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MK615 inhibits pancreatic cancer cell growth by dual inhibition of Aurora A and B kinases

World journal of gastroenterology : WJG, 2008-03, Vol.14 (9), p.1378-1382

2008

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Identification of Potent and Selective Inhibitors of PDGF Receptor Autophosphorylation

Journal of medicinal chemistry, 2006-04, Vol.49 (7), p.2186-2192

2006

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A novel anti-cancer substance, MK615, from ume, a variety of Japanese apricot, inhibits growth of hepatocellular carcinoma cells by suppressing Aurora A kinase activity

Hepato-gastroenterology, 2007-09, Vol.54 (78), p.1770

2007

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The "Prunus mume Sieb. et Zucc" (Ume) is a Rich Natural Source of Novel Anti-Cancer Substance

International journal of food properties, 2007-04, Vol.10 (2), p.375-384

2007

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Synthesis and structure-activity relationship for new series of 4-phenoxyquinoline derivatives as specific inhibitors of platelet-derived growth factor receptor tyrosine kinase

Bioorganic & medicinal chemistry, 2003-11, Vol.11 (23), p.5117-5133

2003

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Orally active anti-proliferation agents : Novel diphenylamine derivatives as FGF-R2 autophosphorylation inhibitors

Bioorganic & medicinal chemistry letters, 2004-02, Vol.14 (4), p.875-879

2004

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Antineoplastic effect of a single oral dose of the novel Flt3 inhibitor KRN383 on xenografted human leukemic cells harboring Flt3-activating mutations

Leukemia research, 2006-12, Vol.30 (12), p.1541-1546

2006

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Corrigendum to “Antineoplastic effect of a single oral dose of the novel Flt3 inhibitor KRN383 on xenografted human leukemic cells harboring Flt3-activating mutations” [Leuk. Res. 30 (2006) 1541–1546]

Leukemia research, 2007-10, Vol.31 (10), p.1457-1457

2007

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Carbohydrate Moieties of Peanut Agglutinin Receptors Isolated from Human Gastric Cancer Cells

Journal of biochemistry (Tokyo), 1987-09, Vol.102 (3), p.657-664

1987

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Ki23819 (KRN383•HCl) Inhibits Kinase Activity of Wild Type and Mutant FLT3 Receptor Tyrosine Kinase In Vitro

Blood, 2004-11, Vol.104 (11), p.1168-1168

2004

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Single Oral Administration of KRN383, a Novel Flt3 Inhibitor, Induces Eradication of the Xenograft Tumor Harboring Flt3 Mutation in Mice

Blood, 2004-11, Vol.104 (11), p.2545-2545

2004

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A convenient synthesis of 4-unsubstituted .beta.-lactams

Journal of the American Chemical Society, 1985-03, Vol.107 (6), p.1698-1701

1985

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Syntheses of α-, β-monoglycosylceramides and four diastereomers of an α-galactosylceramide

Bioorganic & medicinal chemistry letters, 1995-04, Vol.5 (7), p.699-704

1995

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Synthesis and Anti-inflammatory Activity of Antioxidants, 4-Alkylthio-o-anisidine Derivatives

Chemical and Pharmaceutical Bulletin, 1992/02/25, Vol.40(2), pp.351-356

1992

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Carbohydrate Moieties of Peanut Agglutinin Receptors Isolated from Human Gastric Cancer Cells1

Journal of biochemistry (Tokyo), 1987-09, Vol.102 (3), p.657-664

1987

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A novel series of 4-phenoxyquinolines: potent and highly selective inhibitors of PDGF receptor autophosphorylation

Bioorganic & medicinal chemistry letters, 1997-12, Vol.7 (23), p.2935-2940

1997

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Effects of ortho-substituent groups of sulochrin on inhibitory activity to eosinophil degranulation

Bioorganic & medicinal chemistry letters, 1999-07, Vol.9 (14), p.1945-1948

1999

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Selective Inhibition of Platelet-Derived Growth Factor (PDGF) Receptor Autophosphorylation and PDGF-Mediated Cellular Events by a Quinoline Derivative

Experimental cell research, 1997-08, Vol.234 (2), p.285-292

1997

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A convenient synthesis of 4-unsubstituted β-lactams

Journal of the American Chemical Society, 1985, Vol.107 (6), p.1698-1701

1985

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Beneficial Effects of a Novel Inhibitor of Platelet-Derived Growth Factor Receptor Autophosphorylation in the Rat with Mesangial Proliferative Glomerulonephritis

General pharmacology, 1998-11, Vol.31 (5), p.765-773

1998

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Effects of chitosan-coated dialdehyde cellulose, a newly developed oral adsorbent on glomerulonephritis induced by antl-Thy-1 antibody in rats

Japanese journal of pharmacology, 1996, Vol.71, p.287

1996

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Effects of chitosan-coated dialdehyde cellulose, a newly developed oral adsorbent on glomerulonephritis Induced by anti-Thy-1 antibody In rats

Japanese Journal of Pharmacology, 1996, Vol.71 (suppl.2), p.287-287

1996

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P-914 - Effects of chitosan-coated dialdehyde cellulose, a newly developed oral adsorbent on glomerulonephritis induced by antl-Thy-1 antibody in rats

Japanese journal of pharmacology, 1996, Vol.71, p.287-287

1996

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Deep-intronic variant of fukutin is the most prevalent point mutation of Fukuyama congenital muscular dystrophy in Japan

Journal of human genetics, 2017-11, Vol.62 (11), p.945-948

2017

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An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

Nature (London), 1998-07, Vol.394 (6691), p.388-392

1998

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MK615 inhibits pancreatic cancer cell growth by dual inhibition of Aurora A and B kinases

Identification of Potent and Selective Inhibitors of PDGF Receptor Autophosphorylation

A novel anti-cancer substance, MK615, from ume, a variety of Japanese apricot, inhibits growth of hepatocellular carcinoma cells by suppressing Aurora A kinase activity

The "Prunus mume Sieb. et Zucc" (Ume) is a Rich Natural Source of Novel Anti-Cancer Substance

Synthesis and structure-activity relationship for new series of 4-phenoxyquinoline derivatives as specific inhibitors of platelet-derived growth factor receptor tyrosine kinase

Orally active anti-proliferation agents : Novel diphenylamine derivatives as FGF-R2 autophosphorylation inhibitors

Antineoplastic effect of a single oral dose of the novel Flt3 inhibitor KRN383 on xenografted human leukemic cells harboring Flt3-activating mutations

Corrigendum to “Antineoplastic effect of a single oral dose of the novel Flt3 inhibitor KRN383 on xenografted human leukemic cells harboring Flt3-activating mutations” [Leuk. Res. 30 (2006) 1541–1546]

Carbohydrate Moieties of Peanut Agglutinin Receptors Isolated from Human Gastric Cancer Cells

Ki23819 (KRN383•HCl) Inhibits Kinase Activity of Wild Type and Mutant FLT3 Receptor Tyrosine Kinase In Vitro

Single Oral Administration of KRN383, a Novel Flt3 Inhibitor, Induces Eradication of the Xenograft Tumor Harboring Flt3 Mutation in Mice

A convenient synthesis of 4-unsubstituted .beta.-lactams

Syntheses of α-, β-monoglycosylceramides and four diastereomers of an α-galactosylceramide

Synthesis and Anti-inflammatory Activity of Antioxidants, 4-Alkylthio-o-anisidine Derivatives

Carbohydrate Moieties of Peanut Agglutinin Receptors Isolated from Human Gastric Cancer Cells1

A novel series of 4-phenoxyquinolines: potent and highly selective inhibitors of PDGF receptor autophosphorylation

Effects of ortho-substituent groups of sulochrin on inhibitory activity to eosinophil degranulation

Selective Inhibition of Platelet-Derived Growth Factor (PDGF) Receptor Autophosphorylation and PDGF-Mediated Cellular Events by a Quinoline Derivative

A convenient synthesis of 4-unsubstituted β-lactams

Beneficial Effects of a Novel Inhibitor of Platelet-Derived Growth Factor Receptor Autophosphorylation in the Rat with Mesangial Proliferative Glomerulonephritis

Effects of chitosan-coated dialdehyde cellulose, a newly developed oral adsorbent on glomerulonephritis induced by antl-Thy-1 antibody in rats

Effects of chitosan-coated dialdehyde cellulose, a newly developed oral adsorbent on glomerulonephritis Induced by anti-Thy-1 antibody In rats

P-914 - Effects of chitosan-coated dialdehyde cellulose, a newly developed oral adsorbent on glomerulonephritis induced by antl-Thy-1 antibody in rats

Deep-intronic variant of fukutin is the most prevalent point mutation of Fukuyama congenital muscular dystrophy in Japan

An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

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