(RS)-nomifensine

group of stereoisomers
ChemicalSubstance group_of_stereoisomers Q409948
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(RS)-nomifensine

Summary

(RS)-nomifensine is a group of stereoisomers[1]. (RS)-nomifensine draws 152 Wikipedia views per month (group_of_stereoisomers category, ranking #138 of 1,063).[2]

Key Facts

  • (RS)-nomifensine's instance of is recorded as group of stereoisomers[3].
  • (RS)-nomifensine's chemical structure is recorded as Nomifensine.png[4].
  • (RS)-nomifensine's physically interacts with is recorded as solute carrier family 6 member 3[5].
  • (RS)-nomifensine's physically interacts with is recorded as Solute carrier family 6 member 2[6].
  • (RS)-nomifensine's CAS Registry Number is recorded as 24526-64-5[7].
  • (RS)-nomifensine's canonical SMILES is recorded as CN1CC(C2=C(C1)C(=CC=C2)N)C3=CC=CC=C3[8].
  • (RS)-nomifensine's InChI is recorded as InChI=1S/C16H18N2/c1-18-10-14(12-6-3-2-4-7-12)13-8-5-9-16(17)15(13)11-18/h2-9,14H,10-11,17H2,1H3[9].
  • (RS)-nomifensine's InChIKey is recorded as XXPANQJNYNUNES-UHFFFAOYSA-N[10].
  • (RS)-nomifensine's ATC code is recorded as N06AX04[11].
  • (RS)-nomifensine's chemical formula is recorded as C₁₆H₁₈N₂[12].
  • (RS)-nomifensine's subclass of is recorded as medication[13].
  • (RS)-nomifensine's Commons category is recorded as Nomifensine[14].
  • (RS)-nomifensine's MeSH descriptor ID is recorded as D009627[15].
  • (RS)-nomifensine's ChEMBL ID is recorded as CHEMBL273575[16].
  • (RS)-nomifensine's Guide to Pharmacology Ligand ID is recorded as 4792[17].
  • (RS)-nomifensine's Freebase ID is recorded as /m/0932lr[18].
  • (RS)-nomifensine's UNII is recorded as 1LGS5JRP31[19].
  • (RS)-nomifensine's ChemSpider ID is recorded as 4371[20].
  • (RS)-nomifensine's PubChem CID is recorded as 4528[21].
  • (RS)-nomifensine's MeSH tree code is recorded as D03.633.100.531.535[22].
  • (RS)-nomifensine's ChEBI ID is recorded as 116225[23].
  • (RS)-nomifensine's DrugBank ID is recorded as DB04821[24].
  • (RS)-nomifensine's Reaxys registry number is recorded as 484561[25].
  • (RS)-nomifensine's Human Metabolome Database ID is recorded as HMDB0255702[26].
  • (RS)-nomifensine's HSDB ID is recorded as 7702[27].

Why It Matters

(RS)-nomifensine draws 152 Wikipedia views per month (group_of_stereoisomers category, ranking #138 of 1,063).[2] (RS)-nomifensine has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[28] (RS)-nomifensine is known by 13 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] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  5. [7] . Global Substance Registration System. 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] . DrugBank. wikidata.org.
  10. [12] . PubChem. Retrieved . wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . Medical Subject Headings. Retrieved . wikidata.org.
  14. [16] . ChEMBL. Retrieved . wikidata.org.
  15. [17] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  16. [18] . Freebase Data Dumps. 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] . wikidata.org.
  21. [23] . ChEMBL. Retrieved . wikidata.org.
  22. [24] . wikidata.org.
  23. [25] . ChEBI. Retrieved . wikidata.org.
  24. [26] . wikidata.org.
  25. [27] . Hazardous Substances Data Bank. Retrieved . 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). (RS)-nomifensine. Retrieved May 3, 2026, from https://4ort.xyz/entity/rs-nomifensine
MLA “(RS)-nomifensine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/rs-nomifensine.
BibTeX @misc{4ortxyz_rs-nomifensine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{(RS)-nomifensine}}, year = {2026}, url = {https://4ort.xyz/entity/rs-nomifensine}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): (RS)-nomifensine — https://4ort.xyz/entity/rs-nomifensine (retrieved 2026-05-03)

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