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-W1121733
    TFA-Amino-C12-CE-phosphoramidite
    2-Cyanoethyl (12-(2,2,2-trifluoroacetamido)dodecyl) diisopropylphosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
    TFA-Amino-C12-CE-phosphoramidite
  • HY-176891
    Cyslopentenyl cytosine triphosphoric
    Inhibitor
    Cyslopentenyl cytosine triphosphoric is an active metabolite of the antitumor nucleoside analogue cyclopentenyl cytosine (CPEC) within cells. Cyslopentenyl cytosine triphosphoric can inhibit CTP synthetase and deplete the pools of cytidine nucleotides. Cyslopentenyl cytosine triphosphoric can be used for the research of cancer, such as leukemia.
    Cyslopentenyl cytosine triphosphoric
  • HY-W1119956
    5’-(E)-VPG Phosphoramidite
    5'-(E)-VPG Phosphoramidite (5'(E)-VP-2'-OMe-iBu-GPhosphoramidite) is a structurally modified phosphoramidite reagent used to synthesize biologically stable oligonucleotides. 5'-(E)-VPG Phosphoramidite (POM) carries a VP protecting group and can be coupled to the target oligonucleotide at the 5' end via solid-phase synthesis. The modified oligonucleotide is then constructed through oxidation and deprotection steps. 5'-(E)-VPG Phosphoramidite is suitable for RNAi and viral replication research.
    5’-(E)-VPG Phosphoramidite
  • HY-154709
    N-DMTr-N2-Isobutyryl-morpholino-G-5'-O-phosphoramidite
    N-DMTr-N2-Isobutyryl-morpholino-G-5'-O-phosphoramidite is a phosphorite monomer that can be used in the synthesis of oligonucleotides.
    N-DMTr-N2-Isobutyryl-morpholino-G-5'-O-phosphoramidite
  • HY-182148
    dA-Thiophosphoramidite
    dA-Thiophosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
    dA-Thiophosphoramidite
  • HY-145913
    m7GpppApG
    m7GpppApG is a trinucleotide mRNA 5' cap analog that can be used for RNA synthesis in vitro.
    m7GpppApG
  • HY-100468R
    REV7/REV3L-IN-1 (Standard)
    Inhibitor
    REV7/REV3L-IN-1 (Standard) is the analytical standard of REV7/REV3L-IN-1 (HY-100468). This product is intended for research and analytical applications. REV7/REV3L-IN-1 is a REV7/REV3L interaction inhibitor with an IC50 of 78 μM. REV7/REV3L-IN-1 binds directly to REV7 and inhibits its interaction with REV3L. REV7/REV3L-IN-1 inhibits interstrand crosslink repair in cells. REV7/REV3L-IN-1 chemosensitizes cancer cells to Cisplatin (HY-17394). REV7/REV3L-IN-1 can be used in cervical cancer research.
    REV7/REV3L-IN-1 (Standard)
  • HY-W265757R
    4-Ethylcatechol (Standard)
    Inhibitor
    4-Ethylcatechol is a ring-dihydroxylated metabolite of 4-Ethylphenol that leads to oxidative DNA damage.
    4-Ethylcatechol (Standard)
  • HY-W356181
    4,8-DiMeIQx
    Inhibitor
    4,8-DiMeIQx is an orally active mutagen, selective dopaminergic neurotoxicant, and DNA damaging agent. 4,8-DiMeIQx can be isolated from cooked beef, sausage, pork, and chicken. 4,8-DiMeIQx induces reverse mutations in *Salmonella typhimurium* TA98 in the presence or absence of S9 mix, and forms DNA adducts in vivo in rat liver. 4,8-DiMeIQx exhibits selective neurotoxicity toward dopaminergic neurons. 4,8-DiMeIQx shows no activity against non-dopaminergic neurons. 4,8-DiMeIQx can be used in studies related to Parkinson's disease and colorectal cancer.
    4,8-DiMeIQx
  • HY-136597R
    Remdesivir O-desphosphate acetonide impurity (Standard)
    Inhibitor
    Remdesivir O-desphosphate acetonide impurity (Standard) is the analytical standard of Remdesivir O-desphosphate acetonide impurity. This product is intended for research and analytical applications.
    Remdesivir O-desphosphate acetonide impurity (Standard)
  • HY-W714964
    DMTr-TMS-alkynyl-dT phosphoramidite
    (2R,3S,5R)-2-((Bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-5-(2,4-dioxo-5-(8-(trimethylsilyl)octa-1,7-diyn-1-yl)-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-TMS-alkynyl-dT phosphoramidite
  • HY-154388
    5'-O-DMT-2'-O-TBS-5-MeO-U-3'-CE Phosphoramidite
    5’-O-DMTr-2’-O-TBDMS-5-methoxyuridine-3’-(cyanoethyl-N,N-diisopropyl)phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
    5'-O-DMT-2'-O-TBS-5-MeO-U-3'-CE Phosphoramidite
  • HY-14519AR
    Methotrexate disodium (Standard)
    Inhibitor
    Methotrexate (disodium) (Standard) is the analytical standard of Methotrexate (disodium). This product is intended for research and analytical applications. Methotrexate (Amethopterin) disodium, an antimetabolite and antifolate agent, inhibits the enzyme dihydrofolate reductase, thereby preventing the conversion of folic acid into tetrahydrofolate, and inhibiting DNA synthesis. Methotrexate disodium, also an immunosuppressant and antineoplastic agent, is used for the research of rheumatoid arthritis and a number of different cancers (such as acute lymphoblastic leukemia).
    Methotrexate disodium (Standard)
  • HY-W010832R
    Uridine-5'-diphosphate disodium salt (Standard)
    Activator
    Uridine-5'-diphosphate disodium salt is a potent, selective P2Y6 receptor native agonist (EC50=300 nM; pEC50=6.52 for human P2Y6 receptor). Uridine-5'-diphosphate disodium salt, an endogenous metabolite, catalyzes the glucuronidation of a wide array of substrates and is used in nucleic acid (RNA) biosynthesis.
    Uridine-5'-diphosphate disodium salt (Standard)
  • HY-W877828
    2-OMe A(Bz) OMe-amidite
    (2R,3R,4R,5R)-5-(6-Benzamido-9H-purin-9-yl)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-methoxytetrahydrofuran-3-yl methyl diisopropylphosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
    2-OMe A(Bz) OMe-amidite
  • HY-182186
    ACT trimer phosphoramidite
    ACT trimer phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
    ACT trimer phosphoramidite
  • HY-N2033R
    Chebulinic acid (Standard)
    Inhibitor
    Chebulinic acid (Standard) is the analytical standard of Chebulinic acid. This product is intended for research and analytical applications. Chebulinic acid is a potent natural inhibitor of M. tuberculosis DNA gyrase, also can inhibit SMAD-3 phosphorylation, inhibit H+ K+-ATPase activity.
    Chebulinic acid (Standard)
  • HY-10241R
    Simeprevir (Standard)
    Inhibitor
    Simeprevir (Standard) is the analytical standard of Simeprevir (HY-10241). This product is intended for research and analytical applications. Simeprevir (TMC435; TMC435350) is an oral, potent and highly specific hepatitis C virus (HCV) NS3/4A protease inhibitor with a Ki of 0.36 nM. Simeprevir inhibits HCV replication with an EC50 of 7.8 nM. Simeprevir also potently suppresses SARS-CoV-2 replication and synergizes with Remdesivir. Simeprevir inhibits the main protease (Mpro) and the RNA-dependent RNA polymerase (RdRp) of SARS-CoV-2, and also modulates host immune responses.
    Simeprevir (Standard)
  • HY-N19821
    Gangaleoidin
    Inhibitor
    Gangaleoidin is a FOXM1 inhibitor with an IC50 of 2.8 μM. Gangaleoidin inhibits interaction between FOXM1’s DNA-binding domain and target DNA sequence, downregulates FOXM1 and downstream target gene CCNB1 at the transcriptional level. Gangaleoidin suppresses proliferation of FOXM1-overexpressing breast cancer cells. Gangaleoidin can be used for the research of breast cancer.
    Gangaleoidin
  • HY-168345
    Ap4dT tetraammonium
    99.88%
    Ap4dT 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.
    Ap4dT tetraammonium
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