capsazepine

chemical compound
ChemicalSubstance type_of_chemical_entity Q5036336
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capsazepine

Summary

capsazepine is a type of chemical entity[1]. capsazepine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (25 views/month).[2]

Key Facts

  • capsazepine's instance of is recorded as type of chemical entity[3].
  • capsazepine's chemical structure is recorded as Capsazepine.png[4].
  • capsazepine's physically interacts with is recorded as Transient receptor potential cation channel, subfamily M, member 8[5].
  • capsazepine's physically interacts with is recorded as Transient receptor potential cation channel subfamily V member 1[6].
  • capsazepine's CAS Registry Number is recorded as 138977-28-3[7].
  • capsazepine's canonical SMILES is recorded as C1CC2=CC(=C(C=C2CN(C1)C(=S)NCCC3=CC=C(C=C3)Cl)O)O[8].
  • capsazepine's InChI is recorded as InChI=1S/C19H21ClN2O2S/c20-16-5-3-13(4-6-16)7-8-21-19(25)22-9-1-2-14-10-17(23)18(24)11-15(14)12-22/h3-6,10-11,23-24H,1-2,7-9,12H2,(H,21,25)[9].
  • capsazepine's InChIKey is recorded as DRCMAZOSEIMCHM-UHFFFAOYSA-N[10].
  • capsazepine's chemical formula is recorded as C₁₉H₂₁ClN₂O₂S[11].
  • capsazepine's subclass of is recorded as chemical compound[12].
  • capsazepine's part of is recorded as response to capsazepine[13].
  • capsazepine's Commons category is recorded as Capsazepine[14].
  • capsazepine's ChEMBL ID is recorded as CHEMBL391997[15].
  • capsazepine's Guide to Pharmacology Ligand ID is recorded as 2461[16].
  • capsazepine's PDB structure ID is recorded as 5IS0[17].
  • capsazepine's Freebase ID is recorded as /m/02qv683[18].
  • capsazepine's UNII is recorded as LFW48MY844[19].
  • capsazepine's ChemSpider ID is recorded as 2015280[20].
  • capsazepine's PubChem CID is recorded as 2733484[21].
  • capsazepine's ChEBI ID is recorded as 70773[22].
  • capsazepine's Reaxys registry number is recorded as 7047754[23].
  • capsazepine's Human Metabolome Database ID is recorded as HMDB0249598[24].
  • capsazepine's mass is recorded as {'unit': 'Q483261', 'amount': '+376.101'}[25].
  • capsazepine's SureChEMBL ID is recorded as 122421[26].
  • capsazepine's DSSTox substance ID is recorded as DTXSID20160852[27].

Why It Matters

capsazepine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (25 views/month).[2] capsazepine is known by 6 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] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  4. [6] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  5. [7] . ChEBI. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  6. [8] . PubChem. Retrieved . wikidata.org.
  7. [9] . PubChem. Retrieved . wikidata.org.
  8. [10] . PubChem. Retrieved . wikidata.org.
  9. [11] . PubChem. Retrieved . wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . Gene Ontology release 2019-11-16. wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . ChEMBL. Retrieved . wikidata.org.
  14. [16] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  15. [17] . Protein Data Bank. Retrieved . wikidata.org.
  16. [18] . wikidata.org.
  17. [19] . Global Substance Registration System. Retrieved . wikidata.org.
  18. [20] . Q2311683. Retrieved . wikidata.org.
  19. [21] . PubChem. Retrieved . wikidata.org.
  20. [22] . ChEBI. Retrieved . wikidata.org.
  21. [23] . ChEBI. Retrieved . wikidata.org.
  22. [24] . wikidata.org.
  23. [25] . PubChem. 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). capsazepine. Retrieved May 3, 2026, from https://4ort.xyz/entity/capsazepine
MLA “capsazepine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/capsazepine.
BibTeX @misc{4ortxyz_capsazepine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{capsazepine}}, year = {2026}, url = {https://4ort.xyz/entity/capsazepine}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): capsazepine — https://4ort.xyz/entity/capsazepine (retrieved 2026-05-03)

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