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-N14898
    Oudermansin B
    Oudermansin B is an antibiotic. Oudermansin B acts on fungi to inhibit protein, RNA and DNA synthesis.
    Oudermansin B
  • HY-W784559
    DMTr-3'-O-TBDMS-rU-CE Phosphoramidite
    (2S,3S,4S,5S)-2-((Bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-((tert-butyldimethylsilyl)oxy)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
    DMTr-3'-O-TBDMS-rU-CE Phosphoramidite
  • HY-183466
    Morpholino C monomer
    Morpholino C monomer is a morpholino cytosine monomer and can be used for the synthesis of oligonucleotides.
    Morpholino C monomer
  • HY-102020R
    RG3039 (Standard)
    RG3039 (Standard) is the analytical standard of RG3039 (HY-102020). This product is intended for research and analytical applications. RG3039 (PF-06687859) is an orally active, blood-brain barrier-permeable DcpS inhibitor with an IC50 of 4.2 nM against hDcpS. RG3039 inhibits the decapping activity of DcpS and maintains DcpS in a catalytically inactive conformation in the central nervous system and other tissues. RG3039 extends survival and improves function in spinal muscular atrophy mice. RG3039 is applicable to research related to spinal muscular atrophy.
    RG3039 (Standard)
  • HY-W008091A
    5-Methylcytosine hydrochloride
    99.57%
    5-Methylcytosine hydrochloride is a well-characterized DNA modification in prokaryotes and eukaryotes. 5-Methylcytosine hydrochloride forms symmetrical methylation on CpG dinucleotides in DNA, stabilizes tRNA/rRNA structure in RNA, and affects mRNA translation. 5-Methylcytosine hydrochloride can be oxidized to generate 5hmC, 5fC, and 5caC. 5-Methylcytosine hydrochloride can be used in epigenetics, developmental biology, and the study of diseases such as colorectal cancer and hepatocellular carcinoma.
    5-Methylcytosine hydrochloride
  • HY-125650A
    Pseudouridimycin TFA
    Inhibitor
    Pseudouridimycin (PUM) TFA is an antibiotic that selectively inhibits bacterial RNA polymerase (RNAP), with an IC50 of about 0.1 μM and MICs of 4-6 μg/mL. Pseudouridimycin TFA is a C-nucleoside analogue that's effective against both Gram-negative and Gram-positive bacteria. Pseudouridimycin TFA inhibits bacterial growth in vitro and shows activity in a mouse model of purulent streptococcal peritonitis.
    Pseudouridimycin TFA
  • HY-W784611
    3'-NH-Tr-2',3'-ddC(Bz)-5'-CE-Phosphoramidite
    3'-NH-Tr-2',3'-ddC(Bz)-5'-CE-Phosphoramidite is a phosphoramidite monomer used in nucleic acid synthesis, such as oligonucleotides.
    3'-NH-Tr-2',3'-ddC(Bz)-5'-CE-Phosphoramidite
  • HY-N0143R
    Phlorizin (Standard)
    Inhibitor
    Phlorizin (Floridzin) (Standard) is the analytical standard of Phlorizin. This product is intended for research and analytical applications. Phlorizin is an orally active non-selective sodium-glucose cotransporter (SGLT) inhibitor, with an IC50 of 0.04 μM and a Ki of 39 nM against hSGLT2, and an IC50 of 0.17 μM and a Ki of 0.31 μM against hSGLT1. Phlorizin promotes GLUT4 translocation, inhibits gluconeogenesis and promotes glycogen synthesis by activating the PI3K/Akt/mTOR pathway. Phlorizin reduces DNA damage and apoptosis (apoptosis) by inhibiting the NF-κB inflammatory pathway. Phlorizin induces apoptosis via activating the Caspase pathway by antagonizing the JAK/STAT3 and PCK pathways. Phlorizin also exhibits antibacterial, anti-inflammatory and neuroprotective activities.
    Phlorizin (Standard)
  • HY-W1121791
    DMT-2'O-TC-rU Phosphoramidite
    DMT-2'O-TC-rU Phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
    DMT-2'O-TC-rU Phosphoramidite
  • HY-119475
    Satranidazole
    Inhibitor
    Satranidazole is an orally active insecticide and antimicrobial agent with high electron affinity. Satranidazole forms reduced nitro intermediates, which interact with DNA, causing helix instability, strand breakage and release of thymidine derivatives. Satranidazole exhibits antitrichomonal activity against Trichomonas vaginalis and Trichomonas foetus, and antiamoebic activity in rodent models of hepatic amoebiasis and caecal amoebiasis. Satranidazole inhibits the replication of bacteriophage φX174 DNA. Satranidazole can be used in research related to caecal amoebiasis, trichomoniasis and anaerobic bacterial infections.
    Satranidazole
  • HY-168473
    13-TP
    Inhibitor
    13-TP is an inhibitor of SARS-CoV-2. 13-TP effectively inhibits the SARS-CoV-2 central replication transcription complex (C-RTC, nsp12-nsp7-nsp82) catalyzed in vitro RNA synthesis. 13-TP completely inhibits the RdRp polymerization activity. 13-TP blocks the full extension of some of the primer RNA.
    13-TP
  • HY-W592836
    5'-O-DMT-2-F-A-bicyclo[2.2.1]-CE phosphoramidite
    (1R,3R,4R,7S)-3-(6-Amino-2-fluoro-9H-purin-9-yl)-1-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-2,5-dioxabicyclo[2.2.1]heptan-7-yl (2-cyanoethyl) diisopropylphosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
    5'-O-DMT-2-F-A-bicyclo[2.2.1]-CE phosphoramidite
  • HY-W779262
    Cholesteryl-TEG Phosphoramidite
    Cholesteryl-TEG Phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
    Cholesteryl-TEG Phosphoramidite
  • HY-101813R
    Laflunimus (Standard)
    Inhibitor
    Laflunimus (Standard) is the analytical standard of Laflunimus. This product is intended for research and analytical applications. Laflunimus (HR325) is an immunosuppressive agent and an analogue of the Leflunomide-active metabolite A77 1726. Laflunimus is an orally active inhibitor of dihydroorotate dehydrogenase (DHODH). Laflunimus suppresses immunoglobulin (Ig) secretion, with IC50 values of 2.5 and 2 μM for IgM and IgG, respectively. Laflunimus also is a prostaglandin endoperoxide H synthase (PGHS) -1 and -2 inhibitor.
    Laflunimus (Standard)
  • HY-402301
    5'-Amino(Me)-modifier C6
    2-Cyanoethyl (6-(((4-methoxyphenyl)diphenylmethyl)(methyl)amino)hexyl) diisopropylphosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
    5'-Amino(Me)-modifier C6
  • HY-400877
    (E)-Azobenzene phosphoramidite
    (2S,3S)-4-(bis(4-Methoxyphenyl)(phenyl)methoxy)-3-(4-((E)-phenyldiazenyl)benzamido)butan-2-yl (2-cyanoethyl) diisopropylphosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
    (E)-Azobenzene phosphoramidite
  • HY-177385
    Morpholino C phosphoramidite
    Morpholino C phosphoramidite (Compound 4c) is a nucleoside building block that can be used for synthesis of morpholino oligonucleotides. Morpholino C phosphoramidite can be used for oligonucleotide therapies research.
    Morpholino C phosphoramidite
  • HY-164557
    3′-Deoxyadenosine 5′-triphosphate
    3′-Deoxyadenosine 5′-triphosphateCan be used for nucleic acid synthesis.
    3′-Deoxyadenosine 5′-triphosphate
  • HY-131102R
    Mequindox (Standard)
    Inhibitor
    Mequindox (Standard) is the analytical standard of Mequindox. This product is intended for research and analytical applications. Mequindox is an antimicrobial agent. Mequindox acts as an inhibitor of DNA synthesis. Mequindox induces genotoxicity and carcinogenicity in mice.
    Mequindox (Standard)
  • HY-134833
    5'-O-DMT-2'-O-TBS-DIB-Thienopyrimidine-formimidamide-3'-CE phosphoramidite
    (2R,3R,4S,5R)-2-((Bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-((tert-butyldimethylsilyl)oxy)-5-(4-(((E)-(diisobutylamino)methylene)amino)thieno[3,4-d]pyrimidin-7-yl)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
    5'-O-DMT-2'-O-TBS-DIB-Thienopyrimidine-formimidamide-3'-CE phosphoramidite
Cat. No. Product Name / Synonyms Application Reactivity

Your Search Returned No Results.

Sorry. There is currently no product that acts on isoform together.

Please try each isoform separately.