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-W015490R
    1,4-Naphthoquinone (Standard)
    Inhibitor
    1,4-Naphthoquinone is an inhibitor with broad-spectrum inhibitory activity targeting DNA polymerase, NF-κB and monoamine oxidase (MAO-A/B), with antibacterial and anti-biofilm efficacy. 1,4-Naphthoquinone is a competitive inhibitor of MAO-B (Ki=1.4 μM) and a non-competitive inhibitor of MAO-A (Ki=7.7 μM). 1,4-Naphthoquinone inhibits DNA polymerase pol α, β, γ, δ, ε, λ with IC50 ranging from 5.57-128 μM. 1,4-Naphthoquinone inhibits tumor cell proliferation, induces apoptosis and necrosis, and has anti-angiogenic and anti-inflammatory activities by inducing oxidative stress, depleting glutathione (GSH), inhibiting DNA polymerase-mediated DNA synthesis and blocking NF-κB nuclear translocation. 1,4-Naphthoquinone can be used in anti-bacterial , anti-tumor and anti-inflammatory studies, including inhibition of melanoma and colon cancer cell growth and endothelial cell function, as well as LPS-induced inflammation models.
    1,4-Naphthoquinone (Standard)
  • HY-W141393
    2'-OMe-dmf-G-CE-Phosphoramidite
    2'-OMe-dmf-G-CE-Phosphoramidite is a phosphorite monomer that can be used in the synthesis of oligonucleotides.
    2'-OMe-dmf-G-CE-Phosphoramidite
  • HY-W042357
    Ac-rC Phosphoramidite
    98.87%
    Ac-rC Phosphoramidite is a phosphoramidite containing 5’ DMT and the nucleoside cytiding with Acetyl base protection. Ac-rC Phosphoramidite is used for the oligoribonucleotide phosphorodithioate modification (PS2-RNA).
    Ac-rC Phosphoramidite
  • HY-W235043
    Methyl 3-oxodecanoate
    Methyl 3-Oxodecanoate has been shown to have virulence factor activity against human pathogens and is active against fluorescent haplophyllum and culture supernatant. Methyl 3-oxodecanoate has also been shown to inhibit DNA synthesis by inhibiting protein synthesis at the level of translation initiation. Reagent grade, for research purpose.
    Methyl 3-oxodecanoate
  • 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-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-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-N13716
    Lucidenic acid O
    Inhibitor
    Lucidenic acid O is a terpene compound, is a DNA polymerases inhibitor. Lucidenic lactone inhibits calf DNA polymerase-α, rat DNA polymerase-β, and HIV-1 reverse transcriptase with IC50 values of 42 μM, 99 μM, and 69 μM, respectively.
    Lucidenic acid O
  • 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-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-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
  • HY-122462
    Ladirubicin
    Inhibitor
    Ladirubicin (PNU-159548) is a derivative of Daunorubicin (HY-13062A). Ladirubicin exhibits DNA intercalation and DNA alkylating properties, inhibits DNA replication and transcription, causes DNA damage, and thereby exhibits antitumor efficacy. Ladirubicin exhibits the potential to penetrate the blood-brain barrier (BBB) for its high lipophilicity. Ladirubicin exhibits toxicity through suppression of bone marrow activity.
    Ladirubicin
  • HY-120747
    A-65282
    Inhibitor
    A-65282 is an antibacterial agent. A-65282 inhibits P4 DNA unknotting with an IC50 value of 8 µg/mL. A 65281 induces DNA breakage mediated by calf thymus topoisomerase II.
    A-65282
  • HY-154708
    N-DMTr-N6-Benzoyl-morpholino-A-5'-O-phosphoramidite
    N-DMTr-N6-Benzoyl-morpholino-A-5'-O-phosphoramidite is a phosphorite monomer that can be used in the synthesis of oligonucleotides.
    N-DMTr-N6-Benzoyl-morpholino-A-5'-O-phosphoramidite
Cat. No. Product Name / Synonyms Application Reactivity