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128070-78-0
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询盘
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2’,3’-Bis(O-t-butyldimethylsilyl)-4’,5’-didehydro-5’-deoxyuridine
CAS No. : 128070-78-0
MCE 国际站:2’,3’-Bis(O-t-butyldimethylsilyl)-4’,5’-didehydro-5’-deoxyuridine
产品活性:2’,3’-Bis(O-t-butyldimethylsilyl)-4’,5’-didehydro-5’-deoxyuridine 是一种尿嘧啶核苷类似物。尿苷具有潜在的抗癫痫作用,其类似物可用于研究抗惊厥和抗焦虑活性,以及开发新型降压剂。
研究领域:Cell Cycle/DNA Damage
作用靶点:Nucleoside Antimetabolite/Analog
相关产品:2’-dG (iBu)-2’-phosphoramidite | Peldesine dihydrochloride | 3’-Beta-C-Methyl-N6-(m-trifluoromethylbenzyl)adenosine | IBU-DC Phosphoramidite | 8-Methylguanosine | 2'-Deoxy-8-methylamino-adenosine | N6-Isopentenyl-2’-deoxy adenosine, 2’-deoxy riboprine | 7-Ethyl-7,8-dihydro-8-oxo-9-(β-D-xylofuranosyl)guanine | 5’-Deoxy-5’-N-methylaminothymidine | N-Acetyl-2′-deoxycytidine | 5-Carboxymethylaminomethyluridine | 3-Deoxy-1,2-O-isopropylidene-5-p-toluoyl-a-D-glycero-pent-3-enofuranose | 3,5-Di-O-benzoyl-2-deoxy-2-fluoro-5-trifluoromethyl-arabinouridine | 6-Mercaptopurine-13C2,15N | 4′,5′-Didehydro-5′-deoxyadenosine | 2’,3’,5’-Tri-O-acetyl-5,N3-dimethyluridine | 2’-Deoxy-2’-fluoro-N1-methyluridine | 5'-Homocytidine | 2'-Deoxypseudoisocytidine | 3’-O-DMT-N2-isobutyryl-2’-O-(2-methoxyethyl)guanosine | 5’-Deoxy-5’-iodo-2’-O-(2-methoxyethyl)-5-methyluridine | 3’,5’-Di-O-benzoyl-2’-deoxy-2’-fluoro-5-methyl-β-D-arabino-uridine | 2’-Deoxy-2’-fluoro-4-thio-beta-D-arabinouridine | 2’-Deoxy-2’-fluoro-N3-[(pyrid-2-yl)methyl]-beta-D-arabinouridine | Uridine triphosphate-13C9,15N2 (sodium) | 2'-O-Methylinosine | 3-Methylcytidine | Uridine-d | Capecitabine-d11 | 5-Pyrrolidinomethyluridine
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文献和实验RNA Synthesis Using 2-O-(Tert-Butyldimethylsilyl) Protection
This chapter enables the reader to carry out the solid-phase synthesis of ribonucleic acid (RNA) using β-cyanoethyl phosphoramidite chemistry combined with tert -butyldimethylsilyl protection of the ribose 2′-hydroxyl group. Phosphoramidite
describes the preparation of O 4 ?thymidine?alkylene?O 4 ?thymidine dimer bis?phosphoramidites and precursors for incorporation into DNA sequences to produce site?specific DNA interstrand cross?links. Linkers are introduced at the 4?position of thymidine
?isobutyryl?5??O ?(4,4??dimethoxytrityl)?2??O ?(propargyl)guanosine is converted to its 3??O ?levulinyl ester in a yield of 91%. The reaction of commercial N 2 ?isobutyryl?5??O ?(4,4??dimethoxytrityl)?2??O ?tert ?butyldimethylsilyl?3??O ?[(2?cyanoethyl)?N ,N
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