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ceftaroline fosamil

chemical compound
ChemicalSubstance type_of_chemical_entity Q409712
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ceftaroline fosamil

Summary

ceftaroline fosamil is a type of chemical entity[1]. It ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (36 views/month).[2]

Key Facts

  • ceftaroline fosamil's instance of is recorded as type of chemical entity[3].
  • ceftaroline fosamil's chemical structure is recorded as Ceftaroline fosamil2DCSD.svg[4].
  • ceftaroline fosamil's CAS Registry Number is recorded as 229016-73-3[5].
  • ceftaroline fosamil's canonical SMILES is recorded as CCON=C(C1=NSC(=N1)NP(=O)(O)O)C(=O)NC2C3N(C2=O)C(=C(CS3)SC4=NC(=CS4)C5=CC=N+C)C(=O)[O-]N+C)C(=O)[O-]">[6].
  • ceftaroline fosamil's InChI is recorded as InChI=1S/C22H21N8O8PS4/c1-3-38-26-13(16-25-21(43-28-16)27-39(35,36)37)17(31)24-14-18(32)30-15(20(33)34)12(9-40-19(14)30)42-22-23-11(8-41-22)10-4-6-29(2)7-5-10/h4-8,14,19H,3,9H2,1-2H3,(H4-,24,25,27,28,31,33,34,35,36,37)/b26-13-/t14-,19-/m1/s1[7].
  • ceftaroline fosamil's InChIKey is recorded as ZCCUWMICIWSJIX-NQJJCJBVSA-N[8].
  • ceftaroline fosamil's ATC code is recorded as J01DI02[9].
  • ceftaroline fosamil's chemical formula is recorded as C₂₂H₂₁N₈O₈PS₄[10].
  • ceftaroline fosamil's subclass of is recorded as chemical compound[11].
  • ceftaroline fosamil's has use is recorded as medication[12].
  • ceftaroline fosamil's ChEMBL ID is recorded as CHEMBL501122[13].
  • ceftaroline fosamil's Guide to Pharmacology Ligand ID is recorded as 10899[14].
  • ceftaroline fosamil's Freebase ID is recorded as /m/080h3nr[15].
  • ceftaroline fosamil's UNII is recorded as 7P6FQA5D21[16].
  • ceftaroline fosamil's ChemSpider ID is recorded as 8028692[17].
  • ceftaroline fosamil's PubChem CID is recorded as 9852981[18].
  • ceftaroline fosamil's PubChem CID is recorded as 57514685[19].
  • ceftaroline fosamil's KEGG ID is recorded as D08884[20].
  • ceftaroline fosamil's ChEBI ID is recorded as 70718[21].
  • ceftaroline fosamil's DrugBank ID is recorded as DB06590[22].
  • ceftaroline fosamil's Reaxys registry number is recorded as 9535806[23].
  • ceftaroline fosamil's isomeric SMILES is recorded as CCO/N=C(/C1=NSC(=N1)NP(=O)(O)O)\C(=O)N[C@H]2[C@@H]3N(C2=O)C(=C(CS3)SC4=NC(=CS4)C5=CC=N+C)C(=O)[O-]N+C)C(=O)[O-]">[24].
  • ceftaroline fosamil's mass is recorded as {'unit': 'Q483261', 'amount': '+684.01028'}[25].
  • ceftaroline fosamil's NDF-RT ID is recorded as N0000182256[26].
  • ceftaroline fosamil's medical condition treated is recorded as staphylococcal infection[27].

Why It Matters

ceftaroline fosamil ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (36 views/month).[2] It has Wikipedia articles in 14 language editions, a strong signal of global cultural recognition.[28] It 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] ↑ . PubChem. Retrieved . wikidata.org.
  5. [7] ↑ . PubChem. Retrieved . wikidata.org.
  6. [8] ↑ . PubChem. Retrieved . wikidata.org.
  7. [9] ↑ . DrugBank. wikidata.org.
  8. [10] ↑ . PubChem. Retrieved . wikidata.org.
  9. [11] ↑ . wikidata.org.
  10. [12] ↑ . DrugBank. wikidata.org.
  11. [13] ↑ . ChEMBL. Retrieved . wikidata.org.
  12. [14] ↑ . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  13. [15] ↑ . Freebase Data Dumps. wikidata.org.
  14. [16] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  15. [17] ↑ . Q2311683. Retrieved . wikidata.org.
  16. [18] ↑ . PubChem. Retrieved . wikidata.org.
  17. [19] ↑ . wikidata.org.
  18. [20] ↑ . ChEMBL. Retrieved . wikidata.org.
  19. [21] ↑ . ChEMBL. Retrieved . wikidata.org.
  20. [22] ↑ . wikidata.org.
  21. [23] ↑ . ChEBI. Retrieved . wikidata.org.
  22. [24] ↑ . PubChem. Retrieved . wikidata.org.
  23. [25] ↑ . PubChem. Retrieved . wikidata.org.
  24. [26] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  25. [27] ↑ . Drug Indications Extracted from FAERS. Retrieved . 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). ceftaroline fosamil. Retrieved May 3, 2026, from https://4ort.xyz/entity/ceftaroline-fosamil
MLA “ceftaroline fosamil.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/ceftaroline-fosamil.
BibTeX @misc{4ortxyz_ceftaroline-fosamil_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{ceftaroline fosamil}}, year = {2026}, url = {https://4ort.xyz/entity/ceftaroline-fosamil}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): ceftaroline fosamil — https://4ort.xyz/entity/ceftaroline-fosamil (retrieved 2026-05-03)

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