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(+/-)-8-hydroxy-2-(di-N-propylamino)tetralin

group of stereoisomers
ChemicalSubstance group_of_stereoisomers Q4644282
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(+/-)-8-hydroxy-2-(di-N-propylamino)tetralin

Summary

(+/-)-8-hydroxy-2-(di-N-propylamino)tetralin is a group of stereoisomers[1]. (+/-)-8-hydroxy-2-(di-N-propylamino)tetralin draws 11 Wikipedia views per month (group_of_stereoisomers category, ranking #207 of 1,063).[2]

Key Facts

  • (+/-)-8-hydroxy-2-(di-N-propylamino)tetralin's instance of is recorded as group of stereoisomers[3].
  • (+/-)-8-hydroxy-2-(di-N-propylamino)tetralin's chemical structure is recorded as 8-OH-DPAT.svg[4].
  • (+/-)-8-hydroxy-2-(di-N-propylamino)tetralin's physically interacts with is recorded as 5-hydroxytryptamine receptor 1A[5].
  • (+/-)-8-hydroxy-2-(di-N-propylamino)tetralin's physically interacts with is recorded as 5-hydroxytryptamine receptor 1B[6].
  • (+/-)-8-hydroxy-2-(di-N-propylamino)tetralin's physically interacts with is recorded as 5-hydroxytryptamine receptor 1D[7].
  • (+/-)-8-hydroxy-2-(di-N-propylamino)tetralin's CAS Registry Number is recorded as 78950-78-4[8].
  • (+/-)-8-hydroxy-2-(di-N-propylamino)tetralin's canonical SMILES is recorded as CCCN(CCC)C1CCC2=C(C1)C(=CC=C2)O[9].
  • (+/-)-8-hydroxy-2-(di-N-propylamino)tetralin's InChI is recorded as InChI=1S/C16H25NO/c1-3-10-17(11-4-2)14-9-8-13-6-5-7-16(18)15(13)12-14/h5-7,14,18H,3-4,8-12H2,1-2H3[10].
  • (+/-)-8-hydroxy-2-(di-N-propylamino)tetralin's InChIKey is recorded as ASXGJMSKWNBENU-UHFFFAOYSA-N[11].
  • (+/-)-8-hydroxy-2-(di-N-propylamino)tetralin's chemical formula is recorded as C₁₆H₂₅NO[12].
  • (+/-)-8-hydroxy-2-(di-N-propylamino)tetralin's subclass of is recorded as phenols[13].
  • (+/-)-8-hydroxy-2-(di-N-propylamino)tetralin's subclass of is recorded as tertiary amine[14].
  • (+/-)-8-hydroxy-2-(di-N-propylamino)tetralin's subclass of is recorded as tetraline[15].
  • (+/-)-8-hydroxy-2-(di-N-propylamino)tetralin's Commons category is recorded as 8-OH-DPAT[16].
  • (+/-)-8-hydroxy-2-(di-N-propylamino)tetralin's MeSH descriptor ID is recorded as D017371[17].
  • (+/-)-8-hydroxy-2-(di-N-propylamino)tetralin's has part is recorded as carbon[18].
  • (+/-)-8-hydroxy-2-(di-N-propylamino)tetralin's ChEMBL ID is recorded as CHEMBL56[19].
  • (+/-)-8-hydroxy-2-(di-N-propylamino)tetralin's Guide to Pharmacology Ligand ID is recorded as 7[20].
  • (+/-)-8-hydroxy-2-(di-N-propylamino)tetralin's Freebase ID is recorded as /m/03cywtc[21].
  • (+/-)-8-hydroxy-2-(di-N-propylamino)tetralin's UNII is recorded as IWS1724PX6[22].
  • (+/-)-8-hydroxy-2-(di-N-propylamino)tetralin's ChemSpider ID is recorded as 1183[23].
  • (+/-)-8-hydroxy-2-(di-N-propylamino)tetralin's PubChem CID is recorded as 1220[24].
  • (+/-)-8-hydroxy-2-(di-N-propylamino)tetralin's MeSH tree code is recorded as D02.455.426.559.847.638.960.400[25].
  • (+/-)-8-hydroxy-2-(di-N-propylamino)tetralin's MeSH tree code is recorded as D04.615.638.960.400[26].
  • (+/-)-8-hydroxy-2-(di-N-propylamino)tetralin's ChEBI ID is recorded as 73364[27].

Why It Matters

(+/-)-8-hydroxy-2-(di-N-propylamino)tetralin draws 11 Wikipedia views per month (group_of_stereoisomers category, ranking #207 of 1,063).[2] (+/-)-8-hydroxy-2-(di-N-propylamino)tetralin has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[28] (+/-)-8-hydroxy-2-(di-N-propylamino)tetralin is known by 6 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] ↑ . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  7. [9] ↑ . PubChem. Retrieved . wikidata.org.
  8. [10] ↑ . PubChem. Retrieved . wikidata.org.
  9. [11] ↑ . PubChem. Retrieved . 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] ↑ . Medical Subject Headings. Retrieved . wikidata.org.
  16. [18] ↑ . wikidata.org.
  17. [19] ↑ . ChEMBL. Retrieved . wikidata.org.
  18. [20] ↑ . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  19. [21] ↑ . wikidata.org.
  20. [22] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  21. [23] ↑ . Q2311683. Retrieved . wikidata.org.
  22. [24] ↑ . PubChem. Retrieved . wikidata.org.
  23. [25] ↑ . wikidata.org.
  24. [26] ↑ . wikidata.org.
  25. [27] ↑ . ChEMBL. 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.

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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). (+/-)-8-hydroxy-2-(di-N-propylamino)tetralin. Retrieved May 3, 2026, from https://4ort.xyz/entity/8-hydroxy-2-di-n-propylamino-tetralin
MLA “(+/-)-8-hydroxy-2-(di-N-propylamino)tetralin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/8-hydroxy-2-di-n-propylamino-tetralin.
BibTeX @misc{4ortxyz_8-hydroxy-2-di-n-propylamino-tetralin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{(+/-)-8-hydroxy-2-(di-N-propylamino)tetralin}}, year = {2026}, url = {https://4ort.xyz/entity/8-hydroxy-2-di-n-propylamino-tetralin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): (+/-)-8-hydroxy-2-(di-N-propylamino)tetralin — https://4ort.xyz/entity/8-hydroxy-2-di-n-propylamino-tetralin (retrieved 2026-05-03)

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