D-arabinopyranose

group of stereoisomers
ChemicalSubstance group_of_stereoisomers Q27120748
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D-arabinopyranose

Summary

D-arabinopyranose is a group of stereoisomers[1].

Key Facts

  • D-arabinopyranose's instance of is recorded as group of stereoisomers[2].
  • D-arabinopyranose's CAS Registry Number is recorded as 10323-20-3[3].
  • D-arabinopyranose's CAS Registry Number is recorded as 28697-53-2[4].
  • D-arabinopyranose's EC number is recorded as 233-708-5[5].
  • D-arabinopyranose's canonical SMILES is recorded as C1C(C(C(C(O1)O)O)O)O[6].
  • D-arabinopyranose's InChI is recorded as InChI=1S/C5H10O5/c6-2-1-10-5(9)4(8)3(2)7/h2-9H,1H2/t2-,3-,4+,5?/m1/s1[7].
  • D-arabinopyranose's InChIKey is recorded as SRBFZHDQGSBBOR-ZRMNMSDTSA-N[8].
  • D-arabinopyranose's chemical formula is recorded as C₅H₁₀O₅[9].
  • D-arabinopyranose's subclass of is recorded as D-arabinose[10].
  • D-arabinopyranose's subclass of is recorded as pentopyranose[11].
  • D-arabinopyranose's part of is recorded as arabinose isomerase activity[12].
  • D-arabinopyranose's part of is recorded as 3-deoxy-D-manno-octulosonate aldolase activity[13].
  • D-arabinopyranose's part of is recorded as D-arabinokinase activity[14].
  • D-arabinopyranose's part of is recorded as D-arabinose 1-dehydrogenase (NAD+) activity[15].
  • D-arabinopyranose's part of is recorded as D-arabinose 1-dehydrogenase (NADP+) activity[16].
  • D-arabinopyranose's ChEMBL ID is recorded as CHEMBL1222249[17].
  • D-arabinopyranose's UNII is recorded as F0W6ETZ4E5[18].
  • D-arabinopyranose's ChemSpider ID is recorded as 6636[19].
  • D-arabinopyranose's ChemSpider ID is recorded as 32674255[20].
  • D-arabinopyranose's PubChem CID is recorded as 6902[21].
  • D-arabinopyranose's KEGG ID is recorded as C00216[22].
  • D-arabinopyranose's ZVG number is recorded as 124044[23].
  • D-arabinopyranose's ChEBI ID is recorded as 46994[24].
  • D-arabinopyranose's found in taxon is recorded as Psidium guajava[25].
  • D-arabinopyranose's Reaxys registry number is recorded as 2039533[26].

References

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

Direct Wikidata claims

  1. [2] . wikidata.org.
  2. [3] . ChEBI. Retrieved . wikidata.org.
  3. [4] . CAS Common Chemistry. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [5] . ECHA Substance Infocard database. Retrieved . wikidata.org.
  5. [6] . PubChem. Retrieved . wikidata.org.
  6. [7] . PubChem. Retrieved . wikidata.org.
  7. [8] . PubChem. Retrieved . wikidata.org.
  8. [9] . PubChem. Retrieved . wikidata.org.
  9. [10] . wikidata.org.
  10. [11] . wikidata.org.
  11. [12] . Gene Ontology release 2020-05-02. wikidata.org.
  12. [13] . Gene Ontology release 2020-05-02. wikidata.org.
  13. [14] . Gene Ontology release 2020-05-02. wikidata.org.
  14. [15] . Gene Ontology release 2020-05-02. wikidata.org.
  15. [16] . geneontology.org. Retrieved . geneontology.org. Provenance: wikidata.org.
  16. [17] . ChEMBL. Retrieved . wikidata.org.
  17. [18] . wikidata.org.
  18. [19] . Q2311683. Retrieved . wikidata.org.
  19. [20] . Q2311683. Retrieved . wikidata.org.
  20. [21] . PubChem. Retrieved . wikidata.org.
  21. [22] . ChEBI. Retrieved . wikidata.org.
  22. [23] . wikidata.org.
  23. [24] . ChEBI. Retrieved . wikidata.org.
  24. [25] . The hypoglycemic effects of guava leaf (Psidium guajava L.) extract are associated with improving endothelial dysfunction in mice with diet-induced obesity. wikidata.org.
  25. [26] . ChEBI. Retrieved . wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

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APA 4ort.xyz Knowledge Graph. (2026). D-arabinopyranose. Retrieved May 3, 2026, from https://4ort.xyz/entity/d-arabinopyranose
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BibTeX @misc{4ortxyz_d-arabinopyranose_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{D-arabinopyranose}}, year = {2026}, url = {https://4ort.xyz/entity/d-arabinopyranose}, note = {Accessed: 2026-05-03}}
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