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:
154999
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
c1ccc2nc3c(ccc4ccccc34)cc2c1
InChI
1S/C17H11N/c1-3-7-15-12(5-1)9-10-14-11-13-6-2-4-8-16(13)18-17(14)15/h1-11H
InChI key
OAPPEBNXKAKQGS-UHFFFAOYSA-N
分析说明
For more information please see:
BCR158
BCR158
法律信息
BCR is a registered trademark of European Commission
警示用语：
Danger
危险声明
危险分类
Acute Tox. 4 Oral - Eye Dam. 1
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
T Kurihara et al.
Anticancer research, 18(1A), 429-432 (1998-05-06)
On the calculated pi-spin density (rho pi) of benz[c]acridines [1-12], benz[c]acridines [2,8-12] with alternately value of pi-spin density (rho pi) on angular ring, large negative pi-spin density at C-1 and C-3 positions and large positive pi-spin density at C-2 and
T Kurihara et al.
Anticancer research, 16(5A), 2757-2765 (1996-09-01)
In order to clarify the effects of methyl substitution on the carcinogenic activity, each resonance energy (RE) of benz[c]acridines, benzo[a]phenothiazines, chrysene, and their methyl derivatives was calculated by Aihara's TRE theory. Some correlations seem to exist between the values of
M Tanaka et al.
Anticancer research, 16(5A), 2837-2841 (1996-09-01)
The mutagenicity of eleven methylbenz[c]acridines (methyl-B[c]ACRs) was examined by the direct Ames' Salmonella mutagenicity assay on the standard tester strains of TA97a, TA98, TA100 and TA102, each of which is specific to a certain type of mutation. The Benz[c]acridines (B[c]ACRs)
K Kamata et al.
Anticancer research, 9(3), 579-582 (1989-05-01)
Raman spectra of methyl substituted benz[c]acridines (BAc) in the solid state were recorded. Their assignments were proposed for the frequencies of Raman spectra observed. The purpose of this work was to elucidate the mechanisms of interaction between BAc and DNA
H Sakagami et al.
Anticancer research, 15(6B), 2533-2540 (1995-11-01)
A series of phenothiazine, benzo[a]phenothiazine and benz[c]acridine derivatives were compared for their ability to induce nucleosome-sized DNA fragmentation (a biochemical hallmark of apoptosis), using agarose gel electrophoresis and a fluorescence activated cell sorter. Significant DNA fragmentation-inducing activity was detected in
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