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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
30 Results for "
apurinic
" in MedChemExpress (MCE) Product Catalog:
Products (30)
30 Results for "apurinic" in MCE Product Catalog:
4
Research Areas:
Erenapursta (E3330) is a direct, orally active and selective inhibitor of Ape-1 (apurinic/apyrimidinic endonuclease 1)/Ref-1 (redox factor-1) redox. Erenapursta is able to impair tumor growth and blocks the activity of NF-κB, AP-1, and HIF-1α in pancreatic cancer. Erenapursta shows anticancer activities .
3
3 Cited Publications
Cat. No.: HY-W014622
CAS No.: 6960-45-8
Target:
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CRT0044876 is a potent and selective apurinic/apyrimidinic endonuclease 1 (APE1) inhibitor (IC50=~3 μM). CRT0044876 inhibits the AP endonuclease, 3′-phosphodiesterase and 3′-phosphatase activities of APE1, and is a specific inhibitor of the exonuclease III family of enzymes to which APE1 belongs. CRT0044876 potentiates the cytotoxicity of several DNA base-targeting compounds .
3
3 Cited Publications
Cat. No.: HY-P70968
Purity: ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: OGG1; DNA-(apurinic Or Apyrimidinic Site) Lyase; 8-Oxoguanine DNA Glycosylase; DNA-apurinic Or Apyrimidinic Site Lyase; OGH1; OGG1 Type 1e; MUTM; OGG1 Type 1d; N-Glycosylase/DNA Lyase; OGG1 Type 1g; HOGG1; OGG1 Type 1h; HMMH; OGG1 Type 1f; 8-Hydroxyguanin
Species:
Human
Source:
E. coli
2
Hycanthone is an apurinic/apyrimidinic endonuclease 1 (APE1) inhibitor, DNA intercalator and Antischistosomal agent, with an IC50 of 80 nM against APE1. Hycanthone irreversibly inhibits thymidine incorporation into DNA in adult sensitive *Schistosoma mansoni*, while exerts weak inhibitory effects on uridine and leucine incorporation. Hycanthone reduces influenza virus-induced interferon production. Hycanthone exhibits mutagenic effects in various organisms, shows teratogenicity in mice and rabbits, and induces neoplastic liver lesions in partially hepatectomized mice. Hycanthone can be used in research related to schistosomiasis and cancer .
1
1 Cited Publications
Cat. No.: HY-P7523
Purity: ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: APEX1; APE1; Prev. APEX; DNA-(apurinic Or Apyrimidinic Site) Endonuclease; APEN; APEX Nuclease; REF-1; APEX Nuclease (Multifunctional DNA Repair Enzyme); REF1; Deoxyribonuclease (apurinic Or Apyrimidinic); HAP1; apurinic/Apyrimidinic (Abasic) Endonuclease
Species:
Human
Source:
E. coli
1
1 Cited Publications
Cat. No.: HY-P72338
Purity: ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: OGG1; DNA-(apurinic Or Apyrimidinic Site) Lyase; 8-Oxoguanine DNA Glycosylase; DNA-apurinic Or Apyrimidinic Site Lyase; OGH1; OGG1 Type 1e; MUTM; OGG1 Type 1d; N-Glycosylase/DNA Lyase; OGG1 Type 1g; HOGG1; OGG1 Type 1h; HMMH; OGG1 Type 1f; 8-Hydroxyguanin
Species:
Human
Source:
E. coli
Target:
Target:
Research Areas:
APE1-IN-1 is a potent and blood-brain barrier (BBB) penetrant apurinic/apyrimidinic (AP) endonuclease 1 (APE1) inhibitor with an IC50 value of 2 μM. APE1-IN-1 can potentiate the cytotoxicity of the alkylating agents Methylmethane sulfonate and Temozolomide (HY-17364) to cancer cells .
Cat. No.: HY-119993
CAS No.: 510721-85-4
Synonyms: BMH-23
Target:
Research Areas:
AR03 (BMH-23) is an apurinic/apyrimidinic endonuclease 1 (Ape1) inhibitor with an IC50 of 2.1 µM. AR03 has low affinity for double-stranded DNA. AR03 potentiates the cytotoxicity of methyl methanesulfonate and temozolomide in SF767 cells .
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Research Areas:
Exonuclease III is a nuclease for specifically targeting double-stranded DNA (dsDNA). Exonuclease III is a DNA repair-associated nuclease with apurinic/apyrimidinic (AP)-endonuclease and 3'→5' exonuclease activities. Exonuclease III cleaves the ssDNA at 5'-bond of phosphodiester from 3' to 5' end by both exonuclease and endonuclease activities .
APE1-IN-2 (compound AP1) is a Pt(IV) proagent, targeting a critical BER protein, apurinic/apyrimidinic endonuclease 1 (APE1). APE1-IN-2 shows anticancer activity. APE1-IN-2 induces intracellular accumulation of platinum and activates DNA damage response and apoptosis signals .
Cat. No.: HY-23318
CAS No.: 91547-59-0
Research Areas:
1,2-Dideoxy-D-ribofuranose is an abasic deoxyribonucleoside (dRH) and a structural analog of the sugar residue at natural apurinic/apyrimidinic sites. When 1,2-Dideoxy-D-ribofuranose is incorporated into the terminal overhang region of the antisense strand of siRNA, it attenuates RNAi-mediated gene silencing. When 1,2-Dideoxy-D-ribofuranose is incorporated as a dimer at the terminus, it enhances the resistance of oligonucleotides to exonuclease degradation. 1,2-Dideoxy-D-ribofuranose can serve as a building block for oligonucleotide synthesis and siRNA modification. 1,2-Dideoxy-D-ribofuranose is also a commonly used building block in the synthesis of carbapenem antibiotics .
Cat. No.: HY-113056AR
CAS No.: 34450-16-3
Category:
Target:
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Lucanthone N-oxide is the nitrogen oxide of Lucanthone (HY-B2098), an endonuclease inhibitor of Apurinic endonuclease-1 (APE-1) .
Target:
Research Areas:
Lucanthone (Standard) is the analytical standard of Lucanthone. This product is intended for research and analytical applications. Lucanthone is an endonuclease inhibitor of Apurinic endonuclease-1 (APE-1).
Cat. No.: HY-113056AS1
Hycanthone (Standard) is the analytical standard of Hycanthone (HY-B1099). This product is intended for research and analytical applications. Hycanthone is an apurinic/apyrimidinic endonuclease 1 (APE1) inhibitor, DNA intercalator and Antischistosomal agent, with an IC50 of 80 nM against APE1. Hycanthone irreversibly inhibits thymidine incorporation into DNA in adult sensitive *Schistosoma mansoni*, while exerts weak inhibitory effects on uridine and leucine incorporation. Hycanthone reduces influenza virus-induced interferon production. Hycanthone exhibits mutagenic effects in various organisms, shows teratogenicity in mice and rabbits, and induces neoplastic liver lesions in partially hepatectomized mice. Hycanthone can be used in research related to schistosomiasis and cancer .
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
