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Gluroside

chemical compound
ChemicalSubstance group_of_stereoisomers Q82954840
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Gluroside

Summary

Gluroside is a group of stereoisomers[1].

Key Facts

  • Gluroside's instance of is recorded as group of stereoisomers[2].
  • Gluroside's CAS Registry Number is recorded as 55941-48-5[3].
  • Gluroside's canonical SMILES is recorded as OCC1OC(OC2OC=CC3CCC(O)(C)C23)C(O)C(O)C1O[4].
  • Gluroside's InChI is recorded as InChI=1S/C15H24O8/c1-15(20)4-2-7-3-5-21-13(9(7)15)23-14-12(19)11(18)10(17)8(6-16)22-14/h3,5,7-14,16-20H,2,4,6H2,1H3/t7-,8-,9-,10-,11+,12-,13?,14+,15+/m1/s1[5].
  • Gluroside's InChIKey is recorded as BBBYCKMTZMMVAZ-LDADUKJHSA-N[6].
  • Gluroside's chemical formula is recorded as C₁₅H₂₄O₈[7].
  • Gluroside's subclass of is recorded as iridoid[8].
  • Gluroside's PubChem CID is recorded as 180538[9].
  • Gluroside's found in taxon is recorded as Cistanche salsa[10].
  • Gluroside's found in taxon is recorded as Scrophularia umbrosa[11].
  • Gluroside's found in taxon is recorded as Scrophularia oblongifolia[12].
  • Gluroside's found in taxon is recorded as Scrophularia alpestris[13].
  • Gluroside's isomeric SMILES is recorded as C[C@]1(O)CC[C@@H]2C=COC(O[C@@H]3OC@HC@@HC@H[C@H]3O)[C@@H]21C@HC@@HC@H[C@H]3O)[C@@H]21">[14].
  • Gluroside's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+332.14711772799996'}[15].
  • Gluroside's SureChEMBL ID is recorded as 29409790[16].
  • Gluroside's DSSTox substance ID is recorded as DTXSID10971358[17].
  • Gluroside's DSSTOX compound identifier is recorded as DTXCID901398873[18].
  • Gluroside's UniChem compound ID is recorded as 53800628[19].

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] ↑ . wikidata.org.
  8. [9] ↑ . PubChem. Retrieved . wikidata.org.
  9. [10] ↑ . Studies on the constituents of Cistanchis Herba. VI. Isolation and structure of a new iridoid glycoside, 6-deoxycatalpol.. wikidata.org.
  10. [11] ↑ . Late stages in the biosynthesis of aucubin in Scrophularia. wikidata.org.
  11. [12] ↑ . Late stages in the biosynthesis of aucubin in Scrophularia. wikidata.org.
  12. [13] ↑ . Late stages in the biosynthesis of aucubin in Scrophularia. wikidata.org.
  13. [14] ↑ . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . wikidata.org.
  16. [17] ↑ . wikidata.org.
  17. [18] ↑ . wikidata.org.
  18. [19] ↑ . UniChem. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). Gluroside. Retrieved May 3, 2026, from https://4ort.xyz/entity/gluroside
MLA “Gluroside.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/gluroside.
BibTeX @misc{4ortxyz_gluroside_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Gluroside}}, year = {2026}, url = {https://4ort.xyz/entity/gluroside}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Gluroside — https://4ort.xyz/entity/gluroside (retrieved 2026-05-03)

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