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A23609

吖啶

Name: 吖啶
Brand: SIAL

96.5 - 103.5% purity, powder or crystals

别名:

9-氮杂蒽；2,3-苯并喹啉

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关于此项目

经验公式（希尔记法）:

C₁₃H₉N

化学文摘社编号:

260-94-6

分子量:

179.22

NACRES:

NA.47

PubChem Substance ID:

24890478

eCl@ss:

39210107

UNSPSC Code:

12171500

EC Number:

205-971-6

MDL number:

MFCD00005025

Beilstein/REAXYS Number:

120200

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产品名称

吖啶, ≥96.5% (HPLC)

Quality Level

100

assay

≥96.5% (HPLC), 96.5-103.5% (perchloric acid titration)

form

powder or crystals

technique(s)

microbe id | staining: suitable

color

light beige to beige, light brown to brown, light yellow to very dark yellow

bp

346 °C (lit.)

mp

107-110 °C (lit.)

λ_max

392 nm

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

SMILES string

c1ccc2nc3ccccc3cc2c1

InChI

1S/C13H9N/c1-3-7-12-10(5-1)9-11-6-2-4-8-13(11)14-12/h1-9H

InChI key

DZBUGLKDJFMEHC-UHFFFAOYSA-N

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General description

吖啶是一种小的阳离子平面染料，主要与RNA和DNA结合。具有强荧光性。结构与氧杂蒽类似，不过杂原子由氧换成氮。

Application

吖啶可染色核酸，尤其适合细胞周期研究。作为荧光材料，吖啶可用于生物分子可视化和激光领域。

pictograms

GHS07,GHS09

signalword

Warning

hcodes

H302,H315,H319,H335,H410

pcodes

P261 - P264 - P273 - P301 + P312 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

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

dust mask type N95 (US), Eyeshields, Gloves

法规信息

危险化学品

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Design and implementation of an ribonucleic acid (RNA) directed fragment library.

Khaled Bodoor et al.

Journal of medicinal chemistry, 52(12), 3753-3761 (2009-05-19)

The design of RNA binding ligands is complicated by issues of specificity, target flexibility, and the tractability of known RNA inhibitors toward chemical derivitization. To address these difficulties, an RNA-directed fragment compound library is presented. We began with an analysis

Long N and Wong WT

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Molecular properties of psychopharmacological drugs determining non-competitive inhibition of 5-HT3A receptors.

Johannes Kornhuber et al.

European journal of medicinal chemistry, 44(6), 2667-2672 (2009-01-16)

We developed a structure-property-activity relationship (SPAR)-model for psychopharmacological drugs acting as non-competitive 5-HT(3A) receptor antagonists by using a decision-tree learner provided by the RapidMiner machine learning tool. A single molecular descriptor, namely the molecular dipole moment per molecular weight (mu/MW)

Reactivation of latent HIV-1 provirus via targeting protein phosphatase-1.

Mudit Tyagi et al.

Retrovirology, 12, 63-63 (2015-07-17)

HIV-1 escapes antiretroviral drugs by integrating into the host DNA and forming a latent transcriptionally silent HIV-1 provirus. This provirus presents the major hurdle in HIV-1 eradication and cure. Transcriptional activation, which is prerequisite for reactivation and the eradication of

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Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology, 34(4), 1175-1189 (2014-10-04)

Apoptosis and autophagy are two patterns of programmed cell death which play important roles in the intervertebral disc degeneration. Oxidative stress is an important factor for the induction of programmed cell death. However, the cellular reactions linking autophagy to apoptosis

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全球贸易项目编号

货号	GTIN
A23609-25G	04061833350027
A23609-5G	04061833350034

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