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  • Nucleoside Antimetabolite/Analog
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Results for "

oligonucleotide

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    51
    TargetMol | Inhibitors_Agonists
  • Dye Reagents
    25
    TargetMol | Dye_Reagents
  • PROTAC Products
    1
    TargetMol | PROTAC
  • Natural Products
    2
    TargetMol | Natural_Products
  • Recombinant Protein
    4
    TargetMol | Recombinant_Protein
2'-Fluoro-2'-Deoxyadenosine
T972764183-27-3
2'-Fluoro-2'-Deoxyadenosine is efficiently cleaved to the toxic 2-fluoroadenine (FAde) by Escherichia coli purine nucleoside phosphorylase (PNP). 2'-Fluoro-2'-Deoxyadenosine showed good in vivo activity against tumors expressing E. coli PNP. 2'-Fluoro-2'-Deoxyadenosine can be used to synthesize 2'-deoxy-2'-fluoromodified oligonucleotides that can hybridize to RNA.
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TargetMol | Inhibitor Sale
CL097
CL097
T384231026249-18-2
CL097 is an effective agonist of TLR7 and TLR8. CL097 induces pro-inflammatory cytokines in macrophages and NADPH oxidase priming, thereby increasing the fMLF-stimulated ROS production.
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UNC10217938A HCl
UNC7938 HCl, UNC10217938A HCl(1347749-97-6 Free base)
T13254L In house
UNC10217938A HCl (UNC7938 HCl) is a 3-deazapteridine analog. UNC10217938A HCl exhibits strong oligonucleotide enhancing effects. UNC10217938A HCl can modulate their intracellular trafficking and release from endosomes, leading to enhance oligonucleotides effects. UNC10217938A HCl also enhances the effects of siRNA and antisense oligonucleotides.
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Paromomycin Sulfate
Paromomycin sulfate salt, Aminosidine sulfate
T11041263-89-4
Paromomycin binds specifically to the RNA oligonucleotide at the A site of bacterial 30S ribosomes, thereby causing misreading and premature termination of translation of mRNA and inhibition of protein synthesis followed by cell death. Paromomycin Sulfate (Aminosidine sulfate) is the sulfate salt form of paromomycin, a structural derivative of neomycin, an aminoglycoside antibiotic with amebicidal and bactericidal effects against predominantly aerobic gram-negative bacteria.
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TargetMol | Citations Cited
Dmt-2'fluoro-da(bz) amidite
T36752136834-22-5
Dmt-2'fluoro-da(bz) amidite is a 2'-deoxy-2'-fluoro-phosphorothioate oligonucleotide with high affinity and specificity for RNA targets and serves as an intermediate in the synthesis of 5'-DMT-3'-phosphoramidite, an antisense compound resistant to nuclease.
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7-10 days
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5'-O-DMT-N2-ibu-dG
N2-Isobutyryl-5'-O-(4,4'-dimethoxytrityl)-2'-deoxyguanosine, iBu-DMT-dG
T4080068892-41-1
5'-O-DMT-N2-ibu-dG is a deoxynucleoside used in the preparation of oligonucleotides, served as a building block in oligonucleotide synthesis, with protecting groups to prevent unwanted reactions during synthesis.
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7-10 days
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5-Methoxysalicylic acid
5-MeOSA
T58882612-02-4
5-Methoxysalicylic acid (5-MeOSA), a natural product, serves as an effective matrix for oligonucleotide analysis in MALDI MS when used alongside spermine.
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TargetMol | Inhibitor Sale
DMTr-LNA-5MeU-3-CED-phosphoramidite
T13659206055-75-6
DMTr-LNA-5MeU-3-CED-phosphoramidite, a nucleoside derivative, is a modified building block used in oligonucleotide synthesis to enhance stability and binding affinity.
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UNC10217938A
T132541347749-97-6
UNC10217938A is a 3-deazapteridine analog, has strong oligonucleotide enhancing effects.
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1-2 weeks
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Tos-PEG3
T1712977544-68-4
Tos-PEG3, a PEG-based PROTAC linker, is suitable for synthesizing PROTACs and 3'-aminooxy oligonucleotide solid supports[1].
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7-10 days
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Decamethylene glycol
alpha,omega-Decanediol,Decamethylenediol,1,10-Dihydroxydecane,Decane-1,10-diol
T21096112-47-0
Decamethylene glycol is a substance used as a reagent in the biological study of modified oligonucleotide with in vivo antitumoral activity. Also used in the pharmaceutical study on the composition of essential oils obtained from myrrh and frankincense an
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DMT-dC(ac) Phosphoramidite
T36753154110-40-4
DMT-dC(ac) Phosphoramidite is a modified phosphoramidite monomer designed for oligonucleotide synthesis.
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7-10 days
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DMT-dG(dmf) Phosphoramidite
T36755330628-04-1
DMT-dG(dmf) Phosphoramidite is a phosphinamide monomer used in oligonucleotide synthesis.
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7-10 days
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2'-O-Me-C(Bz) Phosphoramidite
T37102110764-78-8
2'-O-Me-C(Bz) Phosphoramidite is a modified phosphoramidite monomer utilized in oligonucleotide synthesis.
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7-10 days
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2'-OMe-A(Bz) Phosphoramidite
T37103110782-31-5
2'-OMe-A(Bz) Phosphoramidite is a modified phosphoramidite monomer used in oligonucleotide synthesis.
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7-10 days
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2'-OMe-G(ibu) Phosphoramidite
T37104150780-67-9
2'-OMe-G(ibu) Phosphoramidite is a modified phosphoramidite monomer suitable for oligonucleotide synthesis.
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7-10 days
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5'-O-DMT-2'-TBDMS-Uridine
T3713381246-80-2
5'-O-DMT-2'-TBDMS-Uridine is a deoxyribonucleoside used for the oligonucleotide synthesis.
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7-10 days
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5'-O-DMT-PAC-dA
T37139110522-82-2
5'-O-DMT-PAC-dA can be used in the synthesis of oligoribonucleotides[1]. [1]. Schulhof JC, et, al. The final deprotection step in oligonucleotide synthesis is reduced to a mild and rapid ammonia treatment by using labile base-protecting groups. Nucleic Acids Res. 1987 Jan 26;15(2):397-416.
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5'-O-DMT-2'-O-TBDMS-N-Bz-Adenosine
T3714681265-93-2
5'-O-DMT-2'-O-TBDMS-N-Bz-Adenosine, an adenosine derivative, functions as an intermediate in oligonucleotide synthesis.
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7-10 days
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Ac-dA Phosphoramidite
T384251027734-01-5
Ac-dA Phosphoramidite is a phosphinamide monomer utilized in oligonucleotide synthesis.
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Bz-rC Phosphoramidite
T38566118380-84-0
Bz-rC Phosphoramidite is a phosphinamide monomer used in oligonucleotide synthesis.
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Nusinersen
T386561258984-36-9
Nusinersen (nusinersen) is an antisense oligonucleotide (ASO) for the treatment of pediatric and adult spinal muscular atrophy (SMA) that alters the way the SMN2 gene is processed and increases the production of SMN proteins, which are deficient in SMA patients.
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7-Deaza-2'-deoxy-7-iodoadenosine
T39141166247-63-8
7-Deaza-2'-deoxy-7-iodoadenosine is a modified oligonucleotide featuring 7-Deazaadenine.
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7-10 days
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5'-O-DMT-dT
5'-O-DMT-dT,5'-O-(4,4'-Dimethoxytrityl)thymidine
T4050640615-39-2
5'-O-DMT-dT (5'-O-(4,4'-Dimethoxytrityl)thymidine) is a nucleoside derivative used in oligonucleotide synthesis.
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7-10 days
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