CAS 13089-48-0
:N4-benzoylcytidine
Description:
N4-benzoylcytidine is a modified nucleoside that features a benzoyl group attached to the nitrogen atom at the 4-position of the cytidine base. This compound is characterized by its structural components, which include a pyrimidine ring and a ribose sugar moiety, typical of nucleosides. The presence of the benzoyl group enhances its lipophilicity and may influence its biological activity, making it of interest in various biochemical and pharmaceutical applications. N4-benzoylcytidine can participate in nucleic acid synthesis and may serve as a substrate or inhibitor in enzymatic reactions involving nucleotides. Its unique structure allows for potential interactions with nucleic acid targets, which can be explored in the context of drug design and development. Additionally, the compound's stability and solubility characteristics are important for its practical applications in research and therapeutic contexts. Overall, N4-benzoylcytidine represents a significant modification of the natural nucleoside cytidine, with implications for molecular biology and medicinal chemistry.
Formula:C16H17N3O6
InChI:InChI=1/C16H17N3O6/c20-8-10-12(21)13(22)15(25-10)19-7-6-11(18-16(19)24)17-14(23)9-4-2-1-3-5-9/h1-7,10,12-13,15,20-22H,8H2,(H,17,18,23,24)/t10-,12-,13-,15-/m1/s1
InChI key:InChIKey=BNXBRFDWSPXODM-BPGGGUHBSA-N
SMILES:O[C@H]1[C@@H](O[C@H](CO)[C@H]1O)N2C(=O)N=C(NC(=O)C3=CC=CC=C3)C=C2
Synonyms:- 4-(benzoylamino)-1-pentofuranosylpyrimidin-2(1H)-one
- Benzamide, N-(1,2-dihydro-2-oxo-1-β-<span class="text-smallcaps">D</span>-ribofuranosyl-4-pyrimidinyl)-
- Cytidine, N-benzoyl-
- N-benzoyl cytidine
- N-benzoylcytidine
- N6-benzoyl cytosine
- N<sup>4</sup>-Benzoylcytidine
- N<sup>6</sup>-Benzoylcytidine
- NSC 242979
- N6-Benzoylcytidine
- Benzamide, N-(1,2-dihydro-2-oxo-1-β-D-ribofuranosyl-4-pyrimidinyl)-
- N4-Benzoylcytidine
- Bz-rC
- N-[1-[3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-2-oxopyrimidin-4-yl]benzamide
- N6-Benzoyl
- N(sup 4)benzoylcytidine
- See more synonyms
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Found 11 products.
N4-Benzoylcytidine
CAS:Formula:C16H17N3O6Purity:>98.0%(T)(HPLC)Color and Shape:White to Almost white powder to crystalMolecular weight:347.33N4-Benzoylcytidine, 99%
CAS:<p>N-Benzoylcytidine is a useful building block for oligoribonucleotide synthesis. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code </p>Formula:C16H17N3O6Purity:99%Molecular weight:347.32N4-Benzoylcytidine
CAS:<p>N4-Benzoylcytidine is a natural product that can be used as a reference standard. The CAS number of N4-Benzoylcytidine is 13089-48-0.</p>Formula:C16H17N3O6Color and Shape:SolidMolecular weight:347.327N-Benzoylcytidine
CAS:<p>N-Benzoylcytidine</p>Formula:C16H17N3O6Purity:97%Color and Shape: white powderMolecular weight:347.32g/molN4-Benzoylcytidine
CAS:<p>N4-Benzoylcytidine is a nucleoside that is used as part of the synthesis of the antiviral drug acyclovir. It is synthesized by reacting uridine with benzoyl chloride in a solid-phase synthesis. N4-Benzoylcytidine has shown to inhibit the growth of virus type-1 and other viruses, including those that cause herpes simplex and varicella zoster. This nucleoside also inhibits epidermal growth factor (EGF) and is a hybridization probe for human immunodeficiency virus (HIV). The benzoate group on this compound reacts with hydroxyl groups on proteins, which may be why it has been shown to stimulate epidermal growth in mammalian cells.</p>Formula:C16H17N3O6Purity:Min. 98 Area-%Color and Shape:White PowderMolecular weight:347.32 g/molN-Benzoylcytidine
CAS:Controlled Product<p>Applications A useful building block for oligoribonucleotide synthesis.<br>References Shestopalov, I., et al.: Nat. Chem. Biol., 3, 650 (2007),<br></p>Formula:C16H17N3O6Color and Shape:NeatMolecular weight:347.32
