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hydroxyprogesterone caproate

chemical compound
ChemicalSubstance type_of_chemical_entity Q3792032
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hydroxyprogesterone caproate

Summary

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

Key Facts

  • hydroxyprogesterone caproate's instance of is recorded as type of chemical entity[3].
  • hydroxyprogesterone caproate's chemical structure is recorded as Hydroxyprogesterone caproate.svg[4].
  • hydroxyprogesterone caproate's CAS Registry Number is recorded as 630-56-8[5].
  • hydroxyprogesterone caproate's EC number is recorded as 211-138-8[6].
  • hydroxyprogesterone caproate's canonical SMILES is recorded as CCCCCC(=O)OC1(CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(=O)C[7].
  • hydroxyprogesterone caproate's InChI is recorded as InChI=1S/C27H40O4/c1-5-6-7-8-24(30)31-27(18(2)28)16-13-23-21-10-9-19-17-20(29)11-14-25(19,3)22(21)12-15-26(23,27)4/h17,21-23H,5-16H2,1-4H3/t21-,22+,23+,25+,26+,27+/m1/s1[8].
  • hydroxyprogesterone caproate's InChIKey is recorded as DOMWKUIIPQCAJU-LJHIYBGHSA-N[9].
  • hydroxyprogesterone caproate's chemical formula is recorded as C₂₇H₄₀O₄[10].
  • hydroxyprogesterone caproate's subclass of is recorded as chemical compound[11].
  • hydroxyprogesterone caproate's has use is recorded as medication[12].
  • hydroxyprogesterone caproate's Commons category is recorded as Hydroxyprogesterone caproate[13].
  • hydroxyprogesterone caproate's MeSH descriptor ID is recorded as D000077713[14].
  • hydroxyprogesterone caproate's ChEMBL ID is recorded as CHEMBL1200848[15].
  • hydroxyprogesterone caproate's Freebase ID is recorded as /m/02q18r0[16].
  • hydroxyprogesterone caproate's UNII is recorded as 276F2O42F5[17].
  • hydroxyprogesterone caproate's ChemSpider ID is recorded as 148552[18].
  • hydroxyprogesterone caproate's PubChem CID is recorded as 169870[19].
  • hydroxyprogesterone caproate's KEGG ID is recorded as C08148[20].
  • hydroxyprogesterone caproate's KEGG ID is recorded as D00949[21].
  • hydroxyprogesterone caproate's MeSH tree code is recorded as D04.210.500.745.745.654.829.395.400.500[22].
  • hydroxyprogesterone caproate's MeSH tree code is recorded as D06.472.334.851.687.750.478.400.250[23].
  • hydroxyprogesterone caproate's ChEBI ID is recorded as 5812[24].
  • hydroxyprogesterone caproate's DrugBank ID is recorded as DB06789[25].
  • hydroxyprogesterone caproate's isomeric SMILES is recorded as CCCCCC(=O)O[C@@]1(CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CCC4=CC(=O)CC[C@]34C)C)C(=O)C[26].
  • hydroxyprogesterone caproate's mass is recorded as {'unit': 'Q483261', 'amount': '+428.29266'}[27].

Why It Matters

hydroxyprogesterone caproate ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (42 views/month).[2] It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[28] It 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] ↑ . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  5. [7] ↑ . PubChem. Retrieved . wikidata.org.
  6. [8] ↑ . PubChem. Retrieved . wikidata.org.
  7. [9] ↑ . PubChem. Retrieved . wikidata.org.
  8. [10] ↑ . PubChem. Retrieved . wikidata.org.
  9. [11] ↑ . wikidata.org.
  10. [12] ↑ . DrugBank. wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . Medical Subject Headings. Retrieved . wikidata.org.
  13. [15] ↑ . ChEMBL. 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] ↑ . wikidata.org.
  21. [23] ↑ . wikidata.org.
  22. [24] ↑ . ChEMBL. Retrieved . wikidata.org.
  23. [25] ↑ . wikidata.org.
  24. [26] ↑ . PubChem. 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). hydroxyprogesterone caproate. Retrieved May 3, 2026, from https://4ort.xyz/entity/hydroxyprogesterone-caproate
MLA “hydroxyprogesterone caproate.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/hydroxyprogesterone-caproate.
BibTeX @misc{4ortxyz_hydroxyprogesterone-caproate_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{hydroxyprogesterone caproate}}, year = {2026}, url = {https://4ort.xyz/entity/hydroxyprogesterone-caproate}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): hydroxyprogesterone caproate — https://4ort.xyz/entity/hydroxyprogesterone-caproate (retrieved 2026-05-03)

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