deguelin

chemical compound
ChemicalSubstance type_of_chemical_entity Q5251862
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deguelin

Summary

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

Key Facts

  • deguelin's instance of is recorded as type of chemical entity[3].
  • deguelin's chemical structure is recorded as Deguelin.png[4].
  • deguelin's CAS Registry Number is recorded as 522-17-8[5].
  • deguelin's canonical SMILES is recorded as CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)C[6].
  • deguelin's InChI is recorded as InChI=1S/C23H22O6/c1-23(2)8-7-12-15(29-23)6-5-13-21(24)20-14-9-17(25-3)18(26-4)10-16(14)27-11-19(20)28-22(12)13/h5-10,19-20H,11H2,1-4H3/t19-,20+/m1/s1[7].
  • deguelin's InChIKey is recorded as ORDAZKGHSNRHTD-UXHICEINSA-N[8].
  • deguelin's chemical formula is recorded as C₂₃H₂₂O₆[9].
  • deguelin's subclass of is recorded as rotenoid[10].
  • deguelin's Commons category is recorded as Deguelin[11].
  • deguelin's ChEMBL ID is recorded as CHEMBL393417[12].
  • deguelin's Freebase ID is recorded as /m/025yttp[13].
  • deguelin's UNII is recorded as K5Z93K66IE[14].
  • deguelin's ChemSpider ID is recorded as 97058[15].
  • deguelin's PubChem CID is recorded as 107935[16].
  • deguelin's KEGG ID is recorded as C10417[17].
  • deguelin's ChEBI ID is recorded as 4357[18].
  • deguelin's found in taxon is recorded as Tephrosia vogelii[19].
  • deguelin's found in taxon is recorded as Amorpha fruticosa[20].
  • deguelin's found in taxon is recorded as Derris malaccensis[21].
  • deguelin's found in taxon is recorded as Derris trifoliata[22].
  • deguelin's found in taxon is recorded as Erycibe expansa[23].
  • deguelin's found in taxon is recorded as Lonchocarpus salvadorensis[24].
  • deguelin's found in taxon is recorded as Millettia pachycarpa[25].
  • deguelin's found in taxon is recorded as Mundulea sericea[26].
  • deguelin's found in taxon is recorded as Piscidia piscipula[27].

Why It Matters

deguelin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (6 views/month).[2]

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] . PubChem. Retrieved . wikidata.org.
  5. [7] . PubChem. Retrieved . wikidata.org.
  6. [8] . PubChem. Retrieved . wikidata.org.
  7. [9] . PubChem. Retrieved . wikidata.org.
  8. [10] . wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . ChEMBL. Retrieved . wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . Global Substance Registration System. Retrieved . wikidata.org.
  13. [15] . Q2311683. Retrieved . wikidata.org.
  14. [16] . PubChem. Retrieved . wikidata.org.
  15. [17] . ChEBI. Retrieved . wikidata.org.
  16. [18] . ChEMBL. Retrieved . wikidata.org.
  17. [19] . Production of rotenoids by heterotrophic and photomixotrophic cell cultures of tephrosia vogelii. wikidata.org.
  18. [20] . Phenolic constituents of Amorpha fruticosa that inhibit NF-kappaB activation and related gene expression.. wikidata.org.
  19. [21] . Derrisin, a new rotenoid from Derris malaccensis plain and anti-Helicobacter pylori activity of its related constituents. wikidata.org.
  20. [22] . 7a-O-methyldeguelol, a modified rotenoid with an open ring-C, from the roots of Derris trifoliata. wikidata.org.
  21. [23] . Structures of new flavonoids, erycibenins D, E, and F, and NO production inhibitors from Erycibe expansa originating in Thailand. wikidata.org.
  22. [24] . Rotenoids of Lonchocarpus salvadorensis: Their effectiveness in protecting seeds against bruchid predation. wikidata.org.
  23. [25] . Chemical constituents of Millettia taiwaniana: structure elucidation of five new isoflavonoids and their cancer chemopreventive activity. wikidata.org.
  24. [26] . Rotenoids and chalcones from Mundulea sericea that inhibit phorbol ester-induced ornithine decarboxylase activity. wikidata.org.
  25. [27] . Two isoflavones from Piscidia erythrina. wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.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). deguelin. Retrieved May 3, 2026, from https://4ort.xyz/entity/deguelin
MLA “deguelin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/deguelin.
BibTeX @misc{4ortxyz_deguelin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{deguelin}}, year = {2026}, url = {https://4ort.xyz/entity/deguelin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): deguelin — https://4ort.xyz/entity/deguelin (retrieved 2026-05-03)

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