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levopropoxyphene

chemical compound
ChemicalSubstance type_of_chemical_entity Q3831365
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levopropoxyphene

Summary

levopropoxyphene is a type of chemical entity[1]. levopropoxyphene ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (38 views/month).[2]

Key Facts

  • levopropoxyphene's instance of is recorded as type of chemical entity[3].
  • levopropoxyphene's chemical structure is recorded as Levopropoxyphene structure.svg[4].
  • levopropoxyphene's CAS Registry Number is recorded as 2338-37-6[5].
  • levopropoxyphene's canonical SMILES is recorded as CCC(=O)OC(Cc1ccccc1)(c2ccccc2)C(C)CN(C)C[6].
  • levopropoxyphene's InChI is recorded as InChI=1S/C22H29NO2/c1-5-21(24)25-22(18(2)17-23(3)4,20-14-10-7-11-15-20)16-19-12-8-6-9-13-19/h6-15,18H,5,16-17H2,1-4H3/t18-,22+/m0/s1[7].
  • levopropoxyphene's InChIKey is recorded as XLMALTXPSGQGBX-PGRDOPGGSA-N[8].
  • levopropoxyphene's chemical formula is recorded as C₂₂H₂₉NO₂[9].
  • levopropoxyphene's subclass of is recorded as DL-propoxyphene[10].
  • levopropoxyphene's Commons category is recorded as Levopropoxyphene[11].
  • levopropoxyphene's MeSH descriptor ID is recorded as D054816[12].
  • levopropoxyphene's Freebase ID is recorded as /m/0bl56t[13].
  • levopropoxyphene's UNII is recorded as U75VZ9PK1J[14].
  • levopropoxyphene's ChemSpider ID is recorded as 21234163[15].
  • levopropoxyphene's PubChem CID is recorded as 200742[16].
  • levopropoxyphene's MeSH tree code is recorded as D02.241.081.751.324[17].
  • levopropoxyphene's ChEBI ID is recorded as 51174[18].
  • levopropoxyphene's DrugBank ID is recorded as DB06793[19].
  • levopropoxyphene's Reaxys registry number is recorded as 3219811[20].
  • levopropoxyphene's isomeric SMILES is recorded as CCC(=O)OC@(C@@HCN(C)C)C2=CC=CC=C2C@(C@@HCN(C)C)C2=CC=CC=C2">[21].
  • levopropoxyphene's isomeric SMILES is recorded as CCC(=O)OC@@(c2ccccc2)C@@HCN(C)CC@@(c2ccccc2)C@@HCN(C)C">[22].
  • levopropoxyphene's HSDB ID is recorded as 3414[23].
  • levopropoxyphene's mass is recorded as {'unit': 'Q483261', 'amount': '+339.21982916800005'}[24].
  • levopropoxyphene's subject has role is recorded as antitussive[25].
  • levopropoxyphene's SureChEMBL ID is recorded as 158770[26].
  • levopropoxyphene's DSSTox substance ID is recorded as DTXSID8023212[27].

Why It Matters

levopropoxyphene ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (38 views/month).[2] levopropoxyphene is known by 4 alternative names across languages and contexts.[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] ↑ . wikidata.org.
  5. [7] ↑ . PubChem. wikidata.org.
  6. [8] ↑ . PubChem. Retrieved . wikidata.org.
  7. [9] ↑ . PubChem. wikidata.org.
  8. [10] ↑ . wikidata.org.
  9. [11] ↑ . wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . Freebase Data Dumps. wikidata.org.
  12. [14] ↑ . ChemIDplus. Retrieved . chem.sis.nlm.nih.gov. Provenance: wikidata.org.
  13. [15] ↑ . wikidata.org.
  14. [16] ↑ . wikidata.org.
  15. [17] ↑ . wikidata.org.
  16. [18] ↑ . ChEBI release 2021-03-01. wikidata.org.
  17. [19] ↑ . wikidata.org.
  18. [20] ↑ . wikidata.org.
  19. [21] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  20. [22] ↑ . wikidata.org.
  21. [23] ↑ . Hazardous Substances Data Bank. Retrieved . wikidata.org.
  22. [24] ↑ . 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 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). levopropoxyphene. Retrieved May 3, 2026, from https://4ort.xyz/entity/levopropoxyphene
MLA “levopropoxyphene.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/levopropoxyphene.
BibTeX @misc{4ortxyz_levopropoxyphene_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{levopropoxyphene}}, year = {2026}, url = {https://4ort.xyz/entity/levopropoxyphene}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): levopropoxyphene — https://4ort.xyz/entity/levopropoxyphene (retrieved 2026-05-03)

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