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1
Sixth plot of the carcinogenic potency database: results of animal bioassays published in the General Literature 1989 to 1990 and by the National Toxicology Program 1990 to 1993.致癌性数据库的第六部分:1989年至1990年发表在普通文献以及1990年至1993年由国家毒理学计划发布的动物生物测定结果。
Environ Health Perspect. 1995 Nov;103 Suppl 8(Suppl 8):3-122. doi: 10.1289/ehp.95103s83.
2
Supplement to the Carcinogenic Potency Database (CPDB): results of animal bioassays published in the general literature in 1993 to 1994 and by the National Toxicology Program in 1995 to 1996.《致癌潜能数据库(CPDB)补编》:1993年至1994年发表于一般文献以及1995年至1996年由美国国家毒理学计划发布的动物生物测定结果。
Environ Health Perspect. 1999 Aug;107 Suppl 4(Suppl 4):527-600. doi: 10.1289/ehp.99107s4527.
3
The fifth plot of the Carcinogenic Potency Database: results of animal bioassays published in the general literature through 1988 and by the National Toxicology Program through 1989.致癌强度数据库的第五部分:1988年之前发表在普通文献以及1989年之前由国家毒理学计划发表的动物生物测定结果。
Environ Health Perspect. 1993 Apr;100:65-168. doi: 10.1289/ehp.9310065.
4
Third chronological supplement to the carcinogenic potency database: standardized results of animal bioassays published through December 1986 and by the National Toxicology Program through June 1987.致癌物致癌强度数据库的第三次按时间顺序排列的补充:截至1986年12月以及截至1987年6月由国家毒理学计划公布的动物生物测定标准化结果。
Environ Health Perspect. 1990 Mar;84:215-86. doi: 10.1289/ehp.9084215.
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The Carcinogenic Potency Database: analyses of 4000 chronic animal cancer experiments published in the general literature and by the U.S. National Cancer Institute/National Toxicology Program.致癌强度数据库:对发表于普通文献以及美国国立癌症研究所/国家毒理学计划的4000项慢性动物癌症实验的分析。
Environ Health Perspect. 1991 Dec;96:11-5. doi: 10.1289/ehp.919611.
6
Second chronological supplement to the Carcinogenic Potency Database: standardized results of animal bioassays published through December 1984 and by the National Toxicology Program through May 1986.《致癌物强度数据库》的第二次按时间顺序排列的补充资料:截至1984年12月以及截至1986年5月由国家毒理学计划公布的动物生物测定标准化结果。
Environ Health Perspect. 1987 Oct;74:237-329. doi: 10.1289/ehp.8774237.
7
Chronological supplement to the Carcinogenic Potency Database: standardized results of animal bioassays published through December 1982.《致癌潜能数据库的时间顺序补充:截至1982年12月发表的动物生物测定标准化结果》
Environ Health Perspect. 1986 Aug;67:161-200. doi: 10.1289/ehp.8667161.
8
Supplement to the Carcinogenic Potency Database (CPDB): results of animal bioassays published in the general literature through 1997 and by the National Toxicology Program in 1997-1998.《致癌潜能数据库(CPDB)补编》:截至1997年发表于一般文献以及1997 - 1998年由美国国家毒理学计划发表的动物生物测定结果。
Toxicol Sci. 2005 Jun;85(2):747-808. doi: 10.1093/toxsci/kfi161. Epub 2005 Mar 30.
9
Compendium of chemical carcinogens by target organ: results of chronic bioassays in rats, mice, hamsters, dogs, and monkeys.按靶器官分类的化学致癌物简编:大鼠、小鼠、仓鼠、狗和猴子的慢性生物测定结果
Toxicol Pathol. 2001 Nov-Dec;29(6):639-52. doi: 10.1080/019262301753385979.
10
A carcinogenic potency database of the standardized results of animal bioassays.一个关于动物生物测定标准化结果的致癌效力数据库。
Environ Health Perspect. 1984 Dec;58:9-319. doi: 10.1289/ehp.84589.

引用本文的文献

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Supplement to the Carcinogenic Potency Database (CPDB): results of animal bioassays published in the general literature in 1993 to 1994 and by the National Toxicology Program in 1995 to 1996.《致癌潜能数据库(CPDB)补编》:1993年至1994年发表于一般文献以及1995年至1996年由美国国家毒理学计划发布的动物生物测定结果。
Environ Health Perspect. 1999 Aug;107 Suppl 4(Suppl 4):527-600. doi: 10.1289/ehp.99107s4527.
3
Allergic contact sensitizing chemicals as environmental carcinogens.作为环境致癌物的变应性接触致敏化学物质。
Environ Health Perspect. 1997 Sep;105(9):940-8. doi: 10.1289/ehp.97105940.
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Prediction of the rodent carcinogenicity of organic compounds from their chemical structures using the FALS method.使用FALS方法从有机化合物的化学结构预测其对啮齿动物的致癌性。
Environ Health Perspect. 1996 Oct;104 Suppl 5(Suppl 5):1051-8. doi: 10.1289/ehp.96104s51051.

本文引用的文献

1
Carcinogenicity of catechol in F344 rats and B6C3F1 mice.儿茶酚对F344大鼠和B6C3F1小鼠的致癌性。
Carcinogenesis. 1993 Mar;14(3):525-9. doi: 10.1093/carcin/14.3.525.
2
The rat urinary bladder as a new target of heterocyclic amine carcinogenicity: tumor induction by 3-amino-1-methyl-5H-pyrido[4,3-b]indole acetate.大鼠膀胱作为杂环胺致癌作用的新靶点:3-氨基-1-甲基-5H-吡啶并[4,3-b]吲哚乙酸诱导肿瘤
Jpn J Cancer Res. 1993 Aug;84(8):852-8. doi: 10.1111/j.1349-7006.1993.tb02057.x.
3
The fifth plot of the Carcinogenic Potency Database: results of animal bioassays published in the general literature through 1988 and by the National Toxicology Program through 1989.致癌强度数据库的第五部分:1988年之前发表在普通文献以及1989年之前由国家毒理学计划发表的动物生物测定结果。
Environ Health Perspect. 1993 Apr;100:65-168. doi: 10.1289/ehp.9310065.
4
How tautological are interspecies correlations of carcinogenic potencies?致癌效力的种间相关性有多赘述?
Risk Anal. 1993 Jun;13(3):265-72. doi: 10.1111/j.1539-6924.1993.tb01078.x.
5
Dose-dependence of 2-amino-1-methyl-6-phenylimidazo[4,5-b]-pyridine (PhIP) carcinogenicity in rats.2-氨基-1-甲基-6-苯基咪唑并[4,5-b]吡啶(PhIP)对大鼠致癌性的剂量依赖性。
Carcinogenesis. 1993 Dec;14(12):2553-7. doi: 10.1093/carcin/14.12.2553.
6
The importance of data on mechanism of carcinogenesis in efforts to predict low-dose human risk.致癌机制数据在预测低剂量人体风险的努力中的重要性。
Risk Anal. 1993 Aug;13(4):399-401. doi: 10.1111/j.1539-6924.1993.tb00739.x.
7
Heterocyclic amines formed by cooking food: comparison of bioassay results with other chemicals in the Carcinogenic Potency Database.烹饪食物形成的杂环胺:生物测定结果与致癌潜能数据库中其他化学物质的比较。
Cancer Lett. 1994 Aug 15;83(1-2):21-9. doi: 10.1016/0304-3835(94)90294-1.
8
Tumor incidence in a chemical carcinogenesis study of nonhuman primates.非人灵长类动物化学致癌研究中的肿瘤发生率。
Regul Toxicol Pharmacol. 1994 Apr;19(2):130-51. doi: 10.1006/rtph.1994.1013.
9
Induction of hepatocellular carcinoma in nonhuman primates by the food mutagen 2-amino-3-methylimidazo[4,5-f]quinoline.食物诱变剂2-氨基-3-甲基咪唑[4,5-f]喹啉诱导非人类灵长类动物发生肝细胞癌
Environ Health Perspect. 1994 Feb;102(2):190-3. doi: 10.1289/ehp.94102190.
10
DNA lesions, inducible DNA repair, and cell division: three key factors in mutagenesis and carcinogenesis.DNA损伤、诱导性DNA修复与细胞分裂:诱变与致癌作用中的三个关键因素。
Environ Health Perspect. 1993 Dec;101 Suppl 5(Suppl 5):35-44. doi: 10.1289/ehp.93101s535.

致癌性数据库的第六部分:1989年至1990年发表在普通文献以及1990年至1993年由国家毒理学计划发布的动物生物测定结果。

Sixth plot of the carcinogenic potency database: results of animal bioassays published in the General Literature 1989 to 1990 and by the National Toxicology Program 1990 to 1993.

作者信息

Gold L S, Manley N B, Slone T H, Garfinkel G B, Ames B N, Rohrbach L, Stern B R, Chow K

机构信息

Life Sciences Division, Lawrence Berkeley Laboratory, California, USA.

出版信息

Environ Health Perspect. 1995 Nov;103 Suppl 8(Suppl 8):3-122. doi: 10.1289/ehp.95103s83.

DOI:10.1289/ehp.95103s83
PMID:8741772
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1518980/
Abstract

This paper presents two types of information from the Carcinogenic Potency Database (CPDB): (a) the sixth chronological plot of analyses of long-term carcinogenesis bioassays, and (b) an index to chemicals in all six plots, including a summary compendium of positivity and potency for each chemical (Appendix 14). The five earlier plots of the CPDB have appeared in this journal, beginning in 1984 (1-5). Including the plot in this paper, the CPDB reports results of 5002 experiments on 1230 chemicals. This paper includes bioassay results published in the general literature between January 1989 and December 1990, and in Technical Reports of the National Toxicology Program between January 1990 and June 1993. Analyses are included on 17 chemicals tested in nonhuman primates by the Laboratory of Chemical Pharmacology, National Cancer Institute. This plot presents results of 531 long-term, chronic experiments of 182 test compounds and includes the same information about each experiment in the same plot format as the earlier papers: the species and strain of test animal, the route and duration of compound administration, dose level and other aspects of experimental protocol, histopathology and tumor incidence, TD50 (carcinogenic potency) and its statistical significance, dose response, author's opinion about carcinogenicity, and literature citation. We refer the reader to the 1984 publications (1,6,7) for a detailed guide to the plot of the database, a complete description of the numerical index of carcinogenic potency, and a discussion of the sources of data, the rationale for the inclusion of particular experiments and particular target sites, and the conventions adopted in summarizing the literature. The six plots of the CPDB are to be used together since results of individual experiments that were published earlier are not repeated. Appendix 14 is designed to facilitate access to results on all chemicals. References to the published papers that are the source of experimental data are reported in each of the published plots. For readers using the CPDB extensively, a combined plot is available of all results from the six separate plot papers, ordered alphabetically by chemical; the combined plot in printed form or on computer tape or diskette is available from the first author. A SAS database is also available.

摘要

本文展示了来自致癌强度数据库(CPDB)的两类信息:(a)长期致癌生物测定分析的第六个按时间顺序排列的图表,以及(b)所有六个图表中化学物质的索引,包括每种化学物质的阳性和强度汇总简编(附录14)。CPDB的前五个图表已发表在本期刊上,始于1984年(1 - 5)。包括本文中的图表在内,CPDB报告了对1230种化学物质进行的5002项实验结果。本文包括1989年1月至1990年12月期间发表在一般文献以及1990年1月至1993年6月期间发表在美国国家毒理学计划技术报告中的生物测定结果。分析包括美国国立癌症研究所化学药理学实验室在非人灵长类动物中测试的17种化学物质。此图表展示了182种受试化合物的531项长期慢性实验结果,并以与早期论文相同的图表格式包含了每个实验的相同信息:受试动物的物种和品系、化合物给药途径和持续时间、剂量水平及实验方案的其他方面、组织病理学和肿瘤发生率、TD50(致癌强度)及其统计学意义、剂量反应、作者对致癌性的看法以及文献引用。我们请读者参考1984年的出版物(1,6,7),以获取关于数据库图表的详细指南、致癌强度数值索引的完整描述,以及关于数据来源、纳入特定实验和特定靶位点的基本原理,和总结文献时采用的惯例的讨论。CPDB的六个图表应一起使用,因为早期发表的单个实验结果不再重复。附录14旨在便于获取所有化学物质的结果。在每个已发表的图表中都报告了作为实验数据来源的已发表论文的参考文献。对于广泛使用CPDB的读者,可提供一份按化学物质字母顺序排列的来自六篇单独图表论文的所有结果的综合图表;印刷版或计算机磁带或软盘形式的综合图表可从第一作者处获取。也可提供一个SAS数据库。