中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
YUANHUACIN-A IS A SELECTIVE ANTAGONIST OF PHORBOL ESTER RECEPTOR IN PROTEIN-KINASE-C

文献类型:期刊论文

作者ZHANG, DC; CAO, CX; ZHANG, CJ; ZHOU, BN
刊名SCIENCE IN CHINA SERIES B-CHEMISTRY
出版日期1993-07
卷号36期号:7页码:803-808
关键词PROTEIN KINASE-C PHORBOL ESTERS YUANHUACIN-A 3H-PHORBOL-12 13-DIBUTYRATE
ISSN号1001-652X
文献子类Article
英文摘要Protein kinase C with a molecular weight of 82 kD has been purified to electrophoresis homogenous from rat brain through a series of chromatography columns including DE-52, Sepharose G-200 and phenyl-Sepharose. The enzyme possessed autophosphorylation activity. Yuanhuacin A inhibited the H-3-phorbol-12, 13-dibutyrate (H-3-PdBu) binding of PKC with an IC50 value of 1.48 +/- 0.28 X 10(-8) mol/L when the concentration of H-3-PdBu was 1.5 X 10(-9) mol/L (K(i) = 1.2 X 10(-8) mol/L). Yuanhuacin A inhibited the PdBu-stimulated PKC activity in the catalysis of the phosphorylation of Histone III-S with an IC50 of 2.82 +/- 0.37 X 10(-9) mol/L (PdBu = 10(-6) mol/L), while it had no effect on the basal and Ca2+-stimulated PKC activity in the same assay system. This result suggests that Yuanhuacin A is a selective antagonist of the phorbol ester receptor in protein kinase C.
WOS关键词SIGNAL TRANSDUCTION ; INHIBITOR ; CALCIUM ; POTENT
WOS研究方向Chemistry
语种英语
WOS记录号WOS:A1993LR67000005
出版者SCIENCE CHINA PRESS
源URL[http://119.78.100.183/handle/2S10ELR8/275130]  
专题中国科学院上海药物研究所
通讯作者ZHANG, DC
作者单位ACAD SINICA,SHANGHAI INST MAT MED,SHANGHAI 200031,PEOPLES R CHINA
推荐引用方式
GB/T 7714
ZHANG, DC,CAO, CX,ZHANG, CJ,et al. YUANHUACIN-A IS A SELECTIVE ANTAGONIST OF PHORBOL ESTER RECEPTOR IN PROTEIN-KINASE-C[J]. SCIENCE IN CHINA SERIES B-CHEMISTRY,1993,36(7):803-808.
APA ZHANG, DC,CAO, CX,ZHANG, CJ,&ZHOU, BN.(1993).YUANHUACIN-A IS A SELECTIVE ANTAGONIST OF PHORBOL ESTER RECEPTOR IN PROTEIN-KINASE-C.SCIENCE IN CHINA SERIES B-CHEMISTRY,36(7),803-808.
MLA ZHANG, DC,et al."YUANHUACIN-A IS A SELECTIVE ANTAGONIST OF PHORBOL ESTER RECEPTOR IN PROTEIN-KINASE-C".SCIENCE IN CHINA SERIES B-CHEMISTRY 36.7(1993):803-808.

入库方式: OAI收割

来源:上海药物研究所

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