chlorpheniramine

chemical compound
ChemicalSubstance group_of_stereoisomers Q420133
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chlorpheniramine

Summary

chlorpheniramine is a group of stereoisomers[1]. chlorpheniramine ranks in the top 4% of group_of_stereoisomers entities by monthly Wikipedia readership (503 views/month).[2]

Key Facts

  • chlorpheniramine's instance of is recorded as group of stereoisomers[3].
  • chlorpheniramine's chemical structure is recorded as Chlorphenamine.svg[4].
  • chlorpheniramine's physically interacts with is recorded as Histamine receptor H1[5].
  • chlorpheniramine's CAS Registry Number is recorded as 132-22-9[6].
  • chlorpheniramine's EC number is recorded as 205-054-0[7].
  • chlorpheniramine's canonical SMILES is recorded as CN(C)CCC(C1=CC=C(C=C1)Cl)C2=CC=CC=N2[8].
  • chlorpheniramine's InChI is recorded as InChI=1S/C16H19ClN2/c1-19(2)12-10-15(16-5-3-4-11-18-16)13-6-8-14(17)9-7-13/h3-9,11,15H,10,12H2,1-2H3[9].
  • chlorpheniramine's InChIKey is recorded as SOYKEARSMXGVTM-UHFFFAOYSA-N[10].
  • chlorpheniramine's ATC code is recorded as R06AB04[11].
  • chlorpheniramine's chemical formula is recorded as C₁₆H₁₉ClN₂[12].
  • chlorpheniramine's subclass of is recorded as chemical compound[13].
  • chlorpheniramine's has use is recorded as essential medicine[14].
  • chlorpheniramine's has use is recorded as medication[15].
  • chlorpheniramine's Commons category is recorded as Chlorphenamine[16].
  • chlorpheniramine's MeSH descriptor ID is recorded as D002744[17].
  • chlorpheniramine's has part is recorded as nitrogen[18].
  • chlorpheniramine's has part is recorded as carbon[19].
  • chlorpheniramine's ChEMBL ID is recorded as CHEMBL505[20].
  • chlorpheniramine's Guide to Pharmacology Ligand ID is recorded as 6976[21].
  • chlorpheniramine's Freebase ID is recorded as /m/0311r3[22].
  • chlorpheniramine's UNII is recorded as 3U6IO1965U[23].
  • chlorpheniramine's ChemSpider ID is recorded as 2624[24].
  • chlorpheniramine's PubChem CID is recorded as 2725[25].
  • chlorpheniramine's KEGG ID is recorded as C06905[26].
  • chlorpheniramine's MeSH tree code is recorded as D03.383.725.620.150[27].

Why It Matters

chlorpheniramine ranks in the top 4% of group_of_stereoisomers entities by monthly Wikipedia readership (503 views/month).[2] chlorpheniramine has Wikipedia articles in 19 language editions, a strong signal of global cultural recognition.[28] chlorpheniramine is known by 38 alternative names across languages and contexts.[29]

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 . commonchemistry.cas.org. Provenance: wikidata.org.
  5. [7] . Global Substance Registration System. Retrieved . wikidata.org.
  6. [8] . PubChem. Retrieved . wikidata.org.
  7. [9] . PubChem. Retrieved . wikidata.org.
  8. [10] . PubChem. Retrieved . wikidata.org.
  9. [11] . DrugBank. wikidata.org.
  10. [12] . PubChem. Retrieved . wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . wikidata.org.
  14. [16] . wikidata.org.
  15. [17] . wikidata.org.
  16. [18] . wikidata.org.
  17. [19] . wikidata.org.
  18. [20] . ChEMBL. Retrieved . wikidata.org.
  19. [21] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  20. [22] . Freebase Data Dumps. wikidata.org.
  21. [23] . Global Substance Registration System. Retrieved . wikidata.org.
  22. [24] . Q2311683. Retrieved . wikidata.org.
  23. [25] . PubChem. Retrieved . wikidata.org.
  24. [26] . ChEMBL. 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.
  2. [28] . Wikidata sitelinks. wikidata.org.
  3. [29] . 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). chlorpheniramine. Retrieved May 3, 2026, from https://4ort.xyz/entity/chlorpheniramine
MLA “chlorpheniramine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/chlorpheniramine.
BibTeX @misc{4ortxyz_chlorpheniramine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{chlorpheniramine}}, year = {2026}, url = {https://4ort.xyz/entity/chlorpheniramine}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): chlorpheniramine — https://4ort.xyz/entity/chlorpheniramine (retrieved 2026-05-03)

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