cephaloglycin

chemical compound
ChemicalSubstance type_of_chemical_entity Q5057214
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cephaloglycin

Summary

cephaloglycin is a type of chemical entity[1]. cephaloglycin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (9 views/month).[2]

Key Facts

  • cephaloglycin's instance of is recorded as type of chemical entity[3].
  • cephaloglycin's CAS Registry Number is recorded as 3577-01-3[4].
  • cephaloglycin's EC number is recorded as 222-696-7[5].
  • cephaloglycin's canonical SMILES is recorded as CC(=O)OCC1=C(N2C(C(C2=O)NC(=O)C(C3=CC=CC=C3)N)SC1)C(=O)O[6].
  • cephaloglycin's InChI is recorded as InChI=1S/C18H19N3O6S/c1-9(22)27-7-11-8-28-17-13(16(24)21(17)14(11)18(25)26)20-15(23)12(19)10-5-3-2-4-6-10/h2-6,12-13,17H,7-8,19H2,1H3,(H,20,23)(H,25,26)/t12-,13-,17-/m1/s1[7].
  • cephaloglycin's InChIKey is recorded as FUBBGQLTSCSAON-PBFPGSCMSA-N[8].
  • cephaloglycin's chemical formula is recorded as C₁₈H₁₉N₃O₆S[9].
  • cephaloglycin's subclass of is recorded as chemical compound[10].
  • cephaloglycin's has use is recorded as medication[11].
  • cephaloglycin's Commons category is recorded as Cefaloglycin[12].
  • cephaloglycin's MeSH descriptor ID is recorded as D002507[13].
  • cephaloglycin's ChEMBL ID is recorded as CHEMBL1200971[14].
  • cephaloglycin's Freebase ID is recorded as /m/0fmkhl[15].
  • cephaloglycin's UNII is recorded as HD2D469W6U[16].
  • cephaloglycin's ChemSpider ID is recorded as 18069[17].
  • cephaloglycin's PubChem CID is recorded as 19150[18].
  • cephaloglycin's KEGG ID is recorded as C13440[19].
  • cephaloglycin's KEGG ID is recorded as D01949[20].
  • cephaloglycin's MeSH tree code is recorded as D02.065.589.099.249.200.180[21].
  • cephaloglycin's MeSH tree code is recorded as D02.886.665.074.200.180[22].
  • cephaloglycin's MeSH tree code is recorded as D03.633.100.300.249.200.180[23].
  • cephaloglycin's ChEBI ID is recorded as 34613[24].
  • cephaloglycin's DrugBank ID is recorded as DB00689[25].
  • cephaloglycin's Reaxys registry number is recorded as 5405868[26].
  • cephaloglycin's isomeric SMILES is recorded as CC(=O)OCC1=C(N2C@@HSC1)C(=O)OC@@HSC1)C(=O)O">[27].

Why It Matters

cephaloglycin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (9 views/month).[2] cephaloglycin has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[28] cephaloglycin is known by 21 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] . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  3. [5] . Global Substance Registration System. Retrieved . wikidata.org.
  4. [6] . PubChem. 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] . wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . ChEMBL. Retrieved . wikidata.org.
  13. [15] . 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] . ChEBI. Retrieved . wikidata.org.
  18. [20] . ChEBI. Retrieved . wikidata.org.
  19. [21] . wikidata.org.
  20. [22] . wikidata.org.
  21. [23] . wikidata.org.
  22. [24] . ChEMBL. Retrieved . wikidata.org.
  23. [25] . wikidata.org.
  24. [26] . ChEBI. Retrieved . wikidata.org.
  25. [27] . PubChem. 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). cephaloglycin. Retrieved May 3, 2026, from https://4ort.xyz/entity/cephaloglycin
MLA “cephaloglycin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/cephaloglycin.
BibTeX @misc{4ortxyz_cephaloglycin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{cephaloglycin}}, year = {2026}, url = {https://4ort.xyz/entity/cephaloglycin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): cephaloglycin — https://4ort.xyz/entity/cephaloglycin (retrieved 2026-05-03)

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