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4-AMINO-5-CARBOXAMIDO-7-(BETA-D-RIBOFURANOSYL)-PYRROLO-[2,3-D]-PYRIMIDINE,SANGIVAMYCIN

Compound with spectra: 3 NMR

4-AMINO-5-CARBOXAMIDO-7-(BETA-D-RIBOFURANOSYL)-PYRROLO-[2,3-D]-PYRIMIDINE,SANGIVAMYCIN
SpectraBase Compound ID EMfHxSf6Mnm
InChI InChI=1S/C12H15N5O5/c13-9-6-4(10(14)21)1-17(11(6)16-3-15-9)12-8(20)7(19)5(2-18)22-12/h1,3,5,7-8,12,18-20H,2H2,(H2,14,21)(H2,13,15,16)
InChIKey OBZJZDHRXBKKTJ-UHFFFAOYSA-N
Mol Weight 309.28 g/mol
Molecular Formula C12H15N5O5
Exact Mass 309.107319 g/mol

View Spectrum of 4-AMINO-5-CARBOXAMIDO-7-(BETA-D-RIBOFURANOSYL)-PYRROLO-[2,3-D]-PYRIMIDINE,SANGIVAMYCIN

13C NMR Spectrum
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent DMSO

View Spectrum of 4-AMINO-5-CARBOXAMIDO-7-(BETA-D-RIBOFURANOSYL)-PYRROLO-[2,3-D]-PYRIMIDINE,SANGIVAMYCIN

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6

View Spectrum of 4-AMINO-5-CARBOXAMIDO-7-(BETA-D-RIBOFURANOSYL)-PYRROLO-[2,3-D]-PYRIMIDINE,SANGIVAMYCIN

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO
  • 4-Amino-5-carboxamido-7-B-D-ribofuranosyl-pyrrolo(2,3-D)pyrimidine
7H-PYRROLO-[2,3-D]-PYRIMIDINE-5-CARBOXAMIDE, 4-AMINO-7-.BETA.-D-RIBOFURANOSYL-
5-(1-HYDROXYETHYL)-TUBERCIDIN
5-[(2-CARBOMETHOXY)-ETHYL]-TUBERCIDIN
(E)-5-(2-PHENYLETHENYL)-TUBERCIDIN
(E)-5-[2-(METHOXYCARBONYL)-ETHENYL]-TUBERCIDIN
(E)-5-(2-CARBOXYETHENYL)-TUBERCIDIN
5-(2-CARBOXAMIDOETHENYL)-TUBERCIDIN
3-CARBAMOYL-1-beta-D-RIBOFURANOSYLPYRIDINIUM HYDROXIDE, 5'TO 5'-ESTER WITH ADENOSINE 5'-(TRIHYDROGEN PYROPHOSPHATE), INNER SALT, TRIHYDRATE
3-CARBAMOYL-1-RIBOFURANOSYLPYRIDINIUM HYDROXIDE, 5' TO 5'-ESTER WITH INOSINE 5'-DIPHOSPHATE, INNER SALT, MONOSODIUM SALT, MONOHYDRATE
3-ACETYL-1-RIBOFURANOSYLPYRIDINIUM HYDROXIDE, 5' TO 5'-ESTER WITH ADENOSINE 5'-DIPHOSPHATE, INNER SALT, DIHYDRATE
Title Journal or Book Year
Pyrrolo[2,3-d]pyrimidine nucleoside antibiotic analogs. Synthesis via organopalladium intermediates derived from 5-mercuritubercidin The Journal of Organic Chemistry 1981
Carbon-13 magnetic resonance. XXV. Basic set of parameters for the investigation of tautomerism in purines established from carbon-13 magnetic resonance studies using certain purines and pyrrolo[2,3-d]pyrimidines Journal of the American Chemical Society 1975
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