(RS)-mianserin

group of stereoisomers
ChemicalSubstance group_of_stereoisomers Q416701
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(RS)-mianserin

Summary

(RS)-mianserin is a group of stereoisomers[1]. (RS)-mianserin ranks in the top 9% of group_of_stereoisomers entities by monthly Wikipedia readership (220 views/month).[2]

Key Facts

  • (RS)-mianserin's instance of is recorded as group of stereoisomers[3].
  • (RS)-mianserin's chemical structure is recorded as Mianserin.svg[4].
  • (RS)-mianserin's physically interacts with is recorded as 5-hydroxytryptamine (serotonin) receptor 1B[5].
  • (RS)-mianserin's physically interacts with is recorded as 5-hydroxytryptamine receptor 2A[6].
  • (RS)-mianserin's physically interacts with is recorded as 5-hydroxytryptamine receptor 2B[7].
  • (RS)-mianserin's physically interacts with is recorded as 5-hydroxytryptamine receptor 2C[8].
  • (RS)-mianserin's physically interacts with is recorded as 5-hydroxytryptamine receptor 6[9].
  • (RS)-mianserin's physically interacts with is recorded as 5-hydroxytryptamine receptor 7[10].
  • (RS)-mianserin's physically interacts with is recorded as 5-hydroxytryptamine (serotonin) receptor 7[11].
  • (RS)-mianserin's physically interacts with is recorded as Adrenoceptor alpha 1A[12].
  • (RS)-mianserin's physically interacts with is recorded as Adrenoceptor alpha 1B[13].
  • (RS)-mianserin's physically interacts with is recorded as Adrenoceptor alpha 1D[14].
  • (RS)-mianserin's CAS Registry Number is recorded as 24219-97-4[15].
  • (RS)-mianserin's EC number is recorded as 246-088-6[16].
  • (RS)-mianserin's canonical SMILES is recorded as CN1CCN2C(C1)C3=CC=CC=C3CC4=CC=CC=C42[17].
  • (RS)-mianserin's InChI is recorded as InChI=1S/C18H20N2/c1-19-10-11-20-17-9-5-3-7-15(17)12-14-6-2-4-8-16(14)18(20)13-19/h2-9,18H,10-13H2,1H3[18].
  • (RS)-mianserin's InChIKey is recorded as UEQUQVLFIPOEMF-UHFFFAOYSA-N[19].
  • (RS)-mianserin's ATC code is recorded as N06AX03[20].
  • (RS)-mianserin's chemical formula is recorded as C₁₈H₂₀N₂[21].
  • (RS)-mianserin's subclass of is recorded as chemical compound[22].
  • (RS)-mianserin's has use is recorded as medication[23].
  • (RS)-mianserin's Commons category is recorded as Mianserin[24].
  • (RS)-mianserin's MeSH descriptor ID is recorded as D008803[25].
  • (RS)-mianserin's ChEMBL ID is recorded as CHEMBL6437[26].
  • (RS)-mianserin's Guide to Pharmacology Ligand ID is recorded as 135[27].

Why It Matters

(RS)-mianserin ranks in the top 9% of group_of_stereoisomers entities by monthly Wikipedia readership (220 views/month).[2] (RS)-mianserin has Wikipedia articles in 18 language editions, a strong signal of global cultural recognition.[28] (RS)-mianserin is known by 8 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] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  6. [8] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  7. [9] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  8. [10] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  9. [11] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  10. [12] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  11. [13] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  12. [14] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  13. [15] . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  14. [16] . Global Substance Registration System. Retrieved . wikidata.org.
  15. [17] . PubChem. Retrieved . wikidata.org.
  16. [18] . PubChem. Retrieved . wikidata.org.
  17. [19] . PubChem. Retrieved . wikidata.org.
  18. [20] . DrugBank. wikidata.org.
  19. [21] . PubChem. Retrieved . wikidata.org.
  20. [22] . wikidata.org.
  21. [23] . wikidata.org.
  22. [24] . wikidata.org.
  23. [25] . wikidata.org.
  24. [26] . ChEMBL. Retrieved . wikidata.org.
  25. [27] . IUPHAR/BPS Guide to PHARMACOLOGY. 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)-mianserin. Retrieved May 3, 2026, from https://4ort.xyz/entity/rs-mianserin
MLA “(RS)-mianserin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/rs-mianserin.
BibTeX @misc{4ortxyz_rs-mianserin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{(RS)-mianserin}}, year = {2026}, url = {https://4ort.xyz/entity/rs-mianserin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): (RS)-mianserin — https://4ort.xyz/entity/rs-mianserin (retrieved 2026-05-03)

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