Schein P S, Panasci L, Woolley P V, Anderson T
Cancer Treat Rep. 1976 Jun;60(6):801-5.
Structure-activity studies of nitrosourea pharmacology have resulted in the synthesis of a new water-soluble agent,chlorozotocin, which has significant antitumor activity against the L1210 leukemia system and produces only a minor degree of inhibition of mouse and human bone marrow DNA synthesis compared to BCNU. It is important to emphasize that the bone marrow sparing feature of chlorozotocin is relative and that if the drug is administered at lethal dose levels in mice, myelosuppression is observed. The potential importance of these studies is the identification of a new and active nitrosourea antiumor agent with modified bone marrow toxicity. If aminoglucose modification of nitrosourea bone marrow toxicity can be confirmed in man without significant loss of antitumor activity, the use of such a compound could facilitate treatment of patients with neoplastic disease who have pre-existing abnormal bone marrow function. It would also allow the more effective use of a nitrosourea agent in combination with anticancer agents possessing more potent myelosuppressive properties.
亚硝基脲药理学的构效关系研究已促成一种新型水溶性药物——氯脲霉素的合成,该药物对L1210白血病系统具有显著的抗肿瘤活性,与卡氮芥相比,对小鼠和人类骨髓DNA合成仅产生轻微程度的抑制。必须强调的是,氯脲霉素的骨髓保护特性是相对的,如果在小鼠中以致死剂量给药,会观察到骨髓抑制。这些研究的潜在重要性在于鉴定出一种具有改良骨髓毒性的新型活性亚硝基脲抗肿瘤药物。如果亚硝基脲骨髓毒性的氨基葡萄糖修饰在人体中得到证实,且抗肿瘤活性无显著损失,那么使用这种化合物将有助于治疗已有骨髓功能异常的肿瘤患者。这也将使亚硝基脲类药物能更有效地与具有更强骨髓抑制特性的抗癌药物联合使用。