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丙亚胺

丙亚胺用途

Razoxane(ICRF 159)是一种抗血管生成拓扑异构酶II抑制剂,可用于肾细胞癌(RCC)的研究[1]。
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丙亚胺名称

[ CAS 号 ]:
21416-67-1

[ 中文名 ]:
丙亚胺

[ 英文名 ]:
Razoxane

[中文别名 ]:

[英文别名 ]:

丙亚胺生物活性

[ 描述 ]:

Razoxane(ICRF 159)是一种抗血管生成拓扑异构酶II抑制剂,可用于肾细胞癌(RCC)的研究[1]。

[ 相关类别 ]:

研究领域 >> 癌症
信号通路 >> 细胞周期/DNA损伤 >> 拓扑异构酶

[ 靶点 ]

Topoisomerase II


[体外研究]

在大鼠骨肉瘤模型中,Razoxane(30 mg/kg;i.p.)具有抗转移作用。

[体内研究]

早期使用Razoxane治疗(第2天至第14天,每天30毫克/千克)比后期治疗(移植后第14天至第28天,每天30毫克/千克,每天30毫克/千克)对肺转移的抑制作用更强【2】。动物模型:Sprague-Dawley大鼠【2】剂量:30毫克/千克或10毫克/千克/天给药:从肿瘤移植前2天到移植后14天腹腔内(i.p.)结果:导致中位生存时间的剂量依赖性延长(分别为83天或48天,而对照组为38天),但对原发肿瘤的生长没有影响。

[参考文献]

[1]. J P Braybrooke, et al. A phase II study of Razoxane, an antiangiogenic topoisomerase II inhibitor, in renal cell cancer with assessment of potential surrogate markers of angiogenesis. Clin Cancer Res.2000; 6(12):4697-704.

[2]. F Wingen, et al. Antimetastatic effects of Razoxane in a rat osteosarcoma model. Clin Exp Metastasis.Jan-Mar 1987; 5(1):9-16.

丙亚胺物理化学性质

[ 密度 ]:
1.333g/cm3

[ 沸点 ]:
531.5ºC at 760mmHg

[ 熔点 ]:
193ºC

[ 分子式 ]:
C11H16N4O4

[ 分子量 ]:
268.26900

[ 闪点 ]:
275.3ºC

[ 精确质量 ]:
268.11700

[ PSA ]:
98.82000

[ 蒸汽压 ]:
1.33E-13mmHg at 25°C

[ 折射率 ]:
1.534

[ 储存条件 ]:
room temp

[ 水溶解性 ]:
DMSO: soluble40mg/mL

丙亚胺MSDS

丙亚胺毒性和生态

CHEMICAL IDENTIFICATION

RTECS NUMBER :
TL6389900
CHEMICAL NAME :
2,6-Piperazinedione, 4,4'-propylenedi-
CAS REGISTRY NUMBER :
21416-67-1
BEILSTEIN REFERENCE NO. :
0821182
LAST UPDATED :
199612
DATA ITEMS CITED :
15
MOLECULAR FORMULA :
C11-H16-N4-O4
MOLECULAR WEIGHT :
268.31
WISWESSER LINE NOTATION :
T6VMV ENTJ EY1&1- ET6VMV ENTJ

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Human - woman
DOSE/DURATION :
3650 mg/kg/2Y-I
TOXIC EFFECTS :
Kidney, Ureter, Bladder - hematuria Blood - aplastic anemia
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Unreported
SPECIES OBSERVED :
Human - woman
DOSE/DURATION :
600 mg/kg/34W-I
TOXIC EFFECTS :
Blood - leukopenia
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Unreported
SPECIES OBSERVED :
Human - man
DOSE/DURATION :
6467 mg/kg/6Y-I
TOXIC EFFECTS :
Blood - normocytic anemia Blood - thrombocytopenia
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
500 mg/kg
TOXIC EFFECTS :
Tumorigenic - active as anti-cancer agent
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Human - man
DOSE/DURATION :
693 mg/kg/77W-I
TOXIC EFFECTS :
Tumorigenic - Carcinogenic by RTECS criteria Blood - leukemia
TYPE OF TEST :
TD - Toxic dose (other than lowest)
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Human - woman
DOSE/DURATION :
4650 mg/kg/2Y-C
TOXIC EFFECTS :
Tumorigenic - Carcinogenic by RTECS criteria Blood - leukemia
TYPE OF TEST :
TD - Toxic dose (other than lowest)
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Human - man
DOSE/DURATION :
2693 mg/kg/3Y-C
TOXIC EFFECTS :
Tumorigenic - Carcinogenic by RTECS criteria Skin and Appendages - tumors
TYPE OF TEST :
TD - Toxic dose (other than lowest)
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Human - woman
DOSE/DURATION :
3650 mg/kg/2Y-I
TOXIC EFFECTS :
Tumorigenic - Carcinogenic by RTECS criteria Blood - leukemia
TYPE OF TEST :
Micronucleus test

MUTATION DATA

TEST SYSTEM :
Rodent - hamster
DOSE/DURATION :
100 mg/kg
REFERENCE :
BJCAAI British Journal of Cancer. (Macmillan Press Ltd., Houndmills, Basingstoke, Hants. RG21 2XS, UK) V.1- 1947- Volume(issue)/page/year: 52,725,1985
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丙亚胺安全信息

[ 危险品运输编码 ]:
NONH for all modes of transport

[ RTECS号 ]:
TL6389900

丙亚胺文献

Quantitative structure-activity relationship and complex network approach to monoamine oxidase A and B inhibitors.

J. Med. Chem. 51 , 6740-51, (2008)

The work provides a new model for the prediction of the MAO-A and -B inhibitor activity by the use of combined complex networks and QSAR methodologies. On the basis of the obtained model, we prepared ...

Development of a phospholipidosis database and predictive quantitative structure-activity relationship (QSAR) models.

Toxicol. Mech. Methods 18 , 217-27, (2008)

ABSTRACT Drug-induced phospholipidosis (PL) is a condition characterized by the accumulation of phospholipids and drug in lysosomes, and is found in a variety of tissue types. PL is frequently manifes...

Changes in cardiac biomarkers during doxorubicin treatment of pediatric patients with high-risk acute lymphoblastic leukemia: associations with long-term echocardiographic outcomes.

J. Clin. Oncol. 30(10) , 1042-9, (2012)

Doxorubicin causes cardiac injury and cardiomyopathy in children with acute lymphoblastic leukemia (ALL). Measuring biomarkers during therapy might help individualize treatment by immediately identify...


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公司名:上海阿拉丁生化科技股份有限公司

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价格:
¥812.0/5mg ¥3238.0/25mg ¥需询单/1g ¥需询单/1g

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产品详情:[Perfemiker]4,4'-(丙烷-1,2-二基)双(哌嗪-2,6-二酮),≥95%


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