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AB120970

NU 7026, DNA-PK inhibitor

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(6 Publications)

MW 281.3 Da, Purity >99%. Novel, specific, reversible DNA-dependent protein kinase (DNA-PK) inhibitor (IC50 = 0.23 μM). Increases G2/M arrest and inhibits double-strand break repair.

View Alternative Names

DNA PK, DNA-PK catalytic subunit, DNA-PKcs, DNA-dependent protein kinase catalytic subunit, DNPK 1, HYRC, HYRC 1, Hyper radiosensitivity of murine scid mutation, complementing 1, Hyperradiosensitivity complementing 1, mouse, homolog of 1, IMD26, PKRDC, PRKDC_HUMAN, Protein Kinase DNA Activated Catalytic Polypeptide, XRCC 7, p350, p460

1 Images
Chemical Structure - NU 7026, DNA-PK inhibitor (AB120970)
  • Chemical Structure

Lab

Chemical Structure - NU 7026, DNA-PK inhibitor (AB120970)

2D chemical structure image of ab120970, NU 7026, DNA-PK inhibitor

Key facts

CAS number

154447-35-5

Purity

>99%

Form

Solid

form

Molecular weight

281.3 Da

Molecular formula

C<sub>1</sub><sub>7</sub>H<sub>1</sub><sub>5</sub>NO<sub>3</sub>

PubChem

9860529

Nature

Synthetic

Solubility

Soluble in DMSO to 10 mM

Biochemical name

2-(Morpholin-4-yl)-benzo[h]chromen-4-one

Biological description

Novel, specific, reversible DNA-dependent protein kinase (DNA-PK) inhibitor (IC50 = 0.23 μM). Increases G2/M arrest and inhibits double-strand break repair.

Canonical smiles

C1COCCN1C2=CC(=O)C3=C(O2)C4=CC=CC=C4C=C3

InChi

InChI=1S/C17H15NO3/c19-15-11-16(18-7-9-20-10-8-18)21-17-13-4-2-1-3-12(13)5-6-14(15)17/h1-6,11H,7-10H2

InChiKey

KKTZALUTXUZPSN-UHFFFAOYSA-N

IUPAC Name

2-morpholin-4-ylbenzo[h]chromen-4-one

Properties and storage information

Shipped at conditions
Ambient - Can Ship with Ice
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
+4°C
Storage information
The product can be stored for up to 12 months

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

DNA-dependent protein kinase catalytic subunit often abbreviated as DNA-PKcs or PKcs is an important component in the cellular machinery responsible for DNA repair. This protein weighs approximately 470 kDa and is predominantly expressed in various tissue types with higher levels found in lymphoid tissues. The DNA-PKcs functions as a serine/threonine protein kinase and becomes active upon binding to DNA contributing to its role in maintaining genome integrity.
Biological function summary

DNA-PKcs plays an essential role in the non-homologous end joining (NHEJ) repair pathway which repairs double-strand breaks in DNA. DNA-PKcs forms a complex with the Ku70/80 heterodimer serving as a critical component of the DNA repair mechanism. This complex recognizes DNA ends facilitates their synapsis and activates other enzymes involved in ligating the broken DNA strands therefore promoting cellular survival following DNA damage.

Pathways

DNA-PKcs deeply integrates into the DNA damage response pathway. It collaborates closely with proteins such as ATM (ataxia-telangiectasia mutated) to sense DNA damage and initiate repair. DNA-PKcs is involved in V(D)J recombination vital for the generation of diverse antibodies in immune cells. Its activity is essential for coordinating with other proteins including XRCC4 and Ligase IV to ensure efficient DNA repair processes are executed.

Defects in DNA-PKcs are linked to severe combined immunodeficiency (SCID) due to its central role in V(D)J recombination. Dysfunction in its pathway also relates to cancer where impaired DNA repair mechanisms substantially increase genomic instability leading to tumorigenesis. DNA-PKcs interacts with other proteins like BRCA1 and p53 in tumors where its overexpression or mutations can contribute to resistance against radiation and chemotherapeutic agents. These interactions highlight the importance of DNA-PK inhibitors as potential therapeutic strategies in oncology.

Product protocols

Publications (6)

Recent publications for all applications. Explore the full list and refine your search

Archives of toxicology 99:2577-2594 PubMed40063242

2025

Replication stress: an early key event in ochratoxin a genotoxicity?

Applications

Unspecified application

Species

Unspecified reactive species

C Klotz,J Borchers,J Brode,P Lambeck,A Mally

Microbiology spectrum 13:e0246824 PubMed39560443

2024

Lack of activity of HIV-1 integrase strand-transfer inhibitors on recombinase activating gene (RAG) activity at clinically relevant concentrations.

Applications

Unspecified application

Species

Unspecified reactive species

Sally Demirdjian,Vincent N Duong,Jennifer N Byrum,Arabinda Nayak,Cooper B McKinney,Jason K Perry,Christian Callebaut,Karla K Rodgers,Brie Falkard,Joy Y Feng

Journal of radiation research 65:315-322 PubMed38648785

2024

Changes in repair pathways of radiation-induced DNA double-strand breaks at the midblastula transition in Xenopus embryo.

Applications

Unspecified application

Species

Unspecified reactive species

Ryosuke Morozumi,Naoto Shimizu,Kouhei Tamura,Makoto Nakamura,Atsushi Suzuki,Hiroko Ishiniwa,Hiroshi Ide,Masataka Tsuda

Cancer discovery 13:880-909 PubMed36700848

2023

Blocking Genomic Instability Prevents Acquired Resistance to MAPK Inhibitor Therapy in Melanoma.

Applications

Unspecified application

Species

Unspecified reactive species

Prashanthi Dharanipragada,Xiao Zhang,Sixue Liu,Shirley H Lomeli,Aayoung Hong,Yan Wang,Zhentao Yang,Kara Z Lo,Agustin Vega-Crespo,Antoni Ribas,Stergios J Moschos,Gatien Moriceau,Roger S Lo

Scientific reports 8:3850 PubMed29497062

2018

Large XPF-dependent deletions following misrepair of a DNA double strand break are prevented by the RNA:DNA helicase Senataxin.

Applications

Unspecified application

Species

Unspecified reactive species

Julien Brustel,Zuzanna Kozik,Natalia Gromak,Velibor Savic,Steve M M Sweet

The Journal of biological chemistry 289:28730-7 PubMed25164823

2014

Nucleotide excision repair-dependent DNA double-strand break formation and ATM signaling activation in mammalian quiescent cells.

Applications

Unspecified application

Species

Unspecified reactive species

Mitsuo Wakasugi,Takuma Sasaki,Megumi Matsumoto,Miyuki Nagaoka,Keiko Inoue,Manabu Inobe,Katsuyoshi Horibata,Kiyoji Tanaka,Tsukasa Matsunaga
View all publications

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