53 Results for "

DSB

" in MedChemExpress (MCE) Product Catalog:
Products (53)

53 Results for "DSB" in MCE Product Catalog:

34
34 Publications Verification
Art. -Nr.: HY-15176A
CAS. Nr.: 1781882-65-2
Reinheit:  98.53%
Synonyms: RR82 hydrochloride
Forschungsgebiete:  

Cancer

Pyridostatin (RR82) hydrochloride is a G-quadruplex DNA stabilizing agent (Kd=490 nM) and can target DNA and RNA G4s in cells. Pyridostatin hydrochloride promotes growth arrest in human cancer cells by inducing replication- and transcription-dependent DNA damage. Pyridostatin hydrochloride targets the proto-oncogene Src. Pyridostatin hydrochloride reduced SRC protein levels and SRC-dependent cellular motility in human breast cancer cells .
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34
34 Publications Verification
Art. -Nr.: HY-15176B
CAS. Nr.: 1472611-44-1
Reinheit:  99.54%
Synonyms: RR82 TFA
Forschungsgebiete:  

Cancer

Pyridostatin (RR82) TFA is a G-quadruplex (G4) inducer/stabilizer with a Kd of 490 nM. Pyridostatin TFA also acts as an inhibitor of Zika virus (ZIKV) NS2B-NS3 protease, with an IC50 of 11.0 μM. Pyridostatin TFA interacts with G-quadruplex structures, regulates the expression of SRC and SUB1, and induces replication- and transcription-dependent DNA damage, growth arrest, and genomic instability. Pyridostatin TFA exhibits antiproliferative and antiviral activities. Pyridostatin TFA can be used in studies related to breast cancer, cervical cancer, and Zika virus infection .
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34
34 Publications Verification
Art. -Nr.: HY-15176C
CAS. Nr.: 2517456-88-9
Synonyms: RR82 trihydrochloride
Forschungsgebiete:  

Cancer

Pyridostatin (RR82) trihydrochloride is a G-quadruplex (G4) inducer/stabilizer with a Kd of 490 nM. Pyridostatin trihydrochloride also acts as an inhibitor of Zika virus (ZIKV) NS2B-NS3 protease, with an IC50 of 11.0 μM. Pyridostatin trihydrochloride interacts with G-quadruplex structures, regulates the expression of SRC and SUB1, and induces replication- and transcription-dependent DNA damage, growth arrest, and genomic instability. Pyridostatin trihydrochloride exhibits antiproliferative and antiviral activities. Pyridostatin trihydrochloride can be used in studies related to breast cancer, cervical cancer, and Zika virus infection .
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10
10 Cited Publications
Art. -Nr.: HY-B1357
CAS. Nr.: 71-63-6
Digitoxin is an anti-cancer agent. Digitoxin induces apoptosis, inhibits influenza cytokine storm, causes DNA double-stranded breaks (DSBs) and blocks the cell cycle at the G2/M phase. Digitoxin induces calcium uptake into cells by forming transmembrane calcium channels and can be used for research of heart failure .
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10
10 Cited Publications
Art. -Nr.: HY-19959
CAS. Nr.: 1198097-97-0
Target:  

ATM/ATR Apoptosis

Forschungsgebiete:  

Cancer

Mirin is a potent Mre11-Rad50-Nbs1 (MRN) complex inhibitor. Mirin prevents MRN-dependent activation of ATM (IC50=12 μM) without affecting ATM protein kinase activity, and it inhibits Mre11-associated exonuclease activity. Mirin abolishes the G2/M checkpoint and homology-dependent repair in mammalian cells. Mirin prevents ATM activation in response to DNA double-strand breaks (DSBs) and blocks homology-directed repair (HDR) in mammalian cells .
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9
9 Cited Publications
Art. -Nr.: HY-117693
CAS. Nr.: 299953-00-7
Reinheit:  98.62%
Target:  

ATM/ATR

Forschungsgebiete:  

Cancer

(E/Z)-Mirin is a mixture of (E)-Mirin and Mirin ((Z)-Mirin) (HY-19959) configurations. Among them, Mirin is an inhibitor of MRN (Mre11-Rad50-Nbs1). Mirin prevents MRN-dependent ATM activation without affecting ATM protein kinase activity .
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5
5 Cited Publications
Art. -Nr.: HY-116770
CAS. Nr.: 1558598-41-6
Reinheit:  99.91%
Target:  

Endonuclease

Forschungsgebiete:  

Cancer

PFM01, N-alkylated Mirin derivative, is a MRE11 endonuclease inhibitor. PFM01 can regulate double-strand break repair (DSBR) by nonhomologous end-joining (NHEJ) versus homologous recombination (HR) .
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4
4 Cited Publications
Art. -Nr.: HY-19939S
CAS. Nr.: 1476074-39-1
Synonyms: M9831
VX-984 is an orally active, potent, selective and BBB-penetrated DNA-PK inhibitor. VX-984 efficiently inhibits NHEJ (non-homologous end joining) and increases DSBs (DNA double-strand breaks). VX-984 can be used for glioblastomas (GBM) and non-small cell lung cancer (NSCLC) research. VX-984 is a de novo deuterium .
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3
3 Cited Publications
Art. -Nr.: HY-110185
CAS. Nr.: 203115-63-3
Reinheit:  99.18%
Target:  

DNA/RNA Synthesis

Forschungsgebiete:  

Cancer

NSC 617145 is a selective werner syndrome helicase (WRN) helicase inhibitor with an IC50 value of 230 nM. NSC 617145 inhibits WRN ATPase, and induces double-strand breaks (DSB) and chromosomal abnormalities. NSC 617145 shows selective for WRN over BLM, FANCJ, ChlR1, RecQ, and UvrD helicases .
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3
3 Cited Publications
Art. -Nr.: HY-10534
CAS. Nr.: 175414-77-4
Reinheit:  99.26%
Synonyms: SNS-595; Vosaroxin; AG 7352
Target:  

Topoisomerase Apoptosis

Forschungsgebiete:  

Cancer

Voreloxin (SNS-595; Vosaroxin; AG 7352) is a first-in-class topoisomerase II inhibitor that intercalates DNA and induces site-selective DNA DSB, G2 arrest, and apoptosis.
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3
3 Cited Publications
Art. -Nr.: HY-17469
CAS. Nr.: 103766-25-2
Synonyms: Gimestat
Gimeracil, a component of an oral fluoropyrimidine derivative S-1, inhibits DNA DSB repair and is a potent inhibitor of DPYD (dihydropyrimidine dehydrogenase, DPD) .
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3
3 Cited Publications
Art. -Nr.: HY-16518
CAS. Nr.: 175519-16-1
Synonyms: SNS-595 Hydrochloride; Vosaroxin Hydrochloride; AG 7352 Hydrochloride
Target:  

Topoisomerase Apoptosis

Forschungsgebiete:  

Cancer

Voreloxin Hydrochloride is a first-in-class topoisomerase II inhibitor that intercalates DNA and induces site-selective DNA DSB, G2 arrest, and apoptosis.
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2
2 Cited Publications
Art. -Nr.: HY-110111
CAS. Nr.: 1380782-27-3
Reinheit:  99.04%
Target:  

DNA/RNA Synthesis

Forschungsgebiete:  

Cancer

T2AA is a monoubiquitinated proliferating cell nuclear antigen (PCNA) inhibitor that prevents DNA repair, increases double-strand break (DSB) formation and promotes necroptosis and cell cycle arrest in G1 phase .
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1
1 Cited Publications
Art. -Nr.: HY-111183
CAS. Nr.: 9014-02-2
Reinheit:  ≥99.0%
Synonyms: Zinostatin; Vinostatin
Forschungsgebiete:  

Infection Cancer

Neocarzinostatin (solution), a potent DNA-damaging, anti-tumor antibiotic, recognizes double-stranded DNA bulge and induces DNA double strand breaks (DSBs). Neocarzinostatin induces apoptosis. Neocarzinostatin has potential for EpCAM-positive cancers treatment .
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1
1 Cited Publications
Art. -Nr.: HY-13703A
CAS. Nr.: 55661-38-6
Reinheit:  98.22%
Synonyms: ACNU
Nimustine hydrochloride (ACNU) is the hydrochloride salt form of Nimustine (HY-13703). Nimustine hydrochloride is an alkylating agent, which induces DNA double-strand breaks (DSBs) and inter-strand crosslinks (ICLs), thereby activating the DNA damage response (DDR) signaling pathway. Nimustine hydrochloride activates p38 MAPK/JNK signaling pathway, and exhibits antitumor activity .
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1
1 Cited Publications
Art. -Nr.: HY-120951
CAS. Nr.: 1310744-67-2
Reinheit:  99.01%
Target:  

Endonuclease

Forschungsgebiete:  

Cancer

PFM39, a Mirin analog, is a potent and selective MRE11 exonuclease inhibitor. PFM39 inhibits phosphate rotation for dsDNA exonuclease activity. PFM39 does not inhibit TmMre11 or human MRE11/MRN endonuclease activity .
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1
1 Cited Publications
Art. -Nr.: HY-113064
CAS. Nr.: 2897-21-4
Reinheit:  ≥99.0%
Selenocystine is a broad-spectrum anti-cancer agent. Selenocystine induces DNA damage in HepG2 cells, particularly in the form of DNA double strand breaks (DSBs). Selenocystine exhibits great promise as a therapeutic or adjuvant agent targeting DNA repair for cancer treatment .
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1
1 Cited Publications
Art. -Nr.: HY-128036B
CAS. Nr.: 72029-21-1
Reinheit:  99.93%
Synonyms: 2',3'-Dideoxyadenosine 5'-triphosphate trisodium
Target:  

DNA/RNA Synthesis HIV

Forschungsgebiete:  

Infection

ddATP (2',3'-Dideoxyadenosine 5'-triphosphate) trisodium, an active metabolite of 2',3'-dideoxyinosine, is a chain-elongating inhibitor of DNA polymerase. ddATP trisodium can be used for Sanger method for DNA sequencing and research of virus infection .
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Art. -Nr.: HY-15176
CAS. Nr.: 1085412-37-8
Reinheit:  96.03%
Synonyms: RR82
Target:  

G-quadruplex

Forschungsgebiete:  

Cancer

Pyridostatin (RR82) is a G-quadruplex DNA stabilizing agent (Kd=490 nM) and can target DNA and RNA G4s in cells. Pyridostatin promotes growth arrest in human cancer cells by inducing replication- and transcription-dependent DNA damage. Pyridostatin targets the proto-oncogene Src. Pyridostatin reduced SRC protein levels and SRC-dependent cellular motility in human breast cancer cells .
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Art. -Nr.: HY-100705
CAS. Nr.: 20357-25-9
Reinheit:  98.76%
Synonyms: 6-Nitroveratraldehyde
Target:  

Drug Intermediate

Forschungsgebiete:  

Neurological Disease

DMNB (6-Nitroveratraldehyde) is a photolabile proton donor that releases acidic substances when excited at a wavelength of 405 nM. DMNB can be used for the synthesis of no-carrier-added 6-[18F]fluoro-L-DOPA (6-FDOPA). DMNB is also applicable to the preparation of o-nitroaryl-bis (5-methylfur-2-yl) methanes and the synthesis of alpha-asarone (HY-N0700). DMNB is an enzyme involved in the non-homologous end joining (NHEJ) pathway responsible for DNA double-strand break (DSB) repair. DMNB can be used in PET studies of the dopaminergic system .
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