2-Deoxy-5'-O-DMT-N2-isobutyryl-8-oxoguanosine 3'-CE phosphoramidite

≥95%

Reagent Code: #180477
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CAS Number 143060-53-1

science Other reagents with same CAS 143060-53-1

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Weight 855.94 g/mol
Formula C₄₄H₅₄N₇O₉P
badge Registry Numbers
MDL Number MFCD08061987
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in solid-phase oligonucleotide synthesis, this phosphoramidite building block enables the site-specific incorporation of 8-oxoguanosine—a modified nucleoside that mimics oxidative DNA damage. It is particularly valuable in preparing DNA probes for studying DNA repair mechanisms, mutagenesis, and oxidative stress-related biological pathways. The DMT and phosphoramidite protecting groups ensure efficient coupling and stepwise chain elongation on automated synthesizers. The 5′-O-DMT group allows for purification by trityl-on methods, while the isobutyryl protection on the exocyclic amine ensures stability during synthesis. Widely applied in the production of modified antisense strands, diagnostic probes, and epigenetic research tools.

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inventory 25mg
10-20 days ฿19,290.00

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2-Deoxy-5'-O-DMT-N2-isobutyryl-8-oxoguanosine 3'-CE phosphoramidite
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Used in solid-phase oligonucleotide synthesis, this phosphoramidite building block enables the site-specific incorporation of 8-oxoguanosine—a modified nucleoside that mimics oxidative DNA damage. It is particularly valuable in preparing DNA probes for studying DNA repair mechanisms, mutagenesis, and oxidative stress-related biological pathways. The DMT and phosphoramidite protecting groups ensure efficient coupling and stepwise chain elongation on automated synthesizers. The 5′-O-DMT group allows for pu

Used in solid-phase oligonucleotide synthesis, this phosphoramidite building block enables the site-specific incorporation of 8-oxoguanosine—a modified nucleoside that mimics oxidative DNA damage. It is particularly valuable in preparing DNA probes for studying DNA repair mechanisms, mutagenesis, and oxidative stress-related biological pathways. The DMT and phosphoramidite protecting groups ensure efficient coupling and stepwise chain elongation on automated synthesizers. The 5′-O-DMT group allows for purification by trityl-on methods, while the isobutyryl protection on the exocyclic amine ensures stability during synthesis. Widely applied in the production of modified antisense strands, diagnostic probes, and epigenetic research tools.

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