camylofin

chemical compound
ChemicalSubstance type_of_chemical_entity Q4725854
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camylofin

Summary

camylofin is a type of chemical entity[1]. camylofin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (13 views/month).[2]

Key Facts

  • camylofin's instance of is recorded as type of chemical entity[3].
  • camylofin's chemical structure is recorded as Camylofin.png[4].
  • camylofin's CAS Registry Number is recorded as 54-30-8[5].
  • camylofin's EC number is recorded as 200-202-0[6].
  • camylofin's canonical SMILES is recorded as CCN(CC)CCNC(C1=CC=CC=C1)C(=O)OCCC(C)C[7].
  • camylofin's InChI is recorded as InChI=1S/C19H32N2O2/c1-5-21(6-2)14-13-20-18(17-10-8-7-9-11-17)19(22)23-15-12-16(3)4/h7-11,16,18,20H,5-6,12-15H2,1-4H3[8].
  • camylofin's InChIKey is recorded as RYOOHIUJEJZCFT-UHFFFAOYSA-N[9].
  • camylofin's ATC code is recorded as A03AA03[10].
  • camylofin's chemical formula is recorded as C₁₉H₃₂N₂O₂[11].
  • camylofin's subclass of is recorded as chemical compound[12].
  • camylofin's MeSH descriptor ID is recorded as C004644[13].
  • camylofin's ChEMBL ID is recorded as CHEMBL253592[14].
  • camylofin's Freebase ID is recorded as /m/04mx98g[15].
  • camylofin's UNII is recorded as 340B6Q764V[16].
  • camylofin's ChemSpider ID is recorded as 5691[17].
  • camylofin's ChemSpider ID is recorded as 21234497[18].
  • camylofin's PubChem CID is recorded as 5902[19].
  • camylofin's ChEBI ID is recorded as 95216[20].
  • camylofin's DrugBank ID is recorded as DB13738[21].
  • camylofin's mass is recorded as {'unit': 'Q483261', 'amount': '+320.246'}[22].
  • camylofin's medical condition treated is recorded as obstetric labor complication[23].
  • camylofin's ECHA Substance Infocard ID is recorded as 100.000.184[24].
  • camylofin's subject has role is recorded as parasympatholytic[25].
  • camylofin's SureChEMBL ID is recorded as 617472[26].
  • camylofin's DSSTox substance ID is recorded as DTXSID7046415[27].

Why It Matters

camylofin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (13 views/month).[2] camylofin has Wikipedia articles in 5 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] . ChemIDplus. Retrieved . chem.sis.nlm.nih.gov. 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] . PubChem. Retrieved . wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . Medical Subject Headings. Retrieved . wikidata.org.
  12. [14] . ChEMBL. Retrieved . wikidata.org.
  13. [15] . wikidata.org.
  14. [16] . ChemIDplus. Retrieved . chem.sis.nlm.nih.gov. Provenance: wikidata.org.
  15. [17] . Q2311683. Retrieved . wikidata.org.
  16. [18] . Q2311683. Retrieved . wikidata.org.
  17. [19] . PubChem. Retrieved . wikidata.org.
  18. [20] . ChEBI. Retrieved . wikidata.org.
  19. [21] . wikidata.org.
  20. [22] . PubChem. Retrieved . wikidata.org.
  21. [23] . Inxight: Drugs Database. Retrieved . drugs.ncats.io. Provenance: wikidata.org.
  22. [24] . ECHA Substance Infocard database. Retrieved . wikidata.org.
  23. [25] . Medical Subject Headings. Retrieved . wikidata.org.
  24. [26] . wikidata.org.
  25. [27] . Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard. 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). camylofin. Retrieved May 3, 2026, from https://4ort.xyz/entity/camylofin
MLA “camylofin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/camylofin.
BibTeX @misc{4ortxyz_camylofin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{camylofin}}, year = {2026}, url = {https://4ort.xyz/entity/camylofin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): camylofin — https://4ort.xyz/entity/camylofin (retrieved 2026-05-03)

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