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CYCLO-(3-METHYLSALIGENYL)-5'-O-(E)-5-(2-BROMOVINYL)-(2'-DEOXY-3'-O-D-PHENYLALANYLURIDINYL)-PHOSPHATE;3-ME-CYCLO-3'-O-D-PHE-BVDUMP

Compound with spectra: 2 NMR

CYCLO-(3-METHYLSALIGENYL)-5'-O-(E)-5-(2-BROMOVINYL)-(2'-DEOXY-3'-O-D-PHENYLALANYLURIDINYL)-PHOSPHATE;3-ME-CYCLO-3'-O-D-PHE-BVDUMP
SpectraBase Compound ID 3wPuPkxx3Ay
InChI InChI=1S/2C28H29BrN3O9P/c2*1-17-6-5-9-20-15-37-42(36,41-25(17)20)38-16-23-22(40-27(34)21(30)12-18-7-3-2-4-8-18)13-24(39-23)32-14-19(10-11-29)26(33)31-28(32)35/h2*2-11,14,21-24H,12-13,15-16,30H2,1H3,(H,31,33,35)/b2*11-10+/t2*21-,22-,23+,24+,42?/m11/s1
InChIKey BVXGBQLJBCCXRP-XFFVBKRNSA-N
Mol Weight 1324.86 g/mol
Molecular Formula C56H58Br2N6O18P2
Exact Mass 1322.164959 g/mol
Enantiomer InChIKey BVXGBQLJBCCXRP-MLRBTMJLSA-N

View Spectrum of CYCLO-(3-METHYLSALIGENYL)-5'-O-(E)-5-(2-BROMOVINYL)-(2'-DEOXY-3'-O-D-PHENYLALANYLURIDINYL)-PHOSPHATE;3-ME-CYCLO-3'-O-D-PHE-BVDUMP

31P NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6

View Spectrum of CYCLO-(3-METHYLSALIGENYL)-5'-O-(E)-5-(2-BROMOVINYL)-(2'-DEOXY-3'-O-D-PHENYLALANYLURIDINYL)-PHOSPHATE;3-ME-CYCLO-3'-O-D-PHE-BVDUMP

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
CYCLO-(3-METHYLSALIGENYL)-5'-O-(E)-5-(2-BROMOVINYL)-(2'-DEOXY-3'-O-L-PHENYLALANYLURIDINYL)-PHOSPHATE;3-ME-CYCLO-3'-O-L-PHE-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-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-ALANYLURIDINYL)-PHOSPHATE;3-ME-CYCLO-3'-O-L-ALA-BVDUMP
CYCLO-(3-METHYLSALIGENYL)-5'-O-(E)-5-(2-BROMOVINYL)-(2'-DEOXY-3'-O-D-ALANYLURIDINYL)-PHOSPHATE;3-ME-CYCLO-3'-O-D-ALA-BVDUMP
CYCLO-(3-METHYLSALIGENYL)-5'-O-(E)-5-(2-BROMOVINYL)-(2'-DEOXY-3'-O-D-PROLINYLURIDINYL)-PHOSPHATE;3-ME-CYCLO-3'-O-D-PRO-BVDUMP
CYCLO-(3-METHYLSALIGENYL)-5'-O-(E)-5-(2-BROMOVINYL)-(2'-DEOXY-3'-O-L-PROLINYLURIDINYL)-PHOSPHATE;3-ME-CYCLO-3'-O-L-PRO-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
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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