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2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol

chemical compound
ChemicalSubstance group_of_stereoisomers Q27165666
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2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol

Summary

2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol is a group of stereoisomers[1].

Key Facts

  • 2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol's instance of is recorded as group of stereoisomers[2].
  • 2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol's canonical SMILES is recorded as C1=NC2=C(C(=N1)N)N=CN2C3C(C(C(O3)CO)O)O[3].
  • 2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol's InChI is recorded as InChI=1S/C10H13N5O4/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(18)6(17)4(1-16)19-10/h2-4,6-7,10,16-18H,1H2,(H2,11,12,13)[4].
  • 2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol's InChIKey is recorded as OIRDTQYFTABQOQ-UHFFFAOYSA-N[5].
  • 2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol's chemical formula is recorded as C₁₀H₁₃N₅O₄[6].
  • 2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol's subclass of is recorded as purine ribonucleoside[7].
  • 2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol's subclass of is recorded as alkaloid[8].
  • 2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol's ChEMBL ID is recorded as CHEMBL11909[9].
  • 2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol's PubChem CID is recorded as 191[10].
  • 2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol's ChEBI ID is recorded as 93913[11].
  • 2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol's found in taxon is recorded as Dendrobium longicornu[12].
  • 2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol's found in taxon is recorded as Polyporus umbellatus[13].
  • 2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol's found in taxon is recorded as Onion[14].
  • 2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol's found in taxon is recorded as Strychnos spinosa[15].
  • 2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol's found in taxon is recorded as Fritillaria przewalskii[16].
  • 2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol's found in taxon is recorded as Zea[17].
  • 2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol's found in taxon is recorded as Fritillaria verticillata[18].
  • 2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol's found in taxon is recorded as Fritillaria walujewii[19].
  • 2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol's found in taxon is recorded as Allium macrostemon[20].
  • 2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol's found in taxon is recorded as Fritillaria pallidiflora[21].
  • 2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol's found in taxon is recorded as Cucumis myriocarpus[22].
  • 2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol's found in taxon is recorded as Vitex negundo[23].
  • 2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol's found in taxon is recorded as Strychnos staudtii[24].
  • 2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol's found in taxon is recorded as Cassytha[25].
  • 2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol's found in taxon is recorded as Allium sativum[26].

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] ↑ . ChEMBL. Retrieved . wikidata.org.
  9. [10] ↑ . PubChem. Retrieved . wikidata.org.
  10. [11] ↑ . ChEBI. Retrieved . wikidata.org.
  11. [12] ↑ . Five new compounds from Dendrobium longicornu. wikidata.org.
  12. [13] ↑ . 1β-hydroxylfriedelin, a new natural pentacylic triterpene from the sclerotia of Polyporus umbellatus. wikidata.org.
  13. [14] ↑ . A steroidal saponin from the seeds of Allium tuberosum. wikidata.org.
  14. [15] ↑ . A quinic acid ester from Strychnos lucida. wikidata.org.
  15. [16] ↑ . Identification and Quantitative Analysis of Nucleosides and Nucleobases in Aqueous Extracts ofFritillaria CirrhosaD. Don. Using HPLC–DAD and HPLC-ESI-MS. wikidata.org.
  16. [17] ↑ . Chemical constituents of the style of Zea mays L. with glycation inhibitory activity. wikidata.org.
  17. [18] ↑ . Identification and Quantitative Analysis of Nucleosides and Nucleobases in Aqueous Extracts ofFritillaria CirrhosaD. Don. Using HPLC–DAD and HPLC-ESI-MS. wikidata.org.
  18. [19] ↑ . Identification and Quantitative Analysis of Nucleosides and Nucleobases in Aqueous Extracts ofFritillaria CirrhosaD. Don. Using HPLC–DAD and HPLC-ESI-MS. wikidata.org.
  19. [20] ↑ . A steroidal saponin from the seeds of Allium tuberosum. wikidata.org.
  20. [21] ↑ . Identification and Quantitative Analysis of Nucleosides and Nucleobases in Aqueous Extracts ofFritillaria CirrhosaD. Don. Using HPLC–DAD and HPLC-ESI-MS. wikidata.org.
  21. [22] ↑ . Two new megastigmanes from the leaves of Cucumis sativus. wikidata.org.
  22. [23] ↑ . Antiestrogenic constituents of the Thai medicinal plants Capparis flavicans and Vitex glabrata. wikidata.org.
  23. [24] ↑ . A quinic acid ester from Strychnos lucida. wikidata.org.
  24. [25] ↑ . Vasorelaxing alkaloids and flavonoids from Cassytha filiformis. wikidata.org.
  25. [26] ↑ . A steroidal saponin from the seeds of Allium tuberosum. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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