Home › Entities › type_of_chemical_entity › lefamulin

lefamulin

chemical compound
ChemicalSubstance type_of_chemical_entity Q24890013
Press Enter · cited answer in seconds

lefamulin

Summary

lefamulin is a type of chemical entity[1]. lefamulin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (24 views/month).[2]

Key Facts

  • lefamulin's instance of is recorded as type of chemical entity[3].
  • lefamulin's chemical structure is recorded as Lefamulin skeletal.svg[4].
  • lefamulin's CAS Registry Number is recorded as 1061337-51-6[5].
  • lefamulin's canonical SMILES is recorded as CC1CCC23CCC(=O)C2C1(C(CC(C(C3C)O)(C)C=C)OC(=O)CSC4CCC(CC4O)N)C[6].
  • lefamulin's InChI is recorded as InChI=1S/C28H45NO5S/c1-6-26(4)14-22(34-23(32)15-35-21-8-7-18(29)13-20(21)31)27(5)16(2)9-11-28(17(3)25(26)33)12-10-19(30)24(27)28/h6,16-18,20-22,24-25,31,33H,1,7-15,29H2,2-5H3/t16-,17+,18-,20-,21-,22-,24+,25+,26-,27+,28+/m1/s1[7].
  • lefamulin's InChIKey is recorded as KPVIXBKIJXZQJX-FCEONZPQSA-N[8].
  • lefamulin's chemical formula is recorded as C₂₈H₄₅NO₅S[9].
  • lefamulin's subclass of is recorded as bc-3781[10].
  • lefamulin's Commons category is recorded as Lefamulin[11].
  • lefamulin's ChEMBL ID is recorded as CHEMBL3291398[12].
  • lefamulin's Guide to Pharmacology Ligand ID is recorded as 10824[13].
  • lefamulin's ChemSpider ID is recorded as 32701544[14].
  • lefamulin's PubChem CID is recorded as 25185057[15].
  • lefamulin's DrugBank ID is recorded as DB12825[16].
  • lefamulin's isomeric SMILES is recorded as C[C@@H]1CC[C@@]23CCC(=O)[C@H]2[C@@]1(C@@HOC(=O)CS[C@@H]4CCC@HN)CC@@HOC(=O)CS[C@@H]4CCC@HN)C">[17].
  • lefamulin's mass is recorded as {'unit': 'Q483261', 'amount': '+507.302'}[18].
  • lefamulin's mass is recorded as {'unit': 'Q483261', 'amount': '+507.30184453999993'}[19].
  • lefamulin's Google Knowledge Graph ID is recorded as /g/11bz0y0w5f[20].
  • lefamulin's SureChEMBL ID is recorded as 19766421[21].
  • lefamulin's DSSTox substance ID is recorded as DTXSID101027896[22].
  • lefamulin's PDB ligand ID is recorded as 62B[23].
  • lefamulin's MedlinePlus drug identifier is recorded as a619059[24].
  • lefamulin's MedlinePlus drug identifier is recorded as a619060[25].
  • lefamulin's UniChem compound ID is recorded as 34040441[26].
  • lefamulin's WikiProjectMed ID is recorded as Lefamulin[27].

Why It Matters

lefamulin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (24 views/month).[2] lefamulin has Wikipedia articles in 12 language editions, a strong signal of global cultural recognition.[28]

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] ↑ . PubChem. Retrieved . wikidata.org.
  8. [10] ↑ . wikidata.org.
  9. [11] ↑ . wikidata.org.
  10. [12] ↑ . ChEMBL. Retrieved . wikidata.org.
  11. [13] ↑ . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  12. [14] ↑ . Q2311683. Retrieved . wikidata.org.
  13. [15] ↑ . PubChem. Retrieved . wikidata.org.
  14. [16] ↑ . wikidata.org.
  15. [17] ↑ . PubChem. Retrieved . wikidata.org.
  16. [18] ↑ . PubChem. Retrieved . wikidata.org.
  17. [19] ↑ . wikidata.org.
  18. [20] ↑ . wikidata.org.
  19. [21] ↑ . wikidata.org.
  20. [22] ↑ . wikidata.org.
  21. [23] ↑ . wikidata.org.
  22. [24] ↑ . wikidata.org.
  23. [25] ↑ . wikidata.org.
  24. [26] ↑ . UniChem. 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.

📑 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). lefamulin. Retrieved May 3, 2026, from https://4ort.xyz/entity/lefamulin
MLA “lefamulin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/lefamulin.
BibTeX @misc{4ortxyz_lefamulin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{lefamulin}}, year = {2026}, url = {https://4ort.xyz/entity/lefamulin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): lefamulin — https://4ort.xyz/entity/lefamulin (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/lefamulin · Last refreshed: