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357774

Sigma-Aldrich

1-苯基咪唑

97%

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About This Item

經驗公式（希爾表示法）:
C9H8N2
CAS號碼:
7164-98-9
分子量：:
144.17
MDL號碼:
MFCD00041204
分類程式碼代碼:
12352005
PubChem物質ID:
24861941
NACRES:
NA.22

化驗

97%

形狀

liquid

bp

142 °C/15 mmHg (lit.)

mp

13 °C (lit.)

密度

1.14 g/mL at 25 °C (lit.)

SMILES 字串

c1ccc(cc1)-n2ccnc2

InChI

1S/C9H8N2/c1-2-4-9(5-3-1)11-7-6-10-8-11/h1-8H

InChI 密鑰

SEULWJSKCVACTH-UHFFFAOYSA-N

相關類別

一般說明

1-苯基咪唑是咪唑衍生物。它在虹鳟鱼（虹鳟鱼）肝细胞中诱导 7-乙氧基试卤灵-O-脱乙基酶（EROD）活化。1-苯咪唑的 S（1）→S（0）跃迁已通过共振双光子电离在超声气流膨胀中进行了研究。据报道，1-苯基咪唑是牛脑和 Ghs 垂体细胞钙调蛋白依赖性一氧化氮合酶的抑制剂。

應用

1-苯基咪唑是一种研究其对牛脑一氧化氮合酶对瓜氨酸形成的影响的合适试剂。

象形圖

Exclamation mark
GHS07

訊號詞

Warning

危險分類

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

10 - Combustible liquids

水污染物質分類（WGK）

WGK 3

閃點（°F）

235.4 °F - closed cup

閃點（°C）

113 °C - closed cup

個人防護裝備

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

分析證明 (COA)

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M R Anari et al.
Chemical research in toxicology, 9(6), 924-931 (1996-09-01)
Organic hydroperoxides are believed to be primarily detoxified in cells by the GSH peroxidase/GSSG reductase system and activated to cytotoxic radical species by non-heme iron. However, organic hydroperoxides seem to be bioactivated by cytochrome P450 (P450) in isolated hepatocytes as
A J Green et al.
Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry, 6(5-6), 523-533 (2001-07-27)
The bioI gene has been sub-cloned and over-expressed in Escherichia coli, and the protein purified to homogeneity. The protein is a cytochrome P450, as indicated by its visible spectrum (low-spin haem iron Soret band at 419 nm) and by the
A Jos et al.
Toxicology in vitro : an international journal published in association with BIBRA, 21(7), 1307-1310 (2007-05-25)
The classical pathway for induction of cytochrome P4501A (CYP1A) by xenobiotics is ligand binding to the aryl hydrocarbon receptor (AhR). However, several studies with mammalian cell systems point out a range of xenobiotics including imidazole derivatives, which are able to
M Murray et al.
Toxicology letters, 25(2), 191-198 (1985-05-01)
Repeated administration of N-phenylimidazole (PI) to rats (3 daily doses of 200 mumol/kg/day) enhanced hepatic microsomal cytochrome P-450 levels (approx. 130%) and aminopyrine N-demethylase (APDM) and aniline p-hydroxylase (APH) activities (approx. 140%); aryl hydrocarbon (benzo[a]pyrene) hydroxylase (AHH) and 7-ethoxycoumarin O-deethylase
Filippo Monti et al.
Inorganic chemistry, 54(6), 3031-3042 (2015-03-06)
A series of cationic iridium(III) complexes with two carbene-based cyclometalating ligands and five different N^N bipyridine and 1,10-phenanthroline ancillary ligands is presented. For the first time--in the frame of a rarely studied class of bis(heteroleptic) iridium complexes with two carbene-based
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