tectoridin

chemical compound
ChemicalSubstance type_of_chemical_entity Q10860610
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tectoridin

Summary

tectoridin is a type of chemical entity[1]. tectoridin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (3 views/month).[2]

Key Facts

  • tectoridin's instance of is recorded as type of chemical entity[3].
  • tectoridin's CAS Registry Number is recorded as 611-40-5[4].
  • tectoridin's EC number is recorded as 683-150-5[5].
  • tectoridin's canonical SMILES is recorded as COC1=C(C=C2C(=C1O)C(=O)C(=CO2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O[6].
  • tectoridin's InChI is recorded as InChI=1S/C22H22O11/c1-30-21-13(32-22-20(29)19(28)17(26)14(7-23)33-22)6-12-15(18(21)27)16(25)11(8-31-12)9-2-4-10(24)5-3-9/h2-6,8,14,17,19-20,22-24,26-29H,7H2,1H3/t14-,17-,19+,20-,22-/m1/s1[7].
  • tectoridin's InChIKey is recorded as CNOURESJATUGPN-UDEBZQQRSA-N[8].
  • tectoridin's chemical formula is recorded as C₂₂H₂₂O₁₁[9].
  • tectoridin's subclass of is recorded as isoflavone[10].
  • tectoridin's ChEMBL ID is recorded as CHEMBL520214[11].
  • tectoridin's Freebase ID is recorded as /m/07s7mbd[12].
  • tectoridin's UNII is recorded as 968X515NZH[13].
  • tectoridin's ChemSpider ID is recorded as 4445121[14].
  • tectoridin's PubChem CID is recorded as 5281810[15].
  • tectoridin's KEGG ID is recorded as C10533[16].
  • tectoridin's ChEBI ID is recorded as 9428[17].
  • tectoridin's found in taxon is recorded as Iris x germanica[18].
  • tectoridin's found in taxon is recorded as Iris tectorum[19].
  • tectoridin's found in taxon is recorded as Dalbergia riparia[20].
  • tectoridin's found in taxon is recorded as Iris leptophylla[21].
  • tectoridin's found in taxon is recorded as Maackia amurensis[22].
  • tectoridin's found in taxon is recorded as Sorbus cuspidata[23].
  • tectoridin's found in taxon is recorded as Iris milesii[24].
  • tectoridin's found in taxon is recorded as Polygonatum odoratum[25].
  • tectoridin's found in taxon is recorded as Platycladus[26].
  • tectoridin's found in taxon is recorded as Griffitharia vestita[27].

Why It Matters

tectoridin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (3 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] . ChEBI. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  3. [5] . ECHA Substance Infocard database. Retrieved . 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] . ChEMBL. Retrieved . wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . Global Substance Registration System. Retrieved . wikidata.org.
  12. [14] . Q2311683. Retrieved . wikidata.org.
  13. [15] . PubChem. Retrieved . wikidata.org.
  14. [16] . ChEBI. Retrieved . wikidata.org.
  15. [17] . ChEBI. Retrieved . wikidata.org.
  16. [18] . Potential Value of Plants as Sources of New Antifertility Agents II *. wikidata.org.
  17. [19] . Potential Value of Plants as Sources of New Antifertility Agents II *. wikidata.org.
  18. [20] . Iso- and neo-flavonoids from Dalbergia riparia. wikidata.org.
  19. [21] . STUDIES ON THE CONSTITUENTS OF TWO IRIS SPECIES. wikidata.org.
  20. [22] . Tectoridin from Maackia amurensis modulates both estrogen and thyroid receptors. wikidata.org.
  21. [23] . Simultaneous analysis of isoflavones and saponins in Pueraria flowers using HPLC coupled to an evaporative light scattering detector and isolation of a new isoflavone diglucoside. wikidata.org.
  22. [24] . Phenolic constituents of Iris milesii rhizomes. wikidata.org.
  23. [25] . Homoisoflavonoids from the fibrous roots of Polygonatum odoratum with glucose uptake-stimulatory activity in 3T3-L1 adipocytes. wikidata.org.
  24. [26] . Flavonoid glucosides from licorice. wikidata.org.
  25. [27] . Simultaneous analysis of isoflavones and saponins in Pueraria flowers using HPLC coupled to an evaporative light scattering detector and isolation of a new isoflavone diglucoside. 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). tectoridin. Retrieved May 3, 2026, from https://4ort.xyz/entity/tectoridin
MLA “tectoridin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/tectoridin.
BibTeX @misc{4ortxyz_tectoridin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{tectoridin}}, year = {2026}, url = {https://4ort.xyz/entity/tectoridin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): tectoridin — https://4ort.xyz/entity/tectoridin (retrieved 2026-05-03)

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Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 20d ago · KaleemBot bot · 2026-05-01 view diff on Wikidata ↗
    Subclass of isoflavone
    Found in taxon Iris x germanica, Iris tectorum, Dalbergia riparia +12
    Mass {'unit': 'Q483261', 'amount': '+462.116212'}
    Stereoisomer of 5-hydroxy-3-(4-hydroxyphenyl)-6-methoxy-7-[(2S,3S,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one
    + 4 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ Added [[wikipedia:ur:ٹیکٹوریڈن]]"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.