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N-acetylcarnosine

chemical compound
ChemicalSubstance type_of_chemical_entity Q4673297
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N-acetylcarnosine

Summary

N-acetylcarnosine is a type of chemical entity[1]. N-acetylcarnosine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (49 views/month).[2]

Key Facts

  • N-acetylcarnosine's instance of is recorded as type of chemical entity[3].
  • N-acetylcarnosine's chemical structure is recorded as Acetylcarnosine.png[4].
  • N-acetylcarnosine's CAS Registry Number is recorded as 56353-15-2[5].
  • N-acetylcarnosine's EC number is recorded as 260-123-2[6].
  • N-acetylcarnosine's canonical SMILES is recorded as CC(=O)NCCC(=O)NC(CC1=CN=CN1)C(=O)O[7].
  • N-acetylcarnosine's InChI is recorded as InChI=1S/C11H16N4O4/c1-7(16)13-3-2-10(17)15-9(11(18)19)4-8-5-12-6-14-8/h5-6,9H,2-4H2,1H3,(H,12,14)(H,13,16)(H,15,17)(H,18,19)/t9-/m0/s1[8].
  • N-acetylcarnosine's InChIKey is recorded as BKAYIFDRRZZKNF-VIFPVBQESA-N[9].
  • N-acetylcarnosine's chemical formula is recorded as C₁₁H₁₆N₄O₄[10].
  • N-acetylcarnosine's subclass of is recorded as N-Acetyl camosine[11].
  • N-acetylcarnosine's Freebase ID is recorded as /m/04y8_5g[12].
  • N-acetylcarnosine's UNII is recorded as 0TPN86OQIF[13].
  • N-acetylcarnosine's ChemSpider ID is recorded as 8079136[14].
  • N-acetylcarnosine's PubChem CID is recorded as 9903482[15].
  • N-acetylcarnosine's ChEBI ID is recorded as 67249[16].
  • N-acetylcarnosine's Reaxys registry number is recorded as 10454928[17].
  • N-acetylcarnosine's isomeric SMILES is recorded as CC(=O)NCCC(=O)NC@@HC(=O)OC@@HC(=O)O">[18].
  • N-acetylcarnosine's mass is recorded as {'unit': 'Q483261', 'amount': '+268.117'}[19].
  • N-acetylcarnosine's ECHA Substance Infocard ID is recorded as 100.054.640[20].
  • N-acetylcarnosine's SureChEMBL ID is recorded as 27675779[21].
  • N-acetylcarnosine's SureChEMBL ID is recorded as 2513184[22].
  • N-acetylcarnosine's CosIng number is recorded as 87128[23].
  • N-acetylcarnosine's DSSTox substance ID is recorded as DTXSID30204897[24].
  • N-acetylcarnosine's RxNorm CUI is recorded as 1796119[25].
  • N-acetylcarnosine's stereoisomer of is recorded as (2R)-2-(3-acetamidopropanoylamino)-3-(1H-imidazol-5-yl)propanoic acid[26].
  • N-acetylcarnosine's Microsoft Academic ID is recorded as 2778563970[27].

Why It Matters

N-acetylcarnosine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (49 views/month).[2]

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] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  12. [14] ↑ . Q2311683. Retrieved . wikidata.org.
  13. [15] ↑ . PubChem. Retrieved . wikidata.org.
  14. [16] ↑ . ChEBI. Retrieved . wikidata.org.
  15. [17] ↑ . ChEBI. Retrieved . wikidata.org.
  16. [18] ↑ . PubChem. Retrieved . wikidata.org.
  17. [19] ↑ . PubChem. Retrieved . wikidata.org.
  18. [20] ↑ . ECHA Substance Infocard database. Retrieved . wikidata.org.
  19. [21] ↑ . wikidata.org.
  20. [22] ↑ . wikidata.org.
  21. [23] ↑ . CosIng database. Retrieved . wikidata.org.
  22. [24] ↑ . Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard. wikidata.org.
  23. [25] ↑ . Global Substance Registration System. 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.

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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). N-acetylcarnosine. Retrieved May 3, 2026, from https://4ort.xyz/entity/n-acetylcarnosine
MLA “N-acetylcarnosine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/n-acetylcarnosine.
BibTeX @misc{4ortxyz_n-acetylcarnosine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{N-acetylcarnosine}}, year = {2026}, url = {https://4ort.xyz/entity/n-acetylcarnosine}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): N-acetylcarnosine — https://4ort.xyz/entity/n-acetylcarnosine (retrieved 2026-05-03)

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