L-gulopyranose

group of stereoisomers
ChemicalSubstance group_of_stereoisomers Q27117232
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L-gulopyranose

Summary

L-gulopyranose is a group of stereoisomers[1].

Key Facts

  • L-gulopyranose's instance of is recorded as group of stereoisomers[2].
  • L-gulopyranose's canonical SMILES is recorded as C(C1C(C(C(C(O1)O)O)O)O)O[3].
  • L-gulopyranose's InChI is recorded as InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3+,4-,5-,6?/m0/s1[4].
  • L-gulopyranose's InChIKey is recorded as WQZGKKKJIJFFOK-QRXFDPRISA-N[5].
  • L-gulopyranose's chemical formula is recorded as C₆H₁₂O₆[6].
  • L-gulopyranose's subclass of is recorded as L-gulose[7].
  • L-gulopyranose's subclass of is recorded as gulopyranose[8].
  • L-gulopyranose's ChemSpider ID is recorded as 8305737[9].
  • L-gulopyranose's ChemSpider ID is recorded as 23942409[10].
  • L-gulopyranose's PubChem CID is recorded as 10130220[11].
  • L-gulopyranose's KEGG ID is recorded as C15923[12].
  • L-gulopyranose's ChEBI ID is recorded as 37704[13].
  • L-gulopyranose's Reaxys registry number is recorded as 1907359[14].
  • L-gulopyranose's isomeric SMILES is recorded as C([C@H]1C@HO)OC@HO)O">[15].
  • L-gulopyranose's Human Metabolome Database ID is recorded as HMDB0012326[16].
  • L-gulopyranose's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+180.063388'}[17].
  • L-gulopyranose's SureChEMBL ID is recorded as 9898186[18].
  • L-gulopyranose's UniChem compound ID is recorded as 1070303[19].

References

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

Direct Wikidata claims

  1. [2] . wikidata.org.
  2. [3] . PubChem. Retrieved . wikidata.org.
  3. [4] . PubChem. Retrieved . wikidata.org.
  4. [5] . PubChem. Retrieved . wikidata.org.
  5. [6] . PubChem. Retrieved . wikidata.org.
  6. [7] . wikidata.org.
  7. [8] . wikidata.org.
  8. [9] . Q2311683. Retrieved . wikidata.org.
  9. [10] . Q2311683. Retrieved . wikidata.org.
  10. [11] . PubChem. Retrieved . wikidata.org.
  11. [12] . ChEBI. Retrieved . wikidata.org.
  12. [13] . ChEBI. Retrieved . wikidata.org.
  13. [14] . ChEBI. Retrieved . wikidata.org.
  14. [15] . PubChem. Retrieved . wikidata.org.
  15. [16] . wikidata.org.
  16. [17] . PubChem. Retrieved . 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). L-gulopyranose. Retrieved May 3, 2026, from https://4ort.xyz/entity/l-gulopyranose
MLA “L-gulopyranose.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/l-gulopyranose.
BibTeX @misc{4ortxyz_l-gulopyranose_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{L-gulopyranose}}, year = {2026}, url = {https://4ort.xyz/entity/l-gulopyranose}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): L-gulopyranose — https://4ort.xyz/entity/l-gulopyranose (retrieved 2026-05-03)

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