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[4]-Gingerdiol 3,5-diacetate

group of stereoisomers with the chemical formula C₁₉H₂₈O₆
ChemicalSubstance group_of_stereoisomers Q104375417
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[4]-Gingerdiol 3,5-diacetate

Summary

[4]-Gingerdiol 3,5-diacetate is a group of stereoisomers[1].

Key Facts

  • [4]-Gingerdiol 3,5-diacetate's instance of is recorded as group of stereoisomers[2].
  • [4]-Gingerdiol 3,5-diacetate's CAS Registry Number is recorded as 53254-50-5[3].
  • [4]-Gingerdiol 3,5-diacetate's canonical SMILES is recorded as O=C(OC(CCC1=CC=C(O)C(OC)=C1)CC(OC(=O)C)CCC)C[4].
  • [4]-Gingerdiol 3,5-diacetate's InChI is recorded as InChI=1S/C19H28O6/c1-5-6-16(24-13(2)20)12-17(25-14(3)21)9-7-15-8-10-18(22)19(11-15)23-4/h8,10-11,16-17,22H,5-7,9,12H2,1-4H3[5].
  • [4]-Gingerdiol 3,5-diacetate's InChIKey is recorded as AUBPDZJRJKZQEX-UHFFFAOYSA-N[6].
  • [4]-Gingerdiol 3,5-diacetate's chemical formula is recorded as C₁₉H₂₈O₆[7].
  • [4]-Gingerdiol 3,5-diacetate's subclass of is recorded as biogenic alkylphenol[8].
  • [4]-Gingerdiol 3,5-diacetate's PubChem CID is recorded as 5318274[9].
  • [4]-Gingerdiol 3,5-diacetate's ChEBI ID is recorded as 172578[10].
  • [4]-Gingerdiol 3,5-diacetate's found in taxon is recorded as Zingiber[11].
  • [4]-Gingerdiol 3,5-diacetate's found in taxon is recorded as ginger[12].
  • [4]-Gingerdiol 3,5-diacetate's Human Metabolome Database ID is recorded as HMDB0039132[13].
  • [4]-Gingerdiol 3,5-diacetate's KNApSAcK ID is recorded as C00062096[14].
  • [4]-Gingerdiol 3,5-diacetate's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+352.188588616'}[15].
  • [4]-Gingerdiol 3,5-diacetate's DSSTox substance ID is recorded as DTXSID701181941[16].
  • [4]-Gingerdiol 3,5-diacetate's UniChem compound ID is recorded as 32021138[17].

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] ↑ . ChEBI release 2022-06-13. wikidata.org.
  10. [11] ↑ . Fresh organically grown ginger (Zingiber officinale): composition and effects on LPS-induced PGE2 production.. wikidata.org.
  11. [12] ↑ . Metabolic Profiles of Ginger, A Functional Food, and Its Representative Pungent Compounds in Rats by Ultraperformance Liquid Chromatography Coupled with Quadrupole Time-of-Flight Tandem Mass Spectrometry.. wikidata.org.
  12. [13] ↑ . wikidata.org.
  13. [14] ↑ . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . wikidata.org.
  16. [17] ↑ . UniChem. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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