1-deaza-3 `-O-methyladenosine: A nucleoside with the syn-conformation in the solid state and in solution
Autor(en): | Seela, F Debelak, H Reuter, H Kastner, G Mikhailopulo, IA |
Stichwörter: | 1-DEAZA-2'-DEOXYADENOSINE; 1-DEAZAADENOSINE ANALOGS; ADENINE NUCLEOSIDES; ADENOSINE-DEAMINASE; Biochemistry & Molecular Biology; CRYSTAL; HOOGSTEEN-DUPLEX DNA; MAGNETIC-RESONANCE; NUCLEOTIDES; PURINE NUCLEOSIDES; SPECTROSCOPY | Erscheinungsdatum: | 1998 | Herausgeber: | TAYLOR & FRANCIS INC | Journal: | NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS | Volumen: | 17 | Ausgabe: | 4 | Startseite: | 729 | Seitenende: | 744 | Zusammenfassung: | The 2'-O-methyl (2) and the 3'-O-methyl (3) derivatives of 1-deazaadenosine (1) were prepared. Single crystal X-ray analysis as well as H-1 and C-13 NMR studies were performed on the 3'-O-methyl-1-deazaadenosine 3. In the solid state, the glycosyl torsion angle (chi = 64.7 degrees) is in the syn-range which is caused by an intramolecular (5')CH2OH ... N(3) hydrogen bond. The ribofuranose moiety adopts a E-2 (C-3'-exo; S) conformation and the orientation of the exocyclic C(4')-C(5') bond is sc (gamma((+)g)). The conformation in solution was found to be very similar to that in solid state. Whereas the 2'-O-methyl derivative of 1 is a strong inhibitor of adenosine deaminase the 3'-O-methyl derivative is neither inhibitor nor substrate. |
ISSN: | 15257770 | DOI: | 10.1080/07328319808004671 |
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geprüft am 02.05.2024