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4-[[(3R,4R,5S)-5-(4-hydroxy-3-methoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methyl]-2-methoxyphenol

group of stereoisomers with the chemical formula C₂₀H₂₄O₆
ChemicalSubstance group_of_stereoisomers Q104171707
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4-[[(3R,4R,5S)-5-(4-hydroxy-3-methoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methyl]-2-methoxyphenol

Summary

4-[[(3R,4R,5S)-5-(4-hydroxy-3-methoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methyl]-2-methoxyphenol is a group of stereoisomers[1].

Key Facts

  • 4-[[(3R,4R,5S)-5-(4-hydroxy-3-methoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methyl]-2-methoxyphenol's instance of is recorded as group of stereoisomers[2].
  • 4-[[(3R,4R,5S)-5-(4-hydroxy-3-methoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methyl]-2-methoxyphenol's CAS Registry Number is recorded as 486-29-3[3].
  • 4-[[(3R,4R,5S)-5-(4-hydroxy-3-methoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methyl]-2-methoxyphenol's canonical SMILES is recorded as OC1=CC=C(C=C1OC)CC2COC(C3=CC=C(O)C(OC)=C3)C2CO[4].
  • 4-[[(3R,4R,5S)-5-(4-hydroxy-3-methoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methyl]-2-methoxyphenol's InChI is recorded as InChI=1S/C20H24O6/c1-24-18-8-12(3-5-16(18)22)7-14-11-26-20(15(14)10-21)13-4-6-17(23)19(9-13)25-2/h3-6,8-9,14-15,20-23H,7,10-11H2,1-2H3[5].
  • 4-[[(3R,4R,5S)-5-(4-hydroxy-3-methoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methyl]-2-methoxyphenol's InChIKey is recorded as MHXCIKYXNYCMHY-UHFFFAOYSA-N[6].
  • 4-[[(3R,4R,5S)-5-(4-hydroxy-3-methoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methyl]-2-methoxyphenol's chemical formula is recorded as C₂₀H₂₄O₆[7].
  • 4-[[(3R,4R,5S)-5-(4-hydroxy-3-methoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methyl]-2-methoxyphenol's subclass of is recorded as chemical compound[8].
  • 4-[[(3R,4R,5S)-5-(4-hydroxy-3-methoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methyl]-2-methoxyphenol's PubChem CID is recorded as 134203[9].
  • 4-[[(3R,4R,5S)-5-(4-hydroxy-3-methoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methyl]-2-methoxyphenol's found in taxon is recorded as Forsythia suspensa[10].
  • 4-[[(3R,4R,5S)-5-(4-hydroxy-3-methoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methyl]-2-methoxyphenol's found in taxon is recorded as Drypetes littoralis[11].
  • 4-[[(3R,4R,5S)-5-(4-hydroxy-3-methoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methyl]-2-methoxyphenol's found in taxon is recorded as Larix gmelinii var. olgensis[12].
  • 4-[[(3R,4R,5S)-5-(4-hydroxy-3-methoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methyl]-2-methoxyphenol's found in taxon is recorded as Araucaria angustifolia[13].
  • 4-[[(3R,4R,5S)-5-(4-hydroxy-3-methoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methyl]-2-methoxyphenol's found in taxon is recorded as Daphne tangutica[14].
  • 4-[[(3R,4R,5S)-5-(4-hydroxy-3-methoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methyl]-2-methoxyphenol's found in taxon is recorded as Balanophora harlandii[15].
  • 4-[[(3R,4R,5S)-5-(4-hydroxy-3-methoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methyl]-2-methoxyphenol's found in taxon is recorded as Daphne odora[16].
  • 4-[[(3R,4R,5S)-5-(4-hydroxy-3-methoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methyl]-2-methoxyphenol's found in taxon is recorded as Daphne mezereum[17].
  • 4-[[(3R,4R,5S)-5-(4-hydroxy-3-methoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methyl]-2-methoxyphenol's found in taxon is recorded as Daphne oleoides[18].
  • 4-[[(3R,4R,5S)-5-(4-hydroxy-3-methoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methyl]-2-methoxyphenol's found in taxon is recorded as Daphne genkwa[19].
  • 4-[[(3R,4R,5S)-5-(4-hydroxy-3-methoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methyl]-2-methoxyphenol's found in taxon is recorded as Picea jezoensis[20].
  • 4-[[(3R,4R,5S)-5-(4-hydroxy-3-methoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methyl]-2-methoxyphenol's found in taxon is recorded as Taxus baccata[21].
  • 4-[[(3R,4R,5S)-5-(4-hydroxy-3-methoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methyl]-2-methoxyphenol's found in taxon is recorded as Rubia cordifolia[22].
  • 4-[[(3R,4R,5S)-5-(4-hydroxy-3-methoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methyl]-2-methoxyphenol's found in taxon is recorded as Rubia yunnanensis[23].
  • 4-[[(3R,4R,5S)-5-(4-hydroxy-3-methoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methyl]-2-methoxyphenol's found in taxon is recorded as Taxus wallichiana[24].
  • 4-[[(3R,4R,5S)-5-(4-hydroxy-3-methoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methyl]-2-methoxyphenol's Human Metabolome Database ID is recorded as HMDB0253982[25].
  • 4-[[(3R,4R,5S)-5-(4-hydroxy-3-methoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methyl]-2-methoxyphenol's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+360.157288488'}[26].

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . Chemical Abstracts Service. Retrieved . wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . wikidata.org.
  8. [9] ↑ . PubChem. Retrieved . wikidata.org.
  9. [10] ↑ . Lignans from the Fruits of Forsythia suspensa (Thunb.) Vahl Protect High-Density Lipoprotein during Oxidative Stress. wikidata.org.
  10. [11] ↑ . Chemical constituents from Drypetes littoralis. wikidata.org.
  11. [12] ↑ . Lignans from bark of Larix olgensis var. koreana. wikidata.org.
  12. [13] ↑ . 13C NMR spectral analysis of lignans from Araucaria angustifolia. wikidata.org.
  13. [14] ↑ . Phenylpropanoids from Daphne feddei and their inhibitory activities against NO production. wikidata.org.
  14. [15] ↑ . A new lignan from Balanophora abbreviata and inhibition of lipopolysaccharide (LPS)-induced inducible nitric oxide synthase (iNOS) expression. wikidata.org.
  15. [16] ↑ . Phenylpropanoids from Daphne feddei and their inhibitory activities against NO production. wikidata.org.
  16. [17] ↑ . Phenylpropanoids from Daphne feddei and their inhibitory activities against NO production. wikidata.org.
  17. [18] ↑ . Phenylpropanoids from Daphne feddei and their inhibitory activities against NO production. wikidata.org.
  18. [19] ↑ . Phenylpropanoids from Daphne feddei and their inhibitory activities against NO production. wikidata.org.
  19. [20] ↑ . Anti-tumor-initiating effects of phenolic compounds isolated from the bark of Picea jezoensis var. jezoensis.. wikidata.org.
  20. [21] ↑ . Structural and spectroscopic characteristics of two lignans from Taxus baccata L.. wikidata.org.
  21. [22] ↑ . Preparative separation of anti-oxidative constituents from Rubia cordifolia by column-switching counter-current chromatography. wikidata.org.
  22. [23] ↑ . Bioactive Constituents from Chinese Natural Medicines. Part 11. Inhibitors on NO Production and Degranulation in RBL-2H3 from Rubia yunnanensis: Structures of Rubianosides II, III, and IV, Rubianol-g, and Rubianthraquinone.. wikidata.org.
  23. [24] ↑ . Cytochrome P450 3A4 inhibitory constituents of the wood of Taxus yunnanensis. wikidata.org.
  24. [25] ↑ . wikidata.org.
  25. [26] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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BibTeX @misc{4ortxyz_4-3r-4r-5s-5-4-hydroxy-3-methoxyphenyl-4-hydroxymethyl-oxolan-3-yl-methyl-2-methoxyphenol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{4-[[(3R,4R,5S)-5-(4-hydroxy-3-methoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methyl]-2-methoxyphenol}}, year = {2026}, url = {https://4ort.xyz/entity/4-3r-4r-5s-5-4-hydroxy-3-methoxyphenyl-4-hydroxymethyl-oxolan-3-yl-methyl-2-methoxyphenol}, note = {Accessed: 2026-05-03}}
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