phenyltoloxamine

chemical compound
ChemicalSubstance type_of_chemical_entity Q7181443
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phenyltoloxamine

Summary

phenyltoloxamine is a type of chemical entity[1]. phenyltoloxamine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (18 views/month).[2]

Key Facts

  • phenyltoloxamine's instance of is recorded as type of chemical entity[3].
  • phenyltoloxamine's CAS Registry Number is recorded as 92-12-6[4].
  • phenyltoloxamine's EC number is recorded as 202-127-9[5].
  • phenyltoloxamine's canonical SMILES is recorded as CN(C)CCOC1=CC=CC=C1CC2=CC=CC=C2[6].
  • phenyltoloxamine's InChI is recorded as InChI=1S/C17H21NO/c1-18(2)12-13-19-17-11-7-6-10-16(17)14-15-8-4-3-5-9-15/h3-11H,12-14H2,1-2H3[7].
  • phenyltoloxamine's InChIKey is recorded as IZRPKIZLIFYYKR-UHFFFAOYSA-N[8].
  • phenyltoloxamine's chemical formula is recorded as C₁₇H₂₁NO[9].
  • phenyltoloxamine's subclass of is recorded as chemical compound[10].
  • phenyltoloxamine's ChEMBL ID is recorded as CHEMBL186720[11].
  • phenyltoloxamine's Freebase ID is recorded as /m/06lxvy[12].
  • phenyltoloxamine's UNII is recorded as K65LB6598J[13].
  • phenyltoloxamine's ChemSpider ID is recorded as 6810[14].
  • phenyltoloxamine's PubChem CID is recorded as 7077[15].
  • phenyltoloxamine's ChEBI ID is recorded as 135047[16].
  • phenyltoloxamine's DrugBank ID is recorded as DB11160[17].
  • phenyltoloxamine's Human Metabolome Database ID is recorded as HMDB0240250[18].
  • phenyltoloxamine's mass is recorded as {'unit': 'Q483261', 'amount': '+255.162'}[19].
  • phenyltoloxamine's NDF-RT ID is recorded as N0000146482[20].
  • phenyltoloxamine's medical condition treated is recorded as urticaria[21].
  • phenyltoloxamine's ECHA Substance Infocard ID is recorded as 100.001.935[22].
  • phenyltoloxamine's subject has role is recorded as H1 antagonist[23].
  • phenyltoloxamine's SureChEMBL ID is recorded as 28854[24].
  • phenyltoloxamine's UMLS CUI is recorded as C0070709[25].
  • phenyltoloxamine's DSSTox substance ID is recorded as DTXSID9023467[26].
  • phenyltoloxamine's RxNorm CUI is recorded as 33408[27].

Why It Matters

phenyltoloxamine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (18 views/month).[2] phenyltoloxamine 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] . 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] . ChEMBL. Retrieved . wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . Global Substance Registration System. Retrieved . wikidata.org.
  12. [14] . Q2311683. Retrieved . wikidata.org.
  13. [15] . PubChem. Retrieved . wikidata.org.
  14. [16] . ChEBI release 2019-10-02. wikidata.org.
  15. [17] . wikidata.org.
  16. [18] . wikidata.org.
  17. [19] . PubChem. Retrieved . wikidata.org.
  18. [20] . Global Substance Registration System. Retrieved . wikidata.org.
  19. [21] . NDF-RT. Retrieved . wikidata.org.
  20. [22] . ECHA Substance Infocard database. Retrieved . wikidata.org.
  21. [23] . NDF-RT. Retrieved . wikidata.org.
  22. [24] . wikidata.org.
  23. [25] . Global Substance Registration System. Retrieved . wikidata.org.
  24. [26] . Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard. wikidata.org.
  25. [27] . Global Substance Registration System. Retrieved . 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). phenyltoloxamine. Retrieved May 3, 2026, from https://4ort.xyz/entity/phenyltoloxamine
MLA “phenyltoloxamine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/phenyltoloxamine.
BibTeX @misc{4ortxyz_phenyltoloxamine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{phenyltoloxamine}}, year = {2026}, url = {https://4ort.xyz/entity/phenyltoloxamine}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): phenyltoloxamine — https://4ort.xyz/entity/phenyltoloxamine (retrieved 2026-05-03)

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