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新型吲哚咔唑化合物6-N-甲酰氨基-12,13-二氢-1,11-二羟基-13-(β-D-吡喃葡萄糖基)-5H-吲哚并[2,3-a]吡咯并[3,4-c]咔唑-5,7(6H)-二酮(NB-506):其在小鼠体内的强效抗肿瘤活性

Novel indolocarbazole compound 6-N-formylamino-12,13-dihydro-1,11-dihydroxy- 13-(beta-D-glucopyranosyl)-5H-indolo[2,3-a]pyrrolo-[3,4-c]carbazole- 5,7(6H)-dione (NB-506): its potent antitumor activities in mice.

作者信息

Arakawa H, Iguchi T, Morita M, Yoshinari T, Kojiri K, Suda H, Okura A, Nishimura S

机构信息

Banyu Tsukuba Research Institute, Tsukuba, Japan.

出版信息

Cancer Res. 1995 Mar 15;55(6):1316-20.

PMID:7882329
Abstract

NB-506 [6-N-formylamino-12,13-dihydro-1,11-dihydroxy-13-(beta-D- glucopyranosyl)-5H-indolo[2,3-a]pyrrolo[3,4-c]carbazole-5,7(6H)-di one d is a new antitumor indolocarbazole compound. The growths of murine M5076 and Ehrlich solid tumors were inhibited 76 and 96%, respectively, by i.v. injection at doses of 300 mg/m2. Furthermore, NB-506 caused regression of nodules of human PC-13 lung cancer and MKN-45 stomach cancer cells at i.v. doses of 90 mg/m2. Human HCT 116 and LS 180 colon cancers also regressed with injections of NB-506. Repeated injections of NB-506 had a stronger antitumor effect than intermittent injections in mice with MKN-45. The cumulative toxicity of NB-506 was low in terms of lethality in mice, i.e., the LD50s on single and 10 repeated i.v. injections into CDF1 mice were 990 and 810 mg/m2/injection, respectively. In conclusion, NB-506 is considered to be an interesting possible candidate as an anticancer drug for treatment of solid tumors in humans.

摘要

NB - 506[6 - N - 甲酰氨基 - 12,13 - 二氢 - 1,11 - 二羟基 - 13 - (β - D - 吡喃葡萄糖基) - 5H - 吲哚并[2,3 - a]吡咯并[3,4 - c]咔唑 - 5,7(6H) - 二酮]是一种新型抗肿瘤吲哚咔唑化合物。静脉注射剂量为300mg/m²时,对小鼠M5076和艾氏实体瘤生长的抑制率分别为76%和96%。此外,静脉注射剂量为90mg/m²时,NB - 506可使人类PC - 13肺癌和MKN - 45胃癌细胞的结节消退。注射NB - 506后,人类HCT 116和LS 180结肠癌也出现消退。在携带MKN - 45的小鼠中,重复注射NB - 506比间歇注射具有更强的抗肿瘤作用。就小鼠致死率而言,NB - 506的累积毒性较低,即对CDF1小鼠单次和10次重复静脉注射的半数致死量分别为990和810mg/m²/注射。总之,NB - 506被认为是一种有潜力的用于治疗人类实体瘤的抗癌药物候选物。

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