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6-aminopenicillanic acid

chemical compound
ChemicalSubstance type_of_chemical_entity Q2823234
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6-aminopenicillanic acid

Summary

6-aminopenicillanic acid is a type of chemical entity[1]. It ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (81 views/month).[2]

Key Facts

  • 6-aminopenicillanic acid's instance of is recorded as type of chemical entity[3].
  • 6-aminopenicillanic acid's canonical SMILES is recorded as CC1(C(N2C(S1)C(C2=O)N)C(=O)O)C[4].
  • 6-aminopenicillanic acid's chemical formula is recorded as C₈H₁₂N₂O₃S[5].
  • 6-aminopenicillanic acid is a type of 6-Amino-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid[6].
  • 6-aminopenicillanic acid's Commons category is recorded as 6-Aminopenicillanic acid[7].
  • 6-aminopenicillanic acid's found in taxon is recorded as Penicillium chrysogenum[8].
  • 6-aminopenicillanic acid's MCN code is recorded as 2934.99.42[9].
  • 6-aminopenicillanic acid's isomeric SMILES is recorded as CC1(C@@HC(=O)O)CC@@HC(=O)O)C">[10].
  • 6-aminopenicillanic acid's mass is recorded as {'unit': 'Q483261', 'amount': '+216.057'}[11].
  • 6-aminopenicillanic acid's stereoisomer of is recorded as 6-aminopenicillanic acid zwitterion[12].
  • 6-aminopenicillanic acid's has active ingredient is recorded as 6-Aminopenicillanic Acid[13].
  • 6-aminopenicillanic acid's tautomer of is recorded as 6-aminopenicillanic acid zwitterion[14].

Why It Matters

6-aminopenicillanic acid ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (81 views/month).[2] It has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[15] It is known by 21 alternative names across languages and contexts.[16]

References

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

Direct Wikidata claims

  1. [3] ↑ . wikidata.org.
  2. [4] ↑ . PubChem. Retrieved . wikidata.org.
  3. [5] ↑ . PubChem. Retrieved . wikidata.org.
  4. [6] ↑ . wikidata.org.
  5. [7] ↑ . wikidata.org.
  6. [8] ↑ . 6-Aminopenicillanic acid II. Formation of 6-aminopenicillanic acid by Emericellopsis minima (Stolk) and related fungi. wikidata.org.
  7. [9] ↑ . wikidata.org.
  8. [10] ↑ . PubChem. Retrieved . wikidata.org.
  9. [11] ↑ . PubChem. Retrieved . wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . ChEBI release 2021-03-01. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.org.
  2. [15] ↑ . Wikidata sitelinks. wikidata.org.
  3. [16] ↑ . 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). 6-aminopenicillanic acid. Retrieved May 3, 2026, from https://4ort.xyz/entity/6-aminopenicillanic-acid
MLA “6-aminopenicillanic acid.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/6-aminopenicillanic-acid.
BibTeX @misc{4ortxyz_6-aminopenicillanic-acid_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{6-aminopenicillanic acid}}, year = {2026}, url = {https://4ort.xyz/entity/6-aminopenicillanic-acid}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): 6-aminopenicillanic acid — https://4ort.xyz/entity/6-aminopenicillanic-acid (retrieved 2026-05-03)

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