(2S,4R)-hypoglycin A

chemical compound
ChemicalSubstance type_of_chemical_entity Q418173
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(2S,4R)-hypoglycin A

Summary

(2S,4R)-hypoglycin An is a type of chemical entity[1]. (2S,4R)-hypoglycin A ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (49 views/month).[2]

Key Facts

  • (2S,4R)-hypoglycin A's instance of is recorded as type of chemical entity[3].
  • (2S,4R)-hypoglycin A's chemical structure is recorded as Hypoglycin A.svg[4].
  • (2S,4R)-hypoglycin A's CAS Registry Number is recorded as 156-56-9[5].
  • (2S,4R)-hypoglycin A's EC number is recorded as 663-646-8[6].
  • (2S,4R)-hypoglycin A's canonical SMILES is recorded as C=C1CC1CC(C(=O)O)N[7].
  • (2S,4R)-hypoglycin A's InChI is recorded as InChI=1S/C7H11NO2/c1-4-2-5(4)3-6(8)7(9)10/h5-6H,1-3,8H2,(H,9,10)/t5-,6+/m1/s1[8].
  • (2S,4R)-hypoglycin A's InChIKey is recorded as OOJZCXFXPZGUBJ-RITPCOANSA-N[9].
  • (2S,4R)-hypoglycin A's chemical formula is recorded as C₇H₁₁NO₂[10].
  • (2S,4R)-hypoglycin A's subclass of is recorded as carbocyclic compound[11].
  • (2S,4R)-hypoglycin A's Commons category is recorded as Hypoglycin[12].
  • (2S,4R)-hypoglycin A's ChEMBL ID is recorded as CHEMBL1615355[13].
  • (2S,4R)-hypoglycin A's Freebase ID is recorded as /m/0dh6c7[14].
  • (2S,4R)-hypoglycin A's UNII is recorded as 7GB7U7M282[15].
  • (2S,4R)-hypoglycin A's ChemSpider ID is recorded as 9943349[16].
  • (2S,4R)-hypoglycin A's PubChem CID is recorded as 11768666[17].
  • (2S,4R)-hypoglycin A's PubChem CID is recorded as 40468186[18].
  • (2S,4R)-hypoglycin A's ChEBI ID is recorded as 195718[19].
  • (2S,4R)-hypoglycin A's found in taxon is recorded as Blighia sapida[20].
  • (2S,4R)-hypoglycin A's isomeric SMILES is recorded as C=C1C[C@@H]1CC@@HNC@@HN">[21].
  • (2S,4R)-hypoglycin A's HSDB ID is recorded as 3496[22].
  • (2S,4R)-hypoglycin A's mass is recorded as {'unit': 'Q483261', 'amount': '+141.079'}[23].
  • (2S,4R)-hypoglycin A's Nikkaji ID is recorded as J85.271F[24].
  • (2S,4R)-hypoglycin A's ECHA Substance Infocard ID is recorded as 100.189.936[25].
  • (2S,4R)-hypoglycin A's NSC number is recorded as 303803[26].
  • (2S,4R)-hypoglycin A's SureChEMBL ID is recorded as 476273[27].

Why It Matters

(2S,4R)-hypoglycin A ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (49 views/month).[2] (2S,4R)-hypoglycin A has Wikipedia articles in 10 language editions, a strong signal of global cultural recognition.[28] (2S,4R)-hypoglycin An is known by 5 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] . 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] . Freebase Data Dumps. wikidata.org.
  13. [15] . Global Substance Registration System. Retrieved . wikidata.org.
  14. [16] . Q2311683. Retrieved . wikidata.org.
  15. [17] . PubChem. Retrieved . wikidata.org.
  16. [18] . wikidata.org.
  17. [19] . wikidata.org.
  18. [20] . Structural characterization of hypoglycin B, a diastereomeric dipeptide from the ackee fruit (Blighia sapida Koenig) by NMR experiments.. wikidata.org.
  19. [21] . PubChem. Retrieved . wikidata.org.
  20. [22] . Hazardous Substances Data Bank. Retrieved . wikidata.org.
  21. [23] . PubChem. Retrieved . wikidata.org.
  22. [24] . wikidata.org.
  23. [25] . ECHA Substance Infocard database. Retrieved . wikidata.org.
  24. [26] . 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). (2S,4R)-hypoglycin A. Retrieved May 3, 2026, from https://4ort.xyz/entity/2s-4r-hypoglycin-a
MLA “(2S,4R)-hypoglycin A.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/2s-4r-hypoglycin-a.
BibTeX @misc{4ortxyz_2s-4r-hypoglycin-a_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{(2S,4R)-hypoglycin A}}, year = {2026}, url = {https://4ort.xyz/entity/2s-4r-hypoglycin-a}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): (2S,4R)-hypoglycin A — https://4ort.xyz/entity/2s-4r-hypoglycin-a (retrieved 2026-05-03)

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