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Merck
CN

A0966

4-氨基-1,8-萘酰亚胺

solid

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关于此项目

经验公式(希尔记法):
C12H8N2O2
化学文摘社编号:
分子量:
212.20
NACRES:
NA.83
PubChem Substance ID:
UNSPSC Code:
12352204
EC Number:
217-110-1
MDL number:
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产品名称

4-氨基-1,8-萘酰亚胺,

InChI

1S/C12H8N2O2/c13-9-5-4-8-10-6(9)2-1-3-7(10)11(15)14-12(8)16/h1-5H,13H2,(H,14,15,16)

InChI key

SSMIFVHARFVINF-UHFFFAOYSA-N

SMILES string

Nc1ccc2C(=O)NC(=O)c3cccc1c23

form

solid

mp

360 °C

density

1.105 g/mL at 25 °C (lit.)

storage temp.

−20°C

Quality Level

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Biochem/physiol Actions

4-氨基-1,8-萘酰亚胺使细胞对辐射诱导的细胞损伤敏感,并增强 1-甲基-3-硝基-1-亚硝基胍的细胞毒性。

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves


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分析证书(COA)

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A Schlicker et al.
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M Banasik et al.
The Journal of biological chemistry, 267(3), 1569-1575 (1992-01-25)
Two classes of enzymes, poly(ADP-ribose) synthetase and mono(ADP-ribosyl)transferases, catalyze covalent attachment of multiple or single residues, respectively, of the ADP-ribose moiety of NAD+ to various proteins. In order to find good inhibitors of poly(ADP-ribose) synthetase free of side actions and
Jun Feng Zhang et al.
Organic letters, 13(5), 1190-1193 (2011-02-09)
A naphthalimide-based highly selective colorimetric and ratiometric fluorescent probe for the fluoride ion displayed both one- and two-photon ratiometric changes. Upon reaction with the F(-) (TBA(+) and Na(+) salts) anion in CH(3)CN as well as in aqueous buffer solution, probe
Marco A Alcala et al.
Nanomedicine : nanotechnology, biology, and medicine, 7(3), 249-258 (2010-10-16)
Surgery is currently the best approach for treating either primary or metastatic hepatic malignancies. Because only 20% of hepatic cancers are operable in patients, several types of regional therapy (RT) are emerging as alternate treatment modalities. However, RTs can have
Emma B Veale et al.
The Journal of organic chemistry, 75(16), 5513-5525 (2010-08-14)
The synthesis and characterization of three bis-1,8-naphthalimide-containing Tröger's bases 1-3, formed from the corresponding 4-amino-1,8-naphthalimide precursors 7-9 in a single step, is described. The photophysical investigation of 1-3 and 7-9 was carried out in various organic solvents as well as

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