B10102
苯并[e]芘
98%
别名:
1,2-苯并芘, 4,5-苯并芘
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关于此项目
经验公式（希尔记法）:
C20H12
化学文摘社编号:
分子量:
252.31
UNSPSC Code:
12352103
NACRES:
NA.23
PubChem Substance ID:
EC Number:
205-892-7
Beilstein/REAXYS Number:
1911334
MDL number:
产品名称
苯并[e]芘, 98%
InChI key
TXVHTIQJNYSSKO-UHFFFAOYSA-N
InChI
1S/C20H12/c1-2-8-16-15(7-1)17-9-3-5-13-11-12-14-6-4-10-18(16)20(14)19(13)17/h1-12H
SMILES string
c1ccc2c(c1)c3cccc4ccc5cccc2c5c34
assay
98%
form
crystals
mp
177-180 °C (lit.)
Quality Level
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Application
用于研究苯并[e]芘对DNP-Ficoll和绵羊红细胞的抗体反应的免疫抑制活性 以及从水样中提取有机化合物的“分散液-液微萃取”技术。
General description
这种多环芳烃可溶于丙酮。它是一种非致癌的苯并芘异构体。 研究显示，它在体内和体外暴露后无免疫抑制活性。在自然界中，它被秀丽隐杆线虫菌株代谢为3-苯并[e]芘硫酸盐、1-羟基-3-苯并[e]芘基硫酸盐和苯并[e]芘3-O-β-吡喃葡萄糖苷。
signalword
Danger
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 1B
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
Mohammad Rezaee et al.
Journal of chromatography. A, 1116(1-2), 1-9 (2006-04-01)
A new microextraction technique termed dispersive liquid-liquid microextraction (DLLME) was developed. DLLME is a very simple and rapid method for extraction and preconcentration of organic compounds from water samples. In this method, the appropriate mixture of extraction solvent (8.0 microL
K L White et al.
Cancer research, 44(8), 3388-3393 (1984-08-01)
The role of metabolic activation of benzo(a)pyrene B(a)P in mediating its suppression of humoral immune responsiveness of the female C57BL/6 X C3H F1 (hereafter called B6C3F1) mouse was addressed in these studies. The model was the in vitro antibody response
Saffar Mansoor et al.
Investigative ophthalmology & visual science, 51(5), 2601-2607 (2009-12-05)
To study the inhibitory effects of some agents or drugs (inhibitors) on benzo(e)pyrene (B(e)P)-induced cell death and apoptosis on human retinal pigment epithelial (ARPE-19) cells in vitro. ARPE-19 cells were pretreated with varying concentrations of different classes of inhibitors (calpain
W H Houser et al.
Molecular carcinogenesis, 5(3), 232-237 (1992-01-01)
In the rat, expression of the CYP1A1 gene is closely associated with arylhydrocarbon hydroxylase (AHH) enzyme activity. AHH is an inducile enzyme activity known to play an important role in the bioactivation of polycyclic aromatic hydrocarbons (PAHs) to mutagenic and
D F Lewis et al.
Toxicology letters, 71(3), 235-243 (1994-05-01)
The present studies were undertaken to provide a rationale for the observation that benzo(a)pyrene and 2-acetylaminofluorene induce the hepatic CYP1A1 protein, whereas their non-carcinogenic isomers benzo(e)pyrene and 4-acetylaminofluorene are, at best, relatively very weak inducers. Using amino acid sequence alignment
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