所有图片(1)
About This Item
经验公式（希尔记法）:
C17H11N
CAS号:
分子量:
229.28
Beilstein:
9262
MDL编号:
UNSPSC代码:
41116107
PubChem化学物质编号:
NACRES:
NA.24
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等级
certified reference material
Agency
BCR®
制造商/商品名称
JRC
技术
HPLC: suitable
gas chromatography (GC): suitable
包装形式
neat
储存温度
2-8°C
SMILES字符串
c1ccc2nc3ccc4ccccc4c3cc2c1
InChI
1S/C17H11N/c1-3-7-14-12(5-1)9-10-17-15(14)11-13-6-2-4-8-16(13)18-17/h1-11H
InChI key
JEGZRTMZYUDVBF-UHFFFAOYSA-N
分析说明
For more information please see:
BCR157
BCR157
法律信息
BCR is a registered trademark of European Commission
警示用语：
Warning
危险声明
危险分类
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
R P Deutsch-Wenzel et al.
Cancer letters, 20(1), 97-101 (1983-08-01)
Using a beeswax/tricaprylin mixture as vehicle, three doses each of acridine, benz[a]acridine (BaAC), benz[c]acridine (BcAC), dibenz[a,h]-acridine (DBa,hAC) and dibenz[a,j]acridine (DBa,jAC) were injected into the lungs of 35 female Osborne-Mendel rats per group. To compare the carcinogenic potency of the heterocycles
Benz[a]acridine.
IARC monographs on the evaluation of the carcinogenic risk of chemicals to humans, 32, 123-127 (1983-12-01)
On the metabolic activation of benz[a]acridine and benz[c]acridine by rat liver and lung microsomes.
J Jacob et al.
Cancer letters, 16(3), 297-306 (1982-09-01)
The metabolism of benz[a]- and benz[c]acridine by liver and lung microsomes from untreated, phenobarbital (PB)-treated and benzo[k]fluoranthene (BkF)-treated rats has been studied by gas chromatography/mass spectrometry (GC/MS). Epoxidation and hydrolysis of the epoxides to dihydrodiols were found to be the
N Motohashi et al.
Anticancer research, 12(1), 135-139 (1992-01-01)
Various synthetic derivatives of phenothiazines, benzo[a]phenothiazines and benz[c]acridines were compared for their abilities to induce antiplasmid activity against E. coli F'lac plasmid. Several phenothiazine derivatives were much more potent in antiplasmid activity than benzo[a]phenothiazine- or benz[c]acridine derivatives. Their antiplasmid activity
G R Southworth et al.
Archives of environmental contamination and toxicology, 10(5), 561-569 (1981-09-01)
The bioconcentration and metabolism of benz(a)acridine in fathead minnows (Pimephales promelas) was investigated using 14C-labelled benz(a)acridine. The rates of uptake, elimination, and metabolic transformation of benz(a)acridine were estimated in the fish. The equilibrium concentration factor [ratio of benz(a)acridine concentration in
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