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CYCLO-(3,5-DIMETHYLSALIGENYL)-5'-O-(E)-5-(2-BROMOVINYL)-3'-O-LEVULINYL-(2'-DEOXYURIDINYL)-PHOSPHATE;3,5-DIME-CYCLO-SAL-3'-O-LEV-BVDUMP

Compound with spectra: 2 NMR

CYCLO-(3,5-DIMETHYLSALIGENYL)-5'-O-(E)-5-(2-BROMOVINYL)-3'-O-LEVULINYL-(2'-DEOXYURIDINYL)-PHOSPHATE;3,5-DIME-CYCLO-SAL-3'-O-LEV-BVDUMP
SpectraBase Compound ID LoC9NR8jn9
InChI InChI=1S/2C25H28BrN2O10P/c2*1-14-8-15(2)23-18(9-14)12-34-39(33,38-23)35-13-20-19(37-22(30)5-4-16(3)29)10-21(36-20)28-11-17(6-7-26)24(31)27-25(28)32/h2*6-9,11,19-21H,4-5,10,12-13H2,1-3H3,(H,27,31,32)/b2*7-6+/t2*19-,20+,21+,39?/m00/s1
InChIKey NONYCHASASMTKQ-RILHQAOQSA-N
Mol Weight 1254.76 g/mol
Molecular Formula C50H56Br2N4O20P2
Exact Mass 1252.13299 g/mol
Enantiomer InChIKey NONYCHASASMTKQ-OFDVVXPWSA-N

View Spectrum of CYCLO-(3,5-DIMETHYLSALIGENYL)-5'-O-(E)-5-(2-BROMOVINYL)-3'-O-LEVULINYL-(2'-DEOXYURIDINYL)-PHOSPHATE;3,5-DIME-CYCLO-SAL-3'-O-LEV-BVDUMP

31P NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of CYCLO-(3,5-DIMETHYLSALIGENYL)-5'-O-(E)-5-(2-BROMOVINYL)-3'-O-LEVULINYL-(2'-DEOXYURIDINYL)-PHOSPHATE;3,5-DIME-CYCLO-SAL-3'-O-LEV-BVDUMP

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
CYCLO-(5-CHLOROSALIGENYL)-5'-O-(E)-5-(2-BROMOVINYL)-3'-O-LEVULINYL-(2'-DEOXYURIDINYL)-PHOSPHATE;5-CL-CYCLO-SAL-3'-O-LEV-BVDUMP
CYCLO-(5-METHOXYSALIGENYL)-5'-O-(E)-5-(2-BROMOVINYL)-3'-O-LEVULINYL-(2'-DEOXYURIDINYL)-PHOSPHATE;5-OME-CYCLO-SAL-3'-O-LEV-BVDUMP
CYCLO-(3-TERT.-BUTYLSALIGENYL)-5'-O-(E)-5-(2-BROMOVINYL)-3'-O-LEVULINYL-(2'-DEOXYURIDINYL)-PHOSPHATE;3-TERT.-BUTYL-CYCLO-SAL-3'-O-LEV-BVDUMP
CYCLO-(3-METHYLSALIGENYL)-5'-O-(E)-5-(2-BROMOVINYL)-(2'-DEOXY-3'-O-D-LEUCINYLURIDINYL)-PHOSPHATE;3-ME-CYCLO-3'-O-D-LEU-BVDUMP
CYCLO-(3-METHYLSALIGENYL)-5'-O-(E)-5-(2-BROMOVINYL)-(2'-DEOXY-3'-O-L-LEUCINYLURIDINYL)-PHOSPHATE;3-ME-CYCLO-3'-O-L-LEU-BVDUMP
CYCLO-(3-METHYLSALIGENYL)-5'-O-(E)-5-(2-BROMOVINYL)-(2'-DEOXY-3'-O-L-ISOLEUCINYLURIDINYL)-PHOSPHATE;3-ME-CYCLO-3'-O-L-ILE-BVDUMP
CYCLO-(3-METHYLSALIGENYL)-5'-O-(E)-5-(2-BROMOVINYL)-(2'-DEOXY-3'-O-D-ISOLEUCINYLURIDINYL)-PHOSPHATE;3-ME-CYCLO-3'-O-D-ILE-BVDUMP
CYCLO-(3-METHYLSALIGENYL)-5'-O-(E)-5-(2-BROMOVINYL)-(2'-DEOXY-3'-O-D-VALYNYLURIDINYL)-PHOSPHATE;3-ME-CYCLO-3'-O-D-VAL-BVDUMP
CYCLO-(3-METHYLSALIGENYL)-5'-O-(E)-5-(2-BROMOVINYL)-(2'-DEOXY-3'-O-L-VALYNYLURIDINYL)-PHOSPHATE;3-ME-CYCLO-3'-O-L-VAL-BVDUMP
CYCLO-(3-METHYLSALIGENYL)-5'-O-(E)-5-(2-BROMOVINYL)-(2'-DEOXY-3'-O-L-PHENYLALANYLURIDINYL)-PHOSPHATE;3-ME-CYCLO-3'-O-L-PHE-BVDUMP
Title Journal or Book Year
CycloSal-BVDUMP Pronucleotides:  How to Convert an Antiviral-Inactive Nucleoside Analogue into a Bioactive Compound against EBV Journal of Medicinal Chemistry 2002

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