Pharmacology & Therapeutics. Part A: Chemotherapy, Toxicology and Metabolic Inhibitors最新文献

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Pharmacology and therapeutics part A 药理学和治疗学
Pharmacology & Therapeutics. Part A: Chemotherapy, Toxicology and Metabolic Inhibitors Pub Date : 1978-01-01 DOI: 10.1016/0362-5478(78)90008-6
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引用次数: 0
Inhibitors of bacterial DNA-dependent RNA polymerase 细菌dna依赖性RNA聚合酶抑制剂
Pharmacology & Therapeutics. Part A: Chemotherapy, Toxicology and Metabolic Inhibitors Pub Date : 1978-01-01 DOI: 10.1016/0362-5478(78)90018-9
Joseph S. Krakow, S. Anand Kumar
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引用次数: 3
Defective interfering viruses and their influence on virus infections 缺陷干扰病毒及其对病毒感染的影响
Pharmacology & Therapeutics. Part A: Chemotherapy, Toxicology and Metabolic Inhibitors Pub Date : 1978-01-01 DOI: 10.1016/0362-5478(78)90014-1
Charlotte Jones, Ian Kennedy, John J. Holland
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引用次数: 1
Interferon action and the cell surface 干扰素作用与细胞表面
Pharmacology & Therapeutics. Part A: Chemotherapy, Toxicology and Metabolic Inhibitors Pub Date : 1978-01-01 DOI: 10.1016/0362-5478(78)90025-6
R. Friedman
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引用次数: 28
Cytochrome P-450—IV. Stability of cytochrome P-450 and conversion to cytochrome P-420: Isolation and properties of cytochrome P-420 细胞色素p - 450 - 4。细胞色素P-450的稳定性及向细胞色素P-420的转化:细胞色素P-420的分离及性质
Pharmacology & Therapeutics. Part A: Chemotherapy, Toxicology and Metabolic Inhibitors Pub Date : 1978-01-01 DOI: 10.1016/0362-5478(78)90010-4
Toshio Yamano, Yoshiyuki Ichikawa
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引用次数: 8
Hydroperoxides and superoxides in microsomal oxidations 微粒体氧化中的氢过氧化物和超氧化物
Pharmacology & Therapeutics. Part A: Chemotherapy, Toxicology and Metabolic Inhibitors Pub Date : 1978-01-01 DOI: 10.1016/0362-5478(78)90004-9
Peter J. O'Brien
{"title":"Hydroperoxides and superoxides in microsomal oxidations","authors":"Peter J. O'Brien","doi":"10.1016/0362-5478(78)90004-9","DOIUrl":"10.1016/0362-5478(78)90004-9","url":null,"abstract":"<div><p>The following scheme summarizes our present knowledge on the mechanism of the reactions carried out by cytochrome P450:</p><p>X<sup>δ+</sup> can be a protein radical or a porphyrin radical cation.</p><p>Donor can be: (i) reduced cytochrome <em>b</em><sub>5</sub> or NADPH:cytochrome <em>c</em> reductase; (ii) tetramethylphenylenediamine, dimethylphenylenediamine, diaminobenzidine; (iii) dimethylaniline or aminopyrine and resulting in N-dealkylation (Griffin, 1977); (iv) ROOH resulting in ROO<sup>.</sup> production and thereby increasing cytochrome P450 destruction, lipid peroxidation, singlet oxygen formation and oxidation of peroxidase donors; (v) unsaturated lipids resulting in lipid peroxidation and singlet oxygen formation; and (vi) various antioxidants.</p><p>S substrate can be amines, drugs, steroids, carcinogens, antioxidants R·CH<sub>2</sub>OH alcohols (from mechanism by Chance and Schonbaum, 1976). Hydroperoxides (e.g. ethyl hydroperoxide) that form alcohol substrates on reduction would be expected to be less effective in catalyzing hydroxylation reactions (Nordblom <em>et al.</em>, 1976).</p><p>R·CHO Aldehyde product from alcohol oxidation ROOH Primary, secondary or tertiary hydroperoxides</p><p>The scheme explains the following three pathways involved in the formation of the oxenoid species: </p><ul><li><span>1.</span><span><p>(1) <em>Organic hydroperoxide catalyzed</em>. This involves first the formation of an enzyme-peroxide complex (Reaction 1) followed by a fast rearrangement by an outer sphere electron transfer mechanism (Chance and Schonbaum, 1976). Some of this complex may be dissociated to the corresponding aldehyde and the original enzyme. The complex may also be hydrated to compound I, the active hydroxylating species, and release the alcohol. The hydroperoxide catalyzed alcohol oxidation (Rahimtula and O'Brien, 1976) can be explained by the reversal of these changes from compound I to the complex and dissociation of this complex (Reaction 4). The hydroperoxide catalyzed substrate hydroxylation involves the transfer of activated oxygen from compound I to the substrate (Reaction 5). It is also possible that alcohol oxidation proceeds by a hydroxylation mechanism, followed by the rearrangement of the ‘hydroxylated’ intermediate to an aldehyde. The hydroperoxide catalyzed oxidation of hydrogen or electron donors, unsaturated lipids or antioxidants involves the protein or porphyrin free radical of compound I and the ferryl iron of compound II. In competition with these donors, ROOH can also convert compound I to compound II (Chance, 1952; Reaction 6) and the resulting peroxy radicals can also oxidize these donors. In the absence of these donors, cytochrome P450 destruction readily occurs as a result of the peroxy radicals or protein or porphyrin radicals.</p></span></li><li><span>2.</span><span><p>(2) H<sub>2</sub>O<sub>2</sub>. The relatively high concentration of H<sub>2</sub>O<sub>2</sub> required compared with that nee","PeriodicalId":101016,"journal":{"name":"Pharmacology & Therapeutics. Part A: Chemotherapy, Toxicology and Metabolic Inhibitors","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1978-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0362-5478(78)90004-9","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84010415","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 37
DNA and RNA polymerases of mammalian cells and tumor viruses 哺乳动物细胞和肿瘤病毒的DNA和RNA聚合酶
Pharmacology & Therapeutics. Part A: Chemotherapy, Toxicology and Metabolic Inhibitors Pub Date : 1978-01-01 DOI: 10.1016/0362-5478(78)90002-5
H.S. Allaudeen
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引用次数: 5
Reconstituted mammalian mixed-function oxidases: Requirements, specificities and other properties 重组哺乳动物混合功能氧化酶:要求、特性和其他性质
Pharmacology & Therapeutics. Part A: Chemotherapy, Toxicology and Metabolic Inhibitors Pub Date : 1978-01-01 DOI: 10.1016/0362-5478(78)90021-9
Anthony Y.H. Lu, Susan B. West
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引用次数: 65
Modulation of immunity by levamisole 左旋咪唑对免疫的调节
Pharmacology & Therapeutics. Part A: Chemotherapy, Toxicology and Metabolic Inhibitors Pub Date : 1978-01-01 DOI: 10.1016/0362-5478(78)90024-4
Gerard Renoux
{"title":"Modulation of immunity by levamisole","authors":"Gerard Renoux","doi":"10.1016/0362-5478(78)90024-4","DOIUrl":"10.1016/0362-5478(78)90024-4","url":null,"abstract":"","PeriodicalId":101016,"journal":{"name":"Pharmacology & Therapeutics. Part A: Chemotherapy, Toxicology and Metabolic Inhibitors","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1978-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0362-5478(78)90024-4","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90439713","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 54
Reconstituted mammalian mixed-function oxidases: Requirements, specificities and other properties 重组哺乳动物混合功能氧化酶:要求、特性和其他性质
Pharmacology & Therapeutics. Part A: Chemotherapy, Toxicology and Metabolic Inhibitors Pub Date : 1978-01-01 DOI: 10.1016/0362-5478(78)90021-9
A. Y. Lu, S. B. West
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引用次数: 65
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