piperacillin

chemical compound
ChemicalSubstance type_of_chemical_entity Q423787
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piperacillin

Summary

piperacillin is a type of chemical entity[1]. piperacillin ranks in the top 5% of type_of_chemical_entity entities by monthly Wikipedia readership (154 views/month).[2]

Key Facts

  • piperacillin's instance of is recorded as type of chemical entity[3].
  • piperacillin's chemical structure is recorded as Piperacillin.svg[4].
  • piperacillin's CAS Registry Number is recorded as 61477-96-1[5].
  • piperacillin's EC number is recorded as 262-811-8[6].
  • piperacillin's canonical SMILES is recorded as CCN1CCN(C(=O)C1=O)C(=O)NC(C2=CC=CC=C2)C(=O)NC3C4N(C3=O)C(C(S4)(C)C)C(=O)O[7].
  • piperacillin's InChI is recorded as InChI=1S/C23H27N5O7S/c1-4-26-10-11-27(19(32)18(26)31)22(35)25-13(12-8-6-5-7-9-12)16(29)24-14-17(30)28-15(21(33)34)23(2,3)36-20(14)28/h5-9,13-15,20H,4,10-11H2,1-3H3,(H,24,29)(H,25,35)(H,33,34)/t13-,14-,15+,20-/m1/s1[8].
  • piperacillin's InChIKey is recorded as IVBHGBMCVLDMKU-GXNBUGAJSA-N[9].
  • piperacillin's Library of Congress authority ID is recorded as sh85102397[10].
  • piperacillin's ATC code is recorded as J01CA12[11].
  • piperacillin's chemical formula is recorded as C₂₃H₂₇N₅O₇S[12].
  • piperacillin's subclass of is recorded as penicillin[13].
  • piperacillin's subclass of is recorded as carboxylic acid[14].
  • piperacillin's has use is recorded as medication[15].
  • piperacillin's Commons category is recorded as Piperacillin[16].
  • piperacillin's MeSH descriptor ID is recorded as D010878[17].
  • piperacillin's ChEMBL ID is recorded as CHEMBL702[18].
  • piperacillin's Guide to Pharmacology Ligand ID is recorded as 10921[19].
  • piperacillin's PDB structure ID is recorded as 3Q07[20].
  • piperacillin's Freebase ID is recorded as /m/073pzq[21].
  • piperacillin's UNII is recorded as 9I628532GX[22].
  • piperacillin's ChemSpider ID is recorded as 39798[23].
  • piperacillin's PubChem CID is recorded as 43672[24].
  • piperacillin's KEGG ID is recorded as C14034[25].
  • piperacillin's KEGG ID is recorded as D08380[26].
  • piperacillin's MeSH tree code is recorded as D02.065.589.099.750.750.050.650[27].

Why It Matters

piperacillin ranks in the top 5% of type_of_chemical_entity entities by monthly Wikipedia readership (154 views/month).[2] piperacillin has Wikipedia articles in 21 language editions, a strong signal of global cultural recognition.[28] piperacillin is known by 22 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] . wikidata.org.
  9. [11] . DrugBank. wikidata.org.
  10. [12] . PubChem. Retrieved . wikidata.org.
  11. [13] . NDF-RT. Retrieved . wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . DrugBank. wikidata.org.
  14. [16] . wikidata.org.
  15. [17] . wikidata.org.
  16. [18] . ChEMBL. Retrieved . wikidata.org.
  17. [19] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  18. [20] . Protein Data Bank. Retrieved . wikidata.org.
  19. [21] . Freebase Data Dumps. wikidata.org.
  20. [22] . Global Substance Registration System. Retrieved . wikidata.org.
  21. [23] . Q2311683. Retrieved . wikidata.org.
  22. [24] . PubChem. Retrieved . wikidata.org.
  23. [25] . ChEBI. Retrieved . wikidata.org.
  24. [26] . ChEBI. Retrieved . 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). piperacillin. Retrieved May 3, 2026, from https://4ort.xyz/entity/piperacillin
MLA “piperacillin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/piperacillin.
BibTeX @misc{4ortxyz_piperacillin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{piperacillin}}, year = {2026}, url = {https://4ort.xyz/entity/piperacillin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): piperacillin — https://4ort.xyz/entity/piperacillin (retrieved 2026-05-03)

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