thymine riboside

chemical compound
ChemicalSubstance type_of_chemical_entity Q425078
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thymine riboside

Summary

thymine riboside is a type of chemical entity[1]. It ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (14 views/month).[2]

Key Facts

  • thymine riboside's instance of is recorded as type of chemical entity[3].
  • thymine riboside's chemical structure is recorded as 5-Methyluridin.svg[4].
  • thymine riboside's CAS Registry Number is recorded as 1463-10-1[5].
  • thymine riboside's EC number is recorded as 215-973-9[6].
  • thymine riboside's canonical SMILES is recorded as CC1=CN(C(=O)NC1=O)C2C(C(C(O2)CO)O)O[7].
  • thymine riboside's InChI is recorded as InChI=1S/C10H14N2O6/c1-4-2-12(10(17)11-8(4)16)9-7(15)6(14)5(3-13)18-9/h2,5-7,9,13-15H,3H2,1H3,(H,11,16,17)/t5-,6-,7-,9-/m1/s1[8].
  • thymine riboside's InChIKey is recorded as DWRXFEITVBNRMK-JXOAFFINSA-N[9].
  • thymine riboside's chemical formula is recorded as C₁₀H₁₄N₂O₆[10].
  • thymine riboside's subclass of is recorded as pyrimidine[11].
  • thymine riboside's Commons category is recorded as Ribothymidine[12].
  • thymine riboside's ChEMBL ID is recorded as CHEMBL106175[13].
  • thymine riboside's PDB structure ID is recorded as 4QSW[14].
  • thymine riboside's Freebase ID is recorded as /m/07jpyf[15].
  • thymine riboside's UNII is recorded as ZS1409014A[16].
  • thymine riboside's ChemSpider ID is recorded as 393058[17].
  • thymine riboside's PubChem CID is recorded as 445408[18].
  • thymine riboside's ChEBI ID is recorded as 45996[19].
  • thymine riboside's found in taxon is recorded as Escherichia coli[20].
  • thymine riboside's found in taxon is recorded as Homo sapiens[21].
  • thymine riboside's found in taxon is recorded as Ctenodiscus crispatus[22].
  • thymine riboside's found in taxon is recorded as Leptasterias (Hexasterias) polaris[23].
  • thymine riboside's found in taxon is recorded as Euphoria longana[24].
  • thymine riboside's catalog is recorded as CAS COVID-19 Anti-Viral Candidate Compounds[25].
  • thymine riboside's isomeric SMILES is recorded as CC1=CN(C(=O)NC1=O)[C@H]2C@@HOC@@HO">[26].
  • thymine riboside's Human Metabolome Database ID is recorded as HMDB0000884[27].

Why It Matters

thymine riboside ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (14 views/month).[2] It has Wikipedia articles in 10 language editions, a strong signal of global cultural recognition.[28] It is known by 37 alternative names across languages and contexts.[29]

References

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

Direct Wikidata claims

  1. [3] . wikidata.org.
  2. [4] . wikidata.org.
  3. [5] . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] . Global Substance Registration System. Retrieved . wikidata.org.
  5. [7] . PubChem. Retrieved . wikidata.org.
  6. [8] . PubChem. Retrieved . wikidata.org.
  7. [9] . PubChem. Retrieved . wikidata.org.
  8. [10] . PubChem. Retrieved . wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . ChEMBL. Retrieved . wikidata.org.
  12. [14] . Protein Data Bank. Retrieved . wikidata.org.
  13. [15] . Freebase Data Dumps. wikidata.org.
  14. [16] . Global Substance Registration System. Retrieved . wikidata.org.
  15. [17] . Q2311683. Retrieved . wikidata.org.
  16. [18] . PubChem. Retrieved . wikidata.org.
  17. [19] . ChEMBL. Retrieved . wikidata.org.
  18. [20] . Transductional mapping of gene trmA responsible for the production of 5-methyluridine in transfer ribonucleic acid of Escherichia coli. wikidata.org.
  19. [21] . Study of normal and modified nucleosides in serum by RP-HPLC. wikidata.org.
  20. [22] . Novel polyhydroxysteroidal glycoside from the starfishLeptasterias polaris acervata. wikidata.org.
  21. [23] . Novel polyhydroxysteroidal glycoside from the starfishLeptasterias polaris acervata. wikidata.org.
  22. [24] . Adenosine, the anxiolytic-like principle of the Arillus of Euphoria longana. wikidata.org.
  23. [25] . wikidata.org.
  24. [26] . PubChem. Retrieved . wikidata.org.
  25. [27] . wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] . Wikidata sitelinks. wikidata.org.
  3. [29] . Wikidata aliases. wikidata.org.

📑 Cite this page

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). thymine riboside. Retrieved May 3, 2026, from https://4ort.xyz/entity/thymine-riboside
MLA “thymine riboside.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/thymine-riboside.
BibTeX @misc{4ortxyz_thymine-riboside_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{thymine riboside}}, year = {2026}, url = {https://4ort.xyz/entity/thymine-riboside}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): thymine riboside — https://4ort.xyz/entity/thymine-riboside (retrieved 2026-05-03)

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