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XZTUSOXSLKTKJQ-CIXPXFMPSA-N
SpectraBase Compound ID GppozhI4kMn
InChI InChI=1S/C23H34O4/c1-21-8-5-16(24)12-15(21)3-4-19-18(21)6-9-22(2)17(7-10-23(19,22)26)14-11-20(25)27-13-14/h11,15-19,24,26H,3-10,12-13H2,1-2H3/t15-,16-,17+,18-,19+,21-,22+,23-/m0/s1
InChIKey XZTUSOXSLKTKJQ-CIXPXFMPSA-N
Mol Weight 374.5 g/mol
Molecular Formula C23H34O4
Exact Mass 374.24571 g/mol
Enantiomer InChIKey XZTUSOXSLKTKJQ-BORMIPFCSA-N
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3:DMSO
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent PYRIDINE-D5
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent PYRIDINE-D5
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C5D5N
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • UZARIGENIN,(3-BETA-OH,5-ALPHA-H)
  • UZARIGENIN;3-BETA,14-DIHYDROXY-5-ALPHA-CARD-20-(22)-ENOLIDE
  • UZARIGENIN(=3-BETA,14-DIHYDROXY-5-ALPHA-CARD-20(22)-ENOLID)
  • 3.beta.-14-Dihydroxy-5.alpha.-17.beta.-H-card-20(22)-enolide
  • 3.beta.-14-Dihydroxy-5.alpha.-card-20(22)-enolide, (uzarigenin)
Title Journal or Book Year
Cardenolide glycosides from Asclepias fruticosa Phytochemistry 1994
Proceragenin, an antibacterial cardenolide from Calotropis procera Phytochemistry 1992
Cardenolide analogues. Part 12. 13C N.m.r. of semi-synthetic glycosides and side-chain modified genins Journal of the Chemical Society, Perkin Transactions 1 1981
Digitoxigenin oleandroside and 5.ALPHA.-adynerin in the leaves of Nerium odorum (Nerium 9). Chemical and Pharmaceutical Bulletin 1978
Carbon-13 NMR of 5.ALPHA.-cardenolides. Chemical and Pharmaceutical Bulletin 1978

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