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S-allylcysteine

chemical compound
ChemicalSubstance type_of_chemical_entity Q7387047
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S-allylcysteine

Summary

S-allylcysteine is a type of chemical entity[1]. S-allylcysteine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (90 views/month).[2]

Key Facts

  • S-allylcysteine's instance of is recorded as type of chemical entity[3].
  • S-allylcysteine's chemical structure is recorded as Allyl cysteine.png[4].
  • S-allylcysteine's CAS Registry Number is recorded as 21593-77-1[5].
  • S-allylcysteine's EC number is recorded as 639-018-4[6].
  • S-allylcysteine's canonical SMILES is recorded as C=CCSCC(C(=O)O)N[7].
  • S-allylcysteine's InChI is recorded as InChI=1S/C6H11NO2S/c1-2-3-10-4-5(7)6(8)9/h2,5H,1,3-4,7H2,(H,8,9)/t5-/m0/s1[8].
  • S-allylcysteine's InChIKey is recorded as ZFAHNWWNDFHPOH-YFKPBYRVSA-N[9].
  • S-allylcysteine's chemical formula is recorded as C₆H₁₁NO₂S[10].
  • S-allylcysteine's subclass of is recorded as DL-S-allylcysteine[11].
  • S-allylcysteine's Commons category is recorded as Allyl cysteine[12].
  • S-allylcysteine's MeSH descriptor ID is recorded as C065299[13].
  • S-allylcysteine's ChEMBL ID is recorded as CHEMBL2048654[14].
  • S-allylcysteine's Freebase ID is recorded as /m/0bn3c4[15].
  • S-allylcysteine's UNII is recorded as 81R3X99M15[16].
  • S-allylcysteine's ChemSpider ID is recorded as 7969672[17].
  • S-allylcysteine's PubChem CID is recorded as 9793905[18].
  • S-allylcysteine's PubChem CID is recorded as 40424388[19].
  • S-allylcysteine's KEGG ID is recorded as C16759[20].
  • S-allylcysteine's ChEBI ID is recorded as 74077[21].
  • S-allylcysteine's ChEBI ID is recorded as 133648[22].
  • S-allylcysteine's found in taxon is recorded as Allium tuberosum[23].
  • S-allylcysteine's found in taxon is recorded as Allium sativum[24].
  • S-allylcysteine's found in taxon is recorded as Allium[25].
  • S-allylcysteine's Reaxys registry number is recorded as 1722895[26].
  • S-allylcysteine's isomeric SMILES is recorded as C=CCSCC@@HNC@@HN">[27].

Why It Matters

S-allylcysteine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (90 views/month).[2] S-allylcysteine has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[28] S-allylcysteine is known by 3 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] ↑ . ChEBI. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] ↑ . ECHA Substance Infocard database. 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] ↑ . Medical Subject Headings. Retrieved . wikidata.org.
  12. [14] ↑ . ChEMBL. Retrieved . wikidata.org.
  13. [15] ↑ . 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] ↑ . wikidata.org.
  18. [20] ↑ . ChEBI. Retrieved . wikidata.org.
  19. [21] ↑ . ChEBI. Retrieved . wikidata.org.
  20. [22] ↑ . wikidata.org.
  21. [23] ↑ . A steroidal saponin from the seeds of Allium tuberosum. wikidata.org.
  22. [24] ↑ . Prevention of liver damage by aged garlic extract and its components in mice. wikidata.org.
  23. [25] ↑ . Analytical methods for bioactive sulfur compounds in Allium: An integrated review and future directions. wikidata.org.
  24. [26] ↑ . ChEBI. Retrieved . wikidata.org.
  25. [27] ↑ . PubChem. Retrieved . 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). S-allylcysteine. Retrieved May 3, 2026, from https://4ort.xyz/entity/s-allylcysteine
MLA “S-allylcysteine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/s-allylcysteine.
BibTeX @misc{4ortxyz_s-allylcysteine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{S-allylcysteine}}, year = {2026}, url = {https://4ort.xyz/entity/s-allylcysteine}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): S-allylcysteine — https://4ort.xyz/entity/s-allylcysteine (retrieved 2026-05-03)

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