5'-DMT-2'-O-TBDMS-N1-Methyl-PseudoUridine-CE-Phosphoramidite MedChemExpress (MCE)

Product Name	N1-Methylpseudouridine CEP
Synonyms	N1-Methylpseudouridine CEP 5'-DMT-2'-O-TBDMS-N1-Me-Pseudouricdine-CE-Phosphoramidite 5'-O-DMT-2'-O-TBDMS-N1-Me-Pseudouridine-CE-Phosphoramidite 5'-DMT-2'-O-TBDMS-N1-Methyl-PseudoUridine-CE-Phosphoramidite Synonyms N1-Methylpseudouridine CEP 5'-DMT-2'-O-TBDMS-N1-Me-Pseudouricdine-CE-Phosphoramidite 5'-O-DMT-2'-O-TBDMS-N1-Me-Pseudouridine-CE-Phosphoramidite 5'-DMT-2'-O-TBDMS-N1-Methyl-PseudoUridine-CE-Phosphoramidite 5'-O-DMTr-2'-O-TBDMS-N1-methylpseudouridine-3'-(cyanoethyl-N,N-diisopropyl)phosphoramidite 5'-Dimethoxytrityl-1-methyl-pseudoUridine, 2'-O-TBDMS-3'-[(2-cyanoethyl)-(N,N-diisopropyl)]-phosphoramidite 2,4(1H,3H)-Pyrimidinedione, 5-[5-O-[bis(4-methoxyphenyl)phenylmethyl]-3-O-[[bis(1-methylethyl)amino](2-cyanoethoxy)phosphino]-2-O-[(1,1-dimethylethyl)dimethylsilyl]-β-D-ribofuranosyl]-1-methyl- 5-?[5-?O-?[bis(4-?methoxyphenyl)?phenylmethyl]?-?3-?O-?[[bis(1-?methylethyl)?amino]?(2-?cyanoethoxy)?phosphino]?-?2-?O-?[(1,?1-?dimethylethyl)?dimethylsilyl]?-?β-?D-?ribofuranosyl]?-?1-?methyl-2,?4(1H,?3H)?-?pyrimidinedione
CAS	875302-45-7
EINECS
Chemical Formula	C46H63N4O9PSi
Molecular Weight	875.09
inchi
Package	25 mg
Price	Get quote
Descriptions	5'-DMT-2'-O-TBDMS-N1-Methyl-PseudoUridine-CE-Phosphoramidite 5'-DMT-2'-O-TBDMS-N1-Methyl-PseudoUridine-CE-Phosphoramidite MedChemExpress (MCE) HY-154366 875302-45-7 N1-Methylpseudouridine CEP 98.0% 4°C, protect from light In solvent : -80°C, 6 months Descriptions 5'-DMT-2'-O-TBDMS-N1-Methyl-PseudoUridine-CE-Phosphoramidite 5'-DMT-2'-O-TBDMS-N1-Methyl-PseudoUridine-CE-Phosphoramidite MedChemExpress (MCE) HY-154366 875302-45-7 N1-Methylpseudouridine CEP 98.0% 4°C, protect from light In solvent : -80°C, 6 months -20°C, 1 month (protect from light) Room temperature in continental US may vary elsewhere. 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. \| \| \| \| \| \| \| \| \| \| [1]. Robak T, Robak P. Purine nucleoside analogs in the treatment of rarer chronic lymphoid leukemias. Curr Pharm Des. 2012 18(23):3373-88. [Content Brief]
Supplier Website	https://www.medchemexpress.com/5-dmt-2-o-tbdms-n1-methyl-pseudouridine-ce-phosphoramidite.html
Last Update	2025-05-21 16:50:25

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