5-carboxamidotryptamine

chemical compound
ChemicalSubstance type_of_chemical_entity Q4639580
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5-carboxamidotryptamine

Summary

5-carboxamidotryptamine is a type of chemical entity[1]. 5-carboxamidotryptamine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (22 views/month).[2]

Key Facts

  • 5-carboxamidotryptamine's instance of is recorded as type of chemical entity[3].
  • 5-carboxamidotryptamine's chemical structure is recorded as 5-Carboxamidotryptamine.png[4].
  • 5-carboxamidotryptamine's physically interacts with is recorded as 5-hydroxytryptamine receptor 1A[5].
  • 5-carboxamidotryptamine's physically interacts with is recorded as 5-hydroxytryptamine (serotonin) receptor 1B[6].
  • 5-carboxamidotryptamine's physically interacts with is recorded as 5-hydroxytryptamine receptor 1B[7].
  • 5-carboxamidotryptamine's physically interacts with is recorded as 5-hydroxytryptamine receptor 1D[8].
  • 5-carboxamidotryptamine's physically interacts with is recorded as 5-hydroxytryptamine receptor 1E[9].
  • 5-carboxamidotryptamine's physically interacts with is recorded as 5-hydroxytryptamine receptor 1F[10].
  • 5-carboxamidotryptamine's physically interacts with is recorded as 5-hydroxytryptamine receptor 2A[11].
  • 5-carboxamidotryptamine's physically interacts with is recorded as 5-hydroxytryptamine receptor 2B[12].
  • 5-carboxamidotryptamine's physically interacts with is recorded as 5-hydroxytryptamine receptor 2C[13].
  • 5-carboxamidotryptamine's physically interacts with is recorded as 5-hydroxytryptamine receptor 5A[14].
  • 5-carboxamidotryptamine's physically interacts with is recorded as 5-hydroxytryptamine (serotonin) receptor 5A[15].
  • 5-carboxamidotryptamine's physically interacts with is recorded as 5-hydroxytryptamine receptor 6[16].
  • 5-carboxamidotryptamine's physically interacts with is recorded as 5-hydroxytryptamine receptor 7[17].
  • 5-carboxamidotryptamine's physically interacts with is recorded as 5-hydroxytryptamine (serotonin) receptor 7[18].
  • 5-carboxamidotryptamine's CAS Registry Number is recorded as 74885-09-9[19].
  • 5-carboxamidotryptamine's canonical SMILES is recorded as C1=CC2=C(C=C1C(=O)N)C(=CN2)CCN[20].
  • 5-carboxamidotryptamine's InChI is recorded as InChI=1S/C11H13N3O/c12-4-3-8-6-14-10-2-1-7(11(13)15)5-9(8)10/h1-2,5-6,14H,3-4,12H2,(H2,13,15)[21].
  • 5-carboxamidotryptamine's InChIKey is recorded as WKZLNEWVIAGNAW-UHFFFAOYSA-N[22].
  • 5-carboxamidotryptamine's chemical formula is recorded as C₁₁H₁₃N₃O[23].
  • 5-carboxamidotryptamine's subclass of is recorded as tryptamine alkaloid[24].
  • 5-carboxamidotryptamine's MeSH descriptor ID is recorded as C047087[25].
  • 5-carboxamidotryptamine's ChEMBL ID is recorded as CHEMBL18840[26].
  • 5-carboxamidotryptamine's Guide to Pharmacology Ligand ID is recorded as 4[27].

Why It Matters

5-carboxamidotryptamine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (22 views/month).[2] 5-carboxamidotryptamine has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[28] 5-carboxamidotryptamine is known by 4 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] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  14. [16] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  15. [17] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  16. [18] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  17. [19] . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  18. [20] . PubChem. Retrieved . wikidata.org.
  19. [21] . PubChem. Retrieved . wikidata.org.
  20. [22] . PubChem. Retrieved . wikidata.org.
  21. [23] . PubChem. Retrieved . wikidata.org.
  22. [24] . wikidata.org.
  23. [25] . Medical Subject Headings. Retrieved . 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). 5-carboxamidotryptamine. Retrieved May 3, 2026, from https://4ort.xyz/entity/5-carboxamidotryptamine
MLA “5-carboxamidotryptamine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/5-carboxamidotryptamine.
BibTeX @misc{4ortxyz_5-carboxamidotryptamine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{5-carboxamidotryptamine}}, year = {2026}, url = {https://4ort.xyz/entity/5-carboxamidotryptamine}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): 5-carboxamidotryptamine — https://4ort.xyz/entity/5-carboxamidotryptamine (retrieved 2026-05-03)

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