product name
2-羟基-1,4-萘醌, 97%
质量水平
检测方案
97%
形式
powder
颜色
faint yellow to dark yellow, and Faint Orange to Dark Orange
mp
192-195 °C (dec.) (lit.)
λmax
452 nm
应用
diagnostic assay manufacturing
hematology
histology
储存温度
room temp
SMILES字符串
OC1=CC(=O)c2ccccc2C1=O
InChI
1S/C10H6O3/c11-8-5-9(12)10(13)7-4-2-1-3-6(7)8/h1-5,12H
InChI key
CSFWPUWCSPOLJW-UHFFFAOYSA-N
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一般描述
2-羟基-1,4-萘醌是用于指纹检测的法医试剂之一。
2-羟基-1,4-萘醌是由惰性劳森氏菌产生的一种橙色染料。属萘醌类染料。2-羟基-1,4-萘醌用于染发和给纺织品着色。具有抗菌、抗真菌、抗炎、抗病毒和抗肿瘤等属性。2-羟基-1,4-萘醌抑制肿瘤细胞生长。刺激活性氧 (ROS) 的产生。
应用
2-羟基-1,4-萘醌已被用作血吸虫蠕虫培养的化合物。
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
Yamin Yasin et al.
Journal of biomedical nanotechnology, 7(3), 486-488 (2011-08-13)
A drug-inorganic nanostructured material involving pharmaceutically active compound lawsone intercalated Zn-Al layered double hydroxides (Law-LDHs) with Zn/AI = 4 has been assembled by co-precipitation and ion exchange methods. Powder X-ray diffraction (XRD) and Fourier transform infrared spectra (FTIR) analysis indicate
Pablo J Almeida et al.
Contact dermatitis, 66(1), 33-37 (2011-10-07)
Very few studies are available in which the components of henna products used by tattoo artists have been analysed. The aim of this study was to quantify the amounts of lawsone (2-hydroxy-1,4-naphthoquinone, the active ingredient in henna) and p-phenylenediamine (PPD)
Francisco L S Bustamante et al.
Inorganic chemistry, 52(3), 1167-1169 (2013-01-25)
Dimerization of lawsone occurs upon reaction with Co(BF(4))(2)·6H(2)O and N,N'-bis(pyridin-2-ylmethyl)ethylenediamine (py(2)en) to produce the mononuclear complex [Co(III)(bhnq)(py(2)en)]BF(4)·H(2)O (1). This complex has been investigated as a prototype of a bioreductive prodrug, where the bhnq(2-) ligand acts as a model for cytotoxic
Trivedi PC
Medicinal Plants: Traditional Knowledge (2006)
Applications of DNA-electrochemical biosensors in cancer research
Chiorcea-Paquim AM, et al.
Past, Present and Future Challenges of Biosensors and Bioanalytical Tools in Analytical Chemistry: A Tribute to Professor Marco Mascini, 77, 287-336 (2017)
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