PROTEIN-TYROSINE KINASE AND PROTEIN-KINASE-C INHIBITION BY FUNGAL ANTHRAQUINONES RELATED TO EMODIN

被引：21

作者：

FREDENHAGEN, A ^{[1
]}

METT, H ^{[1
]}

MEYER, T ^{[1
]}

BUCHDUNGER, E ^{[1
]}

REGENASS, U ^{[1
]}

ROGGO, BE ^{[1
]}

PETERSEN, F ^{[1
]}

机构：

[1] CIBA GEIGY AG,ONCOL RES DEPT,CH-4002 BASEL,SWITZERLAND

来源：

JOURNAL OF ANTIBIOTICS | 1995年 / 48卷 / 11期

关键词：

D O I：

10.7164/antibiotics.48.1355

中图分类号：

Q81 [生物工程学（生物技术）]; Q93 [微生物学];

学科分类号：

071005 ; 0836 ; 090102 ; 100705 ;

摘要：

[No abstract available]

引用

页码：1355 / 1358

页数：4

共 16 条

[1] THERAPEUTIC POTENTIAL OF PROTEIN-KINASE-C INHIBITORS
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[2] 4,5-DIANILINOPHTHALIMIDE - A PROTEIN-TYROSINE KINASE INHIBITOR WITH SELECTIVITY FOR THE EPIDERMAL GROWTH-FACTOR RECEPTOR SIGNAL-TRANSDUCTION PATHWAY AND POTENT IN-VIVO ANTITUMOR-ACTIVITY
BUCHDUNGER, E
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[J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (06) : 2334 - 2338
[3] REQUIREMENT FOR INTRINSIC PROTEIN TYROSINE KINASE IN THE IMMEDIATE AND LATE ACTIONS OF THE EGF RECEPTOR
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[J]. NATURE, 1987, 328 (6133) : 820 - 823
[4] PAECILOQUINONE-A, PAECILOQUINONE-B, PAECILOQUINONE-C, PAECILOQUINONE-D, PAECILOQUINONE-E AND PAECILOQUINONE-F - NEW POTENT INHIBITORS OF PROTEIN-TYROSINE KINASE PRODUCED BY PAECILOMYCES-CARNEUS .2. CHARACTERIZATION AND STRUCTURE DETERMINATION
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[J]. JOURNAL OF ANTIBIOTICS, 1995, 48 (03) : 199 - 204
[5] HANAFUSA H, 1990, ADV SEC MESS PHOSPH, P280
[6] POINT MUTATION AT THE ATP BINDING-SITE OF EGF RECEPTOR ABOLISHES PROTEIN-TYROSINE KINASE-ACTIVITY AND ALTERS CELLULAR ROUTING
HONEGGER, AM
DULL, TJ
FELDER, S
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[J]. CELL, 1987, 51 (02) : 199 - 209
[7] EMODIN, A PROTEIN TYROSINE KINASE INHIBITOR FROM POLYGONUM-CUSPIDATUM
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[J]. JOURNAL OF NATURAL PRODUCTS, 1992, 55 (05): : 696 - 698
[8] LEE JC, 1982, J IMMUNOL, V128, P2393
[9] LYDON NB, 1990, ONCOGENE RES, V5, P161
[10] MARTE BM, 1994, CELL GROWTH DIFFER, V5, P239

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