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(S)-2-azetidinecarboxylic acid

chemical compound
ChemicalSubstance type_of_chemical_entity Q793715
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(S)-2-azetidinecarboxylic acid

Summary

(S)-2-azetidinecarboxylic acid is a type of chemical entity[1]. (S)-2-azetidinecarboxylic acid ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (20 views/month).[2]

Key Facts

  • (S)-2-azetidinecarboxylic acid's instance of is recorded as type of chemical entity[3].
  • (S)-2-azetidinecarboxylic acid's chemical structure is recorded as (S)-Azetidine-2-carboxylic acid-Structural formula V1.svg[4].
  • (S)-2-azetidinecarboxylic acid's CAS Registry Number is recorded as 2133-34-8[5].
  • (S)-2-azetidinecarboxylic acid's EC number is recorded as 218-362-5[6].
  • (S)-2-azetidinecarboxylic acid's canonical SMILES is recorded as C1CNC1C(=O)O[7].
  • (S)-2-azetidinecarboxylic acid's InChI is recorded as InChI=1S/C4H7NO2/c6-4(7)3-1-2-5-3/h3,5H,1-2H2,(H,6,7)/t3-/m0/s1[8].
  • (S)-2-azetidinecarboxylic acid's InChIKey is recorded as IADUEWIQBXOCDZ-VKHMYHEASA-N[9].
  • (S)-2-azetidinecarboxylic acid's chemical formula is recorded as C₄H₇NO₂[10].
  • (S)-2-azetidinecarboxylic acid's subclass of is recorded as 2-azetidinecarboxylic acid[11].
  • (S)-2-azetidinecarboxylic acid's subclass of is recorded as secondary amino acid[12].
  • (S)-2-azetidinecarboxylic acid's MeSH descriptor ID is recorded as D001383[13].
  • (S)-2-azetidinecarboxylic acid's ChEMBL ID is recorded as CHEMBL1165239[14].
  • (S)-2-azetidinecarboxylic acid's Guide to Pharmacology Ligand ID is recorded as 4686[15].
  • (S)-2-azetidinecarboxylic acid's Freebase ID is recorded as /m/05q8p95[16].
  • (S)-2-azetidinecarboxylic acid's UNII is recorded as 5GZ3E0L9ZU[17].
  • (S)-2-azetidinecarboxylic acid's ChemSpider ID is recorded as 15628[18].
  • (S)-2-azetidinecarboxylic acid's PubChem CID is recorded as 16486[19].
  • (S)-2-azetidinecarboxylic acid's PubChem CID is recorded as 11862171[20].
  • (S)-2-azetidinecarboxylic acid's KEGG ID is recorded as C08267[21].
  • (S)-2-azetidinecarboxylic acid's MeSH tree code is recorded as D02.241.081.583.100[22].
  • (S)-2-azetidinecarboxylic acid's MeSH tree code is recorded as D02.491.485.100[23].
  • (S)-2-azetidinecarboxylic acid's MeSH tree code is recorded as D03.383.082.301.100[24].
  • (S)-2-azetidinecarboxylic acid's MeSH tree code is recorded as D12.125.072.401.200[25].
  • (S)-2-azetidinecarboxylic acid's ChEBI ID is recorded as 6198[26].
  • (S)-2-azetidinecarboxylic acid's found in taxon is recorded as Clavulinopsis helvola[27].

Why It Matters

(S)-2-azetidinecarboxylic acid ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (20 views/month).[2] (S)-2-azetidinecarboxylic acid has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[28] (S)-2-azetidinecarboxylic acid is known by 9 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] ↑ . wikidata.org.
  12. [14] ↑ . ChEMBL. Retrieved . wikidata.org.
  13. [15] ↑ . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  14. [16] ↑ . wikidata.org.
  15. [17] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  16. [18] ↑ . Q2311683. Retrieved . wikidata.org.
  17. [19] ↑ . PubChem. Retrieved . wikidata.org.
  18. [20] ↑ . wikidata.org.
  19. [21] ↑ . ChEBI. Retrieved . wikidata.org.
  20. [22] ↑ . wikidata.org.
  21. [23] ↑ . wikidata.org.
  22. [24] ↑ . wikidata.org.
  23. [25] ↑ . wikidata.org.
  24. [26] ↑ . ChEMBL. Retrieved . wikidata.org.
  25. [27] ↑ . A new conjugated diene amino acid, d,l-2-amino-3(cis), 5-hexadienoic acid, from Clavulinopsis helvola. 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)-2-azetidinecarboxylic acid. Retrieved May 3, 2026, from https://4ort.xyz/entity/s-2-azetidinecarboxylic-acid
MLA “(S)-2-azetidinecarboxylic acid.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/s-2-azetidinecarboxylic-acid.
BibTeX @misc{4ortxyz_s-2-azetidinecarboxylic-acid_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{(S)-2-azetidinecarboxylic acid}}, year = {2026}, url = {https://4ort.xyz/entity/s-2-azetidinecarboxylic-acid}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): (S)-2-azetidinecarboxylic acid — https://4ort.xyz/entity/s-2-azetidinecarboxylic-acid (retrieved 2026-05-03)

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