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54824-17-8生产厂家

54824-17-8价格

54824-17-8

54824-17-8结构式
54824-17-8结构式

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中文名 米托萘胺
英文名 2-[2-(dimethylamino)ethyl]-5-nitrobenzo[de]isoquinoline-1,3-dione
英文别名 2-(2-(dimethylamino)ethyl)-3-nitro-1H-benzo[de]isoquinoline-1,3(2H)-dione
Mitonafidum [INN-Latin]
Mitonafida [INN-Spanish]
M 4212 (Pharmaceutical)
2-(2-(dimethylamino) ethyl)-5-nitro-1H-benzo[de]isoquinoline-1,3(2H)-dione
N-(2-(Dimethylamino)ethyl)-3-nitronaphthalimide
M-4212
2-(2-dimethylaminoethyl)-5-nitrobenzo[de]isoquinoline-1,3-dione
Mitonafide
描述 米托那非(NSC 300288)是一种细胞抑制剂。米托那非通过插层与双链DNA结合,并抑制DNA和RNA合成。米托那非是一种抗肿瘤药物,可用于癌症研究,如非小细胞肺癌(NSCLC)、白血病[1][2][3]。
相关类别
靶点

DNA and RNA synthesis[1]

体外研究 米托那非抑制DNA和RNA合成,并诱导中国仓鼠卵巢细胞DNA单链断裂[1]。在厌氧条件下,米托那非与大鼠肝微粒体和NADPH孵育会形成一种被鉴定为5-氨基米托那菲的代谢产物[2]。米托那非(25,50μM,1小时)诱导L1210细胞DNA的单链断裂[2]。米托那非(10-100μM)在HOP-62肺细胞系中显示出细胞毒性作用[4]。细胞活力测定[6]细胞系:SK-OV-3、HepG2、A-549、T-24、SMMC-7721、HL-7702浓度分别为0-100μM。培养时间:48小时结果:抑制细胞活力,IC50值为6.26、10.88、7.94、5.01、6.94、8.51μM。
体内研究 米托那非(0.5和1 mg/kg,腹腔注射,1-7天)在携带S-180的小鼠中显示出抗肿瘤效力[4]。米托那非(5 mg/kg,腹腔注射,每天两次)在HepG2异种移植模型中显示出抗癌活性[6]。米托那非(单次腹腔注射,携带S-180的小鼠)的LD50值为10.0 mg/kg[5]。动物模型:携带S-180的小鼠[4]剂量:0.5 mg/kg和1 mg/kg给药:腹膜内注射(i.p.)1-7天结果:中位生存时间增加。动物模型:HepG2异种移植模型[6]剂量:5 mg/kg给药:腹腔注射(i.p.),每天两次。结果:肿瘤相对增加率(T/C)值为28.8%。
参考文献

[1]. Llombart M, et al. Phase I study of mitonafide in solid tumors. Invest New Drugs. 1992 Aug;10(3):177-81.  

[2]. inha BK, et al. Mechanism of DNA strand breaks by mitonafide, an imide derivative of 3-nitro-1,8-naphthalic acid. Biochem Pharmacol. 1985 Nov 1;34(21):3845-52.  

[3]. Rosell R, et al. Phase I study of mitonafide in 120 hour continuous infusion in non-small cell lung cancer. Invest New Drugs. 1992 Aug;10(3):171-5.  

[4]. Samanta S, et al. Antitumor activity of Nitronaphthal-NU, a novel mixed-function agent. J Exp Ther Oncol. 2005;5(1):15-22.  

[5]. Pain A, et al. Evaluation of naphthalmustine, a nitrogen mustard derivative of naphthalimide as a rationally-designed anticancer agent. J Exp Clin Cancer Res. 2003 Sep;22(3):411-8.  

[6]. Xin M, et al. Design, synthesis and biological evaluation of 3-nitro-1,8-naphthalimides as potential antitumor agents. Bioorg Med Chem Lett. 2020 Apr 15;30(8):127051.  

密度 1.384g/cm3
沸点 496.8ºC at 760 mmHg
分子式 C16H15N3O4
分子量 313.30800
闪点 254.3ºC
精确质量 313.10600
PSA 88.13000
LogP 1.94570
折射率 1.667
储存条件 2-8°C

CHEMICAL IDENTIFICATION

RTECS NUMBER :
QK5650000
CHEMICAL NAME :
Naphthalimide, 2-(2-(dimethylamino)ethyl)-5-nitro-
CAS REGISTRY NUMBER :
54824-17-8
LAST UPDATED :
199612
DATA ITEMS CITED :
6
MOLECULAR FORMULA :
C16-H15-N3-O4
MOLECULAR WEIGHT :
313.34
WISWESSER LINE NOTATION :
T666 1A M CVNVJ D2N1&1 HNW

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
6500 ug/kg
TOXIC EFFECTS :
Tumorigenic - active as anti-cancer agent
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
10000 ug/kg
TOXIC EFFECTS :
Tumorigenic - active as anti-cancer agent

MUTATION DATA

TYPE OF TEST :
Mutation test systems - not otherwise specified
TEST SYSTEM :
Rodent - mouse Ascites tumor
DOSE/DURATION :
4 mg/L
REFERENCE :
CCPHDZ Cancer Chemotherapy and Pharmacology. (Springer-Verlag New York, Inc., Service Center, 44 Hartz Way, Secaucus, NJ 07094) V.1- 1978- Volume(issue)/page/year: 4,61,1980

海关编码 2933990090
上游产品  2

下游产品  3

海关编码 2933990090
中文概述 2933990090. 其他仅含氮杂原子的杂环化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0%
申报要素 品名, 成分含量, 用途, 乌洛托品请注明外观, 6-己内酰胺请注明外观, 签约日期
Summary 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%