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LUCEDENIC-ACID-P;3-BETA,7-BETA-DIHYDROXY-12-BETA-ACETOXY-25,26,27-TRINOR-11,15-DIOXOLANOST-8-EN-24-OIC-ACID
SpectraBase Compound ID FuAJzhZEekm
InChI InChI=1S/C29H42O8/c1-14(8-9-21(34)35)16-12-20(33)29(7)22-17(31)13-18-26(3,4)19(32)10-11-27(18,5)23(22)24(36)25(28(16,29)6)37-15(2)30/h14,16-19,25,31-32H,8-13H2,1-7H3,(H,34,35)/t14-,16-,17+,18+,19+,25-,27+,28+,29+/m1/s1
InChIKey QPEKELRREXLZJP-WGULIUFBSA-N
Mol Weight 518.6 g/mol
Molecular Formula C29H42O8
Exact Mass 518.287968 g/mol
Enantiomer InChIKey QPEKELRREXLZJP-WZCANYOFSA-N
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum G4-66-1585-1a
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • LUCIDENIC-ACID-P;3-BETA,7-BETA-DIHYDROXY-12-BETA-ACETOXY-25,26,27-TRINOR-11,15-DIOXO-LANOST-8-EN-24-OIC-ACID
  • Lucidenic Acid P
Title Journal or Book Year
A Comprehensive Review of the Structure Elucidation and Biological Activity of Triterpenoids from Ganoderma spp. Molecules 2014
Lucidenic Acids P and Q, Methyl Lucidenate P, and Other Triterpenoids from the Fungus Ganoderma lucidum and Their Inhibitory Effects on Epstein−Barr Virus Activation Journal of Natural Products 2003

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