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-17580R
    Fidaxomicin (Standard)
    Inhibitor
    Fidaxomicin (Standard) is the analytical standard of Fidaxomicin. This product is intended for research and analytical applications. Fidaxomicin (OPT-80), a macrocyclic antibiotic, is an orally active and potent RNA polymerase inhibitor. Fidaxomicin has a narrow spectrum of antibacterial activity and a good anti-Clostridium difficile activity (MIC90=0.12 μg/mL). Fidaxomicin can be used for Clostridium difficile infection (CDI) research.
    Fidaxomicin (Standard)
  • HY-145972
    Cyanine 3-dCTP
    Cyanine 3-dCTP is a Cy3-labeled nucleotide and can be used for DNA synthesis.
    Cyanine 3-dCTP
  • HY-W1121746
    PC Linker phosphoramidite
    PC Linker phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
    PC Linker phosphoramidite
  • HY-B0220F
    Erythromycin (glutamate)
    Inhibitor
    Erythromycin glutamate is a macrolide antibiotic produced by actinomycete Streptomyces erythreus with a broad spectrum of antimicrobial activity. Erythromycin glutamate binds to bacterial 50S ribosomal subunits and inhibits RNA-dependent protein synthesis by blockage of transpeptidation and/or translocation reactions, without affecting synthesis of nucleic acid[1][2]. Erythromycin glutamate also exhibits antitumor and neuroprotective effect in different fields of research[3][4].
    Erythromycin (glutamate)
  • HY-164192
    m7(3'AcmG)(5')ppp(5')(2'OMeA)pG ammonium
    m7(3'AcmG)(5')ppp(5')(2'OMeA)pG ammonium, a cap analogue derived from patent WO2023159930A1, can be used for the synthesis of mRNA.
    m7(3'AcmG)(5')ppp(5')(2'OMeA)pG ammonium
  • HY-W725767
    DMTr-Guanosine-(N2-dimethylaminomethylene)-3'-CE-phosphoramidite
    (2R,3S,5R)-2-((Bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-5-(2-(((dimethylamino)methylene)amino)-9H-purin-9-yl)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
    DMTr-Guanosine-(N2-dimethylaminomethylene)-3'-CE-phosphoramidite
  • HY-182139
    2'-OMe-N6-Me-A-CE phosphoramidite
    2'-OMe-N6-Me-A-CE phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
    2'-OMe-N6-Me-A-CE phosphoramidite
  • HY-N15600
    Merulidial
    Inhibitor
    Merulidial (Compound 1) is an antibiotic and cytotoxic agent with a sesquiterpene dialdehyde structure. Merulidial significantly inhibits the germination of spores and the hyphal growth of the wood-roting basidiomycete Heterobasidion annosum (H. annosum) and the saprophytic mould Cladosporium cucumerinum (C.cucumerinum). Merulidial also inhibits a variety of bacteria, algae and DNA synthesis of ECA cells. Merulidial shows a strong anticancer activity with IC50 s of 20 and 10 μg/mL for ECA and L1210 cells, respectively .
    Merulidial
  • HY-107845R
    SCR7 pyrazine (Standard)
    Inhibitor
    SCR7 pyrazine (Standard) is the analytical standard of SCR7 pyrazine (HY-107845). This product is intended for research and analytical applications. SCR7 pyrazine is a DNA ligase IV inhibitor that blocks nonhomologous end-joining (NHEJ) in a ligase IV-dependent manner. SCR7 pyrazine increases the efficiency of Cas9-mediated homology-directed repair (HDR). SCR7 pyrazine induces cell apoptosis and has anticancer activity.
    SCR7 pyrazine (Standard)
  • HY-134013
    Piperitenone oxide
    Inhibitor
    Piperitenone oxide is an orally active monoterpene ketone. Piperitenone oxide can be isolated from the essential oils of plants belonging to Mentha x villosa and Ziziphora clinopodioides. Piperitenone oxide induces differentiation. Piperitenone oxide induces chromosome breakage damage, aneuploidy damage and DNA single-strand breaks. Piperitenone oxide reduces ET-1 levels. Piperitenone oxide exerts antihypertensive effects. Piperitenone oxide can be used in studies related to colon cancer.
    Piperitenone oxide
  • HY-17028R
    Besifloxacin Hydrochloride (Standard)
    Inhibitor
    Besifloxacin (Hydrochloride) (Standard) is a fourth generation fluoroquinolone antibiotic. Besifloxacin Hydrochloride (Standard) is a DNA gyrase and topoisomerase IV inhibitor. Besifloxacin Hydrochloride (Standard) has broad-spectrum antibacterial activity, it is effective against Gram-negative and Gram-positive aerobic and anaerobic strains and reduces the incidence of drug resistance. Besifloxacin Hydrochloride (Standard) has anti-inflammatory activity. Besifloxacin Hydrochloride (Standard) can be used in bacterial conjunctivitis research.
    Besifloxacin Hydrochloride (Standard)
  • HY-108988
    Albicidin
    Inhibitor
    Albicidin is a peptide antibiotic with phytotoxic activity. Albicidin potently inhibits bacterial and plant DNA gyrase at nanomolar concentrations, blocks DNA replication, and exhibits excellent antibacterial efficacy against multidrug-resistant bacteria. Albicidin possesses bactericidal activity against Gram-positive and Gram-negative microorganisms, and acts as a virulence factor for the systemic plant infection by Xanthomonas albilineans. Albicidin can be used in studies related to bacterial infections and sugarcane leaf blight.
    Albicidin
  • HY-W1121753
    5'-Stearyl phosphoramidite
    5'-Stearyl phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
    5'-Stearyl phosphoramidite
  • HY-185069B
    Unylinker-OH Resin (Substitution:250±25 µmol/g)
    Unylinker-OH Resin (Substitution:250±25 µmol/g) is a macroporous polystyrene resin functionalized with Unylinker active groups with uniform particle size and uniform active groups. It is used for oligonucleotides synthesis.
    Unylinker-OH Resin (Substitution:250±25 µmol/g)
  • HY-154068
    N-Trityl-morpholino-T-5’-O-phosphoramidite
    N-Trityl-morpholino-T-5’-O-phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
    N-Trityl-morpholino-T-5’-O-phosphoramidite
  • HY-182180
    8-Amino-dA-CE phosphoramidite
    8-Amino-dA-CE phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
    8-Amino-dA-CE phosphoramidite
  • HY-202321
    Pseudo-u-2ome-evp-pom phosphoramidite
    Pseudo-u-2ome-evp-pom phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
    Pseudo-u-2ome-evp-pom phosphoramidite
  • HY-145287A
    S-MGB-234 TFA
    S-MGB-234 TFA is a minor groove binder used for African Animal Trypanosomiasis (AAT). S-MGB-234 exhibits excellent in vitro activity against the primary pathogens of AAT: Trypanosoma congolense and Trypanosoma vivax. S-MGB-234 TFA does not show cross-resistance with current diamidine active molecules and is not internalized via the transporters used by diamidines.
    S-MGB-234 TFA
  • HY-154067
    N-Trityl-morpholino-U-5’-O-phosphoramidite
    N-Trityl-morpholino-U-5’-O-phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
    N-Trityl-morpholino-U-5’-O-phosphoramidite
  • HY-12926
    ST7612AA1
    ST7612AA1 is a histone deacetylase (HDAC) inhibitor that controls chromatin condensation and DNA transcription by removing acetyl groups from histones. ST7612AA1 is also a potent HIV reactivation inducer, and its reactivation activity is exerted without activating or proliferating CD4+T cells, and can be used in the study of HIV reactivation strategies and elimination of viral reservoirs.
    ST7612AA1
Cat. No. Product Name / Synonyms Application Reactivity

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