• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

N-[4-(5-硝基-2-呋喃基)-2-噻唑基]甲酰胺的应用方式对其在雌性NMRI小鼠中致癌表达定位的影响

Influence of the application mode of N-[4-(5-nitro-2-furyl)-2-thiazolyl]-formamide on the localization of its carcinogenic expression in female NMRI-mice.

作者信息

Berger M R, Petru E, Habs M, Schmähl D

出版信息

Cancer Lett. 1986 Jun;31(3):311-8. doi: 10.1016/0304-3835(86)90153-9.

DOI:10.1016/0304-3835(86)90153-9
PMID:3719571
Abstract

The administration of N-[4-(5-nitro-2-furyl)-2-thiazolyl]-formamide FANFT) by gavage to female NMRI-mice resulted in a high incidence of neoplasms of the forestomach. From 117 effective animals which were pooled from 3 dosed groups, 30 squamous cell carcinomas and 26/117 papillomas of the forestomach were diagnosed. Only 5/117 neoplasms of the urinary bladder occurred. The average cumulative dose administered was 1180 mg/mouse, and the mean latent period for the induction of forestomach tumours was 574 days. The mode of application seems to be an important factor in the carcinogenicity of FANFT.

摘要

通过灌胃法给雌性NMRI小鼠施用N-[4-(5-硝基-2-呋喃基)-2-噻唑基]-甲酰胺(FANFT)会导致前胃肿瘤的高发病率。从3个给药组汇总的117只有效动物中,诊断出30例前胃鳞状细胞癌和26/117例前胃乳头状瘤。仅发生了5/117例膀胱肿瘤。平均累积给药剂量为1180毫克/小鼠,前胃肿瘤诱导的平均潜伏期为574天。施用方式似乎是FANFT致癌性的一个重要因素。

相似文献

1
Influence of the application mode of N-[4-(5-nitro-2-furyl)-2-thiazolyl]-formamide on the localization of its carcinogenic expression in female NMRI-mice.N-[4-(5-硝基-2-呋喃基)-2-噻唑基]甲酰胺的应用方式对其在雌性NMRI小鼠中致癌表达定位的影响
Cancer Lett. 1986 Jun;31(3):311-8. doi: 10.1016/0304-3835(86)90153-9.
2
Effect of aspirin on N-[4-(5-nitro-2-furyl)-2-thiazolyl]-formamide-induced epithelial proliferation in the urinary bladder and forestomach of the rat.阿司匹林对N-[4-(5-硝基-2-呋喃基)-2-噻唑基]-甲酰胺诱导大鼠膀胱和前胃上皮细胞增殖的影响。
Cancer Lett. 1984 Jan;21(3):269-75. doi: 10.1016/0304-3835(84)90005-3.
3
Inhibition by aspirin of N-[4-(5-nitro-2-furyl)-2-thiazolyl] formamide-induced bladder carcinogenesis and enhancement of forestomach carcinogenesis.阿司匹林对N-[4-(5-硝基-2-呋喃基)-2-噻唑基]甲酰胺诱导的膀胱癌发生的抑制作用及对前胃癌发生的促进作用。
Carcinogenesis. 1984 Jan;5(1):53-5. doi: 10.1093/carcin/5.1.53.
4
Effect of avitaminosis A and hypervitaminosis A on urinary bladder carcinogenicity of N-(4-(5-Nitro-2-furyl)-2-thiazolyl)formamide.维生素A缺乏症和维生素A过多症对N-(4-(5-硝基-2-呋喃基)-2-噻唑基)甲酰胺膀胱致癌性的影响。
Cancer Res. 1976 Jul;36(7 PT 1):2334-9.
5
Co-carcinogenicity of sodium saccharin and N-[4-(5-nitro-2-furyl)-2-thiazolyl]formamide for the urinary bladder.糖精钠与N-[4-(5-硝基-2-呋喃基)-2-噻唑基]甲酰胺对膀胱的促癌作用
Carcinogenesis. 1983;4(1):97-9. doi: 10.1093/carcin/4.1.97.
6
Effect of p-hydroxyacetanilide, sodium sulfate, and L-methionine on the leukemogenicity of N-[4-(5-nitro-2-furyl)-2-thiazolyl]acetamide.
Cancer Res. 1978 May;38(5):1398-405.
7
Long term dose response study of N-[4-(5-nitro-2-furyl)-2-thiazolyl] formamide-induced urinary bladder carcinogenesis.
Cancer Lett. 1983 Apr;18(3):261-9. doi: 10.1016/0304-3835(83)90234-3.
8
Enhancement by phenothiazine and 2,5-di-O-acetyl-D-glucosaccharo-(1,4)(6,3)-dilactone of bladder carcinogenicity of N-[4-(5-nitro-2-furyl)-2-thiazolyl]-formamide in rats.
Cancer Lett. 1984 Aug;24(1):37-43. doi: 10.1016/0304-3835(84)90077-6.
9
Effect of dose on the induction of urothelial proliferation by N-[4-(5-nitro-2-furyl)-2-thiazolyl]formamide and its relationship to bladder carcinogenesis in the rat.剂量对N-[4-(5-硝基-2-呋喃基)-2-噻唑基]甲酰胺诱导大鼠尿路上皮增生的影响及其与膀胱癌发生的关系。
Carcinogenesis. 1986 Apr;7(4):633-6. doi: 10.1093/carcin/7.4.633.
10
Mutagenicity of urine of various species fed N-[4-(5-nitro-2-furyl)-2-thiazolyl]formamide or 2-amino-4-(5-nitro-2-furyl)thiazole.喂食N-[4-(5-硝基-2-呋喃基)-2-噻唑基]甲酰胺或2-氨基-4-(5-硝基-2-呋喃基)噻唑的不同物种尿液的致突变性
Mutat Res. 1984 Mar;135(3):169-73. doi: 10.1016/0165-1218(84)90117-4.