• 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

新型广谱药物8-氨甲酰基-3-(2-氯乙基)咪唑并[5,1-d]-1,2,3,5-四嗪-4(3H)-酮(米托唑胺)对小鼠肿瘤模型系统的实验性抗肿瘤活性。

Experimental antitumor activity against murine tumor model systems of 8-carbamoyl-3-(2-chloroethyl)imidazo[5,1-d]-1,2,3,5-tetrazin-4(3 H)-one (mitozolomide), a novel broad-spectrum agent.

作者信息

Hickman J A, Stevens M F, Gibson N W, Langdon S P, Fizames C, Lavelle F, Atassi G, Lunt E, Tilson R M

出版信息

Cancer Res. 1985 Jul;45(7):3008-13.

PMID:4005840
Abstract

8-Carbamoyl-3-(2-chloroethyl)imidazo[5,1-d]-1,2,3,5-tetrazin-4(3H) -one (mitozolomide) demonstrates curative action against a range of murine tumor model systems. At single doses of between 20 and 40 mg/kg, the latter of which approximates the 10% lethal dose value in mice, the compound elicited cures against the L1210 and P388 leukemias irrespective of the route of tumor and/or drug administration; in these tests, animals receiving 10(5) cells i.p. survived greater than 60 days after treatment. Potent effects were also observed against the TLX5 lymphoma (s.c.) and B16 melanoma (i.p.). In other experiments, 7 of 10 animals implanted with 2 X 10(5) Lewis lung carcinoma cells survived greater than 60 days while 10 of 10 animals survived greater than 60 days after implantation of the Colon 26 tumor. Potent inhibition of the solid tumor models was also observed with complete cures of the Colon 38, M5076 sarcoma, and ADJ/PC6A plasmacytoma. In cross-resistance studies, the compound was ineffective against an L1210 leukemia made resistant to 1,3-bis(2-chloroethyl)-1-nitrosourea and against a TLX5 lymphoma resistant to dimethyltriazenes but cured animals bearing the L1210 leukemia with derived resistance to cyclophosphamide.

摘要

8-氨甲酰基-3-(2-氯乙基)咪唑并[5,1-d]-1,2,3,5-四嗪-4(3H)-酮(米托唑胺)对一系列小鼠肿瘤模型系统显示出治愈作用。在20至40毫克/千克的单剂量下,后者接近小鼠的10%致死剂量值,该化合物无论肿瘤接种途径和/或给药途径如何,都能治愈L1210和P388白血病;在这些试验中,腹腔注射10(5)个细胞的动物在治疗后存活超过60天。对TLX5淋巴瘤(皮下接种)和B16黑色素瘤(腹腔注射)也观察到了强效作用。在其他实验中,接种2×10(5)个刘易斯肺癌细胞的10只动物中有7只存活超过60天,而接种结肠26肿瘤的10只动物全部存活超过60天。对实体瘤模型也观察到了强效抑制作用,结肠38、M5076肉瘤和ADJ/PC6A浆细胞瘤完全治愈。在交叉耐药性研究中,该化合物对一株对1,3-双(2-氯乙基)-1-亚硝基脲耐药的L1210白血病和一株对二甲基三嗪耐药的TLX5淋巴瘤无效,但能治愈对环磷酰胺产生衍生耐药性的L1210白血病动物。

相似文献

1
Experimental antitumor activity against murine tumor model systems of 8-carbamoyl-3-(2-chloroethyl)imidazo[5,1-d]-1,2,3,5-tetrazin-4(3 H)-one (mitozolomide), a novel broad-spectrum agent.新型广谱药物8-氨甲酰基-3-(2-氯乙基)咪唑并[5,1-d]-1,2,3,5-四嗪-4(3H)-酮(米托唑胺)对小鼠肿瘤模型系统的实验性抗肿瘤活性。
Cancer Res. 1985 Jul;45(7):3008-13.
2
Antitumor activity of 2-chloroethyl (methylsulfonyl)methanesulfonate (clomesone, NSC 33847) against selected tumor systems in mice.
Cancer Res. 1989 Mar 1;49(5):1182-6.
3
Antitumor activity and pharmacokinetics in mice of 8-carbamoyl-3-methyl-imidazo[5,1-d]-1,2,3,5-tetrazin-4(3H)-one (CCRG 81045; M & B 39831), a novel drug with potential as an alternative to dacarbazine.8-氨基甲酰基-3-甲基-咪唑并[5,1-d]-1,2,3,5-四嗪-4(3H)-酮(CCRG 81045;M&B 39831)是一种有望替代达卡巴嗪的新型药物,对小鼠的抗肿瘤活性及药代动力学研究
Cancer Res. 1987 Nov 15;47(22):5846-52.
4
1,2-Bis(methylsulfonyl)-1-(2-chloroethyl)-2-(methylamino)carbonylhydrazine (101M): a novel sulfonylhydrazine prodrug with broad-spectrum antineoplastic activity.1,2-双(甲基磺酰基)-1-(2-氯乙基)-2-(甲基氨基)甲酰肼(101M):一种具有广谱抗肿瘤活性的新型磺酰肼前药。
Cancer Res. 2001 Apr 1;61(7):3033-8.
5
Antitumor activity of a novel antitumor antibiotic, quinocarmycin citrate (KW2152).新型抗肿瘤抗生素柠檬酸醌霉素(KW2152)的抗肿瘤活性
Cancer Res. 1987 Mar 15;47(6):1516-22.
6
Preclinical antitumor activity of bizelesin in mice.比泽司亭在小鼠体内的临床前抗肿瘤活性。
Clin Cancer Res. 1996 Jul;2(7):1143-9.
7
Activity of a novel anthracenyl bishydrazone, 9,10-anthracenedicarboxyaldehyde Bis[(4,5-dihydro-1H-imidazol-2-yl)hydrazone] dihydrochloride, against experimental tumors in mice.新型蒽基双腙9,10-蒽二甲醛双[(4,5-二氢-1H-咪唑-2-基)腙]二盐酸盐对小鼠实验性肿瘤的活性
Cancer Res. 1982 Feb;42(2):440-4.
8
A fluorine-containing anthracycline (ME2303) as a new antitumor agent against murine and human tumors and their multidrug-resistant sublines.一种含氟蒽环类药物(ME2303)作为一种针对小鼠和人类肿瘤及其多药耐药亚系的新型抗肿瘤药物。
Cancer Res. 1989 Oct 15;49(20):5537-42.
9
Activity of mitozolomide (NSC 353451), a new imidazotetrazine, against xenografts from human melanomas, sarcomas, and lung and colon carcinomas.新型咪唑并四嗪米托唑胺(NSC 353451)对人黑色素瘤、肉瘤以及肺癌和结肠癌异种移植瘤的活性。
Cancer Res. 1985 Apr;45(4):1778-86.
10
Activity of a novel anthracenedione, 1,4-dihydroxy-5,8-bis(((2-[(2-hydroxyethyl)amino]ethyl)amino])-9,10-anthracenedione dihydrochloride, against experimental tumors in mice.一种新型蒽二酮,1,4 - 二羟基 - 5,8 - 双(((2 - [(2 - 羟乙基)氨基]乙基)氨基)) - 9,10 - 蒽二酮二盐酸盐对小鼠实验性肿瘤的活性。
Cancer Res. 1979 May;39(5):1570-4.

引用本文的文献

1
Antitumour imidazotetrazines: past, present… and future?抗肿瘤咪唑并四嗪类药物:过去、现在……以及未来?
RSC Chem Biol. 2023 Aug 29;4(10):736-741. doi: 10.1039/d3cb00076a. eCollection 2023 Oct 4.
2
Novel Imidazotetrazine Evades Known Resistance Mechanisms and Is Effective against Temozolomide-Resistant Brain Cancer in Cell Culture.新型咪唑并四嗪可规避已知耐药机制,并在细胞培养中对替莫唑胺耐药脑肿瘤有效。
ACS Chem Biol. 2022 Feb 18;17(2):299-313. doi: 10.1021/acschembio.2c00022. Epub 2022 Feb 4.
3
A novel mouse model of rectal cancer established by orthotopic implantation of colon cancer cells.
一种通过原位植入结肠癌细胞建立的新型直肠癌小鼠模型。
Cancer Sci. 2004 Jun;95(6):514-9. doi: 10.1111/j.1349-7006.2004.tb03242.x.
4
Marked inactivation of O6-alkylguanine-DNA alkyltransferase activity with protracted temozolomide schedules.使用延长的替莫唑胺给药方案可显著使O6-烷基鸟嘌呤-DNA烷基转移酶活性失活。
Br J Cancer. 2003 Apr 7;88(7):1004-11. doi: 10.1038/sj.bjc.6600827.
5
Mitozolomide activity on human cancer cells in vitro.米托唑胺对人癌细胞的体外活性。
Br J Cancer. 1986 Dec;54(6):925-32. doi: 10.1038/bjc.1986.263.
6
Activity and distribution studies of etoposide and mitozolomide in vivo and in vitro against human choriocarcinoma cell lines.
Cancer Chemother Pharmacol. 1987;19(3):221-5. doi: 10.1007/BF00252976.
7
Mitozolomide (NSC 353451), a new active drug in the treatment of malignant melanoma. Phase II trial in patients with advanced disease.米托唑胺(NSC 353451),一种治疗恶性黑色素瘤的新型活性药物。晚期疾病患者的II期试验。
Br J Cancer. 1987 Apr;55(4):433-5. doi: 10.1038/bjc.1987.85.
8
Phase II evaluation of mitozolomide in ovarian cancer.卵巢癌中米托蒽醌的II期评估。 (注:原文中mitozolomide应为mitoxantrone,即米托蒽醌 )
Br J Cancer. 1988 Jan;57(1):113-4. doi: 10.1038/bjc.1988.21.
9
Mitozolomide-induced sensitisation of mammalian cells in vitro to radiation.米托唑胺体外诱导哺乳动物细胞对辐射的敏感性。
Br J Cancer. 1989 Aug;60(2):182-4. doi: 10.1038/bjc.1989.247.
10
Inhibition of cellular esterases by the antitumour imidazotetrazines mitozolomide and temozolomide: demonstration by flow cytometry and conventional spectrofluorimetry.抗肿瘤咪唑并四嗪类药物米托唑胺和替莫唑胺对细胞酯酶的抑制作用:流式细胞术和传统荧光分光光度法的证明
Cancer Chemother Pharmacol. 1989;25(3):149-55. doi: 10.1007/BF00689574.