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4-amino-1,8-Naphthalimide

 
Catalog No.
C4310
PARP抑制剂
组合的产品项目
规格价格库存 数量
50mg
¥ 3,304.00
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100mg
¥ 5,091.00
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250mg
¥ 11,104.00
Ship with 10-15 days

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背景

4-amino-1,8-Naphthalimide is a novel inhibitor of PARP with IC50 value of 180 nM [1][3].

The poly(ADP-ribose) polymerases (PARPs) is a nuclear enzyme that catalyzes a transfer of the ADP-ribose moiety of NAD+ to acceptor protein with a concomitant release of nicotinamide. PARPs play important roles in DNA repair, cell differentiation, control of cell cycle, transformation, transcription, and alteration of chromatin architecture [2][3][4].

4-amino-1,8-Naphthalimide (4-ANI) is a novel PARP inhibitor and a radiation sensitizer. In exponentially growing hamster lung fibroblasts (V79), rat prostate carcinoma (R3327-AT1) and human prostate carcinoma (DU145) cells, 4-ANI significantly potentiated the cytotoxicity of gamma-irradiation in a dose dependent way and is not cytotoxic in the absence of radiation. 4-ANI was used to study the role of PARP activity in a variety of cell systems [1][3].

References:
[1].  Schlicker A, Peschke P, Bürkle A, et al. 4-Amino-1,8-naphthalimide: a novel inhibitor of poly(ADP-ribose) polymerase and radiation sensitizer. Int J Radiat Biol. 1999 Jan;75(1):91-100.
[2].  Davar D1, Beumer JH, Hamieh L, et al. Role of PARP inhibitors in cancer biology and therapy. Curr Med Chem. 2012;19(23):3907-21.
[3].  Banasik M, Komura H, Shimoyama M,et al. Specific inhibitors of poly(ADP-ribose) synthetase and mono(ADP-ribosyl)transferase. J Biol Chem. 1992 Jan 25;267(3):1569-75.
[4].  Issaeva N, Thomas HD, Djureinovic T, et al. 6-thioguanine selectively kills BRCA2-defective tumors and overcomes PARP inhibitor resistance. Cancer Res. 2010 Aug 1;70(15):6268-76.

化学属性

Physical AppearanceA crystalline solid
StorageStore at -20°C
M.Wt212.2
Cas No.1742-95-6
FormulaC12H8N2O2
Synonyms4-Aminonaphthalimide,4-ANI
Solubility≤1mg/ml in DMSO;0.3mg/ml in dimethyl formamide
Chemical Name6-amino-1H-benz[de]isoquinoline-1,3(2H)-dione
SDFDownload SDF
Canonical SMILESNC1=C2C(C3=CC=C2)=C(C=C1)C(NC3=O)=O
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Chemical structure

4-amino-1,8-Naphthalimide