262 Results for "

breaks

" in MedChemExpress (MCE) Product Catalog:
Products (262)

262 Results for "breaks" in MCE Product Catalog:

Cat. No.: HY-162959
CAS No.: 2254567-00-3
Research Areas:  

Infection

BWC0977 acts as an inhibitor of bacterial Topoisomerase. BWC0977 stabilizes single-strand DNA breaks, inhibits DNA supercoiling and decatenation activities, binds to GyrA and ParC residues, and activates the SOS response. BWC0977 can be used in research related to multidrug-resistant bacterial infections .
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Cat. No.: HY-P2724
CAS No.: 9030-21-1
Synonyms: PNP
Target:  

Endogenous Metabolite

Research Areas:  

Metabolic Disease

Purine nucleoside phosphorylase, Microorganism (PNP) is a key enzyme in purine metabolism, which is involved in the purine rescue pathway. The deficiency of Purine nucleoside phosphorylase resulted in impaired T cell function. In the presence of inorganic orthophosphate as the second substrate, Purine nucleoside phosphorylase catalyzes the breaking of the glycosidic bond between ribose and deoxyribonucleoside to generate purine base and ribose (deoxyribose) -1-phosphate .
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Cat. No.: HY-13550
CAS No.: 64862-96-0
Synonyms: NSC 196473; NSC 290813
Target:  

DNA/RNA Synthesis

Research Areas:  

Cancer

Ametantrone (NSC 196473) is an antitumor agent that intercalates into DNA and induces topoisomerase II (TOP2)-mediated DNA break .
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Cat. No.: HY-164279
CAS No.: 1207615-74-4
Target:  

DNA/RNA Synthesis

Research Areas:  

Cancer

YTR107 is a radiation sensitizer. YTR107 binds to nucleophosmin1 (NPM1) and inhibits pentamer formation. YTR107 inhibits recruitment of nucleophosmin to sites of DNA damage, suppresses repair of DNA double strand breaks, and enhances radiosensitization .
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Cat. No.: HY-129834
CAS No.: 68683-34-1
Purity:  ≥95.0%
Research Areas:  

Inflammation/Immunology

Bilirubin Conjugate disodium is a peroxyl radical scavenger and chain-breaking antioxidant that inhibits lipid peroxidation by undergoing addition reactions with pyrrole moieties and accelerates copper ion-catalyzed decomposition of lipid hydroperoxides. Bilirubin Conjugate disodium is used in oxidative stress-related research .
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Cat. No.: HY-W543137
CAS No.: 727721-37-1
Pt-ttpy, a metallo-organic complex and potent G-quadruplex ligand, effectively triggers substantial telomere-related DNA damage in cancer cells by inhibiting telomerase and/or telomere functions, while also causing various chromatin abnormalities during mitosis, such as chromatin bridges, ultrafine bridges (UFBs), and double-stranded breaks (DSBs).
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Cat. No.: HY-D1023
CAS No.: 102212-99-7
Synonyms: 5-Bromo-2'-deoxyuridine 5'-triphosphate sodium salt
5-BrdUTP sodium salt is a TdT substrate which can be used to label the DNA double-strand breaks.
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Cat. No.: HY-P2892
CAS No.: 9032-88-6
Target:  

Endogenous Metabolite

Research Areas:  

Metabolic Disease

Fumarase catalyses the conversion of l-malic acid to fumaric acid. Fumarase participates in the tricarboxylic acid cycle in mitochondria. Fumarase participates in the cellular response to DNA double strand breaks .
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Cat. No.: HY-138645
CAS No.: 72983-78-9
Purity:  95.34%
Target:  

DNA/RNA Synthesis

Research Areas:  

Cancer

5-Iminodaunorubicin is a quinone-modified anthracycline that retains antitumor activity . 5-Iminodaunorubicin produces protein-concealed DNA strand breaks in cancer cells .
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Cat. No.: HY-N7147
CAS No.: 56495-82-0
Irisquinone, a natural product, is an anticancer agent. Irisquinone is also a radiation sensitizer for cancer. Irisquinone reduces GSH level and inhibits the repair of DNA singular strand breaks .
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Cat. No.: HY-149348
CAS No.: 3052259-89-6
Research Areas:  

Cancer

DiPT-4 is a dual TOP1/PARP1 inhibitor that induces massive DNA double-strand breaks (DSBs), cell cycle arrest, and apoptosis in cancer cells. DiPT-4 has the potential to overcome cancer drug resistance .
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Cat. No.: HY-W076740
CAS No.: 6974-78-3
Synonyms: 8-Bromo-9H-purin-6-amine
8-Bromoadenine (8-Bromo-9H-purin-6-amine) is a DNA radiosensitizer that inhibits DNA single-strand break repair in cells. 8-Bromoadenine is a brominated derivative of adenine, and radioactive adenine can be prepared by replacing bromine with deuterium .
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Cat. No.: HY-16401
CAS No.: 308359-57-1
Synonyms: PM00104
Target:  

Apoptosis

Research Areas:  

Cancer

Zalypsis (PM00104) has anti-tumor activity. Zalypsis binds to DNA and shows cytotoxicity. Zalypsis inhibits cell cycle and transcription, and leads to double stranded DNA breaks .
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Cat. No.: HY-123232
CAS No.: 623578-11-0
Target:  

PARP

Research Areas:  

Cancer

KU-0058684 is a potent PARP inhibitor, with an IC50 of 3.2 nM for PARP-1. KU-0058684 significantly reduces DNA double strand break (DSB) repair .
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Cat. No.: HY-159947
CAS No.: 2736508-94-2
Target:  

PROTACs Btk

Research Areas:  

Cancer

PROTAC BTK Degrader-11 is a PROTAC degrader that can break down BTK, with a DC50 of 1.7 nM. PROTAC BTK Degrader-11 can be used in cancer research .
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Cat. No.: HY-N4120
CAS No.: 51771-49-4
Valechlorine, an iridoid, is an autophagy enhancer. Valechlorine is effective in alleviating fatty liver by acting as an autophagy enhancer to break down lipid droplets. Valechlorine can be used for the study of nonalcoholic fatty liver disease (NAFLD) .
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Cat. No.: HY-W749297
CAS No.: 9060-10-0
Synonyms: Phleomycin D2
Target:  

DNA Stain

Bleomycin B2 (Phleomycin D2) is an anti-cancer agent that targets DNA. Bleomycin B2 causes DNA strand breaks, thereby inhibiting the growth and proliferation of cancer cells. Bleomycin B2 is promising for research of cancers .
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Cat. No.: HY-18626
CAS No.: 208237-49-4
Target:  

Topoisomerase

Research Areas:  

Cancer

NK 314 is an inhibitor for topoisomerase IIα, which generates the break of DNA double-strand. NK 314 arrests the cell cycle at G2 phase in human acute myeloid leukemia cells, inhibits the proliferation of CEM with IC90 of 55 nM .
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Cat. No.: HY-13703
CAS No.: 42471-28-3
Nimustine 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 activates p38 MAPK/JNK signaling pathway, and exhibits antitumor activity .
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Cat. No.: HY-174499
Target:  

mRNA

Research Areas:  

Others

Cas9 Nickase D10A mRNA expresses a version of the Streptococcus pyogenes SF370 Cas9 protein (CRISPR Associated Protein 9) that contains a D10A amino acid substitution. This mRNA also contains a C-terminal nuclear localization signal followed by a HA tag.Cas9 functions as part of the CRISPR (clustered regularly interspaced short palindromic repeats) genome editing system. In the CRISPR system, an RNA guide sequence targets the site of interest and the Cas9 protein is employed to perform the DNA cleavage. While wild-type Cas9 creates a double-stranded break at the target site, Cas9 nickase creates a single-stranded break. This favors homology-directed repair and decreases the occurrence of non-homologous end joining.
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