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Merck
CN

T1264

β-Thionaphthyl acetate

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关于此项目

经验公式(希尔记法):
C12H10OS
化学文摘社编号:
分子量:
202.27
UNSPSC Code:
12352204
PubChem Substance ID:
MDL number:
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storage temp.

2-8°C

SMILES string

CC(=O)Sc1ccc2ccccc2c1

InChI

1S/C12H10OS/c1-9(13)14-12-7-6-10-4-2-3-5-11(10)8-12/h2-8H,1H3

InChI key

NMFMUXYHGNUOAI-UHFFFAOYSA-N



存储类别

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

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B C Payne et al.
The Histochemical journal, 12(1), 71-86 (1980-01-01)
Using the substrate 2-naphthylthiol acetate (NTA), we developed a reproducible method of demonstrating a non-specific esterase while retaining nuclear and cytoplasmic details at the ultrastructural level. The NTA esterase had a distribution and pattern of staining similar to those of
Iu G Zhukovskiĭ et al.
Ukrains'kyi biokhimichnyi zhurnal (1999 ), 75(3), 67-70 (2003-10-28)
1- and 2-thionaphthylacetates were tested as cholinesterase substrates. It was shown that the butyrilcholinesterase from horse serum can hydrolize these compounds. The hydrolysis velocity of 1-thionaphthylacetate was comparable with hydrolysis velocity of acetylthiocholine (the well known cholinesterase substrate), but 2-thionaphthylacetate
H L Li et al.
Experimental and molecular pathology, 46(3), 321-330 (1987-06-01)
Nonspecific esterase activity was localized ultrastructurally within normal and leukemic hematopoietic cells by the use of 2-naphthylthiol acetate (NTA) as a substrate. NTA esterase activity was identified in all cell lines, although mononuclear phagocytes contained the most abundant activity. Monocytes