CRT0044876
CRT0044876 is a potent and selective inhibitor of APE1 with IC50 value of 3.06 μM [1].
Apurinic/apyrimidinic endonuclease-1 (APE1) is a member of the highly conserved exonuclease
III family of AP endonucleases and plays an important role in DNA repair. APE1 exhibits 3’-phosphodiesterase activity and weak 3’-phosphatase activity, 3’-5’-exonuclease activity and RNaseH activity [1].
CRT0044876 is a potent and selective APE1 inhibitor. In HeLa whole cell extract, CRT0044876 inhibited apurinic/apyrimidinic (AP) site cleavage catalyzed by APE1. CRT0044876 inhibited both the AP endonuclease and exonuclease activities of exonuclease III, the bacterial homologue of APE1. CRT0044876 inhibited the 3’-phosphoglycolate diesterase activity of APE1 with IC50 value of 5 μM and also inhibited 3’-phosphatase activity through binding to DNA repair active site of APE1. In HT1080 fibrosarcoma cells, CRT0044876 significantly increased AP site accumulation and was non-toxic at concentrations up to 400 μM. Also, CRT0044876 potentiated the cytotoxicity induced by alkylating agent MMS, temozolomide, hydrogen peroxide and hmdUrd through specific inhibition of the base excision repair (BER) pathway [1].
Reference:
[1]. Madhusudan S, Smart F, Shrimpton P, et al. Isolation of a small molecule inhibitor of DNA base excision repair. Nucleic Acids Res, 2005, 33(15): 4711-4724.
| Physical Appearance | A solid |
| Storage | Store at -20°C |
| M.Wt | 206.15 |
| Cas No. | 6960-45-8 |
| Formula | C9H6N2O4 |
| Solubility | ≥55.56 mg/mL in DMSO; insoluble in H2O; ≥2.85 mg/mL in EtOH with gentle warming and ultrasonic |
| Chemical Name | 7-nitro-1H-indole-2-carboxylic acid |
| SDF | Download SDF |
| Canonical SMILES | C1=CC2=C(C(=C1)[N+](=O)[O-])NC(=C2)C(=O)O |
| Shipping Condition | Small Molecules with Blue Ice, Modified Nucleotides with Dry Ice. |
| General tips | We do not recommend long-term storage for the solution, please use it up soon. |
| Kinase experiment [1]: | |
|
AP site cleavage assay |
BER reaction buffer comprised 40 mM HEPES-KOH (pH 7.8), 5 mM MgCl2, 0.5 mM DTT and 0.1 mM EDTA. A 10 μL AP site cleavage reaction comprised of BER buffer mix, purified protein (3.3 nM final concentration of APE1) and 0.75 ng reduced AP site double-stranded oligonucleotide. The mixture was incubated at 37 °C for 1 hr. A total of 1 μL of stop buffer (50% glycerol, 10 mM Tris–HCl, 1 mM EDTA, 0.1% bromophenol blue and 0.1% Xylene cyanol) was added, and the sample mixture was denatured at 90 ~ 100 °C for 2 mins. The sample was then loaded on a 15% TBE Criterion Pre-Cast Gel, with electrophoresis at a constant current of 30 mA for 30 mins, and the radiolabeled substrate and reaction products were visualized using a phosphorImager. The inhibitory activity of potential APE1-targeting compounds was analyzed at drug concentrations ranging from 0.1 to 100 μM. The resolved radiolabeled bands were quantified using ImageQuant software analysis, and IC50 values were calculated. |
| Cell experiment [1]: | |
|
Cell lines |
Human HT1080 fibrosarcoma cells |
|
Preparation method |
The solubility of this compound in DMSO is > 55.6 mg/mL. General tips for obtaining a higher concentration: Please warm the tube at 37 °C for 10 minutes and/or shake it in the ultrasonic bath for a while. Stock solution can be stored below - 20 °C for several months. |
|
Reacting condition |
1 ~ 2 hrs |
|
Applications |
In Human HT1080 fibrosarcoma cells, CRT0044876 significantly increased apurinic/apyrimidinic (AP) site accumulation. HT1080 cells treated with methylmethane sulfonate (MMS) also elevated the level of AP sites. The combination of CRT0044876 and MMS caused a synergistic increase in the level of AP sites. |
|
References: [1]. Madhusudan S, Smart F, Shrimpton P, et al. Isolation of a small molecule inhibitor of DNA base excision repair. Nucleic Acids Res, 2005, 33(15): 4711-4724. | |
Quality Control & MSDS
- View current batch:
Chemical structure
