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tephrosin

chemical compound
ChemicalSubstance type_of_chemical_entity Q7701343
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tephrosin

Summary

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

Key Facts

  • tephrosin's instance of is recorded as type of chemical entity[3].
  • tephrosin's chemical structure is recorded as Tephrosin.png[4].
  • tephrosin's CAS Registry Number is recorded as 76-80-2[5].
  • tephrosin's EC number is recorded as 804-719-8[6].
  • tephrosin's canonical SMILES is recorded as CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)C[7].
  • tephrosin's InChI is recorded as InChI=1S/C23H22O7/c1-22(2)8-7-12-15(30-22)6-5-13-20(12)29-19-11-28-16-10-18(27-4)17(26-3)9-14(16)23(19,25)21(13)24/h5-10,19,25H,11H2,1-4H3/t19-,23-/m1/s1[8].
  • tephrosin's InChIKey is recorded as AQBZCCQCDWNNJQ-AUSIDOKSSA-N[9].
  • tephrosin's chemical formula is recorded as C₂₃H₂₂O₇[10].
  • tephrosin's subclass of is recorded as rotenoid[11].
  • tephrosin's ChEMBL ID is recorded as CHEMBL241806[12].
  • tephrosin's Freebase ID is recorded as /m/03wh1zr[13].
  • tephrosin's UNII is recorded as 9C081V83CC[14].
  • tephrosin's ChemSpider ID is recorded as 102858[15].
  • tephrosin's PubChem CID is recorded as 114909[16].
  • tephrosin's KEGG ID is recorded as C10535[17].
  • tephrosin's ChEBI ID is recorded as 9442[18].
  • tephrosin's found in taxon is recorded as Tephrosia purpurea[19].
  • tephrosin's found in taxon is recorded as Tephrosia vogelii[20].
  • tephrosin's found in taxon is recorded as Derris malaccensis[21].
  • tephrosin's found in taxon is recorded as Derris trifoliata[22].
  • tephrosin's found in taxon is recorded as Erycibe expansa[23].
  • tephrosin's found in taxon is recorded as Millettia pachycarpa[24].
  • tephrosin's found in taxon is recorded as Mundulea sericea[25].
  • tephrosin's found in taxon is recorded as Amorpha fruticosa[26].
  • tephrosin's found in taxon is recorded as Derris elliptica[27].

Why It Matters

tephrosin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (2 views/month).[2] tephrosin has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[28]

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] ↑ . ChEBI. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] ↑ . ECHA Substance Infocard database. 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] ↑ . 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] ↑ . ChEBI. Retrieved . wikidata.org.
  17. [19] ↑ . Flavonoids of Tephrosia polyphylla. wikidata.org.
  18. [20] ↑ . Production of rotenoids by heterotrophic and photomixotrophic cell cultures of tephrosia vogelii. 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] ↑ . Cancer chemopreventive activity of rotenoids from 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] ↑ . Chemical constituents of Millettia taiwaniana: structure elucidation of five new isoflavonoids and their cancer chemopreventive activity. wikidata.org.
  23. [25] ↑ . Rotenoids and chalcones from Mundulea sericea that inhibit phorbol ester-induced ornithine decarboxylase activity. wikidata.org.
  24. [26] ↑ . Antitumor agents, 138. Rotenoids and isoflavones as cytotoxic constitutents from Amorpha fruticosa. wikidata.org.
  25. [27] ↑ . A Further Rotenoid fromDerris elliptica. 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.

📑 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). tephrosin. Retrieved May 3, 2026, from https://4ort.xyz/entity/tephrosin
MLA “tephrosin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/tephrosin.
BibTeX @misc{4ortxyz_tephrosin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{tephrosin}}, year = {2026}, url = {https://4ort.xyz/entity/tephrosin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): tephrosin — https://4ort.xyz/entity/tephrosin (retrieved 2026-05-03)

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