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用新型细胞毒性免疫抑制剂 3-乙酰基-5-(4-氟亚苄基)-2,5-二氢-4-羟基-2-氧代噻吩(ICI 47776)进行生化研究。

Biochemical studies with a new cytotoxic immunosuppressive agent, 3-acetyl-5-(4-fluorobenzylidene)-2,5-dihydro-4-hydroxy-2-oxothiophen (I.C.I. 47776).

机构信息

Imperial Chemical Industries Limited, Pharmaceuticals Division, Alderley Park, Macclesfield, Cheshire.

出版信息

Biochem J. 1967 Mar;102(3):705-11. doi: 10.1042/bj1020705.

DOI:10.1042/bj1020705
PMID:16742483
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1270317/
Abstract
  1. A new cytotoxic agent, 3-acetyl-5-(4-fluorobenzylidene)-2,5-dihydro-4-hydroxy-2-oxothiophen (I.C.I. 47776), strongly inhibits protein and nucleic acid synthesis and, to a smaller extent, respiration in lymph-node cells and Landschütz ascites-tumour cells in vitro. 2. The activity of I.C.I. 47776 in vitro declines as the pH of the medium is increased and is inversely proportional to the concentration of serum in the medium. 3. The compound has no effect on the incorporation of leucine by a cell-free preparation from Landschütz ascites cells containing ATP and phosphoenolpyruvate. 4. I.C.I. 47776 stimulates glycolysis in suspensions of Landschütz ascites cells in the presence of excess of glucose but has no effect on glycolysis in suspensions of rat lymph-node cells. 5. I.C.I. 47776 markedly depresses ATP concentration in ascites cells in the absence of glucose but has no effect on the ATP concentration in the presence of glucose. The inhibition of protein synthesis by I.C.I. 47776 in ascites cells is, however, only partially reversed by the addition of glucose. 6. The ATP concentration of rat lymph-node cells incubated with I.C.I. 47776 in the absence of glucose is also markedly depressed but the addition of glucose increases the ATP concentration only slightly. Further, glucose has no effect on the inhibition of protein synthesis in lymph-node cells by I.C.I. 47776. 7. It is suggested that I.C.I. 47776 inhibits protein and nucleic acid synthesis in cell suspensions indirectly by acting as a mitochondrial poison. 8. The relevance of studies on the activity of I.C.I. 47776 in vitro to its cytotoxic and immunosuppressive action in vivo is discussed.
摘要
  1. 一种新的细胞毒素剂,3-乙酰基-5-(4-氟亚苄基)-2,5-二氢-4-羟基-2-氧代噻吩(ICI 47776),强烈抑制体外淋巴结细胞和 Lanschütz 腹水肿瘤细胞的蛋白质和核酸合成,并且在较小程度上抑制呼吸。

  2. ICI 47776 在体外的活性随着培养基 pH 值的升高而降低,并且与培养基中血清的浓度成反比。

  3. 该化合物对含有 ATP 和磷酸烯醇丙酮酸的 Landschütz 腹水细胞无细胞制剂中亮氨酸的掺入没有影响。

  4. ICI 47776 在存在过量葡萄糖的情况下刺激 Lanschütz 腹水细胞悬浮液中的糖酵解,但对大鼠淋巴结细胞悬浮液中的糖酵解没有影响。

  5. ICI 47776 在没有葡萄糖的情况下显著降低腹水细胞中的 ATP 浓度,但在有葡萄糖的情况下对 ATP 浓度没有影响。然而,葡萄糖仅部分逆转 ICI 47776 对腹水细胞中蛋白质合成的抑制作用。

  6. 在没有葡萄糖的情况下孵育 ICI 47776 的大鼠淋巴结细胞的 ATP 浓度也明显降低,但葡萄糖仅略微增加 ATP 浓度。此外,葡萄糖对 ICI 47776 抑制淋巴结细胞中蛋白质合成没有影响。

  7. 据认为,ICI 47776 通过作为线粒体毒物间接抑制细胞悬浮液中的蛋白质和核酸合成。

  8. 讨论了在体内对 ICI 47776 的细胞毒性和免疫抑制作用进行体外研究的相关性。

相似文献

1
Biochemical studies with a new cytotoxic immunosuppressive agent, 3-acetyl-5-(4-fluorobenzylidene)-2,5-dihydro-4-hydroxy-2-oxothiophen (I.C.I. 47776).用新型细胞毒性免疫抑制剂 3-乙酰基-5-(4-氟亚苄基)-2,5-二氢-4-羟基-2-氧代噻吩(ICI 47776)进行生化研究。
Biochem J. 1967 Mar;102(3):705-11. doi: 10.1042/bj1020705.
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The inhibition of nucleic acid synthesis by mycophenolic acid.霉酚酸对核酸合成的抑制作用。
Biochem J. 1969 Jul;113(3):515-24. doi: 10.1042/bj1130515.
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[Change in energy metabolism of ascites cancer cells with a decrease in pH].[随着pH值降低腹水癌细胞能量代谢的变化]
Biokhimiia. 1991 Sep;56(9):1652-60.
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A study of the Crabtree effect in Novikoff ascites-hepatoma cells.对 Novikoff 腹水肝癌细胞中 Crabtree 效应的研究。
Biochem J. 1966 May;99(2):413-8. doi: 10.1042/bj0990413.
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On the mechanism of the glucose-induced ATP catabolism in ascites tumour cells and its reversal by pyruvate.关于葡萄糖诱导腹水肿瘤细胞中ATP分解代谢的机制及其被丙酮酸逆转的机制。
Biochem J. 1980 Dec 15;192(3):793-800. doi: 10.1042/bj1920793.
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On the mechanism of the Crabtree effect in mouse ascites tumor cells.关于小鼠腹水肿瘤细胞中巴斯德效应的机制。
J Cell Physiol. 1977 Nov;93(2):313-6. doi: 10.1002/jcp.1040930218.
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The pH-dependence of sugar-transport and glycolysis in cultured Ehrlich ascites-tumour cells.培养的艾氏腹水癌细胞中糖转运和糖酵解的pH依赖性
Biochem J. 1978 Aug 15;174(2):453-9. doi: 10.1042/bj1740453.
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Deoxyribonucleic acid nucleotidyltransferase from Landschütz ascites-tumour cells.来自兰施胡茨腹水瘤细胞的脱氧核糖核酸核苷酸转移酶。
Biochem J. 1966 May;99(2):443-53. doi: 10.1042/bj0990443.
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The time-course of the synthesis of adenosine triphosphate in Ehrlich ascites-tumour cells, and the effect of 2,4-dinitrophenol.艾氏腹水癌细胞中三磷酸腺苷合成的时间进程以及2,4-二硝基苯酚的作用
Biochem J. 1967 Jul;104(1):158-64. doi: 10.1042/bj1040158.
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The stimulus-secretion coupling of glucose-induced insulin release. Metabolism of glucose in K+-deprived islets.葡萄糖诱导的胰岛素释放的刺激-分泌偶联。钾离子缺乏的胰岛中葡萄糖的代谢。
Biochem J. 1980 Jan 15;186(1):183-90. doi: 10.1042/bj1860183.

引用本文的文献

1
The inhibition of nucleic acid synthesis by mycophenolic acid.霉酚酸对核酸合成的抑制作用。
Biochem J. 1969 Jul;113(3):515-24. doi: 10.1042/bj1130515.
2
Immunosuppressive activity of 3-acetyl-5-(4-fluorobenzylidene)-4-hydroxy-2-oxo-2:5-dihydrothiophen (I.C.I. 47,776).3-乙酰基-5-(4-氟亚苄基)-4-羟基-2-氧代-2,5-二氢噻吩(ICI 47,776)的免疫抑制活性
Immunology. 1968 Mar;14(3):393-9.

本文引用的文献

1
Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
J Biol Chem. 1951 Nov;193(1):265-75.
2
Relation of energy processes to the incorporation of amino acids into proteins of the Ehrlich ascites carcinoma.能量过程与氨基酸掺入艾氏腹水癌蛋白质的关系。
J Biol Chem. 1955 Mar;213(1):1-9.
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CHEMOTHERAPY OF ARTHRITIS INDUCED IN RATS BY MYCOBACTERIAL ADJUVANT.分枝杆菌佐剂诱导大鼠关节炎的化学疗法
Br J Pharmacol Chemother. 1963 Aug;21(1):127-36. doi: 10.1111/j.1476-5381.1963.tb01508.x.
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The inhibition of incorporation of leucine into protein of cell-free systems from rat liver and Escherichia coli by chlortetracycline.金霉素对大鼠肝脏及大肠杆菌无细胞系统中亮氨酸掺入蛋白质的抑制作用。
Biochem J. 1963 Jun;87(3):449-53. doi: 10.1042/bj0870449.
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Regulatory mechanisms in carbohydrate metabolism. III. Limiting factors in glycolysis of ascites tumor cells.碳水化合物代谢中的调节机制。III. 腹水肿瘤细胞糖酵解中的限制因素。
J Biol Chem. 1959 May;234(5):1029-35.
6
A new type of cytotoxic immunosuppressive agent: 3-acetyl-5-(4-fluorbenzylidiene)4-hydroxy-2-oxo-2:5-dihydrothiophen.一种新型细胞毒性免疫抑制剂:3-乙酰基-5-(4-氟亚苄基)-4-羟基-2-氧代-2,5-二氢噻吩
Nature. 1966 May 7;210(5036):638-9. doi: 10.1038/210638a0.