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| Product | Description | |
|---|---|---|
| N-Benzoylcytidine | A useful building block for oligoribonucleotide synthesis. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1g. US Biological Life Sciences. |  Worldwide |
| N-Benzoylcytidine | N-Benzoylcytidine is a substrate for uracil-cytidine kinase 1 (UCK1) and UCK2. N-Benzoylcytidine can be used to synthesize 2-OH protective groups for solid-phase RNA synthesis, as well as synthetic oligonucleotides for UV induction and targeted gene silencing in zebrafish embryos [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 13089-48-0. Pack Sizes: 10 mM * 1 mL; 5 g; 25 g. Product ID: HY-78574. |  |
| N-Benzoylcytidine | Synonyms: hydrochloricacid; hydrogenchloride; Muriaticacid; 7647-01-0; Chlorohydricacid; Acidechlorhydrique. Grades: 95%. CAS No. 13098-48-0. Molecular formula: ClH. Mole weight: 36.46094. |  |
| N4-Benzoyl-2'-O-tert-butyldimethylsilyl-5'-O-DMT-cytidine | N4-Benzoyl-2'-O-tert-butyldimethylsilyl-5'-O-DMT-cytidine is a valuable compound extensively used in the biomedical industry acting as a key intermediate for the synthesis of nucleotides and nucleosides. This product finds application in the development of antiviral drugs targeting various diseases caused by viral infections. Synonyms: 5'-DMT-2'-TBDMS-Bz-rC; 5'-O-DMT-2'-O-TBDMS-N-Bz-Cytidine; N- (1- ( (2R, 3R, 4R, 5R)-5- ( (Bis (4-methoxyphenyl) (phenyl)methoxy)methyl)-3- ( (tert-butyldimethylsilyl)oxy)-4-hydroxytetrahydrofuran-2-yl)-2-oxo-1, 2-dihydropyrimidin-4-yl)benzamide; 5'-O-(4,4'-Dimethoxytrityl)-2'-O-(tert-butyldimethylsilyl)-N-benzoylcytidine; N-Benzoyl-5'-O-[bis(4-methoxyphenyl)(phenyl)methyl]-2'-O-[tert-butyl(dimethyl)silyl]cytidine; N4-Benzoyl-2'-O-(tert-butyldimethylsilyl)-5'-O-(4,4'-dimethoxytrityl)cytidine. Grades: ≥98% by HPLC. CAS No. 81256-87-3. Molecular formula: C43H49N3O8Si. Mole weight: 763.95. | |
| N-Benzoyl-5'-O-tritylcytidine | N-Benzoyl-5'-O-tritylcytidine, a nucleoside analogue, has garnered interest in the development of antiviral agents targeting RNA viruses like hepatitis C and HIV. Its potential in the treatment of solid tumors including lung and breast cancer has also been observed. Moreover, this compound's structural attributes make it a valuable asset in the synthesis of modified nucleosides for a slew of biomedical uses. Synonyms: 5'-Trt-N4-Bz-rC; N-Benzoyl-5'-O-(triphenylmethyl)-Cytidine; 5'-O-trityl-4-N-benzoylcytidine; 5'-O-Trt-N4-Bz-rC; Cytidine, N-benzoyl-5'-O-(triphenylmethyl)-. Grades: ≥98% by HPLC. CAS No. 41092-41-5. Molecular formula: C35H31N3O6. Mole weight: 589.65. | |
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