70800
1-萘胺-5-磺酸
technical, ≥60.0% (T)
别名:
5-氨基-1-萘磺酸, Laurent 酸
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关于此项目
经验公式（希尔记法）:
C10H9NO3S
化学文摘社编号:
分子量:
223.25
Beilstein:
2214149
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
等级
technical
表单
powder
浓度
≥60.0% (T)
SMILES字符串
Nc1cccc2c(cccc12)S(O)(=O)=O
InChI
1S/C10H9NO3S/c11-9-5-1-4-8-7(9)3-2-6-10(8)15(12,13)14/h1-6H,11H2,(H,12,13,14)
InChI key
DQNAQOYOSRJXFZ-UHFFFAOYSA-N
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警示用语：
Danger
危险声明
危险分类
Acute Tox. 4 Dermal - Skin Corr. 1B
储存分类代码
8B - Non-combustible corrosive hazardous materials
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
新产品
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Yuta Takigawa et al.
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Oxo-octadecadienoic acids (OxoODEs) act as peroxisome proliferator-activated receptor (PPAR) agonists biologically, and are known to be produced in the lipoxygenase/linoleate system. OxoODEs seem to originate from the linoleate alkoxyl radicals that are generated from (E/Z)-hydroperoxy octadecadienoic acids ((E/Z)-HpODEs) by a
J Fick et al.
European journal of biochemistry, 126(2), 367-372 (1982-08-01)
Fluorescence studies of the intramolecular and intermolecular interactions between aminonaphthylsulfonate and nucleotides of uracil or adenine are described. The fluorescence originates solely from the naphthyl moiety and is intramolecularly quenched by the base, uracil being more effective than adenine. The
Brent A Mulder et al.
Nucleic acids research, 33(15), 4865-4873 (2005-09-06)
The mechanism by which HIV-1 reverse transcriptase (HIV-RT) discriminates between the correct and incorrect nucleotide is not clearly understood. Chemically modified nucleotides containing 1-aminonaphthalene-5-sulfonate (ANS) attached to their gamma-phosphate were synthesized and used to probe nucleotide selection by this error
U Bhattacharyya et al.
The Journal of biological chemistry, 274(21), 14573-14578 (1999-05-18)
In the previous paper we demonstrated that uridine-5'-beta-1-(5-sulfonic acid) naphthylamidate (UDPAmNS) is a stacked and quenched fluorophore that shows severalfold enhancement of fluorescence in a stretched conformation. UDPAmNS was found to be a powerful competitive inhibitor (Ki = 0.2 mM)
Y T Kim et al.
The Journal of biological chemistry, 263(27), 13712-13717 (1988-09-25)
Physical interactions between pyridoxal kinase and aspartate aminotransferase were detected by means of emission anisotropy and affinity chromatography techniques. Binding of aspartate aminotransferase (apoenzymes) to pyridoxal kinase tagged with a fluorescent probe was detected by emission anisotropy measurements at pH
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