1. Signaling Pathways
  2. Cell Cycle/DNA Damage
  3. 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.

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-N14130
    Cyclothialidine B
    Inhibitor
    Cyclothialidine B inhibits escherichia coli DNA helicases with an IC50 of 0.7 μM.
    Cyclothialidine B
  • HY-N0112S
    Dihydromyricetin-d4
    Inhibitor
    Dihydromyricetin-d4 (Ampelopsin-d4) is deuterium labeled Dihydromyricetin. Dihydromyricetin is a potent inhibitor with an IC50 of 48 μM on dihydropyrimidinase. Dihydromyricetin can activate autophagy through inhibiting mTOR signaling. Dihydromyricetin suppresses the formation of mTOR complexes (mTORC1/2). Dihydromyricetin is also a potent influenza RNA-dependent RNA polymerase inhibitor with an IC50 of 22 μM.
    Dihydromyricetin-d<sub>4</sub>
  • HY-N14131
    Cyclothialidine D
    Inhibitor
    Cyclothialidine D inhibits escherichia coli DNA helicases with an IC50 of 0.7 μM.
    Cyclothialidine D
  • HY-154031
    3'-F-3'-dA(Bz)-2'-Phosphoramidite
    3'-F-3'-dA(Bz)-2'-Phosphoramidite is a phosphorite monomer that can be used in the synthesis of oligonucleotides.
    3'-F-3'-dA(Bz)-2'-Phosphoramidite
  • HY-W794486
    5'-O-DMTr-2'-O-tert-Butyldimethylsilyl-nebularine-3′-CE phosphoramidite
    (2r,3r,4r,5r)-2-((Bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-((tert-Butyldimethylsilyl)oxy)-5-(9h-purin-9-yl)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
    5'-O-DMTr-2'-O-tert-Butyldimethylsilyl-nebularine-3′-CE phosphoramidite
  • HY-164181
    Fmoc-protected DMT-Dt PEG2 NH2 amidite
    Fmoc-protected DMT-Dt PEG2 NH2 amidite is a phosphoramidite monomer.
    Fmoc-protected DMT-Dt PEG2 NH2 amidite
  • HY-154080
    5'-O-DMTr-2'-FU-methyl phosphonamidite
    5’-O-DMTr-2’-FU-methyl phosphonamidite, 5’-O-DMTr-2’-deoxy-2’-fluorouridine-3’-O-(P-methyl-N,N-diisopropylamino) phosphonamidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
    5'-O-DMTr-2'-FU-methyl phosphonamidite
  • HY-157904
    Abasic II phosphoramidite
    Abasic II phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
    Abasic II phosphoramidite
  • HY-154368
    DMTr-MOE-Inosine-3-CED-phosphoramidite
    DMTr-MOE-Inosine-3-CED-phosphoramidite is a phosphorite monomer that can be used in the synthesis of oligonucleotides.
    DMTr-MOE-Inosine-3-CED-phosphoramidite
  • HY-182154
    8-Oxo-dA-CE phosphoramidite
    8-Oxo-dA-CE phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
    8-Oxo-dA-CE phosphoramidite
  • HY-174226
    RNA binder 2
    Ligand
    RNA binder 2 (Compound 20) is a covalent inhibitor targeting the r(CUG)exp RNA in myotonic dystrophy type 1 (DM1). RNA binder 2 binds to RNA via a Hoechst scaffold, blocking MBNL1 binding and restoring normal splicing. RNA binder 2 is promising for research of DM1.
    RNA binder 2
  • HY-117247
    5,6,7,8-Tetrahydro-8-deazahomofolic acid
    5,6,7,8-Tetrahydro-8-deazahomofolic acid is a potential thymidylate synthase (TS) inhibitor with inhibitory activity against other folate-related enzymes. 5,6,7,8-Tetrahydro-8-deazahomofolic acid showed mild growth inhibition against enterococci, lactic acid bacteria, and L1210 cells in culture. 5,6,7,8-Tetrahydro-8-deazahomofolic acid also showed weak inhibition against thymidylate synthase, dihydrofolate reductase, glycyl-ribonucleoside aminotransferase, and aminoimidazole-carboxyacyl-ribonucleoside aminotransferase. 5,6,7,8-Tetrahydro-8-deazahomofolic acid showed low substrate activity for thymidylate synthase.
    5,6,7,8-Tetrahydro-8-deazahomofolic acid
  • HY-182193
    5-I-dC-CE Phosphoramidite
    5-I-dC-CE Phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
    5-I-dC-CE Phosphoramidite
  • HY-116113
    SJP-L-5
    Inhibitor
    SJP-L-5 is an HIV-1 capsid dissociation inhibitor. SJP-L-5 exhibits inhibitory activity against multiple HIV-1 strains, with an EC50 ranging from 0.16 to 0.97 μg/mL. SJP-L-5 inhibits viral infection by blocking HIV-1 viral DNA entry into the nucleus. SJP-L-5 can be used in HIV-1 infection research.
    SJP-L-5
  • HY-43049
    DMT-2'O-TBDMS-rA(bz) Phosphoramidite enantiomer
    DMT-2'O-TBDMS-rA(bz) Phosphoramidite enantiomer is a phosphoramidite that can be used in the synthesis of oligonucleotides.
    DMT-2'O-TBDMS-rA(bz) Phosphoramidite enantiomer
  • HY-W579407
    DMT-2'-OMe-dA(bz) phosphoramidite
    DMT-2'-OMe-dA(bz) phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
    DMT-2'-OMe-dA(bz) phosphoramidite
  • HY-W013514R
    2-Acetamidofluorene (Standard)
    Inhibitor
    2-Acetamidofluorene is a potent carcinogenan. 2-Acetamidofluorene is can be used fot induction of hepatocellular carcinoma (HCC) and multiple primary tumours.
    2-Acetamidofluorene (Standard)
  • HY-W784560
    DMTr-3'-O-TBDMS-rG(iBu)-CE Phosphoramidite
    (2S,3S,4S,5S)-2-((Bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-((tert-butyldimethylsilyl)oxy)-5-(2-isobutyramido-6-oxo-3,6-dihydro-9H-purin-9-yl)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
    DMTr-3'-O-TBDMS-rG(iBu)-CE Phosphoramidite
  • HY-204951
    5'-O-DMT-2'-OMe-5-F-4-S-CE-U-3'-CE Phosphoramidite
    (2R,3R,4R,5R)-2-((Bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-5-(4-((2-cyanoethyl)thio)-5-fluoro-2-oxopyrimidin-1(2H)-yl)-4-methoxytetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
    5'-O-DMT-2'-OMe-5-F-4-S-CE-U-3'-CE Phosphoramidite
  • HY-175468
    RNA polymerase-IN-3
    Inhibitor
    RNA polymerase-IN-3 (Compound 28) is a bacterial RNA polymerase (RNAP) inhibitor with antibacterial activity. RNA polymerase-IN-3 inhibits RNA synthesis by competitively blocking the binding of UTP to RNAP (IC50= 0.28 μM). RNA polymerase-IN-3 is promising for research of bacterial infections.
    RNA polymerase-IN-3
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