CAS 251647-48-0: N-Benzoyl-5′-O-[bis(4-methoxyphenyl)phenylmethyl]-2′-O-(2-methoxyethyl)adenosine
Description:N-Benzoyl-5′-O-[bis(4-methoxyphenyl)phenylmethyl]-2′-O-(2-methoxyethyl)adenosine is a complex organic compound that belongs to the class of modified nucleosides. It features a purine base, specifically adenine, which is linked to a ribose sugar and further modified with various functional groups. The presence of the benzoyl group and methoxyphenyl substituents indicates that this compound may exhibit unique solubility and reactivity characteristics, potentially enhancing its biological activity. The methoxyethyl group contributes to its lipophilicity, which may influence its ability to cross cellular membranes. Such modifications are often designed to improve pharmacokinetic properties, such as stability and bioavailability. This compound may be of interest in medicinal chemistry, particularly in the development of antiviral or anticancer agents, due to its structural similarities to naturally occurring nucleosides. However, specific biological activities and applications would require further investigation through empirical studies.
Formula:C41H41N5O8
InChI:InChI=1S/C41H41N5O8/c1-49-22-23-52-36-35(47)33(54-40(36)46-26-44-34-37(42-25-43-38(34)46)45-39(48)27-10-6-4-7-11-27)24-53-41(28-12-8-5-9-13-28,29-14-18-31(50-2)19-15-29)30-16-20-32(51-3)21-17-30/h4-21,25-26,33,35-36,40,47H,22-24H2,1-3H3,(H,42,43,45,48)/t33-,35-,36-,40-/m1/s1
InChI key:InChIKey=KEVMXGNDTKPSMC-MUMPVVMASA-N
SMILES:O=C(NC1=NC=NC2=C1N=CN2C3OC(COC(C=4C=CC=CC4)(C5=CC=C(OC)C=C5)C6=CC=C(OC)C=C6)C(O)C3OCCOC)C=7C=CC=CC7
- Synonyms:
- 5′-Dimethoxytrityl-2′-O-(2-Methoxyethyl)-N<sup>6</sup>-benzoyl adenosine
- Adenosine, N-benzoyl-5′-O-[bis(4-methoxyphenyl)phenylmethyl]-2′-O-(2-methoxyethyl)-
- N-Benzoyl-5'-O-(Bis(4-Methoxyphenyl)Phenylmethyl)-2'-O-(2-Methoxyethyl)Adenosine
- 24: PN: WO03106645 PAGE: 73 claimed sequence
- 23: PN: US20040014699 PAGE: 20 claimed sequence
- 17: PN: US20030211606 PAGE: 19 claimed sequence