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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
201-571-0
Beilstein/REAXYS Number:
2214149
MDL number:
Form:
powder
InChI key
DQNAQOYOSRJXFZ-UHFFFAOYSA-N
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)
SMILES string
Nc1cccc2c(cccc12)S(O)(=O)=O
grade
technical
form
powder
concentration
≥60.0% (T)
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Dermal - Skin Corr. 1B
存储类别
8B - Non-combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
新产品
此项目有
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
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
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
S C Tyagi et al.
The Journal of biological chemistry, 262(22), 10684-10688 (1987-08-05)
New fluorescent derivatives of dinucleoside monophosphates, (5'-AmNS)UpA/ApU/GpU/CpA, with a fluorophore, 1-aminonaphthalene-5-sulfonic acid (AmNS), attached to the first nucleotide of the dinucleoside monophosphates via a 5'-secondary amine linkage were synthesized in good yield. The chemical structure of (5'-AmNS)ApU was proved by
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