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9-[4-(DIFLUOROMETHYLDIPHOSPHONYL)-OXYPHOSPHONYLMETHOXY)-CYCLOPENT-2-ENYL]-GUANINE

Compound with spectra: 2 NMR

9-[4-(DIFLUOROMETHYLDIPHOSPHONYL)-OXYPHOSPHONYLMETHOXY)-CYCLOPENT-2-ENYL]-GUANINE
SpectraBase Compound ID HY7M303vKMf
InChI InChI=1S/C12H16F2N5O10P3/c13-12(14,31(23,24)25)32(26,27)29-30(21,22)5-28-7-2-1-6(3-7)19-4-16-8-9(19)17-11(15)18-10(8)20/h1-2,4,6-7H,3,5H2,(H,21,22)(H,26,27)(H2,23,24,25)(H3,15,17,18,20)/t6-,7+/m0/s1
InChIKey KKHRRYOJOJNVLH-NKWVEPMBSA-N
Mol Weight 521.2 g/mol
Molecular Formula C12H16F2N5O10P3
Exact Mass 521.007809 g/mol
Enantiomer InChIKey KKHRRYOJOJNVLH-RQJHMYQMSA-N

View Spectrum of 9-[4-(DIFLUOROMETHYLDIPHOSPHONYL)-OXYPHOSPHONYLMETHOXY)-CYCLOPENT-2-ENYL]-GUANINE

19F NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent D2O

View Spectrum of 9-[4-(DIFLUOROMETHYLDIPHOSPHONYL)-OXYPHOSPHONYLMETHOXY)-CYCLOPENT-2-ENYL]-GUANINE

31P NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent D2O
(1'S,4'R)-9-[4'-(HYDROXY)-[[(DIFLUORO)-(PHOSPHONO)-METHYL]-HYDROXYPHOSPHORYLOXY]-PHOSPHORYLMETHOXY)-CYCLOPENT-2'-ENYL]-GUANINE-(TRIS-AMMONIUM-SALT)
(1'S,4'R)-9-[4'-(HYDROXY-([(DIFLUORO)-(METHYLHYDROXYPHOSPHORYL)-METHYL]-HYDROXYPHOSPHORYLOXY)-PHOSPHORYLMETHOXY)-CYClOPENT-2'-ENYL]-GUANINE-(TRIS-A
9-[4-(DIBROMOMETHYLDIPHOSPHONYLOXY)-OXYPHOSPHONYLMETHOXY)-CYCLOPENT-2-ENYL]-GUANINE
3',5'-(TERT.-BUTYLDIMETHYLSILYLOXY)-2'-DEOXYGUANOSINE
GUANOSINE 5'-PHOSPHATE, DISODIUM SALT, MONOHYDRATE
Guanosine 5'-monophosphate disodium salt hydrate
[(2S,3R,4S,5S)-5-(2-amino-6-keto-3H-purin-9-yl)-3,4-dihydroxy-tetrahydrofuran-2-yl]methoxy-trihydroxy-phosphonium
3',5'-DI-O-LEVULINYL-2'-DEOXYGUANOSINE
[(2R,3S,5R)-5-(2-amino-6-oxo-3H-purin-9-yl)-3-butanoyloxy-tetrahydrofuran-2-yl]methyl butanoate
deoxy-N-acetyl-2-amino-9.beta.- D-(diacetyl)ribofuranosyl)-9H-purine-6(1H)-one
Title Journal or Book Year
Carbocyclic Dinucleoside Polyphosphonates:  Interaction with HIV Reverse Transcriptase and Antiviral Activity Journal of Medicinal Chemistry 2002
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