cephalosporin C

chemical compound
ChemicalSubstance type_of_chemical_entity Q5063335
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cephalosporin C

Summary

cephalosporin C is a type of chemical entity[1]. It ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (32 views/month).[2]

Key Facts

  • cephalosporin C's instance of is recorded as type of chemical entity[3].
  • cephalosporin C's chemical structure is recorded as Cephalosporin C.svg[4].
  • cephalosporin C's CAS Registry Number is recorded as 61-24-5[5].
  • cephalosporin C's EC number is recorded as 200-501-6[6].
  • cephalosporin C's canonical SMILES is recorded as CC(=O)OCC1=C(N2C(C(C2=O)NC(=O)CCCC(C(=O)O)N)SC1)C(=O)O[7].
  • cephalosporin C's InChI is recorded as InChI=1S/C16H21N3O8S/c1-7(20)27-5-8-6-28-14-11(13(22)19(14)12(8)16(25)26)18-10(21)4-2-3-9(17)15(23)24/h9,11,14H,2-6,17H2,1H3,(H,18,21)(H,23,24)(H,25,26)/t9-,11-,14-/m1/s1[8].
  • cephalosporin C's InChIKey is recorded as HOKIDJSKDBPKTQ-GLXFQSAKSA-N[9].
  • cephalosporin C's chemical formula is recorded as C₁₆H₂₁N₃O₈S[10].
  • cephalosporin C's subclass of is recorded as (7R)-3-(acetyloxymethyl)-7-[[(5R)-5-amino-5-carboxypentanoyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid[11].
  • cephalosporin C's part of is recorded as cephalosporin C metabolic process[12].
  • cephalosporin C's part of is recorded as cephalosporin C catabolic process[13].
  • cephalosporin C's part of is recorded as cephalosporin C biosynthetic process[14].
  • cephalosporin C's Commons category is recorded as Cephalosporin C[15].
  • cephalosporin C's ChEMBL ID is recorded as CHEMBL482858[16].
  • cephalosporin C's Freebase ID is recorded as /m/0h98wx_[17].
  • cephalosporin C's UNII is recorded as 3XIY7HJT5L[18].
  • cephalosporin C's ChemSpider ID is recorded as 58980[19].
  • cephalosporin C's PubChem CID is recorded as 65536[20].
  • cephalosporin C's KEGG ID is recorded as C00916[21].
  • cephalosporin C's ChEBI ID is recorded as 15776[22].
  • cephalosporin C's found in taxon is recorded as Cephalosporium acremonium[23].
  • cephalosporin C's found in taxon is recorded as Acremonium[24].
  • cephalosporin C's found in taxon is recorded as Streptomyces clavuligerus[25].
  • cephalosporin C's found in taxon is recorded as Sarocladium strictum[26].
  • cephalosporin C's found in taxon is recorded as Acremonium strictum[27].

Why It Matters

cephalosporin C ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (32 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] . Gene Ontology release 2019-11-16. wikidata.org.
  11. [13] . Gene Ontology release 2019-11-16. wikidata.org.
  12. [14] . Gene Ontology release 2019-11-16. wikidata.org.
  13. [15] . wikidata.org.
  14. [16] . ChEMBL. Retrieved . wikidata.org.
  15. [17] . wikidata.org.
  16. [18] . Global Substance Registration System. Retrieved . wikidata.org.
  17. [19] . Q2311683. Retrieved . wikidata.org.
  18. [20] . PubChem. Retrieved . wikidata.org.
  19. [21] . wikidata.org.
  20. [22] . ChEMBL. Retrieved . wikidata.org.
  21. [23] . Cephalosporin C biosynthesis : On the mechanism of hydroxylation of deacetoxycephalosporin C to deacetylcephalosporin C.. wikidata.org.
  22. [24] . The structure of cephalesporin C. wikidata.org.
  23. [25] . Different proteins bind to the butyrolactone receptor protein ARE sequence located upstream of the regulatory ccaR gene of Streptomyces clavuligerus. wikidata.org.
  24. [26] . Cephalosporin C biosynthesis; stereochemistry of the incorporation ofD,L,D-α-aminodipoyl-cysteinyl-(3S)-[2-2H,4-13C]valine into β-lactam compounds. wikidata.org.
  25. [27] . The stereochemical fate of chiral-methyl valines in cephalosporin C biosynthesis. wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.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). cephalosporin C. Retrieved May 3, 2026, from https://4ort.xyz/entity/cephalosporin-c
MLA “cephalosporin C.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/cephalosporin-c.
BibTeX @misc{4ortxyz_cephalosporin-c_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{cephalosporin C}}, year = {2026}, url = {https://4ort.xyz/entity/cephalosporin-c}, note = {Accessed: 2026-05-03}}
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Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 5w ago · Shuaib-bot bot · 2026-05-02 view diff on Wikidata ↗
    Subclass of (7R)-3-(acetyloxymethyl)-7-[[(5R)-5-amino-5-carboxypentanoyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
    Found in taxon Cephalosporium acremonium, Acremonium, Streptomyces clavuligerus +2
    Mass {'unit': 'Q483261', 'amount': '+415.105'}
    Part of cephalosporin C metabolic process, cephalosporin C catabolic process, cephalosporin C biosynthetic process
    + 6 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update-languages-and-other-short:0||ur */"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.