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A0966

Sigma-Aldrich

4-Amino-1,8-naphthalimide

solid

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About This Item

Fórmula empírica (notación de Hill):
C12H8N2O2
Número de CAS:
1742-95-6
Peso molecular:
212.20
EC Number:
217-110-1
MDL number:
MFCD00006921
UNSPSC Code:
12352204
PubChem Substance ID:
24277696
NACRES:
NA.83

product name

4-Amino-1,8-naphthalimide,

form

solid

mp

360 °C

density

1.105 g/mL at 25 °C (lit.)

storage temp.

−20°C

SMILES string

Nc1ccc2C(=O)NC(=O)c3cccc1c23

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

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Biochem/physiol Actions

4-Amino-1,8-naphthalimide sensitizes cells to radiation-induced cell damage and enhances the cytotoxicity of 1-methyl-3-nitro-1-nitrosoguanidine.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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A Schlicker et al.
International journal of radiation biology, 75(1), 91-100 (1999-02-11)
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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
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
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
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