- Signaling Pathways
- Cell Cycle/DNA Damage
- DNA/RNA Synthesis
DNA/RNA Synthesis
RNA synthesis, which is also called DNA transcription, is a highly selective process. Transcription by RNA polymerase II extends beyond RNA synthesis, towards a more active role in mRNA maturation, surveillance and export to the cytoplasm.
Single-strand breaks are repaired by DNA ligase using the complementary strand of the double helix as a template, with DNA ligase creating the final phosphodiester bond to fully repair the DNA.DNA ligases discriminate against substrates containing RNA strands or mismatched base pairs at positions near the ends of the nickedDNA. Bleomycin (BLM) exerts its genotoxicity by generating free radicals, whichattack C-4′ in the deoxyribose backbone of DNA, leading to opening of the ribose ring and strand breakage; it is an S-independentradiomimetic agent that causes double-strand breaks in DNA.
First strand cDNA is synthesized using random hexamer primers and M-MuLV Reverse Transcriptase (RNase H). Second strand cDNA synthesis is subsequently performed using DNA Polymerase I and RNase H. The remaining overhangs are converted into blunt ends using exonuclease/polymerase activity. After adenylation of the 3′ ends of DNA fragments, NEBNext Adaptor with hairpin loop structure is ligated to prepare the samples for hybridization. Cell cycle and DNA replication are the top two pathways regulated by BET bromodomain inhibition. Cycloheximide blocks the translation of mRNA to protein.
DNA/RNA Synthesis Isoform Specific Products
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DNA/RNA Synthesis Inhibitors
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DNA/RNA Synthesis Inducers
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DNA/RNA Synthesis Substrates
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DNA/RNA Synthesis Ligands
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DNA/RNA Synthesis Related Products (2944)
Related Products (2944)
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Antibodies (248)
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DNA/RNA Synthesis Isoform Comparison
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Ibulocydine
0 ImagesCat. No.: HY-116054CAS No.: 1314096-68-8Ibulocydine is an isobutyrate prodrug of the Cdk inhibitor BMK-Y101 (HY-188159), with oral activity, and exhibits IC50 values of approximately 50 nM against CDK1/CDK2, 530 nM against CDK7/cyclin H/Mat1, and 85 nM against CDK9/cyclin T. Ibulocydine reduces the phosphorylation levels of Rb, nucleolin, and RNA polymerase II CTD Ser-5 and Ser-2, downregulates the expression of Mcl-1, survivin, and XIAP, decreases MMP-9 expression, and lowers the Bcl-2/Bax ratio, activates calpain-mediated Bax cleavage, cytochrome c release, and caspase activation. Ibulocydine induces apoptosis, inhibits the growth of cancer cells and xenografts, enhances the sensitivity of cancer cells to TRAIL and radiotherapy, and blocks cancer cell metastasis. Ibulocydine can be used in research related to various cancers, including hepatocellular carcinoma, triple-negative breast cancer, lung cancer, and colon cancer. -
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Antibacterial agent 345
0 ImagesCat. No.: HY-183712Antibacterial agent 345 is a Ciprofloxacin (HY-B0356)-lipophilic derivative and is an antibacterial agent. Antibacterial agent 345 inhibits DNA gyrase and inhibits bacterial DNA replication and transcription. Antibacterial agent 345 inhibits bacterial biofilm formation. Antibacterial agent 345 can be used for the research of bacterial infections, such as Pseudomonas aeruginosa infection. -
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- 5'-O-DMT-2'-F-5-MeO-U-3'-CE Phosphoramidite
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Ap4dT
0 ImagesCat. No.: HY-168345ACAS No.: 13457-68-6Ap4dT is an inhibitor for human adenylate kinase isozyme 1 (hAK1), that inhibits the ATP and ADP synthesis with IC50s of 42 μM and 38 μM. -
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TH287 hydrochloride
0 ImagesCat. No.: HY-16965ACAS No.: 1638211-05-8TH287 hydrochloride is a potent and selective inhibitor of MTH1, with an IC50 of 0.8 nM. TH287 hydrochloride is highly selective towards MTH1, with no relevant inhibition of MTH2, NUDT5, NUDT12, NUDT14, NUDT16, dCTPase, dUTPase and ITPA at 100 μM. TH287 hydrochloride could act as a chemotherapeutic agent for cancer research. -
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CMX-521
0 ImagesCat. No.: HY-160704CAS No.: 2077178-99-3CMX-521, a nucleoside analog, is a potent inhibitor for RNA-dependant RNA polymerase (RdRp) of norovirus. CMX-521 suppresses murine norovirus (MNV) and human norovirus. -
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Gimeracil (Standard)
0 ImagesSynonyms: Gimestat (Standard)Gimeracil (Standard) is the analytical standard of Gimeracil. This product is intended for research and analytical applications. 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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- Guanosine 5'-triphosphate-5'-adenosine
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R-1479 (Standard)
0 ImagesSynonyms: 4'-Azidocytidine (Standard)R-1479 (Standard) is the analytical standard of R-1479 (HY-10444). This product is intended for research and analytical applications. R-1479 (4'-Azidocytidine), a nucleoside analogue, is a specific inhibitor of RNA-dependent RNA polymerase (RdRp) of HCV. R-1479 inhibits HCV replication in the HCV subgenomic replicon system (IC50=1.28 μM). R-1479 is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups. -
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SNA T amidite
0 ImagesCat. No.: HY-185384CAS No.: 179472-04-9SNA T amidite is a phosphoramidite that can be used in the synthesis of oligonucleotides. -
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tCnitro-CE phosphoramidite
0 ImagesCat. No.: HY-182118CAS No.: 1139889-28-3tCnitro-CE phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides. -
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HAMNO (Standard)
0 ImagesCat. No.: HY-111285RCAS No.: 138736-73-9Synonyms: NSC111847 (Standard) -
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Sennidin A
0 ImagesSennidin A is an anthraquinone derivative and a HCV NS3 helicase inhibitor with an IC50 of 0.8 μM against HCV NS3 helicase. Sennidin A induces Akt phosphorylation at Ser-473 and Thr-308 and promotes GLUT4 translocation to the plasma membrane. Sennidin A inhibits HCV replication. Sennidin A stimulates glucose incorporation and 2-Deoxyglucose uptake in cells. Sennidin A does not induce tyrosine phosphorylation of the insulin receptor or insulin receptor substrate-1. Sennidin A can be used for research on type 2 diabetes and hepatitis C. -
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(R)-GNA-U phosphoramidite
0 ImagesCat. No.: HY-177335CAS No.: 2940934-04-1(R)-GNA-U phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides. -
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CHD1L-IN-2
0 ImagesCat. No.: HY-185041CAS No.: 1251542-88-7CHD1L-IN-2 is a CHD1L inhibitor and exhibits cytotoxicity against tumor cells. -
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rU Phosphoramidite, 99%, ≤0.2%(K.F.)
0 ImagesCat. No.: HY-W048482ACAS No.: 118362-03-1Synonyms: DMT-2'O-TBDMS-rU phosphoramidite, 99%, ≤0.2%(K.F.)rU Phosphoramidite, 99%, ≤0.2%(K.F.) is a phosphoramidite that can be used in the synthesis of oligonucleotides. -
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TGC Trimer phosphoramidite
0 ImagesCat. No.: HY-182214CAS No.: 1446702-65-3TGC Trimer phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides. -
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Gemcitabine 5'-diphosphate
0 ImagesCat. No.: HY-W791041CAS No.: 116371-66-5Synonyms: dFdCDPGemcitabine 5'-diphosphate (dFdCDP) is a core active metabolic intermediate of Gemcitabine (HY-17026) and a potent ribonucleotide reductase (RNR) inhibitor. Gemcitabine 5'-diphosphate depletes deoxyribonucleotide pools, consumes deoxycytidine triphosphate and increases the phosphorylation level of gemcitabine. Gemcitabine 5'-diphosphate prolongs the intracellular retention duration of gemcitabine metabolites, enhances the nucleic acid incorporation of gemcitabine, and exerts anti-tumor/cytotoxic effects. -
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2'-F-ANA-rC(N-Ac) Phosphoramidite
0 ImagesCat. No.: HY-W11432222'-F-ANA-rC(N-Ac) Phosphoramidite is a modified phosphoramidite monomer that can be used for the synthesis of oligonucleotides. -
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dX-CE Phosphoramidite
0 ImagesCat. No.: HY-182107CAS No.: 292050-43-2dX-CE Phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides. -
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