flesinoxan

chemical compound
ChemicalSubstance type_of_chemical_entity Q5458730
Press Enter · cited answer in seconds

flesinoxan

Summary

flesinoxan is a type of chemical entity[1]. flesinoxan ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (10 views/month).[2]

Key Facts

  • flesinoxan's instance of is recorded as type of chemical entity[3].
  • flesinoxan's chemical structure is recorded as Flesinoxan.png[4].
  • flesinoxan's physically interacts with is recorded as 5-hydroxytryptamine receptor 1A[5].
  • flesinoxan's CAS Registry Number is recorded as 98206-10-1[6].
  • flesinoxan's canonical SMILES is recorded as C1CN(CCN1CCNC(=O)C2=CC=C(C=C2)F)C3=C4C(=CC=C3)OC(CO4)CO[7].
  • flesinoxan's InChI is recorded as InChI=1S/C22H26FN3O4/c23-17-6-4-16(5-7-17)22(28)24-8-9-25-10-12-26(13-11-25)19-2-1-3-20-21(19)29-15-18(14-27)30-20/h1-7,18,27H,8-15H2,(H,24,28)/t18-/m0/s1[8].
  • flesinoxan's InChIKey is recorded as NYSDRDDQELAVKP-SFHVURJKSA-N[9].
  • flesinoxan's chemical formula is recorded as C₂₂H₂₆FN₃O₄[10].
  • flesinoxan's subclass of is recorded as chemical compound[11].
  • flesinoxan's Commons category is recorded as Flesinoxan[12].
  • flesinoxan's MeSH descriptor ID is recorded as C056895[13].
  • flesinoxan's ChEMBL ID is recorded as CHEMBL1742477[14].
  • flesinoxan's Guide to Pharmacology Ligand ID is recorded as 1[15].
  • flesinoxan's Freebase ID is recorded as /m/047mjln[16].
  • flesinoxan's UNII is recorded as 3V574S89E1[17].
  • flesinoxan's ChemSpider ID is recorded as 51700[18].
  • flesinoxan's PubChem CID is recorded as 57347[19].
  • flesinoxan's KEGG ID is recorded as D02568[20].
  • flesinoxan's isomeric SMILES is recorded as C1CN(CCN1CCNC(=O)C2=CC=C(C=C2)F)C3=C4C(=CC=C3)OC@HCOC@HCO">[21].
  • flesinoxan's mass is recorded as {'unit': 'Q483261', 'amount': '+415.190735'}[22].
  • flesinoxan's subject has role is recorded as antihypertensive drug[23].
  • flesinoxan's subject has role is recorded as antidepressant[24].
  • flesinoxan's subject has role is recorded as anxiolytic[25].
  • flesinoxan's subject has role is recorded as serotonin receptor agonists[26].
  • flesinoxan's SureChEMBL ID is recorded as 220401[27].

Why It Matters

flesinoxan ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (10 views/month).[2]

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] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . 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] . PubChem. Retrieved . wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . Medical Subject Headings. Retrieved . wikidata.org.
  12. [14] . ChEMBL. Retrieved . wikidata.org.
  13. [15] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  14. [16] . wikidata.org.
  15. [17] . Global Substance Registration System. Retrieved . wikidata.org.
  16. [18] . Q2311683. Retrieved . wikidata.org.
  17. [19] . PubChem. Retrieved . wikidata.org.
  18. [20] . wikidata.org.
  19. [21] . PubChem. Retrieved . wikidata.org.
  20. [22] . PubChem. Retrieved . wikidata.org.
  21. [23] . Medical Subject Headings. Retrieved . wikidata.org.
  22. [24] . Medical Subject Headings. Retrieved . wikidata.org.
  23. [25] . Medical Subject Headings. Retrieved . wikidata.org.
  24. [26] . Medical Subject Headings. Retrieved . wikidata.org.
  25. [27] . wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.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). flesinoxan. Retrieved May 3, 2026, from https://4ort.xyz/entity/flesinoxan
MLA “flesinoxan.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/flesinoxan.
BibTeX @misc{4ortxyz_flesinoxan_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{flesinoxan}}, year = {2026}, url = {https://4ort.xyz/entity/flesinoxan}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): flesinoxan — https://4ort.xyz/entity/flesinoxan (retrieved 2026-05-03)

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