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N-(羟甲基)三聚氰胺

N-(Hydroxymethyl) melamines.

作者信息

Coley H M

机构信息

CRC Center for Cancer Therapeutics, Institute of Cancer Research, Belmont, Sutton, Surrey, UK.

出版信息

Gen Pharmacol. 1997 Feb;28(2):177-82. doi: 10.1016/s0306-3623(96)00172-3.

Abstract
  1. The N-(hydroxymethyl) melamines are analogs of the antitumor agent hexamethylmelamine (HMM) which do not require bioactivation to exert their antitumor effects. 2. Trimelamol (N2,N4,N6-trihydroxymethyl-N2,N4,N6-trimethylmelamine; TM) was developed as a water-soluble antitumor agent for intravenous administration. 3. Phase I and II trials of TM showed promising activity versus platinum-refractory ovarian cancer, but unfortunately further clinical development was halted due to formulation difficulties. 4. Stable analogs of TM were synthesized in an effort to overcome this shortcoming and these were evaluated in a number of in vitro and in vivo studies. 5. While the stable analogs showed good in vitro cytotoxicity in tumor cell lines, only one analog, CB7646 [bis-N-(hydroxymethyl)trimethylmelamine], showed comparable in vivo antitumor activity to that seen for TM. 6. Both TM and CB7646 were curative in human ovarian and breast cancer xenograft models, including the HX110P ovarian cancer xenograft with acquired resistance to carboplatin. 7. As CB7646 possesses favorable formulation characteristics, relating to its superior stability over that for TM, it is currently being developed for phase I clinical trial. 8. The N-(hydroxymethyl) melamines are capable of overcoming many forms of drug resistance, based on data obtained in in vitro and in vivo studies, and thus show promise as agents in the treatment of heavily pretreated, refractive tumors.
摘要
  1. N-(羟甲基)三聚氰胺是抗肿瘤药物六甲蜜胺(HMM)的类似物,它们无需生物活化即可发挥抗肿瘤作用。2. 曲美仑(N2,N4,N6-三羟甲基-N2,N4,N6-三甲基三聚氰胺;TM)被开发为一种用于静脉给药的水溶性抗肿瘤药物。3. TM的I期和II期试验显示出对铂耐药卵巢癌有良好的活性,但不幸的是,由于制剂困难,进一步的临床开发停止了。4. 为了克服这一缺点,合成了TM的稳定类似物,并在多项体外和体内研究中对其进行了评估。5. 虽然稳定类似物在肿瘤细胞系中显示出良好的体外细胞毒性,但只有一种类似物CB7646 [双-N-(羟甲基)三甲基三聚氰胺] 在体内显示出与TM相当的抗肿瘤活性。6. TM和CB7646在人卵巢癌和乳腺癌异种移植模型中都具有治愈性,包括对卡铂获得性耐药的HX110P卵巢癌异种移植模型。7. 由于CB7646具有良好的制剂特性,与其比TM具有更高的稳定性有关,它目前正在进行I期临床试验开发。8. 根据体外和体内研究获得的数据,N-(羟甲基)三聚氰胺能够克服多种形式的耐药性,因此有望成为治疗经过大量预处理的难治性肿瘤的药物。

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