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ChemicalBook > Product Catalogue >Biochemical Engineering >Inhibitors >DNA damage >DNA-PK inhibitors >NU7026

NU7026

NU7026 Structure
  • ₹27365.6 - ₹28240
  • Product name: NU7026
  • CAS: 154447-35-5
  • MF: C17H15NO3
  • MW: 281.31
  • EINECS:
  • MDL Number:MFCD06798345
  • Synonyms:2-MORPHOLINO-4H-BENZO[H]CHROMEN-4-ONE;NU7026, >=98%;2-(4-Morpholinyl)-4H-naphthol[1,2-b]pyran-4-one;NU7026;LY293646; NU-7026;LY 293646;2-(4-Morpholinyl)-4H-naphtho[1,2-b]pyran-4-one;4H-Naphtho[1,2-b]pyran-4-one, 2-(4-morpholinyl)-;2-(4-Morpholinyl)-4H-naphtho[1,2-b]pyran-4-one NU7026
3 prices
Selected condition:

Brand

  • Sigma-Aldrich
  • Sigma-Aldrich(India)

Package

  • 5MG
  • ManufacturerSigma-Aldrich
  • Product number260961
  • Product descriptionDNA-PK Inhibitor II - CAS 154447-35-5 - Calbiochem The DNA-PK Inhibitor II, also referenced under CAS 154447-35-5, controls the biological activity of DNA-PK. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation appl
  • Packaging5MG
  • Price₹28240
  • Updated2022-06-14
  • Buy
  • ManufacturerSigma-Aldrich(India)
  • Product numberN1537
  • Product descriptionNU7026 ≥98% (HPLC), solid
  • Packaging5MG
  • Price₹27365.6
  • Updated2022-06-14
  • Buy
  • ManufacturerSigma-Aldrich(India)
  • Product number260961
  • Product descriptionDNA-PK Inhibitor II - CAS 154447-35-5 - Calbiochem The DNA-PK Inhibitor II, also referenced under CAS 154447-35-5, controls the biological activity of DNA-PK. This small molecule/inhibitor is primarily
  • Packaging5MG
  • Price₹28240
  • Updated2022-06-14
  • Buy
Manufacturer Product number Product description Packaging Price Updated Buy
Sigma-Aldrich 260961 DNA-PK Inhibitor II - CAS 154447-35-5 - Calbiochem The DNA-PK Inhibitor II, also referenced under CAS 154447-35-5, controls the biological activity of DNA-PK. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation appl 5MG ₹28240 2022-06-14 Buy
Sigma-Aldrich(India) N1537 NU7026 ≥98% (HPLC), solid 5MG ₹27365.6 2022-06-14 Buy
Sigma-Aldrich(India) 260961 DNA-PK Inhibitor II - CAS 154447-35-5 - Calbiochem The DNA-PK Inhibitor II, also referenced under CAS 154447-35-5, controls the biological activity of DNA-PK. This small molecule/inhibitor is primarily 5MG ₹28240 2022-06-14 Buy

Properties

Melting point :267-269 °C(Solv: methanol (67-56-1); water (7732-18-5))
Boiling point :459.9±45.0 °C(Predicted)
Density :1.330
storage temp. :2-8°C
solubility :DMSO: 3 mg/mL at 60 °C, soluble
form :solid
pka :0.49±0.20(Predicted)
color :tan

Safety Information

Symbol(GHS): GHS hazard pictograms
Signal word: Danger
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
H314 Causes severe skin burns and eye damage Skin corrosion/irritation Category 1A, B, C Danger GHS hazard pictograms P260,P264, P280, P301+P330+ P331,P303+P361+P353, P363, P304+P340,P310, P321, P305+ P351+P338, P405,P501
Precautionary statements:
P264 Wash hands thoroughly after handling.
P264 Wash skin thouroughly after handling.
P280 Wear protective gloves/protective clothing/eye protection/face protection.
P301+P330+P331 IF SWALLOWED: Rinse mouth. Do NOT induce vomiting.
P303+P361+P353 IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.
P363 Wash contaminated clothing before reuse.
P405 Store locked up.

Description

DNA-dependent protein kinase (DNA-PK) binds to strand breaks produced during normal cellular processes or in response to genotoxic stresses, such as ionizing radiation, targeting substrates that facilitate DNA repair. NU 7026 is a cell-permeable, potent, specific, and ATP-competitive inhibitor of DNA-PK (IC50 = 230 nM). It poorly inhibits phosphioinositide 3 kinase (IC50 = 13 μM) and is inactive against ataxia telangiectasia mutated kinase, ATR, and poly (ADP-ribose) polymerase. NU 7026 impairs cellular DNA double strand break repair and decreases survival in cells exposed to ionizing radiation. It also potentiates the cytotoxicity of topoisomerase II poisons used in the treatment of leukemia. For example, it potentiates the growth inhibitory effects of mitoxantrone in K562 cells more than 10-fold.

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