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75059-22-2

75059-22-2 Structure

75059-22-2 Structure
IdentificationBack Directory
[Name]

3'-fluoro-3'-deoxyadenosine
[CAS]

75059-22-2
[Synonyms]

3'-F-3'-rA
3'-fluoro-3'-deoxyadenosine
Adenosine, 3'-deoxy-3'-fluoro-
(2R,3S,4S,5R)-2-(6-Amino-9H-purin-9-yl)-4-fluoro-5-(hydroxymethyl)tetrahydrofuran-3-ol
[Molecular Formula]

C10H12FN5O3
[MDL Number]

MFCD20134043
[MOL File]

75059-22-2.mol
[Molecular Weight]

269.23
Chemical PropertiesBack Directory
[Melting point ]

211-212 °C
[Boiling point ]

628.6±65.0 °C(Predicted)
[density ]

2.01±0.1 g/cm3(Predicted)
[form ]

Solid
[pka]

12.45±0.70(Predicted)
[color ]

White to off-white
[InChI]

InChI=1S/C10H12FN5O3/c11-5-4(1-17)19-10(7(5)18)16-3-15-6-8(12)13-2-14-9(6)16/h2-5,7,10,17-18H,1H2,(H2,12,13,14)/t4-,5-,7-,10-/m1/s1
[InChIKey]

QCDAWXDDXYQEJJ-QYYRPYCUSA-N
[SMILES]

OC[C@H]1O[C@@H](N2C3C(=C(N=CN=3)N)N=C2)[C@H](O)[C@@H]1F
Hazard InformationBack Directory
[Uses]

3'-deoxy-3'-fluoroadenosine can be used as pharmaceutical intermediates for pharmaceutical experimental research.
[Biological Activity]

3'-Fluoro-3'-deoxyadenosine was active against a broad range of viruses, encompassing both DNA viruses [pox (vaccinia)], single-stranded (+) RNA viruses [picorna (polio, Coxsackie B), toga (sindbis, Semliki Forest)] and double-stranded RNA viruses (reo). Its antiviral activity spectrum, 3'-fluoro-3'-deoxyadenosine, clearly differed from those adenosine analogs known as inhibitors of S-adenosylhomocysteine hydrolase. 3'-Fluoro-3'-deoxyadenosine also proved effective in vivo in inhibiting tail lesion formation in mice inoculated intravenously with vaccinia virus[1].
[References]

[1] A. Van Aerschot. “Synthesis and antiviral activity evaluation of 3′-fluoro-3′-deoxyribonucleosides: broad-spectrum antiviral activity of 3′-fluoro-3′-deoxyadenosine.” Antiviral research 12 3 (1989): Pages 133-150.
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