carbetocin

chemical compound
ChemicalSubstance type_of_chemical_entity Q5037853
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carbetocin

Summary

carbetocin is a type of chemical entity[1]. carbetocin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (42 views/month).[2]

Key Facts

  • carbetocin's instance of is recorded as type of chemical entity[3].
  • carbetocin's CAS Registry Number is recorded as 37025-55-1[4].
  • carbetocin's EC number is recorded as 253-312-6[5].
  • carbetocin's canonical SMILES is recorded as CCC(C)C1C(=O)NC(C(=O)NC(C(=O)NC(CSCCCC(=O)NC(C(=O)N1)CC2=CC=C(C=C2)OC)C(=O)N3CCCC3C(=O)NC(CC(C)C)C(=O)NCC(=O)N)CC(=O)N)CCC(=O)N[6].
  • carbetocin's InChI is recorded as InChI=1S/C45H69N11O12S/c1-6-25(4)38-44(66)51-28(15-16-34(46)57)40(62)52-31(21-35(47)58)41(63)54-32(23-69-18-8-10-37(60)50-30(42(64)55-38)20-26-11-13-27(68-5)14-12-26)45(67)56-17-7-9-33(56)43(65)53-29(19-24(2)3)39(61)49-22-36(48)59/h11-14,24-25,28-33,38H,6-10,15-23H2,1-5H3,(H2,46,57)(H2,47,58)(H2,48,59)(H,49,61)(H,50,60)(H,51,66)(H,52,62)(H,53,65)(H,54,63)(H,55,64)/t25-,28-,29-,30-,31-,32-,33-,38-/m0/s1[7].
  • carbetocin's InChIKey is recorded as NSTRIRCPWQHTIA-DTRKZRJBSA-N[8].
  • carbetocin's ATC code is recorded as H01BB03[9].
  • carbetocin's chemical formula is recorded as C₄₅H₆₉N₁₁O₁₂S[10].
  • carbetocin's subclass of is recorded as synthetic peptide[11].
  • carbetocin's has use is recorded as medication[12].
  • carbetocin's MeSH descriptor ID is recorded as C020731[13].
  • carbetocin's ChEMBL ID is recorded as CHEMBL3301668[14].
  • carbetocin's Guide to Pharmacology Ligand ID is recorded as 11169[15].
  • carbetocin's Freebase ID is recorded as /m/02pzj2z[16].
  • carbetocin's UNII is recorded as 88TWF8015Y[17].
  • carbetocin's ChemSpider ID is recorded as 16736854[18].
  • carbetocin's PubChem CID is recorded as 16681432[19].
  • carbetocin's KEGG ID is recorded as D07229[20].
  • carbetocin's KEGG ID is recorded as C18365[21].
  • carbetocin's ChEBI ID is recorded as 59204[22].
  • carbetocin's DrugBank ID is recorded as DB01282[23].
  • carbetocin's Reaxys registry number is recorded as 9985308[24].
  • carbetocin's isomeric SMILES is recorded as CCC@H[C@H]1C(=O)NC@HCCC(=O)NC@H[C@H]1C(=O)NC@HCCC(=O)N">[25].
  • carbetocin's Human Metabolome Database ID is recorded as HMDB0015402[26].
  • carbetocin's mass is recorded as {'unit': 'Q483261', 'amount': '+987.484788'}[27].

Why It Matters

carbetocin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (42 views/month).[2] carbetocin has Wikipedia articles in 10 language editions, a strong signal of global cultural recognition.[28] carbetocin is known by 10 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] . Global Substance Registration System. Retrieved . wikidata.org.
  3. [5] . Global Substance Registration System. Retrieved . wikidata.org.
  4. [6] . PubChem. Retrieved . wikidata.org.
  5. [7] . PubChem. Retrieved . wikidata.org.
  6. [8] . PubChem. Retrieved . wikidata.org.
  7. [9] . DrugBank. wikidata.org.
  8. [10] . PubChem. Retrieved . wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . DrugBank. wikidata.org.
  11. [13] . Medical Subject Headings. Retrieved . wikidata.org.
  12. [14] . ChEMBL. Retrieved . wikidata.org.
  13. [15] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  14. [16] . wikidata.org.
  15. [17] . Global Substance Registration System. Retrieved . wikidata.org.
  16. [18] . Q2311683. Retrieved . wikidata.org.
  17. [19] . PubChem. Retrieved . wikidata.org.
  18. [20] . ChEBI. Retrieved . wikidata.org.
  19. [21] . ChEBI. Retrieved . wikidata.org.
  20. [22] . ChEMBL. Retrieved . wikidata.org.
  21. [23] . wikidata.org.
  22. [24] . ChEBI. Retrieved . wikidata.org.
  23. [25] . PubChem. Retrieved . wikidata.org.
  24. [26] . 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). carbetocin. Retrieved May 3, 2026, from https://4ort.xyz/entity/carbetocin
MLA “carbetocin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/carbetocin.
BibTeX @misc{4ortxyz_carbetocin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{carbetocin}}, year = {2026}, url = {https://4ort.xyz/entity/carbetocin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): carbetocin — https://4ort.xyz/entity/carbetocin (retrieved 2026-05-03)

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