1-o-p-Coumaroyl-beta-d-glucose

group of stereoisomers with the chemical formula C₁₅H₁₈O₈
ChemicalSubstance group_of_stereoisomers Q104987909
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Summary

1-o-p-Coumaroyl-beta-d-glucose is a group of stereoisomers[1].

Key Facts

  • 1-o-p-Coumaroyl-beta-d-glucose's instance of is recorded as group of stereoisomers[2].
  • 1-o-p-Coumaroyl-beta-d-glucose's canonical SMILES is recorded as O=C(OC1OC(CO)C(O)C(O)C1O)C=CC2=CC=C(O)C=C2[3].
  • 1-o-p-Coumaroyl-beta-d-glucose's InChI is recorded as InChI=1S/C15H18O8/c16-7-10-12(19)13(20)14(21)15(22-10)23-11(18)6-3-8-1-4-9(17)5-2-8/h1-6,10,12-17,19-21H,7H2/b6-3+[4].
  • 1-o-p-Coumaroyl-beta-d-glucose's InChIKey is recorded as DSNCQKUYZOSARM-ZZXKWVIFSA-N[5].
  • 1-o-p-Coumaroyl-beta-d-glucose's chemical formula is recorded as C₁₅H₁₈O₈[6].
  • 1-o-p-Coumaroyl-beta-d-glucose's subclass of is recorded as chemical compound[7].
  • 1-o-p-Coumaroyl-beta-d-glucose's PubChem CID is recorded as 14158116[8].
  • 1-o-p-Coumaroyl-beta-d-glucose's ChEBI ID is recorded as 168167[9].
  • 1-o-p-Coumaroyl-beta-d-glucose's found in taxon is recorded as Capsicum annuum[10].
  • 1-o-p-Coumaroyl-beta-d-glucose's found in taxon is recorded as Fragaria[11].
  • 1-o-p-Coumaroyl-beta-d-glucose's found in taxon is recorded as Malus domestica[12].
  • 1-o-p-Coumaroyl-beta-d-glucose's found in taxon is recorded as Ribes nigrum[13].
  • 1-o-p-Coumaroyl-beta-d-glucose's found in taxon is recorded as Ribes rubrum[14].
  • 1-o-p-Coumaroyl-beta-d-glucose's found in taxon is recorded as Ribes uva-crispa[15].
  • 1-o-p-Coumaroyl-beta-d-glucose's found in taxon is recorded as Rubus[16].
  • 1-o-p-Coumaroyl-beta-d-glucose's found in taxon is recorded as Vaccinium corymbosum[17].
  • 1-o-p-Coumaroyl-beta-d-glucose's found in taxon is recorded as Malus pumila[18].
  • 1-o-p-Coumaroyl-beta-d-glucose's isomeric SMILES is recorded as O=C(/C=C/c1ccc(O)cc1)OC1OC(CO)C(O)C(O)C1O[19].
  • 1-o-p-Coumaroyl-beta-d-glucose's Human Metabolome Database ID is recorded as HMDB0036936[20].
  • 1-o-p-Coumaroyl-beta-d-glucose's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+326.100167536'}[21].
  • 1-o-p-Coumaroyl-beta-d-glucose's SureChEMBL ID is recorded as 9942496[22].
  • 1-o-p-Coumaroyl-beta-d-glucose's DSSTox substance ID is recorded as DTXSID901341858[23].
  • 1-o-p-Coumaroyl-beta-d-glucose's UniChem compound ID is recorded as 32011095[24].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . PubChem. Retrieved . wikidata.org.
  8. [9] ↑ . ChEBI release 2022-06-13. wikidata.org.
  9. [10] ↑ . Characterization and quantitation of antioxidant constituents of sweet pepper (Capsicum annuum L.).. wikidata.org.
  10. [11] ↑ . Cultural system affects fruit quality and antioxidant capacity in strawberries. wikidata.org.
  11. [12] ↑ . Phenolic compounds in apples: varietal differences. wikidata.org.
  12. [13] ↑ . Hydroxybenzoic and hydroxycinnamic acid derivatives in soft fruits. wikidata.org.
  13. [14] ↑ . Hydroxybenzoic and hydroxycinnamic acid derivatives in soft fruits. wikidata.org.
  14. [15] ↑ . Hydroxybenzoic and hydroxycinnamic acid derivatives in soft fruits. wikidata.org.
  15. [16] ↑ . Hydroxybenzoic and hydroxycinnamic acid derivatives in soft fruits. wikidata.org.
  16. [17] ↑ . Hydroxybenzoic and hydroxycinnamic acid derivatives in soft fruits. wikidata.org.
  17. [18] ↑ . Quality of Commercial Apple Juices Evaluated on the Basis of the Polyphenol Content and the TEAC Antioxidant Activity. wikidata.org.
  18. [19] ↑ . wikidata.org.
  19. [20] ↑ . wikidata.org.
  20. [21] ↑ . wikidata.org.
  21. [22] ↑ . wikidata.org.
  22. [23] ↑ . wikidata.org.
  23. [24] ↑ . UniChem. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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