2. Oligonucleotides
  3. Nucleosides and their Analogs Nucleotides and their Analogs Nucleoside Phosphoramidites
  4. U

U

Uracil

U (34):

Cat. No. Product Name CAS No. Purity Chemical Structure
  • HY-148506
    5'-ODMT cEt m5U Phosphoramidite (Amidite) 1197033-22-9 99.25%
    5'-ODMT cEt m5U Phosphoramidite Amidite is a locked nucleic acid (LNA) analog. 5'-ODMT cEt m5U Phosphoramidite Amidite shows excellent safety and antisense activity in mice.
    5'-ODMT cEt m5U Phosphoramidite (Amidite)
  • HY-45409
    DMT-2′Fluoro-dU Phosphoramidite 146954-75-8 99.98%
    DMT-2’ Fluoro-dU Phosphoramidite (2'-F-dU Phosphoramidite) is a uridine phosphoramidite with a fluorine in the 2’ position. DMT-2’ Fluoro-dU Phosphoramidite could be used for nucleoside modification and synthesis of DNA.
    DMT-2′Fluoro-dU Phosphoramidite
  • HY-W570886
    2'-O-MOE-U 163759-97-5
    2'-O-MOE-U is a phosphoramidite, can be used for oligonucleotide synthesis.
    2'-O-MOE-U
  • HY-W101391
    DMT-2'O-Methyl-rU Phosphoramidite 110764-79-9 99.70%
    DMT-2'O-Methyl-rU Phosphoramidite (2'-O-Me-U Phosphoramidite) is a 2'-O-Me derivative, and can be used for oligonucleotide synthesis.
    DMT-2'O-Methyl-rU Phosphoramidite
  • HY-W102322
    5'-O-DMT-2'-TBDMS-Uridine 81246-80-2 99.11%
    5'-O-DMT-2'-TBDMS-Uridine is a deoxyribonucleoside used for the oligonucleotide synthesis.
    5'-O-DMT-2'-TBDMS-Uridine
  • HY-W048482
    rU Phosphoramidite 118362-03-1 99.22%
    rU Phosphoramidite is a phosphorite monomer that can be used in the synthesis of oligonucleotides.
    rU Phosphoramidite
  • HY-111531
    DMTr-LNA-5MeU-3-CED-phosphoramidite 206055-75-6 98.75%
    DMTr-LNA-5MeU-3-CED-phosphoramidite is a nucleoside derivative.
    DMTr-LNA-5MeU-3-CED-phosphoramidite
  • HY-154366
    5'-DMT-2'-O-TBDMS-N1-Methyl-PseudoUridine-CE-Phosphoramidite 875302-45-7 ≥98.0%
    5'-DMT-2'-O-TBDMS-N1-Methyl-PseudoUridine-CE-Phosphoramidite is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc.
    5'-DMT-2'-O-TBDMS-N1-Methyl-PseudoUridine-CE-Phosphoramidite
  • HY-104016
    2'-O-MOE-5MeU-3'-phosphoramidite 163878-63-5
    2'-O-MOE-5MeU-3'-phosphoramidite is a phosphorite monomer that can be used in the synthesis of oligonucleotides.
    2'-O-MOE-5MeU-3'-phosphoramidite
  • HY-W570892
    DMTr-LNA-U-3-CED-Phosphora 206055-76-7
    DMTr-LNA-U-3-CED-phosphora is a phosphorite monomer that can be used in the synthesis of oligonucleotides.
    DMTr-LNA-U-3-CED-Phosphora
  • HY-150017
    2'-O-Methyl-5-methyl-U CEP 153631-20-0 ≥98.0%
    2'-O-Methyl-5-methyl-U CEP is a uridine, can be used for synthesis nucleic acid.
    2'-O-Methyl-5-methyl-U CEP
  • HY-132136
    DMT-dU-CE Phosphoramidite 109389-30-2 99.75%
    DMT-dU-CE Phosphoramidite is a nucleoside molecule that can be used in DNA synthesis and DNA sequencing.
    DMT-dU-CE Phosphoramidite
  • HY-D1409
    DMTr-4'-F-U-CED-TBDMS phosphoramidite
    DMTr-4'-F-U-CED-TBDMS phosphoramidite (DMTr-4'-F-uridine-CED-TBDMS phosphoramidite), a dye reagent for oligonucleotide labeling, can be used for the research of applications in RNA therapeutics, RNA aptamers, and ribozymes for elucidating RNA structure. DMTr-4'-F-U-CED-TBDMS phosphoramidite represents a probe with wide utility for elucidation of RNA structure.
    DMTr-4'-F-U-CED-TBDMS phosphoramidite
  • HY-D1408
    DMTr-4'-Me-U-CED-TBDMS phosphoramidite 1260508-74-4
    DMTr-4'-Me-U-CED-TBDMS phosphoramidite (DMTr-4'-Methyluridine-CED-TBDMS phosphoramidite), a dye reagent for oligonucleotide labeling, can be used for the research of applications in RNA therapeutics, RNA aptamers, and ribozymes for elucidating RNA structure. DMTr-4'-Me-U-CED-TBDMS phosphoramidite represents a probe with wide utility for elucidation of RNA structure.
    DMTr-4'-Me-U-CED-TBDMS phosphoramidite
  • HY-D1410
    DMTr-4'-F-5-Me-U-CED phosphoramidite 2758388-05-3
    DMTr-4'-F-5-Me-U-CED phosphoramidite (DMTr-4'-F-5-Methyluridine-CED phosphoramidite), a dye reagent for oligonucleotide labeling, acts as efficient as the incorporation of native deoxyribonucleoside phosphoramidites. DMTr-4'-F-5-Me-U-CED phosphoramidite is a building block.
    DMTr-4'-F-5-Me-U-CED phosphoramidite
  • HY-151750
    Pyrene phosphoramidite dU 199920-17-7
    Pyrene phosphoramidite Du is a click chemistry reagent containing pyrene groups. The pyrene group in Pyrene phosphoramidite Du can be inserted into DNA with strong blue fluorescence.
    Pyrene phosphoramidite dU
  • HY-134337
    5'-O-DMTr-3'-O-methyl uridine-3'-CED-phosphoramidite 179479-05-1
    5'-O-DMTr-3'-O-methyl uridine-3'-CED-phosphoramidite is a uridine analog. Uridine has potential antiepileptic effects, and its analogs can be used to study anticonvulsant and anxiolytic activities, as well as to develop new antihypertensive agents.
    5'-O-DMTr-3'-O-methyl uridine-3'-CED-phosphoramidite
  • HY-154223
    5'-O-(4,4'-Dimethoxytrityl)-2'-O-methyl-2-thiouridine 302918-83-8
    5'-O-(4,4'-Dimethoxytrityl)-2'-O-methyl-2-thiouridine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc.
    5'-O-(4,4'-Dimethoxytrityl)-2'-O-methyl-2-thiouridine
  • HY-154525
    2’-Deoxy-2’-(N-trifluoroacetyl)amino-5’-O-DMTr-uridine 3’-CED phosphoramidite 126139-44-4
    2’-Deoxy-2’-(N-trifluoroacetyl)amino-5’-O-DMTr-uridine 3’-CED phosphoramidite is a uridine analog. Uridine has potential antiepileptic effects, and its analogs can be used to study anticonvulsant and anxiolytic activities, as well as to develop new antihypertensive agents.
    2’-Deoxy-2’-(N-trifluoroacetyl)amino-5’-O-DMTr-uridine 3’-CED phosphoramidite
  • HY-154238
    5’-O-DMTr-3’-deoxyuridine 2’-CED phosphoramidite 161503-98-6
    5’-O-DMTr-3’-deoxyuridine 2’-CED phosphoramidite is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc.
    5’-O-DMTr-3’-deoxyuridine 2’-CED phosphoramidite