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Volumn 127, Issue 3, 2000, Pages 485-491

Development of a new inhibitor of glucosylceramide synthase

Author keywords

Ceramide; Glucosylceramide synthase; Glycosphingolipids; Inhibitor; PBPP; PDMP

Indexed keywords

1 PHENYL 2 BENZYLOXYCARBONYLAMINO 3 PYRROLIDINO 1 PROPANOL; 2 DECANOYLAMINO 3 MORPHOLINO 1 PHENYL 1 PROPANOL; CERAMIDE GLUCOSYLTRANSFERASE; CERAMIDE GLUCOSYLTRANSFERASE INHIBITOR; UNCLASSIFIED DRUG;

EID: 0034126244     PISSN: 0021924X     EISSN: None     Source Type: Journal    
DOI: 10.1093/oxfordjournals.jbchem.a022631     Document Type: Article
Times cited : (21)

References (22)
  • 1
    • 0023258056 scopus 로고
    • Preparation of active isomer of 1-phenyl-2-decanoylamino-3-morpholino-1-propanol, inhibitor of murine glucocerebroside synthetase
    • Inokuchi, J. and Radin, N.S. (1987) Preparation of active isomer of 1-phenyl-2-decanoylamino-3-morpholino-1-propanol, inhibitor of murine glucocerebroside synthetase. J. Lipid. Res. 28, 565-571
    • (1987) J. Lipid. Res. , vol.28 , pp. 565-571
    • Inokuchi, J.1    Radin, N.S.2
  • 2
    • 0031534616 scopus 로고
    • Roles of glycosphingolipids revealed by D-PDMP, an inhibitor of glucosylceramide synthase
    • Inokuchi, J. (1987) Roles of glycosphingolipids revealed by D-PDMP, an inhibitor of glucosylceramide synthase. Trends Glycosci. Glycotechnol. 9, S37-S45
    • (1987) Trends Glycosci. Glycotechnol. , vol.9
    • Inokuchi, J.1
  • 4
    • 0000255378 scopus 로고    scopus 로고
    • Expression of glucosylceramide synthase, converting ceramide to glucosylceramide, confers adriamycin resistance in human breast cancer cells
    • Liu, Y., Han, T.Y., Giuliano, A.E., and Cabot, M.C. (1999) Expression of glucosylceramide synthase, converting ceramide to glucosylceramide, confers adriamycin resistance in human breast cancer cells. J. Biol. Chem. 274, 1140-1146
    • (1999) J. Biol. Chem. , vol.274 , pp. 1140-1146
    • Liu, Y.1    Han, T.Y.2    Giuliano, A.E.3    Cabot, M.C.4
  • 6
    • 0027355755 scopus 로고
    • Metabolic effects of inhibiting glucosylceramide synthesis with PDMP and other substances
    • Radin, N.S., Shayman, J.A., and Inokuchi, J. (1993) Metabolic effects of inhibiting glucosylceramide synthesis with PDMP and other substances. Adv. Lipid Res. 26, 183-213
    • (1993) Adv. Lipid Res. , vol.26 , pp. 183-213
    • Radin, N.S.1    Shayman, J.A.2    Inokuchi, J.3
  • 7
    • 0026338405 scopus 로고
    • New direction in cancer therapy based on aberant expression of glycosphingolipids: Anti-adhesion and ortho-signaling therapy
    • Hakomori, S. (1991) New direction in cancer therapy based on aberant expression of glycosphingolipids: anti-adhesion and ortho-signaling therapy Cancer Cells 3, 461-470
    • (1991) Cancer Cells , vol.3 , pp. 461-470
    • Hakomori, S.1
  • 8
    • 0025027772 scopus 로고
    • Inhibition of experimental metastasis of murine Lewis lung carcinoma by an inhibitor of glucosylceramide synthetase on and its possible mechanism of action
    • Inokuchi, J., Jimbo, M., Momosaki, K., Shimeno, H., Nagamatsu, A., and Radin, N.S. (1990) Inhibition of experimental metastasis of murine Lewis lung carcinoma by an inhibitor of glucosylceramide synthetase on and its possible mechanism of action. Cancer Res. 50, 6731-6737
    • (1990) Cancer Res. , vol.50 , pp. 6731-6737
    • Inokuchi, J.1    Jimbo, M.2    Momosaki, K.3    Shimeno, H.4    Nagamatsu, A.5    Radin, N.S.6
  • 9
    • 0030039399 scopus 로고    scopus 로고
    • Glucosylceramide synthase inhibitor, D-threo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol (D-PDMP) exhibits a novel decarcinogenic activity against Shope carcinoma cells
    • Kyogashima, M., Inoue, M., Seto, A., and Inokuchi, J. (1996) Glucosylceramide synthase inhibitor, D-threo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol (D-PDMP) exhibits a novel decarcinogenic activity against Shope carcinoma cells. Cancer Lett. 101, 25-30
    • (1996) Cancer Lett. , vol.101 , pp. 25-30
    • Kyogashima, M.1    Inoue, M.2    Seto, A.3    Inokuchi, J.4
  • 10
    • 0029795428 scopus 로고    scopus 로고
    • Abrogation of shedding of immunosuppressive neuroblastoma gangliosides
    • Li, R. and Ladish, S. (1996) Abrogation of shedding of immunosuppressive neuroblastoma gangliosides. Cancer Res. 56, 4602-4605
    • (1996) Cancer Res. , vol.56 , pp. 4602-4605
    • Li, R.1    Ladish, S.2
  • 11
    • 0031887067 scopus 로고    scopus 로고
    • Synthesis, shedding, and intercellular transfer of human medulloblastoma gangliosides: Abrogation by a new inhibitor of glucosylceramide synthase
    • Olshefski, R. and Ladish, S. (1998) Synthesis, shedding, and intercellular transfer of human medulloblastoma gangliosides: abrogation by a new inhibitor of glucosylceramide synthase. J. Neurochem. 70, 467-472
    • (1998) J. Neurochem. , vol.70 , pp. 467-472
    • Olshefski, R.1    Ladish, S.2
  • 12
    • 0032836990 scopus 로고    scopus 로고
    • Preferential killing of multidrug-resistant KB cells by inhibitors of glucosylceramide synthase
    • Nicholson, K.M., Quinn, D.M., Kellett, G.L., and Warr, J.R. (1999) Preferential killing of multidrug-resistant KB cells by inhibitors of glucosylceramide synthase. Br. J . Cancer 81, 423-430
    • (1999) Br. J . Cancer , vol.81 , pp. 423-430
    • Nicholson, K.M.1    Quinn, D.M.2    Kellett, G.L.3    Warr, J.R.4
  • 14
    • 0028316588 scopus 로고
    • Studies on morpholinosphingolipids: Potent inhibitors of glucosylceramide synthase
    • Carson, K.G. and Ganem, B. (1994) Studies on morpholinosphingolipids: potent inhibitors of glucosylceramide synthase. Tetrahedron Lett. 35, 2659-2662
    • (1994) Tetrahedron Lett. , vol.35 , pp. 2659-2662
    • Carson, K.G.1    Ganem, B.2
  • 16
    • 0030744022 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of four stereoisomers of PDMP-analogue, N-(2-decylamino-3-hydroxy-3-phenylprop-1-yl)-β-valienamine, and related compounds
    • Ogawa, S., Tamai, M., Taiji, E., Jimbo, M., Yamagishi, K., and Inokuchi, J. (1997) Synthesis and biological evaluation of four stereoisomers of PDMP-analogue, N-(2-decylamino-3-hydroxy-3-phenylprop-1-yl)-β-valienamine, and related compounds. Bioorg. Med. Chem. Lett. 7, 1915-1920
    • (1997) Bioorg. Med. Chem. Lett. , vol.7 , pp. 1915-1920
    • Ogawa, S.1    Tamai, M.2    Taiji, E.3    Jimbo, M.4    Yamagishi, K.5    Inokuchi, J.6
  • 17
    • 0033591332 scopus 로고    scopus 로고
    • Improved inhibitors of glucosylceramide synthase
    • Lee, L., Abe, A., and Shayman, J.A. (1999) Improved inhibitors of glucosylceramide synthase. J. Biol. Chem. 274, 14662-14669
    • (1999) J. Biol. Chem. , vol.274 , pp. 14662-14669
    • Lee, L.1    Abe, A.2    Shayman, J.A.3
  • 18
    • 0029891058 scopus 로고    scopus 로고
    • A novel enzyme that catalyzes the esterification of N-acetylsphingosine
    • Abe, A., Shayman, J.A., and Radin, N.S. (1996) A novel enzyme that catalyzes the esterification of N-acetylsphingosine. J. Biol. Chem. 271, 14383-14389
    • (1996) J. Biol. Chem. , vol.271 , pp. 14383-14389
    • Abe, A.1    Shayman, J.A.2    Radin, N.S.3
  • 19
    • 0019003203 scopus 로고
    • Analogs of ceramide that inhibit glucocerebroside synthase in mouse brain
    • Vunnam, R.R. and Radin, N.S. (1980) Analogs of ceramide that inhibit glucocerebroside synthase in mouse brain. Chem. Phys. Lipids 26, 265-278
    • (1980) Chem. Phys. Lipids , vol.26 , pp. 265-278
    • Vunnam, R.R.1    Radin, N.S.2
  • 20
    • 0032541179 scopus 로고    scopus 로고
    • The multidrug resistance modulator SDZ PSC 833 is a potent activator of cellular ceramide formation
    • Cabot, M.C., Han, T.Y., and Giuliano, A.E. (1998) The multidrug resistance modulator SDZ PSC 833 is a potent activator of cellular ceramide formation. FEBS Lett. 17, 185-188
    • (1998) FEBS Lett. , vol.17 , pp. 185-188
    • Cabot, M.C.1    Han, T.Y.2    Giuliano, A.E.3
  • 22
    • 0029761340 scopus 로고    scopus 로고
    • Accumulation of glucosylceramides in multidrug-resistant cancer cells
    • Lavie, Y., Cao, H., Bursten, S.L., Giuliano, A.E., and Cabot, M.C. (1996) Accumulation of glucosylceramides in multidrug-resistant cancer cells. J. Biol. Chem. 271, 19530-19536
    • (1996) J. Biol. Chem. , vol.271 , pp. 19530-19536
    • Lavie, Y.1    Cao, H.2    Bursten, S.L.3    Giuliano, A.E.4    Cabot, M.C.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.