15 Results for "

nucleoside modification

" in MedChemExpress (MCE) Product Catalog:
Products (15)

15 Results for "nucleoside modification" in MCE Product Catalog:

4
4 Cited Publications
Cat. No.: HY-113137
CAS No.: 2140-67-2
Purity:  99.40%
N2,N2-Dimethylguanosine is a methylated modified nucleoside present in RNA and serves as a structural modification component of tRNA. N2,N2-Dimethylguanosine inhibits reverse transcriptase-mediated cDNA synthesis and is one of the key modifications affecting sequencing efficiency in high-throughput RNA sequencing. N2,N2-Dimethylguanosine can be selectively demethylated at one methyl group by AlkB mutant enzymes (such as D135S/L118V) and converted to N2-methylguanosine, thereby reducing the inhibition of reverse transcription .
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Cat. No.: HY-148503
CAS No.: 1197033-19-4
Purity:  98.55%
Research Areas:  

Others

5'-ODMT cEt N-Bz A Phosphoramidite (Amidite) is a nucleoside phosphoramidite monomer used to synthesize locked nucleic acid (LNA) analog oligonucleotides. It can be used as a building block of antisense oligonucleotides (ASOs) to target complementary RNA sequences. 5'-ODMT cEt N-Bz A Phosphoramidite (Amidite) locks the furanose ring into an N-type conformation through 2',4'-constrained ethyl (cEt) modification, enhancing hybridization affinity and mismatch discrimination with RNA, while significantly improving the resistance of oligonucleotides to exonuclease digestion. 5'-ODMT cEt N-Bz A Phosphoramidite (Amidite) mediates RNase H-dependent mRNA degradation or inhibits translation by forming a stable hybrid with RNA, thereby achieving gene expression regulation. 5'-ODMT cEt N-Bz A Phosphoramidite (Amidite) is mainly used in the development of antisense drugs, gene function research and oligonucleotide synthesis related to disease treatment .
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Cat. No.: HY-45409
CAS No.: 146954-75-8
Synonyms: 2'-F-dU Phosphoramidite
Research Areas:  

Cancer

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 .
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Cat. No.: HY-Y0973
CAS No.: 56602-33-6
BOP hexafluorophosphate is a phosphonium-type condensing agent. BOP hexafluorophosphate activates the carboxylic acid component to form a highly reactive O-benzotriazole ester (active ester) intermediate, which then reacts with the amino component to form an amide bond (peptide bond). BOP hexafluorophosphate is applicable to solid-phase polypeptide synthesis and nucleoside modification .
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Cat. No.: HY-138603
CAS No.: 146954-77-0
Purity:  99.85%
5'-O-DMT-N4-Bz-2'-F-dC is a nucleoside with protective and modification effects.
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Cat. No.: HY-138597
CAS No.: 40733-28-6
Purity:  99.43%
5'-O-TBDMS-dT is a nucleoside with protective and modification effects.
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Cat. No.: HY-138595
CAS No.: 51549-39-4
Purity:  98.37%
5'-O-TBDMS-Bz-dA is a nucleoside with protective and modification effects.
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Cat. No.: HY-100096A
CAS No.: 2733287-29-9
Synonyms: (Rac)-Emtricitabine sulfoxide; (Rac)-Emtricitabine Degradant-III
Research Areas:  

Infection

(Rac)-Emtricitabine S-oxide ((Rac)-Emtricitabine sulfoxide; (Rac)-Emtricitabine Degradant-III) is Emtricitabine S-oxide (HY-100096) racemic modification. Emtricitabine S-oxide is a major degradation product of Emtricitabine. Emtricitabine is a potent nucleoside reverse transcriptase inhibitor used for the treatment of HIV infection.
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Cat. No.: HY-15350
CAS No.: 148311-89-1
Synonyms: LY 300046 hydrochloride
Target:  

Reverse Transcriptase

Research Areas:  

Others

Trovirdine hydrochloride, a phenethylthiazolylthiourea (PETT) derivative, is an HIV reverse transcriptase (RT) non-nucleoside inhibitor (NNI). A novel computer model of the RT/NNI binding pocket revealed spatial gaps around Trovirdine hydrochloride's pyridyl ring. Docking studies suggested that replacing this planar ring with a nonplanar piperidinyl or piperazinyl ring could better occupy the binding pocket, enhancing anti-HIV activity. Synthesized heterocyclic compounds based on this modification demonstrated greater potency than Trovirdine hydrochloride, effectively inhibiting HIV replication at nanomolar concentrations without cytotoxicity in infected peripheral blood mononuclear cells .
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Cat. No.: HY-W1119950
CAS No.: 1644649-86-4
3'-NH-Tr-2',3'-DMF-ddA-5'-CE-Phosphoramidite is an adenine nucleotide monomer precursor used in solid-phase synthesis of oligonucleotides, particularly modified oligonucleotides, such as those with DNA chain end modifications. 3'-NH-Tr-2',3'-DMF-ddA-5'-CE-Phosphoramidite, with trityl (Tr), cyanoethyl (CE), and dimethylformamidine (DMF) protecting groups, is a ddNTP adenosine nucleoside useful in applications such as solid-phase oligonucleotide synthesis, probe design, and chain-termination sequencing .
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Cat. No.: HY-160199
CAS No.: 213206-31-6
Research Areas:  

Others

3'-L-Histidyl-AMP is applicable for nucleoside modification (DNA, RNA) .
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Cat. No.: HY-160199A
Target:  

Drug Derivative

Research Areas:  

Others

3'-L-histidyl-AMP (disodium) is applicable for nucleoside modification (DNA, RNA) .
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Cat. No.: HY-W018179
CAS No.: 81256-88-4
Research Areas:  

Others

5'-DMT-3'-TBDMS-Bz-rA is a nucleoside with protective and modification effects.
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Cat. No.: HY-138604
CAS No.: 98056-69-0
Purity:  98.00%
5'-O-DMT-N6-Me-2'-dA is a nucleoside with protective and modification effects.
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Cat. No.: HY-Z15868
CAS No.: 39638-73-8
Research Areas:  

Infection

5-Hydroxycytidine is the RNA modified nucleoside that can be found in the 23S rRNA of bacteria E. coli. 5-Hydroxycytidine modifies at the C2501 site, exhibits a higher modification level in stationary cells. 5-Hydroxycytidine exhibits a higher modification level in radiation resistant Radius than in E. coli .
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