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afamelanotide

chemical compound
ChemicalSubstance type_of_chemical_entity Q410794
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afamelanotide

Summary

afamelanotide is a type of chemical entity[1]. afamelanotide ranks in the top 5% of type_of_chemical_entity entities by monthly Wikipedia readership (161 views/month).[2]

Key Facts

  • afamelanotide's instance of is recorded as type of chemical entity[3].
  • afamelanotide's physically interacts with is recorded as melanocortin 1 receptor[4].
  • afamelanotide's physically interacts with is recorded as Melanocortin 3 receptor[5].
  • afamelanotide's physically interacts with is recorded as Melanocortin 4 receptor[6].
  • afamelanotide's physically interacts with is recorded as Melanocortin 5 receptor[7].
  • afamelanotide's CAS Registry Number is recorded as 75921-69-6[8].
  • afamelanotide's canonical SMILES is recorded as CCCCC(C(=O)NC(CCC(=O)O)C(=O)NC(CC1=CN=CN1)C(=O)NC(CC2=CC=CC=C2)C(=O)NC(CCCNC(=N)N)C(=O)NC(CC3=CNC4=CC=CC=C43)C(=O)NCC(=O)NC(CCCCN)C(=O)N5CCCC5C(=O)NC(C(C)C)C(=O)N)NC(=O)C(CO)NC(=O)C(CC6=CC=C(C=C6)O)NC(=O)C(CO)NC(=O)C[9].
  • afamelanotide's InChI is recorded as InChI=1S/C78H111N21O19/c1-5-6-19-52(91-75(116)61(41-101)97-72(113)57(34-46-24-26-49(103)27-25-46)94-74(115)60(40-100)88-44(4)102)68(109)92-54(28-29-64(105)106)70(111)96-59(36-48-38-83-42-87-48)73(114)93-56(33-45-16-8-7-9-17-45)71(112)90-53(22-14-31-84-78(81)82)69(110)95-58(35-47-37-85-51-20-11-10-18-50(47)51)67(108)86-39-63(104)89-55(21-12-13-30-79)77(118)99-32-15-23-62(99)76(117)98-65(43(2)3)66(80)107/h7-11,16-18,20,24-27,37-38,42-43,52-62,65,85,100-101,103H,5-6,12-15,19,21-23,28-36,39-41,79H2,1-4H3,(H2,80,107)(H,83,87)(H,86,108)(H,88,102)(H,89,104)(H,90,112)(H,91,116)(H,92,109)(H,93,114)(H,94,115)(H,95,110)(H,96,111)(H,97,113)(H,98,117)(H,105,106)(H4,81,82,84)/t52-,53-,54-,55-,56+,57-,58-,59-,60-,61-,62-,65-/m0/s1[10].
  • afamelanotide's InChIKey is recorded as UAHFGYDRQSXQEB-LEBBXHLNSA-N[11].
  • afamelanotide's ATC code is recorded as D02BB02[12].
  • afamelanotide's chemical formula is recorded as C₇₈H₁₁₁N₂₁O₁₉[13].
  • afamelanotide's subclass of is recorded as tryptamine alkaloid[14].
  • afamelanotide's MeSH descriptor ID is recorded as C534526[15].
  • afamelanotide's ChEMBL ID is recorded as CHEMBL441738[16].
  • afamelanotide's Guide to Pharmacology Ligand ID is recorded as 1324[17].
  • afamelanotide's Freebase ID is recorded as /m/05h5nc0[18].
  • afamelanotide's UNII is recorded as QW68W3J66U[19].
  • afamelanotide's ChemSpider ID is recorded as 17310725[20].
  • afamelanotide's PubChem CID is recorded as 16197727[21].
  • afamelanotide's PubChem CID is recorded as 44285019[22].
  • afamelanotide's PubChem CID is recorded as 57514683[23].
  • afamelanotide's PubChem CID is recorded as 16154396[24].
  • afamelanotide's PubChem CID is recorded as 91898441[25].
  • afamelanotide's ChEBI ID is recorded as 136034[26].
  • afamelanotide's DrugBank ID is recorded as DB04931[27].

Why It Matters

afamelanotide ranks in the top 5% of type_of_chemical_entity entities by monthly Wikipedia readership (161 views/month).[2] afamelanotide has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[28] afamelanotide is known by 9 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] ↑ . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . 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] ↑ . DrugBank. Retrieved . wikidata.org.
  7. [9] ↑ . PubChem. Retrieved . wikidata.org.
  8. [10] ↑ . wikidata.org.
  9. [11] ↑ . PubChem. Retrieved . wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . PubChem. Retrieved . 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] ↑ . wikidata.org.
  17. [19] ↑ . DrugBank. Retrieved . wikidata.org.
  18. [20] ↑ . Q2311683. Retrieved . 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] ↑ . ChEBI release 2019-10-02. wikidata.org.
  25. [27] ↑ . 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). afamelanotide. Retrieved May 3, 2026, from https://4ort.xyz/entity/afamelanotide
MLA “afamelanotide.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/afamelanotide.
BibTeX @misc{4ortxyz_afamelanotide_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{afamelanotide}}, year = {2026}, url = {https://4ort.xyz/entity/afamelanotide}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): afamelanotide — https://4ort.xyz/entity/afamelanotide (retrieved 2026-05-03)

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