3
Riley, R.T.4
-
16
-
-
0019452896
-
Phytotoxins. II. Characterization of a phytotoxic fraction from Alternaria alternata f. sp. lycopersici
-
Bottini AT, Bowen JR, Gilchrist DG. Phytotoxins. II. Characterization of a phytotoxic fraction from Alternaria alternata f. sp. lycopersici. Tetrahedron Lett 22: 2723-2726 (1981)
-
(1981)
Tetrahedron Lett
, vol.22
, pp. 2723-2726
-
-
Bottini, A.T.1
Bowen, J.R.2
Gilchrist, D.G.3
-
17
-
-
0037203347
-
Fumonisins and fumonisin analogs as inhibitors of ceramide synthase and inducers of apoptosis
-
Desai K, Sullards MC, Allegood J, Wang E, Schmelz EM, Hartl M, Humpf H-U, Liotta DC, Peng Q, Merrill AH Jr. Fumonisins and fumonisin analogs as inhibitors of ceramide synthase and inducers of apoptosis. Biochim Biophy Acta 1585: 188-192 (2002)
-
(2002)
Biochim Biophy Acta
, vol.1585
, pp. 188-192
-
-
Desai, K.1
Sullards, M.C.2
Allegood, J.3
Wang, E.4
Schmelz, E.M.5
Hartl, M.6
Humpf, H.-U.7
Liotta, D.C.8
Peng, Q.9
Merrill Jr., A.H.10
-
18
-
-
0015298713
-
Myriocin, a new antifungal antibiotic from Myriococcum albomyces
-
Kluepfel D, Bagli J, Baker H, Charest MP, Kudelski A, Sehgal SN, Vezina C. Myriocin, a new antifungal antibiotic from Myriococcum albomyces. J. Antibiot 25: 109-115 (1972)
-
(1972)
J. Antibiot
, vol.25
, pp. 109-115
-
-
Kluepfel, D.1
Bagli, J.2
Baker, H.3
Charest, M.P.4
Kudelski, A.5
Sehgal, S.N.6
Vezina, C.7
-
19
-
-
0028372227
-
Fungal metabolites. Part 11. A potent immunosuppressive activity found in Isaria sinclairii metabolite
-
Fujita T, Inoue K, Yamamoto S, Ikumoto T, Sasaki S, Toyama R, Chiba K, Hoshino Y, Okumoto T. Fungal metabolites. Part 11. A potent immunosuppressive activity found in Isaria sinclairii metabolite. J. Antibiot 47: 208-215 (1994)
-
(1994)
J. Antibiot
, vol.47
, pp. 208-215
-
-
Fujita, T.1
Inoue, K.2
Yamamoto, S.3
Ikumoto, T.4
Sasaki, S.5
Toyama, R.6
Chiba, K.7
Hoshino, Y.8
Okumoto, T.9
-
20
-
-
0029075192
-
Serine palmitoyltransferase is the primary target of a sphingosine-like immunosuppressant, ISP-1/myriocin
-
Miyake Y, Kozutsumi Y, Nakamura S, Fujita T, Kawasaki T. Serine palmitoyltransferase is the primary target of a sphingosine-like immunosuppressant, ISP-1/myriocin. Biochem Biophys Res Commun 211: 396-403 (1995)
-
(1995)
Biochem Biophys Res Commun
, vol.211
, pp. 396-403
-
-
Miyake, Y.1
Kozutsumi, Y.2
Nakamura, S.3
Fujita, T.4
Kawasaki, T.5
-
21
-
-
20544456156
-
FTY720, a novel immunomodulator: Efficacy and safety results from the first phase 2A study in de novo renal transplantation
-
Tedesco-Silva H, Mourad G, Kahan BD, Boira JG, Weimar W, Mulgaonkar S, Nashan B, Madsen S, Charpentier B, Pellet P, Vanrenterghem Y. FTY720, a novel immunomodulator: efficacy and safety results from the first phase 2A study in de novo renal transplantation. Transplantation 77: 1826-1833 (2004)
-
(2004)
Transplantation
, vol.77
, pp. 1826-1833
-
-
Tedesco-Silva, H.1
Mourad, G.2
Kahan, B.D.3
Boira, J.G.4
Weimar, W.5
Mulgaonkar, S.6
Nashan, B.7
Madsen, S.8
Charpentier, B.9
Pellet, P.10
Vanrenterghem, Y.11
-
22
-
-
0023891786
-
Inhibition of cytochrome c oxidase and hemolysis caused by lysosphingolipids
-
Igisu H, Hamasaki N, Ito A, Ou W. Inhibition of cytochrome c oxidase and hemolysis caused by lysosphingolipids. Lipids 23: 345-348 (1988)
-
(1988)
Lipids
, vol.23
, pp. 345-348
-
-
Igisu, H.1
Hamasaki, N.2
Ito, A.3
Ou, W.4
-
23
-
-
0034612304
-
Ceramide interaction with the respiratory chain of heart mitochondria
-
Di Paola M, Cocco T, Lorusso M. Ceramide interaction with the respiratory chain of heart mitochondria. Biochemistry 39: 6660-6668 (2000)
-
(2000)
Biochemistry
, vol.39
, pp. 6660-6668
-
-
Di Paola, M.1
Cocco, T.2
Lorusso, M.3
-
24
-
-
20044370261
-
A γ-lactone form nafuredin, nafuredin-γ, also inhibits helminth complex I
-
Shiomi K, Ui H, Suzuki H, Hatano H, Nagamitsu T, Takano D, Miyadera H, Yamashita T, Kita K, Miyoshi H, Harder A, Tomoda H, Ōmura S. A γ-lactone form nafuredin, nafuredin-γ, also inhibits helminth complex I. J Antibiot 58: 50-55 (2005)
-
(2005)
J Antibiot
, vol.58
, pp. 50-55
-
-
Shiomi, K.1
Ui, H.2
Suzuki, H.3
Hatano, H.4
Nagamitsu, T.5
Takano, D.6
Miyadera, H.7
Yamashita, T.8
Kita, K.9
Miyoshi, H.10
Harder, A.11
Tomoda, H.12
Omura, S.13
-
25
-
-
0035027370
-
Isolation of a new antibiotic oligomycin G produced by Streptomyces sp. WK-6150
-
Enomoto Y, Shiomi K, Matsumoto A, Takahashi Y, Iwai Y, Harder A, Kölbl H, Woodruff HB, Ōmura S. Isolation of a new antibiotic oligomycin G produced by Streptomyces sp. WK-6150. J Antibiot 54: 308-313 (2001)
-
(2001)
J Antibiot
, vol.54
, pp. 308-313
-
-
Enomoto, Y.1
Shiomi, K.2
Matsumoto, A.3
Takahashi, Y.4
Iwai, Y.5
Harder, A.6
Kölbl, H.7
Woodruff, H.B.8
Omura, S.9
|