(RS)-oxybutynin

bladder medication
ChemicalSubstance group_of_stereoisomers Q1060922
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(RS)-oxybutynin

Summary

(RS)-oxybutynin is a group of stereoisomers[1]. (RS)-oxybutynin ranks in the top 5% of group_of_stereoisomers entities by monthly Wikipedia readership (460 views/month).[2]

Key Facts

  • (RS)-oxybutynin's instance of is recorded as group of stereoisomers[3].
  • (RS)-oxybutynin's chemical structure is recorded as Oxybutynin.svg[4].
  • (RS)-oxybutynin's physically interacts with is recorded as Cholinergic receptor muscarinic 1[5].
  • (RS)-oxybutynin's physically interacts with is recorded as Cholinergic receptor muscarinic 2[6].
  • (RS)-oxybutynin's physically interacts with is recorded as Cholinergic receptor muscarinic 3[7].
  • (RS)-oxybutynin's physically interacts with is recorded as Cholinergic receptor muscarinic 4[8].
  • (RS)-oxybutynin's physically interacts with is recorded as Cholinergic receptor muscarinic 5[9].
  • (RS)-oxybutynin's physically interacts with is recorded as Muscarinic acetylcholine receptor M3[10].
  • (RS)-oxybutynin's CAS Registry Number is recorded as 5633-20-5[11].
  • (RS)-oxybutynin's EC number is recorded as 630-332-7[12].
  • (RS)-oxybutynin's canonical SMILES is recorded as CCN(CC)CC#CCOC(=O)C(C1CCCCC1)(C2=CC=CC=C2)O[13].
  • (RS)-oxybutynin's InChI is recorded as InChI=1S/C22H31NO3/c1-3-23(4-2)17-11-12-18-26-21(24)22(25,19-13-7-5-8-14-19)20-15-9-6-10-16-20/h5,7-8,13-14,20,25H,3-4,6,9-10,15-18H2,1-2H3[14].
  • (RS)-oxybutynin's InChIKey is recorded as XIQVNETUBQGFHX-UHFFFAOYSA-N[15].
  • (RS)-oxybutynin's ATC code is recorded as G04BD04[16].
  • (RS)-oxybutynin's chemical formula is recorded as C₂₂H₃₁NO₃[17].
  • (RS)-oxybutynin's subclass of is recorded as chemical compound[18].
  • (RS)-oxybutynin's has use is recorded as medication[19].
  • (RS)-oxybutynin's Commons category is recorded as Oxybutynin[20].
  • (RS)-oxybutynin's MeSH descriptor ID is recorded as C005419[21].
  • (RS)-oxybutynin's ChEMBL ID is recorded as CHEMBL1231[22].
  • (RS)-oxybutynin's Guide to Pharmacology Ligand ID is recorded as 359[23].
  • (RS)-oxybutynin's Freebase ID is recorded as /m/0bgvbn[24].
  • (RS)-oxybutynin's UNII is recorded as K9P6MC7092[25].
  • (RS)-oxybutynin's ChemSpider ID is recorded as 4473[26].
  • (RS)-oxybutynin's PubChem CID is recorded as 4634[27].

Why It Matters

(RS)-oxybutynin ranks in the top 5% of group_of_stereoisomers entities by monthly Wikipedia readership (460 views/month).[2] (RS)-oxybutynin has Wikipedia articles in 19 language editions, a strong signal of global cultural recognition.[28] (RS)-oxybutynin is known by 11 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 . platform.opentargets.org. Provenance: 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] . Open Targets Platform. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  9. [11] . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  10. [12] . ECHA Substance Infocard database. Retrieved . wikidata.org.
  11. [13] . PubChem. Retrieved . wikidata.org.
  12. [14] . PubChem. Retrieved . wikidata.org.
  13. [15] . PubChem. Retrieved . wikidata.org.
  14. [16] . DrugBank. wikidata.org.
  15. [17] . PubChem. Retrieved . wikidata.org.
  16. [18] . wikidata.org.
  17. [19] . wikidata.org.
  18. [20] . wikidata.org.
  19. [21] . Medical Subject Headings. Retrieved . wikidata.org.
  20. [22] . ChEMBL. Retrieved . wikidata.org.
  21. [23] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  22. [24] . Freebase Data Dumps. wikidata.org.
  23. [25] . Global Substance Registration System. Retrieved . wikidata.org.
  24. [26] . Q2311683. Retrieved . wikidata.org.
  25. [27] . PubChem. 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)-oxybutynin. Retrieved May 3, 2026, from https://4ort.xyz/entity/rs-oxybutynin
MLA “(RS)-oxybutynin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/rs-oxybutynin.
BibTeX @misc{4ortxyz_rs-oxybutynin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{(RS)-oxybutynin}}, year = {2026}, url = {https://4ort.xyz/entity/rs-oxybutynin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): (RS)-oxybutynin — https://4ort.xyz/entity/rs-oxybutynin (retrieved 2026-05-03)

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